Remarkable drug-release enhancement with an elimination-based AB3 self-immolative dendritic amplifier

被引:58
作者
Sagi, Amit
Segal, Ehud
Satchi-Fainaro, Ronit [1 ]
Shabat, Doron
机构
[1] Tel Aviv Univ, Dept Physiol & Pharmacol, Sackler Sch Med, IL-69978 Tel Aviv, Israel
[2] Tel Aviv Univ, Dept Organ Chem, Sch Chem, Raymond & Beverly Sackler Fac Exact Sci, IL-69978 Tel Aviv, Israel
关键词
prodrug; dendrimer; enzyme; self-immolative;
D O I
10.1016/j.bmc.2007.03.054
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Self-immolative dendritic prodrugs, activated through a single catalytic reaction by a specific enzyme, could offer significant advantages in inhibition of tumor growth relative to monomeric prodrug, especially if the targeted or secreted enzyme exists at relatively low levels in the malignant tissue. We have designed and synthesized new AB(3) self-immolative dendritic prodrug system that releases three active drugs by a single cleavage of the enzyme penicillin-G-amidase. The cleavage signal is transferred from the dendron focal point to its periphery through fast elimination reactions and the design leads to three-fold signal amplification. In cell-growth inhibition assays, the elimination-based AB(3) self-immolative dendritic prodrug was significantly more effective than a cyclization-based AB(3) dendritic prodrug. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3720 / 3727
页数:8
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