Drug Targeting Strategies Based on Charge Dependent Uptake of Nanoparticles into Cancer Cells

The aim of this review was to describe the preferred charged nano-particles (CNPs) for targeted delivery in tumor cells. Zeta Potential (ZP), which represents the surface charge of NPs was highlighted in cell entrance and interactions. In this regard, various types of endocytosis pathways which are...

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Main Authors: Maryam Saadat (Author), Fahimeh Zahednezhad (Author), Parvin Zakeri-Milani (Author), Hamid Reza Heidari (Author), Javid Shahbazi-Mojarrad (Author), Hadi Valizadeh (Author)
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Published: Frontiers Media S.A., 2019-05-01T00:00:00Z.
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100 1 0 |a Maryam Saadat  |e author 
700 1 0 |a Fahimeh Zahednezhad  |e author 
700 1 0 |a Parvin Zakeri-Milani  |e author 
700 1 0 |a Hamid Reza Heidari  |e author 
700 1 0 |a Javid Shahbazi-Mojarrad  |e author 
700 1 0 |a Hadi Valizadeh  |e author 
245 0 0 |a Drug Targeting Strategies Based on Charge Dependent Uptake of Nanoparticles into Cancer Cells 
260 |b Frontiers Media S.A.,   |c 2019-05-01T00:00:00Z. 
500 |a 10.18433/jpps30318 
500 |a 1482-1826 
520 |a The aim of this review was to describe the preferred charged nano-particles (CNPs) for targeted delivery in tumor cells. Zeta Potential (ZP), which represents the surface charge of NPs was highlighted in cell entrance and interactions. In this regard, various types of endocytosis pathways which are involved in NPs' uptake were first introduced. Then, significance of positively charged NPs (PCNPs) in proton sponge effect corresponding to lysosomal escape was discussed. Cells prefer to endocyte the NPs with positive charge in passive targeting and gene delivery, while in active targeting; the charge of receptors' ligand binding site determines the NPs cellular uptake. Moreover, pH-sensitive NPs represent charge reversible behavior depending on pH changes which leads to longer blood circulation residence and higher uptake at acidic microenvironment of the cancer media. Role of the CNPs in overcoming multidrug resistance (MDR) and bypassing p-glycoprotein was further investigated. 
546 |a EN 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Journal of Pharmacy & Pharmaceutical Sciences, Vol 22, Iss 1 (2019) 
787 0 |n https://journals.library.ualberta.ca/jpps/index.php/JPPS/article/view/30318 
787 0 |n https://doaj.org/toc/1482-1826 
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