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用于高效递送亚甲基蓝的温敏/酸碱响应性明胶/多酚单宁/氧化石墨烯水凝胶。

Thermo- and pH-Responsive Gelatin/Polyphenolic Tannin/Graphene Oxide Hydrogels for Efficient Methylene Blue Delivery.

机构信息

Group of Polymeric Materials and Composites, Department of Chemistry, State University of Maringá (UEM), Maringá 87020-900, PR, Brazil.

Chemistry Department, Institute of Exact Sciences, Federal University of Juiz de Fora, Juiz de Fora 36036-900, MG, Brazil.

出版信息

Molecules. 2021 Jul 27;26(15):4529. doi: 10.3390/molecules26154529.

Abstract

Gelatin (GE), amino-functionalized polyphenolic tannin derivative (TN), and graphene oxide (GO) were associated to yield thermo- and pH-responsive hydrogels for the first time. Durable hydrogel assemblies for drug delivery purposes were developed using the photosensitizer methylene blue (MB) as a drug model. The cooling GE/TN blends provide brittle physical assemblies. To overcome this disadvantage, different GO contents (between 0.31% and 1.02% /) were added to the GE/TN blend at 89.7/10.3 /. FTIR and RAMAN spectroscopy analyses characterized the materials, indicating GO presence in the hydrogels. Incorporation studies revealed a total MB (0.50 mg/mL) incorporation into the GE/TN-GO hydrogel matrices. Additionally, the proposed systems present a mechanical behavior similar to gel. The GO presence in the hydrogel matrices increased the elastic modulus from 516 to 1650 Pa. SEM revealed that hydrogels containing MB present higher porosity with interconnected pores. Dissolution and swelling degree studies revealed less stability of the GE/TN-GO-MB hydrogels in SGF medium (pH 1.2) than SIF (pH 6.8). The degradation increased in SIF with the GO content, making the polymeric matrices more hydrophilic. MB release studies revealed a process controlled by Fickian diffusion. Our results point out the pH-responsible behavior of mechanically reinforced GE/TN-GO-MB hydrogels for drug delivery systems purposes.

摘要

首次将明胶(GE)、氨基功能化多酚单宁衍生物(TN)和氧化石墨烯(GO)结合在一起,生成热响应和 pH 响应水凝胶。使用作为药物模型的光敏剂亚甲蓝(MB)开发了用于药物输送目的的耐用水凝胶组件。冷却的 GE/TN 混合物提供易碎的物理组件。为了克服这一缺点,在 89.7/10.3 / 的 GE/TN 混合物中添加了不同含量的 GO(0.31% 至 1.02%/)。FTIR 和拉曼光谱分析对材料进行了表征,表明 GO 存在于水凝胶中。掺入研究表明,MB(0.50 mg/mL)完全掺入到 GE/TN-GO 水凝胶基质中。此外,所提出的系统表现出类似于凝胶的机械行为。GO 的存在增加了水凝胶基质的弹性模量,从 516 增加到 1650 Pa。SEM 显示,含有 MB 的水凝胶具有更高的孔隙率和相互连接的孔。溶胀度和降解度研究表明,GE/TN-GO-MB 水凝胶在 SGF 介质(pH 1.2)中的稳定性低于 SIF(pH 6.8)。GO 含量的增加增加了聚合物基质的亲水性,导致降解增加。MB 释放研究表明这是一个由菲克扩散控制的过程。我们的结果指出了用于药物输送系统的机械增强 GE/TN-GO-MB 水凝胶的 pH 响应行为。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/940d/8347097/8ce9e5407821/molecules-26-04529-g001.jpg

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