Microcapsules for immune response

• US 4,650,769 A
• Filed: 03/08/1984
• Issued: 03/17/1987
• Est. Priority Date: 07/09/1980
• Status: Expired due to Term

• Current Assignee: Fuji Photo Film Co Limited (Fujifilm Holdings Corporation)
• Original Assignee: Fuji Photo Film Co Limited (Fujifilm Holdings Corporation)
• Inventors: Kakimi, Fujio, Akiyoshi, Yutaka, Matsukawa, Hiroharu, Kobayashi, Shinzo
• Primary Examiner(s): Nucker, Christine M.
• Application Number:
  US06/585,634
• Time in Patent Office: 1,104 Days
• Field of Search: 436/518, 436/532, 436/533, 436/534, 436/535, 436/823, 436/824, 436/829, 252/315.1, 428/402.2
• US Class Current: 436/533
• CPC Class Codes: B01J 13/16 Interfacial polymerisation
• CPC Class Codes: G01N 33/54346 Nanoparticles
• CPC Class Codes: Y10S 436/823 Immunogenic carrier or carrier per se
• CPC Class Codes: Y10S 436/829 Liposomes, e.g. encapsulation
• CPC Class Codes: Y10T 428/2984 Microcapsule with fluid core [includes liposome]

Abstract

Microcapsules for effecting an immune response, especially through agglutination reaction, comprise an antigen or antibody bound to functional groups, such as amino groups, carboxy groups, etc., on a wall surface of the microcapsules via cross linking agents, such as polyfunctional isocyanates, isothiocyanates, etc. The antigen or antibody is strongly bound to the wall surface of the microcapsules to thereby achieve excellent detection sensitivity.

Claims

1. Microcapsules for effecting an immune response which comprise a wall having an oily substance encapsulated therein as a core and an antigen or antibody bound to a functional group of the wall surface of the microcapsules via a cross linking agent, wherein the average particle size of the microcapsule is in the range of from 0.1 to 30 μ

m and the microcapsules have a variable specific gravity ranging from about 0.80 to about 1.20.

2. The microcapsules of claim 1 wherein said functional group is selected from the group consisting of an amino group, a carboxy group, a hydroxy group and a mercapto group.

3. The microcapsules of claim 1 wherein said wall is prepared by reacting a compound selected from the group consisting of a polyfunctional isocyanate, a polyfunctional isothiocyanate, a polyfunctional acid chloride and a polyfunctional epoxy compound with an aminocontaining substance selected from the group consisting of ethylenediamine, hexamethylene diamine, cyclic amines, arginine, lysine and cystine.

4. The microcapsules of claim 1 wherein said wall is prepared by reacting a compound selected from the group consisting of a polyfunctional isocyanate, a polyfunctional isothiocyanate, a polyfunctional acid chloride and a polyfunctional epoxy compound with a carboxy-containing substance selected from the group consisting of carboxymethyl cellulose, polyacrylic acid, polymethacrylic acid and polystyrene carboxylic acid.

5. The microcapsules of claim 1 wherein said wall is prepared by reacting a compound selected from the group consisting of a polyfunctional isocyanate, a polyfunctional isothiocyanate, a polyfunctional acid chloride and a polyfunctional epoxy compound with thiourea to form microcapsule walls and then reducing the thus formed microcapsules.

6. The microcapsules of claim 1 wherein said wall is prepared by reacting a compound selected from the group consisting of a polyfunctional isocyanate, a polyfunctional isothiocyanate, a polyfunctional acid chloride and a polyfunctional epoxy compound with an ester compound selected from the group consisting of a polyacrylate and a polymethacrylate to form the microccapsule wall, and then the microcapsule wall thus formed is hydrolyzed under acidic conditions.

7. The microcapsules of claim 3, 4, 5 or 6 wherein said polyfunctional isothiocyanate is selected from the group consisting of phenylene diisothiocyanate and ethylene diisothiocyanate.

8. The microcapsules of claim 3, 4, 5 or 6 wherein said polyfunctional isocyanate is selected from the group consisting of toluene diisocyanate, xylene diisocyanate, tolylene diisocyanate and hexamethylene diisocyanate.

9. The microcapsules of claim 3, 4, 5 or 6 wherein said polyfunctional acid chloride is 1-hydroxy-2,4-disulfonyl chloride.

10. The microcapsules of claim 3, 4, 5 or 6 wherein said polyfunctional epoxy compound is diepoxybenzene.

11. The microcapsules of claim 1 wherein said cross linking agent is employed in an amount of 5 to 25 wt% and a compound introducing said functional group into the microcapsule in a range of 2 to 20 wt%, based upon a core of the microcapsule.

12. The microcapsules of claim 1 wherein said functional group is present in a concentration of at least 10^-9 mol. per 1 mg. of the solids content of the microcapsules.

13. The microcapsules of claim 12 wherein said functional group is present in a concentration of from 10^-9 to 10^-5 ml. per 1 mg. of solids content of the microcapsules.

14. The microcapsules of claim 1 wherein the cross linking agent is a compound selected from the group consisting of a dialdehyde, a diisocyanate, an amide ester, a disulfonyl chloride, a halonitrobenzene, a water-soluble carbodiamide, an isoxazolium salt, an alkyl chloroformate, a N,N'"'"'-o-phenylenedimaleimide ester or an m-maleimidobenzoyl-N-hydroxysuccinimide ester.

15. The microcapsules of claim 1 wherein the cross linking agent is a compound selected from the group consisting of glutaraldehyde, toluene-2,4-diisocyanate, p-phenylenedithioisocyanate, diethyl maloneimidate, 1-hydroxy-2,4-disulfonyl chloride, p,p'"'"'-difluoro-m,m'"'"'-dinitrophenylsulfonic acid, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride, 1-cyclohexyl-3-(2-morpholinyl-4-ethyl)carbodiimidomethyl-p-toluenesulfonic acid, N-ethyl-5-phenylisoxazolium-3'"'"'-sulfonic acid, and ethyl chloroformate.

16. The microcapsules of claim 1, having an average particle size of from 0.5 to 10 μ

m.