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核心和表面微凝胶力学对不同的交联浓度具有不同的敏感性。

Core and surface microgel mechanics are differentially sensitive to alternative crosslinking concentrations.

机构信息

Division of Pharmaceutics and Translational Therapeutics, College of Pharmacy, The University of Iowa, Iowa City, IA 52242, USA.

出版信息

Soft Matter. 2017 Aug 30;13(34):5684-5695. doi: 10.1039/c7sm00727b.

Abstract

Microgel mechanics are central to the swelling of stimuli-responsive materials and furthermore have recently emerged as a novel design space for tuning the uptake of nanotherapeutics. Despite this importance, the techniques available to assess mechanics, at the sub-micron scale, remain limited. In this report, all mechanical moduli for a series of air-dried, polystyrene-co-poly(N-isopropylacrylamide) (pS-co-NIPAM) microgels of varying composition in monomer and crosslinker (N,N'-methylene-bisacrylamide (BIS)) mol% have been determined using Brillouin light scattering (BLS) and AFM nanoindentation. These techniques sample the material through distinct means and provide complementary nanomechanical data. An initial demonstration of this combined approach is used to evaluate size-dependent nanomechanics in pS particles of varying diameter. For the pS-co-NIPAM series, our BLS results demonstrate an increase in Young's (E) and shear moduli with increasing NIPAM and/or BIS mol%, while the Poisson's ratio decreased. The same rank order in E was observed from AFM and the two techniques correlate well. However, at low BIS crosslinking, an inverted particle structure persists and small increases in BIS yield a higher increase in E from AFM relative to BLS, consistent with a higher density at the particle surface. At higher BIS incorporation, the microgel reverts to a typical, dense-core structure and further increasing BIS yields changes to core-particle mechanics reflected in BLS. Lastly, at 75 mol% NIPAM, the microgels displayed a broad volume phase transition and increased crosslinking resulted in a minor, yet unexpected, increase in swelling ratio. This complementary approach offers new insight into nanomechanics critical for microgel design and application.

摘要

微凝胶力学对于刺激响应材料的溶胀至关重要,此外,它最近已成为调节纳米治疗剂摄取的新型设计空间。尽管如此重要,但在亚微米尺度上评估力学的可用技术仍然有限。在本报告中,使用布里渊光散射(BLS)和原子力显微镜(AFM)纳米压痕法测定了一系列具有不同单体和交联剂(N,N'-亚甲基双丙烯酰胺(BIS))摩尔%组成的空气干燥的聚苯乙烯-co-聚(N-异丙基丙烯酰胺)(pS-co-NIPAM)微凝胶的所有机械模量。这些技术通过不同的手段对材料进行采样,并提供互补的纳米力学数据。这种组合方法的初步演示用于评估不同直径的 pS 颗粒的尺寸依赖性纳米力学。对于 pS-co-NIPAM 系列,我们的 BLS 结果表明,杨氏(E)和剪切模量随 NIPAM 和/或 BIS 摩尔%的增加而增加,而泊松比降低。AFM 也观察到相同的 E 顺序,两种技术相关性良好。然而,在低 BIS 交联时,仍然存在反相颗粒结构,并且 BIS 的少量增加会导致 AFM 相对于 BLS 产生更高的 E 增加,这与颗粒表面更高的密度一致。在更高的 BIS 掺入下,微凝胶恢复到典型的密集核结构,并且进一步增加 BIS 会导致 BLS 反映的核-颗粒力学发生变化。最后,在 75 mol%NIPAM 下,微凝胶显示出宽的体积相转变,并且增加交联导致溶胀比的微小但意外增加。这种互补方法为微凝胶设计和应用至关重要的纳米力学提供了新的见解。

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