S
Sanjeeb K. Sahoo
Researcher at University of Nebraska Medical Center
Publications - 15
Citations - 5927
Sanjeeb K. Sahoo is an academic researcher from University of Nebraska Medical Center. The author has contributed to research in topics: PLGA & Drug carrier. The author has an hindex of 12, co-authored 15 publications receiving 5598 citations. Previous affiliations of Sanjeeb K. Sahoo include Nebraska Medical Center.
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Nanotech approaches to drug delivery and imaging.
TL;DR: This review considers different nanotechnology-based drug delivery and imaging approaches, and their economic impact on pharmaceutical and biomedical industries.
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Rapid endo-lysosomal escape of poly(dl-lactide-co-glycolide) nanoparticles: implications for drug and gene delivery
TL;DR: The mechanism of rapid escape is by selective reversal of the surface charge of NPs (from anionic to cationic) in the acidic endolysosomal compartment, which causes the NPs to interact with the endo‐lysosomal membrane and escape into the cytosol.
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Residual polyvinyl alcohol associated with poly (D,L-lactide-co-glycolide) nanoparticles affects their physical properties and cellular uptake.
TL;DR: The residual PVA associated with nanoparticles is an important formulation parameter that can be used to modulate the pharmaceutical properties of PLGA nanoparticles.
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Iron oxide nanoparticles for sustained delivery of anticancer agents.
TL;DR: A novel water-dispersible oleic acid-Pluronic-coated iron oxide magnetic nanoparticle formulation that can be loaded easily with high doses of water-insoluble anticancer agents and demonstrated sustained intracellular drug retention relative to drug in solution and a dose-dependent antiproliferative effect in breast and prostate cancer cell lines.
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Polymer degradation and in vitro release of a model protein from poly(D,L-lactide-co-glycolide) nano- and microparticles.
Jayanth Panyam,Manisha M. Dali,Sanjeeb K. Sahoo,Wenxue Ma,Sudhir S. Chakravarthi,Gordon L. Amidon,Robert J. Levy,Vinod Labhasetwar +7 more
TL;DR: The polymer degradation rates in vitro were not substantially different for different size particles despite a 10- and 100-fold greater surface area to volume ratio for 0.1 microm size nanoparticles as compared to 1 and 10microm size microparticles, respectively.