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Chinmay Ghoroi
Researcher at Indian Institute of Technology Gandhinagar
Publications - 65
Citations - 1499
Chinmay Ghoroi is an academic researcher from Indian Institute of Technology Gandhinagar. The author has contributed to research in topics: Chemistry & Surface energy. The author has an hindex of 16, co-authored 50 publications receiving 1029 citations. Previous affiliations of Chinmay Ghoroi include Indian Institute of Technology Bombay & New Jersey Institute of Technology.
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Large Reductions in Solar Energy Production Due to Dust and Particulate Air Pollution
TL;DR: In this article, the influence of dust and anthropogenic sources (e.g., fossil and biomass fuel combustion) on solar electricity generation is estimated. But, the results show that solar energy production is currently reduced by ∼17-25% across these regions, with roughly equal contributions from ambient PM and PM deposited on photovoltaic surfaces.
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Simultaneous micronization and surface modification for improvement of flow and dissolution of drug particles.
TL;DR: The surface modified, micronized powders showed improved dispersion, higher bulk densities, reduced electrostatic, and higher flowability, indicating they may be used in high drug loaded formulations amenable to direct compression.
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Improvement of flow and bulk density of pharmaceutical powders using surface modification.
TL;DR: A limited design of experiment was conducted to establish a standardized dry coating procedure that limits the extent of powder attrition, while providing the most consistent improvement in angle of repose (AOR), which indicated a significant positive shift due to dry coating.
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Influence of surface modification on wettability and surface energy characteristics of pharmaceutical excipient powders.
Vikram Karde,Chinmay Ghoroi +1 more
TL;DR: The study successfully demonstrated that surface wettability and energetics of powders can be modified by varying the level of surface coating.
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Dry coating of micronized API powders for improved dissolution of directly compacted tablets with high drug loading.
TL;DR: The most significant advantage is in tablet dissolution where the t(80) for the tablets with dry coated APIs was well under 5 min, indicating that this approach can produce nearly instant release direct compacted tablets at high drug loadings.