自愈水凝胶
肽
低临界溶液温度
药物输送
药品
化学工程
聚合物
化学
毒品携带者
高分子化学
共聚物
生物物理学
药理学
有机化学
生物化学
工程类
生物
医学
作者
Meiwen Cao,Yu Wang,Xuzhi Hu,Haoning Gong,Ruiheng Li,Henry Cox,Jing Zhang,Thomas Andrew Waigh,Hai Xu,Jian R. Lu
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2019-07-31
卷期号:20 (9): 3601-3610
被引量:223
标识
DOI:10.1021/acs.biomac.9b01009
摘要
Mixed thermoreversible gels were successfully fabricated by the addition of a thermosensitive polymer, poly(N-isopropylacrylamide) (PNIPAM), to fibrillar nanostructures self-assembled from a short peptide I3K. When the temperature was increased above the lower critical solution temperature of the PNIPAM, the molecules collapsed to form condensed globular particles, which acted as cross-links to connect different peptide nanofibrils and freeze their movements, resulting in the formation of a hydrogel. Since these processes were physically driven, such hydrogels could be reversibly switched between the sol and gel states as a function of temperature. As a model peptide, I3K was formulated with PNIPAM to produce a thermoreversible sol-gel system with a transition temperature of ∼33 °C, which is just below the body temperature. The antibacterial peptide of G(IIKK)3I-NH2 could be conveniently encapsulated in the hydrogel by the addition of the solution at lower temperatures in the sol phase and then increasing the temperature to be above 33 °C for gelation. The hydrogel gave a sustained and controlled linear release of G(IIKK)3I-NH2 over time. Using the peptide nanofibrils as three-dimensional scaffolds, such thermoresponsive hydrogels mimic the extracellular matrix and could potentially be used as injectable hydrogels for minimally invasive drug delivery or tissue engineering.
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