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通过快速灵敏的放大发光邻近均相测定法检测冈田酸。

Okadaic Acid Detection through a Rapid and Sensitive Amplified Luminescent Proximity Homogeneous Assay.

机构信息

College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, 310018, China.

出版信息

Toxins (Basel). 2023 Aug 14;15(8):501. doi: 10.3390/toxins15080501.

Abstract

Okadaic acid (OA), a marine biotoxin produced by microalgae, poses a significant threat to mariculture, seafood safety, and human health. The establishment of a novel, highly sensitive detection method for OA would have significant practical and scientific implications. Therefore, the purpose of this study was to develop an innovative approach for OA detection. A competitive amplified luminescent proximity homogeneous assay (AlphaLISA) was developed using the principle of specific antigen-antibody binding based on the energy transfer between chemiluminescent microspheres. The method was non-washable, sensitive, and rapid, which could detect 2 × 10-200 ng/mL of OA within 15 min, and the detection limit was 4.55 × 10 ng/mL. The average intra- and inter-assay coefficients of variation were 2.54% and 6.26%, respectively. Detection of the actual sample results exhibited a good correlation with high-performance liquid chromatography. In conclusion, a simple, rapid, sensitive, and accurate AlphaLISA method was established for detecting OA and is expected to significantly contribute to marine biotoxin research.

摘要

冈田酸(OA)是一种由微藻产生的海洋生物毒素,对海水养殖业、海鲜安全和人类健康构成重大威胁。建立一种新型的、高灵敏度的 OA 检测方法具有重要的实际意义和科学意义。因此,本研究旨在开发一种 OA 检测的新方法。基于化学发光微球之间的能量转移,利用特定抗原-抗体结合的原理,建立了竞争性扩增发光邻近均相分析(AlphaLISA)方法。该方法无需洗涤,灵敏且快速,可在 15 分钟内检测到 2×10-200ng/mL 的 OA,检测限为 4.55×10ng/mL。平均批内和批间变异系数分别为 2.54%和 6.26%。实际样品检测结果与高效液相色谱法具有良好的相关性。总之,建立了一种简单、快速、灵敏、准确的 AlphaLISA 方法来检测 OA,有望为海洋生物毒素研究做出重要贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1e/10467062/42611d697130/toxins-15-00501-g001.jpg

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