羟基重盐的控释动力学:宿主阴离子结构的影响

Stephen Majoni, J. Hossenlopp
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引用次数: 4

摘要

纳米层状金属氢氧化物如层状双氢氧化物(LDHs)和羟基双盐(hds)可以进行阴离子交换反应,释放插层阴离子。正因为如此,这些金属氢氧化物在生物活性物质如药物和农药的控释递送中得到了应用。本研究以羟基肉桂酸同分异构体为模型化合物,系统探讨了阴离子结构对hds阴离子释放速率和程度的影响。在同分异构体的插入和释放之后,已经证明了插入阴离子上取代基的性质和位置对释放的速度和程度有深远的影响。释放的程度与偶极矩的大小有关,而反应速率则与层内氢键的程度密切相关。与其他异构体相比,正位异构体表现出更持久和完全的释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Controlled Release Kinetics in Hydroxy Double Salts: Effect of Host Anion Structure
Nanodimensional layered metal hydroxides such as layered double hydroxides (LDHs) and hydroxy double salts (HDSs) can undergo anion exchange reactions releasing intercalated anions. Because of this, these metal hydroxides have found applications in controlled release delivery of bioactive species such as drugs and pesticides. In this work, isomers of hydroxycinnamate were used as model compounds to systematically explore the effects of anion structure on the rate and extent of anion release in HDSs. Following intercalation and subsequent release of the isomers, it has been demonstrated that the nature and position of substituent groups on intercalated anions have profound effects on the rate and extent of release. The extent of release was correlated with the magnitude of dipole moments while the rate of reaction showed strong dependence on the extent of hydrogen bonding within the layers. The orthoisomer showed a more sustained and complete release as compared to the other isomers.
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