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Development of an enzyme-linked immunosorbent assay for the determination of the linear alkylbenzene sulfonates and long-chain sulfophenyl carboxylates using antibodies generated by pseudoheterologous immunization

机译:酶联免疫吸附测定方法的开发,该方法使用伪异源免疫产生的抗体测定直链烷基苯磺酸盐和长链磺基苯基羧酸盐

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摘要

ELISA methods have been developed for screening contamination of water resources by linear alkyl benzene sulfonates (LAS) or the most immediate degradation products, the long chain sulfophenyl carboxylates, SPCs. The assay uses antibodies raised through pseudoheterologous immunization strategies using an equimolar mixture of two immunogens (SFA-IUR and 13C(13)-SPC-KLH) prepared by coupling N-(4-alkylphenyl)sulfonyl-3aminopropanoic acid (SFA) and p-(1-carboxy-13-tridecyl)phenylsulfonic acid (13C(13)-SPC) to keyhole limpet hemocyanin (KLH). The immunizing haptens have been designed to address recognition versus two different epitopes of the molecule. The SFA hapten maximizes recognition of the alkyl moiety while preserving the complexity of the different alkyl chains present in the LAS technical mixture. The 13C(13)-SPC hapten addresses recognition of the common and highly antigenic phenylsulfonic group. The antisera raised using this strategy have been shown to be superior to those obtained through homologous immunization procedures using a single substance. By using an indirect ELISA format, LAS and long-chain SPCs can be detected down to 1.8 and 0.2 mu g L-1, respectively. Coefficients of variation of 6 and 12% within and between assays, respectively, demonstrate immunoassay reproducibility. The assay can be used in media with a wide range of pH and ionic strength values. Preliminary experiments performed to assess matrix effects have demonstrated the potential applicability of the method as a screening tool to assess contamination by these types of surfactants in natural water samples.
机译:已开发出ELISA方法来筛选线性烷基苯磺酸盐(LAS)或最直接降解的产物长链磺基苯基羧酸盐SPC对水资源的污染。该测定使用通过伪异源免疫策略产生的抗体,使用两种免疫原(SFA-IUR和13C(13)-SPC-KLH)的等摩尔混合物,通过偶联N-(4-烷基苯基)磺酰基-3氨基丙酸(SFA)和p- (1-羧基-13-十三烷基)苯磺酸(13C(13)-SPC)到匙孔血蓝蛋白(KLH)。已经设计了免疫半抗原来解决与分子的两个不同表位相比的识别。 SFA半抗原最大程度地提高了烷基部分的识别率,同时保留了LAS技术混合物中存在的不同烷基链的复杂性。 13C(13)-SPC半抗原解决了常见的和高度抗原性的苯基磺酸基团的识别。已经显示出使用这种策略产生的抗血清优于通过使用单一物质的同源免疫程序获得的抗血清。通过使用间接ELISA格式,可以分别检测低至1.8和0.2μg L-1的LAS和长链SPC。在测定中和测定之间的变异系数分别为6%和12%,证明了免疫测定的可重复性。该测定法可用于pH和离子强度值范围很宽的介质中。为评估基质效应而进行的初步实验表明,该方法作为评估天然水样品中这些类型表面活性剂污染的筛选工具的潜在适用性。

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