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基于壳聚糖的响应性杂化纳米凝胶,用于集成光学 pH 传感、肿瘤细胞成像和控制药物释放。

Chitosan-based responsive hybrid nanogels for integration of optical pH-sensing, tumor cell imaging and controlled drug delivery.

机构信息

Department of Chemistry, College of Staten Island, and The Graduate Center, The City University of New York, Staten Island, NY 10314, USA.

出版信息

Biomaterials. 2010 Nov;31(32):8371-81. doi: 10.1016/j.biomaterials.2010.07.061. Epub 2010 Aug 10.

Abstract

We report a new class of chitosan-based hybrid nanogels by in-situ immobilization of CdSe quantum dots (QDs) in the chitosan-poly(methacrylic acid) (chitosan-PMAA) networks. The covalently crosslinked hybrid nanogels with chitosan chains semi-interpenetrating in the crosslinked PMAA networks exhibit excellent colloidal and structural stability as well as reversible physical property change in response to a pH variation cross the physiological condition. In contrast, the hybrid nanogels formed by non-covalent physical association exhibit a significant change in the structure and composition upon exposure to physiological pH. This distinction in the structural stability of hybrid nanogels produces very different outcomes for their biomedical applications. The covalently crosslinked hybrid nanogels are low-cytotoxic and could illuminate the B16F10 cells, sense the environmental pH change, and regulate the release of anticancer drug in the typical abnormal pH range of 5-7.4 found in pathological zone, thus successfully combine multiple functionality into a single nano-object. However, the physically associated hybrid nanogels exhibit a non-reversible pH-sensitive PL property and a significant cytotoxicity after 24 h treatment. It is critical to construct a highly stable biopolymer-QD hybrid nanogel, via a rational design for safe bionanomaterials, to simultaneously combine the biosensing, bioimaging, and effective therapy functions.

摘要

我们通过将 CdSe 量子点(QDs)原位固定在壳聚糖-聚(甲基丙烯酸)(chitosan-PMAA)网络中,报告了一类新的壳聚糖基杂化纳米凝胶。通过壳聚糖链在交联的 PMAA 网络中的半互穿,共价交联的杂化纳米凝胶表现出优异的胶体和结构稳定性,以及对生理条件下 pH 值变化的可逆物理性质变化。相比之下,通过非共价物理缔合形成的杂化纳米凝胶在暴露于生理 pH 值时,其结构和组成会发生显著变化。这种杂化纳米凝胶结构稳定性的区别,为它们的生物医学应用产生了非常不同的结果。共价交联的杂化纳米凝胶具有低细胞毒性,可以照亮 B16F10 细胞,感测环境 pH 值的变化,并在病理区域中发现的典型异常 pH 值 5-7.4 范围内调节抗癌药物的释放,从而将多种功能成功结合到单个纳米物体中。然而,物理缔合的杂化纳米凝胶在 24 小时处理后表现出不可逆的 pH 敏感 PL 性质和显著的细胞毒性。通过合理设计安全的生物纳米材料来构建高度稳定的生物聚合物-QD 杂化纳米凝胶对于同时结合生物传感、生物成像和有效治疗功能至关重要。

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