...
首页> 外文期刊>Chemistry of Materials: A Publication of the American Chemistry Society >Bis-Aliphatic Hydrazone-Linked Hydrogels Form Most Rapidly at Physiological pH: Identifying the Origin of Hydrogel Properties with Small Molecule Kinetic Studies
【24h】

Bis-Aliphatic Hydrazone-Linked Hydrogels Form Most Rapidly at Physiological pH: Identifying the Origin of Hydrogel Properties with Small Molecule Kinetic Studies

机译:双亲脂Hy连接的水凝胶在生理pH值上形成最快:通过小分子动力学研究确定水凝胶性质的起源

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Rheological and small molecule kinetic studies were performed to study the formation and hydrolysis of the bis-aliphatic hydrazone bond. The rate of gelation was found to correspond closely with the rate of bond formation and the rate of gel relaxation with the rate of hydrolysis, indicating that small molecule kinetic studies can play an important role in material design. Furthermore, unlike aryl or acyl hydrazone bonds, the bis-aliphatic hydrazone bond forms rapidly under physiological conditions without requiring aniline catalysis yet maintains a pH-dependent rate of hydrolysis. These results suggest the bis-aliphatic hydrazone bond should find use alongside existing bioorthogonal click chemistries for bioconjugation, biomaterial synthesis, and controlled release applications.
机译:进行了流变学和小分子动力学研究,以研究双脂族键的形成和水解。发现凝胶化速率与键形成速率和凝胶松弛速率与水解速率密切相关,这表明小分子动力学研究可以在材料设计中发挥重要作用。此外,与芳基或酰基键不同,双脂族键在生理条件下快速形成,而无需苯胺催化,但仍保持pH依赖的水解速率。这些结果表明,双脂族键应与现有的生物正交点击化学一起用于生物缀合,生物材料合成和控释应用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号