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dc.contributor.authorMuniruzzaman, Md.
dc.contributor.authorMarin, Alexander
dc.contributor.authorLuo, Yi
dc.contributor.authorPrestwich, Glenn D.
dc.contributor.authorPitt, William G.
dc.contributor.authorHusseini, Ghaleb
dc.contributor.authorRapoport, Natalya Y.
dc.date.accessioned2020-12-21T05:44:53Z
dc.date.available2020-12-21T05:44:53Z
dc.date.issued2002
dc.identifier.citationMuniruzzaman, M., Marin, A., Luo, Y., Prestwich, G. D., Pitt, W. G., Husseini, G., & Rapoport, N. Y. (2002). Intracellular uptake of Pluronic copolymer: effects of the aggregation state. Colloids and Surfaces B: Biointerfaces, 25(3), 233–241. https://doi.org/10.1016/s0927-7765(01)00329-0en_US
dc.identifier.issn0927-7765
dc.identifier.urihttp://hdl.handle.net/11073/19831
dc.description.abstractThe effect of the Pluronic P-105 aggregation state on its uptake by HL-60 cells was studied by flow cytometry, fluorescence spectroscopy, and confocal and fluorescence microscopy using a fluorescently labeled Pluronic P105. In the low concentration region below the critical micelle concentration (CMC), Pluronic uptake was proportional to the concentration in the incubation medium. The proportionality broke sharply above the CMC, revealing a less efficient intracellular uptake of Pluronic micelles than that of unimers. The data suggested that Pluronic micelles were internalized via fluid-phase endocytosis while unimers were internalized via diffusion through plasma membranes. Based on the above findings, the shielding effect of Pluronic micelles on drug intracellular uptake was explained.en_US
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.urihttps://doi.org/10.1016/S0927-7765(01)00329-0en_US
dc.subjectPluronic micellesen_US
dc.subjectHL-60 cellsen_US
dc.subjectUltrasounden_US
dc.subjectIntracellular uptakeen_US
dc.titleIntracellular uptake of Pluronic copolymer: effects of the aggregation stateen_US
dc.typePeer-Revieweden_US
dc.typeArticleen_US
dc.typePostprinten_US
dc.identifier.doi10.1016/s0927-7765(01)00329-0


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