The present invention relates generally to threads of hyaluronic acid, and/or derivatives thereof, methods of making thereof and uses thereof, for example, in aesthetic applications (e.g., dermal fillers), surgery (e.g., sutures), drug delivery, negative pressure wound therapy, moist wound dressing, etc.
Hyaluronic acid is a linear polysaccharide (i.e., non-sulfated glycosaminoglycan) consisting of a repeated disaccharide unit of alternately bonded β-D-N-acetylglucosamine and β-D-glucuronic acid (i.e., (-4GlcUAβ1-3GlcNAcβ1-)n) which is a chief component of the extracellular matrix and is found, for example, in connective, epithelial and neural tissue. Natural hyaluronic acid is highly biocompatible because of its lack of species and organ specificity and thus is often used as a biomaterial in tissue engineering and as a common ingredient in various dermal fillers.
Various chemically modified forms of hyaluronic acid (e.g., cross linked forms, ionically modified forms, esterified forms, etc.) have been synthesized to address a significant problem associated with natural hyaluronic acid which has poor in vivo stability due to rapid enzymatic degradation and hydrolysis. Currently, hyaluronic acid or cross linked versions thereof are used in various gel forms, for example as dermal fillers, adhesion barriers, etc.
However, substantial issues exist with the use of gels of hyaluronic acid or cross linked versions thereof. First, the force required to dispense gels of hyaluronic acid or cross linked versions thereof is non-linear which causes the initial “glob” that many physicians report when injecting hyaluronic acid or cross linked versions thereof. Second, precisely dispensing hyaluronic gels to specific locations is very difficult because such gels have little mechanical strength. Further, the gel will occupy the space of least resistance which makes its use in many applications (e.g., treatment of fine wrinkles) problematic.
Accordingly, what is needed are new physical forms of hyaluronic acid or cross linked versions thereof which can be dispensed uniformly to specific locations regardless of tissue resistance. Such new forms may have particular uses, for example, in aesthetic and surgical applications, drug delivery, wound therapy and wound dressing.
The present invention satisfies these and other needs by providing, in one aspect, a thread of hyaluronic acid or salts, hydrates or solvates thereof and, in a second aspect, a thread of cross linked hyaluronic acid or salts, hydrates or solvates thereof. In some embodiments, the thread is a combination of a thread of hyaluronic acid or salts, hydrates or solvates thereof and a thread of cross linked hyaluronic acid or salts, hydrates or solvates thereof.
In a third aspect, a method of making a thread of hyaluronic acid or salts, hydrates or solvates thereof is provided. Hyaluronic acid or salts, hydrates or solvates thereof are mixed with water or a buffer to form a gel. The gel is extruded to form a thread. The thread is then dried to provide a thread of hyaluronic acid.
In a fourth aspect, a method of making a thread of cross linked hyaluronic acid or salts, hydrates or solvates thereof is provided. Hyaluronic acid or salts, hydrates or solvates thereof are mixed with water or a buffer and a cross linking agent to form a gel. The gel is extruded to form a thread. The thread is then dried to provide a thread of cross linked hyaluronic acid.
In a fifth aspect a method of treating a wrinkle in a subject in need thereof is provided. A thread of hyaluronic acid or salts, hydrates or solvates thereof or a thread of cross linked hyaluronic acid or salts, hydrates or solvates thereof or a combination thereof is attached to the proximal aspect of a needle. The distal end of the needle is inserted through the skin surface of the subject into the dermis adjacent to or within the wrinkle. The dermis of the subject in the base of the wrinkle is traversed with the needle. The needle then exits the skin surface of the subject and is pulled distally until it is removed from the skin of the subject such that the thread is pulled into the location previously occupied by the needle. The excess thread is cut from the needle at the skin surface of the subject.
In still other aspects, methods of using threads of hyaluronic acid or salts, hydrates or solvates thereof or threads of cross linked hyaluronic acid or salts, hydrates or solvates thereof or combinations thereof, for example, as dermal fillers, adhesion barriers, wound dressings including negative pressure wound dressings, sutures, etc. is provided. Further provided are methods of using threads of hyaluronic acid or salts, hydrates or solvates thereof or threads of cross linked hyaluronic acid or salts, hydrates or solvates thereof or combinations thereof, for example, in surgery, ophthalmology, wound closure, drug delivery, etc.
Definitions
“Buffer” includes, but is not limited to, 2-amino-2-methyl-1,3-propanediol, 2-amino-2-methyl-1-propanol, L-(+)-tartaric acid, D-(−)-tartaric acid, ACES, ADA, acetic acid, ammonium acetate, ammonium bicarbonate, ammonium citrate, ammonium formate, ammonium oxalate, ammonium phosphate, ammonium sodium phosphate, ammonium sulfate, ammonium tartrate, BES, BICINE, BIS-TRIS, bicarbonate, boric acid, CAPS, CHES, calcium acetate, calcium carbonate, calcium citrate, citrate, citric acid, diethanolamine, EPP, ethylenediaminetetraacetic acid disodium salt, formic acid solution, Gly-Gly-Gly, Gly-Gly, glycine, HEPES, imidazole, lithium acetate, lithium citrate, MES, MOPS, magnesium acetate, magnesium citrate, magnesium formate, magnesium phosphate, oxalic acid, PIPES, phosphate buffered saline, phosphate buffered saline, piperazine potassium D-tartrate, potassium acetate, potassium bicarbonate, potassium carbonate, potassium chloride, potassium citrate, potassium formate, potassium oxalate, potassium phosphate, potassium phthalate, potassium sodium tartrate, potassium tetraborate, potassium tetraoxalate dehydrate, propionic acid solution, STE buffer solution, sodium 5,5-diethylbarbiturate, sodium acetate, sodium bicarbonate, sodium bitartrate monohydrate, sodium carbonate, sodium citrate, sodium formate, sodium oxalate, sodium phosphate, sodium pyrophosphate, sodium tartrate, sodium tetraborate, TAPS, TES, TNT, TRIS-glycine, TRIS-acetate, TRIS buffered saline, TRIS-HCl, TRIS phosphate-EDTA, tricine, triethanolamine, triethylamine, triethylammonium acetate, triethylammonium phosphate, trimethylammonium acetate, trimethylammonium phosphate, Trizma® acetate, Trizma® base, Trizma® carbonate, Trizma® hydrochloride or Trizma® maleate.
“Salt” refers to a salt of hyaluronic acid, which possesses the desired activity of the parent compound. Such salts include, but are not limited to: (1) acid addition salts, formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid and the like; or formed with organic acids such as acetic acid, propionic acid, hexanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, 3-(4-hydroxybenzoyl)benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 1,2-ethane-disulfonic acid, 2-hydroxyethanesulfonic acid, benzenesulfonic acid, 4-chlorobenzenesulfonic acid, 2-naphthalenesulfonic acid, 4-toluenesulfonic acid, camphorsulfonic acid, 4-methylbicyclo[2.2.2]-oct-2-ene-1-carboxylic acid, glucoheptonic acid, 3-phenylpropionic acid, trimethylacetic acid, t-butylacetic acid, lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxynaphthoic acid, salicylic acid, stearic acid, muconic acid and the like; or (2) salts formed when an acidic proton present in the parent compound is replaced by an ammonium ion, a metal ion, e.g., an alkali metal ion (e.g., sodium or potassium), an alkaline earth ion (e.g., calcium or magnesium), or an aluminum ion; or coordinates with an organic base such as ethanolamine, diethanolamine, triethanolamine, N-methylglucamine, morpholine, piperidine, dimethylamine, diethylamine and the like. Also included are salts of amino acids such as arginates and the like, and salts of organic acids like glucurmic or galacturonic acids and the like.
Threads of Hyaluronic Acid and Derivatives Thereof
The present invention generally provides threads of hyaluronic acid or salts, hydrates or solvates thereof, threads of cross linked hyaluronic acid or salts, hydrates or solvates thereof and combinations thereof. In some embodiments, the hyaluronic acid is isolated from an animal source. In other embodiments, the hyaluronic acid is isolated from bacterial fermentation.
In some embodiments, the lifetime of the threads of hyaluronic acid or salts, hydrates or solvates thereof, in vivo is between about 1 minute and about 1 month. In other embodiments, the lifetime of the thread of hyaluronic acid or salts, hydrates or solvates thereof, in vivo is between about 10 minutes and about 1 week. In still other embodiments, the lifetime of the thread of hyaluronic acid or salts, hydrates or solvates thereof, in vivo is between about 1 hour and about 3 days.
In some embodiments, the lifetime of the thread of cross linked hyaluronic acid or salts, hydrates or solvates thereof, in vivo is between about 1 week and about 24 months. In other embodiments, the lifetime of the thread of cross linked hyaluronic acid or salts, hydrates or solvates thereof, in vivo is between about 1 month and about 12 months. In still other embodiments, the lifetime of the thread of hyaluronic acid or salts, hydrates or solvates thereof, in vivo is between about 3 months and about 9 months.
In some embodiments, hyaluronic acid or salts, hydrates or solvates thereof have been cross linked with butanediol diglycidyl ether (BDDE), divinyl sulfone (DVS) or 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC). Those of skill in the art will appreciate that many other cross linking agents may be used to crosslink hyaluronic acid or salts, hydrates or solvates thereof. Accordingly, the above list of cross linking agents is illustrative rather than comprehensive.
In some of the above embodiments, the degree of cross linking between hyaluronic acid or salts, hydrates or solvates thereof and the cross linking agent is between about 0.01% and about 20%. In other of the above embodiments, the degree of cross linking between hyaluronic acid or salts, hydrates or solvates thereof and the cross linking agent is between about 0.1% and about 10%. In still other of the above embodiments, the degree of cross linking between hyaluronic acid or salts, hydrates or solvates thereof and the cross linking agent is between about 1% and about 8%.
