Okra polysaccharides/gelatin complex coacervate as pH-responsive and intestine-targeting delivery protects isoquercitin bioactivity.


Journal

International journal of biological macromolecules
ISSN: 1879-0003
Titre abrégé: Int J Biol Macromol
Pays: Netherlands
ID NLM: 7909578

Informations de publication

Date de publication:
15 Sep 2020
Historique:
received: 29 11 2019
revised: 30 04 2020
accepted: 10 05 2020
pubmed: 19 5 2020
medline: 20 3 2021
entrez: 19 5 2020
Statut: ppublish

Résumé

Okra polysaccharides (OPs) belong to RG I pectin branched with neutral saccharide side chains, which possesses distinctive structure and physicochemical properties from the commonly used HG pectin. Until now, the application of RG I pectin as wall material of microcapsule remains unclear. Here, we obtained OPs/gelatin complex coacervate at the maximum yield of 86.8% (pH 3.5, gelatin/OPs ratio 9:1 and 2% (w/v) total polymer concentration) by response surface methodology. Isoquercitin (IQ)-loaded OPs/gelatin complex coacervate (OGIQ) showed porous spongy-like surface structure with average particle size, encapsulation efficiency and surface porosity at 334 nm, 81.6% and 31.9%, respectively. OGIQ was found to be pH-responsive and intestine-targeting. The IQ-release rate of OGIQ was assayed to be 89.4% in intestine fluid and below 2% in acidic and simulated gastric digestion, respectively. Accordingly, embedding in OGIQ protected IQ in digestion and improved its postdigestive α-glucosidase inhibitory rate by 88.7%. The differential scanning calorimetry curves showed that OGIQ effectively prevented IQ from thermal decomposition. The XRD, FT-IR and CD spectra indicated that IQ was embedded in OGIQ in amorphous state by hydrogen bonds and electrostatic interaction. Compared with HG, the neutral saccharide side chains of OPs could induce different secondary conformation change of gelatin during complex coacervation.

Identifiants

pubmed: 32422271
pii: S0141-8130(20)33213-X
doi: 10.1016/j.ijbiomac.2020.05.067
pii:
doi:

Substances chimiques

Drug Carriers 0
Macromolecular Substances 0
Polymers 0
Polysaccharides 0
isoquercitrin 0YX10VRV6J
Gelatin 9000-70-8
Quercetin 9IKM0I5T1E

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

487-496

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare no conflict of interest.

Auteurs

Jingwen Li (J)

Department of Food Engineering, College of Biomass Science and Engineering & Healthy Food Evaluation Research Center, Sichuan University, Chengdu 610065, PR China.

Xiaoran Yang (X)

Department of Food Engineering, College of Biomass Science and Engineering & Healthy Food Evaluation Research Center, Sichuan University, Chengdu 610065, PR China.

Xiao Li (X)

Department of Food Engineering, College of Biomass Science and Engineering & Healthy Food Evaluation Research Center, Sichuan University, Chengdu 610065, PR China.

Zihan Zhang (Z)

Department of Food Engineering, College of Biomass Science and Engineering & Healthy Food Evaluation Research Center, Sichuan University, Chengdu 610065, PR China.

Zeliang Wei (Z)

Laboratory of Ethnopharmacology, West China Hospital, West China Medical School, Sichuan University, Chengdu 610041, PR China.

Zhihua Xing (Z)

Laboratory of Ethnopharmacology, West China Hospital, West China Medical School, Sichuan University, Chengdu 610041, PR China.

Sha Deng (S)

Department of Food Engineering, College of Biomass Science and Engineering & Healthy Food Evaluation Research Center, Sichuan University, Chengdu 610065, PR China.

Feixia Duan (F)

Department of Food Engineering, College of Biomass Science and Engineering & Healthy Food Evaluation Research Center, Sichuan University, Chengdu 610065, PR China. Electronic address: duanfeixia@126.com.

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Classifications MeSH