Chinese Journal of Clinical Pharmacology and Therapeutics ›› 1997, Vol. 2 ›› Issue (1): 53-56.
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Received:
1996-11-11
Online:
1997-03-26
Published:
2020-12-04
CLC Number:
1 Gibaldi M,Perrier D.Pharmacokinetics. 2nd ed,Marcel Dekker,1982 2 Gibaldi M,McNamara. Steady-state concentrations of drugs with short half-lives when administered in oral sustained-rclease formulations. Int J Pharm,1979,2:167 3 Purich E.Bioavailability/Bioequivalency regulations:An FDA perspective. In Albert KS ed“Drug Absorption and disposition:Statistical Considerations",Americal Pharmaeutical Association,W ashington DC,1980:115 4 Cohen A. Gonzalen MA,Mroszozak EJ,et al.Evaluation of the pharmacokinetios of Naproxen from a 500-mg controlled relcased tablets. Current Therapeutic Research,1988,43(6):1109 5 Wanwimolruk S,W anwimolruk SZ,Zoest AR. Sensitive HPLC assay for ketoprofen in human plasma and its application to pharmacokinetic study. Journal of Liquid Chromatography,1991,14(20):3685 6 American Pharmaceutical Magnufacturers Association. Bioequivalence of soild oral dosage forms. Washington DC,1986 7 Skelly JP.AmidonA,Barr WH. et al. In viro and in vivo lesting and coreation for dorsage forms.Report of the 2nd Workshop bheld Dec. Washinnton DC. U.S.A. J Controlled Reseale,1988,14:95 8 ShargeiL,Yu ABC. Applied Biopharmacy and Pharmacokinetics. 2nd ed,1985 9 Interc hageable multi-source pharmaceutical products. WHO 6 Dec,1993 10 Untied States Pharmacopeoia 23 ed. 1995:1919 11 黄圣凯,韩可勤.生物等效性评价的几种方法.中国临床药理学杂志,1993,9:246. 12 张霖泽,王兰勤,Shah NH.口服控释制剂的质量评价中国药学杂志1995,30(6):366 |
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