Cargando…
Data demonstrating the challenges of determining the kinetic parameters of P-gp mediated transport of low-water soluble substrates
The presented data are related to the research article entitled “Characterization of the IPEC-J2 MDR1 (iP-gp) cell line as a tool for identification of P-gp substrates” by Ozgur et al. (2017) [1]. This data report describes the challenges of investigating the concentration-dependent transport of P-g...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5848149/ https://www.ncbi.nlm.nih.gov/pubmed/29541662 http://dx.doi.org/10.1016/j.dib.2017.11.092 |
_version_ | 1783305833775366144 |
---|---|
author | Ozgür, Burak Saaby, Lasse Langthaler, Kristine Brodin, Birger |
author_facet | Ozgür, Burak Saaby, Lasse Langthaler, Kristine Brodin, Birger |
author_sort | Ozgür, Burak |
collection | PubMed |
description | The presented data are related to the research article entitled “Characterization of the IPEC-J2 MDR1 (iP-gp) cell line as a tool for identification of P-gp substrates” by Ozgur et al. (2017) [1]. This data report describes the challenges of investigating the concentration-dependent transport of P-glycoprotein (P-gp) substrates with relatively low aqueous solubility. Thus, we provide solubility data on two prototypical P-gp substrates, digoxin and rhodamine 123, representing P-gp substrates with a relatively low- and high-aqueous solubility, respectively. We present a hypothetical Michaelis-Menten curve of the P-gp mediated transport of digoxin to demonstrate that the maximal donor concentration, which can be reached in the experimental transport buffer, is too low to yield transport data in the saturable range of the Michaelis-Menten relationship. Furthermore, we present data on the bidirectional transport of digoxin and rhodamine 123 across cell monolayers of the MDCK II MDR1 cell line and iP-pg cell line in the presence of the selective P-gp inhibitor, zosuquidar/LY335979. |
format | Online Article Text |
id | pubmed-5848149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-58481492018-03-14 Data demonstrating the challenges of determining the kinetic parameters of P-gp mediated transport of low-water soluble substrates Ozgür, Burak Saaby, Lasse Langthaler, Kristine Brodin, Birger Data Brief Pharmacology, Toxicology and Pharmaceutical Science The presented data are related to the research article entitled “Characterization of the IPEC-J2 MDR1 (iP-gp) cell line as a tool for identification of P-gp substrates” by Ozgur et al. (2017) [1]. This data report describes the challenges of investigating the concentration-dependent transport of P-glycoprotein (P-gp) substrates with relatively low aqueous solubility. Thus, we provide solubility data on two prototypical P-gp substrates, digoxin and rhodamine 123, representing P-gp substrates with a relatively low- and high-aqueous solubility, respectively. We present a hypothetical Michaelis-Menten curve of the P-gp mediated transport of digoxin to demonstrate that the maximal donor concentration, which can be reached in the experimental transport buffer, is too low to yield transport data in the saturable range of the Michaelis-Menten relationship. Furthermore, we present data on the bidirectional transport of digoxin and rhodamine 123 across cell monolayers of the MDCK II MDR1 cell line and iP-pg cell line in the presence of the selective P-gp inhibitor, zosuquidar/LY335979. Elsevier 2017-12-06 /pmc/articles/PMC5848149/ /pubmed/29541662 http://dx.doi.org/10.1016/j.dib.2017.11.092 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Pharmacology, Toxicology and Pharmaceutical Science Ozgür, Burak Saaby, Lasse Langthaler, Kristine Brodin, Birger Data demonstrating the challenges of determining the kinetic parameters of P-gp mediated transport of low-water soluble substrates |
title | Data demonstrating the challenges of determining the kinetic parameters of P-gp mediated transport of low-water soluble substrates |
title_full | Data demonstrating the challenges of determining the kinetic parameters of P-gp mediated transport of low-water soluble substrates |
title_fullStr | Data demonstrating the challenges of determining the kinetic parameters of P-gp mediated transport of low-water soluble substrates |
title_full_unstemmed | Data demonstrating the challenges of determining the kinetic parameters of P-gp mediated transport of low-water soluble substrates |
title_short | Data demonstrating the challenges of determining the kinetic parameters of P-gp mediated transport of low-water soluble substrates |
title_sort | data demonstrating the challenges of determining the kinetic parameters of p-gp mediated transport of low-water soluble substrates |
topic | Pharmacology, Toxicology and Pharmaceutical Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5848149/ https://www.ncbi.nlm.nih.gov/pubmed/29541662 http://dx.doi.org/10.1016/j.dib.2017.11.092 |
work_keys_str_mv | AT ozgurburak datademonstratingthechallengesofdeterminingthekineticparametersofpgpmediatedtransportoflowwatersolublesubstrates AT saabylasse datademonstratingthechallengesofdeterminingthekineticparametersofpgpmediatedtransportoflowwatersolublesubstrates AT langthalerkristine datademonstratingthechallengesofdeterminingthekineticparametersofpgpmediatedtransportoflowwatersolublesubstrates AT brodinbirger datademonstratingthechallengesofdeterminingthekineticparametersofpgpmediatedtransportoflowwatersolublesubstrates |