Controlled submicro particle formation of ampicillin by supercritical antisolvent precipitation

被引:57
作者
Tenorio, A. [1 ]
Gordillo, M. D. [1 ]
Pereyra, C. [1 ]
Martinez de la Ossa, E. J. [1 ]
机构
[1] Univ Cadiz, Fac Sci, Dept Chem Engn, Cadiz 11510, Spain
关键词
supercritical antisolvent; ampicillin; drug; precipitation; particle size;
D O I
10.1016/j.supflu.2006.07.003
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A supercritical antisolvent (SAS) technique has been used in the precipitation of ampicillin (APC), one of the world's most widely prescribed antibiotics, to control its particle size (PS) and particle size distribution (PSD). The influences of different solvents and pressure on morphologies, PS and PSD have been investigated. Three different solvents: N-methylpyrrolidone (NMP), dimethylsuffoxide (DMSO), and ethyl alcohol (EtOH) have been assayed. Experimental conditions (150 bar, 313 K, 20 mg/mL and ratio of CO2 flow rate/liquid flow rate equal to 15, on a mass basis at the process operating conditions) were kept constant throughout the course of this investigation. Through simply changing the APC-liquid solvent system we observed large variations in PS and PSD, accompanied by different particles morphologies. The APC-NMP proved to be the best system for controlling the precipitation of ampicillin; both compact particles and spherical microparticles (mean diameter = 0.26 mu m and standard deviation = 0.08 mu m) were obtained. In a second study, ampicillin has been successfully processed in the range of 80-150 bar using NMP as liquid solvent under constant experimental conditions. A change from 80 to 100 bar led to a large reduction of the mean PS and PSD, and no significant differences were found at pressures higher than 100 bar. Conversely, an increase in pressure produced better sphericity in particle shape. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:308 / 316
页数:9
相关论文
共 39 条
[1]   Analysis of the supersaturation and precipitation process with supercritical CO2 [J].
Bristow, S ;
Shekunov, T ;
Shekunov, BY ;
York, P .
JOURNAL OF SUPERCRITICAL FLUIDS, 2001, 21 (03) :257-271
[2]   Dense gas anti-solvent processes for pharmaceutical formulation [J].
Dehghani, F ;
Foster, NR .
CURRENT OPINION IN SOLID STATE & MATERIALS SCIENCE, 2003, 7 (4-5) :363-369
[3]   Droplet mass transfer, intradroplet nucleation and submicron particle production in two-phase flow of solvent-supercritical antisolvent emulsion [J].
Dukhin, SS ;
Shen, Y ;
Dave, R ;
Pfeffer, R .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2005, 261 (1-3) :163-176
[4]  
EVGENYI GZ, 1996, J PHARM SCI, V85, P1137
[5]   Polymorphic properties of micronized carbamazepine produced by RESS [J].
Gosselin, PM ;
Thibert, R ;
Preda, M ;
McMullen, JN .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 252 (1-2) :225-233
[6]   Measurements and correlation of high-pressure VLE of binary CO2-alcohol systems (methanol, ethanol, 2-methoxyethanol and 2-ethoxyethanol) [J].
Joung, SN ;
Yoo, CW ;
Shin, HY ;
Kim, SY ;
Yoo, KP ;
Lee, CS ;
Huh, WS .
FLUID PHASE EQUILIBRIA, 2001, 185 (1-2) :219-230
[7]   Micronization of ibuprofen by RESS [J].
Kayrak, D ;
Akman, U ;
Hortaçsu, Ö .
JOURNAL OF SUPERCRITICAL FLUIDS, 2003, 26 (01) :17-31
[8]   Micronization of drugs using supercritical carbon dioxide [J].
Kerc, J ;
Srcic, S ;
Knez, Z ;
Sencar-Bozic, P .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 182 (01) :33-39
[9]   A novel insulin microcrystals preparation using a seed zone method [J].
Kwon, JH ;
Kim, CW .
JOURNAL OF CRYSTAL GROWTH, 2004, 263 (1-4) :536-543
[10]   Encapsulation and sustained release of a model drug, indomethacin, using CO2-based microencapsulation [J].
Liu, H ;
Finn, N ;
Yates, MZ .
LANGMUIR, 2005, 21 (01) :379-385