Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University , 199 Ren'ai Road, Suzhou, 215123 Jiangsu, China.
State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau , Avenida da Universidad, Taipa, Macau 999078, China.
ACS Appl Mater Interfaces. 2017 Jul 19;9(28):23555-23563. doi: 10.1021/acsami.7b07535. Epub 2017 Jul 3.
Nanoscale coordination polymers (NCPs), with inherent biodegradability, chemical diversities, and porous structures, are a promising class of nanomaterials in the nanomedicine field. Herein, a unique type of redox-sensitive NCPs is constructed with manganese ions (Mn) and dithiodiglycolic acid as the disulfide (SS)-containing organic bridging ligand. The obtained Mn-SS NCPs with a mesoporous structure could be efficiently loaded with doxorubicin (DOX), a chemotherapeutics. The yielded Mn-SS/DOX nanoparticles are coated with a layer of polydopamine (PDA) and then modified by poly(ethylene glycol) (PEG). In such a Mn-SS/DOX@PDA-PEG NCP structure, the disulfide linkage (SS) within dithiodiglycolic acid can be cleaved in the presence of glutathione (GSH), leading to efficient redox-responsive dissociation of NCPs and the subsequent drug release. Meanwhile, Mn in Mn-SS/DOX@PDA-PEG NCPs would offer a strong T1 contrast in magnetic resonance (MR) imaging, Upon intravenous injection, these Mn-SS/DOX@PDA-PEG NCPs show efficient tumor homing, as revealed by MR imaging, and offer an obviously improved in vivo therapeutic outcome compared to that achieved with free DOX.
纳米级配位聚合物(NCPs)具有内在的生物降解性、化学多样性和多孔结构,是纳米医学领域一类很有前途的纳米材料。本文构建了一种独特的氧化还原敏感型 NCPs,其以锰离子(Mn)和二硫代二甘酸作为含有二硫键(SS)的有机桥联配体。所得的具有介孔结构的 Mn-SS NCPs 可以高效负载阿霉素(DOX),这是一种化疗药物。所生成的 Mn-SS/DOX 纳米粒子被一层聚多巴胺(PDA)包裹,然后用聚乙二醇(PEG)进行修饰。在这种 Mn-SS/DOX@PDA-PEG NCP 结构中,二硫键(SS)在谷胱甘肽(GSH)存在的情况下可以被切断,导致 NCPs 的有效氧化还原响应性解离和随后的药物释放。同时,Mn-SS/DOX@PDA-PEG NCPs 中的 Mn 会在磁共振(MR)成像中提供强烈的 T1 对比。静脉注射后,这些 Mn-SS/DOX@PDA-PEG NCPs 通过 MR 成像显示出高效的肿瘤归巢,并与游离 DOX 相比,在体内治疗效果上有明显改善。