This study aims to enhance the antidiabetic potential of Vanadium pentoxide (VO) by synthesizing chitosan-based nanoparticles (NPs). Chitosan and its derivatives were used to fabricate VO NPs, ensuring enhanced antioxidant and antidiabetic activity. Surface topography was analyzed using atomic force microscopy (AFM), revealing bioactive sites on the NPs with improved electron-transfer capability, as confirmed by cyclic voltammetry (CV). Furthermore, NPs were exploited for their possible antioxidant and antidiabetic potency by using different in-vitro assays. Among the fabricated NPs, chitosan-salicylaldehyde decorated VO NPs (CHVD) exhibited highest antidiabetic activity with 72.69 ± 0.76 % inhibition against α-amylase, 69.15 ± 0.58 % inhibition against α-glucosidase, and glycemic diffusion retardation index (GDRI) of 60.33 ± 0.47 %. Importantly, CHVD did not inhibit the growth of Bifidobacterium bacteria, as shown by disc-diffusion assay and exhibit least cytotoxicity among all NPs as tested on HacaT cell line. Molecular docking studies revealed strong binding interactions between CHVD and the target enzymes, α-amylase, and α-glucosidase supporting its inhibitory potential. This work demonstrates the promising enhanced antidiabetic and antioxidant properties of chitosan-coated VO NPs.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ijbiomac.2025.139986DOI Listing

Publication Analysis

Top Keywords

molecular docking
8
vanadium pentoxide
8
nps
8
antioxidant antidiabetic
8
antidiabetic activity
8
antidiabetic
6
in-vitro assay
4
assay studies
4
studies molecular
4
docking functionalized
4

Similar Publications

Catheter-associated urinary tract infections (CAUTIs), often caused by biofilm-forming Staphylococcus aureus, present significant clinical challenges. Skt35, a dioxopiperidinamide derivative of cinnamic acid, was investigated for its potential antibacterial and antibiofilm activities against S. aureus biofilms.

View Article and Find Full Text PDF

CD47, a cell surface protein, serves as a "don't eat me" signal that prevents immune cells from engulfing healthy cells upon its interaction with SIRPα. Cancer cells exploit this mechanism by overexpressing CD47 to evade immune destruction. Blocking the interaction between CD47 and its receptor, SIRPα, is a promising therapeutic strategy.

View Article and Find Full Text PDF

The quinazoline scaffold serves as a fundamental framework, demonstrating potent anti-tumor activity. Employing the pharmacophore-based scaffold hopping principle, we successfully synthesized a series of FAK/PLK1 inhibitors incorporating the quinazoline scaffold. The synthesized compounds were characterized using H NMR, C NMR, and HRMS techniques.

View Article and Find Full Text PDF

Succinate dehydrogenase (SDH) has been identified as one of the ideal targets for the development of novel nematicides. However, the resistance of nematodes to fluopyram, one of the commercialized SDH inhibitors, is becoming a growing concern. Since expanding the structural diversity around an active scaffold is a useful strategy for drug development, herein a series of fluopyram analogues with a broad, biologically relevant indole moiety were synthesized and evaluated for nematicidal activity against C.

View Article and Find Full Text PDF

Sea buckthorn is a model of medicine and food homology, but the chemical composition and mechanism of anti-inflammatory effects are limited. In this study, the key components and mechanisms of the anti-inflammatory effects of sea buckthorn were identified based on UPLC-Q-TOF-MS, network pharmacology, molecular docking, molecular dynamics and RAW264.7 cells.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!