WO2008069961A1 - Medical devices incorporating collagen inhibitors - Google Patents

Abstract

Provided herein are implantable or insertable biomedical devices comprising a substrate and a collagen inhibitor on or in said substrate, and methods of treatment using the same. In some embodiments, the device is a urethral, ureteral, or nephroureteral catheter or stent. In some embodiments, the device is an absorbable esophageal or tracheal stent. Wound closure devices are also provided herein, including a substrate and a collagen inhibitor on or in the substrate. Also provided are surgical packings, including a substrate and a collagen inhibitor on or in the substrate. A barrier material for preventing adhesions in a subject is further provided, including a preformed or in situ formable barrier substrate and a collagen inhibitor on or in the substrate.

Description

MEDICAL DEVICES INCORPORATING COLLAGEN INHIBITORS

Related Applications

This application claims the benefit of United States Provisional Patent Application Serial No. 60/868,217, filed December 1, 2006, the disclosure of which is incorporated by reference herein in its entirety.

Field of the Invention

The present invention concerns medical devices, including implantable devices such as catheters and stents, as well as wound closure devices such as staples and sutures.

Background of the Invention

Scar tissue forms in response to tissue injury after trauma. This response is mediated by multiple inflammatory pathways and involves the development of a complex matrix of collagen, hyaluronic acid, fibronectin, and proteoglycans (Salamone et al. Current Otolaryngology. McGraw Hill, 2006). Though relatively expedient, healing by scar tissue deposition (cicatrization) does not replace functional tissue by multi-germ layer regeneration.

Forty-five million surgeries are performed annually in the United States, and with every surgery there is inevitable formation of scar tissue (DeFrances et al. Advance Data From Vital and Health Statistics. 2006 May; 371 : 14). Fibrous adhesion formation after surgery or other trauma to tubular structures such as the esophagus, tracheobronchial tree, ureter, fallopian tubes and gut can lead to chronic illness and death. Scar tissue that forms in muscle, bone and skin tissue may lead to chronic orthopedic conditions, chronic pain, cosmetic deformity and decreased quality of life.

An example is paranasal sinus surgery. The paranasal sinuses are air spaces in the mammalian facial skeleton. These spaces can become obstructed due to various conditions such as allergy, infection, tumor, and radiation therapy. When conventional medical therapy fails, paranasal sinus surgery is a common procedure used to establish sinus drainage and to relieve the symptoms of sinus obstruction. Nearly 200,000 chronic sinus disease patients undergo sinus surgery that fails in more than 50% of cases due to unfavorable scar formation (Musy et al. American Journal of Otolaryngology. 2004 Nov-Dec;25(6):418-22). Revision surgery has a higher complication rate than initial surgery, is less successful, and is associated with a perceived decrease in quality of life (Jiang et al. Annals of Otology, Rhinology, and Laryngology. 2002 Feb;l 11(2): 155-59).

Attempts to decrease scar tissue formation during wound healing such as with antiinflammatory agents and inhibitors of fibroblast proliferation, are indirect and largely ineffective. These agents are non-specific, and not only inhibit fibroblasts, but also inhibit epithelial cell migration. In paranasal sinus surgery in particular, a cavity is created that must re-epithelialize with functional sinus lining (mucosa) that will promote active mucociliary clearance of sinus debris; therefore agents that inhibit re-epithelialization are counter productive to optimal healing in the paranasal sinus.

There is need for new approaches that will specifically target scar tissue without inhibiting germ layer regenerative tissue processes in order to alleviate scar tissue formation and other problems associated with medical interventions.

Summary of the Invention

Provided herein are implantable or insertable biomedical devices comprising a substrate and a collagen inhibitor on or in said substrate. In some embodiments, the device is a urethral, ureteral, or nephroureteral catheter or stent. In some embodiments, the substrate includes a material selected from the group consisting of vinyl, polyethylene, poly(vinyl chloride) (PVC), ethylene vinyl acetate (EVA), silicone, latex, and polypropylene. In some embodiments, the collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

Methods of treating urethral or ureteral strictures in a subject in need thereof are also provided, including topically administering a collagen inhibitor in an amount effective to treat the urethral strictures. In some embodiments, the administering step is carried out by stenting with a catheter (e.g., a silicone catheter) coated with the collagen inhibitor. In some embodiments, the collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

Wound closure devices are also provided herein, including a substrate and a collagen inhibitor on or in the substrate. In some embodiments, the substrate is selected from the group consisting of biodegradable substrates and non-biodegradable (inert) substrates. In some embodiments, the device is a suture, staple, tape, or bandage. In some embodiments, the substrate includes a biodegradable polymer, e.g., poly(lactide)s, poly(glycolide)s, poly(lactide-coglycolide)s, poly(lactic acid)s, poly(glycolic acid)s, poly(lactic acid-co- glycolic acid)s, poly(caprolactone), polycarbonates, polyesteramides, polyanhydrides, poly(amino acid)s, poly(ortho ester)s, polycyanoacrylates, polyamides, polyacetals, poly(ether ester)s, copolymers of poly(ethylene glycol) and poly(ortho ester)s, poly(dioxanone)s, poly(alkylene alkylate)s, biodegradable polyurethanes, blends and copolymers thereof, etc. In some embodiments, the substrate is a suture formed of braided, woven, or non-woven fiber material, e.g., silk, cotton, rayon, linen, wool, satin, nylon, polyester, polypropylene, polytetrafluoroethylene or combinations thereof. In some embodiments, the collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

Also provided are surgical packings (e.g., sinus packings), including a substrate and a collagen inhibitor on or in the substrate. In some embodiments, the substrate includes a material selected from the group consisting of oxycellulose, methylcellulose, hydroxypropylmethylcellulose, hydroxybutylmethylcellulose, hydroxyethylmethylcellulose, ethylhydroxyethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, carboxymethylcellulose, microcrystalline cellulose, xanthan gum, silicon dioxide, and mixtures thereof. In some embodiments, the substrate is in the form of a dry powder. In some embodiments, the collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

Methods of treating a paranasal sinus wound in a subject in need thereof are provided, including topically administering a collagen inhibitor in an amount effective to treat said wound. In some embodiments, the administering step is carried out by packing the paranasal sinus with a sinus packing material (e.g., a cellulose compound or gel) that includes a collagen inhibitor. In some embodiments, the collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

Methods of treating esophageal or tracheal stricture in a subject in need thereof are also provided, comprising topically administering a collagen inhibitor in an amount effective to treat the stricture in said subject. In some embodiments, the administering step is carried out by stenting the stricture with a biodegradable stent comprising said collage inhibitor. In some embodiments, the collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

A barrier material for preventing adhesions in a subject is further provided, including a preformed or in situ formable barrier substrate and a collagen inhibitor on or in the substrate. In some embodiments, the collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof. Methods of treating abdominal adhesions in a subject in need thereof are provided, including topically administering into the abdominal cavity of tje subject a collagen inhibitor in an amount effective to treat said abdominal adhesions in said subject. In some embodiments, the collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

Further provided are the uses of a substrate that includes a collagen inhibitor in the methods of treatment as described above.

Kits including the implantable or insertable biomedical devices are also provided.

The present invention is explained in greater detail in the specification set forth below.

Brief Description of the Drawings

Figure 1. Schematic diagram of the three phases of wound healing. A: Inflammation, B: Fibroplasia, C: Maturation

Figure 2. Scanning electron microscopy of HF-Br coated 3-0 Vicryl sutures (A) and uncoated 3-0 Vicryl sutures (B) at 20Ox magnification.

Figure 3. Elution of HF-Br in vitro shows rapid drug release detected by UV spectroscopy at 243nm.

Figure 4. Histology results. 4A: Wound Areas. 4B: Fibroblast Counts. Vic: uncoated 3-0 Vicryl suture. VicNBC: uncoated 3-0 Vicryl suture; then 7V-butyl-2- cyanoacrylate glue applied topically. HF Vic: 3-0 Vicryl suture coated with halofuginone bromide. VicNBCHF: uncoated 3-0 Vicryl suture; then mixture of N-butyl-2-cyanoacrylate glue and halofuginone bromide applied topically. HF-Br: Halofuginone Bromide.

