B
Bhushan S. Pattni
Researcher at Northeastern University
Publications - 14
Citations - 1803
Bhushan S. Pattni is an academic researcher from Northeastern University. The author has contributed to research in topics: Drug delivery & Cancer cell. The author has an hindex of 9, co-authored 14 publications receiving 1423 citations.
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Journal ArticleDOI
New Developments in Liposomal Drug Delivery.
TL;DR: Bhushan S. Pattni,† Vladimir V. Chupin,‡ and Vladimir P. Torchilin study the role of phosphorous in the biosynthesis of Membrane Proteins and found that phosphorous binds to polypeptide A in a manner similar to that of polymethine.
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Nanopreparations to overcome multidrug resistance in cancer
TL;DR: Nanoparticles, up to 400 nm in size, have shown great promise for carrying, protecting and delivering potential therapeutic molecules with diverse physiological properties, and the use of nanotechnology to overcome the MDR is discussed in detail.
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Transferrin-targeted, resveratrol-loaded liposomes for the treatment of glioblastoma.
TL;DR: Overall, the liposomal nanomedicines of RES developed in this project exhibited favorable in vitro and in vivo efficacies, which warrant their further investigation for the treatment of GBMs.
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Transferrin and octaarginine modified dual-functional liposomes with improved cancer cell targeting and enhanced intracellular delivery for the treatment of ovarian cancer
TL;DR: DOX-loaded liposomes, surface-modified with, R8 and transferrin (Tf) (Dual DOX-L), are reported on to improve targeting of A2780 ovarian carcinoma cells via the over-expressed transferrin receptors with R8-mediated intracellular DOX delivery.
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Solid lipid nanoparticles co-loaded with doxorubicin and α-tocopherol succinate are effective against drug-resistant cancer cells in monolayer and 3-D spheroid cancer cell models.
Mariana Silva Oliveira,Bhawani Aryasomayajula,Bhushan S. Pattni,Samuel V. Mussi,Lucas Antônio Miranda Ferreira,Vladmir P. Torchilin +5 more
TL;DR: Solid lipid nanoparticles co-loaded with doxorubicin and TS showed a prominent cytotoxicity and a greater penetration of doxorbicin in cancer cell spheroids and in the monolayer model, suggesting a bypassing of P-glycoprotein bomb efflux.