Imaging modification of colon carcinoma cells exposed to lipid based nanovectors for drug delivery: a scanning electron microscopy investigation.
Nicoletta DepaloElisabetta FanizzaFabio VischioNunzio DenoraValentino LaquintanaAnnalisa CutrignelliMarinella StriccoliGianluigi GiannelliAngela AgostianoMaria Lucia CurriMaria Principia ScavoPublished in: RSC advances (2019)
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.
Keyphrases
- drug delivery
- electron microscopy
- induced apoptosis
- cancer therapy
- high resolution
- cell cycle arrest
- drug release
- cell therapy
- endoplasmic reticulum stress
- single cell
- emergency department
- signaling pathway
- oxidative stress
- metal organic framework
- radiation therapy
- atomic force microscopy
- squamous cell carcinoma
- mesenchymal stem cells
- neoadjuvant chemotherapy
- lymph node
- aqueous solution
- amino acid
- climate change
- cystic fibrosis
- small molecule
- staphylococcus aureus
- mass spectrometry
- fatty acid
- molecularly imprinted
- high speed
- adverse drug