Keywords

Doxorubicin, Hl-60 Cells, Micellar Drug Delivery, N, N-Diethylacrylamide, Pluronic, Ultrasound

Abstract

Controlled drug delivery from micelles requires that the micelles remain stable when diluted below their critical micelle concentration, such as upon injection into blood. A cross-linked, interpenetrating network of N,N-diethylacrylamide (NNDEA) was polymerized in the core of Pluronic P105 micelles to stabilize temporarily the micelles at concentrations below the critical micellar concentration of free P105. The stabilized Pluronic micelles (called Plurogels) were able to sequester the drug doxorubicin (Dox) and protect HL-60 cells from the drug at concentrations where non-stabilized Pluronic provided no protection. The protection lasted ~ 12 hr, which is similar to the half-life of the particles. Application of low-frequency ultrasound resulted in a synergistic killing effect with Dox and low concentrations of either Pluronic P105 or stabilized Plurogels, most probably due to release of Dox and permeabilization of the cell membrane.

Original Publication Citation

Pruitt, J.D. and Pitt*, W.G., “Sequestration and Ultrasound-Induced Release of Doxorubicin from Stabilized Pluronic P105 Micelles”, Drug Delivery 9(4), 253-259 (2002).

Document Type

Peer-Reviewed Article

Publication Date

2008-09-29

Publisher

Taylor & Francis

Language

English

College

Ira A. Fulton College of Engineering

Department

Chemical Engineering

University Standing at Time of Publication

Full Professor

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