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Erschienen in: Investigational New Drugs 1/2024

21.12.2023 | Research

Targeted delivery of liposomal Ribociclib to SLC7A5 transporters in breast cancer cells

verfasst von: Mahtab Afsharzadeh, Jaleh Varshosaz, Mina Mirian, Farshid Hasanzadeh

Erschienen in: Investigational New Drugs | Ausgabe 1/2024

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Summary

This study aimed to prepare SLC7A5 transporters targeted liposomes of Ribociclib (RB) by stear(o)yl conjugation of Phe, Asp, Glu amino acids to liposomes as targeting moieties. The liposomes were optimized for their formulations. Cell analysis on two cell lines of MCF-7 and NIH-3T3 were done including; cell viability test by MTT assay, cellular uptake, and cell cycle arrest by flow cytometry. The optimal liposomes showed the particle size of 123.6 ± 1.3 nm, drug loading efficiency and release efficiency of 83.87% ± 1.33% and 60.55% ± 0.46%, respectively. The RB loaded liposomes showed no hemolysis activity. Targeted liposomes increased cytotoxicity on MCF-7 cells more significantly than NIH-3T3 cells. Cell flow cytometry indicated that targeted liposomes uptake was superior to plain (non-targted) liposomes and free drug. Free drug and RB-loaded liposomes interrupted cell cycle in G1. However, amino acid-targeted liposomes arrested cells more than the free drug at this stage. Targeted liposomes reduced cell cycle with more interruption in the G2/M phase compared to the negative control.

Graphical abstract

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Metadaten
Titel
Targeted delivery of liposomal Ribociclib to SLC7A5 transporters in breast cancer cells
verfasst von
Mahtab Afsharzadeh
Jaleh Varshosaz
Mina Mirian
Farshid Hasanzadeh
Publikationsdatum
21.12.2023
Verlag
Springer US
Erschienen in
Investigational New Drugs / Ausgabe 1/2024
Print ISSN: 0167-6997
Elektronische ISSN: 1573-0646
DOI
https://doi.org/10.1007/s10637-023-01409-9

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