In some of the above embodiments, the thread includes one or more therapeutic or diagnostic agents. In other of the above embodiments, the diagnostic agent is soluble TB (tuberculosis) protein. In still other of the above embodiments, the therapeutic agent is an anesthetic, including but not limited to, lidocaine, xylocaine, novocaine, benzocaine, prilocaine, ropivacaine, propofol or combinations thereof. In still other of the above embodiments, the therapeutic agent is epinephrine, adrenaline, ephedrine, aminophylline, theophylline or combinations thereof. In still other of the above embodiments, the therapeutic agent is botulism toxin. In still other of the above embodiments, the therapeutic agent is laminin-511. In still other of the above embodiments, the therapeutic agent is glucosamine, which can be used, for example, in the treatment of regenerative joint disease. In still other of the above embodiments, the therapeutic agent is an antioxidant, including but not limited to, vitamin E or all-trans retinoic acid such as retinol. In still other of the above embodiments, the therapeutic agent includes stem cells. In still other of the above embodiments, the therapeutic agent is insulin, a growth factor such as, for example, NGF (nerve growth factor), BDNF (brain-derived neurotrophic factor), PDGF (platelet-derived growth factor) or Purmorphamine Deferoxamine NGF (nerve growth factor), dexamethasone, ascorbic acid, 5-azacytidine, 4,6-disubstituted pyrrolopyrimidine, cardiogenols, cDNA, DNA, RNAi, BMP-4 (bone morphogenetic protein-4), BMP-2 (bone morphogenetic protein-2), an antibiotic agent such as, for example, β lactams, quinolones including fluoroquinolones, aminoglycosides or macrolides, an anti-fibrotic agent, including but not limited to, hepatocyte growth factor or Pirfenidone, an anti-scarring agent, such as, for example, anti-TGF-b2 monoclonal antibody (rhAnti-TGF-b2 mAb), a peptide such as, for example, GHK copper binding peptide, a tissue regeneration agent, a steroid, fibronectin, a cytokine, an analgesic such as, for example, Tapentadol HCl, opiates, (e.g., morphine, codone, oxycodone, etc.) an antiseptic, alpha- beta or gamma-interferon, EPO, glucagons, calcitonin, heparin, interleukin-1, interleukin-2, filgrastim, a protein, HGH, luteinizing hormone, atrial natriuretic factor, Factor VIII, Factor IX, or a follicle-stimulating hormone. In still other of the above embodiments, the thread contains a combination of more than one therapeutic agent or diagnostic agent. In some of these embodiments, different threads comprise different therapeutic agents or diagnostic agents.
In some of the above embodiments, the thread has an ultimate tensile strength of between about 0 kpsi and about 250 kpsi. In other of the above embodiments, the thread has an ultimate tensile strength of between about 1 kpsi and about 125 kpsi. In still other of the above embodiments, the thread has an ultimate tensile strength of between about 5 kpsi and about 100 kpsi.
In some of the above embodiments, the thread has an axial tensile strength of between about 0.01 lbs and about 10 lbs. In other of the above embodiments, the thread has an axial tensile strength of between about 0.1 lbs and about 5 lbs. In still other of the above embodiments, the thread has an axial tensile strength of between about 0.5 lbs and about 2 lbs.
In some of the above embodiments, the thread has a cross-section area of between about 1*106 in2 and about 1,000*106 in2. In other of the above embodiments, the thread has a cross-section area of between about 10*106 in2 and about 500*106 in2. In still other of the above embodiments, the thread has a cross-section area of between about 50*106 in2 and about 250*106 in2.
In some of the above embodiments, the thread has a diameter of between about 0.0001 in and about 0.100 in. In other of the above embodiments, the thread has a diameter of between about 0.001 in and about 0.020 in. In still other of the above embodiments, the thread has a diameter of between about 0.003 and about 0.010 in.
In some of the above embodiments, the thread has an elasticity of between about 1% and 200%. In other of the above embodiments, the thread has an elasticity of between about 5% and about 100%. In still other of the above embodiments, the thread has an elasticity of between about 10% and 50%. Herein, elasticity is the % elongation of the thread while retaining ability to return to the initial length of the thread.
In some of the above embodiments, the thread has a molecular weight of between about 0.1 MD and about 8 MD (MD is a million Daltons). In other of the above embodiments, the thread has a molecular weight of between about 0.5 MD to about 4 MD. In still other of the above embodiments, the thread has a molecular weight of between about 1 MD to about 2 MD.
In some of the above embodiments, the thread has a persistent chain length of between about 10 nm and about 250 nm. In other of the above embodiments, the thread has a persistent chain length of between about 10 nm and about 125 nm. In still other of the above embodiments, the thread has a persistent chain length of between about 10 nm and about 75 nm.
In some of the above embodiments, the cross-sectional area of the thread when fully hydrated swells to between about 0% to about 10,000%. In other of the above embodiments, the cross-sectional area of the thread when fully hydrated swells to between about 0% to about 2,500%. In still other of the above embodiments, the cross-sectional area of the thread when fully hydrated swells to between about 0% to about 900%.
In some of the above embodiments, the thread elongates when fully hydrated to between about 0% to about 1,000%. In other of the above embodiments, the thread elongates when fully hydrated to between about 0% to about 100%. In still other of the above embodiments, the thread elongates when fully hydrated to between about 0% to about 30%.
In some of the above embodiments, the thread is fully hydrated after submersion in an aqueous environment in between about 1 second and about 24 hours. In other of the above embodiments, the thread is fully hydrated after submersion in an aqueous environment in between about 1 second and about 1 hour. In still other of the above embodiments, the thread is fully hydrated after submersion in an aqueous environment in between about 1 second to about 5 minutes.
In some embodiments, the thread is cross linked and has an ultimate tensile strength of between about 50 kpsi and about 75 kpsi, a diameter of between 0.005 in and about 0.015 in, the thickness or diameter of the thread when fully hydrated swells between about 50% to about 100% and the lifetime of the thread in vivo is about 6 months.
In some embodiments, braids may be formed from the threads described above. In other embodiments, cords may be formed from the threads described above. In still other embodiments, a woven mesh may be formed from the threads described above. In still other embodiments, a woven mesh may be formed from the braids or cords described above.
In some embodiments, a three-dimensional structure may be constructed by weaving or wrapping or coiling or layering the threads described above. In other embodiments, a three-dimensional structure may be constructed by weaving or wrapping or coiling or layering the braids described above. In still other embodiments, a three-dimensional structure may be constructed by weaving or wrapping or coiling or layering the cords described above. In still other embodiments, a three-dimensional structure may be constructed by weaving or wrapping or coiling or layering the meshes described above.
In some embodiments, a three-dimensional, cylindrical implant is made of any of the threads is provided. An exemplary use for such an implant is for nipple reconstruction. In some embodiments, the threads used to make the cylindrical implant are cross linked and include chondrocyte adhesion compounds. In other embodiments, the cylindrical shape is provided by multiple, concentric coils of threads.
Threads of hyaluronic acid and/or derivatives thereof may contain one or more chiral centers and therefore, may exist as stereoisomers, such as enantiomers or diastereomers. In general, all stereoisomers (i.e., all possible enantiomers and stereoisomers of the illustrated compounds including the stereoisomerically pure form (e.g., enantiomerically pure or diastereomerically pure) and enantiomeric and stereoisomeric mixtures are within the scope of the present invention.
Threads of hyaluronic acid and/or derivatives thereof may exist in several tautomeric forms and mixtures thereof all of which are within the scope of the present invention. Threads of hyaluronic acid and/or derivatives thereof may exist in unsolvated forms as well as solvated forms, including hydrated forms. In general, hydrated and solvated forms are within the scope of the present invention. Accordingly, all physical forms of threads of hyaluronic acid and/or derivatives thereof are equivalent for the uses contemplated by the present invention and are intended to be within the scope of the present invention.
Methods of Making Threads of Hyaluronic Acid and Derivatives Thereof
The present invention also provides methods for making threads of hyaluronic acid and derivatives thereof as described above. In some embodiments, a method of making threads of hyaluronic acid or salts, hydrates or solvates thereof, is provided Hyaluronic acid or salts, hydrates or solvates thereof are mixed with water or a buffer to form a gel. The gel is then extruded to form a thread of gel. The gel can be extruded, for example, by placing the gel in a syringe with a nozzle, pressurizing the syringe, and linearly translating the syringe as gel is extruded from the nozzle. Nozzle characteristics such as taper, length and diameter, the syringe pressure, and the speed of linear translation may be adjusted to make threads of different sizes and mechanical characteristics. Another method of making a thread of gel is by rolling the gel, i.e., like dough, or by placing it into a mold. Still another method of making a thread of gel is to allow the gel to stretch into a thread under the influence of gravity or using centrifugal force. Still another method of making a thread of gel is by shearing the gel in between charged parallel glass plates. Yet another method of making a thread of gel is by confining the gel into a groove patterned on an elastomer and then stretching the elastomer. Yet another method of making a thread of gel is by confining the gel into a permeable tubular structure that allows dehydration of the thread, and if necessary controlling the nature of the dehydration by adjusting environmental parameters such as temperature, pressure and gaseous composition. The thread of hyaluronic acid or salts, hydrates or solvates thereof is then dried after preparation.
In other embodiments, a method of making threads of cross linked hyaluronic acid or salts, hydrates or solvates thereof, is provided. Hyaluronic acid or salts, hydrates or solvates thereof are mixed with water or a buffer and a cross linking agent to form a gel. The gel is then extruded to form a thread as described above or the thread can be made by any of the methods described above. Generally, the gel should be extruded or otherwise manipulated soon after addition of the cross linking agent so that cross linking occurs as the thread dries. The thread of cross linked hyaluronic acid or salts, hydrates or solvates thereof is then dried after preparation.
In some embodiments, the ratio of cross linking agent to hyaluronic acid is between about 0.01% and about 10%. In other embodiments, the ratio of cross linking agent to hyaluronic acid is between about 0.02% and about 5%. In still other embodiments, the ratio of cross linking agent to hyaluronic acid is between about 0.1% and about 3%.
In some of the above embodiments, one or more therapeutic or diagnostic agents are included in the gel forming step.
In some of the above embodiments, the gel has a concentration by weight of hyaluronic acid of between about 0.1% and about 10%. In other of the above embodiments, the gel has a concentration by weight of hyaluronic acid of between about 1% and about 7%. In still other of the above embodiments, the gel has a concentration by weight of hyaluronic acid of between about 4% and about 6%.
