Synthesis and characterization of antioxidant-enriched Moringa oil-based edible oleogel

Author:

Yaqoob Nazia1,Rehman Saima2,Shafiq Nusrat3,Mohsin Muhammad2,Akbar Aleena1,Ibenmoussa Samir4,Wondmie Gezahign Fentahun5,Bin Jardan Yousef A.6,Bourhia Mohammed7

Affiliation:

1. Green Chemistry Lab., Department of Chemistry, Government College Women University , Faisalabad , 38000 , Pakistan

2. Department of Chemistry, Government College University , Faisalabad , 38000 , Pakistan

3. Synthetic and Natural Product Discovery Lab., Department of Chemistry, Government College Women University , Faisalabad , 38000 , Pakistan

4. Laboratory of Therapeutic and Organic Chemistry, Faculty of Pharmacy, University of Montpellier , Montpellier , 34000 , France

5. Department of Biology, Bahir Dar University , P.O. Box 79 , Bahir Dar , Ethiopia

6. Department of Pharmaceutics, College of Pharmacy, King Saud University , P.O. Box 11451 , Riyadh , Saudi Arabia

7. Department of Chemistry and Biochemistry, Faculty of Medicine and Pharmacy, Ibn Zohr University , Laayoune , 70000 , Morocco

Abstract

Abstract This study aims to formulate and optimize Moringa oleifera (Moringa) oil oleogels using pectin (PC) and chitosan (CS) as gelling agents. These include monogelator oleogels, utilizing either PC or CS as a single gelling agent, and binary gelator oleogels, incorporating a combination of both PC and CS. Among the binary gelator oleogel compositions, the most stable oleogel OPCCS2 was further studied with the addition of antioxidants. The important antioxidant compounds of gallic acid equivalents (GAEs)/Moringa antioxidant extracts (MAEs) were quantified by the use of various assays. The oil-binding capacity (OBC) of the most stable oleogel MCPC1.5% was 99.94 ± 0.05. The lower peroxide value of antioxidant-rich oleogels at 1.5% concentration of GAEs (4.34 ± 0.025) and MAEs (4.32 ± 0.03) suggested its richness of phenols to retard the lipid peroxidation of oil. The opaque appearances of the formulations were studied via polarizing light microscopy. The molecular interaction study through FTIR analysis revealed the hydrogen bond interactions between the carboxyl groups of fatty acids and hydroxyl groups of polysaccharide chains. The differential scanning calorimeter analysis further confirmed the presence of strong interactions between polysaccharide chains and the oil phase. These findings indicate that the optimized oleogel formulations have the potential for imminent advances by exhibiting improved texture, biocompatibility, enhanced OBC, and stability.

Publisher

Walter de Gruyter GmbH

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