Tailoring micellar nanocarriers for pemetrexed in breast cancer: design, fabrication and in vitro evaluation.

Nanomedicine (London, England) Pub Date : 2024-01-01 Epub Date: 2024-05-03 DOI:10.2217/nnm-2024-0013
Nalla Usha Kumari, Padakanti Sandeep Chary, Ekta Pardhi, Neelesh Kumar Mehra
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Abstract

Aim: To investigate the pemetrexed encapsulated polymeric mixed micelles (PMMs) against breast cancer treatment.Methods: We meticulously optimized the formulation and conducted extensive characterizations, including photon correlation spectroscopy for micellization, advanced analytical techniques and in vitro cell line assessments.Results: The PMM exhibited favorable characteristics, with a spherical morphology, hydrodynamic particle size of 19.58 ± 0.89 nm, polydispersity index of 0.245 ± 0.1, and a surface charge of -9.70 ± 0.61 mV. Encapsulation efficiency and drug payload reached 96.16 ± 0.37% and 4.5 ± 0.32%, respectively. Cytotoxicity analysis indicated superior efficacy of the PMM over the drug solution.Conclusion: The PMM formulation exhibited controlled release of the drug, and demonstrated enhanced cytotoxicity against breast cancer cells, highlighting its therapeutic promise.

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定制用于乳腺癌培美曲塞的胶束纳米载体:设计、制造和体外评估。
目的:研究培美曲塞包裹的聚合物混合胶束(PMMs)对乳腺癌的治疗作用。方法:我们精心优化了配方,并进行了广泛的表征,包括胶束化的光子相关光谱、先进的分析技术和体外细胞系评估。结果PMM 具有良好的特性,呈球形,水动力粒径为 19.58 ± 0.89 nm,多分散指数为 0.245 ± 0.1,表面电荷为 -9.70 ± 0.61 mV。封装效率和药物有效载荷分别达到 96.16 ± 0.37% 和 4.5 ± 0.32%。细胞毒性分析表明,PMM 的药效优于药物溶液。结论PMM 制剂可控制药物的释放,对乳腺癌细胞的细胞毒性也有所增强,突出了其治疗前景。
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