liposomes as gene delivery vectors for human placental cells

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ID: 225380
2018
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Abstract
Nanomedicine as a therapeutic approach for pregnancy-related diseases could offer improved treatments for the mother while avoiding side effects for the fetus. In this study, we evaluated the potential of liposomes as carriers for small interfering RNAs to placental cells. Three neutral formulations carrying rhodamine-labelled siRNAs were evaluated on an in vitro model, i.e., human primary villous cytotrophoblasts. siRNA internalization rate from lipoplexes were compared to the one in the presence of the lipofectamine reagent and assessed by confocal microscopy. Results showed cellular internalization of nucleic acid with all three formulations, based on two cationic lipids, either DMAPAP or CSL-3. Moreover, incubation with DMAPAP+AA provided a rate of labelled cells as high as with lipofectamine (53 ± 15% and 44 ± 12%, respectively) while being more biocompatible. The proportion of cells which internalized siRNA were similar when using DMAPAP/DDSTU (16 ± 5%) and CSL-3 (22 ± 5%). This work highlights that liposomes could be a promising approach for gene therapy dedicated to pregnant patients.
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valero2018moleculesliposomes Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Lucie Valero;Khair Alhareth;Jenifer Espinoza Romero;Warren Viricel;Jeanne Leblond;Audrey Chissey;Hélène Dhotel;Caroline Roques;Danielle Campiol Arruda;Virginie Escriou;Nathalie Mignet;Thierry Fournier;Karine Andrieux
Journal Journal of ethnopharmacology
Year 2018
DOI
10.3390/molecules23051085
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