Light scatter-based immunoassay

Details Light scatter-based immunoassay Light scatter-based immunoassay

1995-06-07

2001-03-13

Le, Long V. (Department: 1641)

Chemistry: analytical and immunological testing

Involving an insoluble carrier for immobilizing immunochemicals

Carrier is particulate and the particles are of...

C435S007100, C435S006120, C436S501000, C436S518000, C436S525000, C436S527000, C436S534000, C436S164000

Reexamination Certificate

active

06200820

ABSTRACT:

BACKGROUND OF THE INVENTION
1 .Field of the Invention
The invention relates broadly to immunoassay methods for measuring one or more analytes in a fluid sample by measuring light scatter signals from particles in a flow particle analyzer. More particularly, the invention relates to measuring changes in light scatter signals from monodisperse microspheres as the result of analyte-mediated binding to such microspheres of colloidal particles.
2. Description of the Prior Art
Antibodies, antigens and many haptens exhibit high affinities, not only for their complementary proteins, but also for certain solid surfaces such as those found in the wells of plastic microtiter plates, walls of plastic test tubes, polymeric microspheres, and colloidal metal particles. Exploitation of these properties has led to a revolution in the field of diagnostic assay methods for the aforementioned analytes in fluid samples such as serum.
The ability to carry out antigen-antibody interactions on solid supports has greatly simplified the separation of analyte-containing immunocomplexes from unused reactants and interfering substances, such as those often present in biological fluids. Such systems are generally referred to as “solid phase immunoassays” or “immunosorbent assays”, and fall within the genus of “heterogeneous immunoassays.” While the phase separation steps in heterogeneous immunoassays are valuable in reducing interferences by nonspecific binding substances that generally have an adverse effect on the sensitivity of the assay method, such assays are cumbersome and expensive, and are a focal point for reliability problems in automated systems.
Additionally, such heterogeneous systems have the additional disadvantage of requiring that one or another member of the immunocomplex be labeled with a molecule that can be easily quantified. Such molecules are generally referred to as “reporter molecules” and include radioisotopes (radioimmunoassays, RIA), enzymes (enzyme-linked immunoassays generally coupled with a chromophore, ELISA), fluorescent molecules (fluorescence immunoassays, FIA), chemiluminescent molecules (CIA), gold particles, photosensitive molecules, and the like. For a review, see Kemeny, D. M., et al., Immunology Today 7, 67 (1986). Further, because of the limited number of chromophores and fluorophores available as reporter molecules, and the extensive overlap of emission spectra of such molecules, simultaneous assay of multiple analytes are not suitable using these reporters. For example, Cambridge Biotech's simultaneous EIA assays for HIV-
1
and HIV-
2
are not separable.
“Homogeneous immunoassay” is the term applied to immunoassays in which no phase separation occurs. Such systems, which include binding protein-coated particle agglutination assays, are useful because they have fewer steps to automate, and automation is mechanically, fluidically and electrically simple. Examples of immunoassays requiring no phase separation steps include: latex microsphere agglutination, hemagglutination, and fluorescence depolarization assays. Examples of latex bead agglutination assays for single analytes are found in U.S. Pat. Nos. 4,521,521; 4,184,849; 4,279,617; 4,191,739; and 4,851,329, and for multiple analytes in a single fluid sample in Hansen, copending U.S. patent application Ser. No. 07/883,574, now U.S. Pat. No. 5,286,452. Nephelometric or turbidimetric automated systems for agglutination or fluorescence depolarization assays are simple, inexpensive to construct, and, unlike heterogeneous assays, do not require frequent maintenance of the complicated phase separation apparatus.
The presence of interfering substances in body fluids however, has inhibited otherwise promising homogeneous immunoassay approaches from meeting the high sensitivity requirements of many medically important tests, such as aremet by ELISA and RIA. For reviews of this problem see, for example, Masson et al.,
Methods in Enzymology
, 74:115(1981) and Collett-Cassart et al.,
Clin Chem
., 27:64 (1981). By contrast, methods according to preferred embodiments of the present invention provide immunoassays that can be free from non-specific interferences, at least to a sensitivity level of about 5×10
−13
M. This level of sensitivity is two to three orders of magnitude greater than prior art homogeneous; latex bead agglutination assays. See, e.g., alpha-fetoprotein (3×10
−10
M, Collett-Cassart et al., above), urinary HCG (6×10
−11
M, Lentrichia et al.,
J. Immunol Meth
., 89:657(1986) (but exhibiting only an 87% correlation with RIA at analyte levels 20 times the claimed sensitivity limit), and serum digoxin by a fluorescence depolarization method (3×10
−10
M, S. Wong in D. Chan, ed.,
Immunoassay Automation
, Academic Press, 1992, p. 329).
Prior art approaches to eliminating or decreasing the undesirable effects of non-specific interfering substance on homogeneous immunoassays have been generally unsatisfactory. These include: high dilution of body fluid sample (Fritz et al.,
J. Immunol
., 108:110(1972), but this proportionally decreases sensitivity; using antibody fragments (Masson, Id.), but this approach is expensive and unpredictable; and, use of special conditions of pH, ionic strength, and buffer type, and/or addition of chelators or other scavengers (Masson, Id.), but these introduce multiple dependent factors that must be optimized for each analyte, and can become prohibitively expensive and cumbersome (Lim et al.,
J. Clin. Chem. Clin. Biochem
., 20:141(1982).
Other approaches to solving the non-specific interference problem have included using IgG-coated latex ultramicrospheres to inhibit non-specific reactions in a latex sphere agglutination assay that uses antibody fragments. The sensitivity of one such agglutination method using a Coulter principle electronic resistance flow particle analyzer with a 30 &mgr;m orifice was reported to be about 5×10
−13
to 4×10
−12
M. Sakai et al.,
Chem. Pharm. Bull
., 37:3010 (1989). The disadvantages of this approach is that the additional reagent (non-specific, IgG coated ultramicrospheres) has an incremental manufacturing, quality control and storage cost associated with it. Preferred methods according to the present invention remove this important disadvantage by combining the action of specific immunoreactivity with an action that can improve specificity, all in one reagent. In addition, although the Coulteic principle particle counter used by Sakai et al. yields quantitative results, the need for the small (30 &mgr;m) orifice in order to sense agglutination has the problem of clogging during agglutination reactions (Masson, Id.). Certain methods according to the present invention can use a sheath flow particle analyzer with a large orifice, which eliminates clogging. However, in the Sakai et al. approach, the frequency distribution of the amplitude of the detected signals from light scattering of specifically agglutinated particles (dimers, trimers, etc) presents a problem in Coulter volume overlap if simultaneous assays of more than one analyte are attempted, a problem not encountered in the present invention as multimers generally are not formed and multiple simultaneous assays can be performed without complex: signal processing algorithms to remove the problem of detection signal overlap.
Another problem encountered in prior art agglutination immunoassays is the need for agitation by mechanical mixers during the entire reaction period of reaction mixtures containing particles of one micron or greater (Masson, Id.). A further advantage of the preferred methods according to the present invention, insofar as automation is concerned, is that agitation of samples is not needed to complete the reaction during useful time frames.
Schutt et al., EP 0254430 and U.S. Pat. No. 5,017,009, show a scattered total internal reflectance (STIR) assay method for an analyte in which colloidal gold particles are used as a label for proteins that bind to a coated macroscopic plastic plate of optical qu

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