Fabrication, characterization of carboxymethyl konjac glucomannan/ovalbumin-naringin nanoparticles with improving in vitro bioaccessibility

•A new nano-delivery system (OVA/CKGM-Naringin NPs) consisting of ovalbumin (OVA) and carboxymethyl konjac glucomannan (CKGM) to embedding naringin.•Bioavailability and encapsulation efficiency were used as indexes to evaluate the processing parameters of OVA/CKGM-Naringin NPs, including proportion...

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Veröffentlicht in:Food Chemistry: X 2022-12, Vol.16, p.100477-100477, Article 100477
Hauptverfasser: Tang, Weimin, Wei, Yanjun, Lu, Wenjing, Chen, Di, Ye, Qin, Zhang, Cen, Chen, Yufeng, Xiao, Chaogeng
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Sprache:eng
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Zusammenfassung:•A new nano-delivery system (OVA/CKGM-Naringin NPs) consisting of ovalbumin (OVA) and carboxymethyl konjac glucomannan (CKGM) to embedding naringin.•Bioavailability and encapsulation efficiency were used as indexes to evaluate the processing parameters of OVA/CKGM-Naringin NPs, including proportion of OVA: CKGM, pH and naringin concentration.•The bioavailability of naringin in OVA/CKGM-Naringin NPs system is significantly advanced to two folds of naringin as control.•High OVA concentration in OVA/CKGM system showed different fluorescence behaviors compared with that of low OVA concentration. Naringin is potential functional and therapeutic ingredient, has low bioavailability because of poor aqueous solubility. In this study, an ovalbumin (OVA)-carboxymethyl konjac glucomannan (CKGM) nano-delivery system was developed to enhance the bioavailability of naringin. The effects of proportion (OVA: CKGM), pH and naringin concentration were studied on the formation, encapsulation efficiency (EE) and bioaccessibility of OVA/CKGM-Naringin nanoparticles (OVA/CKGM-Naringin NPs). Its morphology and size were viewed by Scanning Electron Microscope (SEM) and Transmission Electron Microscopy (TEM). The cross-linkage between OVA and CKGM was verified by Fourier Transform Infrared Spectroscopy (FTIR) and Fluorescence Intensity analysis. The size of OVA/CKGM-Naringin NPs were 463.83 ± 18.50 nm (Polydispersity Index-PDI, 0.42 ± 0.05). It indicated that 2:1 of OVA: CKGM, pH 3 and 7 mg/mL of naringin concentration were optimized processing parameters of OVA/CKGM-Naringin NPs with EE (97.90 ± 2.97 %) and remarkably improved bioaccessibility (85.01 ± 2.52 %). The OVA/CKGM-Naringin NPs was energy efficiently prepared and verified as an ideal carrier of naringin.
ISSN:2590-1575
2590-1575
DOI:10.1016/j.fochx.2022.100477