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用于测定人血浆中普伐他汀的新型高灵敏度酶免疫测定法。

New highly sensitive enzyme immunoassay for the determination of pravastatin in human plasma.

作者信息

Darwish Ibrahim A, Al-Obaid Abdul-Rahman M, Al-Malaq Hamoud A

机构信息

Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.

出版信息

Talanta. 2009 Oct 15;79(5):1478-83. doi: 10.1016/j.talanta.2009.06.021. Epub 2009 Jun 16.

Abstract

New highly sensitive enzyme immunoassay (EIA) has been developed and validated for the determination of pravastatin (PRV) in human plasma samples. PRV was coupled to keyhole limpt hemocyanin (KLH) and bovine serum albumin (BSA) via its terminal carboxylic acid group by carbodiimide reagent. PRV-KLH conjugate was used as an immunogen for raising anti-PRV polyclonal antibody in rabbits. The generated anti-PRV antibody recognized PRV with high affinity and selectivity. PRV-BSA conjugate was immobilized onto microwell plates and used as a solid phase. The assay involved a competitive binding reaction between PRV, in plasma sample, and the immobilized PRV-BSA for the binding sites on a limited amount of the anti-PRV antibody. The anti-PRV antibody bound to the plate wells was quantified with horseradish peroxidase-labeled anti-immunoglobulin second anti-rabbit IgG antibody and 3,3',5,5'-tetramethylbenzidine as a substrate for the peroxidase enzyme. The concentration of PRV in the sample was quantified by its ability to inhibit the binding of the anti-PRV antibody to the immobilized PRV-BSA and subsequently the color development in the assay wells. The conditions of the proposed EIA were investigated and the optimum conditions were employed in the determination of PRV in plasma samples. The assay limit of detection was 0.2 ng mL(-1) and the effective working range at relative standard deviation (RSD) of <or=5% was 0.5-20 ng mL(-1). The mean analytical recovery of PRV from spiked plasma was 100.9+/-2.98%. The precision of the assay was satisfactory; RSD was 2.61-3.70 and 3.96-4.17% for intra- and inter-assay precision, respectively. The analytical procedure is convenient, and one can analyze approximately 200 samples per working day, facilitating the processing of large-number batch of samples. The proposed EIA has a great value in the routine analysis of PRV in plasma samples for its therapeutic monitoring and pharmacokinetic studies.

摘要

已开发并验证了一种新型高灵敏度酶免疫分析法(EIA),用于测定人血浆样本中的普伐他汀(PRV)。通过碳二亚胺试剂,PRV经其末端羧酸基团与钥孔血蓝蛋白(KLH)和牛血清白蛋白(BSA)偶联。PRV - KLH偶联物用作免疫原,在兔体内产生抗PRV多克隆抗体。所产生的抗PRV抗体以高亲和力和选择性识别PRV。PRV - BSA偶联物固定在微孔板上,用作固相。该分析涉及血浆样本中的PRV与固定化的PRV - BSA之间针对有限量抗PRV抗体上的结合位点的竞争性结合反应。用辣根过氧化物酶标记的抗免疫球蛋白第二抗兔IgG抗体和3,3',5,5'-四甲基联苯胺作为过氧化物酶的底物,对结合到板孔上的抗PRV抗体进行定量。样本中PRV的浓度通过其抑制抗PRV抗体与固定化PRV - BSA结合以及随后测定孔中显色的能力来定量。研究了所提出的EIA的条件,并将最佳条件用于血浆样本中PRV的测定。该分析方法的检测限为0.2 ng mL(-1),相对标准偏差(RSD)≤5%时的有效工作范围为0.5 - 20 ng mL(-1)。加标血浆中PRV的平均分析回收率为100.9±2.98%。该分析方法的精密度令人满意;批内精密度的RSD为2.61 - 3.70%,批间精密度的RSD分别为3.96 - 4.17%。该分析程序简便,每个工作日可分析约200个样本,便于大量样本的处理。所提出的EIA在血浆样本中PRV的治疗监测和药代动力学研究的常规分析中具有重要价值。

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