Adhesive sealant composition

a technology of adhesive sealant and composition, which is applied in the field of adhesive sealant composition, can solve the problems of limited adhesive composition, unsuitable tissue adhesive or sealant, and inability to meet the needs of paper after-treatment,

Inactive Publication Date: 2003-06-24
NEOMEND INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

Two component adhesives were prepared according to the process described in Example 6 except that the pH of the buffer in the protein solution was changed as listed in Table 2. The data indicate that a preferred pH range is about 8.44-10.0.
TABLE 2 Crosslinking agent Cure Protein PEG-SS2 Time Constistency HSA 130 mg/ml 10 min Initially softer Baxter 3400 mw adhesive, hardens Lot 2837A238AA with aging 40% 0.1 M pH 7.4 Carb/Bicarb HSA 130 mg/ml 20 sec Very elastic, good Sigma 3400 mw adhesive strength Lot 63H9041 not sticky 40% 0.1 M pH 8.44 Carb/Bicarb HSA 130 mg/ml 10 sec Hard gel, not sticky Sigma 3400 mw Lot 63H9041 40% 0.15 M pH 9.07 Carb/Bicarb HSA 130 mg/ml 5 sec Hard gel, not sticky Sigma 3400 mw Lot 63H9041 40% 0.2 M pH 9.52 Carb/Bicarb HSA 260 mg/ml 5 sec Hard gel, not sticky Sigma 3400 mw Lot 63H9041 40% 0.2 M pH 9.52 Carb/Bicarb HSA 130 mg/ml 7 sec Elastic to hard gel, Sigma 10,000 mw slightly sticky Lot 63H9041 40% 0.2 M pH 9.52 Carb/Bicarb HSA 260 mg/ml 7 sec Elastic to hard gel, Sigma 10,000 mw slightly sticky Lot 63H9041 40% 0.2 M pH 9.52 Carb/Bicarb HSA 130 mg/ml 25 s

Problems solved by technology

In sum, there are few available adhesive compositions that have sufficient strength, biocompatibility and bioabsorbability as well as other desired properties that would allow such compositions to be readi

Method used

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Examples

Experimental program
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Effect test

example 1

Synthesis of Polyethylene Glycol Disuccinimidyl Succinate PEG-SS2

Polyethylene glycol, PEG, (50 g, Aldrich Chemical Company, Milwaukee, Wis., sold as 3,400 average molecular weight, GPC analysis M.sub.n was 2,980, M.sub.w, was 3,480) was dissolved in 1,2-dichloroethane (250 ml) containing succinic arthydride (14.7 g) and anhydrous pyridine (12 ml). The mixture was refluxed under nitrogen for three days. After filtration and evaporation of the solvent, the residue was dissolved in 100 ml water and treated with the cation exchange resin Dowex.TM. 50 (H.sup.+) (50 g) for 30 minutes. The mixture was then filtered and the Dowex.TM. 50 was washed with water (50 ml 1.times.). The combined filtrate was washed with anhydrous diethyl ether (50 ml 2.times.). The PEG-disuccinate was then extracted from the water phase with two 100 ml chloroform washes. Evaporation of chloroform yielded about 49 g of PEG-disuccinate.

The PEG-disuccinate was dissolved in 200 ml N,N-dimethylformamide (DMF) at 37.deg...

example 2

Synthesis of N-hydroxysuccinimide Ester of Dicarboxymethyl Polyethylene Glycol

Dicarboxymethyl poly(ethylene glycol) (mol. wt. 3400) purchased from Shearwater Polymers, Inc., Huntsville, Ala. (5 g) and N-hydroxysuccinimide purchased from Sigma Chemical Co., St. Louis, Mo. (1 g) were dissolved in 30 ml of anhydrous DMF with mechanical stirring under nitrogen. The solution was cooled to 0.degree. C. and a solution of dicyclohexylcarbodiimide (1.79 g) in 5 ml DMF was added dropwise. The stirring was continued in the cold for 3 hours then at room temperature overnight (16 hrs). Dicyclohexylurea which precipitated was removed by filtration. Toluene (100 ml) was added to the filtrate and cooled to 0.degree. C. The product was then precipitated by addition of petroleum ether. The precipitate was collected on a sintered glass filter. Dissolution in toluene and reprecipitation with petroleum ether was repeated three times. The product was dried under vacuum in a desiccator.

example 3

Synthesis of Polyethylene Glycol-di-oligoglycolide Disuccinimidyl Succinate

A 500 ml three neck round bottom flask was flame dried under nitrogen. 50 g of PEG (mol. wt. 3400), 300 ml of xylene, and 1 drop of 0.33M stannous ottoate solution in xylene were charged into the flask with a continuous nitrogen purge. The flask was heated to boil the solution and 50 ml of xylene were removed by distillation. The solution was then cooled to room temperature. 17 g of glycolide (Boehfinger Ingleheim KG, Ingleheim, Germany) was added to the flask and the reaction mixture was refluxed under nitrogen for 16 hours. The copolymer reaction mixture was filtered hot to remove polyglycolide homopolymer. The copolymer then precipitated from the filtrate upon cooling and collected by filtration. The copolymer was placed in a flask with 500 ml of dichloromethane and 7 g of succinyl chloride. The solution was refluxed under nitrogen overnight (16 hours). 8.5 g of N-hydroxysuccinimide was added to the flask ...

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Abstract

This invention is related to an adhesive composition which may be used to bond or seal tissue in vivo. The adhesive composition is readily formed from a two component mixture which includes a first part of a protein, preferably a serum albumin protein, in an aqueous buffer having a pH in the range of about 8.0-11.0 and a second part of a water-compatible or water-soluble bifunctional crosslinking agent. When the two parts of the mixture are combined, the mixture is initially a liquid which cures in vivo on the surface of tissue in less than about one minute to give a strong, flexible, pliant substantive composition which bonds to the tissue and is absorbed in about four to sixty days. The adhesive composition may be used either to bond tissue, to seal tissue or to prevent tissue adhesions caused by surgery.

Description

BACKGROUNDA variety of techniques have been used to bond or seal tissue. For example, different types of tissues have been mechanically bound or sealed with a number of procedures, materials and methods including sutures, staples, tapes and bandages. In some applications, these materials are made of absorbable materials which are intended to bond and / or seal tissue as it heals and then to be absorbed over a period of time.The common use of a medical adhesive or "tissue glue" has not found widespread application. To date, some adhesive materials are known which may be used to adhere or stick tissue such as skin. For example, cyanoacrylate adhesives such as HISTOACRYL adhesive available from B. Braun, Melsungen, Germany or VETBOND tissue adhesive available from 3M, St. Paul, Minn. may be used to bond tissue. In addition to cyanoacrylate adhesives, other types of materials have been reported to adhere to stick to skin. For example, U.S. Pat. No. 4,839,345 to Doi et al. reports a hydrat...

Claims

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Application Information

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IPC IPC(8): A61L24/00A61L24/04C09J189/00A61L24/10
CPCA61L24/043A61L24/046A61L24/10A61L24/106C09J189/00Y10S530/83C08L89/00
Inventor BARROWS, THOMAS H.LEWIS, TERRY W.TRUONG, MYHANH T.SCHOLZ, MATTHEW T.
Owner NEOMEND INC
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