Figure 5. Alpha 1 Collagen Gene Expression. Relative quantities of alpha 1 collagen gene expression were normalized with expression levels of 18S (5A) and GAPDH (5B) RNA. These values were then divided by the relative quantity of alpha 1 collagen gene expression in normal skin.

Figure 6. Inflammation grading for weeks 2, 6 and 12.

Figure 7. Wound areas for weeks 2, 6 and 12.

Figure 8. Percent masses of salt soluble collagen in HF-Br treated and control wounds was determined by the Sircol™ Soluble Collagen Assay. Salt soluble collagen is representative of newly formed collagen.

Figure 9. Stiffness (9A), Ultimate Tensile Load (9B) and % Elongation (9C) of samples at 2 and 12 weeks. Figure 10. Sinus Packing in vitro elution study. 80% of drug eluted in 1 hour.

Figure 11. Fibroblast Counts decreased in HF sinus pack wounds.

Figure 12. A: Non-HFBr PLA implant (4X), B: HFBr electrospun implant (4X). Masson trichrome stain (blue is collagen). Note reduced thickness of collagen capsule (marked with arrows).

Figure 13. SEM image of HFBr coating on silicone urethral stent used in rat model.

Figure 14. Masson' s Trichrome Stain of 2-Week Rat Urethra. A: Samples had HF- coated stent. B: Samples had uncoated stent. In slides Al (2.5x) and A2 (1Ox), there is no new collagen deposition (no spongiofibrosis), but only an inflammatory response. In slides Bl (2.5x) and B2 (1Ox), there is obvious new collagen deposition (spongiofibrosis).

Figure 15. Masson's Trichrome Stain of 3-month Rabbit Urethra. A: Sample had HF- coated stent. B: Sample had uncoated stent. In slide A, there is less collagen deposition (less blue stain) with normal urethral architecture. In slide B, there is greater collagen deposition (more blue stain), but note that at 3 months the collagen has become more organized, unlike the amorphous collagen seen at 2 weeks.

Figure 16. Rat Halofuginone Levels in vivo. The concentration of HF was determined in both the penile tissue and blood serum. There is almost a ten-fold difference between HF levels in the serum vs. the penile tissue. Standard error bars are included.

Figure 17. HF Elution.

Detailed Description of the Preferred Embodiments

The disclosures of all United States Patent references cited herein are to be incorporated by reference herein as if fully set forth.

Healing through the deposition of scar (fibrous) tissue is the normal response to injury. In humans, the wound healing response is divided into three phases: inflammation, fibroplasias and maturation. The steps of the process overlap broadly and are best understood as a continuum rather than a series of discrete steps (Figure 1).

Without wishing to be bound to any particular theory, the wound healing process begins with a disturbance of blood vessel integrity that exposes the subendothelial collagen to blood platelets. This event is the initiating step that leads to blood extravasation and triggers the acute inflammatory response. This response activates local and systemic factors that lead to an orderly and predictable migration of cells into the wound. The first cells to appear in the wound are neutrophils, followed by monocytes and fibroblasts. Fibroblasts are the dominant cell type during fibroplasia. This phase is characterized by fibroblast proliferation and migration. The major function of the fibroblast during this stage is to elaborate interstitial matrix and collagen type-1. It is this collagen that makes up the fibrous tissue that characterizes the clinical entity referred to as scar tissue. When the fibroplasia stage is complete, the final stage of maturation occurs during which the wound becomes acellular and undergoes remodeling over months to years. During the remodeling phase the wound gathers tensile strength. Under the influence of various mediators and enzymes, remodeling is thought to represent the interplay between matrix synthesis and degradation.

Provided herein are compositions, devices and methods of treatment to improve wound healing after medical procedures such as surgery, or other trauma. In some embodiments, the present invention provides collagen inhibitors topically administered to the wound or site of injury. "Stenosis" or "stricture" refers to the narrowing of a bodily canal, passageway or tubular structure or organ.

"Subjects" that may be treated by the present invention include both human subjects for medical purposes and animal subjects for veterinary and laboratory purposes. Other suitable animal subjects are, in general, mammalian subjects such as primates, bovines, ovines, caprines, porcines, equines, felines, canines, lagomorphs, rodents (e.g., rats and mice), etc. Human subjects are the most preferred. Human subjects include fetal, neonatal, infant, juvenile, adult and geriatric subjects.

"Treat" as used herein refers to any type of treatment or prevention that imparts a benefit to a subject afflicted with or at risk of developing scarring or complications involving scar tissue production and/or collagen production, including improvement in the condition of the subject (e.g., in one or more symptoms), delay in the progression of the scarring, delay the onset of symptoms or slow the progression of symptoms, etc. As such, the term "treatment" also includes prophylactic treatment of the subject to prevent the onset of symptoms. As used herein, "treatment" and "prevention" are not necessarily meant to imply cure or complete abolition of symptoms, but refer to any type of treatment that imparts a benefit to a patient afflicted with a disease, including improvement in the condition of the patient (e.g., in one or more symptoms), delay in the progression of the disease, etc.

"Treatment effective amount", "amount effective to treat" or the like as used herein means an amount of the collagen inhibitor sufficient to produce a desirable effect upon a patient inflicted with wounds or site of injury. This includes improvement in the condition of the patient (e.g., in one or more symptoms), delay in the progression of the disease, etc.

"Pharmaceutically acceptable" as used herein means that the compound or composition is suitable for administration to a subject to achieve the treatments described herein, without unduly deleterious side effects in light of the severity of the disease and necessity of the treatment.

I. Collagen Inhibitors

"Collagen inhibitors" useful for carrying out the present invention are known and include all agents that inhibit the synthesis of collagen. See, e.g., US Patent No. 6,046,340 and 5,092,841; PCT Publication No. WO/2005/112999. Collagen is the major protein component of the extracellular matrix in organisms. There are at least 12 types of collagens, with types I, II and III being the most common. They are primarily synthesized in the body by fibroblasts during healing, and are formed by processing of the precursor procollagen proteins.

In some embodiments, inhibitors of type- 1 collagen (also known as type I collagen) are preferred. The primary component of scar tissue, collagen type-1 alpha, typically forms a protein rod 300nm long composed of 3 subunits: two αl(I) chains and one α2(I) chain. Within the fibroblast, elaboration of type-1 collagen is controlled by activation of the alpha- 1 collagen gene. Therefore, in some embodiments, inhibitors of the alpha- 1 collagen gene expression are preferred.

Examples of "collagen inhibitors" as used herein include, but are not limited to, mithramycin, mitomycin-c, tranilast, halofuginone, d-penicillamine, beta-aminopropionitrile, okadaic acid, LY294002 (PI-3K inhibitor), 5-fluorouracil, analogs thereof, etc.

Mithramycin (MIT or plicamycin) is an aureolic acid polyketide antibiotic that binds to GC-rich areas of DNA, and is typically used as a chemotherapeutic agent. See, e.g., US Patent No. 5,723,448. Mitomycin-c is a known fibroblast inhibitor with known scar inhibitory effects in the eye, sinus and trachea.

Tranilast (2-(2,3-dimethoxycinnamoyl)aminobenzoic acid) is also known and described in, for example, US Patent Nos. 5,385,935; 6,239,177; and 6,376,543.

"Halofuginone" or halofuginone bromide (7-bromo-6-chloro-3-[3-(3-hydroxy-2- piperidinyl)-2-oxopropyl]-4(3H) is known and described in, for example, US Patent Nos. 5,449,678, 6,420,371; 6,028,078; 6,090,814; and 6,159,488. Halofuginone is a quinazolinone compound that has been used in the cattle and poultry industries as an anti-coccidal agent. Serendipitously, it was discovered that dermal thinning was occurring in chickens that were administered the drug systemically. Further study of this phenomenon led to the discovery that the mechanism of action of halofuginone was inhibition of the alpha- 1 collagen gene promoter (Granot I et al. Poult Sci. 1991 Jul;70(7): 1559-63). The pharmacology of this compound has been extensively studied for veterinary use and has FDA orphan drug approval for use in humans to treat scleroderma.

