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Hexosomes as Efficient Platforms for Possible Fluoxetine Hydrochloride Repurposing with Improved Cytotoxicity against HepG2 Cells

Hend Mohamed Abdel‐Bar, Shaymaa Elsayed Khater, Dalia Ghorab, Abdulaziz Mohsen Al-mahallawi

2020ACS Omega23 citationsDOIOpen Access PDF

Abstract

FH release, where only 19.5 ± 2.3% released in phosphate-buffered saline (PBS) pH 7.4 after 24 h. Contrarily, HEX rapidly released FH in acetate buffer pH 5.5 and achieved a 90.5 ± 4.7% release after 24 h. The obtained HEX showed an improved cellular internalization in a time-dependent manner and enhanced the cytotoxicity (2-fold higher than FH solution). The current study suggests the potential of FH-HEX as a possible anticancer agent against hepatocellular carcinoma.

Topics & Concepts

CytotoxicityChemistryPoloxamerParticle sizeOleic acidHydrochlorideIn vitroNuclear chemistryChromatographyCombinatorial chemistryBiochemistryOrganic chemistryCopolymerPhysical chemistryPolymerLung Cancer Research StudiesNeuroendocrine Tumor Research AdvancesProteoglycans and glycosaminoglycans research
Hexosomes as Efficient Platforms for Possible Fluoxetine Hydrochloride Repurposing with Improved Cytotoxicity against HepG2 Cells | Litcius