Cargando…
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...
Autores principales: | , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1782355868836167680 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4318625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT azadmohammadak significantaccumulationofpolymyxininsinglerenaltubularcellsamedicinalchemistryandtriplecorrelativemicroscopyapproach AT robertskaded significantaccumulationofpolymyxininsinglerenaltubularcellsamedicinalchemistryandtriplecorrelativemicroscopyapproach AT yuheidih significantaccumulationofpolymyxininsinglerenaltubularcellsamedicinalchemistryandtriplecorrelativemicroscopyapproach AT liuboyin significantaccumulationofpolymyxininsinglerenaltubularcellsamedicinalchemistryandtriplecorrelativemicroscopyapproach AT schofieldalicev significantaccumulationofpolymyxininsinglerenaltubularcellsamedicinalchemistryandtriplecorrelativemicroscopyapproach AT jamessimona significantaccumulationofpolymyxininsinglerenaltubularcellsamedicinalchemistryandtriplecorrelativemicroscopyapproach AT howarddaryll significantaccumulationofpolymyxininsinglerenaltubularcellsamedicinalchemistryandtriplecorrelativemicroscopyapproach AT nationrogerl significantaccumulationofpolymyxininsinglerenaltubularcellsamedicinalchemistryandtriplecorrelativemicroscopyapproach AT rogerskelly significantaccumulationofpolymyxininsinglerenaltubularcellsamedicinalchemistryandtriplecorrelativemicroscopyapproach AT dejongemartind significantaccumulationofpolymyxininsinglerenaltubularcellsamedicinalchemistryandtriplecorrelativemicroscopyapproach AT thompsonphilipe significantaccumulationofpolymyxininsinglerenaltubularcellsamedicinalchemistryandtriplecorrelativemicroscopyapproach AT fujing significantaccumulationofpolymyxininsinglerenaltubularcellsamedicinalchemistryandtriplecorrelativemicroscopyapproach AT velkovtony significantaccumulationofpolymyxininsinglerenaltubularcellsamedicinalchemistryandtriplecorrelativemicroscopyapproach AT lijian significantaccumulationofpolymyxininsinglerenaltubularcellsamedicinalchemistryandtriplecorrelativemicroscopyapproach |