Chitosan-olive oil microparticles for phenylethyl isothiocyanate delivery

• Main Author: Coscueta, Ezequiel R.
• Publication Date: 2021
• Other Authors: Reis, Celso A., Pintado, Manuela
• Language: eng
• Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
• Download full: http://hdl.handle.net/10400.14/36563
• topic: Nanotechnology; Nanoparticle; Phenylethyl isothiocyanate (PEITC); Chitosan

Phenylethyl isothiocyanate (PEITC) is released from the enzymatic hydrolysis of gluconasturtiin, the most abundant glucosinolate found in watercress (a vegetable from the family Brassicaceae) by the enzyme myrosinase. Among all the isothiocyanates, PEITC is one of the most extensively studied with various biological activities such as antimicrobial, antioxidant and anti-inflammatory. Several studies suggested that PEITC exhibits cancer preventive and therapeutic effects on multiple types of cancers and is one of the isothiocyanates that is being tested in clinical trials. PEITC is highly reactive due to its considerably electrophilic nature. Furthermore, it is hydrophobic and has low stability, bioavailability and bioaccessibility, restricting its use in biomedical and nutraceutical or food applications. Thus, the encapsulation of this agent has the function of overcoming these limitations, promoting its solubility in water, and stabilizing it, preserving its bioactivity. So, polymeric microparticles were developed using chitosan-olive oil-PEITC systems. For this, an optimisation process (factors: olive oil: chitosan ratio and PEITC: chitosan ratio) were implemented through a 3-level (32) factorial experimental design. The responses were: the particle size, zeta-potential, polydisperse index, and entrapment efficiency. The optimal formulation was further characterized by FTIR and biocompatibility in Caco-2 cells. Optimal conditions were olive oil: chitosan and PEITC: chitosan ratios of 1.46 and 0.25, respectively. These microparticles had a size of 629 nm, a zeta-potential of 32.3 mV, a polydispersity index of 0.329, and an entrapment efficiency of 98.49%. We found that the inclusion process affected the optical behaviour of the PEITC, as well as the microparticles themselves and their interaction with the medium. Furthermore, the microparticles did not show cytotoxicity within the therapeutic values of PEITC. Thus, PEITC was microencapsulated with characteristics suitable for potential biomedical, nutraceutical and food applications.