Controlled release of 18-β-Glycyrrhetic Acid by nanodelivery systems increases Cytotoxicity On Oral Carcinoma Cell Line.

Massimo Cordaro, Carlo Lajolo, Cinzia Anna Maria Calla', Patrizia Gallenzi, Alessandro Sgambato, Giuseppina Nocca, Alessandro Arcovito, Adriana Amalfitano, Monica Cantiani, Alma Boninsegna Lucarelli, Donatella Lucchetti, Ilaria Cacciotti, Laura Chronopoulou, Cleofe Palocci

Research output: Contribution to journalArticlepeer-review

25 Citations (Scopus)

Abstract

The topical treatment for oral mucosal diseases is often based on products optimized for dermatologic applications; consequently, a lower therapeutic effect may be present. 18-β-Glycyrrhetic Acid (GA) is extracted from Glycirrhiza glabra. The first aim of this study was to test the cytotoxicity of GA on PE/CA-PJ15 cells. The second aim was to propose and test two different delivery systems, i.e. nanoparticles and fibers, to guarantee a controlled release of GA in vitro. We used chitosan and poly(lactic-co-glycolic) acid based nanoparticles and polylactic acid fibers. We tested both delivery systems in vitro on PE/CA-PJ15 cells and on normal human gingival fibroblasts (HGFs). The morphology of GA-loaded nanoparticles (GA-NPs) and fibers (GA-FBs) was investigated by electron microscopy and dynamic light scattering; GA release kinetics was studied spectrophotometrically. MTT test was used to assess GA cytotoxicity on both cancer and normal cells. Cells were exposed to different concentrations of GA (20 - 500 µmol/L) administered as free GA (GA-f), and to GA-NPs or GA-FBs. ROS production was evaluated using dichlorodihydrofluorescein as a fluorescent probe. Regarding the cytotoxic effect of GA on PE/CA-PJ15 cells, the lowest TC50 value was 200 µmol/L when GA was added as GA-NPs. No cytotoxic effects were observed when GA was administered to HGFs. N-acetyl Cysteine reduced mortality induced by GA-f in PE/CA-PJ15 cells. The specific effect of GA on PE/CA-PJ15 cells is mainly due to the different sensitivity of cancer cells to ROS over-production; GA-NPs and GA-FBs formulations increase, in vitro, this toxic effect on oral cancer cells.
Original languageEnglish
Pages (from-to)1-29
Number of pages29
JournalNanotechnology
Volume29
DOIs
Publication statusPublished - 2018

Keywords

  • 18-β-Glycyrrhetic Acid
  • Oral cavity pathologies.
  • PLA nanofibers
  • PLGA nanoparticles
  • ROS production
  • molecular targeted therapies
  • targeted drug

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