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Significant Accumulation of Polymyxin in Single Renal Tubular Cells: A Medicinal Chemistry and Triple Correlative Microscopy Approach

[Image: see text] Polymyxin is the last-line therapy against Gram-negative ‘superbugs’; however, dose-limiting nephrotoxicity can occur in up to 60% of patients after intravenous administration. Understanding the accumulation and concentration of polymyxin within renal tubular cells is essential for...

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Autores principales: Azad, Mohammad A. K., Roberts, Kade D., Yu, Heidi H., Liu, Boyin, Schofield, Alice V., James, Simon A., Howard, Daryl L., Nation, Roger L., Rogers, Kelly, de Jonge, Martin D., Thompson, Philip E., Fu, Jing, Velkov, Tony, Li, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4318625/
https://www.ncbi.nlm.nih.gov/pubmed/25553489
http://dx.doi.org/10.1021/ac504516k
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author Azad, Mohammad A. K.
Roberts, Kade D.
Yu, Heidi H.
Liu, Boyin
Schofield, Alice V.
James, Simon A.
Howard, Daryl L.
Nation, Roger L.
Rogers, Kelly
de Jonge, Martin D.
Thompson, Philip E.
Fu, Jing
Velkov, Tony
Li, Jian
author_facet Azad, Mohammad A. K.
Roberts, Kade D.
Yu, Heidi H.
Liu, Boyin
Schofield, Alice V.
James, Simon A.
Howard, Daryl L.
Nation, Roger L.
Rogers, Kelly
de Jonge, Martin D.
Thompson, Philip E.
Fu, Jing
Velkov, Tony
Li, Jian
author_sort Azad, Mohammad A. K.
collection PubMed
description [Image: see text] Polymyxin is the last-line therapy against Gram-negative ‘superbugs’; however, dose-limiting nephrotoxicity can occur in up to 60% of patients after intravenous administration. Understanding the accumulation and concentration of polymyxin within renal tubular cells is essential for the development of novel strategies to ameliorate its nephrotoxicity and to develop safer, new polymyxins. We designed and synthesized a novel dual-modality iodine-labeled fluorescent probe for quantitative mapping of polymyxin in kidney proximal tubular cells. Measured by synchrotron X-ray fluorescence microscopy, polymyxin concentrations in single rat (NRK-52E) and human (HK-2) kidney tubular cells were approximately 1930- to 4760-fold higher than extracellular concentrations. Our study is the first to quantitatively measure the significant uptake of polymyxin in renal tubular cells and provides crucial information for the understanding of polymyxin-induced nephrotoxicity. Importantly, our approach represents a significant methodological advancement in determination of drug uptake for single-cell pharmacology.
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spelling pubmed-43186252016-01-01 Significant Accumulation of Polymyxin in Single Renal Tubular Cells: A Medicinal Chemistry and Triple Correlative Microscopy Approach Azad, Mohammad A. K. Roberts, Kade D. Yu, Heidi H. Liu, Boyin Schofield, Alice V. James, Simon A. Howard, Daryl L. Nation, Roger L. Rogers, Kelly de Jonge, Martin D. Thompson, Philip E. Fu, Jing Velkov, Tony Li, Jian Anal Chem [Image: see text] Polymyxin is the last-line therapy against Gram-negative ‘superbugs’; however, dose-limiting nephrotoxicity can occur in up to 60% of patients after intravenous administration. Understanding the accumulation and concentration of polymyxin within renal tubular cells is essential for the development of novel strategies to ameliorate its nephrotoxicity and to develop safer, new polymyxins. We designed and synthesized a novel dual-modality iodine-labeled fluorescent probe for quantitative mapping of polymyxin in kidney proximal tubular cells. Measured by synchrotron X-ray fluorescence microscopy, polymyxin concentrations in single rat (NRK-52E) and human (HK-2) kidney tubular cells were approximately 1930- to 4760-fold higher than extracellular concentrations. Our study is the first to quantitatively measure the significant uptake of polymyxin in renal tubular cells and provides crucial information for the understanding of polymyxin-induced nephrotoxicity. Importantly, our approach represents a significant methodological advancement in determination of drug uptake for single-cell pharmacology. American Chemical Society 2015-01-01 2015-02-03 /pmc/articles/PMC4318625/ /pubmed/25553489 http://dx.doi.org/10.1021/ac504516k Text en Copyright © 2015 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Azad, Mohammad A. K.
Roberts, Kade D.
Yu, Heidi H.
Liu, Boyin
Schofield, Alice V.
James, Simon A.
Howard, Daryl L.
Nation, Roger L.
Rogers, Kelly
de Jonge, Martin D.
Thompson, Philip E.
Fu, Jing
Velkov, Tony
Li, Jian
Significant Accumulation of Polymyxin in Single Renal Tubular Cells: A Medicinal Chemistry and Triple Correlative Microscopy Approach
title Significant Accumulation of Polymyxin in Single Renal Tubular Cells: A Medicinal Chemistry and Triple Correlative Microscopy Approach
title_full Significant Accumulation of Polymyxin in Single Renal Tubular Cells: A Medicinal Chemistry and Triple Correlative Microscopy Approach
title_fullStr Significant Accumulation of Polymyxin in Single Renal Tubular Cells: A Medicinal Chemistry and Triple Correlative Microscopy Approach
title_full_unstemmed Significant Accumulation of Polymyxin in Single Renal Tubular Cells: A Medicinal Chemistry and Triple Correlative Microscopy Approach
title_short Significant Accumulation of Polymyxin in Single Renal Tubular Cells: A Medicinal Chemistry and Triple Correlative Microscopy Approach
title_sort significant accumulation of polymyxin in single renal tubular cells: a medicinal chemistry and triple correlative microscopy approach
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4318625/
https://www.ncbi.nlm.nih.gov/pubmed/25553489
http://dx.doi.org/10.1021/ac504516k
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