中药组分与组分生物药剂学分类系统构建(4)
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[28] He X, Kadomura S, Takekuma Y, et al. A new system forthe prediction of drug absorption using a pHcontrolled Caco2 model: evaluation of pHdependent soluble drugabsorption and pHrelated changes in absorption[J]. J Pharm Sci, 2004, 93 (1):71.
[29] 郁丹红,刘丹,张振海,等基于生物药剂学性质的中药组分剂型的设计技术[J]中国中药杂志,2012,37(19):2993, http://www.100md.com(刘丹 郁丹红 孙娥 贾晓斌)
[24] Amidon G L, LennernasH, Shah V P, et al. A theroretical basis for biopharmaceutical drug classification system: the correlation of dissolution and in vivo bioavailability[J]. Pharm Res, 1995, 12(3):413.
[25] FDA Center for Drug Evaluation and Research. Guidance for industry: waiver of in vivo bioavailability and bioequivalence studies for immediaterelease solid oral dosage forms based on a biopharmaceuticals classification system[EB/OL]. 20000113 http// www.fda.gov/ cder/guidance/ 3618fnl.pdf.
[26] 平其能. 中药成分的胃肠转运与剂型设计[M]. 北京:化学工业出版社, 2010.
[27] Li Z Q, He X, Gao X, et al. Study on dissolution and absorption of four dosage forms of isosorbidemononitrate: level A in vitroin vivo correlation[J]. Eur J Pharm Biopharm, 2011, 79(2): 364.
[28] He X, Kadomura S, Takekuma Y, et al. A new system forthe prediction of drug absorption using a pHcontrolled Caco2 model: evaluation of pHdependent soluble drugabsorption and pHrelated changes in absorption[J]. J Pharm Sci, 2004, 93 (1):71.
[29] 郁丹红,刘丹,张振海,等基于生物药剂学性质的中药组分剂型的设计技术[J]中国中药杂志,2012,37(19):2993, http://www.100md.com(刘丹 郁丹红 孙娥 贾晓斌)