Spray freezing into liquid (SFL) particle engineering technology to enhance dissolution of poorly water soluble drugs: organic solvent versus organic/aqueous co-solvent systems

被引:107
作者
Hu, JH
Johnston, KP
Williams, RO
机构
[1] Univ Texas, Coll Pharm, Div Pharmaceut, Austin, TX 78712 USA
[2] Univ Texas, Dept Chem Engn, Austin, TX 78712 USA
关键词
spray freezing into liquid; dissolution; poorly water soluble drug; particle engineering; SFL organic system;
D O I
10.1016/S0928-0987(03)00203-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A spray freezing into liquid (SFL) particle engineering technology has been developed to produce micronized powders to enhance the dissolution of poorly water soluble active pharmaceutical ingredients (APIs). Previously, a tetrahydrofuran (THF)/water co-solvent was used as the solution source in the SFL process. In the present study, an organic system was developed to further enhance the properties of particles produced by SFL. The influence of solution type (e.g. organic versus organic/water) on the physicochemical properties of SFL powders was investigated and compared. The physicochemical properties of SFL carbamazepine (CBZ)/poloxamer 407/PVP K 15 (2: 1:1 ratio) powders were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), particle size distribution, surface area analysis, contact angle measurement, Karl-Fisher (KF) titration, gas chromatography (GC) analysis, HPLC analysis, and dissolution testing. The CBZ loading in the feed solution of the SFL acetonitrile system was 2.2% (w/w), which was greater than 0.22% (w/w) loading of the THF/water co-solvent system. XRD results indicated CBZ was amorphous in SFL powders produced by either system. SEM micrographs indicated that SFL powders from acetonitrile appeared less porous with a smaller primary particle size than particles from the co-solvent. The M50 (50% cumulative percent undersize) of micronized powder from the SFL acetonitride system and the THF/water co-solvent system with 0.22% CBZ loading were 680 nm and 7.06 mum, respectively. The surface area of SFL powders from the acetonitrile and co-solvent systems were 12.89 and 13.31 m(2)/g, respectively. The contact angle of the SFL powders against purified water was about 35degrees for both systems. The SFL powders from both systems exhibited similar and significantly enhanced dissolution rates compared to the bulk CBZ. Acetonitrile was an effective alternative solvent to THF/water co-solvent for use with the SFL micronization process to produce free flowing particles containing CBZ with significantly enhanced wetting and dissolution properties. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:295 / 303
页数:9
相关论文
共 28 条
[1]   A THEORETICAL BASIS FOR A BIOPHARMACEUTIC DRUG CLASSIFICATION - THE CORRELATION OF IN-VITRO DRUG PRODUCT DISSOLUTION AND IN-VIVO BIOAVAILABILITY [J].
AMIDON, GL ;
LENNERNAS, H ;
SHAH, VP ;
CRISON, JR .
PHARMACEUTICAL RESEARCH, 1995, 12 (03) :413-420
[2]   CLINICAL PHARMACOKINETICS OF CARBAMAZEPINE [J].
BERTILSSON, L .
CLINICAL PHARMACOKINETICS, 1978, 3 (02) :128-143
[3]   Adsorption of gases in multimolecular layers [J].
Brunauer, S ;
Emmett, PH ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 :309-319
[4]   Protein spray freeze drying. 2. Effect of formulation variables on particle size and stability [J].
Costantino, HR ;
Firouzabadian, L ;
Wu, CC ;
Carrasquillo, KG ;
Griebenow, K ;
Zale, SE ;
Tracy, MA .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 91 (02) :388-395
[5]   Protein spray-freeze drying.: Effect of atomization conditions on particle size and stability [J].
Costantino, HR ;
Firouzabadian, L ;
Hogeland, K ;
Wu, CC ;
Beganski, C ;
Carrasquillo, KG ;
Córdova, M ;
Griebenow, K ;
Zale, SE ;
Tracy, MA .
PHARMACEUTICAL RESEARCH, 2000, 17 (11) :1374-1383
[6]  
CULLITY D, 2001, ELEMENTS XRAY DIFFRA, P397
[7]   In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs [J].
Dressman, JB ;
Reppas, C .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2000, 11 :S73-S80
[8]  
Gold PM, 1998, Patent, Patent No. [5770230, US5770230]
[9]   Improvement of dissolution rates of poorly water soluble APIs using novel spray freezing into liquid technology [J].
Hu, JH ;
Rogers, TL ;
Brown, J ;
Young, T ;
Johnston, KP ;
Williams, RO .
PHARMACEUTICAL RESEARCH, 2002, 19 (09) :1278-1284
[10]  
HUBBARD WK, 1997, FED REGISTER, V62, P67377