应用化学 ›› 2019, Vol. 36 ›› Issue (2): 146-154.DOI: 10.11944/j.issn.1000-0518.2019.02.180106

• 研究论文 • 上一篇    下一篇

双重响应性生物基自修复凝胶的制备及其性能

黄河,李雅瑜,郭子砚,施冬健(),张洪吉,陈明清   

  1. 江南大学化学与材料工程学院,合成与生物胶体教育部重点实验室 江苏 无锡 214122
  • 收稿日期:2018-04-10 出版日期:2019-02-01 发布日期:2019-01-31
  • 通讯作者: 施冬健
  • 基金资助:
    江苏省研究生科研与实践创新计划项目(KYCX_1470)资助课题

Preparation and Properties of Dual Responsive Self-healing Bio-based Hydrogels

HUANG He,LI Yayu,GUO Ziyan,SHI Dongjian(),ZHANG Hongji,CHEN Mingqing   

  1. The Key Laboratory of Synthetic and Biological Colloids,Ministry of Education,School of Chemical and Material Engineering,Jiangnan University,Wuxi,Jiangsu 214122,China
  • Received:2018-04-10 Published:2019-02-01 Online:2019-01-31
  • Contact: SHI Dongjian
  • Supported by:
    Supported by the Postgraduate Research & Practice Innovation Program of Jiangsu Province(No.KYCX_1470)

摘要:

为拓宽多重响应性凝胶在生物医学领域中的应用,本文基于生物大分子构筑具有pH响应、糖响应性的可自修复性水凝胶。 本文选用3-氨基苯硼酸(APBA)和2,3-环氧丙基三甲基氯化铵(CHGTA)分别对聚谷氨酸(γ-PGA)和瓜尔胶(GG)进行改性制备了聚谷氨酸-g-氨基苯硼酸(γ-PGA-g-APBA)和阳离子瓜尔胶,在此基础上,对γ-PGA-g-APBA和阳离子瓜尔胶进行物理共混制备生物基凝胶。 通过傅里叶变换红外光谱仪(FTIR)、核磁共振波谱仪(1H NMR)和流变仪对聚合物化学结构、接枝率、流变性能和力学性能进行表征,并考察了凝胶在不同pH值及糖浓度下刺激响应性。 结果表明,凝胶具有自修复性,修复效率可达100%;具有pH响应性,在环境pH值较高时更易形成凝胶,且凝胶强度随pH值升高而增大;同时所制凝胶具有糖响应性,在4 g/L的葡萄糖溶液中浸泡后即可导致凝胶解体。 这些结果说明功能基团APBA的引入可赋予凝胶多重响应性。 所制的双重响应性生物基凝胶具有良好的生物相容性,有望应用于生物医学、功能器件、传感等领域。

关键词: 自修复, 响应性凝胶, 聚谷氨酸, 瓜尔胶

Abstract:

Phenylboronic acid and derivatives that conjugate with diol units to form a reversible ester bond can be used to prepare self-healing and stimuli-responsive materials. Stimuli-responsive hydrogels based on phenylboronic acid have been reported to have excellent self-healing properties. However, in these examples, employed polymers are not fully degradable nor have low biocompatibility. Therefore, this study aims to prepare a bio-based hydrogel for potential biomedical applications. Poly(γ-glutamic acid-g-3-aminophenylboronic acid)(γ-PGA-g-APBA) was synthesized by grafting 3-aminophenylboronic acid(APBA) in the presence of 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide(EDC) and N-hydroxysuccinimide(NHS) as catalysts, and guar gum was modified by cationic etherification agent, 2,3-epoxypropyltrimethylammonium chloride(CHGTA). These two modified bio-polymers were characterized by Fourier transform infrared(FT-IR) spectroscopy, nuclear magnetic resonance(1H NMR), and ultraviolet-visible(UV-Vis) spectrophotometer, and were mixed to form hydrogels. Mechanical properties of the prepared hydrogels were characterized by the rheometer. The results show that(γ-PGA-g-APBA/CGG) hydrogels have self-healing and pH-responsive properties. The structure of the gels is damaged with large strain and reconstructed completely with small strain, indicating that the hydrogel have the self-healing property and the repeatability. With the increase of pH value from 7 to 9, the hydrogels are formed and their strengths increase with pH, due to the conversion of the trigonal boronic-ester bond to tetrahedral boronic-ester bond. In the presence of 4 g/L glucose, the formed gel dissociates and changes to sol, because of the competing reaction between glucose and guar gum with PBA group. Moreover, rheology test indicates the shear-thinning and injectable properties of the hydrogels. Thus, the bio-based(γ-PGA-g-APBA/CGG) hydrogels have the potential applications in sensors, medicine and tissue engineering.

Key words: self-healing, stimuli-responsive gel, polyglutamic acid, guar gum