Jamali F
Faculty of Pharmacy, University of Alberta, Edmonton, Canada.
J Clin Pharmacol. 1992 Oct;32(10):930-4. doi: 10.1002/j.1552-4604.1992.tb04641.x.
Despite the fact that many important drugs are chiral, for a variety of reasons they are marketed as racemates (i.e., an equal proportion of two enantiomers). Although enantiomers of racemic drugs often differ from one another in their pharmacodynamic and pharmacokinetic properties, bioequivalence assessments are made using nonstereospecific assays. Such an approach may provide a poor assessment of therapeutic equality. This can be true particularly for drugs with complicated pharmacokinetics and those that exhibit extensive stereoselectivity in their disposition kinetics. Accordingly, examples of bioequivalence studies based on stereospecific assays have started to appear in the literature. Fortunately, facile stereospecific assays have become available in the last several years for many drugs. Consequently, regulatory agencies have started to take the issue of stereochemistry into consideration in the assessment of bioequivalence, particularly from the standpoint of generic substitution.
尽管许多重要药物是手性的,但由于各种原因,它们以消旋体形式上市(即两种对映体的比例相等)。虽然外消旋药物的对映体在药效学和药代动力学性质上往往彼此不同,但生物等效性评估是使用非立体特异性分析方法进行的。这种方法可能无法很好地评估治疗等效性。对于药代动力学复杂的药物以及在处置动力学中表现出广泛立体选择性的药物来说尤其如此。因此,基于立体特异性分析的生物等效性研究实例已开始出现在文献中。幸运的是,在过去几年中,许多药物都有了简便的立体特异性分析方法。因此,监管机构在评估生物等效性时已开始考虑立体化学问题,特别是从仿制药替代的角度。