Synthesis and characterization of curcumin-encapsulated loaded on carboxymethyl cellulose with docking validation as α-amylase and α-glucosidase inhibitors

Author:

Almehizia Abdulrahman A.1,Al-Omar Mohamed A.1,Al-Obaid Abdulrahman M.1,Naglah Ahmed M.1,Bhat Mashooq A.1,Ghabbour Hazem A.23,Khatab Tamer K.4,Hassan Ashraf S.4

Affiliation:

1. Department of Pharmaceutical Chemistry, College of Pharmacy , King Saud University , P.O. Box 2457, Riyadh 11451 , Saudi Arabia

2. School of health and biomedical sciences , RMIT University , Melbourne 3083 , Australia

3. Department of Medicinal Chemistry, Faculty of Pharmacy , University of Mansoura , Mansoura , Egypt

4. Organometallic and Organometalloid Chemistry Department, National Research Centre , Dokki 12622, Cairo , Egypt

Abstract

Abstract In reaction to the expanding predominance of diabetes mellitus, curcumin nanoparticles stacked on carboxymethyl cellulose (CMC) composite were effectively synthesized, characterized, and examined utilizing UV/Vis and FTIR spectroscopy combined with transmission electron microscopy (TEM). The bioactivity of curcumin (Cur), carboxymethyl cellulose (CMC), and curcumin nanoparticles stacked with carboxymethyl cellulose (CUR-CMC) was tried through atomic docking approval as an α-amylase and α-glucosidase inhibitor. The conclusion illustrated that the curcumin-supported CMC is more potent than CUR itself self the validation presented is compared with acarbose as a reference molecule and then CUR-CMC can presented as promising in curing hyperglycemia by decreasing the absorption of glucose.

Publisher

Walter de Gruyter GmbH

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