In some of the above embodiments, the polymer chains are further oriented along the axis of the thread by being stretched axially. In other of the above embodiments, the polymer chains are oriented along the axis of the thread by gravimetric force or centrifugal force. In still other of the above embodiments, gravimetric force is applied by hanging the thread vertically. In still other of the above embodiments, the polymer chains are oriented along the axis of the thread by application of an electric potential along the length of the thread. In still other of the above embodiments, the polymer chains are oriented along the axis of the thread by a combination of the above methods.
In some of the above embodiments, the threads are hydrated with water and then dried again. In other of the above embodiments, the hydration and drying steps are repeated multiple times. In still other of the above embodiments, the polymer chains are oriented along the axis of the thread by being stretched axially, by application of gravimetric force or centrifugal force, by application of an electric potential along the length of the thread or by combinations thereof. In still other of the above embodiments, a therapeutic agent or a diagnostic agent or a cross linking agent is applied to the thread during the hydration step.
In some of the above embodiments, the gel is extruded over a previously made thread to provide a layered thread.
In another of the above embodiments, after the drying step, the thread is submerged or rinsed with an agent. In some of the above embodiments, the agent is a cross linking agent, therapeutic or diagnostic agent.
In another of the above embodiments, while the thread is hydrated, for example after a rinsing step, the thread is submerged or rinsed with an agent. In some of the above embodiments, the agent is a cross linking agent, therapeutic or diagnostic agent.
In still other of the above embodiments, the thread is frozen and then thawed. In still other of the above embodiments, the thread is frozen and then thawed at least more than once.
In still other of the above embodiments, a dried thread is irradiated to promote cross linking. In some of the above embodiments, a hydrated thread is irradiated to promote cross linking.
In still other of the above embodiments, a dried or hydrated thread is coated to alter the properties of the thread, with a bioabsorbable biopolymer, such as for example, collagen, PEG or PLGA. Alternatively, woven constructs, whether single layer or 3D, can be coated in their entirety to create weaves or meshes with altered physical properties from that of a free-woven mesh.
Methods of Using Threads of Hyaluronic Acid and Derivatives Thereof
The threads, braids, cords, woven meshes or three-dimensional structures described herein can be used, for example, to fill aneurysms, occlude blood flow to tumors, (i.e., tumor occlusion), in eye-lid surgery, in penile augmentation (e.g., for enlargement or for sensitivity reduction, i.e., pre-mature ejaculation treatment), inter-nasal (blood-brain barrier) delivery devices for diagnostic and/or therapeutic agents, corneal implants for drug delivery, nose augmentation or reconstruction, lip augmentation or reconstruction, facial augmentation or reconstruction, ear lobe augmentation or reconstruction, spinal implants (e.g., to support a bulging disc), root canal filler (medicated with therapeutic agent), glottal insufficiency, laser photo-refractive therapy (e.g., hyaluronic acid thread/weave used as a cushion), scaffolding for organ regrowth, spinal cord treatment (BDNF and NGF), in Parkinson's disease (stereotactic delivery), precise delivery of therapeutic or diagnostic molecules, in pulp implantation, replacement pulp root canal treatment, shaped root canal system, negative pressure wound therapy, adhesion barriers and wound dressings.
In some embodiments, the threads, braids, cords, woven meshes or three-dimensional structures described herein are used as dermal fillers in various aesthetic applications. In other embodiments, the threads, braids, cords, woven meshes or three-dimensional structures described herein are used as sutures in various surgical applications. In still other embodiments, the threads, braids, cords, woven meshes or three-dimensional structures described herein are used in ophthalmologic surgery, drug delivery and intra-articular injection.
In some embodiments, the threads, braids, cords, woven meshes or three-dimensional structures described herein are used in wound dressings including negative pressure wound dressings.
In some embodiments, wound dressing remains in contact with the wound for at least 72 hours. In other embodiments, the negative pressure wound dressing remains in contact with the wound for at least 1 week. In still other embodiments, the wound dressing remains in contact with the wound for at least 2 weeks. In still other embodiments, the wound dressing remains in contact with the wound for at least 3 weeks. In still other embodiments, the wound dressing remains in contact with the wound for at least 4 weeks. In the above embodiments, it should be understood that granulation tissue is not retaining the threads, braids, cords, woven meshes or three-dimensional structures described herein as these components are fully absorbable. In some of these embodiments, the wound dressing is between about 1 cm and about 5 cm thick. Accordingly, in some of these embodiments, wound bed closure may be achieved without changing the dressing.
In some embodiments, the woven meshes described herein are used in wound dressings including negative pressure wound dressings. In other embodiments, the dressing include between 2 and about 10 layers of woven meshes.
In still other embodiments, the woven meshes comprise identical threads. In still other embodiments, the woven meshes comprise different threads.
In some embodiments, the woven meshes are between about 1 mm and about 2 mm thick when dry. In other embodiments, the woven meshes are between about 2 mm and about 4 mm thick when dry.
In some embodiments, the pore size of the woven mesh is between about 1 mm and about 10 mm in width. In other embodiments, the pore size of the woven mesh is between about 0.3 mm and about 0.6 mm in width. In still other embodiments, the pores of the woven mesh are aligned. In still other embodiments, the pores of the woven mesh are staggered. In still other embodiments, the woven meshes are collimated to create pores of desired size.
In some embodiments, the woven mesh is mechanically stable at a vacuum up to about 75 mm Hg. In other embodiments, the woven mesh is mechanically stable at a vacuum up to about 150 mm Hg.
In some embodiments, the woven mesh includes collagen. In other embodiments, the dressing is attached to a polyurethane foam. In still other embodiments, the polyurethane foam is open celled. In still other embodiments, the dressing is attached to a thin film. In still other embodiments, the thin film is silicone or polyurethane. In still other embodiments, the dressing is attached to the thin film with a water soluble adhesive.
In some embodiments, the thread used in the dressing includes a therapeutic agent or a diagnostic agent.
In some embodiments, a negative pressure wound dressing (Johnson et al., U.S. Pat. No. 7,070,584, Kemp et al., U.S. Pat. No. 5,256,418, Chatelier et al., U.S. Pat. No. 5,449,383, Bennet et al., U.S. Pat. No. 5,578,662, Yasukawa et al., U.S. Pat. Nos. 5,629,186 and 5,780,281 and Ser. No. 08/951,832) is provided for use in vacuum induced healing of wounds, particularly open surface wounds (Zamierski U.S. Pat. Nos. 4,969,880, 5,100,396, 5,261,893, 5,527,293 and 6,071,267 and Argenta et al., U.S. Pat. Nos. 5,636,643 and 5,645,081). The dressing includes a pad which conforms to the wound location, an air-tight seal which is removably adhered to the pad, a negative pressure source in fluid communication with the pad and the threads, braids, cords, woven meshes or three-dimensional structures described herein attached to the wound contacting surface of the pad. The pad, seal and vacuum source are implemented as described in the prior art.
In other embodiments, the threads, braids, cords, woven meshes or three-dimensional structures described herein are mechanically stable at a vacuum up to about 75 mm Hg. In still other embodiments, the threads, braids, cords, woven meshes or three-dimensional structures described herein are mechanically stable at a vacuum up to about 150 mm Hg. In still other embodiments, the dressing includes at least one layer of woven mesh. In still other embodiments, the dressing include between 2 and about 10 layers of woven mesh. In still other embodiments, the pad is a foam. In still other embodiments, the pad is an open cell polyurethane foam.
In some embodiments a tube connects the pad to the negative pressure source. In still other embodiments, a removable canister is inserted between the pad and the negative pressure source and is in fluid communication with both the pad and the negative pressure source.
In some embodiments, the threads, braids, cords, woven meshes or three-dimensional structures described herein are not hydrated. Accordingly, in these embodiments, the dressing could absorb wound exudates when placed in contact with the wound. In other embodiments, the threads, braids, cords, woven meshes or three-dimensional structures described herein are hydrated. Accordingly, in these embodiments, the dressing could keep the wound moist when placed in contact with the wound.
In some embodiments, an input port attached to a fluid is connected with the pad. Accordingly, in these embodiments, fluid could be dispensed in the wound. In some embodiments, the fluid is saline. In other embodiments, the fluid contains diagnostic or therapeutic agents.
In some embodiments, the threads, braids, cords, woven meshes or three-dimensional structures described herein are used as adhesion barriers. In some embodiments, the woven meshes described herein are used in adhesion barriers.
In some embodiments, a method of treating a wrinkle in a subject is provided. For example, the wrinkle may be in the peri-orbital region as illustrated in
While not wishing to be bound by theory, the method above may successfully treat wrinkles as shown in
In some embodiments, the above method may be used to rejuvenate the skin of a subject in need thereof. In many of these embodiments, the thread includes substantial amounts of non-cross linked hyaluronic acid. In some of these embodiments, the thread includes antioxidants, vitamin E or retinol or combinations thereof.
In some embodiments, a method of treating hair loss in a subject is provided. A subject such as, for example, a male with typical male-pattern baldness is illustrated in
In some embodiments, a method for treating tumors in a subject in need thereof is provided. The thread may be attached to a needle as illustrated, for example, in
In an exemplary embodiment, methods of the current invention may be used to treat pancreatic tumors.
In some embodiments, a method for treating a varicose vein in subject in need thereof is provided. The thread may be attached to a needle as illustrated, for example, in
In some embodiments, a method for nipple reconstruction is provided where a three-dimensional, cylindrical implant comprised of cross linked threads is implanted underneath the skin. The implant may include therapeutic agents, for example chondrocyte adhesion compounds.
In some embodiments, methods for nerve or vessel regrowth are provided. As illustrated in
The present invention is further defined by reference to the following examples. It will be apparent to those skilled in the art that many modifications, both to materials and methods, may be practiced without departing from the scope of the current invention.
