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Reversal of multidrug resistance by surfactants.

Cremophor EL, a pharmacologically inactive solubilising agent, has been shown to reverse multidrug resistance (MDR). Using flow cytometric evaluation of equilibrium intracellular levels of daunorubicin (DNR), we found that eight other surface active agents will also reverse MDR. All the active deter...

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Autores principales: Woodcock, D. M., Linsenmeyer, M. E., Chojnowski, G., Kriegler, A. B., Nink, V., Webster, L. K., Sawyer, W. H.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1992
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977900/
https://www.ncbi.nlm.nih.gov/pubmed/1637678
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author Woodcock, D. M.
Linsenmeyer, M. E.
Chojnowski, G.
Kriegler, A. B.
Nink, V.
Webster, L. K.
Sawyer, W. H.
author_facet Woodcock, D. M.
Linsenmeyer, M. E.
Chojnowski, G.
Kriegler, A. B.
Nink, V.
Webster, L. K.
Sawyer, W. H.
author_sort Woodcock, D. M.
collection PubMed
description Cremophor EL, a pharmacologically inactive solubilising agent, has been shown to reverse multidrug resistance (MDR). Using flow cytometric evaluation of equilibrium intracellular levels of daunorubicin (DNR), we found that eight other surface active agents will also reverse MDR. All the active detergents contain polyethoxylated moieties but have no similarities in their hydrophobic components. The properties of three polyethoxylated surfactants that showed the lowest toxicities, Cremophor, Tween 80 and Solutol HS15, were examined in more detail. The concentrations of Tween 80 and Solutol required to reverse DNR exclusion were 10-fold lower than for Cremophor. However while concentrations greater than or equal to 1:10(2) of the former two surfactants resulted in breakdown of cells, even 1:10 of Cremophor did not lyse cells. Studies of the effects of Cremophor on the uptake and efflux of DNR in normal and MDR cell types showed that Cremophor increases intracellular DNR primarily by locking the rapid efflux from the cells. This blockage of drug efflux may be mediated by a substantial alteration in the fluidity of cell membranes induced by Cremophor, as shown by decreased fluorescence anisotropy of a membrane probe. Consistent with these data, coinjection of adriamycin plus Cremophor into mice carrying a multidrug resistant P388 transplantable tumour significantly increased the survival time of the mice compared with adriamycin treatment alone.
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spelling pubmed-19779002009-09-10 Reversal of multidrug resistance by surfactants. Woodcock, D. M. Linsenmeyer, M. E. Chojnowski, G. Kriegler, A. B. Nink, V. Webster, L. K. Sawyer, W. H. Br J Cancer Research Article Cremophor EL, a pharmacologically inactive solubilising agent, has been shown to reverse multidrug resistance (MDR). Using flow cytometric evaluation of equilibrium intracellular levels of daunorubicin (DNR), we found that eight other surface active agents will also reverse MDR. All the active detergents contain polyethoxylated moieties but have no similarities in their hydrophobic components. The properties of three polyethoxylated surfactants that showed the lowest toxicities, Cremophor, Tween 80 and Solutol HS15, were examined in more detail. The concentrations of Tween 80 and Solutol required to reverse DNR exclusion were 10-fold lower than for Cremophor. However while concentrations greater than or equal to 1:10(2) of the former two surfactants resulted in breakdown of cells, even 1:10 of Cremophor did not lyse cells. Studies of the effects of Cremophor on the uptake and efflux of DNR in normal and MDR cell types showed that Cremophor increases intracellular DNR primarily by locking the rapid efflux from the cells. This blockage of drug efflux may be mediated by a substantial alteration in the fluidity of cell membranes induced by Cremophor, as shown by decreased fluorescence anisotropy of a membrane probe. Consistent with these data, coinjection of adriamycin plus Cremophor into mice carrying a multidrug resistant P388 transplantable tumour significantly increased the survival time of the mice compared with adriamycin treatment alone. Nature Publishing Group 1992-07 /pmc/articles/PMC1977900/ /pubmed/1637678 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Woodcock, D. M.
Linsenmeyer, M. E.
Chojnowski, G.
Kriegler, A. B.
Nink, V.
Webster, L. K.
Sawyer, W. H.
Reversal of multidrug resistance by surfactants.
title Reversal of multidrug resistance by surfactants.
title_full Reversal of multidrug resistance by surfactants.
title_fullStr Reversal of multidrug resistance by surfactants.
title_full_unstemmed Reversal of multidrug resistance by surfactants.
title_short Reversal of multidrug resistance by surfactants.
title_sort reversal of multidrug resistance by surfactants.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977900/
https://www.ncbi.nlm.nih.gov/pubmed/1637678
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