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).
BYU ScholarsArchive Citation
Pruitt, John D. and Pitt, William G., "Sequestration and Ultrasound-Induced Release of Doxorubicin from Stabilized Pluronic P105 Micelles" (2008). Faculty Publications. 7673.
https://scholarsarchive.byu.edu/facpub/7673
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
Copyright Use Information
https://lib.byu.edu/about/copyright/