Development of novel 5-FU-loaded poly(methylidene malonate 2.1.2)-based microspheres for the treatment of brain cancers

被引:66
作者
Fournier, E
Passirani, C
Colin, N
Breton, P
Sagodira, S
Benoit, JP
机构
[1] INSERM, Ingn Vecorisat Particulaire, ERIT M 0104, F-49100 Angers, France
[2] Virsol, Paris, France
关键词
poly(methylidene malonate 2.1.2); microsphere; 5-fluorouracil; long term delivery; experimental design;
D O I
10.1016/s0939-6411(03)00146-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In order to treat malignant brain tumors by local delivery of antineoplastic agents, the feasibility of 5-fluorouracil (5-FU)-sustained release biodegradable microspheres with a novel material, poly(methylidene malonate 2.1.2), was investigated using an emulsion/extraction method. This polymer was expected to present a slow degradation rate, thus leading to a long term local delivery system. Microparticles were successfully obtained and characterized in terms of drug loading, size, morphology and release profile. The size of the particles was between 40 and 50 mum, which was compatible with a stereotactic injection through a needle. Sufficient drug loadings were obtained (i.e. compatible with the preparation of therapeutic 5-FU doses in a minimal volume of injection), and perfectly spherical microspheres were observed. The respective influences of the polymer molecular weight, the polymer concentration, and the emulsion time on the release profiles were studied using a 2(3) factorial design. In the same objective, the solvent extraction time was extended while keeping all the previous parameters fixed at their optimal values. The in vitro study of these different parameters allowed a reduction of the initial burst release, with a percentage of 5-FU released after 24 h that was lowered from 90 to 65%, and the achievement of a long term drug delivery system, since the release was still ongoing after 43 days. Moreover, the microparticles could be gamma-sterilized (25 kGy) without modification of the release kinetics. Thus, the requested specifications to perform animal experiments were attained. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:189 / 197
页数:9
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