II. Substrates

Substrates include any biocompatible substrate, and may be biodegradable or nonbiodegradable.

Biodegradable or bioabsorbable substrates may be formed of biodegradable polymers. Any suitable polymer may be employed, including, but not limited to, poly(lactide)s, poly(glycolide)s, poly(lactide-coglycolide)s, poly(lactic acid)s, poly(glycolic acid)s, poly(lactic acid-co-glycolic acid)s, poly(caprolactone), polycarbonates, polyesteramides, polyanhydrides, poly(amino acid)s, poly(ortho ester)s, polycyanoacrylates, polyamides, polyacetals, poly(ether ester)s, copolymers of poly(ethylene glycol) and poly(ortho ester)s, poly(dioxanone)s, poly(alkylene alkylate)s, biodegradable polyurethanes, as well as blends and copolymers thereof. See, e.g., US Patent No. 7,097,857.

According to some embodiments, the present invention provides a wound closure device comprising a substrate and a collagen inhibitor on or in said substrate. The substrate may comprise, consist of or consist essentially of a biodegradable substrate (such as albumin, collagen, synthetic polyamino acids, prolamines, polysaccharides, etc., or biodegradable polymers such as polylactides, polyglycolic acids, poly(lactide-co-glycolides), polycaprolactones, polycarbonates, polyamides, polyanhydrides, polyamino acids, polyortho esters, polyacetals, polycyanoacrylates, and degradable polyurethanes) or a nonbiodegradable (inert) substrates such as silicone and silk, or polyvinyl alcohol, polyethylene, polyurethane, polypropylene, polycaprolactone, polyacrylates, ethylene-vinyl acetates, polystyrenes, polyvinyl oxides, polyvinyl fluorides, poly(vinyl imidazoles), chlorosulphonated polyolefins, polyethylene oxides, polytetrafluoroethylenes, nylons, and copolymers and combinations thereof. The device may take any suitable form, such as a suture, staple, tape, or bandage. In some embodiments the collagen inhibitor is carried in a biodegradable polymer which is coated on an inert or non-biodegradable substrate.

In some embodiments the device is a suture. Sutures may be formed of biodegradable polymers as described above (which may be in the form of a unitary solid), or may be formed from braided, woven, or non-woven fiber material (e.g., silk, cotton, rayon, linen, wool, satin, nylon, polyester or mixtures thereof). See, e.g., US Patent Nos. 5,685,860 and 6,224,630. In some embodiments, sutures include polypropylene (e.g., prolene or marlex) and/or polytetrafluoroethylene (PTFE) (e.g., Gore-Tex).

The present invention also provides surgical packings (e.g., sinus packings) that include a substrate and a collagen inhibitor on or in said substrate. The packing may take any suitable form, including, but not limited to, those described in US Patents Nos. 5,263,927 and 4,291,687.

The substrate material for the packing may be formed of any suitable material, including but not limited to methylcellulose, hydroxypropylmethylcellulose, hydroxybutylmethylcellulose, hydroxyethylmethylcellulose, ethylhydroxyethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, carboxymethylcellulose, microcrystalline cellulose, xanthan gum, silicon dioxide, and mixtures thereof. See, e.g., US Patent No. 7,135,197. Oxycellulose is currently used as a wound packing to achieve hemostatis. In some embodiments the substrate may be provided in the form of a dry, preferably sterile, powder (e.g., with which the collagen inhibitor may be mixed).

In some embodiments, a barrier material is used for preventing adhesions in a subject, comprising in combination, a preformed or in situ formable barrier substrate and a collagen inhibitor on or in said substrate. The substrate may be any suitable material, and when formed in situ any suitable cross-linking agent may be employed. Suitable examples include but are not limited to those described in US Patent No. 6,638,917. The substrate or material may be bioabsorbable (e.g., a hemostatic matieral) or non-bioabsorbable (e.g., a non-absorbable mesh, such as is currently used in hernia repair).

A further aspect of the invention is an implantable or insertable biomedical device comprising a substrate and a collagen inhibitor on or in said substrate. In some embodiments, the device is a urethral, ureteral, or nephroureteral catheter or stent. Various nasal, esophageal and tracheal stents are also known. Cranial, maxillary and mandibular bone plates include bioabsorble substrates (such as poly-L-lactic-polyglycolic plates (PLLA/PGA)) and non- bioabsorbable substrates (such as titanium).

In some embodiments, a non-bioabsorbable stent (i.e., a tube designed to prevent luminal strictures) anywhere in the body. Examples include, but are not limited to, Urethral catheter, Ureteral stent, Nephroureteral catheter, Esophageal stent, Tracheostomy stent, Gastric feeding tube, Nasogastric tube, Laryngeal/tracheal/pulmonary stent, Myringotomy tube, Nasal stent, Salivary duct stent, Biliary stent, Enteric stents, Nasolacrimal stents.

Still other examples are described below. The substrate may be comprised of any suitable biodegradable or non-biodegradable material. In some embodiments the substrate (e.g., from which the catheter is formed) comprises a material such as vinyl, polyethylene, poly(vinyl chloride) (PVC), ethylene vinyl acetate (EVA), silicone, latex, or polypropylene. See, e.g., US Patent No. 7,025,753. The collagen inhibitor may be coated on such a substrate material, with or without a carrier (such as a biodegradable polymer), by any suitable technique as discussed further below.

Specific examples of devices or products that can be used to carry out the present invention by including a collagen inhibitor on or in a substrate from which the product or device is formed include, but are not limited to (for various fields):

UROLOGY:

Coated Urethral Catheter

Coated Ureteral Stent

Coated Nephroureteral Catheter

ENT:

Coated Sinus Packing Material

Injectable sinus packing material

Coated Esophageal Stent

Coated Tracheostomy Tube

Coated Gastric Feeding Tube

Coated Nasogastric Tube

Coated Laryngeal/Tracheal/Pulmonary Stent

Injectable Material for Vocal Fold Augmentation

Coated Myringotomy Tube

Coated Nasal Septal Splint

Coated Nasal Stent

Coated Salivary Duct Stent

Coated Laryngeal Implant

Injectable gel for salivary radiation fibrosis

Coated cranial, maxillary, mandibular absorbable and nonabsorbable bone plates

PLASTIC SURGERY/DERMATOLOGY:

Coated Silicone Implants (or Coated Implants of other Composition)

Injectable Material for Cosmetic Augmentation (Bulking Agent)

Cream/Gel/Spray for Prevention of Hypertrophic Scar

Coated Silicone Sheets for the Prevention of Scarring

Cream/Gel/Spray/Silicone Sheets to Prevent Burn Scarring/Contractures

Coated skin graft material

Coated Suture for Wound Closure

Coated Skin Staples/ Intracorporeal Staples

Coated "Steri-Strips" Wound Closure Adhesives

GENERAL SURGERY:

Coated Sheets or Sprays for the Prevention of Surgical Adhesions Coated Biliary Stents Coated Enteric Stents OPHTHALMOLOGY

Coated Nasolacrimal Stents

VASCULAR SURGERY:

Coated Endovascular Stents

CARDIOLOGY:

Coated Endovascular Cardiac Stents

ORTHOPAEDIC:

Coated absorbable and nonabsorbable bone plates

MISCELLANEOUS:

Coating for other Implanted Artificial Medical Devices (vascular access devices, insulin pumps, etc)

Coated synthetic polymers [e.g., polyglycolic acid (PGA), polylactic acid (PLA), and poly(lactic-co-glycolic acid) (PLGA)], used to make absorbable vascular stent, cardiovascular stents, staples, suture

Devices, materials, and compositions of the invention may be used in the treatment of both human subjects and animal subjects such as dogs, cats, horses, cattle, sheep, monkeys, etc. for veterinary or laboratory purposes.

III. Formulations

In some embodiments, collagen inhibitors of the present invention are provided as a coating on a substrate. Collagen inhibitors may be coated on a substrate by any suitable technique, such as dipping, spraying, spray drying, etc. The collagen inhibitor may be applied per se or concurrently with a carrier material or film-forming material, such as a biodegradable polymer (e.g., as described above). Collagen inhibitors may be combined into materials (such as powders or biodegradable materials) by any suitable technique, such as mixing, co-extruding, etc. In some embodiments, the collagen inhibitor is included in an amount effective to inhibit scar formation and/or collagen formation on or adjacent the implanted or inserted substrate.

