BISACYLPHOSPHONATES INHIBIT HYDROXYAPATITE FORMATION AND DISSOLUTION INVITRO AND DYSTROPHIC CALCIFICATION INVIVO

被引:46
作者
GOLOMB, G
SCHLOSSMAN, A
SAADEH, H
LEVI, M
VANGELDER, JM
BREUER, E
机构
[1] HEBREW UNIV JERUSALEM,SCH PHARM,DEPT PHARMACEUT CHEM,IL-91120 JERUSALEM,ISRAEL
[2] HEBREW UNIV JERUSALEM,SCH PHARM,DEPT PHARM,IL-91120 JERUSALEM,ISRAEL
关键词
BISPHOSPHONATES; PHOSPHONATES; ACYLPHOSPHONATES; KETOPHOSPHONATES; CALCIFICATION; CALCINOSIS; HYDROXYAPATITE;
D O I
10.1023/A:1018956516640
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Some geminal bisphosphonates are used clinically for a number of important bone/calcium related diseases; however, side effects and lack of selectivity impede their wide use. This work reports the synthesis and evaluation of bisacylphosphonates (e.g., adipoyl- and suberoylbisphosphonate). These compounds were found to inhibit significantly hydroxyapatite formation and dissolution in vitro and the calcification of bioprosthetic tissue implanted subdermally in rats. These are the first instances of nongeminal bisphosphonates [P-(C)n-P, n greater-than-or-equal-to 2] that have been reported to be active in calcium-related disorders. The reported bisacylphosphonates possess apparent lower toxicity, and their calcium complexes/salts have improved solubility properties. Therefore, they are of potential importance for clinical applications.
引用
收藏
页码:143 / 148
页数:6
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