A process for the preparation of reconstituted collagen sponge |
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| An improved process for the preparation of collagen sponge | |
| A process for the preparation of a novel chemically modified fibrin-fibrillar-protein (FFP) composite sheet | |
| A process for the preparation of plant based reconstituted collagen substratum | |
| A process for the preparation of reconstituted collagen substratum | |
| A process for the preparation of biopolymer scaffold for medical applications | |
| A process for the preparation of a novel collagen scaffold useful for wound dressing | |
A process for the preparation of collagen-chitosan bilayer material |
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A process for extraction of atelopeptide collagen from a collagenous source by microbial treatment |
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An improved process for the preparation of fibroplast A process for the preparation of reconstituted collagen sponge An improved process for the preparation of collagen sponge A process for the preparation of collagen sponge without lyophilisation is disclosed, whereby the collagen solution obtained from a conventional collagenous source is treated with a non-ionic wetting agent under specified conditions to enable the treated solution to be air dried, thereby reducing the high cost involved in conventional lyophilisation. It is envisaged to have enormous potential application in the pharmaceutical industry in preparing cost effective collagenous biomaterial useful for medical applications. The sponge obtained by this process can be used for different medical applications including burn management, wound cover, drug delivery device etc. A process for the preparation of plant based reconstituted collagen substratum The process involves purification of proteolytic enzyme solubilized collagen and preparation of Aloe vera extract from its parenchymal tissue. The purified collagen and Aloe vera extract are mixed together and reconstituted. Subsequently, the solution mixture is spread to form sheets, followed by sterilization to obtain plant based reconstituted collagen substratum. The product finds potential medical application as biological cover for non-healing ulcers as well as burn injuries. A process for the preparation of reconstituted collagen substratum A process for the preparation of biopolymer scaffold for medical applications. The invention relates to a scaffold to aid in the tissue regeneration of tissue, such as bone, cartilage or soft tissue and as a container for delivery of bioactive molecules like growth factors. The scaffold is formed by the combination of the soluble biopolymer with a glycol, alkaline earth metal chloride and a cross linker. It comprises a polymer network having active agents, such as wound healing agents, incorporated therein. The compositions are suitable for use as or in wound dressings as it comprises methods and compositions for treating wounds. The matrix may be formed into any desired shape for treatment of wounds. The composition comprises a single density foam, either with or without cell seeding, which is not freeze dried, can be used to build living tissue equivalents or model tissue systems. A process for the preparation of a novel collagen scaffold useful for wound dressing. The process involves purification of collagen from fetal calfskin by conventional method. Development of antibacterial agent loaded alginate microsphere by water/oil emulsion technique through ionic gelation of alginate, thus entrapping antibacterial agent in the alginate polymer matrix followed by rigidization and drying of the drug loaded microspheres. The prepared drug loaded microsphere was impregnated in the prepared collagen and subsequently initiating fibrillation. The drug impregnated fibrillated collagen was cast as a thin scaffold under controlled temperature and aseptic environment. The developed novel collagen scaffold impregnated with antibacterial agent delivers the drug in a controlled manner thus reducing frequency of dressing and makes wound assessment easier. A process for the preparation of collagen-chitosan bilayer material. Collagen purified to the necessary extent (with or without telopeptide) in acid soluble form at a concentration of 1-10 mg/ml is made to gel around physiological conditions and crosslinked with appropriate chemicals in very low concentrations of 10-5 to 10-2 percent. An attachment to a layer of chitosan is effected at the same time resulting in a bilayer material. The composite matrix is further processed as appropriate to make four types of bilayer matrices ie. collagen film – chitosan film, collagen sponge – chitosan film, collagen film – chitosan sponge and collagen sponge – chitosan sponge. The bilayer material is envisaged to have enormous application in pharmaceutical industry as wound healing agent. It also finds potential application in biomedical area as efficient tissue engineering matrix. A process for extraction of atelopeptide collagen from a collagenous source by microbial treatment. The invention relates to an extraction process to derive collagen fibres of high tensile strength from collagenous tissue. This microbial extraction procedure ensures degradation of non-collagenous components, leaving the collagenous matter intact. The resulting atelopeptide collagen exhibits largely monomeric triple helical conformation.The collagen is rendered non-immunogenic by the removal of certain terminal peptide chains. The non-cytotoxic fibres can be fabricated into various physical forms for biomedical applications. |
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Ophthalmic related |
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A process for the preparation of ionically charged collagen sponge |
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A process for the preparation of viscoelastic, bio-erodible ophthalmic shield |
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A process for the preparation of bio-erodible insert for ophthalmic applications |
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| A process for the preparation of transparent soft collagen film. | |
A process for the preparation of ionically charged collagen sponge The process relates to modifying the polar sites of collagen using charged ligands under inert atmosphere to prepare ionically charged collagenous solution, which is cast into sponge of desired shape and size after incorporating foaming agent, crosslinkers and pharmaceutically active components. The resulting collagen sponge is either cationic or anionic at physiological pH and it can be effectively used at the sites of ionic nature. The ionic property of the sponge is of paramount importance in several surgical requirements where charge plays an important role. The ionically charged collagen sponge finds potential application as corneal shields in ophthamological treatment. It may also be used as effective haemostat for wound dressing. It may even be used as bone-cartilage substitute, surgical tampons, laparatomy pads and containers for drug release. The product is capable of entrapping different drugs and the controlled release of entrapped drugs is facilitated. Moreover, the soluble collagen, which is obtained as an intermediate product while making the sponge, finds a very high demand as a component of skin care products such as creams, shampoo etc, in the cosmetic and pharmaceutical industry. A process for the preparation of viscoelastic, bio-erodible ophthalmic shield. A process for the preparation of visco-elastic bio-erodible ophthalmic shield is disclosed, whereby pure collagen is obtained from bovine tissues by pH alteration and enzyme treatment this is followed by succinylation with succinic anhydride. The pure succinylated collagen is treated with hydrophilic polymers and antioxidant to get a viscoelastic solution. The solution is dried in moulds in a dust free chamber, cross-linked with UV irradiation and sterilised to get a bio-erodible ophthalmic shield for the treatment of infected eyes, injured eyes, dry eyes and traumatic and non-traumatic eyes. This can include one or more therapeutically active substances that will be released in the eye. The ophthalmic shield is biocompatible, bio-erodible, visco-elastic and transparent which can be used for ophthalmic application. A novel bio-erodible insert for ophthalmic applications and a process for the preparation thereof A novel bio-erodible insert for ophthalmic applications has been developed. The invention further relates to a process for the preparation of the insert. In the said process, collagen is treated with organic polar solvents, hydrophilic polymers and therapeutically active substances under controlled conditions. The resulting solution is air dried in a dust free chamber to make collagen film. This film is cut into shape to obtain insert, which is subjected to cross-linking with UV irradiation followed by conventional sterilization. The resulting insert is very effective for temporary punctual occlusion in various corneal conditions and is very effective for treating dry eye syndrome resulting due to occupational conditions. The invention has been applied for Patent protection (Indian Patent application no. 2064DEL2006).A process for the preparation of transparent soft collagen film |
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