Nanostructured Poly-l-lactide and Polyglycerol Adipate Carriers for the Encapsulation of Usnic Acid: A Promising Approach for Hepatoprotection

Author:

Brugnoli Benedetta1ORCID,Perna Greta1,Alfano Sara1ORCID,Piozzi Antonella1ORCID,Galantini Luciano1ORCID,Axioti Eleni2ORCID,Taresco Vincenzo2ORCID,Mariano Alessia3ORCID,Scotto d’Abusco Anna3ORCID,Vecchio Ciprioti Stefano4ORCID,Francolini Iolanda1ORCID

Affiliation:

1. Department of Chemistry, Sapienza University of Rome, P.le A. Moro, 00185 Rome, Italy

2. School of Chemistry, University of Nottingham, Nottingham NG7 2RD, UK

3. Department of Biochemical Sciences, Sapienza University of Rome, P.le A. Moro, 5, 00185 Rome, Italy

4. Department of Basic and Applied Science for Engineering, Sapienza University of Rome, Via del Castro Laurenziano 7, 00161 Rome, Italy

Abstract

The present study investigates the utilization of nanoparticles based on poly-l-lactide (PLLA) and polyglycerol adipate (PGA), alone and blended, for the encapsulation of usnic acid (UA), a potent natural compound with various therapeutic properties including antimicrobial and anticancer activities. The development of these carriers offers an innovative approach to overcome the challenges associated with usnic acid’s limited aqueous solubility, bioavailability, and hepatotoxicity. The nanosystems were characterized according to their physicochemical properties (among others, size, zeta potential, thermal properties), apparent aqueous solubility, and in vitro cytotoxicity. Interestingly, the nanocarrier obtained with the PLLA-PGA 50/50 weight ratio blend showed both the lowest size and the highest UA apparent solubility as well as the ability to decrease UA cytotoxicity towards human hepatocytes (HepG2 cells). This research opens new avenues for the effective utilization of these highly degradable and biocompatible PLLA-PGA blends as nanocarriers for reducing the cytotoxicity of usnic acid.

Funder

Sapienza University of Rome

Publisher

MDPI AG

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