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Ed Luther

Researcher at Northeastern University

Publications -  19
Citations -  403

Ed Luther is an academic researcher from Northeastern University. The author has contributed to research in topics: Cancer cell & Doxorubicin. The author has an hindex of 9, co-authored 19 publications receiving 316 citations.

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Nanomedicine based curcumin and doxorubicin combination treatment of glioblastoma with scFv-targeted micelles: In vitro evaluation on 2D and 3D tumor models.

TL;DR: The increased efficacy of combination nanoformulations on the spheroids compared to a single agent loaded, or to non-targeted formulations, reinforces the rationale for selection of this combination and successful utilization of GLUT1 scFv as a targeting agent for glioblastoma treatment.
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Reversal of Chemoresistance in Ovarian Cancer by Co-Delivery of a P-Glycoprotein Inhibitor and Paclitaxel in a Liposomal Platform

TL;DR: It is found that overexpression of P-gp in ovarian cancer is associated with a shorter progression-free and overall survival, and co-delivery of a P- gp inhibitor and paclitaxel using a liposomal platform can sensitize pac litaxel-resistant ovarian cancer cells to paclitAXel.
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Enhanced Cytotoxicity of Folic Acid-Targeted Liposomes Co-Loaded with C6 Ceramide and Doxorubicin: In Vitro Evaluation on HeLa, A2780-ADR, and H69-AR Cells

TL;DR: Overall, this study clearly shows that the co-delivery of C6 ceramide and Dox using a liposomal platform significantly correlates with an antiproliferative effect due to cell cycle regulation and subsequent induction of apoptosis and thus warrants its further evaluation in preclinical animal models.
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Surface-engineered polyethyleneimine-modified liposomes as novel carrier of siRNA and chemotherapeutics for combination treatment of drug-resistant cancers.

TL;DR: Novel liposomal formulations surface-modified with a low molecular weight, branched polyethyleneimine (bPEI)–lipid conjugate for use as an alternative to PEG had very good stability characteristics in ion- and protein-rich mediums and tumor growth inhibition was observed in a mouse ovarian xenograft tumor model.