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解析载有替莫唑胺的 PLGA 纳米粒的细胞毒性潜力。

Unraveling the cytotoxic potential of Temozolomide loaded into PLGA nanoparticles.

机构信息

Department of Pharmaceutics, C,U, Shah College of Pharmacy, SNDT Women's University, Juhu Tara Road, Santacruz (West), Mumbai 400 049, India.

出版信息

Daru. 2014 Jan 10;22(1):18. doi: 10.1186/2008-2231-22-18.

Abstract

BACKGROUND

Nanotechnology has received great attention since a decade for the treatment of different varieties of cancer. However, there is a limited data available on the cytotoxic potential of Temozolomide (TMZ) formulations. In the current research work, an attempt has been made to understand the anti-metastatic effect of the drug after loading into PLGA nanoparticles against C6 glioma cells.Nanoparticles were prepared using solvent diffusion method and were characterized for size and morphology. Diffusion of the drug from the nanoparticles was studied by dialysis method. The designed nanoparticles were also assessed for cellular uptake using confocal microscopy and flow cytometry.

RESULTS

PLGA nanoparticles caused a sustained release of the drug and showed a higher cellular uptake. The drug formulations also affected the cellular proliferation and motility.

CONCLUSION

PLGA coated nanoparticles prolong the activity of the loaded drug while retaining the anti-metastatic activity.

摘要

背景

自十年前以来,纳米技术因其在治疗各种癌症方面的应用而受到广泛关注。然而,关于替莫唑胺(TMZ)制剂的细胞毒性潜力的数据有限。在当前的研究工作中,我们试图了解载药 PLGA 纳米颗粒对 C6 神经胶质瘤细胞的抗转移作用。采用溶剂扩散法制备纳米粒,并对其粒径和形态进行了表征。采用透析法研究药物从纳米粒中的扩散情况。还使用共聚焦显微镜和流式细胞术评估了设计的纳米粒的细胞摄取情况。

结果

PLGA 纳米粒可使药物持续释放,并表现出更高的细胞摄取。药物制剂还影响细胞增殖和迁移。

结论

PLGA 包被的纳米粒在保持抗转移活性的同时延长了载药的活性。

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