According to some embodiments, for suture and/or packing materials the coating process includes one or more of the following steps: (a) prepare materials to desired size and shape for implantation; (b) prepare a solution of a collagen inhibitor (e.g., HFBr at 0.5μg/ml); (c) materials are then dipped and immediately frozen at -80F for approximately 24 hours; (d) Frozen materials are then lyophilized (i.e., vacuum dried); (e) materials are sterilized, e.g., using ethylene oxide or gamma irradiation. According to some embodiments, coating and/or impregnating stent materials (e.g., for esophagus, trachea, vascular, etc.) with a collagen inhibitor includes one or more of the following steps: (a) dry collagen inhibitor (e.g., HFBr) in powder form is mixed (e.g., in a 50:50 ratio) with stent material also in powder form (e.g., PLLA, PGA, Vicryl (polygalactin)); (b) powder material is then electrospun into desired shape (in some embodiments, this process results in a collagen inhibitor impregnated stent that allows freedom to make the desired shape for implantation); (c) stent is sterilized, e.g., using ethylene oxide or gamma irradiation.

According to some embodiments, wound glue including a collagen inhibitor includes one or more of the following steps: (a) the collagen inhibitor (e.g., HFBr at 0.5μg/ml) is mixed 50:50 with a suitable glue material (e.g., acrylate material); and (b) applied directly to the wound.

According to some embodiments, coating of stents (e.g., permanent catheters) with a collagen inhibitor includes one or more of the following steps, (a) Weigh stent; (b) Modify surface of the stent with a plasma reactor, or alternatively microwave water wet stent for about 30-60 seconds; (c) Imerse stent in collagen inhibitor (e.g., halofuginone) and freeze in liquid nitrogen or -80C); (d) Lyophilize stent (e.g., overnight); (e) Weigh stent; (f) Immerse stent in 1% PEG (3500-5000g/mol filtered in 0.2um filter); (g) Freeze PEG in liquid nitrogen or -80C, and lyophilize overnight; (h) Immerse stent in collagen inhibitor (e.g., halofuginone) and freeze and lyophilize overnight; (i) Weigh stent; and Q) Sterilize.

According to some embodiments, coating of stents (e.g., permanent catheters) with a collagen inhibitor includes one or more of the following steps, (a) Weigh stent (b) Modify surface of the stent with a plasma reactor, or alternatively microwave wet stent (e.g., wet with PBS and covered with PBS soaked gauze) for about 30-60 seconds; (c) Dip stent in 2% PLGA-COOH to cool; (d) Dry under hood; (e) Cover with soaked gauze (e.g., with PBS) and microwave for about 30-60 seconds (or use plasma reactor); (f) Coat stent with halofuginone (e.g., immerse) and freeze in liquid nitrogen and lyophilize overnight; (g) Weight stent to estimate drug content; and Qi) Sterilize.

Those of skill in the art will appreciate that all of the above methods can be modified and optimized as desired by routine methods without departing from the spirit of the invention disclosed herein. IV. Dosages and Routes of Administration

In preferred embodiments, collagen inhibitors of the present invention are administered topically (i.e., locally) to the wound or site of injury. In some embodiments, compositions including collagen inhibitors may be administered via a coated suture, via combination with a gel or suitable wound glue, via coatings and/or impregnating collagen inhibitors onto a suitable substrate as described herein.

In some embodiments, topical application of one or more collagen inhibitors in nano (10^"9) or pico (10^"12) molar doses is sufficient to inhibit collagen type-1 production in an open wound. In some embodiments, collagen inhibitors is used topically as a packing material (e.g., in the sinus after paranasal sinus surgery) to prevent post-operative scar tissue formation.

In some embodiments, collagen inhibitors are administered by elution/absorption of the drug in less than 30 minutes. In some embodiments, administration is performed over a longer period of time, e.g., substantial elution over 30 minutes, 1, 2 or 3 hours, and up to 5, 6, 7 or 8 days. In some embodiments, collagen inhibitors are eluted over time to capture as much of the early fibroplasia stage of wound healing as possible (e.g., over 3-7 days).

In some embodiments, HF is administered in a single or total dosage over time of 0.5, 1.0 or 1.5 to 2.0, 2.5, 3.0, 3.5 or 4.0 mg/kg. In some embodiments, the total dosage is 0.5 to 10 mg. In some embodiments, HF is administered in nano (10^"9) or pico (10^~12) molar doses.

Some embodiments of present invention are explained in greater detail in the following non-limiting examples.

EXAMPLES

EXAMPLE 1: Effect of a collagen type-I inhibitor on dermal wound healing.

Halofuginone has been used in experimental animal models as a systemic agent to inhibit scar formation (Pines et al. General Pharmacology. 1998 Apr;30(4):445-50; Pines et al. Biol Blood Marrow Transplant. 2003 Ju;9(7):417-25). However, little is know about its effectiveness as a topical agent for this purpose.

Experimental models for wound healing and scar tissue formation are well described in the rat, and all incorporate dorsal skin incisions (Kapoor et al. The American Journal of Pathology. 2004; 165:299-307). The rat has a relatively thick dermis on the dorsum that approximates the thickness of human dermis.

A total of nine animals underwent surgery: three controls and six treatment animals. On each control animal four full thickness dermal incisions were made on the dorsum. The two anterior incisions were closed with uncoated 3-0 Vicryl and N-butyl-2-cyanoacrylate glue; the posterior incisions were closed with Vicryl alone. In the experimental animals four full thickness wounds were made on the dorsum; the two anterior incisions were closed uncoated Vicryl and a mixture of HF-Br and iV-butyl-2-cyanoacrylate (0.5cc of HF-Br was added to 0.5cc of N-butyl cyanoacrylate glue) was applied topically to the closed wound. The two posterior wounds were closed with HF-Br coated 3-0 Vicryl. Two treatment animals and one control animal were then euthanized at 2, 6, and 12 weeks and soft tissue specimens were taken for analysis.

Suture Coating: 3-0 Vicryl absorbable sutures were weighed and placed in 1 ml serological pipettes. The pipettes were then filled with Ice of Halocur™ Halofuginone Bromide 0.5 mg/ml (Halocur ® (Oral Halofuginone. 0.5 mg/mL) from Intervet International BV of Norway) and frozen at -8O⁰C for 24 hours and lyophilized. Pre and post coating weights were recorded and scanning electron microscopy (SEM) was used to show drug coating (particulate matter) on sutures (Figure 2). Visual inspection of the coated sutures demonstrated a yellow coating, providing further evidence that the yellow Halocur had adhered.

Sutures were sterilized in ethylene oxide for surgical use. Weight recordings taken before and after coating showed an average of 96 μg/cm of drug on coated sutures.

To determine halofuginone elution, an in vitro elution study was performed. The release of halofuginone from coated Vicryl sutures into phosphate buffered saline (PBS) was used to estimate kinetics of drug release in vivo. A 2.5cm segment of HF-Br coated Vicryl was placed in 1.5 mL of PBS and incubated at 37 ⁰C. At 5, 15, 30, and 45 minutes and 1, 2, 4, 8, 24, 48, 72, and 96 hours the segment was transferred into a new 1.5 mL aliquot of PBS, and the amount of halofuginone from the previous aliquot was measured with UV spectrophotometry at 243 nm. Data from UV spectrophotometry indicated a rapid release of HF-Br into PBS in vitro (Figure 3). It was approximated that 90% of the total drug mass was released in 30 minutes and that the drug was nearly eliminated in 2 hours.

Gross Appearance of Wounds: More erythema and induration were visible in control wounds at two weeks than HF-Br treated wounds (data not shown). No significant difference in appearance was visible at later time points. Soft tissue samples were harvested, embedded in paraffin and sectioned (5μm). Sections were stained with Hematoxylin and Eosin (H&E) and Masson's Trichrome. Inflammation scores were recorded according to the method of Storch (Surgical Infections. 2002; 3: 89-98). The area of scar tissue deposition was approximated and calculated with light microscopy and a Zeiss™ digital image capture software system. Results are shown in Figure 4.

