Docetaxel delivery using folate-targeted liposomes: in vitro and in vivo studies | ||
Nanomedicine Journal | ||
مقاله 3، دوره 7، شماره 2، تیر 2020، صفحه 108-114 اصل مقاله (595.76 K) | ||
نوع مقاله: Research Paper | ||
شناسه دیجیتال (DOI): 10.22038/nmj.2020.07.003 | ||
نویسندگان | ||
Roghayyeh Vakili-Ghartavol1؛ Mahmoud Reza Jaafari2، 3؛ Amin Reza Nikpoor4؛ Seyed Mahdi Rezayat* 1، 5 | ||
1Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran | ||
2Department of Pharmaceutical Nanotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran | ||
3Nanotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran | ||
4Molecular Medicine Research Center Hormozgan Health Institute, Hormozgan University of Medical Sciences, Bandar Abbas, Iran | ||
5Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran | ||
چکیده | ||
Objective(s): Folate-targeted liposomes have been well considered in folate receptor (FR) overexpressing cells including MCF-7 and 4T1 cells in vitro and in vivo. The objective of this study is to design an optimum folate targeted liposomal formulations which show the best liposome cell uptake to tumor cells. Material and Methods: In this study, we prepared and characterized different targeted formulations and a nontargeted form as a control. Physicochemical analysis showed that the liposomes had homogeneous population and appropriate size to accumulate to tumor sites through the enhanced permeation and retention (EPR) mechanism. Moreover, we compared the cell uptake of folate targeted liposomal docetaxel compared to nontargeted liposomes in vitro. Results: The in vitro drug release profile of the formulations at different time points showed none of the formulations did not has burst release. However, targeted liposomes accumulated in tumor tissue in vivo less than nontargeted formulations which could be attributed to their uptake by RES due to relatively greater size of targeted formulations. It is presumable that analyze the biodistribution process at longer time points and the molecular mechanisms behind the tissue accumulation could clear the issue. Conclusion: We conclude that success in vitro studies holds the promise of folate targeting strategy and in vivo study merits further investigations. | ||
کلیدواژهها | ||
Docetaxel Encapsulation؛ Folate Targeting؛ Liposomes؛ Tumor Drug Delivery | ||
مراجع | ||
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