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聚(甲基丙烯酸 2-羟乙酯-丙烯酰胺)水凝胶在湿介质中的合成、表征及基于儿茶酚的仿生粘附性能

Synthesis, Characterization and Catechol-Based Bioinspired Adhesive Properties in Wet Medium of Poly(2-Hydroxyethyl Methacrylate--Acrylamide) Hydrogels.

作者信息

Romero-Gilbert Sebastian, Castro-García Matías, Díaz-Chamorro Héctor, Marambio Oscar G, Sánchez Julio, Martin-Trasancos Rudy, Inostroza Matías, García-Herrera Claudio, Pizarro Guadalupe Del C

机构信息

Departamento de Química, Facultad de Ciencias Naturales, Matemáticas y Medio Ambiente, Universidad Tecnológica Metropolitana (UTEM), J. P. Alessandri 1242, Santiago 7800002, Chile.

Departamento de Ciencias del Ambiente, Facultad de Química y Biología, Universidad de Santiago de Chile (USACH), Santiago 9170022, Chile.

出版信息

Polymers (Basel). 2024 Jan 8;16(2):187. doi: 10.3390/polym16020187.

DOI:10.3390/polym16020187
PMID:38256986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10820396/
Abstract

Hydrogels consist of crosslinked hydrophilic polymers from which their mechanical properties can be modulated for a wide variety of applications. In the last decade, many catechol-based bioinspired adhesives have been developed following the strategy of incorporating catechol moieties into polymeric backbones. In this work, in order to further investigate the adhesive properties of hydrogels and their potential advantages, several hydrogels based on poly(2-hydroxyethyl methacrylate--acrylamide) with '-methylene-bisacrylamide (MBA), without/with L-3,4-dihydroxyphenylalanine (DOPA) as a catecholic crosslinker, were prepared via free radical copolymerization. 2-Hydroxyethyl methacrylate (HEMA) and acrylamide (AAm) were used as comonomers and MBA and DOPA both as crosslinking agents at 0.1, 0.3, and 0.5 mol.-%, respectively. The polymeric hydrogels were characterized by Fourier transform infrared spectroscopy (FT-IR), thermal analysis and swelling behavior analysis. Subsequently, the mechanical properties of hydrogels were determined. The elastic properties of the hydrogels were quantified using Young's modulus (stress-strain curves). According to the results herein, the hydrogel with a feed monomer ratio of 1:1 at 0.3 mol.-% of MBA and DOPA displayed the highest rigidity and higher failure shear stress (greater adhesive properties). In addition, the fracture lap shear strength of the biomimetic polymeric hydrogel was eight times higher than the initial one (only containing MBA); however at 0.5 mol.-% MBA/DOPA, it was only two times higher. It is understood that when two polymer surfaces are brought into close contact, physical self-bonding (Van der Waals forces) at the interface may occur in an -OH interaction with wet contacting surfaces. The hydrogels with DOPA provided an enhancement in the flexibility compared to unmodified hydrogels, alongside reduced swelling behavior on the biomimetic hydrogels. This approach expands the possible applications of hydrogels as adhesive materials, in wet conditions, within scaffolds that are commonly used as biomaterials in cartilage tissue engineering.

摘要

水凝胶由交联的亲水性聚合物组成,其机械性能可针对各种应用进行调节。在过去十年中,许多基于儿茶酚的仿生粘合剂已按照将儿茶酚部分引入聚合物主链的策略开发出来。在这项工作中,为了进一步研究水凝胶的粘附性能及其潜在优势,通过自由基共聚制备了几种基于聚(甲基丙烯酸2-羟乙酯-丙烯酰胺)与N,N'-亚甲基双丙烯酰胺(MBA)、不含/含有L-3,4-二羟基苯丙氨酸(DOPA)作为儿茶酚交联剂的水凝胶。甲基丙烯酸2-羟乙酯(HEMA)和丙烯酰胺(AAm)用作共聚单体,MBA和DOPA均用作交联剂,分别为0.1、0.3和0.5摩尔-%。通过傅里叶变换红外光谱(FT-IR)、热分析和溶胀行为分析对聚合物水凝胶进行了表征。随后,测定了水凝胶的机械性能。使用杨氏模量(应力-应变曲线)对水凝胶的弹性性能进行了量化。根据本文的结果,在0.3摩尔-%的MBA和DOPA条件下,进料单体比为1:1的水凝胶表现出最高的刚性和更高的破坏剪切应力(更大的粘附性能)。此外,仿生聚合物水凝胶的断裂搭接剪切强度比初始水凝胶(仅含MBA)高八倍;然而,在0.5摩尔-% MBA/DOPA时,仅高两倍。据了解,当两个聚合物表面紧密接触时,在与湿接触表面的-OH相互作用中,界面处可能会发生物理自粘合(范德华力)。与未改性的水凝胶相比,含DOPA的水凝胶在柔韧性方面有所增强,同时仿生水凝胶的溶胀行为有所降低。这种方法扩展了水凝胶作为粘合剂材料在潮湿条件下、在通常用作软骨组织工程生物材料的支架内的可能应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0752/10820396/c767f153bd13/polymers-16-00187-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0752/10820396/e9fd6e126c48/polymers-16-00187-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0752/10820396/7d392a75aebf/polymers-16-00187-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0752/10820396/cc16935bea6c/polymers-16-00187-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0752/10820396/158e354cd8b2/polymers-16-00187-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0752/10820396/c767f153bd13/polymers-16-00187-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0752/10820396/e9fd6e126c48/polymers-16-00187-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0752/10820396/7d392a75aebf/polymers-16-00187-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0752/10820396/cc16935bea6c/polymers-16-00187-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0752/10820396/158e354cd8b2/polymers-16-00187-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0752/10820396/c767f153bd13/polymers-16-00187-g005.jpg

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