Microencapsulated ciliary neurotrophic factor: Physical properties and biological activities

被引:45
作者
Maysinger, D
Krieglstein, K
FilipovicGrcic, J
Sendtner, M
Unsicker, K
Richardson, P
机构
[1] MGH, MONTREAL, PQ H3G 1Y6, CANADA
[2] UNIV HEIDELBERG, DEPT ANAT & CELL BIOL, D-69120 HEIDELBERG, GERMANY
[3] UNIV WURZBURG, DEPT CLIN NEUROL, D-97080 WURZBURG, GERMANY
关键词
D O I
10.1006/exnr.1996.0056
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Controlled drug release in the CNS and PNS is still an obstacle to the treatment of neurodegenerative disorders. We have prepared a variety of microspheres containing either ciliary neurotrophic factor (CNTF) or genetically engineered cells able to synthesize and release this cytokine. CNTF is a multifunctional cytokine that can regulate the survival and differentiation of many types of developing and adult neurons. However, when given in therapeutically effective doses by systemic injections, it produces numerous adverse side effects. In order to minimize these effects we have microencapsulated it in biopolymers (chitosans, alginates, and copolymers in various proportions to achieve different kinetic properties). Size distribution profiles were determined by an image analysis system and surface characteristics were assessed by electron microscopy. The total content of CNTF as well as the amounts released per day were determined by ELISA and in vitro bioassays. The results from the release kinetics demonstrate that long-term secretion (up to 24 days) of CNTF is achieved by combining chitosan with copolymerized lactic and glycolic acid, whereas microspheres made of alginate provided only relatively short-term release (2-12 days). Neuron survival and neurite outgrowth in cultures of ciliary ganglia were supported by microencapsulated CNTF, indicating biological stability of CNTF. Genetically engineered human kidney cells 293 continued synthesizing CNTF within spheres and the released amounts of CNTF in the culture medium were comparable to the amounts secreted from monolayers (1 ng/ml of supernatant from confluent cultures) or even higher. These studies provide a basis for future testing of CNTF in encapsulated preparations using animal models of neurodegenerative disorders. (C) 1996 Academic Press, Inc.
引用
收藏
页码:177 / 188
页数:12
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