Toon S
Medeval Ltd, University of Manchester, UK.
Eur J Drug Metab Pharmacokinet. 1996 Apr-Jun;21(2):93-103. doi: 10.1007/BF03190257.
Biotechnology derived medicines will have an increasing impact not only upon medical practice but also upon the working lives of many pharmaceutical scientists. Whilst such medicines may be viewed as highly sophisticated to the clinician and scientist, the computer will still rightly demand that they are both efficacious and safe. Impacting as it does upon all phases of drug development and facilitating quantitative relationship between administered dose and systemic drug concentration, pharmacokinetics has an important role to play in the development of all medicines. Bioanalysis is an essential prelude to any pharmacokinetic investigation. For many biotechnology products the immunoassay and bioassay methodologies employed are often relatively non-specific and imprecise and yield assay dependent pharmacokinetic parameters. Other factors may also confound the pharmacokinetic evaluation of biotechnological products. In vivo binding proteins (including antibodies) may not only interfere with bioanalytical methodology but also have a significant effect on the pharmacokinetics and biological activity of certain macromolecules. Antibody formation is a particular problem in the preclinical evaluation of human proteins. Unlike most conventional pharmaceuticals, the rate and time of delivery into the systemic circulation is a fundamental component of the biological activity of many biological molecules.
生物技术衍生药物不仅将对医学实践产生越来越大的影响,也将对许多制药科学家的工作生活产生影响。虽然这类药物对临床医生和科学家来说可能被视为高度复杂,但计算机仍将合理地要求它们既有效又安全。由于药代动力学对药物研发的各个阶段都有影响,并促进给药剂量与全身药物浓度之间的定量关系,因此在所有药物的研发中都发挥着重要作用。生物分析是任何药代动力学研究的重要前奏。对于许多生物技术产品,所采用的免疫分析和生物分析方法往往相对不特异且不精确,得出的药代动力学参数依赖于分析方法。其他因素也可能混淆生物技术产品的药代动力学评估。体内结合蛋白(包括抗体)不仅可能干扰生物分析方法,还可能对某些大分子的药代动力学和生物活性产生重大影响。在人源蛋白的临床前评估中,抗体形成是一个特别的问题。与大多数传统药物不同,许多生物分子的生物活性的一个基本组成部分是其进入体循环的速度和时间。