Claims
- 1. A method of detecting or determining relative amounts of target antibodies or antigens by reaction with specific binding partners thereto, wherein one of either the target or the binding partner is bound to a carrier and the other is unbound, wherein a complex of the carrier-bound target and the binding partner, or of the target and the carrier-bound binding partner, form an agglutinate which is optically detectable, said method comprising:
- providing a microreaction vessel, sized to receive at least one fluid sample or about 10-50 .mu.l, containing a slurry or suspension of inert particles and the known unbound target or binding partner thereto;
- adding about 10-50 .mu.l of a solution containing the carrier-bound target or binding partner to the vessel to form a target-binding partner complex which is carrier-bound and optically detectable;
- centrifuging the vessel; and
- observing the location of the carrier-bound complex to determine the presence of the target antibody or antigen to be detected, with a strongly positive reaction being indicated by a complex lying upon or in a top portion of a layer of the inert particles, a weakly positive reaction being indicated by a complex located within a lower portion of the layer of inert particles, and a negative reaction being indicated by the absence of a complex, with the carrier-bound target or carrier-bound binding partner lying beneath the inert particles.
- 2. The method of claim 1, wherein said inert particles have a particle size of from 10-200 microns.
- 3. The method of claim 2, wherein the inert particles are cross-linked polymers, glass or silica gel.
- 4. The method of claim 1, wherein the carrier is erythrocytes, leukocytes, platelets, latex particles or polymerized agarose.
- 5. The method of claim 1, wherein the microreaction vessel is mounted on or forms part of a centrifugable card comprising a card member and a plurality of elongated microreaction vessels lying side by side along an upper portion of the card member, said card member having a lower identifying indicia-receiving portion.
- 6. A method of detecting or determining relative amounts of analyte antibodies or antigens in a fluid sample by reaction with known antigen or antibody, respectively, binding partners exhibiting specific binding affinity thereto, wherein either the analyte or known antigens or antibodies are bound to a carrier, wherein a complex of the carrier-bound antigen and the analyte antibody, or of the carrier-bound antibody and the analyte antigen, form an agglutinate which is optically detectable, said method comprising:
- providing a microreaction vessel containing a slurry or suspension of inert particles;
- centrifuging the fluid sample and the binding partner in said vessel in the presence of the inert particles; and
- determining the presence of analyte antibodies or antigens by observing the location of any agglutinate, with a strongly positive reaction being indicated by an antigen-antibody complex lying upon a top portion of a layer of the inert particles, a weakly positive reaction being indicated by an antigen-antibody complex located within a lower portion of the layer of inert particles, and a negative reaction being indicated by the absence of an antigen-antibody complex with the carrier-bound antigen or antibody lying beneath the inert particles.
- 7. The method of claim 6, wherein the microreaction vessel is mounted on or forms part of a centrifugable card comprising a planar card member and a plurality of elongated microreaction vessels lying side by side along an upper portion of the card member, said card member having a lower identifying indicia-receiving portion.
- 8. Method of claim 7, wherein the antibodies or antigens detected are antigens or antibodies of blood groups, with different microreaction vessels on the card detecting a different antigen or antibody of the groups comprising A.sub.1, A.sub.2, A.sub.1 B, A.sub.2 B, A.sub.3, A.sub.3 B, A.sub.x, B, O, Du, C, E, c, e, or Cw.
- 9. Method of claim 8, wherein the antigen or the antibody is bound to erythrocytes.
- 10. The method of claim 6, wherein said inert particles have a particle size of from 10-200 microns.
- 11. The method of claim 6, wherein the inert particles are cross-linked polymers, glass or silica gel.
- 12. The method of claim 6, wherein the carrier is erythrocytes, leukocytes, platelets, latex particles or polymerized agarose.
- 13. Method of claim 6, wherein the carrier material is naturally colored or tagged.
- 14. Method of claim 6, wherein the carrier material is stained or is isotope, fluorescent, or enzyme labeled.
- 15. Method of claim 6, wherein the carrier material is erythrocytes, leukocytes or platelets.
- 16. Method of claim 6, wherein the inert particles are porous globules of polyacrylamide gel, of cross-linked dextran, of glass or of silica gel, having a particle size of from 10-200 microns.
- 17. The method of claim 6, wherein the antibodies or antigens detected are blood group antibodies or antigens.
- 18. The method of claim 6, wherein the antibodies are carrier bound and are antibodies against proteins, viruses, bacteria, or synthetically produced proteins.
- 19. The method of claim 6, wherein the antigens are carrier-bound and the components of body fluids.
- 20. The method of claim 19, wherein the body fluid is blood, serum components, or plasma components.
- 21. Method of claim 6, wherein the fluid sample is a blood specimen, and the antibody is specific for blood-group antigens.
- 22. Method of claim 6, wherein the microreaction vessel contains antibodies for determining the presence or absence of Rh antigens in a blood specimen.
Priority Claims (1)
Number |
Date |
Country |
Kind |
3240/87 |
Aug 1987 |
CHX |
|
Parent Case Info
This application is a continuation of U.S. application Ser. No. 08/140,494 filed Oct. 25, 1993, now abandoned which is a divisional of U.S. application Ser. No. 07/969,532 filed Oct. 30, 1992, now U.S. Pat. No. 5,338,689, which is a continuation of Ser. No. 07/684,459 filed Apr. 11, 1991, now abandoned, which is a continuation of Ser. No. 07/122,152, filed Nov. 11, 1987, now abandoned.
US Referenced Citations (13)
Foreign Referenced Citations (10)
Number |
Date |
Country |
39195 |
Nov 1981 |
EPX |
0194156 |
Sep 1986 |
EPX |
2236181 |
Jan 1975 |
FRX |
2554240 |
May 1985 |
FRX |
8502010 |
Aug 1986 |
FRX |
0194212 |
Sep 1986 |
FRX |
0224439 |
Jun 1987 |
FRX |
1005759 |
Apr 1957 |
DEX |
2017910 |
Oct 1979 |
GBX |
8300296 |
Mar 1983 |
WOX |
Non-Patent Literature Citations (6)
Entry |
Yapa, et al., "Use of papain treatment of NR latex to produce superior-quality rubbers," Chemical Abstracts 94 (18):59 May 4, 1981. |
Fudenberg et al. (ed), Basic and Clinical Immunology (3rd edition), Lange Medical Publications, Los Altos, Calif. (1980), pp. 373-376 and 398-404. |
Fisher Scientific Catalog (1983), pp. 180-184, 187-189 and 694. |
Stedman's Medical Dictionary (24th edition), Williams & Wilkins, Baltimore, p. 770. |
Lehninger, Biochemistry, Worth Publishers, Inc., New York, N.Y. (1970), pp. 141-143. |
Tietz, Fundamentals of Clinical Chemistry, W. B. Saunders Company, Philadelphia, Pa. (1970), p. 234. |
Divisions (1)
|
Number |
Date |
Country |
Parent |
969532 |
Oct 1992 |
|
Continuations (3)
|
Number |
Date |
Country |
Parent |
140494 |
Oct 1993 |
|
Parent |
684459 |
Apr 1991 |
|
Parent |
122152 |
Nov 1987 |
|