A Novel Approach for the Synthesis of Responsive Core–Shell Nanogels with a Poly(N-Isopropylacrylamide) Core and a Controlled Polyamine Shell

IF 4.7 3区 工程技术 Q1 POLYMER SCIENCE Polymers Pub Date : 2024-09-13 DOI:10.3390/polym16182584
Anna Harsányi, Attila Kardos, Pinchu Xavier, Richard A. Campbell, Imre Varga
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Abstract

Microgel particles can play a key role, e.g., in drug delivery systems, tissue engineering, advanced (bio)sensors or (bio)catalysis. Amine-functionalized microgels are particularly interesting in many applications since they can provide pH responsiveness, chemical functionalities for, e.g., bioconjugation, unique binding characteristics for pollutants and interactions with cell surfaces. Since the incorporation of amine functionalities in controlled amounts with predefined architectures is still a challenge, here, we present a novel method for the synthesis of responsive core–shell nanogels (dh < 100 nm) with a poly(N-isopropylacrylamide) (pNIPAm) core and a polyamine shell. To achieve this goal, a surface-functionalized pNIPAm nanogel was first prepared in a semi-batch precipitation polymerization reaction. Surface functionalization was achieved by adding acrylic acid to the reaction mixture in the final stage of the precipitation polymerization. Under these conditions, the carboxyl functionalities were confined to the outer shell of the nanogel particles, preserving the core’s temperature-responsive behavior and providing reactive functionalities on the nanogel surface. The polyamine shell was prepared by the chemical coupling of polyethyleneimine to the nanogel’s carboxyl functionalities using a water-soluble carbodiimide (EDC) to facilitate the coupling reaction. The efficiency of the coupling was assessed by varying the EDC concentration and reaction temperature. The molecular weight of PEI was also varied in a wide range (Mw = 0.6 to 750 kDa), and we found that it had a profound effect on how many polyamine repeat units could be immobilized in the nanogel shell. The swelling and the electrophoretic mobility of the prepared core–shell nanogels were also studied as a function of pH and temperature, demonstrating the successful formation of the polyamine shell on the nanogel core and its effect on the nanogel characteristics. This study provides a general framework for the controlled synthesis of core–shell nanogels with tunable surface properties, which can be applied in many potential applications.
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合成具有聚(N-异丙基丙烯酰胺)核和可控多胺壳的响应性核壳纳米凝胶的新方法
微凝胶颗粒可在药物输送系统、组织工程、先进(生物)传感器或(生物)催化等方面发挥关键作用。胺功能化微凝胶在许多应用中尤其引人关注,因为它们可以提供 pH 值响应性、用于生物共轭等的化学功能性、与污染物的独特结合特性以及与细胞表面的相互作用。由于在预定结构中加入数量可控的胺官能团仍是一项挑战,我们在此介绍一种新方法,用于合成具有聚(N-异丙基丙烯酰胺)(pNIPAm)内核和聚胺外壳的响应性核壳纳米凝胶(dh < 100 nm)。为实现这一目标,首先通过半批次沉淀聚合反应制备了表面功能化的 pNIPAm 纳米凝胶。在沉淀聚合反应的最后阶段,通过向反应混合物中添加丙烯酸实现了表面功能化。在这些条件下,羧基官能团被限制在纳米凝胶颗粒的外壳中,从而保留了核心的温度响应特性,并在纳米凝胶表面提供了反应性官能团。多胺外壳的制备方法是将聚乙烯亚胺与纳米凝胶的羧基官能团进行化学偶联,使用水溶性碳二亚胺(EDC)促进偶联反应。通过改变 EDC 浓度和反应温度来评估偶联效率。我们还在很大范围内改变了 PEI 的分子量(Mw = 0.6 至 750 kDa),发现这对纳米凝胶外壳中能固定多少个多胺重复单元有很大影响。我们还研究了所制备的核壳纳米凝胶的溶胀性和电泳迁移率与 pH 值和温度的函数关系,证明了纳米凝胶核上多胺壳的成功形成及其对纳米凝胶特性的影响。这项研究为可控合成具有可调表面性质的核壳纳米凝胶提供了一个总体框架,它可以应用于许多潜在的应用领域。
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来源期刊
Polymers
Polymers POLYMER SCIENCE-
CiteScore
8.00
自引率
16.00%
发文量
4697
审稿时长
1.3 months
期刊介绍: Polymers (ISSN 2073-4360) is an international, open access journal of polymer science. It publishes research papers, short communications and review papers. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Polymers provides an interdisciplinary forum for publishing papers which advance the fields of (i) polymerization methods, (ii) theory, simulation, and modeling, (iii) understanding of new physical phenomena, (iv) advances in characterization techniques, and (v) harnessing of self-assembly and biological strategies for producing complex multifunctional structures.
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