Hu Jie, Fu Shaozhi, Peng Qiuxia, Han YunWei, Xie Jie, Zan Ning, Chen Yue, Fan Juan
Department of Oncology, The Affiliated Hospital of Southwest Medical University, Luzhou 646000, China.
Department of Orthopedics, The Affiliated Hospital of Southwest Medical University, Luzhou 646000, China.
Int J Pharm. 2017 Jan 10;516(1-2):313-322. doi: 10.1016/j.ijpharm.2016.11.047. Epub 2016 Nov 21.
The objective of our study was to examine the anti-tumor effect of paclitaxel (PTX)-loaded polymeric nanoparticles (PTX-NPs) combined with circadian chronomodulated chemotherapy. Our intention was to screen out the best time of the day for the drug to be administered. PTX-NPs with a diameter of approximately 168nm were prepared through a thin film dispersion technique. The PTX in PTX-NPs showed an initial fast release subsequently a slower and sustained release. The cytotoxicity of chronomodulated administration of PTX-NPs in vitro confirmed that its cytotoxic effect was lower than that of PTX injection, and showed a time-dependent effect. In addition, anti-tumor effect was examined by analysing tumor growth inhibition rate, micro-vessel density (MVD), cell proliferation and cell apoptosis, following either injection with PTX or administration of PTX-NPs. Micro fluorine-18-deoxyglucose PET/computed tomography (F-FDG PET/CT) was used to evaluate tumor reactivity to PTX-NPs combined with chronomodulated chemotherapy. Taken these results into consideraion, our experiment indicates that PTX-NPs exhibit greater anti-tumor activity against A549 cells, in comparison with PTX injection, and the anti-tumor effect at 15h after light onset (HALO) administration is the best in all groups. Therefore, prepared PTX-NPs combined with chronomodulated chemotherapy could be a potential treatment for lung cancer.
我们研究的目的是考察载有紫杉醇(PTX)的聚合物纳米粒(PTX-NPs)联合昼夜节律时辰化疗的抗肿瘤效果。我们的意图是筛选出一天中给药的最佳时间。通过薄膜分散技术制备了直径约为168nm的PTX-NPs。PTX-NPs中的PTX呈现出初始快速释放,随后是较慢的持续释放。PTX-NPs时辰调制给药在体外的细胞毒性证实其细胞毒性作用低于PTX注射,并呈现出时间依赖性效应。此外,在注射PTX或给予PTX-NPs后,通过分析肿瘤生长抑制率、微血管密度(MVD)、细胞增殖和细胞凋亡来考察抗肿瘤效果。使用微型氟-18-脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(F-FDG PET/CT)来评估肿瘤对PTX-NPs联合时辰化疗的反应性。综合这些结果,我们的实验表明,与PTX注射相比,PTX-NPs对A549细胞表现出更大的抗肿瘤活性,并且在光照开始后15小时(HALO)给药时的抗肿瘤效果在所有组中最佳。因此,制备的PTX-NPs联合时辰化疗可能是肺癌的一种潜在治疗方法。
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