To determine alpha 1 collagen gene expression (in suture only animals), 2mm punch biopsies of skin were taken at the border of wounds adjacent to suture material. Samples were flash frozen, pulverized, and RNA was extracted with Trizol reagent. Real time qPCR was employed to measure gene expression using rat l-alpha-2 collagen ampliset. Relative quantities of alpha 1 collagen gene expression were normalized with expression levels of 18S and GAPDH RNA. These values were then divided by the relative quantity of alpha 1 collagen gene expression in normal skin. Results showed that l-alpha-2 collagen gene expression is inhibited in wounds treated topically with HF (Figure 5).

The inflammatory response was visualized with H&E staining (not shown) and inflammation scores were consistently lower in HF-Br treated samples than in controls (Figure 6). Masson's trichrome staining showed that cross sectional areas of collagen deposition (scar) were also consistently smaller in HF-Br treated samples than in controls (not shown).

Wound area approximations of Week 2 showed a 2.7 fold difference in collagen staining between HF-Br treated (322,107 μm²) and control (865,743 μm²) (not shown). Wound areas for weeks 2, 6 and 12 are shown in Figure 7.

To evaluate levels of newly formed collagen, tissue samples were digested in IM NaCl in 0.05M Tris. Salt soluble collagen was then bound with a Sircol™ dye detection system and content was measured with UV spectrophotometry at 243 nm. Percent tissue masses of salt soluble collagen were higher in all week 2 samples. No significant difference in salt soluble collagen levels could be detected between HF-Br treated and control samples over each time point (Figure 8).

Tensile strength of dermal wound tissue specimens is assessed by measuring the breaking point with a tensometer. Tissue specimens are harvested and analyzed immediately after animals are sacrificed. The specimens are attached to the tensometer and pressure is applied until the wound breaks. This breaking pressure is recorded as tensile strength.

Skin samples were harvested so that the plane of the scar would be perpendicular to the direction of force applied. Samples were frozen, re-thawed, and secured by clamps in an tensometer (Instron™ Norwood, MA ). Force was then applied until samples broke. Ultimate tensile load, percent elongation, and stiffness were then calculated for three control and three HF-Br treated samples at 2 and 12 weeks. Averages were reported. Average stiffness, ultimate tensile load, and percent elongation for all tissue samples increased from 2 to 12 weeks (Figure 9). No significant difference was detected between treatment and control samples.

Conclusions: HF-Br coated suture delivers drug topically to dermal wounds, reducing scar tissue formation while maintaining tensile strength relative to control wounds. Type 1 Collagen content was the same in control and experimental wounds. HF can also be applied topically in the form of a cyanoacrylate based wound glue for effective wound closure.

EXAMPLE 2: Paranasal sinus packing.

The ability of halofuginone bromide (HF-Br), an inhibitor of the alpha- 1 collagen gene, to prevent scar tissue formation was examined in a rodent model of paranasal sinus surgery. Systemic administration of this compound has been found to inhibit scar tissue formation in animal and human studies, though none have examined its effects on scar tissue formation in sinonasal surgery. It was the objective of this study to determine if topical application of HF-Br will prevent scarring in an animal model of paranasal sinus surgery.

The potency of halofuginone bromide has led us to hypothesize that topical application in low doses would be more than sufficient to inhibit collagen type-1 production in an open wound and would have virtually no systemic risk of side effects. Based upon this hypothesis, we have compounded a formulation of halofuginone bromide that can be used topically as a packing material in the sinus to prevent post-operative scar tissue formation.

The use of rodent models in the study of paranasal sinus injury and wound healing has been established by previous studies in mice (Bomer et al. Arch Otolaryngol Head Neck Surg. 1998 Nov; 124(11): 1227-32), but none have examined the role of halofuginone bromide in this context. We have developed a rat model of sinus surgery useful in the study of wound healing, in which micro CT evaluation and histological data confirmed removal of ethmoid tissue similar to that seen after sinus surgery in a human while sparing critical structures (data not shown).

Halofuginone is combined with a suitable material that will absorb blood and fluid to help with hemostasis and to act as a drug delivery vehicle. We have chosen a cellulose derivative for this purpose. The packing materials were prepared as follows, step 1 : prepare materials to desired size and shape for implantation. Cellulose sinus packing material (Merocel) was cut into 5mm strips, step 2: prepare a solution of HFBr 0.5μg/ml (Halocur ® (Oral Halofuginone. 0.5 mg/mL), Intervet International BV of Norway), step 3: materials are then dipped and immediately frozen at -80F for 24 hours, step 4: frozen materials are then lyophilized (vacuum dried), step 5: materials are sterilized using ethylene oxide or gamma irradiation. Visual inspection of the coated Merocel demonstrated a yellow coating, providing further evidence that the yellow Halocur had adhered.

Topical application of a halofuginone/cellulose derivative packing was tested for the prevention of scar tissue formation in the paranasal sinuses of a rat. The paired, anatomically identical paranasal sinuses of the rat allow one side to serve as a control and the other to serve as experimental. The control sinus was packed with an uncoated cellulose derivative packing material (Merocel). The other (experimental) sinus cavity was packed with a halofuginone bromide coated cellulose derivative compound packing material. A second set of animals underwent paranasal sinus surgery and no packing material of any kind was placed. Both packing preparations provide adequate homeostasis and require removal, as in the human clinical scenario. The surgical wound was closed using absorbable subcuticular sutures. Sinus surgery was performed in the rat and packs placed for 5 days. Sinus specimens were harvested and analyzed.

Table 1 below represents the weight of drug on the Merocel packs that were placed in the rat sinuses. Dry mass is weight of pack prior to coating with drug. Wet mass represents weight of pack after coating with drug. Drug mass represents total amount of drug applied as a coating to pack. This figure is calculated by subtracting dry mass from wet mass. Mean drug mass is the average of drug masses 1-10, with standard deviation as shown.

Table 1: Mass of HFBr-coated Cellulose Derivative (Merocel) Sinus Pack Pack Dry Mass (g) Wet Mass (q) Druq Mass (q)

1 0.0243 0.0301 0.0058

2 0.0244 0.0309 0.0065

3 0.0276 0.037 0.0094

4 0.0253 0.0326 0.0073

5 0.0245 0.0351 0.0106

6 0.0264 0.0344 0.008

7 0.0246 0.0315 0.0069

8 0.0282 0.0347 0.0065

9 0.0266 0.0344 0.0078

10 0.0274 0.0397 0.0123 Mean Drug Mass (g) 0.00811

Standard Dev 0.00201

Elution studies in vitro showed that 80% of the drug eluted in 1 hour (Figure 10). In vivo elution studies were performed on packs removed 5 days post-operatively, placed in 1OmL PBS for 8 hrs, and 30OuL aliquot placed in spectrophotometer (blanked with a control pack removed post-operatively). No drug could be identified on post-op day 5 packing (not shown), suggesting that total amount of drug was given.

Fibroblast counts revealed decreased fibroblast counts in HF sinus pack wounds (Figure 11). Collagen staining with Masson's trichrome staining showed decreased collagen staining in HF sinus pack wounds when compared to non-HF-coated cellulose pack (not shown).

Conclusions: Topical administration of HF-Br reduced post-operative scar formation in the paranasal sinus.

EXAMPLE 3: Paranasal sinus packing gel.

An alternative to using a coated cellulose pack in the sinus is a sinus packing gel. This formulation was made by combining halofuginone (HF-Br) (Halocur ® (Oral Halofuginone. 0.5 mg/mL), Intervet International BV of Norway) with carboxymethylcellulose (CMC) and storing as a sterile powder. The mixture is reconstituted with sterile water to form a gel and is then instilled in the sinus at the time of surgery for hemostasis and scar control.

Halofuginone in a liquid form is combined with a powder form of cellulose derivative to form an injectable gel. This gel is lyophilized and set aside for reconstitution with distilled water at the time of surgery. The amount of halofuginone present in the drug compound will be carefully controlled by weight and will represent 0.03% of the total compound dry weight.

EXAMPLE 4: Treatment of esophageal stenosis with an absorbable drug eluting esophageal stent.

