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dc.contributor.authorLiang, X.
dc.contributor.authorWang, H.
dc.contributor.authorGrice, J.
dc.contributor.authorLi, L.
dc.contributor.authorLiu, Jian
dc.contributor.authorXu, Z.
dc.contributor.authorRoberts, M.
dc.date.accessioned2018-12-13T09:11:05Z
dc.date.available2018-12-13T09:11:05Z
dc.date.created2018-12-12T02:46:48Z
dc.date.issued2016
dc.identifier.citationLiang, X. and Wang, H. and Grice, J. and Li, L. and Liu, J. and Xu, Z. and Roberts, M. 2016. Physiologically Based Pharmacokinetic Model for Long-Circulating Inorganic Nanoparticles. Nano Letters: a journal dedicated to nanoscience and nanotechnology. 16 (2): pp. 939-945.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/71707
dc.identifier.doi10.1021/acs.nanolett.5b03854
dc.description.abstract

© 2016 American Chemical Society. A physiologically based pharmacokinetic model was developed for accurately characterizing and predicting the in vivo fate of long-circulating inorganic nanoparticles (NPs). This model is built based on direct visualization of NP disposition details at the organ and cellular level. It was validated with multiple data sets, indicating robust inter-route and interspecies predictive capability. We suggest that the biodistribution of long-circulating inorganic NPs is determined by the uptake and release of NPs by phagocytic cells in target organs.

dc.publisherAmerican Chemical Society
dc.titlePhysiologically Based Pharmacokinetic Model for Long-Circulating Inorganic Nanoparticles
dc.typeJournal Article
dcterms.source.volume16
dcterms.source.number2
dcterms.source.startPage939
dcterms.source.endPage945
dcterms.source.issn1530-6984
dcterms.source.titleNano Letters: a journal dedicated to nanoscience and nanotechnology
curtin.departmentWASM: Minerals, Energy and Chemical Engineering (WASM-MECE)
curtin.accessStatusFulltext not available


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