A cross linked thread of a diameter between 0.004 in and 0.006 in was made by forming a gel with a concentration of 5% hyaluronic acid and 0.4% BDDE, by weight with the remainder comprised of water. A tapered tip nozzle with an inner diameter of 0.02 in, a syringe pressure of 20 psi and a linear translation speed commensurate with the speed of gel ejection from the syringe was used to extrude the gel into a thread form. However, numerous combinations of extrusion parameters that can make a thread of the desired thickness exist. The thread was dried and then rinsed with water which hydrated the thread, which was then stretched during drying. Over the course of multiple rinsing and drying cycles the overall length of the thread was increased by between about 25% and about 100%. The thread made as described above will fail at a tensile force of about between about 0.25 kg and about 1.50 kg and will swell in diameter by about 25% and about 100% when hydrated. It may persist as a thread in vivo between 1 and 9 months.
Hypodermic needles (22 to 25 Ga) were affixed with single or double strands of hyaluronic acid threads, ranging from thicknesses of 0.004 in to 0.008 in. Both non-crosslinked threads and threads crosslinked using BDDE were used. The needles were able to traverse wrinkles in a cadaveric head of a 50 y/o woman such as the naso-labial fold, peri-orals, peri-orbitals, frontalis (forehead), and glabellar. The needle was able to pull the thread through the skin such that the thread was located where the needle was previously inserted.
Acute and chronic canine studies were performed. Hypodermic needles (22 to 25 Ga) were affixed with single or double strands of hyaluronic acid threads, ranging from thicknesses of 0.004 in to 0.008 in. Both non-crosslinked threads and threads cross linked using BDDE were used. In all cases, the needle was able to pull the attached thread or threads into the dermis. Within minutes most threads produced a visible impact on the skin surface of the animals in the form of a linear bump.
The tensile strength of an autocrosslinked thread of hyaluronic acid was compared to a thread cross linked using the method of Example 1. A thread of non-crosslinked hyaluronic acid was repeatedly frozen and thawed, replicating a method of autocrosslinking hyaluronic acid (Ref. U.S. Pat. No. 6,387,413). All such samples had less tensile force at failure than a thread made using the same extrusion parameters and cross-linked using BDDE as described above.
Finally, it should be noted that there are alternative ways of implementing the present invention. Accordingly, the present embodiments are to be considered as illustrative and not restrictive, and the invention is not to be limited to the details given herein, but may be modified within the scope and equivalents of the appended claims. All references and publications cited herein are incorporated by reference in their entirety.
This application is a continuation of United States National Stage application Ser. No. 13/060,919, filed May 19, 2011 which is a 371 of PCT/US09/55704, filed Sep. 2, 2009, which claims benefit under 35 U.S.C. §119(e) from U.S. Provisional Application Ser. No. 61/190,866, filed Sep. 2, 2008.
Number | Name | Date | Kind |
---|---|---|---|
1558037 | Morton | Oct 1925 | A |
1960117 | Lydeard | May 1934 | A |
2128827 | Killian | Aug 1938 | A |
3548056 | Eigen | Dec 1970 | A |
3611551 | Shave et al. | Oct 1971 | A |
3763009 | Suzuki et al. | Oct 1973 | A |
3949073 | Daniels et al. | Apr 1976 | A |
4060081 | Yannas et al. | Nov 1977 | A |
4140537 | Luck et al. | Feb 1979 | A |
4233360 | Luck et al. | Nov 1980 | A |
4273705 | Kato | Jun 1981 | A |
4279812 | Cioca | Jul 1981 | A |
4424208 | Wallace et al. | Jan 1984 | A |
4500676 | Balazs et al. | Feb 1985 | A |
4501306 | Chu et al. | Feb 1985 | A |
4582640 | Smestad et al. | Apr 1986 | A |
4582865 | Balazs et al. | Apr 1986 | A |
4605691 | Balazs et al. | Aug 1986 | A |
4636524 | Balazs et al. | Jan 1987 | A |
4642117 | Nguyen et al. | Feb 1987 | A |
4713448 | Balazs et al. | Dec 1987 | A |
4716154 | Matson et al. | Dec 1987 | A |
4772419 | Matson et al. | Sep 1988 | A |
4803075 | Wallace et al. | Feb 1989 | A |
4851521 | della Valle et al. | Jul 1989 | A |
4886787 | De Belder et al. | Dec 1989 | A |
4896787 | Delamour et al. | Jan 1990 | A |
4902508 | Badylak et al. | Feb 1990 | A |
4956178 | Badylak et al. | Sep 1990 | A |
4957744 | della Valle et al. | Sep 1990 | A |
4963666 | Malson | Oct 1990 | A |
4965353 | della Valle et al. | Oct 1990 | A |
5009013 | Wiklund | Apr 1991 | A |
5041128 | Korthoff | Aug 1991 | A |
5087446 | Suzuki et al. | Feb 1992 | A |
5091171 | Yu et al. | Feb 1992 | A |
5143724 | Leshchiner et al. | Sep 1992 | A |
5211644 | VanBeek et al. | May 1993 | A |
5246698 | Leshchiner et al. | Sep 1993 | A |
5281422 | Badylak et al. | Jan 1994 | A |
5314874 | Miyata et al. | May 1994 | A |
5328955 | Rhee et al. | Jul 1994 | A |
5336767 | della Valle et al. | Aug 1994 | A |
5352463 | Badylak et al. | Oct 1994 | A |
5356883 | Kuo et al. | Oct 1994 | A |
5372821 | Badylak et al. | Dec 1994 | A |
5399351 | Leshchiner et al. | Mar 1995 | A |
5403345 | Spingler | Apr 1995 | A |
5428024 | Chu et al. | Jun 1995 | A |
5445833 | Badylak et al. | Aug 1995 | A |
5516533 | Badylak et al. | May 1996 | A |
5520916 | Dorigatti et al. | May 1996 | A |
5527856 | Rhee et al. | Jun 1996 | A |
5531716 | Luzio et al. | Jul 1996 | A |
5550187 | Rhee et al. | Aug 1996 | A |
5565519 | Rhee et al. | Oct 1996 | A |
5571503 | Mausner | Nov 1996 | A |
5573784 | Badylak et al. | Nov 1996 | A |
5614587 | Rhee et al. | Mar 1997 | A |
5616568 | Pouyani et al. | Apr 1997 | A |
5616611 | Yamamoto et al. | Apr 1997 | A |
5616689 | Shenoy et al. | Apr 1997 | A |
5622707 | Dorigatti et al. | Apr 1997 | A |
5633001 | Bengt Agerup | May 1997 | A |
5641518 | Badylak et al. | Jun 1997 | A |
5643464 | Rhee et al. | Jul 1997 | A |
5644049 | Giusti et al. | Jul 1997 | A |
5645860 | Knapp, Jr. et al. | Jul 1997 | A |
5668288 | Storey et al. | Sep 1997 | A |
5676964 | Della Valle et al. | Oct 1997 | A |
5695998 | Badylak et al. | Dec 1997 | A |
5711969 | Patel et al. | Jan 1998 | A |
5718012 | Cavallaro | Feb 1998 | A |
5730933 | Peterson | Mar 1998 | A |
5733868 | Peterson et al. | Mar 1998 | A |
5735863 | Della Valle et al. | Apr 1998 | A |
5753267 | Badyiak et al. | May 1998 | A |
5755791 | Whitson et al. | May 1998 | A |
5762966 | Knapp, Jr. et al. | Jun 1998 | A |
5782913 | Schindler et al. | Jul 1998 | A |
5788625 | Plouhar et al. | Aug 1998 | A |
5823671 | Mitchell et al. | Oct 1998 | A |
5824333 | Scopelianos et al. | Oct 1998 | A |
5824335 | Dorigatti et al. | Oct 1998 | A |
5827529 | Ono et al. | Oct 1998 | A |
5827937 | Agerup | Oct 1998 | A |
5843907 | Sakai et al. | Dec 1998 | A |
5866414 | Badylak et al. | Feb 1999 | A |
5879359 | Dorigatti et al. | Mar 1999 | A |
5880107 | Buenter | Mar 1999 | A |
5885619 | Patel et al. | Mar 1999 | A |
5886042 | Yu et al. | Mar 1999 | A |
5922028 | Plouhar et al. | Jul 1999 | A |
5935164 | Iverson | Aug 1999 | A |
5941910 | Schindler et al. | Aug 1999 | A |
5972326 | Galin et al. | Oct 1999 | A |
5980930 | Fenton et al. | Nov 1999 | A |
6013679 | Kuo et al. | Jan 2000 | A |
6056777 | McDowell | May 2000 | A |
6066325 | Wallace et al. | May 2000 | A |
6086578 | Adamyan et al. | Jul 2000 | A |
6139520 | McCrory et al. | Oct 2000 | A |
6140257 | Kershaw et al. | Oct 2000 | A |
6224857 | Romeo et al. | May 2001 | B1 |
6312421 | Boock | Nov 2001 | B1 |
6335035 | Drizen et al. | Jan 2002 | B1 |
6339074 | Cialdi et al. | Jan 2002 | B1 |
6372494 | Naughton et al. | Apr 2002 | B1 |
6383218 | Sourdille et al. | May 2002 | B1 |
