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新型 pH 响应β-环糊精接枝胶束共递送阿霉素和康氟酮引发转移性人乳腺癌细胞凋亡。

Co-delivery of doxorubicin and conferone by novel pH-responsive β-cyclodextrin grafted micelles triggers apoptosis of metastatic human breast cancer cells.

机构信息

Department of Applied Chemistry, Faculty of Chemistry, Semnan University, Semnan, Iran.

Department of Electrical Engineering, University of Bonab, Bonab, Iran.

出版信息

Sci Rep. 2021 Nov 2;11(1):21425. doi: 10.1038/s41598-021-00954-8.

Abstract

Adjuvant-aided combination chemotherapy is one of the most effective ways of cancer treatment by overcoming the multidrug resistance (MDR) and reducing the side-effects of anticancer drugs. In this study, Conferone (Conf) was used as an adjuvant in combination with Doxorubicin (Dox) for inducing apoptosis to MDA-MB-231 cells. Herein, the novel biodegradable amphiphilic β-cyclodextrin grafted poly maleate-co-PLGA was synthesized by thiol-ene addition and ring-opening process. Micelles obtained from the novel copolymer showed exceptional properties such as small size of around 34.5 nm, CMC of 0.1 μg/mL, and cell internalization of around 100% at 30 min. These novel engineered micelles were used for combination delivery of doxorubicin-conferone with high encapsulation efficiency of near 100% for both drugs. Our results show that combination delivery of Dox and Conf to MDA-MB-231 cells had synergistic effects (CI < 1). According to cell cycle and Annexin-V apoptosis analysis, Dox-Conf loaded micelle significantly induce tumor cell apoptosis (more than 98% of cells population showed apoptosis at IC = 0.259 μg/mL). RT-PCR and western-blot tests show that Dox-Conf loaded βCD-g-PMA-co-PLGA micelle induced apoptosis via intrinsic pathway. Therefore, the unique design of multi-functional pH-sensitive micelles open a new perspective for the development of nanomedicine for combination chemo-adjuvant therapy against malignant cancer.

摘要

辅助联合化疗是克服多药耐药性(MDR)和降低抗癌药物副作用的最有效癌症治疗方法之一。在这项研究中,Conferone(Conf)被用作与多柔比星(Dox)联合使用的佐剂,以诱导 MDA-MB-231 细胞凋亡。在此,通过硫醇-烯加成和开环过程合成了新型可生物降解的两亲性β-环糊精接枝聚马来酸-co-PLGA。从新型共聚物获得的胶束表现出出色的性能,例如约 34.5nm 的小尺寸、CMC 为 0.1μg/mL,以及在 30 分钟时约 100%的细胞内化。这些新型工程胶束用于阿霉素-康佛酮的联合递药,两种药物的包封效率接近 100%。我们的结果表明,Dox 和 Conf 联合递药对 MDA-MB-231 细胞具有协同作用(CI<1)。根据细胞周期和 Annexin-V 凋亡分析,载有 Dox 和 Conf 的胶束显著诱导肿瘤细胞凋亡(在 IC=0.259μg/mL 时,超过 98%的细胞群显示凋亡)。RT-PCR 和 Western blot 测试表明,载有 Dox-Conf 的βCD-g-PMA-co-PLGA 胶束通过内在途径诱导细胞凋亡。因此,多功能 pH 敏感胶束的独特设计为开发用于联合化疗佐剂治疗恶性癌症的纳米医学开辟了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74fa/8563731/f6a8c0c50702/41598_2021_954_Fig1_HTML.jpg

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