Levinson S S
J Clin Microbiol. 1979 Sep;10(3):334-8. doi: 10.1128/jcm.10.3.334-338.1979.
Soluble, group A, B, C, and G beta-hemolytic streptococcal antigens were successfully identified in a prototype spectrophotometric system by an immunochemical turbidimetric assay. Any spectrophotometic system which can take a zero reading followed by a second reading 2 or more min later can be used for the assay. Maximum absorbance was obtained near a wavelength of 340 nm. A wide range of linearity between antigen concentration and absorbance was observed at some antibody dilutions, resulting in a simple assay which can be used to quantitate amounts of antigen in solution. Minimal cross-reactions that present no problem in interpretation was observed. Simulated emergency samples were solubilized and assayed for group A and B bacteria within 3 h of colony recognition. Reproducibility of the absorbance resulting from the antibody-antigen reaction was great, with low coefficients of variation over a period of 50 days. The simplicity of the assay solutions, requiring only antisera and a buffer, and the accessibility to high levels of quality control are among the greatest assets of the technique to clinical laboratories.
通过免疫化学比浊法在一个原型分光光度系统中成功鉴定出可溶性A、B、C和G组β溶血性链球菌抗原。任何能够进行零读数,然后在2分钟或更长时间后进行第二次读数的分光光度系统都可用于该测定。在340nm波长附近获得最大吸光度。在某些抗体稀释度下,观察到抗原浓度与吸光度之间有很宽的线性范围,从而形成了一种可用于定量溶液中抗原量的简单测定方法。观察到最小的交叉反应,这在解释中没有问题。模拟紧急样本在识别菌落的3小时内进行溶解,并对A组和B组细菌进行检测。抗体-抗原反应产生的吸光度的重现性很好,在50天内变异系数很低。该测定方法的溶液简单,只需要抗血清和缓冲液,并且易于进行高水平的质量控制,这些都是该技术对临床实验室最大的优势。