6383219 | Telandro et al. | May 2002 | B1 |
6387413 | Miyata et al. | May 2002 | B1 |
6418934 | Chin | Jul 2002 | B1 |
6432710 | Boss, Jr. et al. | Aug 2002 | B1 |
6521223 | Calias et al. | Feb 2003 | B1 |
6544503 | Vanderhoff et al. | Apr 2003 | B1 |
6579978 | Renier et al. | Jun 2003 | B1 |
6602859 | Miyarnoto et al. | Aug 2003 | B2 |
6627620 | Nielsen | Sep 2003 | B1 |
6630486 | Royer | Oct 2003 | B1 |
6632802 | Bellini et al. | Oct 2003 | B2 |
6638538 | Hashimoto et al. | Oct 2003 | B1 |
6685963 | Taupin et al. | Feb 2004 | B1 |
6716251 | Asius et al. | Apr 2004 | B1 |
6734298 | Barbucci et al. | May 2004 | B1 |
6767924 | Yu et al. | Jul 2004 | B2 |
6767928 | Murphy et al. | Jul 2004 | B1 |
6790438 | Constancis et al. | Sep 2004 | B1 |
6833488 | Bucevschi et al. | Dec 2004 | B2 |
6852255 | Yang et al. | Feb 2005 | B2 |
6872819 | Pavesio et al. | Mar 2005 | B1 |
6893466 | Trieu | May 2005 | B2 |
6903199 | Moon et al. | Jun 2005 | B2 |
6921819 | Piron et al. | Jul 2005 | B2 |
6924273 | Pierce | Aug 2005 | B2 |
6939562 | Spiro et al. | Sep 2005 | B2 |
6979440 | Shefer et al. | Dec 2005 | B2 |
7014860 | Kawata et al. | Mar 2006 | B1 |
7087745 | Pallado et al. | Aug 2006 | B1 |
7119062 | Avis et al. | Oct 2006 | B1 |
7125860 | Renier et al. | Oct 2006 | B1 |
7166570 | Hunter et al. | Jan 2007 | B2 |
7192984 | Berg et al. | Mar 2007 | B2 |
7196180 | Aeschlimann et al. | Mar 2007 | B2 |
7214765 | Ringeisen et al. | May 2007 | B2 |
7244270 | Lesh | Jul 2007 | B2 |
7314636 | Caseres et al. | Jan 2008 | B2 |
7323425 | Chu et al. | Jan 2008 | B2 |
7491709 | Carey | Feb 2009 | B2 |
7504386 | Pressato et al. | Mar 2009 | B2 |
7559952 | Pinchuk | Jul 2009 | B2 |
7637900 | Burgess | Dec 2009 | B2 |
7666339 | Chaouk et al. | Feb 2010 | B2 |
7741476 | Lebreton | Jun 2010 | B2 |
7807656 | Reinmuller | Oct 2010 | B2 |
7850965 | Patel et al. | Dec 2010 | B2 |
7902171 | Reinmuller et al. | Mar 2011 | B2 |
7910690 | Ringeisen et al. | Mar 2011 | B2 |
7998202 | Lesh | Aug 2011 | B2 |
3021323 | Arora et al. | Sep 2011 | A1 |
3033665 | Burgess | Oct 2011 | A1 |
8052990 | Hermitte et al. | Nov 2011 | B2 |
8124120 | Sadozai et al. | Feb 2012 | B2 |
8147811 | Dalle Carbonare et al. | Apr 2012 | B1 |
8240314 | Fletcher | Aug 2012 | B2 |
8318695 | Stroumpoulis et al. | Nov 2012 | B2 |
8338375 | Schroeder et al. | Dec 2012 | B2 |
8338388 | Lebreton | Dec 2012 | B2 |
8357795 | Lebreton | Jan 2013 | B2 |
8394782 | Stroumpoulis et al. | Mar 2013 | B2 |
8394783 | Stroumpoulis et al. | Mar 2013 | B2 |
8394784 | Stroumpoulis et al. | Mar 2013 | B2 |
8450475 | Lebreton | May 2013 | B2 |
8455465 | Gavard Molliard | Jun 2013 | B2 |
8513216 | Stroumpoulis et al. | Aug 2013 | B2 |
8524213 | Leshchiner et al. | Sep 2013 | B2 |
8563532 | Lebreton et al. | Oct 2013 | B2 |
8575129 | Bellini et al. | Nov 2013 | B2 |
8586562 | Lebreton | Nov 2013 | B2 |
8901202 | Pastorello et al. | Dec 2014 | B2 |
9228027 | Gurtner | Jan 2016 | B2 |
20010008937 | Callegaro et al. | Jul 2001 | A1 |
20020026039 | Bellini et al. | Feb 2002 | A1 |
20020102311 | Gustavsson et al. | Aug 2002 | A1 |
20020160109 | Yeo et al. | Oct 2002 | A1 |
20030031638 | Joshi et al. | Feb 2003 | A1 |
20030068297 | Jain | Apr 2003 | A1 |
20030093157 | Casares et al. | May 2003 | A1 |
20030119985 | Sehl et al. | Jun 2003 | A1 |
20030148995 | Piron et al. | Aug 2003 | A1 |
20040006319 | Lina et al. | Jan 2004 | A1 |
20040032056 | Vang et al. | Feb 2004 | A1 |
20040101959 | Marko et al. | May 2004 | A1 |
20040127698 | Tsai et al. | Jul 2004 | A1 |
20040127699 | Zhao et al. | Jul 2004 | A1 |
20040192643 | Pressato et al. | Sep 2004 | A1 |
20040199241 | Gravett et al. | Oct 2004 | A1 |
20040265389 | Yul et al. | Dec 2004 | A1 |
20050033362 | Grafton | Feb 2005 | A1 |
20050101582 | Lyons et al. | May 2005 | A1 |
20050136122 | Sadozai et al. | Jun 2005 | A1 |
20050142152 | Leshchiner et al. | Jun 2005 | A1 |
20050181007 | Hunter et al. | Aug 2005 | A1 |
20050186261 | Avelar et al. | Aug 2005 | A1 |
20050186673 | Geistlich et al. | Aug 2005 | A1 |
20050187185 | Reinmuller | Aug 2005 | A1 |
20050226936 | Agerup et al. | Oct 2005 | A1 |
20050271729 | Wang | Dec 2005 | A1 |
20050281880 | Wang | Dec 2005 | A1 |
20050287180 | Chen | Dec 2005 | A1 |
20060040894 | Hunter et al. | Feb 2006 | A1 |
20060041320 | Matsuda | Feb 2006 | A1 |
20060073207 | Masters et al. | Apr 2006 | A1 |
20060095137 | Chung et al. | May 2006 | A1 |
20060105022 | Yokokawa et al. | May 2006 | A1 |
20060122147 | Wohlrab et al. | Jun 2006 | A1 |
20060136070 | Pinchuk | Jun 2006 | A1 |
20060141049 | Lyons et al. | Jun 2006 | A1 |
20060147483 | Chaouk et al. | Jul 2006 | A1 |
20060148755 | Bailleul | Jul 2006 | A1 |
20060166928 | Moon et al. | Jul 2006 | A1 |
20060189516 | Yang et al. | Aug 2006 | A1 |
20060194758 | Lebreton | Aug 2006 | A1 |
20060246137 | Hermitte et al. | Nov 2006 | A1 |
20060257488 | Hubbard | Nov 2006 | A1 |
20060264698 | Kondonis et al. | Nov 2006 | A1 |
20060286769 | Tsuchiya et al. | Dec 2006 | A1 |
20070026070 | Vonwiller et al. | Feb 2007 | A1 |
20070032805 | Therin et al. | Feb 2007 | A1 |
20070066816 | Tsai et al. | Mar 2007 | A1 |
20070077292 | Pinsky | Apr 2007 | A1 |
20070196426 | Hermitte et al. | Aug 2007 | A1 |
20070197754 | White et al. | Aug 2007 | A1 |
20070203095 | Sadozai et al. | Aug 2007 | A1 |
20070212385 | David | Sep 2007 | A1 |
20070224247 | Chudzik et al. | Sep 2007 | A1 |
20070224278 | Lyons et al. | Sep 2007 | A1 |
20070298005 | Thibault | Dec 2007 | A1 |
20080044476 | Lyons et al. | Feb 2008 | A1 |
20080057091 | Abdellaoui et al. | Mar 2008 | A1 |
20080089918 | Lebreton | Apr 2008 | A1 |
20080097605 | Pastorello et al. | Apr 2008 | A1 |
20080118563 | Muzzarelli et al. | May 2008 | A1 |
20080188416 | Bernstein | Aug 2008 | A1 |
20080193538 | Kitazono et al. | Aug 2008 | A1 |
20080200430 | Bitterrnan et al. | Aug 2008 | A1 |
20080207560 | Harada et al. | Aug 2008 | A1 |
20080207794 | Wright et al. | Aug 2008 | A1 |
20080241252 | Lyons et al. | Oct 2008 | A1 |
20080248079 | Dempsey et al. | Oct 2008 | A1 |
20080268051 | Hughes et al. | Oct 2008 | A1 |
20080274946 | Giampapa | Nov 2008 | A1 |
20080279806 | Cho | Nov 2008 | A1 |
20080293637 | Schroeder et al. | Nov 2008 | A1 |
20090017091 | Daniloff et al. | Jan 2009 | A1 |
20090018102 | Moutet et al. | Jan 2009 | A1 |
20090022808 | Champion et al. | Jan 2009 | A1 |
20090028817 | Niklason et al. | Jan 2009 | A1 |
20090030367 | Arora et al. | Jan 2009 | A1 |
20090036403 | Stroumpoulis et al. | Feb 2009 | A1 |
20090042834 | Karageozian et al. | Feb 2009 | A1 |
20090043268 | Eddy et al. | Feb 2009 | A1 |
20090093755 | Schroeder et al. | Apr 2009 | A1 |
20090110671 | Miyata et al. | Apr 2009 | A1 |
20090110736 | Boutros | Apr 2009 | A1 |
20090143331 | Stoumpoulis et al. | Jun 2009 | A1 |
20090143348 | Tezel et al. | Jun 2009 | A1 |
20090148527 | Robinson et al. | Jun 2009 | A1 |
20090155314 | Tezel et al. | Jun 2009 | A1 |
20090155362 | Longin et al. | Jun 2009 | A1 |
20090169615 | Pinsky | Jul 2009 | A1 |
20090204101 | Wortzman et al. | Aug 2009 | A1 |
20090209456 | Sweis | Aug 2009 | A1 |
20090263447 | Asius et al. | Oct 2009 | A1 |
20090291986 | Puppas et al. | Nov 2009 | A1 |
20090297632 | Waugh | Dec 2009 | A1 |
20100004198 | Stroumpoulis et al. | Jan 2010 | A1 |
20100028435 | Gavard Molliard | Feb 2010 | A1 |
20100028437 | Lebreton | Feb 2010 | A1 |
20100035838 | Heber et al. | Feb 2010 | A1 |
20100041788 | Voigts et al. | Feb 2010 | A1 |
20100098764 | Stroumpoulis et al. | Apr 2010 | A1 |
20100098794 | Armand | Apr 2010 | A1 |
20100099623 | Schroeder et al. | Apr 2010 | A1 |
20100111919 | Abuzaina et al. | May 2010 | A1 |
20100136070 | Dobak et al. | Jun 2010 | A1 |
