Comparison of Three Dissolution Apparatuses for Testing Calcium Phosphate Pellets used as Ibuprofen Delivery Systems

被引:17
作者
Chevalier, Emilie [1 ]
Viana, Marylene [1 ]
Artaud, Aymeric [2 ]
Chomette, Lisette [3 ]
Haddouchi, Samir [2 ]
Devidts, Gille [3 ]
Chulia, Dominique [1 ]
机构
[1] Univ Limoges, Pharm Galen Lab, Fac Pharm, CNRS SPCTS UMR 6638, F-87025 Limoges, France
[2] SPS Pharma Serv, F-63000 Clermont Ferrand, France
[3] Varian SA, F-91941 Les Ulis, France
来源
AAPS PHARMSCITECH | 2009年 / 10卷 / 02期
关键词
calcium phosphate pellets; flow-through cell; ibuprofen delivery system; in vitro drug release; paddle apparatus; reciprocating cylinder; IN-VITRO; DRUG DISSOLUTION; RELEASE; INVIVO; SIMILARITY; APATITE; SURFACE; VIVO;
D O I
10.1208/s12249-009-9252-z
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Porous calcium phosphate pellets were produced according to two granulation processes (low and high shear wet granulations) and drug loaded with five ibuprofen contents (1.75%, 7%, 12.5%, 22%, and 36%) in order to ensure both bone defect filling and local drug delivery. The drug-release kinetics from the two types of pellets was studied using three dissolution apparatuses: paddle apparatus, reciprocating cylinder, and flow-through cell. The paper compared the three dissolution methods and considered the effect of the granulation process on the ibuprofen-release kinetics. Dissolution data were analyzed using the Weibull function as well as the difference (f1) and similarity (f2) factors. Dissolution kinetics was not influenced by the granulation process, regardless of the dissolution apparatus and of the drug content. The comparison of the three dissolution devices indicated that ibuprofen was released faster from granules loaded with 36% of drug content with the reciprocating apparatus, due to the disintegration of the granules occurring during the dissolution test. For the other drug contents, dissolution profiles were not significantly different from one apparatus to another. However, the flow-through cell seemed to be more suitable for the drug-release study of implantable materials.
引用
收藏
页码:597 / 605
页数:9
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