Department of Mechanical Engineering, University of Wisconsin—Milwaukee, Milwaukee, Wisconsin 53211, United States.
ACS Nano. 2010 Nov 23;4(11):6805-17. doi: 10.1021/nn101670k. Epub 2010 Oct 19.
A multifunctional stable and pH-responsive polymer vesicle nanocarrier system was developed for combined tumor-targeted delivery of an anticancer drug and superparamagnetic iron oxide (SPIO) nanoparticles (NPs). These multifunctional polymer vesicles were formed by heterofunctional amphiphilic triblock copolymers, that is, R (folate (FA) or methoxy)-poly(ethylene glycol)(M(w):5000)-poly(glutamate hydrozone doxorubicin)-poly(ethylene glycol) (M(w):2000)-acrylate (i.e., R (FA or methoxy)-PEG(114)-P(Glu-Hyd-DOX)-PEG(46)-acrylate). The amphiphilic triblock copolymers can self-assemble into stable vesicles in aqueous solution. It was found that the long PEG segments were mostly segregated into the outer hydrophilic PEG layers of the vesicles, thereby providing active tumor targeting via FA, while the short PEG segments were mostly segregated into the inner hydrophilic PEG layer of the vesicles, thereby making it possible to cross-link the inner PEG layer via the acrylate groups for enhanced in vivo stability. The therapeutic drug, DOX, was conjugated onto the polyglutamate segment, which formed the hydrophobic membrane of the vesicles using a pH-sensitive hydrazone bond to achieve pH-responsive drug release, while the hydrophilic SPIO NPs were encapsulated into the aqueous core of the stable vesicles, allowing for ultrasensitive magnetic resonance imaging (MRI) detection. The SPIO/DOX-loaded vesicles demonstrated a much higher r(2) relaxivity value than Feridex, a commercially available SPIO-based T(2) contrast agent, which was attributed to the high SPIO NPs loading level and the SPIO clustering effect in the aqueous core of the vesicles. Results from flow cytometry and confocal laser scanning microscopy (CLSM) analysis showed that FA-conjugated vesicles exhibited higher cellular uptake than FA-free vesicles which also led to higher cytotoxicity. Thus, these tumor-targeting multifunctional SPIO/DOX-loaded vesicles will provide excellent in vivo stability, pH-controlled drug release, as well as enhanced MRI contrast, thereby making targeted cancer therapy and diagnosis possible.
一种多功能稳定且 pH 响应的聚合物囊泡纳米载体系统被开发出来,用于联合递送抗癌药物和超顺磁性氧化铁 (SPIO) 纳米颗粒 (NPs) 进行肿瘤靶向治疗。这些多功能聚合物囊泡由杂功能两亲性嵌段共聚物形成,即 R(叶酸(FA)或甲氧基)-聚(乙二醇)(Mw:5000)-聚(谷氨酸羟肟酸)-聚(乙二醇)(Mw:2000)-丙烯酰胺(即,R(FA 或甲氧基)-PEG(114)-P(Glu-Hyd-DOX)-PEG(46)-丙烯酰胺)。两亲性嵌段共聚物可以在水溶液中自组装成稳定的囊泡。研究发现,长 PEG 链段主要被分隔到囊泡的外亲水 PEG 层中,从而通过 FA 提供主动肿瘤靶向,而短 PEG 链段主要被分隔到囊泡的内亲水 PEG 层中,从而可以通过丙烯酰胺基团交联内 PEG 层,以提高体内稳定性。治疗药物 DOX 与聚谷氨酸段连接,通过 pH 敏感的腙键形成囊泡的疏水性膜,实现 pH 响应性药物释放,而亲水性 SPIO NPs 则被包裹在稳定囊泡的水核中,允许进行超灵敏磁共振成像 (MRI) 检测。SPIO/DOX 负载的囊泡的 r2 弛豫率值明显高于 Feridex,Feridex 是一种市售的基于 SPIO 的 T2 对比剂,这归因于 SPIO NPs 的高负载水平和 SPIO 在囊泡水核中的聚集效应。流式细胞术和共聚焦激光扫描显微镜 (CLSM) 分析的结果表明,与 FA 非负载囊泡相比,FA 修饰的囊泡具有更高的细胞摄取率,这也导致了更高的细胞毒性。因此,这些肿瘤靶向多功能 SPIO/DOX 负载的囊泡将提供出色的体内稳定性、pH 控制的药物释放以及增强的 MRI 对比度,从而实现靶向癌症治疗和诊断。
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