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US4427808A Expired / Lapsed US ⏱️ 0.0 years remaining

Composite polymeric material for biological and medical applications and the method for its preparation

Assignee: Czech Academy of Sciences
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Filing: 1981-07-15
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Granted: 1984-01-24
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Expires: 2001-07-15
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Abstract

Abstract The invention relates to a composite polymeric material suitable for biological and medical applications and to the method for preparation thereof. The composite material consists of 1-99 wt. % of hydrophilic polymer or copolymer based on methacrylic or acrylic esters, 1-99 wt. % of fibrillar collagen, and up to 2.5 wt. % of a crosslinking agent, based on both polymeric components. The composite material may further comprise biologically active compounds and other auxiliary materials, as fillers and/or plasticizers. The composite material is prepared by dispersing the fibrillar collagen in a solution or a highly swollen dispersion of the synthetic hydrophilic polymer or copolymer in a lyotropic agent and the subsequent removal of the lyotropic agent, thus forming a matrix of the synthetic polymer or copolymer penetrated by fibrillar collagen or vice versa. The composite material may be applied on a solid support or reinforced with glass, plastics, cellulose, or metallic materials. A method for the preparation of the composite material consists in dispersing of fibrillar collagen in a solution or a highly swollen dispersion of the synthetic hydrophilic polymer or copolymer in a lyotropic agent, e.g. in water diluted carboxylic acids, strongly acidified aqueous mixtures of ethanol and methanol, high-concentrated aqueous solutions of lyotropic salts, and high-concentrated aqueous solutions of urea or guanidinium chloride, at temperature not exceeding 37° C., and the subsequent removing of the lyotropic agent from the viscous dispersion at temperature not exceeding 37° C. using the known methods. The crosslinking agent, e.g. trimethylolurea, formaldehyde, acetaldehyde, glutaraldehyde, starch dialdehyde, glyoxal, or Cr(III) salts, may be added in the course of preparation of the dispersion or after removal of the lyotropic agent.

Inventors

  • 👤 Miroslav Stol
  • 👤 Miroslav Tolar
  • 👤 Milan Adam
  • 👤 Pavel Cefelin
  • 👤 Jaroslav Kalal

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 08:10
CPC Classifications
C; C12; C12N; C12N5/00; C12N5/0068; A; A61; A61L; A61L15/00; A61L15/16; A61L15/22; A61L15/225; A61L27/00; A61L27/14; A61L27/26; A61L33/00; A61L33/0005; A61L33/0011; C08; C08L; C08L33/00; C08L33/04; C08L33/06; C08L33/08; C08L89/00; C08L89/04; C12N2533/00; C12N2533/30; C12N2533/50; C12N2533/54; Y; Y10; Y10S; Y10S128/00; Y10S128/08; Y10S525/00; Y10S525/937

Claims Analysis

Total Claims: 4
Claim 1
Independent Claim 96 words
A method for the preparation of a composite polymeric material for biological and medical applications, wherein fibrillar collagen is dispersed in a solution or a high-swollen dispersion of the synthetic hydrophilic polymer or copolymer in a lyotropic agent selected from the group comprising carboxylic acids diluted with water, strongly acidified aqueous mixtures of ethanol and methanol, high-concentrated aqueous solutions of lyotropic salts, and high-concentrated aqueous solutions of urea or guanidinium chloride, under stirring at temperature not exceeding 37° C. and then the lyotropic agent is removed from the viscous dispersion at temperature not exceeding 37° C.
Claim 2
Independent Claim 96 words
A method for the preparation of a composite polymeric material for biological and medical applications, wherein fibrillar collagen is dispersed in a solution or a high-swollen dispersion of the synthetic hydrophilic polymer or copolymer in a lyotropic agent selected from the group comprising carboxylic acids diluted with water, strongly acidified aqueous mixtures of ethanol and methanol, high-concentrated aqueous solutions of lyotropic salts, and high-concentrated aqueous solutions of urea or guanidinium chloride, under stirring at temperature not exceeding 37° C. and then the lyotropic agent is removed from the viscous dispersion at temperature not exceeding 37° C.
Claim 3
Dependent Claim 62 words
The method according to claim 1, wherein a crosslinking agent selected from the group comprising trimethylolurea, formaldehyde, acetaldehyde, glutaraldehyde, starch dialdehyde, glyoxal, and chromium(III) salts, is added, during the preparation of dispersion or after the lyotropic agent has been removed, in the amount of 2.5 weight percent at utmost, related to the total amount of the synthetic polymer or copolymer and collagen.
Claim 4
Dependent Claim 36 words
The method according to claim 2, wherein a biologically active compound, and if it is desired, a filler and/or a plasticizer are added during the preparation of dispersion or after the lyotropic agent has been removed.

References Cited (Backward Citations)

US4264155A Cited
US4388428A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-01-23 1987-07-25 1988-01-24 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-01-23 1991-07-25 1992-01-24 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-01-23 1995-07-25 1996-01-24 $7700.00 Window Closed / Lapsed

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