Dinesh Kumar on Muck Rack

Dinesh Kumar

As seen in: The Times of India, India Times, PLOS, American Chemical Society, Royal Society of Chemistry, Data Science Central, Chemistry World, The Sunday Guardian, HR.com

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Articles

N-Methyl-D-aspartate receptors as novel M1 macrophage-specific biomedical imaging nanoplatform agents: Feasibility of targeted imaging in an inflammatory mice model

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By Hui-Jeon Jeon, Dinesh Kumar, Hoon Hyun, Yong hyun Jeon
| Royal Society of Chemistry Verified
N-Methyl-D-aspartate receptors as novel M1 macrophage-specific biomedical imaging nanoplatform agents: Feasibility of targeted imaging in an inflammatory mice model N-methyl-D-aspartate receptor (NMDAR)-antibody-labeled mesoporous silica nanoparticles (NMDAR-PEG-DID@MSNs) were developed as a fluorescence imaging tool for M1 macrophage-associated inflammatory diseases.
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Increasing electron density through n-type semiconductor to accelerate hot electrons from plasmonic Au nanospheres for artificial photosynthesis and cross-coupling reactions

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By Dinesh Kumar, Suresh Kumar, Richa Jaswal, Devendra Shrestha
| Royal Society of Chemistry Verified
Increasing electron density through n-type semiconductor to accelerate hot electrons from plasmonic Au nanospheres for artificial photosynthesis and cross-coupling reactions Here, we report the synthesis of an n-type semiconductor (SnO2) and gold nanospheres (GNSs) based core-satellite heterostructures (SnO2@GNSs) composed of GNSs as core and ultra-small SnO2 nanodots as a satellite with multiple thicknesses which then utilized for artificial photosynthesis and Suzuki-Miyaura coupling reaction.
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Review on novel targeted enzyme drug delivery systems: enzymosomes

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By Dinesh Kumar, Sunita Devi, Komal Sachdeva, Rajni Tanwar
| Royal Society of Chemistry Verified
Review on novel targeted enzyme drug delivery systems: enzymosomes The goal of this review is to present enzymosomes as an innovative means for site-specific drug delivery. Enzymosomes make use of an enzyme's special characteristics, such as its capacity to accelerate the reaction rate and bind to a particular substrate at a regulated rate. Enzymosomes are created when an enzyme forms a covalent linkage with a liposome or lipid vesicle surface.
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