Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang 453007, People's Republic of China.
Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Sciences, Xiamen University, Xiamen 154007, China.
Mater Sci Eng C Mater Biol Appl. 2020 Mar;108:110464. doi: 10.1016/j.msec.2019.110464. Epub 2019 Nov 20.
Multifunctional mixed micelles possessing targeting folates on the periphery and stable radicals in the core were prepared from the mixture of folate-poly(ethylene glycol)-block-poly(d-lactide) (FA-PEG-b-PDLA) and poly(ethylene glycol) methyl ether-block-poly(l-lactide)- 2,2,6,6-tetramethylpiperidine-1-oxyl (mPEG-b-PLLA-TEMPO). FA-PEG-b-PDLA and mPEG-b-PLLA-TEMPO were prepared by combining ring-opening polymerization (ROP) of lactide with a series of conversion of the end functional groups. The synthesized block copolymers and their intermediates were well characterized by gel permeation chromatography (GPC) and H nuclear magnetic resonance (H NMR) spectroscopy. The mixture of FA-PEG-b-PDLA and mPEG-b-PLLA-TEMPO self-assembled into spherical micelles with the average diameter about 200 nm through PLA stereocomplexation, which were characterized by dynamic light scattering (DLS), transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). The formed micelles were confirmed to emit electron paramagnetic resonance (EPR) signals by EPR spectroscopy. Additionally, the formed micelles exhibited high loading capacity of hydrophobic anticancer drug, controlled in vitro drug release, satisfied biocompatibility and a significantly higher cellular uptake, indicating promising applications in smart drug delivery.
具有靶向叶酸的多功能混合胶束,其外围为聚乙二醇封端的聚(乳酸)-嵌段-聚(D-乳酸)(FA-PEG-b-PDLA),内核为稳定自由基,是由叶酸-聚乙二醇-嵌段-聚(L-乳酸)-2,2,6,6-四甲基哌啶-1-氧自由基(mPEG-b-PLLA-TEMPO)混合物制备的。FA-PEG-b-PDLA 和 mPEG-b-PLLA-TEMPO 通过丙交酯的开环聚合(ROP)和一系列端基转化反应制备。合成的嵌段共聚物及其中间体通过凝胶渗透色谱(GPC)和 H 核磁共振(H NMR)光谱进行了很好的表征。FA-PEG-b-PDLA 和 mPEG-b-PLLA-TEMPO 的混合物通过 PLA 立构复合自组装成平均直径约为 200nm 的球形胶束,通过动态光散射(DLS)、透射电子显微镜(TEM)和差示扫描量热法(DSC)进行了表征。电子顺磁共振(EPR)光谱证实形成的胶束可发出电子顺磁共振(EPR)信号。此外,形成的胶束表现出对疏水性抗癌药物的高载药量、体外药物控制释放、良好的生物相容性和显著提高的细胞摄取,表明在智能药物输送中有很好的应用前景。