20100221684 | Asius et al. | Sep 2010 | A1 |
20100226988 | Lebreton | Sep 2010 | A1 |
20100255068 | Stroumpoulis et al. | Oct 2010 | A1 |
20100303873 | Piron et al. | Dec 2010 | A1 |
20100310631 | Domard et al. | Dec 2010 | A1 |
20100316683 | Piron et al. | Dec 2010 | A1 |
20110034684 | Yokokawa et al. | Feb 2011 | A1 |
20110077737 | Stroumpoulis et al. | Mar 2011 | A1 |
20110113206 | Lebreton | May 2011 | A1 |
20110171286 | Cecile et al. | Jul 2011 | A1 |
20110171311 | Gousse et al. | Jul 2011 | A1 |
20110172180 | Gousse et al. | Jul 2011 | A1 |
20110224164 | Lebreton | Sep 2011 | A1 |
20110229574 | Guillen et al. | Sep 2011 | A1 |
20110263724 | Gurtner et al. | Oct 2011 | A1 |
20120010146 | Han et al. | Jan 2012 | A1 |
20120013959 | Andersson et al. | Jan 2012 | A1 |
20120034462 | Stroumpoulis et al. | Feb 2012 | A1 |
20120071437 | Stroumpoulls et al. | Mar 2012 | A1 |
20120095206 | Chen et al. | Apr 2012 | A1 |
20120100217 | Green et al. | Apr 2012 | A1 |
20120164098 | Schroeder et al. | Jun 2012 | A1 |
20120172328 | Lebreton | Jul 2012 | A1 |
20120189589 | Van Epps et al. | Jul 2012 | A1 |
20120189590 | Van Epps et al. | Jul 2012 | A1 |
20120189708 | Van Epps et al. | Jul 2012 | A1 |
20120190644 | D'este et al. | Jul 2012 | A1 |
20120208890 | Gousse et al. | Aug 2012 | A1 |
20120225842 | Cecile et al. | Sep 2012 | A1 |
20120232030 | Gousse et al. | Sep 2012 | A1 |
20130013415 | Brown et al. | Jan 2013 | A1 |
20130023653 | Stroumpoulis et al. | Jan 2013 | A1 |
20130041038 | Lebreton | Feb 2013 | A1 |
20130041039 | Lebreton | Feb 2013 | A1 |
20130072453 | Gousse et al. | Mar 2013 | A1 |
20130096081 | Njikang et al. | Apr 2013 | A1 |
20130116188 | Pollock et al. | May 2013 | A1 |
20130116190 | Pollock et al. | May 2013 | A1 |
20130116411 | Pollock et al. | May 2013 | A1 |
20130122063 | Fermanian et al. | May 2013 | A1 |
20130123210 | Liu et al. | May 2013 | A1 |
20130131011 | Lebreton | May 2013 | A1 |
20130136780 | Tezel et al. | May 2013 | A1 |
20130142731 | Gurtner et al. | Jun 2013 | A1 |
20130203696 | Njikang et al. | Aug 2013 | A1 |
20130209532 | Stroumpoulis et al. | Aug 2013 | A1 |
20130210760 | Liu et al. | Aug 2013 | A1 |
20130226235 | Fermanian et al. | Aug 2013 | A1 |
20130237615 | Meunier et al. | Sep 2013 | A1 |
20130244943 | Yu et al. | Sep 2013 | A1 |
20130244970 | Lebreton | Sep 2013 | A1 |
20130274222 | Horne et al. | Oct 2013 | A1 |
20140011980 | Chitre et al. | Jan 2014 | A1 |
20140011990 | Lebreton | Jan 2014 | A1 |
20140228971 | Kim | Aug 2014 | A1 |
Number | Date | Country |
---|---|---|
0949965 | Jun 1974 | CA |
104144714 | Nov 2014 | CA |
2912043 | Jan 1980 | DE |
0273823 | Jul 1988 | EP |
0193510 | Nov 1988 | EP |
0341745 | Nov 1989 | EP |
0416250 | Mar 1991 | EP |
0416846 | Mar 1991 | EP |
1217008 | Jun 2002 | EP |
1247522 | Oct 2002 | EP |
1398131 | Mar 2004 | EP |
1419792 | May 2004 | EP |
1532991 | May 2005 | EP |
1614696 | Jan 2006 | EP |
1640026 | Mar 2006 | EP |
1712228 | Oct 2006 | EP |
1726299 | Nov 2006 | EP |
2236523 | Jun 2010 | EP |
2733427 | Oct 1996 | FR |
2920000 | Feb 2009 | FR |
2924615 | Jun 2009 | FR |
550153711 | Nov 1980 | JP |
11-511344 | Oct 1999 | JP |
2000-210376 | Aug 2000 | JP |
2000-271207 | Oct 2000 | JP |
2000-516978 | Dec 2000 | JP |
2002-080501 | Mar 2002 | JP |
2003-521962 | Jul 2003 | JP |
2006-504930 | Feb 2006 | JP |
2006-522851 | Oct 2006 | JP |
2007-502430 | Feb 2007 | JP |
2007-063177 | Mar 2007 | JP |
2007-516333 | Jun 2007 | JP |
2007-520612 | Jul 2007 | JP |
2007-262595 | Oct 2007 | JP |
2009-503281 | Jan 2009 | JP |
20080062092 | Jul 2008 | KR |
1986000079 | Jan 1986 | WO |
1986000912 | Feb 1986 | WO |
1992000105 | Jan 1992 | WO |
199213579 | Aug 1992 | WO |
1992020349 | Nov 1992 | WO |
1996033751 | Oct 1993 | WO |
1994001468 | Jan 1994 | WO |
1994002517 | Mar 1994 | WO |
199524497 | Sep 1995 | WO |
199637519 | Nov 1996 | WO |
1997004012 | Feb 1997 | WO |
199737613 | Oct 1997 | WO |
199808876 | Mar 1998 | WO |
1998035639 | Aug 1998 | WO |
1998035640 | Aug 1998 | WO |
199904828 | Feb 1999 | WO |
199956799 | Nov 1999 | WO |
2000001428 | Jan 2000 | WO |
200100190 | Jan 2001 | WO |
2001079342 | Oct 2001 | WO |
2002005753 | Jan 2002 | WO |
2002006350 | Jan 2002 | WO |
2002009792 | Feb 2002 | WO |
200217979 | Mar 2002 | WO |
2003007782 | Jan 2003 | WO |
2002017713 | Mar 2003 | WO |
2004020473 | Mar 2004 | WO |
2004022603 | Mar 2004 | WO |
2004073759 | Sep 2004 | WO |
2004092222 | Oct 2004 | WO |
2004092223 | Oct 2004 | WO |
2005012364 | Feb 2005 | WO |
2005040224 | Jun 2005 | WO |
2005067994 | Jul 2005 | WO |
2005074913 | Aug 2005 | WO |
2005085329 | Sep 2005 | WO |
2005097218 | Oct 2005 | WO |
2005112888 | Dec 2005 | WO |
2006023645 | Mar 2006 | WO |
2006067608 | Jun 2006 | WO |
2007018124 | Feb 2007 | WO |
2007070617 | Jun 2007 | WO |
2007077399 | Jul 2007 | WO |
2007128923 | Nov 2007 | WO |
2007136738 | Nov 2007 | WO |
2008034176 | Mar 2008 | WO |
2008056069 | May 2008 | WO |
2008068297 | Jun 2008 | WO |
2008072230 | Jun 2008 | WO |
2008077172 | Jul 2008 | WO |
2008098019 | Aug 2008 | WO |
2008139122 | Nov 2008 | WO |
2008147817 | Dec 2008 | WO |
2008148967 | Dec 2008 | WO |
2008157280 | Dec 2008 | WO |
2008157608 | Dec 2008 | WO |
2009024719 | Feb 2009 | WO |
2009026158 | Feb 2009 | WO |
2009028764 | Mar 2009 | WO |
2009034559 | Mar 2009 | WO |
2009073437 | Jun 2009 | WO |
2010003797 | Jan 2010 | WO |
2010015900 | Feb 2010 | WO |
2010027471 | Mar 2010 | WO |
2010028025 | Mar 2010 | WO |
2010029344 | Mar 2010 | WO |
2010038771 | Apr 2010 | WO |
2010051641 | May 2010 | WO |
2010052430 | May 2010 | WO |
2010053918 | May 2010 | WO |
2010061005 | Jun 2010 | WO |
2011109129 | Sep 2011 | WO |
2011109130 | Sep 2011 | WO |
2012054301 | Apr 2012 | WO |
2012054311 | Apr 2012 | WO |
2012077055 | Jun 2012 | WO |
2012089179 | Jul 2012 | WO |
2013055832 | Apr 2013 | WO |
2012174464 | May 2014 | WO |
Entry |
---|
Adams, Mark, An Analysis of Clinical Studies of the Use of Crosslinked Hyaluronan, Hylan, in the Treatment of Osteoarthritis, The Journal of Rheumatology, 1993, 16-18, 20 (39). |
Aesthetic Buyers Guide, Juvederm Raises Standards, 2007, 1, 4-7; miinews.com. |
Albano, Emanuele et al., Hydroxyethyl Radicals in Ethanol Hepatotoxicity, Frontiers in Bioscience, 1999, 533-540, 4. |
Allemann, Inja Bogdan, Hyaluronic Acid Gel (Juvederm) Preparations in the Treatment of Facial Wrinkles and Folds, Clinical Interventions in Aging, 2008, 629-634, 3 (4). |
Andre, Pierre MD, Hyaluronic Acid and Its Use as a “Rejuvenation” Agent in Cosmetic Dermatology, Seminars in Cutaneous Medicine and Surgery, 2004, 218-222, Elsevier, Inc. |
Antunes, Alberto et al., Efficacy of Intrarectal Lidocaine Hydrochloride Gel for Pain Control in Patients Undergoing Transrectal Prostate Biopsy, Clinical Urology, 2004, 380-383, 30. |
Atanassoff, Peter et al., The Effect of Intradermal Administration of Lidocaine and Morphine on the Response to Thermal Stimulation, Anesth Analg, 1997, 1340-1343, 84. |
Baumann, Leslie et al., Comparison of Smooth-Gel Hyaluronic Acid Dermal Fillers with Cross-linked Bovine Collagen: A Multicenter, Double-Masked, Randomized, Within-Subject Study, Dermatologic Surgery, 2007, S128-135, 33 (2). |
Beasley, Karen et al., Hyaluronic Acid Fillers: A Comprehensive Review, Facial Plast. Surg., 2009, 86-94, 25(2). |
Beer, Kenneth, Dermal Fillers and Combinations of Fillers for Facial Rejuvenation, Dermatologic Clin, 2009, 427-432, 27 (4). |
Belda, Jose et al., Hyaluronic Acid Combined With Mannitol to Improve Protection Against Free-Radical Endothelial Damage: Experimental Model, J Cataract Refract Surg, 2005, 1213-1218, 31. |
Bircher, Andres et al., Delayed-type Hypersensitivity to Subcutaneous Lidocaine With Tolerance to Articaine: Confirmation by In Vivo and In Vitro Tests, Contact Dermatitis, 1996, 387-389, 34. |
