Mukesh Kumar Kumawat

ORCID: 0000-0002-8847-3691
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About
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Research Areas
  • Synthesis and biological activity
  • Graphene and Nanomaterials Applications
  • Carbon and Quantum Dots Applications
  • Synthesis and Characterization of Heterocyclic Compounds
  • Malaria Research and Control
  • Computational Drug Discovery Methods
  • Nanocluster Synthesis and Applications
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Synthesis and Biological Evaluation
  • Click Chemistry and Applications
  • Molecular Sensors and Ion Detection
  • Graphene research and applications
  • Diverse Scientific Research Studies
  • Quinazolinone synthesis and applications
  • Synthesis of heterocyclic compounds
  • Electric Motor Design and Analysis
  • Advanced biosensing and bioanalysis techniques
  • Nanoplatforms for cancer theranostics
  • Gold and Silver Nanoparticles Synthesis and Applications
  • Sensorless Control of Electric Motors
  • Pharmaceutical Economics and Policy
  • Engineering and Technology Innovations
  • Advancements in Transdermal Drug Delivery
  • Natural Antidiabetic Agents Studies

Dr. Hari Singh Gour University
2025

Apeejay Stya University
2021-2024

Shree Guru Gobind Singh Tricentenary University
2024

Indian Institute of Technology Bombay
2016-2023

Directorate of Medicinal and Aromatic Plants Research
2011-2017

Dibrugarh University
2015-2016

Alliance for a Green Revolution in Africa
2015

Anand Agricultural University
2013-2014

NIMS University
2010

We report a simple one-pot microwave-assisted green-synthesis route for the fabrication of bright red-luminescent graphene quantum dots (GQDs) using ethanolic extracts Mangifera indica (mango) leaves, hence addressing them as mGQDs. The mGQDs were quantum-sized ranging from 2 to 8 nm and exhibited excitation-independent fluorescence emission in near-infrared (NIR) region between 650 750 nm. showed defects their structure highly crystalline nature confirmed by Raman spectroscopy powdered...

10.1021/acssuschemeng.6b01893 article EN ACS Sustainable Chemistry & Engineering 2016-12-19

We report a simple one-pot microwave assisted "green synthesis" of Graphene Quantum Dots (GQDs) using grape seed extract as green therapeutic carbon source. These GQDs readily self-assemble, hereafter referred to "self-assembled" (sGQDs) in the aqueous medium. The sGQDs enter via caveolae and clathrin-mediated endocytosis target themselves into cell nucleus within 6-8 h without additional assistance external capping/targeting agent. tendency self-localize also remains consistent different...

10.1038/s41598-017-16025-w article EN cc-by Scientific Reports 2017-11-14

An Indian fig tree serves as a green factory by providing withered leaves carbon source for graphene quantum dots synthesis. The are multi-functional and have tremendous theranostic biomedical applications.

10.1039/c6ra25976f article EN cc-by-nc RSC Advances 2017-01-01

Abstract Developing a nanotheranostic agent with better image resolution and high accumulation into solid tumor microenvironment is challenging task. Herein, we established light mediated phototriggered strategy for enhanced of nanohybrids. A multifunctional liposome based nanotheranostics loaded gold nanoparticles (AuNPs) emissive graphene quantum dots (GQDs) were engineered named as NFGL. Further, doxorubicin hydrochloride was encapsulated in NFGL to exhibit chemotherapy functionalized...

10.1038/s42003-020-1016-z article EN cc-by Communications Biology 2020-06-05

Background: Agricultural waste clearance and reutilization is a significant problem today. Objective: Successful extraction purification of cellulose its derivatives (methylcellulose) from agri-waste pollution. This an innovative polymer (cellulose & derivatives) that can be used in pharmaceutical technical applications eco-friendly manner. Aim: Isolate characterize derived prominent agricultural (sugarcane bagasse) utilization various biomedical fields. Method: Eco-friendly Soxhlet...

10.69857/joapr.v13i1.942 article EN cc-by-nc Journal of Applied Pharmaceutical Research 2025-02-28

A novel series of phenyl hydrazone bearing pyrazole and pyrimidine hybrid compounds has been designed using the molinspiration toolkit based on Lipinski's rule five developed via sequential reactions starting from diazotization different anilines further active methylation with acetyl acetone, ethyl acetoacetate cyanoacetate to generate hydrazono derivatives. The target were synthesized cyclisation resulting derivatives hydrazine, hydrazine urea. These molecules have subsequently tested for...

10.1039/c3ra41604f article EN RSC Advances 2013-01-01

An efficient and general one-pot reaction to a novel series of hybrid thiazolidine-4-one-1,3,5-triazine derivatives was developed. The easy work-up the products, rapid reaction, mild conditions are notable features this protocol. These molecules were found exhibit potent activity against panel Gram-positive Gram-negative micro-organisms.

10.1039/c2nj41028a article EN New Journal of Chemistry 2013-01-01

Herein, we report the synthesis and characterization of ESIPT-based benzothiazole substituted tetraphenylethylene molecules. We also studied their emission behavior in aggregation solid state.

10.1039/c6qm00374e article EN Materials Chemistry Frontiers 2017-01-01

Some novel derivatives of 3-(3-(7-chloroquinolin-4-ylamino)propyl)-1,3-thiazinan-4-one were synthesized and characterized by their physical spectral data. All the compounds subsequently screened for in vitro antimalarial activity against chloroquine sensitive strain Plasmodium falciparum (RKL-2) employing as reference drug. Most exhibited mild to moderate susceptibilities towards parasite comparison standard. It was found that...

10.1016/j.arabjc.2011.07.007 article EN cc-by-nc-nd Arabian Journal of Chemistry 2011-08-01
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