生物粘附
体内
氢键
纳米技术
水下
材料科学
凝聚力(化学)
药物输送
化学
分子
有机化学
地质学
海洋学
生物
生物技术
作者
Hao Wang,Xiang Ke,Shuxian Tang,Kai Ren,Qi Chen,Chichi Li,Wenbin Ran,Chunmei Ding,Jiaojiao Yang,Jun Luo,Jianshu Li
出处
期刊:Small
[Wiley]
日期:2024-01-08
卷期号:20 (24)
被引量:3
标识
DOI:10.1002/smll.202307628
摘要
Abstract Injectable bioadhesives are attractive for managing gastric ulcers through minimally invasive procedures. However, the formidable challenge is to develop bioadhesives that exhibit high injectability, rapidly adhere to lesion tissues with fast gelation, provide reliable protection in the harsh gastric environment, and simultaneously ensure stringent standards of biocompatibility. Here, a natural bioadhesive with tunable cohesion is developed based on the facile and controllable gelation between silk fibroin and tannic acid. By incorporating a hydrogen bond disruptor (urea or guanidine hydrochloride), the inherent network within the bioadhesive is disturbed, inducing a transition to a fluidic state for smooth injection (injection force <5 N). Upon injection, the fluidic bioadhesive thoroughly wets tissues, while the rapid diffusion of the disruptor triggers instantaneous in situ gelation. This orchestrated process fosters the formed bioadhesive with durable wet tissue affinity and mechanical properties that harmonize with gastric tissues, thereby bestowing long‐lasting protection for ulcer healing, as evidenced through in vitro and in vivo verification. Moreover, it can be conveniently stored (≥3 m) postdehydration. This work presents a promising strategy for designing highly injectable bioadhesives utilizing natural feedstocks, avoiding any safety risks associated with synthetic materials or nonphysiological gelation conditions, and offering the potential for minimally invasive application.
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