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人唾液中分泌型过氧化物酶和髓过氧化物酶的灵敏免疫分析方法。

Sensitive immunometric assays for secretory peroxidase and myeloperoxidase in human saliva.

作者信息

Vilja P, Lumikari M, Tenovuo J, Sievers G, Tuohimaa P

机构信息

Department of Biomedical Sciences, University of Tampere, Finland.

出版信息

J Immunol Methods. 1991 Aug 9;141(2):277-84. doi: 10.1016/0022-1759(91)90154-8.

Abstract

We have developed specific immunoassays for secretory peroxidase (SP) and for myeloperoxidase (MP) (polymorphonuclear leukocyte-derived peroxidase) in human saliva. Antibodies against SP and MP were produced using bovine milk lactoperoxidase (LP) and human MP as the immunogens, respectively. The methods developed are non-isotopic immunometric assays using biotinylated antibodies and avidin-enzyme conjugate. The detection limit was 0.1 ng/ml and the performance time less than 3 h for both assays. The determination ranges were 0.5-100 ng LP (SP)/ml and 0.5-200 ng MP/ml with intra- and interassay CVs of 4.3% and 15.6% for SP and 3.7% and 10.8% for MP, respectively. The mean analytical recoveries were 108.9% (SP) and 91.5% (MP). These assays correlated well (r = 0.849-0.871) with the colorimetric assays based on the oxidation of thiocyanate or chloride by peroxidases. However, compared to the colorimetric methods the new immunometric assays are much more sensitive and specific for salivary SP and MP. The assays are also more rapid since extensive dialysis to remove endogenous thiocyanate is not required.

摘要

我们已经开发出了针对人唾液中分泌型过氧化物酶(SP)和髓过氧化物酶(MP,多形核白细胞衍生的过氧化物酶)的特异性免疫测定法。分别使用牛乳过氧化物酶(LP)和人MP作为免疫原制备了抗SP和抗MP的抗体。所开发的方法是使用生物素化抗体和抗生物素蛋白 - 酶缀合物的非同位素免疫测定法。两种测定法的检测限均为0.1 ng/ml,检测时间均少于3小时。SP的测定范围为0.5 - 100 ng LP(SP)/ml,MP的测定范围为0.5 - 200 ng MP/ml,SP的批内和批间变异系数分别为4.3%和15.6%,MP的批内和批间变异系数分别为3.7%和10.8%。平均分析回收率分别为108.9%(SP)和91.5%(MP)。这些测定法与基于过氧化物酶氧化硫氰酸盐或氯化物的比色测定法相关性良好(r = 0.849 - 0.871)。然而,与比色法相比,新的免疫测定法对唾液中的SP和MP更敏感、更特异。该测定法也更快,因为不需要进行广泛的透析来去除内源性硫氰酸盐。

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