I. Garthwaite, K. M. Ross, C. Miles, R. P. Hansen, D. Foster, A. Wilkins, N. Towers
{"title":"Polyclonal antibodies to domoic acid, and their use in immunoassays for domoic acid in sea water and shellfish.","authors":"I. Garthwaite, K. M. Ross, C. Miles, R. P. Hansen, D. Foster, A. Wilkins, N. Towers","doi":"10.1002/(SICI)1522-7189(199805/08)6:3/4<93::AID-NT15>3.0.CO;2-9","DOIUrl":null,"url":null,"abstract":"Ovine antibodies raised against conjugates linked through the secondary amino group of domoic acid (1) were used, together with activated-ester-derived conjugates of domoic acid (DA) as the plate coater, to develop a robust indirect competitive enzyme-linked immunosorbent assay (cELISA) for DA in shellfish and seawater. The ELISA was used to analyze shellfish samples for DA, and was compatible with several extraction procedures. The ELISA had a detection limit below 0.01 ng ml(-1), a limit of quantitation (LOQ) of 0.15 ng ml(-1) and a working range of 0.15-15 ng ml(-1) DA. The LOQ is equivalent to 38 ng g(-1) DA in shellfish flesh, assuming a 250-fold dilution during extraction. This is more than 500 times lower than the maximum permitted level (20 microg g(-1) flesh). The ELISA is designed for use alongside regulatory analyses, and, following formal validation, should be available for pre-screening of regulatory shellfish flesh samples. The ELISA was also shown to be appropriate for analysis of DA in algal cultures and in samples of seawater, and thus has the potential to provide early warning of developing algal blooms.","PeriodicalId":18777,"journal":{"name":"Natural toxins","volume":"22 1","pages":"93-104"},"PeriodicalIF":0.0000,"publicationDate":"1998-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"91","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural toxins","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/(SICI)1522-7189(199805/08)6:3/4<93::AID-NT15>3.0.CO;2-9","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 91
Abstract
Ovine antibodies raised against conjugates linked through the secondary amino group of domoic acid (1) were used, together with activated-ester-derived conjugates of domoic acid (DA) as the plate coater, to develop a robust indirect competitive enzyme-linked immunosorbent assay (cELISA) for DA in shellfish and seawater. The ELISA was used to analyze shellfish samples for DA, and was compatible with several extraction procedures. The ELISA had a detection limit below 0.01 ng ml(-1), a limit of quantitation (LOQ) of 0.15 ng ml(-1) and a working range of 0.15-15 ng ml(-1) DA. The LOQ is equivalent to 38 ng g(-1) DA in shellfish flesh, assuming a 250-fold dilution during extraction. This is more than 500 times lower than the maximum permitted level (20 microg g(-1) flesh). The ELISA is designed for use alongside regulatory analyses, and, following formal validation, should be available for pre-screening of regulatory shellfish flesh samples. The ELISA was also shown to be appropriate for analysis of DA in algal cultures and in samples of seawater, and thus has the potential to provide early warning of developing algal blooms.
利用针对软骨藻酸(1)二级氨基连接偶联物的羊抗体,以及软骨藻酸(DA)的活化酯衍生偶联物作为板涂剂,建立了一种针对贝类和海水中DA的间接竞争性酶联免疫吸附试验(cELISA)。该酶联免疫吸附法用于贝类样品的DA分析,并与几种提取方法兼容。ELISA的检出限小于0.01 ng ml(-1),定量限为0.15 ng ml(-1),工作范围为0.15 ~ 15 ng ml(-1) DA。假设提取过程中稀释250倍,LOQ相当于贝类肉中的38 ng g(-1) DA。这比最大允许水平(20微克g(-1)肉)低500多倍。ELISA设计用于与监管分析一起使用,并且在正式验证之后,应可用于监管贝类肉样品的预筛选。该酶联免疫吸附试验也被证明适用于分析藻类培养物和海水样品中的DA,因此有可能提供发生藻华的早期预警。