Pvlova I S, Lukin Iu V, Kovalenko V A, Avdeev D N, Kul'shin V A, Zubov V P
Bioorg Khim. 1994 Jul;20(7):731-9.
Non-instrumental immunoassays based on immunofiltration and microtiter particle agglutination (MPA) techniques have been developed using coloured polyacrolein latex. These methods have been applied to the quantification of the group-specific polysaccharide (PS) of S. pyogenes (group A streptococcus) and compared with standard ELISA tests. The most efficient method was MPA; as little as 0.05 ng A-PS/ml could be detected in 1.5 h. In comparison with ELISA test, the sensitivity of MPA was 10 times higher and the procedure was much simpler. The sensitivity of immunofiltration assay using both enzyme and latex conjugates was shown to be the same (50 ng/ml A-PS) and the duration of the assay 3-5 min. No cross-reactions of latex conjugates with non A streptococcus cell lysates have been observed. The developed methods are rapid, robust, easy to perform, don't need any sophisticated equipment and specially trained staff.
基于免疫过滤和微量滴定板颗粒凝集(MPA)技术,使用彩色聚丙烯醛乳胶开发了非仪器免疫测定法。这些方法已应用于化脓性链球菌(A组链球菌)群特异性多糖(PS)的定量分析,并与标准ELISA试验进行了比较。最有效的方法是MPA;在1.5小时内可检测到低至0.05 ng A-PS/ml。与ELISA试验相比,MPA的灵敏度高10倍,且操作过程要简单得多。使用酶和乳胶偶联物的免疫过滤测定法的灵敏度相同(50 ng/ml A-PS),测定持续时间为3-5分钟。未观察到乳胶偶联物与非A组链球菌细胞裂解物的交叉反应。所开发的方法快速、稳健、易于操作,不需要任何复杂设备和经过专门培训的人员。