Self‐assembled α‐lactalbumin nanostructures: encapsulation and controlled release of bioactive molecules in gastrointestinal in vitro model

Author:

de Oliveira Bianchi Jhonatan Rafael1ORCID,Fabrino Daniela Leite1ORCID,Quintão Cristiane Medina Finzi2ORCID,dos Reis Coimbra Jane Selia3ORCID,Santos Igor José Boggione1ORCID

Affiliation:

1. Department of Chemistry, Biotechnology and Bioprocess Engineering Federal University of São João del Rei (UFSJ), Alto Paraopeba Campus Ouro Branco Brazil

2. Department of Chemical Engineering Federal University of São João del Rei (UFSJ), Alto Paraopeba Campus Ouro Branco Brazil

3. Department of Food Technology Federal University of Viçosa (UFV) Viçosa Brazil

Abstract

AbstractBACKGROUNDImplementing encapsulation techniques is pivotal in safeguarding bioactive molecules against environmental conditions for drug delivery systems. Moreover, the food‐grade nanocarrier is a delivery system and food ingredient crucial in creating nutraceutical foods. Nano α‐lactalbumin has been shown to be a promissory nanocarrier for hydrophobic molecules. Furthermore, the nanoprotein can enhance the tecno‐functional properties of food such as foam and emulsion. The present study investigated the nanostructured α‐lactalbumin protein (nano α‐la) as a delivery and controlled release system for bioactive molecules in a gastric‐intestinal in vitro mimic system.RESULTSThe nano α‐la was synthesized by a low self‐assembly technique, changing the solution ionic strength by NaCl and obtaining nano α‐la 191.10 ± 21.33 nm and a spherical shape. The nano α‐la showed higher encapsulation efficiency and loading capacity for quercetin than riboflavin, a potential carrier for hydrophobic compounds. Thermal analysis of nano α‐la resulted in a ΔH of −1480 J g−1 for denaturation at 57.44 °C. The nanostructure formed by self‐assembly modifies the foam volume increment and stability. Also, differences between nano and native proteins in emulsion activity and stability were noticed. The release profile in vitro showed that the nano α‐la could not hold the molecules in gastric fluid. The Weibull and Korsmeyer‐Peppas model better fits the release profile behavior in the studied fluids.CONCLUSIONThe present study shows the possibility of nano α‐la as an alternative to molecule delivery systems and nutraceutical foods' formulation because of the high capacity to encapsulate hydrophobic molecules and the improvement of techno‐functional properties. However, the nanocarrier is not perfectly suitable for the sustainable delivery of molecules in the gastrointestinal fluid, demanding improvements in the nanocarrier. © 2024 Society of Chemical Industry.

Publisher

Wiley

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