Microspheres containing insulin-like growth factor I for treatment of chronic neurodegeneration

被引:37
作者
Carrascosa, C
Torres-Aleman, I
Lopez-Lopez, C
Carro, E
Espejo, L
Torrado, S
Torrado, JJ
机构
[1] Univ Complutense, Inst Cajal, Sch Pharm, Dept Pharmaceut Technol,CSIC, Madrid, Spain
[2] CSIC, Inst Cajal, Neuroendocrinol Lab, E-28002 Madrid, Spain
关键词
microsphere; PLGA IGF-I; pharmacokinetic; neurodegeneration;
D O I
10.1016/S0142-9612(03)00562-3
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The therapeutic potential of peptide growth factors as insulin-like growth factor I (IGF-I) is currently under intense scrutiny in a wide variety of diseases, including neurodegenerative illnesses. A new poly(lactic-co-glycolide)-based microsphere IGF-I controlled release formulation for subcutaneous (SC) delivery has been developed by a triple emulsion method. The resulting microspheres displayed a mean diameter of 1.5 mum, with an encapsulation efficiency of 74.3%. The protein retained integrity after the microencapsulation process as evaluated by circular dichroism and SDS-PAGE. The administration of IGF-I in microspheres caused at least a 30-fold increase in IGF-I mean residence time in rats and mice when compared with the conventional SC solution. Therefore, dosing can be changed from the conventional twice a day to once every 2 weeks. Therapeutic efficacy of this new formulation has been studied in mutant mice with inherited Purkinje cell degeneration (PCD). These mice show a chronic limb discoordination that is resolved after continuous systemic delivery of IGF-1. Normal motor coordination was maintained as long as IGF-I microsphere therapy is continued. Moreover, severely affected PCD mice, with marked ataxia, muscle wasting and shortened life-span showed a significant improvement after continuous IGF-I microsphere therapy as determined by enhanced motor coordination, marked weight gain and extended survival. This new formulation can be considered of great therapeutic promise for some chronic brain diseases. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:707 / 714
页数:8
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