Esophageal stenosis or stricture refers to narrowing of the esophagus secondary to the deposition of scar tissue in response to disruption of the epithelial lining. Deposition of scar tissue can occur secondary to gastroesophageal reflux disease (GERD), radiation or chemotherapy for cancer, surgery, trauma or inflammatory diseases. Contraction of this scar reduces the esophageal lumen, and can lead to the inability to swallow, inanition, aspiration and death (Ruigomez et al. Am J Gastroenterol. 2006;101 :2685-2692). When a tubular (luminal) structure is traumatized, the protective epithelial lining is disrupted and replaced by scar tissue that forms a circular scar. This circular scar contracts and reduces the luminal cross sectional area, which reduces flow through that structure.

Current treatments for luminal stricture conditions seek to stretch (dilate) and stent the involved segment of strictured organ, to remove the involved segment of the organ, to bypass the involved organ or replace the organ entirely (organ transplant). The tissue trauma associated with these approaches inevitably leads to the formation of more scar tissue and an uninterrupted cycle of tissue trauma followed by scar tissue deposition, contraction and stenosis. Metallic stents have been used with limited success to try to resist contractile forces, but the chief drawback associated with this approach is that the stent causes continued tissue trauma that stimulates more collagen production and ultimately must be removed. For this reason, in some embodiments of the present invention, an absorbable stent is provided.

The gold standard, first line treatment for esophageal stricture disease has been endoscopic dilatation. Failure of such endoscopic procedures is common and necessitates a highly morbid open approach to remove the esophagus and reconstruct with gastric or free tissue transfer. The most common complication of either treatment is recurrence of stricture and need for repeat dilatation and stenting (Pereira-Lima et al. Am J Gastroenterol. 1999;94:1497-1501).

Because of the poor success rate of operative approaches to esophageal stenosis, adjunctive surgical techniques have been employed to oppose the process of wound contraction and to prevent stricture recurrence. These methods include long term stenting with non-absorbable stents following stricture therapy as well as the local injection of various pharmacologic agents (corticosteroids, mitomycin C, colchicine, etc), in an effort to reduce the incidence of recurrence. None of these efforts have been successful and therefore a new treatment paradigm for dealing with this problem must be sought.

An absorbable esophageal stent is placed that administers topical collagen inhibitor after stricture lysis. These stents do not need to be removed, which minimizes risk to the patient. The drug eluting, absorbable esophageal stent will not only improve the treatment of esophageal stricture, but also have translational implications for treating other luminal strictures in anatomic sites such as the urethra, tracheobronchial tree, intestine, and blood vessels. There is evidence that orally administered or locally injected halofuginone can safely treat and prevent luminal stricture disease. Less is known about its effectiveness as a topical agent, but topical application is advantageous as it would deliver drug directly to tissue and it would avoid systemic doses which could interfere with systemic collagen homeostasis and blood coagulation. For example, in a recent Phase I clinical trial, systemic doses of 3.5mg per day were associated with bleeding. Based upon this evidence, we believe that the ideal method of drug delivery would be topical on an absorbable, drug coated stent. Such a stent would administer drug directly to the area of injury with little or no systemic effect and the stent itself would be digested with no harmful effect.

Toward the goal of developing such a stent, investigators in Japan have recently showed promising results in a small human clinical trial in which an absorbable woven non- drug coated polylactic acid (PLA) stent was effective and safe for the treatment of benign esophageal stricture (Tanaka et al. Digestion 2006Oct;74: 199-205).

We hypothesize that an absorbable HFBr coated esophageal stent will moderate scar tissue formation in a rat model of esophageal stricture formation, and we applied topical HF- Br in the form of an absorbable drug eluting esophageal stent in order to prevent cicatrization and luminal stenosis.

Previous animal models have used a caustic burn model (Sodium Hydroxide) to achieve esophageal injury. We were concerned that the pH of the esophagus would be sufficiently altered by sodium hydroxide so as to effectively alter the activity of a topical HFBr application and we therefore will use an electrocautery burn model.

Electrospinning technology was used to make a polylactic acid (PLA)/HFBr impregnated material that we have implanted subcutaneously in a rat. We found that this material was readily absorbed with reduced fibrous (scar) capsule formation (Figure 12). Electrospinning uses an electrical charge to form a mat of fine fibers. The standard setup for electrospinning consists of a spinneret with a metallic needle, a syringe pump, a high-voltage power supply, and a grounded collector. A polymer, sol-gel, composite solution (in our case PLA/HFBr melt solution) is loaded into the syringe and this liquid is driven to the needle tip by a syringe pump, forming a droplet at the tip. When a voltage is applied to the needle, the droplet is first stretched and then an electrified liquid jet is formed. The jet is then elongated and whipped continuously by electrostatic repulsion until it is deposited on the grounded collector. Whipping due to a bending instability in the electrified jet and concomitant evaporation of solvent allow this jet to be stretched to desired diameters.

For the esophageal stent we use this same procedure to spin a tubular structure that will have an outer diameter of 2.5 - 3mm (the approximate diameter of an adult rat esophagus). We record the mass of PLA used and control the amount of drug used (0.5mg maximum based on human data (de Jonge et al. Eur J Cancer. 2006 Aug;42(12):1768-74) and our existing experience with HFBr in rats). Once the stent is fabricated, we study the material using scanning electron microscopy to look for even distribution of PLA and HFBr. We weigh and measure the length of each specimen and then perform drug elution studies in vitro as previously performed on paranasal sinus and suture materials. Briefly, we place the fabricated stent in PBS and measure drug levels using spectrophotometry at defined time points to establish a drug distribution (μg/ml) curve. Initially we measure time points of 5min, 10 min, 20 min, 40 min, 60 min, 2h, 4h, 8hr, 12h 24h 48h 72h and 96h or until greater than 80% of drug has been released. These data allow us to estimate the amount of drug per unit length of stent.

The rat model described above is used to test our hypothesis that topical HFBr will inhibit scar tissue formation in the esophagus. Three groups of animals are used: Group 1 is normal rats, Group 2 is caustic esophageal injury without stent placement and Group 3 is caustic esophageal injury with PLA/HFBr stent placement. All animals undergo pre-operative weight, esophagram and serum blood draws for drug (HFBr) levels.

Animals in Groups 2 and 3 undergo surgery. In Group 3, the prefabricated stent is inserted through a small esophagotomy incision just distal to the burn injury at the time of burn injury and is secured with a single 6.0 monocryl suture to assure that the stent remains at the site of injury. The esophagotomy incision is closed with an interrupted absorbable suture. Wounds are closed in a standard fashion with absorbable suture, and animals are awakened and allowed to recover. In Group 3, 5 animals are euthanized at days 1, 2, 3, 4 and 5 for transcardiac serum blood draw to measure systemic levels of HFBr. In these same animals, the esophagus is opened and gross evaluation for stent integrity will be carried out. At 2, 6, 12 and 24 weeks remaining animals in all groups are weighed, euthanized and esophagram is performed. Esophageal specimens are harvested fixed in formalin, embedded in paraffin, sectioned and stained with hematoxylin and eosin and Masson's trichrome. We quantify the amount of scar tissue deposition using light microscopy and digital technology to measure scar areas. Real time PCR measurements are performed to quantify the activity of the Type- lα collagen activity. Pre and post weights are used as a marker of swallowing functionality and are compared across groups.

EXAMPLE 5: Treatment of abdominal adhesions in a rat model

During surgery on large body cavities such as the abdomen, scar tissue forms and causes vital organs in that cavity to stick together in a process called adhesion formation. These adhesions cause loss of normal organ function and can lead to chronic pain and death. Prevention of adhesion formation would improve outcomes after surgery. Therefore one or more collagen inhibitors are topically applied to internal organs during or post surgery.

Adhesions are created in the abdominal cavity of animals are treated with a collagen inhibitor (e.g., halofuginone bromide) that blocks scar tissue formation. The drug is placed directly in the abdominal cavity by implanting an absorbable material or non-absorbable mesh in order to prevent adhesion formation between vital organs after surgery. The abdominal cavity is surgically opened and adhesions are created by gently rubbing the vital organs with a gauze sponge. Halofuginone bromide-coated absorbable hemostatic material is then applied directly into the abdominal cavity and the wounds are sewn shut.

