Development of Poly(Lactic Acid)/Chitosan Co-Matrix Microspheres: Controlled Release of Taxol-Heparin for Preventing Restenosis

Development of Poly(Lactic Acid)/Chitosan Co-Matrix Microspheres: Controlled Release of Taxol-Heparin for Preventing Restenosis
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聚乳酸/壳聚糖复合基质微球的开发:控制释放紫杉醇-肝素以预防再狭窄

DOI:
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发表时间:
2001
期刊:
影响因子:
6
通讯作者:
G. S. Das
G. S. Das
中科院分区:
医学2区
文献类型:
--
作者:
T. Chandy;Gundu H. R. Rao;Robert F. Wilson;G. S. Das

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Smooth muscle cell proliferation plays a major role in the genesis of restenosis after angioplasty or vascular injury. Controlled release of appropriate drugs alone and in combinations is one approach for treating coronary obstructions, balloon angioplasty, restenosis associated with thrombosis, and calcification. We demonstrated the possibility of encapsulating taxol-loaded polylactic acid (PLA) microspheres within heparin-chitosan spheres to develop a prolonged release co-matrix form. The in vitro release profile of taxol and heparin from this co-matrix system was monitored in phosphate buffered saline pH 7.4, using an ultraviolet spectrophotometer. The amount of taxol/heparin release was initially much higher, followed by a constant slow release profile for a prolonged period. The initial burst release of taxol (15.8%) and heparin (32.7%) from the co-matrix was modified with polyethylene glycol coatings (13.5% and 25.4%, respectively, for 24 hr). From scanning electron microscopy studies, it appears that these drugs diffuse out slowly to the dissolution medium through the micropores of the co-matrix. However, the surface micropores were modified with polyethylene glycol (PEG) coatings for a constant slow release profile. This PEG-coated PLA/chitosan co-matrix may target drug combinations having synergestic effects for prolonged periods to treat restenosis.
DOI: 10.1016/s0142-9612(00)00154-x
发表时间: 2000-11-01
期刊: BIOMATERIALS
影响因子: 14
作者:
Edelman, ER;Nathan, A;Karnovsky, MJ
通讯作者: Karnovsky, MJ
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DOI: 10.1161/01.cir.94.7.1733
发表时间: 1996
期刊: Circulation
影响因子: 37.8
作者:
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