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采用酶联免疫吸附测定法对人体血液中的石房蛤毒素进行定量分析。

Quantification of saxitoxin in human blood by ELISA.

作者信息

Wharton Rebekah E, Feyereisen Melanie C, Gonzalez Andrea L, Abbott Nicole L, Hamelin Elizabeth I, Johnson Rudolph C

机构信息

Battelle Memorial Institute at the Centers for Disease Control and Prevention, Atlanta, GA, USA.

Oak Ridge Institute for Science and Education Fellow at the Centers for Disease Control and Prevention, Atlanta, GA, USA.

出版信息

Toxicon. 2017 Jul;133:110-115. doi: 10.1016/j.toxicon.2017.05.009. Epub 2017 May 7.

Abstract

Saxitoxin (STX) is a potent marine toxin that causes paralytic shellfish poisoning (PSP) which can result in significant morbidity and mortality in humans. Low lethal doses, rapid onset of PSP symptoms, and brief STX half-life in vivo require sensitive and rapid diagnostic techniques to monitor human exposures. Our laboratory has validated an enzyme-linked immunosorbent assay (ELISA) for quantitative detection of STX from 0.020 to 0.80 ng/mL in human whole blood and from 0.06 to 2.0 ng/mL in dried human blood which is simple, sensitive, rapid, and cost-effective. To our knowledge, this is the first validated method for the quantitation of saxitoxin in whole blood. Microsampling devices were used in sample collection which allows for standardized collection of blood, stable storage, and cost-efficient shipping. Quality control precision and accuracy were evaluated over the course of validation and were within 20% of theoretical concentrations. No detectable background concentrations of STX were found among fifty whole blood and dried blood convenience samples. Additionally, ten spiked individual whole blood and dried blood samples were tested for accuracy and precision and were within 20% of theoretical concentrations. Gonyautoxins 2&3 (GTX2&3) cross-reacted with this ELISA by 21%, but all other structurally related PSP toxins tested cross-reacted less than two percent. While clinical diagnosis or treatment of PSP would be unaffected by GTX2&3 cross-reactivity by ELISA, to accurately quantify individual PSP toxins, these results should be coupled with high performance liquid chromatography mass spectrometry measurements.

摘要

石房蛤毒素(STX)是一种强效海洋毒素,可导致麻痹性贝类中毒(PSP),进而可能在人类中引发严重发病和死亡。PSP症状的低致死剂量、快速发作以及STX在体内的短暂半衰期,都需要灵敏且快速的诊断技术来监测人类接触情况。我们实验室已验证了一种酶联免疫吸附测定法(ELISA),可用于定量检测人全血中0.020至0.80纳克/毫升以及干血中0.06至2.0纳克/毫升的STX,该方法简便、灵敏、快速且经济高效。据我们所知,这是首个经过验证的全血中石房蛤毒素定量方法。样本采集采用了微量采样装置,可实现血液的标准化采集、稳定储存以及经济高效的运输。在验证过程中评估了质量控制的精密度和准确度,结果在理论浓度的20%以内。在五十份全血和干血便利样本中未发现可检测到的STX背景浓度。此外,对十个加标的个体全血和干血样本进行了准确度和精密度测试,结果在理论浓度的20%以内。膝沟藻毒素2和3(GTX2&3)与该ELISA的交叉反应率为21%,但测试的所有其他结构相关的PSP毒素交叉反应率均低于2%。虽然ELISA对GTX2&3的交叉反应性不会影响PSP的临床诊断或治疗,但为了准确量化个体PSP毒素,这些结果应与高效液相色谱质谱测量相结合。

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