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Imaging modification of colon carcinoma cells exposed to lipid based nanovectors for drug delivery: a scanning electron microscopy investigation

The adsorption at cell surfaces and cell internalization of two drug delivery lipid based nanovectors has been investigated by means of Field Emission Scanning Electron Microscopy (FE-SEM) operating at low beam voltage on two different colon carcinoma cell lines, CaCo-2 and CoLo-205, that were compa...

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Autores principales: Depalo, Nicoletta, Fanizza, Elisabetta, Vischio, Fabio, Denora, Nunzio, Laquintana, Valentino, Cutrignelli, Annalisa, Striccoli, Marinella, Giannelli, Gianluigi, Agostiano, Angela, Curri, Maria Lucia, Scavo, Maria Principia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066453/
https://www.ncbi.nlm.nih.gov/pubmed/35518842
http://dx.doi.org/10.1039/c9ra02381j
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author Depalo, Nicoletta
Fanizza, Elisabetta
Vischio, Fabio
Denora, Nunzio
Laquintana, Valentino
Cutrignelli, Annalisa
Striccoli, Marinella
Giannelli, Gianluigi
Agostiano, Angela
Curri, Maria Lucia
Scavo, Maria Principia
author_facet Depalo, Nicoletta
Fanizza, Elisabetta
Vischio, Fabio
Denora, Nunzio
Laquintana, Valentino
Cutrignelli, Annalisa
Striccoli, Marinella
Giannelli, Gianluigi
Agostiano, Angela
Curri, Maria Lucia
Scavo, Maria Principia
author_sort Depalo, Nicoletta
collection PubMed
description The adsorption at cell surfaces and cell internalization of two drug delivery lipid based nanovectors has been investigated by means of Field Emission Scanning Electron Microscopy (FE-SEM) operating at low beam voltage on two different colon carcinoma cell lines, CaCo-2 and CoLo-205, that were compared with the M14 melanoma cell line, as a reference. The cells were incubated with the investigated multifunctional nanovectors, based on liposomes and magnetic micelles loaded with 5-fluorouracil, as a chemotherapeutic agent, and a FE-SEM systematic investigation was performed, enabling a detailed imaging of any morphological changes of the drug exposed cells as a function of time. The results of the FE-SEM investigation were validated by MTS assay and immunofluorescence staining of the Ki-67 protein performed on the investigated cell lines at different times. The two nanoformulations resulted in a comparable effect on CaCo-2 and M14 cell lines, while for CoLo 205 cells, the liposomes provided an cytotoxic activity higher than that observed in the case of the micelles. The study highlighted the high potential of FE-SEM as a valuable complementary technique for imaging and monitoring in time the drug effects on the selected cells exposed to the two different nanoformulations.
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spelling pubmed-90664532022-05-04 Imaging modification of colon carcinoma cells exposed to lipid based nanovectors for drug delivery: a scanning electron microscopy investigation Depalo, Nicoletta Fanizza, Elisabetta Vischio, Fabio Denora, Nunzio Laquintana, Valentino Cutrignelli, Annalisa Striccoli, Marinella Giannelli, Gianluigi Agostiano, Angela Curri, Maria Lucia Scavo, Maria Principia RSC Adv Chemistry The adsorption at cell surfaces and cell internalization of two drug delivery lipid based nanovectors has been investigated by means of Field Emission Scanning Electron Microscopy (FE-SEM) operating at low beam voltage on two different colon carcinoma cell lines, CaCo-2 and CoLo-205, that were compared with the M14 melanoma cell line, as a reference. The cells were incubated with the investigated multifunctional nanovectors, based on liposomes and magnetic micelles loaded with 5-fluorouracil, as a chemotherapeutic agent, and a FE-SEM systematic investigation was performed, enabling a detailed imaging of any morphological changes of the drug exposed cells as a function of time. The results of the FE-SEM investigation were validated by MTS assay and immunofluorescence staining of the Ki-67 protein performed on the investigated cell lines at different times. The two nanoformulations resulted in a comparable effect on CaCo-2 and M14 cell lines, while for CoLo 205 cells, the liposomes provided an cytotoxic activity higher than that observed in the case of the micelles. The study highlighted the high potential of FE-SEM as a valuable complementary technique for imaging and monitoring in time the drug effects on the selected cells exposed to the two different nanoformulations. The Royal Society of Chemistry 2019-07-15 /pmc/articles/PMC9066453/ /pubmed/35518842 http://dx.doi.org/10.1039/c9ra02381j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Depalo, Nicoletta
Fanizza, Elisabetta
Vischio, Fabio
Denora, Nunzio
Laquintana, Valentino
Cutrignelli, Annalisa
Striccoli, Marinella
Giannelli, Gianluigi
Agostiano, Angela
Curri, Maria Lucia
Scavo, Maria Principia
Imaging modification of colon carcinoma cells exposed to lipid based nanovectors for drug delivery: a scanning electron microscopy investigation
title Imaging modification of colon carcinoma cells exposed to lipid based nanovectors for drug delivery: a scanning electron microscopy investigation
title_full Imaging modification of colon carcinoma cells exposed to lipid based nanovectors for drug delivery: a scanning electron microscopy investigation
title_fullStr Imaging modification of colon carcinoma cells exposed to lipid based nanovectors for drug delivery: a scanning electron microscopy investigation
title_full_unstemmed Imaging modification of colon carcinoma cells exposed to lipid based nanovectors for drug delivery: a scanning electron microscopy investigation
title_short Imaging modification of colon carcinoma cells exposed to lipid based nanovectors for drug delivery: a scanning electron microscopy investigation
title_sort imaging modification of colon carcinoma cells exposed to lipid based nanovectors for drug delivery: a scanning electron microscopy investigation
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066453/
https://www.ncbi.nlm.nih.gov/pubmed/35518842
http://dx.doi.org/10.1039/c9ra02381j
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