Biowaiver Monographs for Immediate Release Solid Oral Dosage Forms: Piroxicam

被引:31
|
作者
Shohin, Igor E. [1 ,2 ]
Kulinich, Julia I. [1 ,2 ]
Ramenskaya, Galina V. [1 ,2 ]
Abrahamsson, Bertil [3 ]
Kopp, Sabine [4 ]
Langguth, Peter [5 ]
Polli, James E. [6 ]
Shah, Vinod P. [7 ]
Groot, D. W. [8 ]
Barends, Dirk M. [8 ]
Dressman, Jennifer B. [9 ]
机构
[1] Sechenov First Moscow State Med Univ, Moscow, Russia
[2] Inst Clin Pharmacol, Sci Ctr Expertise Med Prod, Moscow, Russia
[3] AstraZeneca R&D, Molndal, Sweden
[4] WHO, Geneva, Switzerland
[5] Johannes Gutenberg Univ Mainz, D-55122 Mainz, Germany
[6] Univ Maryland, Baltimore, MD 21201 USA
[7] Int Pharmaceut Federat FIP, The Hague, Netherlands
[8] RIVM Natl Inst Publ Hlth & Environm, Bilthoven, Netherlands
[9] Goethe Univ Frankfurt, Inst Pharmaceut Technol, D-60054 Frankfurt, Germany
关键词
piroxicam; absorption; biopharmaceutics classification system (BCS); permeability; solubility; dissolution; regulatory science; DISSOLUTION; BIOAVAILABILITY; PERMEABILITY; EQUILIBRIA; ADULT; AGENT; DRUGS; BCS;
D O I
10.1002/jps.23799
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Literature and experimental data relevant to the decision to allow a waiver of in vivo bioequivalence (BE) testing for the approval of immediate release (IR) solid oral dosage forms containing piroxicam in the free acid form are reviewed. Piroxicam solubility and permeability, its therapeutic use and therapeutic index, pharmacokinetic properties, data related to the possibility of excipient interactions and reported BE/bioavailability (BA), and corresponding dissolution data are taken into consideration. The available data suggest that according to the current biopharmaceutics classification system (BCS) and all current guidances, piroxicam would be assigned to BCS Class II. The extent of piroxicam absorption seems not to depend on manufacturing conditions or excipients, so the risk of bioinequivalence in terms of area under the curve (AUC) is very low, but the rate of absorption (i.e., BE in terms of C-max) can be affected by the formulation. Current in vitro dissolution methods may not always reflect differences in terms of Cmax for BCS Class II weak acids; however, minor differences in absorption rate of piroxicam would not subject the patient to unacceptable risks: as piroxicam products may be taken before or after meals, the rate of absorption cannot be considered crucial to drug action. Therefore, a biowaiver for IR piroxicam solid oral dosage form is considered feasible, provided that (a) the test product contains only excipients, which are also present in IR solid oral drug products containing piroxicam, which have been approved in ICH or associated countries, for instance, those presented in Table 3 of this paper; (b) both the test and comparator drug products dissolve 85% in 30 min or less at pH 1.2, 4.5, and 6.8; and (c) the test product and comparator show dissolution profile similarity in pH 1.2, 4.5, and 6.8. When not all of these conditions can be fulfilled, BE of the products should be established in vivo. (C) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:367 / 377
页数:11
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