SCHEDULED MAINTENANCE
Cholyl-l-lysine-carboxylbutyryl adriamycin prodrugs targeting chemically induced liver injury†
a
Ming
Zhao,
*ab
Yuji
Wang,
a
Haimei
Zhu,
a
Yaonan
Wang,
a
Shurui
Zhao,
a
Jianhui
Wu
a
and
Shiqi
Peng
*a
Abstract
By use of carboxylbutyryl as a linker, adriamycin (ADR) and cholyl-L-Lys (an anti-inflammatory agent) were covalently conjugated and Nα-cholyl-Nε-(N-carbonylpropionoadriamycin)-L-Lys (BCBALys) was constructed as a liver-targeting nano-delivery system to release cholyl-L-Lys and protect the liver from CCl4-induced injury. In ultrapure water and rat plasma, 10−6 M BCBALys formed nanoparticles of 42–231 nm in diameter and ∼116 nm in height. In a CCl4-injured mouse model, however, only 2 µmol kg−1 of BCBALys effectively protected the liver of the mice from injury, and the mouse liver histology showed no hepatic architecture loss and inflammatory cell infiltration. BCBALys selectively accumulated in the liver of CCl4-injured mice, but not in other vital organs, and released cholyl-L-Lys. These data demonstrated that BCBALys exhibited high efficacy for treating CCl4-induced liver injury in a targeted manner. The chemical mechanism of BCBALys nanoparticle formation and the pharmacological mechanism of BCBALys mouse liver protection from CCl4-induced injury were also revealed by experiments.
- This article is part of the themed collection: 2017 Journal of Materials Chemistry B HOT Papers
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