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一种用于测定格列本脲和其他磺酰脲类药物的放射免疫分析法。

A radioimmunoassay for determination of glibenclamide and other sulfonylureas.

机构信息

, Hoechst AG, D-6230, Frankfurt 80.

出版信息

Pharm Res. 1984 Sep;1(5):215-20. doi: 10.1023/A:1016321313510.

Abstract

An antiserum was prepared for the determination of glibenclamide and for the estimation of other commercially available sulfonylureas. Rabbits were immunized with a glibenclamide-BSA conjugate. Tritiated glibenclamide was used as the tracer. The assay was performed in the presence of 8-anilinonaphthalenesulfonic acid to displace glibenclamide bound to serum protein, and free and antibody bound tracer were separated by dextran-coated charcoal. For glibenclamide determination in serum and plasma the limit of detection was 3 ng/ml. Sensitivity calculated for the whole determination range was 102 cpm for a 10 % concentration difference. Specificity studies showed a cross-reaction of less than 0.1 % for glibenclamide metabolite M1 and 9 % for metabolite M2. Other sulfonylurea drugs display cross-reactivities from 0.1% (chlorpropamide) to 190% (gliquidone). Both intra-assay and inter-assay imprecision were below 10 %. Accuracy was established by comparison of the present method with HPLC. The assay was applied to the specific determination of glibenclamide in clinical trials and for diagnosing factitious hypoglycemia caused by sulfonylureas.

摘要

制备了一种用于测定格列本脲和其他市售磺酰脲类药物的抗血清。兔子用格列本脲-BSA 缀合物免疫。氚标记的格列本脲被用作示踪剂。该测定法在 8-苯胺基萘磺酸的存在下进行,以置换与血清蛋白结合的格列本脲,并用葡聚糖包被的活性炭分离游离和抗体结合的示踪剂。用于血清和血浆中格列本脲的检测限为 3ng/ml。计算整个测定范围内的灵敏度为 10%浓度差异时为 102 cpm。特异性研究表明,格列本脲代谢物 M1 的交叉反应小于 0.1%,代谢物 M2 的交叉反应为 9%。其他磺酰脲类药物的交叉反应率从 0.1%(氯丙嗪)到 190%(格列喹酮)不等。内和间测定精密度均低于 10%。通过将本方法与 HPLC 进行比较来确定准确性。该测定法已应用于临床试验中格列本脲的特异性测定以及诊断磺酰脲类药物引起的假性低血糖。

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