Synthesis and Biological Activity Evaluations of Green ZnO-Decorated Acid-Activated Bentonite-Mediated Curcumin Extract (ZnO@CU/BE) as Antioxidant and Antidiabetic Agents

Author:

Rudayni Hassan Ahmed1ORCID,Shemy Marwa H.23,Aladwani Malak1,Alneghery Lina M.1,Abu-Taweel Gasem M.4,Allam Ahmed A.5,Abukhadra Mostafa R.36ORCID,Bellucci Stefano7ORCID

Affiliation:

1. Department of Biology, College of Science, Imam Muhammad bin Saud Islamic University, Riyadh 11623, Saudi Arabia

2. Chemistry Department, Faculty of Science, Beni-Suef University, Beni-Suef 65211, Egypt

3. Materials Technologies and Their Applications Lab, Geology Department, Faculty of Science, Beni-Suef University, Beni-Suef 65214, Egypt

4. Department of Biology, College of Science, Jazan University, P.O. Box 2079, Jazan 45142, Saudi Arabia

5. Zoology Department, Faculty of Science, Beni-Suef University, Beni-Suef 62514, Egypt

6. Geology Department, Faculty of Science, Beni-Suef University, Beni-Suef 65214, Egypt

7. INFN-Laboratori Nazionali di Frascati, Via. E. Fermi 54, 00044 Frascati, Italy

Abstract

Green ZnO-decorated acid-activated bentonite-mediated curcumin extract (ZnO@CU/BE) was prepared as a multifunctional antioxidant and antidiabetic agent based on the extract of curcumin, which was used as a reducing and capping reagent. ZnO@CU/BE showed notably enhanced antioxidant properties against nitric oxide (88.6 ± 1.58%), 1,1-diphenyl-2-picrylhydrazil (90.2 ± 1.76%), 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid (87.3 ± 1.61%), and superoxide (39.5 ± 1.12%) radicals. These percentages are higher than the reported values of ascorbic acid as a standard and the integrated components of the structure (CU, BE/CU, and ZnO). This signifies the impact of the bentonite substrate on enhancing the solubility, stability, dispersion, and release rate of the intercalated curcumin-based phytochemicals, in addition to enhancing the exposure interface of ZnO nanoparticles. Therefore, effective antidiabetic properties were observed, with significant inhibition effects on porcine pancreatic α-amylase (76.8 ± 1.87%), murine pancreatic α-amylase (56.5 ± 1.67%), pancreatic α-glucosidase (96.5 ± 1.07%), murine intestinal α-glucosidase (92.5 ± 1.10%), and amyloglucosidase (93.7 ± 1.55%) enzymes. These values are higher than those determined using commercial miglitol and are close to the values measured using acarbose. Hence, the structure can be applied as an antioxidant and antidiabetic agent.

Funder

Deanship of Scientific Research at Imam Mohammad Ibn Saud Islamic University

Publisher

MDPI AG

Subject

Biomedical Engineering,Biomaterials

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