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高灵敏度酶联免疫吸附测定法检测多种人体生物体液中的紫杉醇

High sensitivity ELISA determination of taxol in various human biological fluids.

作者信息

Svojanovsky S R, Egodage K L, Wu J, Slavik M, Wilson G S

机构信息

Department of Chemistry, University of Kansas, Lawrence 66045, USA.

出版信息

J Pharm Biomed Anal. 1999 Jul;20(3):549-55. doi: 10.1016/s0731-7085(99)00073-4.

Abstract

Taxol (paclitaxel)--the natural product isolated from Pacific yew (Taxus brevifolia)--is a novel agent with high activity in the treatment of patients with several malignant tumors including those resistant to other cytotoxic drugs. The therapeutic index of this promising anticancer drug could be further increased by the exploration of its pharmacokinetic pharmacodynamic relationship in cancer patients. Since taxol is highly protein bound, a very specific and highly sensitive analytical method is required in order to determine free, protein unbound and biologically active taxol species in human physiological fluids: plasma; plasma ultrafiltrate; and salivary fluids. In order to accomplish this, a new indirect competitive enzyme-linked immunosorbent assay (ELISA), for quantitating such a low bioactive taxol concentration level, has been developed in our laboratories. This method uses taxol competitive inhibition of mouse anti-taxol antibodies binding to the solid phase coated antigen 7-succinyltaxol-bovine serum albumin. This indicates recognition of the active taxol in the solution phase, where a diluted horseradish peroxidase labeled goat anti-mouse enzyme conjugate is used. While employing this technique, after systematic optimization of the experimental conditions, we are able to detect the anticipated taxol in plasma ultrafiltrate and salivary fluids at the concentration level of subpicogram per milliliter. The working range of the assay is approximately five orders in magnitude, i.e. from pg ml(-1) to 100 ng ml(-1). The clinical part of this study verified the working range of the ELISA method using samples of physiological fluids from a cancer patient treated with 3 h intravenous (i.v.) infusion of this drug. Our results of taxol determination in plasma, plasma ultrafiltrate and saliva demonstrate the applicability of the newly developed ELISA method for further pharmacokinetic studies of free, biologically active taxol species in cancer patients.

摘要

紫杉醇(paclitaxel)——从太平洋紫杉(短叶红豆杉,Taxus brevifolia)中分离出的天然产物——是一种新型药物,对包括那些对其他细胞毒性药物耐药的多种恶性肿瘤患者具有高活性。通过探索其在癌症患者中的药代动力学与药效学关系,这种有前景的抗癌药物的治疗指数有望进一步提高。由于紫杉醇与蛋白质高度结合,为了测定人体生理体液(血浆、血浆超滤物和唾液)中游离的、未与蛋白质结合的以及具有生物活性的紫杉醇种类,需要一种非常特异且高度灵敏的分析方法。为此,我们实验室开发了一种新的间接竞争酶联免疫吸附测定法(ELISA),用于定量如此低的生物活性紫杉醇浓度水平。该方法利用紫杉醇竞争性抑制小鼠抗紫杉醇抗体与固相包被抗原7 - 琥珀酰紫杉醇 - 牛血清白蛋白的结合。这表明在溶液相中能够识别活性紫杉醇,在此相中使用稀释的辣根过氧化物酶标记的山羊抗小鼠酶结合物。在采用该技术时,经过系统优化实验条件后,我们能够在血浆超滤物和唾液中检测到预期的紫杉醇,其浓度水平为每毫升亚皮克。该测定法的工作范围约为五个数量级,即从皮克/毫升(pg ml⁻¹)到100纳克/毫升(ng ml⁻¹)。本研究的临床部分使用了一名接受该药物3小时静脉输注治疗的癌症患者的生理体液样本,验证了ELISA方法的工作范围。我们在血浆、血浆超滤物和唾液中测定紫杉醇的结果表明,新开发的ELISA方法适用于进一步研究癌症患者中游离的、具有生物活性的紫杉醇种类的药代动力学。

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