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一种用于检测麦角酸二乙酰胺(LSD)的在线免疫分析方法:与气相色谱 - 质谱联用(GC-MS)及阿布斯creen放射免疫分析(RIA)的比较

An online immunoassay for LSD: comparison with GC-MS and the Abuscreen RIA.

作者信息

McNally A J, Goc-Szkutnicka K, Li Z, Pilcher I, Polakowski S, Salamone S J

机构信息

Roche Diagnostic Systems, Somerville, New Jersey 08876, USA.

出版信息

J Anal Toxicol. 1996 Oct;20(6):404-8. doi: 10.1093/jat/20.6.404.

Abstract

A homogenous microparticle-based immunoassay has been developed for the detection of d-lysergic acid diethylamide (LSD) in human urine using the Online technology. This immunoassay is based on the principle of the kinetic interaction of microparticles in a solution where the drug content of the urine is directly proportional to the inhibition of the microparticle aggregation. Antibodies to LSD were obtained by immunizing goats with an LSD analogue derivatized through the indole nitrogen and conjugated to bovine thyroglobulin. The assay cutoff is 0.5 ng/mL LSD, and the clinical sensitivity for the detection of LSD and its metabolites in human urine samples is equivalent to the LSD Abuscreen RIA. Thirty-one samples previously screened LSD positive by Abuscreen RIA and confirmed by gas chromatography-mass spectrometry were analyzed by the Abuscreen OnLine LSD and Abuscreen LSD RIA assays. All thirty-one samples screened positive in the Abuscreen OnLine and Abuscreen RIA. OnLine's cross-reactivity to nor-LSD is greater than thirty-five percent; other structurally related compounds have similar cross-reactivity to that of the Abuscreen RIA. One thousand presumed negative urine samples were also analyzed; 992 (99.2%) of these gave negative results. The eight OnLine positive samples from this set were found to be negative by Abuscreen RIA. Typical qualitative within-run precision on the Hitachi 717 (at x = cutoff of 0.5 ng/mL; 0.5x, 1.0x, and 1.5x) was found to be less than 2.5%. Between-run precision was less than 3.0%.

摘要

已开发出一种基于均质微粒的免疫测定法,利用在线技术检测人尿中的d-麦角酸二乙酰胺(LSD)。这种免疫测定法基于溶液中微粒动力学相互作用的原理,其中尿液中的药物含量与微粒聚集的抑制呈正比。通过用经吲哚氮衍生化并与牛甲状腺球蛋白偶联的LSD类似物免疫山羊,获得了LSD抗体。该测定法的临界值为0.5 ng/mL LSD,在人尿样中检测LSD及其代谢物的临床灵敏度与LSD Abuscreen放射免疫测定法相当。通过Abuscreen在线LSD和Abuscreen LSD放射免疫测定法对31个先前经Abuscreen放射免疫测定法筛查为LSD阳性并经气相色谱-质谱法确证的样品进行了分析。所有31个样品在Abuscreen在线和Abuscreen放射免疫测定法中均筛查为阳性。在线法对去甲-LSD的交叉反应性大于35%;其他结构相关化合物与Abuscreen放射免疫测定法的交叉反应性相似。还对1000份假定为阴性的尿样进行了分析;其中992份(99.2%)结果为阴性。这组中8份在线法阳性的样品经Abuscreen放射免疫测定法检测为阴性。在日立717上(在x = 0.5 ng/mL临界值处;0.5x、1.0x和1.5x)典型的批内定性精密度小于2.5%。批间精密度小于3.0%。

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