Tan Qinggang, Chu Yanyan, Bie Min, Wang Zihao, Xu Xiaoyan
Key Laboratory for Advanced Civil Engineering Materials (Ministry of Education), School of Materials Science and Engineering, Tongji University, Caoan Road 4800, Shanghai 201804, China.
Materials (Basel). 2017 Feb 16;10(2):192. doi: 10.3390/ma10020192.
Biopolymer/inorganic material nanocomposites have attracted increasing interest as nanocarriers for delivering drugs owing to the combined advantages of both biopolymer and inorganic materials. Here, amphiphilic block copolymer/fullerene nanocomposites were prepared as nanocarriers for hydrophobic drug by incorporation of C60 in the core of methoxy polyethylene glycol-poly(d,l-lactic acid) (MPEG-PDLLA) micelles. The structure and morphology of MPEG-PDLLA/C60 nanocomposites were characterized using transmission electron microscopy, dynamic light scattering, high-resolution transmission electron microscopy, and thermal gravimetric analysis. It was found that the moderate amount of spherical C60 incorporated in the MPEG-PDLLA micelles may cause an increase in the molecular chain space of PDLLA segments in the vicinity of C60 and, thus, produce a larger cargo space to increase drug entrapment and accelerate the drug release from nanocomposites. Furthermore, sufficient additions of C60 perhaps resulted in an aggregation of C60 within the micelles that decreased the drug entrapment and produced a steric hindrance for DOX released from the nanocomposites. The results obtained provide fundamental insights into the understanding of the role of C60 in adjusting the drug loading and release of amphiphilic copolymer micelles and further demonstrate the future potential of the MPEG-PDLLA/C60 nanocomposites used as nanocarriers for controlled drug-delivery applications.
由于生物聚合物和无机材料的综合优势,生物聚合物/无机材料纳米复合材料作为药物递送的纳米载体越来越受到关注。在此,通过将C60掺入甲氧基聚乙二醇-聚(d,l-乳酸)(MPEG-PDLLA)胶束的核心中,制备了两亲性嵌段共聚物/富勒烯纳米复合材料作为疏水性药物的纳米载体。使用透射电子显微镜、动态光散射、高分辨率透射电子显微镜和热重分析对MPEG-PDLLA/C60纳米复合材料的结构和形态进行了表征。结果发现,掺入MPEG-PDLLA胶束中的适量球形C60可能会导致C60附近的PDLLA链段的分子链空间增加,从而产生更大的载药空间以增加药物包封率并加速药物从纳米复合材料中的释放。此外,足够量的C60添加可能导致C60在胶束内聚集,从而降低药物包封率并对从纳米复合材料中释放的阿霉素产生空间位阻。所获得的结果为理解C60在调节两亲共聚物胶束的药物负载和释放中的作用提供了基本见解,并进一步证明了MPEG-PDLLA/C60纳米复合材料作为可控药物递送应用的纳米载体的未来潜力。