Method for making carrier systems for biologically active materials

• US 5,342,646 A
• Filed: 11/19/1992
• Issued: 08/30/1994
• Est. Priority Date: 08/25/1990
• Status: Expired due to Fees

• Current Assignee: Huls AG (Evonik Degussa GmbH)
• Original Assignee: ROHM Co., Ltd.
• Inventors: Kleese, Wolfgang, Lehmann, Klaus, Petereit, Hans-Ulrich, Siol, Werner, Kraemer, Dieter
• Primary Examiner(s): Beck, Shrive
• Assistant Examiner(s): DUDASH, DIANA L
• Application Number:
  US07/979,425
• Time in Patent Office: 649 Days
• Field of Search: 427/2, 427/212, 427/221, 427/421, 427/430.1, 427/220, 427/214
• US Class Current: 427/2.1
• CPC Class Codes: C07K 17/08 the carrier being a synthetic polymer
• CPC Class Codes: C12N 11/087 Acrylic polymers
• CPC Class Codes: G01N 33/545 Synthetic resin

Abstract

What is disclosed is a method for preparing carrier systems, adaptable to the covalent bonding thereto of biologically active materials, consisting of a known solid support material having a surface coated with a polymer containing functional groups suitable for covalent bonding, by coating the support material with a film-forming polymer dispersion and a non-film-forming polymer dispersion, suitably in admixture, at least one of the two polymer dispersions containing a polymer having functional groups suitable for covalent bonding with a biologically active material.

Claims

1. A method for making a carrier for the covalent bonding thereto of a biologically active material, which method comprises coating a solid support with a dispersion of a film-forming polymer and with another dispersion of a non-film-forming polymer, at least one of the polymers including a monomer having at least one functional group capable of covalently bonding with the biologically active material.

2. A method as in claim 1 wherein the support is coated with a mixture of the dispersions.

3. A method as in claim 1 wherein the support is inorganic.

4. A method as in claim 1 wherein the support is organic.

5. A method as in claim 1 wherein the support is in the form of spherical particles.

6. A method as in claim 5 wherein the spherical particles have an average diameter from 0.01 to 10 millimeters.

7. A method as in claim 1 wherein the polymers each comprise at least one monomer selection from the group consisting of acrylates, methacrylates, styrene, alkyl styrenes, vinyl esters, and vinyl halides.

8. A method as in claim 1 where the polymer in at least one of the dispersions comprises at least one monomer of the formula

Z-(R)_n -X ,

wherein X is a functional group selected from the group consisting of sulfonic acid halide, thioisocyanate, thiocarbonyldioxy, carbonyl-imidoyldioxy, haloethoxy, aziridine, epoxy, formyl, keto, acryloyl, anhydride, and active ester groups, R is a chemically inert spacer, n is 0 or 1, and Z is a polymerizable entity.

9. A method as in claim 1 wherein the polymers each comprise at least one monomer, different from the monomer having at least one functional group, selected from the group consisting of acrylates, methacrylates, styrene, alkyl styrenes, vinyl esters, and vinyl halides.

10. A method as in claim 9 where the polymer in at least one of the dispersions comprises at least one monomer of the formula

Z-(R)_n -X ,

wherein X is a functional group selected from the group consisting of sulfonic acid halide, thioisocyanate, thiocarbonyldioxy, carbonyl-imidoyldioxy, haloethoxy, aziridine, epoxy, formyl, keto, acryloyl, anhydride, and active ester groups, R is a chemically inert spacer, n is 0 or 1, and Z is a polymerizable entity.

11. A method as in claim 1 wherein the monomer having at least one functional group is present in the non-film-forming polymer.

12. A method as in claim 1 wherein the monomer having at least one functional group is present in an amount from 0.1 to 80 percent by weight of the film-forming polymer or of the non-film-forming polymer.

13. A method as in claim 1 wherein the polymers each further comprise at least 50 percent by weight of monomers of the formula ##STR8## wherein R₁ is hydrogen, methyl, or --CH₂ --COOR₂, R₂ is alkyl having 1 to 4 carbon atoms, and R₃ is linear or branched alkyl having 1 to 18 carbon atoms or is cycloalkyl having 3 to 12 ring members.

14. A method as in claim 11 wherein the film-forming polymer has a minimum film forming temperature below 60°

C.

15. A method as in claim 14 wherein the non-film-forming polymer has a freezing point of at least 30°

C.

16. A method as in claim 1 wherein the film-forming polymer is present in the film-forming dispersion as particles having an average particle size from 0.02 to 5 microns.

17. A method as in claim 1 wherein the non-film-forming polymer is present in the non-film-forming polymer dispersion as particles having an average particle size from 0.04 to 5 microns.

18. A method as in claim 11 wherein the polymers in the film-forming and non-film-forming dispersions are present as particles and the average size of the particles in the non-film-forming dispersion is larger than the average size of the particles in the film-forming dispersion by a factor of 1.2 to 20.

19. A method as in claim 11 wherein the ratio by dry weight of polymer in the non-film-forming dispersion to dry weight of polymer in the film-forming dispersion is from 50:

50 to 99;

1.

20. A method as in claim 1 wherein the support is coated by immersion or spraying.

21. A method as in claim 2 wherein the support is coated by immersion or spraying.