Bleyer, Mark, SIS Facial Implant 510(k) Summary, Cook Biotech Inc., May 19, 2005. |
Bluel, K. et al., Evaluation of Reconstituted Collagen Tape as a Model for Chemically Modified Soft Tissues, Biomat., Med. Dev., Art. Org., 1981, 37-46, 9(1). |
Boulle et al., Lip Augmentation and Contour Correction With a Ribose Cross-linked Collagen Dermal Filler, Journal of Drugs in Dermatology, Mar. 2009, 1-8, vol. 8 Issue 3. |
Buck, Donald, Injectable Fillers for Facial Rejuvenation: A Review, Journal of Plastic, Reconstructive & Aesthetic Surgery, 2009, 11-18, 62. |
Capozzi, Angelo et al., Distant Migration of Silicone Gel From a Ruptured Breast Implant, Silicone Gel Migration, 1978, 302-3, 62 (2). |
Carlin, G. et al., Effect of Anti-Inflammatory Drugs on Xanthine Oxidase and Xanthine Oxidase Induced Depolyrnerization of Hyaluronic Acid, Agents and Actions, 1985, 377-384 16 (5). |
Carruthers et al., The Science and Art of Dermal Fillers for Soft-Tissue Augmentation, Journal of Drugs in Dermatology, Apr. 2009, 335-350, vol. 8 Issue 4. |
Champion, Julie et al., Role of Target Geometry in Phagocytosis, Proc. Nat. Acad. Sci., 2006, 4930-4934, 103 (13). |
Chin, Thomas et al., Allergic Hypersensitivity to Lidocaine Hydrochloride, International Society of Tropical Dermatology, 1980, 147-148. |
Chvapil, Milos, Collagen Sponge: Theory and Practice of Medical Applications, J. Biomed. Mater. Res., 1977, 721-741, 11. |
Clark, D. Dick et al., The Influence of Triamcinolone Acetonide on Joint Stiffness in the Rat, The Journal of Bone and Joint Surgery, 1971, 1409-1414, 53A (7). |
Cohen, Miriam et al., Organization and Adhesive Properties of the Hyaluronan Pericellular Coat of Chondrocytes and Epithelial Cells, Biophysical Journal, 2003, 1996-2005, 85. |
Conley et al., Thread Augmentation for Facial Rhytides, Annals of Plastic Surgery, Aug. 1979, 118-126. |
Cui, Yu et al., The Comparison of Physicochemical Properties of Four Cross-linked Sodium Hyaluronate Gels With Different Cross-linking Agents, Advanced Materials Research, 2012, 1506-1512, 396-398. |
Deland, Frank, Intrathecal Toxicity Studies with Benzyl Alcohol, Toxicology and Applied Pharmacology, 1973, 153-6, 25, Academic Press, Inc. |
Desai, Ur et al., Molecular Weight of Heparin Using 13C Nuclear Magnetic Resonance Spectroscopy, J Pharm Sci., 1995, 212-5, 84 (2). |
Elvassore et al., Production of Different Morphologies of Biocompatible Polymeric Materials by Supercritical CO2 Antisolvent Techniques, Biotechnology and Bioengineering, 2001, 449-457. |
Eyre, David R. et al., Collagen Cross-Links, Topics in Current Chemistry, 2005, 207-229, 247, US. |
Falcone et al., Temporary Polysaccharide Dermal Fillers: A Model for Persistence Based on Physical Properties, Dermatologic Surgery, Aug. 2009, 1238-1243, 35; 8. |
Falcone, Samuel et al., Crosslinked Hyaluronic Acid Dermal Fillers: A Comparison of Rheological Properties, Journal of Biomedical Materials Research, 2008, 264-271, 87 (1). |
Farley, Jon et al., Diluting Lidocaine and Mepivacaine in Balanced Salt Solution Reduces the Pain of Intradermal Injection, Regional Anesthesia, 1994, 48-51, 19 (1). |
Frati, Elena et al., Degradation of Hyaluronic Acid by Photosensitized Riboflavin In Vitro. Modulation of the Effect by Transition Metals, Radical Quenchers, and Metal Chelators, Free Radical Biology Medicine, 1996, 1139-1144, 22 (7). |
Fujinaga, Masahiko et al., Reproductive and Teratogenic Effects of Lidocaine in Sprague-Dawley Rats, Anesthesiology, 1986, 626-632, 65. |
Gammaitoni, Arnold et al., Pharmacokinetics and Safety of Continuously Applied Lidocaine Patches 5%, Am J Health Syst Pharm, 2002, 2215-2220, 59. |
Ginshicel MH, Hydroxy Propyl Methyl Cellulose, Retrieved on Nov. 12, 2008 http://www.ginshicel.cn/MHPC.html, 2007, p. 1-3, 2 (3). |
Gold, Michael, Use of Hyaluronic Acid Fillers for the Treatment of the Aging Face, Clin. Interventions Aging, 2007, 369-376, 2 (3). |
Goldberg, David, Breakthroughs in US dermal fillers for facial soft-tissue augmentation, Journal of Cosmetic and Laser Therapy, 2009, 240-247, 11, Informa UK Ltd. |
Graefe, Hendrik et al., Sensitive and Specific Photometric Determination of Mannitol, Clin Chem Lab Med, 2003, 1049-1055, 41 (8). |
Grecomoro, G. et al., Intra-articular treatment with sodium hyaluronate in gonarthrosis: a controlled clinical trial versus placebo, Pharmatherapeutica, 1987, 137-141, 5 (2). |
Grillo, Hermes et al., Thermal Reconstitution of Collagen From Solution and the Response to Its Heterologous Implantation, JSR, 1962, 69-82, 2 (1). |
Haaf et al., Resorbable suture material in the human skin: tissue reaction and modified suture technic, Hautarzt, Jan. 1988, 39(1), (Abstract only). |
Hassan, HG et al., Effects of Adjuvants to Local Anaesthetics on Their Duration. III. Experimental Studies of Hyaluronic Acid, Acta Anaesthesiol Scand., 1985, 1, 29 (4). |
Hayashibara, AA2G, Sep. 23, 2007, Retrieved on Jan. 17, 2012, http://web.archive.org/web/20070923072010/http://www.hayashibara-intl.cosmetics/aa2g.html. |
Helary, Christophe et al., Concentrated Collagen Hydrogels as Dermal Substitutes, Biomaterials, 2010, 481-490, 31. |
Helliwell, Philip, Use of an objective measure of articular stiffness to record changes in finger joints after intra-articular injection of corticosteroid, Annals of Rheumatic Diseases, 1997, 71-73, 56. |
Hertzberger-Ten, Cate et al., Intra-articular steroids in pauciarticular juvenile chronic arthritis, type 1, European Journal of Pediatrics, 1991, 170-172, 150. |
Hetherington, NJ et al., Potential for Patient Harm from Intrathecal Administration of Preserved Solutions, Med J Aust., 2000, 1, 173(3). |
Holzheimer, R.G., Adverse Events of Sutures: Possible Interactions of Biomaterials?, European Journal of Medical Research, 2006, 521-526, 10, I. Holzapfel Publishers. |
Hurst, E., Adhesive Arachnoiditis and Vascular Blockage Caused by Detergents and Other Chemical Irritants: An Experimental Study, J Path. Bact., 1955, 167, 70. |
Intramed (PTY) Ltd, Intramed Mannitol 20% m/v Infusion, Package Insert, Jan. 1979, 4 pages, 12-214/8-94, ZA. |
Jones, Adrian C. et al., Intra-articular hyaluronic acid compared to intra-articular triamcinolone hexacetonide in inflammatory knee osteoarthritis, Osteoarthritis and Cartilage, 1995, 269-273, 3. |
Kablik, Jeffrey et al., Comparative Physical Properties of Hyaluronic Acid Dermal Fillers, Dermatol Surg, 2009, 302-312, 35. |
Klein, Arnold William, Skin Filling Collagen and Other Injectables of the Skin, Dermatologic Clinics, Jul. 2001, 491-508, 19 (3), US. |
Kopp, et al., The Short-term Effect of Intra-articular Injections of Sodium Hyaluronate and Corticosteroid on Temporomandibular Joint Pain and Dysfunction, Journal of Oral and Maxillofacial Surgery, 1985, 429-435, 43. |
Kulicke, Werner-Michael et al., Visco-Elastic Properties of Sodium Hyaluronate Solutions, Institute for Technical and Macromolecular Chemistry, 2008, 585-587, DE. |
Laeschke, Klaus, Biocompatibility of Microparticies Into Soft Tissue Fillers, Semin Cutan Med Surg, 2004, 214-217, 23. |
Lamar, PD et al., Antifibrosis Effect of Novel Gels in Anterior Ciliary Sclerotomy (ACS), 2002, 1 Page, The Association for Research in Vision and Ophthalrnology, Inc. |
Lapcik et al., Hyaluronan: Preparation, Structure, Properties, and Applications, Chemical Reviews, Dec. 1998. 2663-2684. vol. 98. No. 8. |
Leach et al., Hyaluronan, Encyclopedia of Biomaterials and Biomedical Engineering, 2004, 779-789. |
Levy, Jaime et al., Lidocaine Hypersensitivity After Subconjunctival Injection, Can J Ophthalmol, 2006, 204-206, 41. |
