Hydrodynamic investigation of USP dissolution test apparatus II

被引:95
作者
Bai, Ge
Armenante, Piero M.
Plank, Russell V.
Gentzler, Michael
Ford, Kenneth
Harmon, Paul
机构
[1] New Jersey Inst Technol, Dept Chem Engn, Newark, NJ 07102 USA
[2] Merck & Co Inc, West Point, PA 19486 USA
关键词
dissolution; testing; pharmaceutical testing; USP dissolution test apparatus; hydrodynamics; laser doppler velocimetry; LDV; computational fluid dynamics; CFD; coning;
D O I
10.1002/jps.20818
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
The USP Apparatus II is the device commonly used to conduct dissolution testing in the pharmaceutical industry. Despite its widespread use, dissolution testing remains susceptible to significant error and test failures, and limited information is available on the hydrodynamics of this apparatus. In this work, laser-Doppler velocimetry (LDV) and computational fluid dynamics (CFD) were used, respectively, to experimentally map and computationally predict the velocity distribution inside a standard USP Apparatus II under the typical operating conditions mandated by the dissolution test procedure. The flow in the apparatus is strongly dominated by the tangential component of the velocity. Secondary flows consist of an upper and lower recirculation loop in the vertical plane, above and below the impeller, respectively. A low recirculation zone was observed in the lower part of the hemispherical vessel bottom where the tablet dissolution process takes place. The radial and axial velocities in the region just below the impeller were found to be very small. This is the most critical region of the apparatus since the dissolving tablet will likely be at this location during the dissolution test. The velocities in this region change significantly over short distances along the vessel bottom. This implies that small variations in the location of the tablet on the vessel bottom caused by the randomness of the tablet descent through the liquid are likely to result in significantly different velocities and velocity gradients near the tablet. This is likely to introduce variability in the test. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:2327 / 2349
页数:23
相关论文
共 32 条
[1]
Experimentally-validated micromixing-based CFD model for fed-batch stirred-tank reactors [J].
Akiti, O ;
Armenante, PM .
AICHE JOURNAL, 2004, 50 (03) :566-577
[2]
ARMENANTE P, 1994, ICHEME S SER, V136, P349
[3]
Velocity profiles in a closed, unbaffled vessel: comparison between experimental LDV data and numerical CFD predictions [J].
Armenante, PM ;
Luo, CG ;
Chou, CC ;
Fort, I ;
Medek, J .
CHEMICAL ENGINEERING SCIENCE, 1997, 52 (20) :3483-3492
[4]
ARMENANTE PM, 1994, AICHE S SER, V90, P33
[5]
Ballard J., 2003, Dissolution Technology, V10, P6, DOI DOI 10.14227/DTL00303P6
[6]
Hydrodynamics-induced variability in the USP apparatus II dissolution test [J].
Baxter, JL ;
Kukura, J ;
Muzzio, FJ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 292 (1-2) :17-28
[7]
FLUID AND PARTICLE LASER DOPPLER VELOCITY-MEASUREMENTS AND MASS-TRANSFER PREDICTIONS FOR THE USP PADDLE METHOD DISSOLUTION APPARATUS [J].
BOCANEGRA, LM ;
MORRIS, GJ ;
JUREWICZ, JT ;
MAUGER, JW .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1990, 16 (09) :1441-1464
[8]
Turbulent flow in closed and free-surface unbaffled tanks stirred by radial impellers [J].
Ciofalo, M ;
Brucato, A ;
Grisafi, F ;
Torraca, N .
CHEMICAL ENGINEERING SCIENCE, 1996, 51 (14) :3557-3573
[9]
THE DEVELOPMENT OF USP DISSOLUTION AND DRUG RELEASE STANDARDS [J].
COHEN, JL ;
HUBERT, BB ;
LEESON, LJ ;
RHODES, CT ;
ROBINSON, JR ;
ROSEMAN, TJ ;
SHEFTER, E .
PHARMACEUTICAL RESEARCH, 1990, 7 (10) :983-987
[10]
Influence of dissolution medium agitation on release profiles of sustained-release tablets [J].
Costa, P ;
Lobo, JMS .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2001, 27 (08) :811-817