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工程化高溶胀双响应蛋白基可注射水凝胶:体内分子结构和组成的影响。

Engineering highly swellable dual-responsive protein-based injectable hydrogels: the effects of molecular structure and composition in vivo.

机构信息

School of Chemical Engineering, Theranostic Macromolecules Research Center, Sungkyunkwan University, Suwon, Republic of Korea.

出版信息

Biomater Sci. 2017 Oct 24;5(11):2285-2294. doi: 10.1039/c7bm00707h.

Abstract

Stimuli-responsive hydrogels, known as smart hydrogels, are three-dimensional amphiphilic or hydrophilic polymer networks that are able to change their volume or phase, and other properties, including viscosity, structure, and dimension, in response to changes in pH, temperature, and magnetic or electric field. Highly swellable, dual-responsive bovine serum albumin (BSA)-based injectable hydrogels are prepared here by the chemical conjugation of pH- and temperature-responsive oligo(sulfamethazine acrylate-co-N-isopropylacrylamide) (oligo(SMA-co-NIPAM)) copolymers on the surface of BSA through carbodiimide-mediated chemistry. The pH- and temperature-responsive oligomer-bearing BSA conjugates show rapid sol-to-gel phase transition properties. Specifically, the free-flowing conjugates at high pH (pH 8.4, 23 °C) are transformed to a viscoelastic gel under physiological conditions (pH 7.4, 37 °C). The swelling ratio, gel strength, and pore size of the BSA hydrogel were tuned by altering the conjugation ratio of the oligo(SMA-co-NIPAM) copolymers of various lengths and compositions to BSA. Subcutaneously administered BSA conjugate sols into the dorsal region of Sprague-Dawley rats formed an in situ gel. When the oligo(NIPAM) content in the hydrogel was high, the degradation rate of BSA hydrogels was remarkably slow, and two weeks after in vivo administration, the hydrogels with high oligo(NIPAM) had swollen more than 4-fold. An in vivo biodegradation study demonstrated that no necrosis or hemorrhage was observed in the tissues with the hydrogels. The concurrent stimuli-responsivity under physiological conditions and high elasticity suggest that these smart hydrogels may open a new avenue for hydrogel applications.

摘要

刺激响应水凝胶,也称为智能水凝胶,是一种三维两亲性或亲水性聚合物网络,能够响应 pH 值、温度和磁场或电场等变化,改变其体积或相以及其他性质,包括粘度、结构和尺寸。本文通过碳二亚胺介导的化学方法,在牛血清白蛋白(BSA)表面化学接枝 pH 和温度响应性寡聚物(磺胺嘧啶丙烯酰胺-co-N-异丙基丙烯酰胺)(oligo(SMA-co-NIPAM))共聚物,制备了高度溶胀的双响应性牛血清白蛋白(BSA)基可注射水凝胶。具有 pH 和温度响应性的寡聚物接枝的 BSA 缀合物表现出快速的溶胶-凝胶相转变特性。具体而言,在高 pH(23°C,pH 8.4)下呈自由流动的缀合物在生理条件下(pH 7.4,37°C)转变为粘弹性凝胶。通过改变不同长度和组成的寡聚物(SMA-co-NIPAM)共聚物与 BSA 的接枝比,可以调节 BSA 水凝胶的溶胀率、凝胶强度和孔径。将 BSA 缀合物溶液皮下注入 Sprague-Dawley 大鼠的背部区域,形成原位凝胶。当水凝胶中的寡聚(NIPAM)含量较高时,BSA 水凝胶的降解速度明显较慢,体内给药两周后,具有高寡聚(NIPAM)的水凝胶溶胀超过 4 倍。体内生物降解研究表明,水凝胶所在的组织没有观察到坏死或出血。在生理条件下的协同刺激响应性和高弹性表明,这些智能水凝胶可能为水凝胶的应用开辟新途径。

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