Lindvall, Sven et al., Influence of Various Compounds on the Degradation of Hyaluronic Acid by a Myeloperoxidase System, Chemico-Biological Interactions, 1994, 1-12, 90. |
Lupo, Mary, Hyaluronic Acid Fillers in Facial Rejuvenation, Seminars in Cutaneous Medicine and Surgery, 2006, 122-126, 25. |
Mackley, Christine et al., Delayed-Type Hypersensitivity to Lidocaine, Arch Dermatol, 2003, 343-346, 139. |
Mancinelli, Laviero et al., Intramuscular High-dose Triamcinolone Acetonide in the Treatment of Severe Chronic Asthma, West J Med, 1997, 322-329, 167 (5). |
Matsumoto, Alan et al., Reducing the Discomfort of Lidocaine Administration Through pH Buffering, Journal of Vascular and Interventional Radiology, 1994, 171-175, 5 (1). |
McCarty, Dj, et al., Inflammatory Reaction After Intrasynovial Injection of Microcrystalline Andrenocorticosteroid Esters, Arthritis and Rheumatism, Aug. 1964, 359-367, vol. VII, No. 4, Grune & Stratton. |
McCleland, Marcee et al., Evaluation of Artecoll Polymethylmethacrylate Implant for Soft-Tissue Augmentation: Biocompatibility and Chemical Characterization, Plastic & Reconstructive Surgery, 1997, 1466-1474, 100 (6). |
McPherson, John et al., Development and Biochemical Characterization of Injectable Collagen, Journal of Dermatol Surg Oncol, 1988, 13-20, 14 (Suppl) 1) 7. |
Millay, Donna et al., Vasoconstrictors in Facial Plastic Surgery, Arch Otolaryngol Head Neck Surg., 1991, 160-163, 117. |
Niamtu III, DMD, Joseph, Advanta Facial Implants, Oral Maxillofacial Surg Clin N Am, 2005, 29-39, 17. |
Orvisky, E. et al., High-molecular-weight Hyaluronan—a Valuable Tool in Testing the Antioxidative Activity of Amphiphilic Drugs Stobadine and Vinpocetine, Journal of Pharm. Biomed. Anal., 1997, 419-424 16. |
Osmitrol (generic name Mannitol), Official FDA Information, side effects and uses, http://www.drugs.com/pro/osmitrol.html, 2010, 10 Pages. |
Osol, Arthur, Remington's Pharmaceutical Sciences, Mack Publishing Company, 1980, 10 pgs, 16th Edition, Easton, Pennsylvania, US. |
Park, DJ et al., In Vitro Evaluation of Conjugated Hyaluronic Acid With Ascorbic Acid, Journal of Bone and Joint Surgery, 2010, 115, 92. |
Park, Si-Nae et al., Biological Characterization of EDC-Crosslinked Collagen-Hyaluronic Acid Matrix in Dermal Tissue Restoration, Biomaterials, 2003, 1631-1641, 24. |
Park, Si-Nae et al., Characterization of Porous Collagen/Hyaluronic Acid Scaffold Modified by 1-Ethyl-3-(3-Dimethylaminopropyl)Carbodiimide Cross-Linking, Biomaterials, 2002, 1205-1212, 23. |
Powell, Michael, Stability of Lidocaine in Aqueous Solution: Effect of Temperature, pH, Buffer, and Metal Ions on Amide Hydrolysis, Pharmaceutical Research, 1987, 42-45, 4 (1). |
Prestwich, Glenn, Evaluating Drug Efficacy and Toxicology in Three Dimensions: Using Synthetic Extracellular Matrices in Drug Discovery, Accounts of Chemical Research, Jan. 2008, 139-148, 41(1). |
Rehakova, Milena et al., Properties of Collagen and Hyaluronic Acid Composite Materials and Their Modification by Chemical Crosslinking, Journal of Biomedical Materials Research, 1996, 369-372, 30, US. |
Rinaudo, Marguerite, Main properties and current applications of some polysaccharides as biomaterials, Polymer international. 2008, 397-430, 57. |
Rosenblatt, J. et al., Chain Rigidity and Diffusional Release in Biopolymer Gels, Controlled Release Society, 1993, 264-265, 20. |
Rosenblatt, J. et al., The Effect of Collagen Fiber Size Distribution on the Release Rate of Proteins From Collagen Matrices by Diffusion, J Controlled Release, 1989, 195-203, 9. |
Sannino, A. et al., Crosslinking of Cellulose Derivatives and Hyaluronic Acid With Water-Soluble Carbodiimide, Polymer, 2005, 11206-11212, 46. |
Sculptra Product Information, Dermik Laboratories, Jun. 1-10, 2004. |
Segura, Tatiana et al., Crosslinked Hyaluronic Add Hydrogels: A Strategy to Functionalize and Pattern, Biomaterials, 2005, 359-371, 26 (4). |
Selvi, Enrico et al., Arthritis Induced by Corticosteroid Crystals, The Journal of Rheumatology, 2004, 622, 31 (3). |
Semchyshyn, N.L., Dermatologic Surgical Complications, Drugs, Diseases and Procedures, 2012, 1-20. |
Serban, Monica et al., Modular Extracellular Matrices: Solutions for the Puzzle, Methods, 2008, 93-98, 45 (1). |
Shu, Xiao et al, Synthesis and evaluation of injectable, in situ crosslinkable synthetic extracellular matrices for tissue engineering, Journal of Biomedical Materials Research, 2006, 902-912, 79A. |
Silver, Frederick et al., Physical Properties of Hyaluronic Acid and Hydroxypropylmethylcellulose in Solution: Evaluation of Coating Ability, Journal of Applied Biomaterials, 1994, 89-98, 5. |
Skardal, Aleksander et al., Bioprinting Vessel-Like Constructs Using Hyaluronan Hydrogels Crosslinked With Tetrahedral Polyethylene Glycol Tetracrylates, Biomaterials, 2010, 6173-6181, 31. |
Smith, Kevin et al., Five Percent Lidocaine Cream Applied Simultaneously to the Skin and Mucosa of the Lips Creates Excellent Anesthesia for Filler Injections, Dermatol Surg, 2005, 1635-1637, 31. |
Tezel et al., The science of hyaluronic acid dermal fillers, Journal of Cosmetic and Laser Therapy, 2008, 35-42, 10. |
Thermo Scientific Pierce Crosslinking Technical Handbook, Apr. 2009, 1-48. |
Truswell, MD, William H., Dual-Porosity Expanded Polytetrafluoroethylene Soft Tissue Implant, Arch Facial Plast Surg, Apr. 2002, 92-97, 4(2). |
Visiol, Viscoelstic Gel for Use in Ocular Surgery, http://www.trbchemedica.com/index.php/option=com—content&tas, 2010, 1 Page. |
Wahl, Gregor, European Evaluation of a New Hyaluronic Acid Filler Incorporating Lidocaine, Journal of Cosmetic Dermatology, 2008, 298-303, 7. |
Wang, Frank et al., In Vivo Stimulation of De Novo Collagen Production Caused by Cross-Linked Hyaluronic Acid Dermal Filler Injections in Photodamaged Human Skin, Arch Dermatol, Feb. 2007, 155-163, 143. |
Waraszkiewicz, Sigmund et al., Stability-Indicating High-Performance Liquid Chromatographic Analysis of Lidocaine Hydrochloride and Lidocaine Hydrochloride with Epinephrine Injectable Solutions, J of Pharmaceutical Sciences, 1981, 1215-1218, 70 (11). |
Weidmann, Michael, New Hyaluronic Acid Filler for Subdermal and Long-lasting Volume Restoration of the Face, European Dermatology, 2009, 65-68. |
Xia, Yun et al., Comparison of Effects of Lidocaine Hydrochloride, Buffered Lidocaine, Diphenhydramine, and Normal Saline After Intradermal Injection, J of Clinical Anesthesia, 2002, 339-343, 14. |
Yeom, Junseok et al., Effect of Cross-linking Reagents for Hyaluronic Acid Hydrogel Dermal Fillers on Tissue Augmentation and Regeneration, Bioconjugate Chemistry, 2010, 240, 21, American Chemical Society. |
Yui, Nobuhiko et al., Inflammation Responsive Degradation of Crosslinked Hyaluronic Acid Gels, Journal of Controlled Release, 1992, 105-116, 26. |
Yui, Nobuhiko et al., Photo-Responsive Degradation of Heterogeneous Hydrogels Comprising Crosslinked Hyaluronic Acid and Lipid Microspheres for Temporal Drug Delivery, Journal of Controlled Release, 1993, 141-145, 26. |
Yun, Yang H. et al., Hyaluronan Microspheres for Sustained Gene Delivery and Site-Specific Targeting, Biomaterials, 2004, 147-157, 25, US. |
Zheng et al., In Situ Crosslinkable Hyaluronan Hydrogels for Tissue Engineering, Biomaterials, 2004, 1339-1348, 25. |
Zulian, F. et al., Triamcinolone Acetonide and Hexacetonide Intra-Articular Treatment of Symmetrical Joints in Juvenile Idiopathic Arthritis: A Double-Blind Trial, Rheumatology, 2004, 1288-1291, 43. |
Number | Date | Country | |
---|---|---|---|
20160074307 A1 | Mar 2016 | US |
Number | Date | Country | |
---|---|---|---|
61190866 | Sep 2008 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 13060919 | US | |
Child | 14947409 | US |