SCANNING ELECTRON-MICROSCOPY STUDIES OF THE PREVENTION OF BIOPROSTHETIC HEART-VALVE CALCIFICATION WITH CONTROLLED RELEASE POLYMERIC MATRICES

被引:0
|
作者
PATHAK, YV
BOYD, J
JOHNSTON, TP
LEVY, JT
GOLOMB, G
SCHOEN, FJ
LEVY, RJ
机构
[1] UNIV MICHIGAN, DEPT PEDIAT & PHARMACEUT, R-5014 KRESGE II, ANN ARBOR, MI 48109 USA
[2] UNIV ILLINOIS, COLL PHARM, DEPT PHARMACEUT, CHICAGO, IL 60612 USA
[3] EASTERN MICHIGAN UNIV, DEPT CHEM, YPSILANTI, MI 48197 USA
[4] BRIGHAM & WOMENS HOSP, BOSTON, MA 02115 USA
[5] HARVARD UNIV, SCH MED, BOSTON, MA 02115 USA
[6] HEBREW UNIV JERUSALEM, SCH PHARM, IL-91120 JERUSALEM, ISRAEL
来源
CELLS AND MATERIALS | 1991年 / 1卷 / 01期
关键词
BIOPROSTHETIC HEART VALVE CALCIFICATION; POLYMERIC MATRICES; CONTROLLED RELEASE DEVICES; ANTICALCIFICATION AGENTS; EHDP; ALUMINUM; IRON;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Pathologic calcification is the principal failure mode of bioprosthetic heart valves fabricated from glutaraldehyde pretreated porcine aortic valves. Bovine pericardial bioprosthetic valves also fail frequently by calcification. This review covers the novel uses of the scanning electron microscope (SEM) for investigating the pathology and prevention of bioprosthetic heart valve calcification. The progression and growth of calcific lesions in the bioprosthetic heart valve tissues has been documented using SEM with elemental localization by energy dispersive X-ray analysis (EDX). Controlled release polymeric matrices consisting of either ethanehydroxydiphosphonate, FeCl3 or Al(NO3)3 coimplanted with bioprosthetic tissue prevent experimental bioprosthetic calcification. SEM has also been used to study the drug particle distribution in the controlled release matrices. Furthermore, matrix drug release in vitro and in vivo has also been characterized and quantified using SEM techniques.
引用
收藏
页码:65 / 72
页数:8
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