The rat is used as the animal model. Experimental models for abdominal adhesion formation are well described in the rat and all incorporate ventral midline incisions. One incision is made on the abdomen of each rat and then a visceral abrasion is created to mimic human surgery. Separate control and experimental rats are used. In each experimental animal, a HF-Br coated absorbable material is implanted. In each control animal a non-HF-Br coated absorbable material is implanted. In a third control group no absorbable material is implanted. At 2, 6, 12 and 24 weeks, animals are euthanized, the amount of adhesion formation is quantified by percent area of adhesion formed in the abdominal wall, and the gross appearance of the adhesions is evaluated. Soft tissue specimens are harvested and analyzed for adhesion formation using hematoxylin and eosin staining, Masson's Trichrome staining and collagen content assay. Tensile strength of the abdominal wall is also measured at 12 weeks. On days 1,2,3, and 4, one rat from each experimental group is euthanized for intracardiac blood drawing to access plasma levels of HF-Br.

We have coated oxycellulose with HF-Br (not shown), and this is used as the packing material for the abdominal adhesion.

EXAMPLE 6: Coated ureteral and urethral catheter material

Luminal strictures, such as urethral or ureteral strictures, represent a vexing problem for urologists. Urethral strictures result from spongiofibrosis, most of which is composed of type I collagen, and are due to the imbalance of collagen formation and destruction following urethral injury (Baskin et al. J Urol. 1993. Aug. 150 (2 Pt 2): 642-7). Urethral strictures are commonly treated with dilation and/or incision followed by stenting, but such techniques have suffered from high failure rates. The use of pharmacologic agents to prevent stricture formation (e.g. MMC, steroids, colchicine) have improved treatment results only marginally. Orally administered and locally injected halofuginone has also been shown to prevent collagen deposition and stricture formation in the ureter and urethra in animal models of urologic strictures (Turk et al. J Endourol. 2000 Mar;14(2):145-7; Nagler et al. J Urol. 2000 Nov; 164(5): 1776-80; Jaidane et al. J Urol. 2003 Nov;170(5):2049-52).

However, oral administration or administration by injection is not ideal. Though it has been shown that oral doses of up to 3.5mg/day were administered to patients with solid tumors with minimal ill effects (Jianng et al. Antimicrob Agents Chemother. 2005 Mar;49(3): 1169-76), in some embodiments of the present invention collagen inhibitors such as halofuginone are provided via a coated stent. In the case of urethral stricture disease, this would be the best possible therapy because it could be incorporated into current treatment techniques with little modifications, while providing improved results.

Short urethral strictures are typically treated with a direct visual internal urethrotomy (DVIU), or incision of the stricture, followed by catheter stenting for approximately 4 days, in hopes that the new scar will heal around the stent, leaving a large caliber urethra. Unfortunately, wound healing cannot be well controlled, and the new incision heals via the deposition of type-I collagen, which may contract, causing a high rate of stricture recurrence. A collagen inhibitor coated catheter would be an ideal adjunct to this therapy, as it could be inserted following stricture incision, preventing recurrence by delivering a small amount of collagen inhibitor to the specific area of interest.

Halofuginone bromide (HF) is a substance known to be a potent Collagen Type I inhibiter, and previous studies have demonstrated that oral and local halofuginone administration can prevent luminal strictures, including urethral strictures. However, no previous studies have demonstrated the ability of HF coated stents to prevent urethral stricture formation. The objectives of this study were to successfully coat urethral stents with HF, and then to test whether HF coated stents could prevent spongiofibrosis in a small animal model of urethral stricture disease.

Halocur ® (Oral Halofuginone. 0.5 mg/mL) was obtained from Intervet International BV of Norway. The rat stents were made of silicone tubing (0.30 mm X 0.64 mm) from SMI, while the rabbit stents were 8fr silicone foley catheters (Bard). The stents were coated as follows: 1. Wet stent with PBS and cover with PBS soaked gauze and microwave for 40 sec; 2. Dip stent in 2% PLGA-COOH to cool; 3. Dry under hood; 4. Cover with PBS soaked gauze and microwave (or plasma) for 30 sec; 5. Coat stent with halofuginone (immerse) and freeze in liquid nitrogen and lyophilize overnight; 6. Weight should be measured before and after coating to estimate drug content. The presence of halofuginone on the catheters was documented by measuring changes in stent weight, gross and SEM imaging studies, and elution kinetics.

The simplest method of measuring drug coating, namely determinations of changes in weight, was performed first. Silicone tubing of 3cm in length was weighed before and after coating with Halocur. The average weight change following coating was approximately lmg, demonstrating the coating of a small amount of drug on the tubing. Visual inspection of the coated catheters also demonstrated a yellow coating over the usual white appearance of the silicone, providing further evidence that the yellow Halocur had adhered to the tubing.

Scanning electron microscopy of the silicone tubing was also performed before and after coating with Halocur. The coated tube clearly demonstrates a layer of drug on its surface, while the uncoated tube is completely smooth. This provides further evidence that the Halocur was successfully coated on the silicone tubing.

Drug release studies were then performed to determine the amount of halofuginone released by the coated stents, and the timing of drug release. Stents approximately 3cm in length were coated with halofuginone using our proprietary technique. These stents were then placed in PBS solution at room temperature for 24-hour intervals. After each 24-hour interval, the stents were placed in a new PBS solution, and the previous solution was analyzed for halofuginone concentration using UV spectroscopy (absorption at 243nm). This process was continued daily until the amount of halofuginone in the PBS dropped to immeasurable levels. There was a sustained release of halofuginone from the stents for approximately 4 days, with a large burst release the first 24 hours, and progressively less the following 3 days (Figure 17). These results provided further evidence that the silicone stents had been successfully coated with Halocur, and that this coating provided a sustained release of drug over a several day period.

Animal Surgeries (Rat and Rabbit): Urethral scars were formed in the urethra via electrocautery using an established animal model (Jaidane et al. J. Urol. 2003 Nov. 170(5):2049-52). Uncoated (control) or HF-coated (experimental) stent was inserted into the urethrae and secured with permanent sutures. The rabbits had perineal urethrostomies. The rats were euthanized at 2 weeks and the rabbits at 3 months post-surgery, at which point the penes (containing the urethral stents) and surrounding subcutaneous tissues were excised.

The specimens were fixed in 10% paraformalin and embedded in paraffin blocks. The specimen was then sectioned (5 μm), made into slides, and stained with Masson's trichrome and alpha 1 collagen antibody staining. HF Analysis in Local Tissues and Serum (in Rat): The tissue specimens were morcellated, incubated for 24 hours in 40 mL of PBS, centrifuged, and a sample was taken for HF concentration analysis via spectrophotometry. Blood was also drawn (1 mL) from the heart post-mortem, added to 5 mL of PBS, centrifuged, and the serum analyzed for HF concentration via spectrophotometry.

Results: The silicone stents were successfully coated with halofuginone. Scars were effectively induced in both animal models, utilizing the electrocautery technique, and scar formation was characterized by increased collagen deposition within damaged tissues (see Figure 14 and Figure 15). On gross examination, there was obvious collagen deposition (spongiofibrosis) seen in the penes with the uncoated stents, while there was no new collagen deposition in the spongiosal tissue of the penes with the HF-coated stent. This result was observed in both the rat and rabbit animal model (Figure 14 and Figure 15, respectively). HF was detected in both the surrounding penile tissues and in the bloodstream serum, but the level of HF was significantly higher in the tissues than in the serum (Figure 16).

Conclusions: HF coated stents resulted in no new periurethral collagen deposition in response to injury, thereby causing less scarring of the insulted area. This may correlate to reduced stricture formation. HF is present in both tissues adjacent to the drug-eluting stent and in the blood serum, and significantly higher concentrations are seen in local tissues than in the blood serum.

EXAMPLE 7: Human Testing

Ten male patients with comparable urethral strictures amenable to treatment by DVIU therapy (<2cm length) are recruited and divided into 2 treatment groups. Group A (5 men) are treated with DVIU and then stented for 4 days with a silicone urethral Foley catheter. Group B (5 men) are treated with DVIU and then stented for 4 days with a type-I collagen inhibitor coated silicone catheter.

