Preparation and Characterization of Resveratrol Loaded Pectin/Alginate Blend Gastro-Resistant Microparticles

被引:23
作者
Gartziandia, Oihane [1 ,2 ]
Lasa, Arrate [3 ,4 ,5 ]
Luis Pedraz, Jose [1 ,2 ]
Miranda, Jonatan [3 ,4 ,5 ]
Puy Portillo, Maria [3 ,4 ,5 ]
Igartua, Manoli [1 ,2 ]
Maria Hernandez, Rosa [1 ,2 ]
机构
[1] Univ Basque Country, UPV EHU, Sch Pharm, NanoBiocel Grp,Lab Pharmaceut, Vitoria 01006, Spain
[2] CIBER BBN, Biomed Res Networking Ctr Bioengn Biomat & Nanome, Vitoria 01006, Spain
[3] Univ Basque Country, UPV EHU, Fac Pharm, Nutr & Obes Grp,Dept Nutr & Food Sci, Vitoria 01006, Spain
[4] Univ Basque Country, UPV EHU, Lucio Lascaray Res Inst, Vitoria 01006, Spain
[5] Inst Hlth Carlos III, ISCIII, CIBEROBN Physiopathol Obes & Nutr, Vitoria 01006, Spain
关键词
resveratrol; dietary supplement; gastro-resistant; microparticles; obesity; HPLC; FAT MOBILIZATION; SUPPLEMENTATION; BIOAVAILABILITY; ENCAPSULATION; ABSORPTION; DELIVERY; HUMANS; LIVER; RATS;
D O I
10.3390/molecules23081886
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: The use of resveratrol as a dietary supplement is limited because it is easily oxidized and, after oral ingestion, it is metabolized into enterocytes and hepatocytes. Thus, new formulations are needed in order to improve its oral bioavailability. Objective: The objective of this study was to develop and characterize a gastro-resistant formulation of resveratrol for oral administration as a dietary supplement. Method: Resveratrol was encapsulated in Eudragit-coated pectin-alginate microparticles. Results: The microparticle size was about 1450 mu m, with an encapsulation efficiency of 41.72% +/- 1.92%. The dissolution assay conducted, as specified in the European Pharmacopoeia for delayed-release dosage forms, revealed that our microparticles were gastro-resistant, because the resveratrol percentage released from microparticles in acid medium was less than 10%. In addition, the high-performance liquid chromatographic (HPLC) method developed for resveratrol content quantification in the microparticles was validated according to International Council for Harmonisation (ICH) Q2 (R1) guidelines. Finally, the biological activity of resveratrol was investigated in 3T3-L1 mature adipocytes, concluding that the encapsulation process does not affect the activity of resveratrol. Conclusion: In summary, the gastro-resistant microparticles developed could represent a suitable method of including resveratrol in dietary supplements and in functional foods used in obesity therapy.
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页数:10
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