Department of Polymer and Materials Chemistry, Faculty of Chemistry & Petroleum Sciences, Shahid Beheshti University, Tehran, Iran.
Department of Polymer and Materials Chemistry, Faculty of Chemistry & Petroleum Sciences, Shahid Beheshti University, Tehran, Iran.
J Pharm Sci. 2021 May;110(5):2196-2209. doi: 10.1016/j.xphs.2020.12.029. Epub 2020 Dec 26.
Novel dual redox/pH-sensitive star-like amphiphilic sucrose-oligo(butyl fumarate) (thioglycolic acid conjugate)-SS-poly(ethylene glycol) (Suc-OBF(TGA)-SS-PEG) copolymers and their self-assembled micelles were prepared and utilized for intracellular doxorubicin delivery. Importance of changing the hydrophobic chain length on micelles properties was investigated. Results showed that the micelles with longer hydrophobic chain exhibited smaller size and were more stable in aqueous solution. The redox and pH sensitivity of the micelles was confirmed by the change of micelle diameter/diameter distribution measured by dynamic light scattering and the change of micellar morphology observed by scanning electron microscope. The micelles display a decent doxorubicin loading capacity. In vitro release studies showed that only 14.3% doxorubicin was released from doxorubicin-loaded micelles under physiological conditions in 30 h. The release of doxorubicin was accelerated at pH 5.5 or in the presence of 10 mM glutathione at pH 7.4 (46.9% and 76.9% of doxorubicin was released, respectively, in 30 h). The doxorubicin release was further expedited under pH 5.5 and 10 mM GSH conditions (91.4%). Suc-OBF(TGA)-SS-PEG micelles displayed no cytotoxicity toward HDF cells. MTT assays indicated that doxorubicin-loaded micelles had good cytotoxicity against MCF-7 cells. This work suggested that star-like amphiphilic Suc-OBF(TGA)-SS-PEG copolymer micelles may provide a promising platform for delivering doxorubicin and other hydrophobic anticancer drugs.
新型双氧化还原/pH 敏感星型两亲性蔗糖-聚(丁烯富马酸)(巯基乙酸)-SS-聚(乙二醇)(Suc-OBF(TGA)-SS-PEG)共聚物及其自组装胶束被制备并用于细胞内阿霉素的递送。研究了改变胶束性质的疏水性链长的重要性。结果表明,具有较长疏水性链的胶束表现出较小的尺寸,并且在水溶液中更加稳定。通过动态光散射测量的胶束粒径/粒径分布的变化和扫描电子显微镜观察的胶束形态的变化证实了胶束的氧化还原和 pH 敏感性。胶束显示出良好的阿霉素载药能力。体外释放研究表明,在生理条件下,载有阿霉素的胶束在 30 小时内仅释放了 14.3%的阿霉素。在 pH5.5 或在 pH7.4 时存在 10mM 谷胱甘肽的条件下,阿霉素的释放速度加快(分别在 30 小时内释放了 46.9%和 76.9%的阿霉素)。在 pH5.5 和 10mM GSH 条件下,阿霉素的释放进一步加快(91.4%)。Suc-OBF(TGA)-SS-PEG 胶束对 HDF 细胞没有细胞毒性。MTT 测定表明,载有阿霉素的胶束对 MCF-7 细胞具有良好的细胞毒性。这项工作表明,星型两亲性 Suc-OBF(TGA)-SS-PEG 共聚物胶束可能为递送阿霉素和其他疏水性抗癌药物提供了一个有前途的平台。