Midha Kamal K, Shah Vinod P, Singh Gur Jai Pal, Patnaik Rabi
College of Pharmacy and Medicine, University of Saskatchewan, Saskatoon, SK, Canada.
J Pharm Sci. 2007 Apr;96(4):747-54. doi: 10.1002/jps.20786.
This is a summary report of the International Pharmaceutical Federation/Board of Pharmaceutical Sciences (FIP/BPS) international conference, Bio-International 2005, which was held October 24-26, 2005 at the Royal Pharmaceutical Society, in London, UK. Bioequivalence (BE) issues related to multisource locally delivered topical dosage forms, oral inhalation drug products, highly variable drug products (HVDP), and endogenously occurring drugs were discussed. The conference also focused on alternate approaches to assess BE for some of these drug products. Pharmacokinetic (PK) approaches like, dermatopharmacokinetics (DPK) for dermatological topical dosage forms, scaled average BE (s-ABE) where within-subject variability is considered for estimation of 90% confidence intervals to document BE for highly variable drugs (HVD) were recommended. In addition, issues and difficulties related to the BE assessment of oral inhalation products, role, and appropriateness of metabolites in BE assessment, importance of base line correction in BE assessment of endogenously occurring drugs, and waiver of BE study requirements for certain drugs based on a Biopharmaceutics Classification System (BCS), were also discussed.
这是国际药学联合会/药学科学委员会(FIP/BPS)国际会议——2005年生物国际会议的总结报告。该会议于2005年10月24日至26日在英国伦敦的皇家药学会举行。会议讨论了与多源局部给药的局部剂型、口腔吸入药品、高变异药品(HVDP)以及内源性药物相关的生物等效性(BE)问题。会议还重点探讨了评估其中一些药品生物等效性的替代方法。推荐了药代动力学(PK)方法,如用于皮肤科局部剂型的皮肤药代动力学(DPK),以及在估计90%置信区间以证明高变异药物(HVD)的生物等效性时考虑受试者内变异性的标化平均生物等效性(s-ABE)。此外,还讨论了与口腔吸入产品生物等效性评估相关的问题和困难、代谢物在生物等效性评估中的作用和适用性、内源性药物生物等效性评估中基线校正的重要性,以及基于生物药剂学分类系统(BCS)对某些药物豁免生物等效性研究要求的情况。