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Bivash Mandal

Researcher at University of Tennessee Health Science Center

Publications -  17
Citations -  761

Bivash Mandal is an academic researcher from University of Tennessee Health Science Center. The author has contributed to research in topics: Targeted drug delivery & Drug delivery. The author has an hindex of 10, co-authored 17 publications receiving 648 citations. Previous affiliations of Bivash Mandal include Indian Institute of Chemical Biology & Jadavpur University.

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Core–shell-type lipid–polymer hybrid nanoparticles as a drug delivery platform

TL;DR: This comprehensive review covers the current applications of core-shell-type lipid-polymer hybrid nanoparticles, which combine the mechanical advantages of biodegradable polymeric nanoparticles and biomimetic advantages of liposomes to enable an efficient drug delivery system.
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Development and in vitro evaluation of core–shell type lipid–polymer hybrid nanoparticles for the delivery of erlotinib in non-small cell lung cancer

TL;DR: Evaluated in vitro cellular efficacy results indicated enhanced uptake and efficacy of erlotinib loaded CSLPHNPs compared to erlotInib solution in A549 cells, a human lung adenocarcinoma cell line, and CSL PHNPs could be a potential delivery system for erlot inib in the therapy of NSCLC.
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Preparation and Physicochemical Characterization of Eudragit ® RL100 Nanosuspension with potential for Ocular Delivery of Sulfacetamide

TL;DR: In this paper, a formulation of sulfacetamide in Eudragit® RL100 nanosuspension could be used as potential delivery system for treating ocular bacterial infections.
Journal Article

Sulfacetamide loaded Eudragit® RL100 nanosuspension with potential for ocular delivery.

TL;DR: The results indicate that the formulation of sulfacetamide in Eudragit® RL100 nanosuspension could be utilized as potential delivery system for treating ocular bacterial infections.
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Chloramphenicol-incorporated poly lactide-co-glycolide (PLGA) nanoparticles: formulation, characterization, technetium-99m labeling and biodistribution studies.

TL;DR: The CHL-loaded PLGA NPs coated with PS-80 exhibited relatively high brain uptake with comparatively low accumulation in bone marrow to that of free drug and CHL/PVA NPs (PVA, used as emulsion stabilizer) at 24 h post injection time period indicates the usefulness of the above delivery system for prolonged use of the antibiotic.