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In vitro caco-2 cell permeability studies of ziprasidone hydrochloride monohydrate nanocrystals

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dc.contributor.author Karaküçük, A.
dc.contributor.author Taşhan, E.
dc.contributor.author Öztürk, N.
dc.contributor.author Çelebi, N.
dc.date.accessioned 2022-10-06T12:50:31Z
dc.date.available 2022-10-06T12:50:31Z
dc.date.issued 2021
dc.identifier.issn 1304530X (ISSN)
dc.identifier.uri http://hdl.handle.net/11616/71835
dc.description.abstract Objectives: The current study focused on the evaluation of the cytotoxic effect and permeability of ziprasidone hydrochloride monohydrate (ZHM) nanocrystals on Caco-2 cells. Materials and Methods: ZHM nanocrystals were prepared by the microfluidization method in the presence of polyvinylpyrrolidone as a stabilizer. Particle size (PS), particle size distribution (PDI), and zeta potential (ZP) values were measured in characterization studies. In vitro cytotoxic effects of ZHM nanocrystals were investigated using the 3-(4,5-dimetylthiazol-2-yl)-2,5-diphenyltetrazolium bromide test. Caco-2 transport studies were conducted with formulations of ZHM coarse powder and nanocrystals. Results: Nanocrystals were obtained with 400-600 nm PS, 0.1-0.4 PDI, and >20 mV ZP values. The cell viability remained 100% for all sample groups. The permeability value of ZHM nanocrystals through Caco-2 cells increased 2.3-fold in comparison with ZHM coarse powder. Cumulative drug transport also increased at the end of the sampling period. Conclusion: Nanocrystal technology helps to increase the permeability of drug particles by increasing the saturation solubility. © Turk J Pharm Sci, Published by Galenos Publishing House.
dc.source Turkish Journal of Pharmaceutical Sciences
dc.title In vitro caco-2 cell permeability studies of ziprasidone hydrochloride monohydrate nanocrystals


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