Multifunctional Polymeric Biodegradable and Biocompatible Coatings Based on Silver Nanoparticles: A Comparative In Vitro Study on Their Cytotoxicity towards Cancer and Normal Cell Lines of Cytostatic Drugs versus Essential-Oil-Loaded Nanoparticles and on Their Antimicrobial and Antibiofilm Activities

We report on a comparative in vitro study of selective cytotoxicity against MCF7 tumor cells and normal VERO cells tested on silver-based nanocoatings synthesized by the matrix-assisted pulsed laser evaporation (MAPLE) technique. Silver nanoparticles (AgNPs) were loaded with five representative cyto...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Rebecca Alexandra Puiu (VerfasserIn), Alexandra Cătălina Bîrcă (VerfasserIn), Valentina Grumezescu (VerfasserIn), Liviu Duta (VerfasserIn), Ovidiu Cristian Oprea (VerfasserIn), Alina Maria Holban (VerfasserIn), Ariana Hudiță (VerfasserIn), Bianca Gălățeanu (VerfasserIn), Paul Cătălin Balaure (VerfasserIn), Alexandru Mihai Grumezescu (VerfasserIn), Ecaterina Andronescu (VerfasserIn)
Format: Buch
Veröffentlicht: MDPI AG, 2023-07-01T00:00:00Z.
Schlagworte:
Online-Zugang:Connect to this object online.
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_c0d91d9f7d7f44c7aeef0b6a4ae0f862
042 |a dc 
100 1 0 |a Rebecca Alexandra Puiu  |e author 
700 1 0 |a Alexandra Cătălina Bîrcă  |e author 
700 1 0 |a Valentina Grumezescu  |e author 
700 1 0 |a Liviu Duta  |e author 
700 1 0 |a Ovidiu Cristian Oprea  |e author 
700 1 0 |a Alina Maria Holban  |e author 
700 1 0 |a Ariana Hudiță  |e author 
700 1 0 |a Bianca Gălățeanu  |e author 
700 1 0 |a Paul Cătălin Balaure  |e author 
700 1 0 |a Alexandru Mihai Grumezescu  |e author 
700 1 0 |a Ecaterina Andronescu  |e author 
245 0 0 |a Multifunctional Polymeric Biodegradable and Biocompatible Coatings Based on Silver Nanoparticles: A Comparative In Vitro Study on Their Cytotoxicity towards Cancer and Normal Cell Lines of Cytostatic Drugs versus Essential-Oil-Loaded Nanoparticles and on Their Antimicrobial and Antibiofilm Activities 
260 |b MDPI AG,   |c 2023-07-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics15071882 
500 |a 1999-4923 
520 |a We report on a comparative in vitro study of selective cytotoxicity against MCF7 tumor cells and normal VERO cells tested on silver-based nanocoatings synthesized by the matrix-assisted pulsed laser evaporation (MAPLE) technique. Silver nanoparticles (AgNPs) were loaded with five representative cytostatic drugs (i.e., doxorubicin, fludarabine, paclitaxel, gemcitabine, and carboplatin) and with five essential oils (EOs) (i.e., oregano, rosemary, ginger, basil, and thyme). The as-obtained coatings were characterized by X-ray diffraction, thermogravimetry coupled with differential scanning calorimetry, Fourier-transform IR spectroscopy, IR mapping, and scanning electron microscopy. A screening of the impact of the prepared nanocoatings on the MCF7 tumor and normal VERO cell lines was achieved by means of cell viability MTT and cytotoxicity LDH assays. While all nanocoatings loaded with antitumor drugs exhibited powerful cytotoxic activity against both the tumor and the normal cells, those embedded with AgNPs loaded with rosemary and thyme EOs showed remarkable and statistically significant selective cytotoxicity against the tested cancercells. The EO-loaded nanocoatings were tested for antimicrobial and antibiofilm activity against <i>Staphylococcus aureus</i>, <i>Escherichia coli</i>, and <i>Candida albicans</i>. For all studied pathogens, the cell viability, assessed by counting the colony-forming units after 2 and 24 h, was significantly decreased by all EO-based nanocoatings, while the best antibiofilm activity was evidenced by the nanocoatings containing ginger and thyme EOs. 
546 |a EN 
690 |a cancer therapy 
690 |a silver nanoparticles 
690 |a MAPLE 
690 |a essential oil 
690 |a nanocoatings 
690 |a cytostatic drugs 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 15, Iss 7, p 1882 (2023) 
787 0 |n https://www.mdpi.com/1999-4923/15/7/1882 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/c0d91d9f7d7f44c7aeef0b6a4ae0f862  |z Connect to this object online.