The type-I collagen inhibitor coated silicone urethral catheter consists of a Bard AIl- Silicone 16 french Foley catheter (already in widespread use in humans), coated with the specific type-I collagen inhibitor halofuginone, approximately 0.375 mg of halofuginone in the form of the solution Halocur. The catheters used will be Bard 16 frenchlOO% silicone Foley catheters, purchased for hospital use through the usual vendors, and therefore packaged sterilely. The catheter will then be removed from its packaging and coated with the drug Halocur (0.5mg/ml halofuginone solution) as described above. The Halocur is obtained from the Intervet Corporation, which produces Halocur in large quantities with excellent quality control for use in the treatment of Crytosporidium parvum in newborn calves. Once the catheter is coated, it is packaged and sterilized under UV or gamma irradiation in preparation for patient use.

Immediately following removal of the catheter (and then every 3 months for a year), the patients undergo uroflowmetry evaluation in the standard fashion. At the end of the year, all patients undergo a retrograde urethrogram to evaluate urethral patency.

Qualitatively, the safety of the type-I collagen inhibitor coated catheter is assessed, as patients are observed for any untoward effects from the use of the stent. Quantitatively, recurrence of the urethral stricture is assessed by measuring uroflow rates as well as urethral caliber on retrograde urethrograms.The uroflowmetry results will be objectively compared by measuring the maximal flow rate (or Qmax), and subjectively compared by analyzing the shape of the flow curve (unimodal with normal monotonic increase, stable period, and monotonic decrease signifying normal flow, versus a multimodal extended pattern signifying obstructed flow). The retrograde urethrography studies will be objectively compared by measuring the urethral width at its most narrow point to evaluate for stricture recurrence in each case.

EXAMPLE 8: Catheter coating.

The following is a list of ureteral and urethral catheter material that we have demonstrated the ability to coat with halofuginone using imaging studies (microscopic and gross), weight changes, and elution data over 4 days:

General device material: Silicone, Silastic, Latex, Polyurethane, Nitinol, PLGA.

Boston Scientific products: Percuflex stents, Flexima stents, Pebax material.

Cook stents: Polyurethane, Sof-flex, AQ stents, Endo-sof stents.

Bard stents: Polyurethane, Latex, Woven stents, Lubricath foley, Inlay stent, Elastomer coated catheters, Silver coated catheters.

The stents were coated as follows: 1. Wet stent with PBS and cover with PBS soaked gauze and microwave for 40 sec; 2. Dip stent in 2% PLGA-COOH to cool; 3. Dry under hood; 4. Cover with PBS soaked gauze and microwave (or plasma) for 30 sec; 5. Coat stent with halofuginone (immerse) and freeze in liquid nitrogen and lyophilize overnight; 6. Weight should be measured before and after coating to estimate drug content.

Stents and other substrates made of the same materials (e.g., esophageal and tracheal products) are coated in the same fashion. The foregoing is illustrative of the present invention, and is not to be construed as limiting thereof. The invention is defined by the following claims, with equivalents of the claims to be included therein.

Claims

THAT WHICH IS CLAIMED IS:

1. An implantable or insertable biomedical device comprising a non-bioabsorbable substrate and a collagen inhibitor on or in said substrate.

2. The device of claim 1, wherein said device is a urethral, ureteral, or nephroureteral catheter or stent.

3. The device of claim 1 or claim 2, wherein said substrate is comprised of a material selected from the group consisting of vinyl, polyethylene, poly(vinyl chloride) (PVC), ethylene vinyl acetate (EVA), silicone, latex, and polypropylene.

4. The device of any of claims 1-3, wherein said collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

5. A method of treating urethral or ureteral strictures in a subject in need thereof comprising topically administering a collagen inhibitor in an amount effective to treat said urethral strictures in said subject.

6. The method of claim 5, wherein said administering step is carried out by stenting with a catheter coated with said collagen inhibitor.

7. The method of claim 6, wherein said catheter comprises silicone.

8. The method of any of claims 5-7, wherein said collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

9. A wound closure device comprising a substrate and a collagen inhibitor on or in said substrate.

10. The device of claim 9, wherein said substrate is selected from the group consisting of biodegradable substrates and non-biodegradable (inert) substrates.

1 1. The device of claim 9 or claim 10, wherein said device is a suture, staple, tape, or bandage.

12. The device of any of claims 9-11, wherein said substrate comprises a biodegradable polymer.

13. The device of any of claims 9-12, wherein said substrate comprises a biodegradable polymer is selected from the group consisting of poly(lactide)s, poly(glycolide)s, poly(lactide-coglycolide)s, poly(lactic acid)s, poly(glycolic acid)s, poly(lactic acid-co-glycolic acid)s, poly(caprolactone), polycarbonates, polyesteramides, polyanhydrides, poly(amino acid)s, poly(ortho ester)s, polycyanoacrylates, polyamides, polyacetals, poly(ether ester)s, copolymers of poly(ethylene glycol) and poly(ortho ester)s, poly(dioxanone)s, poly(alkylene alkylate)s, biodegradable polyurethanes, and blends and copolymers thereof.

14. The device of any of claims 9-13, wherein said substrate is a suture formed of braided, woven, or non-woven fiber material.

15. The device of claim 14, wherein said fiber material is silk, cotton, rayon, linen, wool, satin, nylon, polyester, polypropylene, polytetrafluoroethylene or a combination thereof.

16. The device of any of claims 9-15, wherein said collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

17. A surgical packing comprising a substrate and a collagen inhibitor on or in said substrate.

18. The packing of claim 17, wherein said substrate comprises a material selected from the group consisting of oxycellulose, methylcellulose, hydroxypropylmethylcellulose, hydroxybutylmethylcellulose, hydroxyethylmethylcellulose, ethylhydroxyethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, carboxymethylcellulose, microcrystalline cellulose, xanthan gum, silicon dioxide, and mixtures thereof.

19. The packing of claim 17 or claim 18, wherein said substrate is in the form of a dry powder.

20. The packing of any of claims 17-19, wherein said packing is a sinus packing.

21. The packing of any of claims 17-20, wherein said collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

22. A method of treating a paranasal sinus wound in a subject in need thereof comprising topically administering a collagen inhibitor in an amount effective to treat said wound.

23. The method of claim 22, wherein said administering step is carried out by packing said paranasal sinus with a sinus packing material comprising said collagen inhibitor.

24. The method of claim 23, wherein said sinus packing material comprises a cellulose compound.

25. The method of claim 23 or claim 24, wherein said sinus packing material comprises a sinus packing gel.

26. The method of any of claims 22-25, wherein said collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

27. A method of treating esophageal or tracheal stricture in a subject in need thereof comprising topically administering a collagen inhibitor in an amount effective to treat said stricture in said subject.

28. The method of claim 27, wherein said administering step is carried out by stenting with a biodegradable stent comprising said collage inhibitor.

29. The method of claim 27 or claim 28, wherein said collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

30. A barrier material for preventing adhesions in a subject, comprising a preformed or in situ formable barrier substrate and a collagen inhibitor on or in said substrate.

31. The barrier material of claim 30, wherein said collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

32. A method of treating abdominal adhesions in a subject in need thereof comprising topically administering into the abdominal cavity of said subject a collagen inhibitor in an amount effective to treat said abdominal adhesions in said subject.

33. The method of claim 32, wherein said collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.

34. A kit comprising:

(a) a substrate coated with a collagen inhibitor; and

(b) a container in which said substrate is packaged in sterile form.

35. The kit of claim 34, wherein said container comprises a plastic or foil container.

36. The kit of claim 34, wherein said container is vacuum-packed.

37. The kit of claim 34, wherein said substrate is coated with a single unit dose of said collagen inhibitor.

38. The kit of claim 34, wherein said substrate is biodegradable or non-biodegradable.

39. The kit of claim 34, wherein said collagen inhibitor is selected from the group consisting of: mithramycin, mitomycin-c, tranilast, halofuginone and analogs thereof.