18β-glycyrrhetinic acid (GA) is a pentacyclic triterpene with promising hepatoprotective and anti-Hepatocellular carcinoma effects. GA low water solubility however reduces its biodistribution and bioavailability, limiting its applications in biomedicine. In this work we used core-shell NPs made of PolyD-L-lactide-co-glycolide (PLGA) coated with chitosan (CS), prepared through an osmosis-based methodology, to efficiently entrap GA. NPs morphology was investigated with SEM and TEM and their GA payload was evaluated with a spectrophotometric method. GA-loaded NPs were administered to HepG2 cells and their efficiency in reducing cell viability was compared with that induced by the free drug in in vitro tests. Cell viability was evaluated by the MTT assay, as well as with Electric Cells-Substrate Impedance Sensing (ECIS), that provided a real-time continuous monitoring. It was possible to correlate the toxic effect of the different forms of GA with the bioavailability of the drug, evidencing the importance of real-time tests for studying the effects of bioactive substances on cell cultures

Controlled release of 18-β-Glycyrrhetinic acid from core-shell nanoparticles: effects on cytotoxicity and intracellular concentration in HepG2 cell line / Nocca, Giuseppina; D’Avenio, Giuseppe; Amalfitano, Adriana; Chronopoulou, Laura; Mordente, Alvaro; Palocci, Cleofe; Grigioni, Mauro. - In: MATERIALS. - ISSN 1996-1944. - 14:14(2021). [10.3390/ma14143893]

Controlled release of 18-β-Glycyrrhetinic acid from core-shell nanoparticles: effects on cytotoxicity and intracellular concentration in HepG2 cell line

Chronopoulou, Laura
;
Palocci, Cleofe;
2021

Abstract

18β-glycyrrhetinic acid (GA) is a pentacyclic triterpene with promising hepatoprotective and anti-Hepatocellular carcinoma effects. GA low water solubility however reduces its biodistribution and bioavailability, limiting its applications in biomedicine. In this work we used core-shell NPs made of PolyD-L-lactide-co-glycolide (PLGA) coated with chitosan (CS), prepared through an osmosis-based methodology, to efficiently entrap GA. NPs morphology was investigated with SEM and TEM and their GA payload was evaluated with a spectrophotometric method. GA-loaded NPs were administered to HepG2 cells and their efficiency in reducing cell viability was compared with that induced by the free drug in in vitro tests. Cell viability was evaluated by the MTT assay, as well as with Electric Cells-Substrate Impedance Sensing (ECIS), that provided a real-time continuous monitoring. It was possible to correlate the toxic effect of the different forms of GA with the bioavailability of the drug, evidencing the importance of real-time tests for studying the effects of bioactive substances on cell cultures
2021
nanoparticles; drug delivery; ECIS; cytotoxicity
01 Pubblicazione su rivista::01a Articolo in rivista
Controlled release of 18-β-Glycyrrhetinic acid from core-shell nanoparticles: effects on cytotoxicity and intracellular concentration in HepG2 cell line / Nocca, Giuseppina; D’Avenio, Giuseppe; Amalfitano, Adriana; Chronopoulou, Laura; Mordente, Alvaro; Palocci, Cleofe; Grigioni, Mauro. - In: MATERIALS. - ISSN 1996-1944. - 14:14(2021). [10.3390/ma14143893]
File allegati a questo prodotto
File Dimensione Formato  
Nocca_Controlled-release_2021.pdf

accesso aperto

Note: https://www.mdpi.com/1996-1944/14/14/3893
Tipologia: Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza: Creative commons
Dimensione 2.53 MB
Formato Adobe PDF
2.53 MB Adobe PDF

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1562277
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 5
  • ???jsp.display-item.citation.isi??? 5
social impact