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Int J Biol Macromol ; 172: 133-142, 2021 Mar 01.
Article in English | MEDLINE | ID: mdl-33450338

ABSTRACT

Ursolic acid (UA) is a naturally occurring triterpene that has been investigated for its antitumor activity. However, its lipophilic character hinders its oral bioavailability, and therapeutic application. To overcome these limitations, chitosan (CS) modified poly (lactic acid) (PLA) nanoparticles containing UA were developed, characterized, and had their oral bioavailability assessed. The nanoparticles were prepared by emulsion-solvent evaporation technique and presented a mean diameter of 330 nm, zeta potential of +28 mV, spherical shape and 90% encapsulation efficiency. The analysis of XRD and DSC demonstrated that the nanoencapsulation process induced to UA amorphization. The in vitro release assay demonstrated that 53% of UA was released by diffusion after 144 h, following a second-order release kinetics. In simulated gastrointestinal fluids and mucin interaction tests, CS played an important role in stability and mucoadhesiveness improvement of PLA nanoparticles, respectively. In the presence of erythrocytes, nanoparticles proved their hemocompatibility. In tumor cells, nanoparticles presented lower cytotoxicity than free UA, due to slow UA release. After a single oral dose in rats, CS modified PLA nanoparticles increased the UA absorption, reduced its clearance and elimination, resulting in increased bioavailability. The results show the potential application of these nanoparticles for UA oral delivery for cancer therapy.


Subject(s)
Chitosan/chemistry , Nanoparticles/chemistry , Polyesters/chemistry , Triterpenes/chemistry , Triterpenes/metabolism , Animals , Biological Availability , Cell Line, Tumor , Emulsions/chemistry , Erythrocytes/drug effects , Humans , Male , Rats , Rats, Wistar , Solvents/chemistry , Ursolic Acid
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