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The use of molecular descriptors to model pharmaceutical uptake by a fish primary gill cell culture epithelium

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The use of molecular descriptors to model pharmaceutical uptake by a fish primary gill cell culture epithelium. / Chang, Elisabeth D.; Hogstrand, Christer; Miller, Thomas H.; Owen, Stewart F.; Bury, Nic R.

In: Environmental science & technology, Vol. 53, No. 3, 05.02.2019, p. 1576-1584.

Research output: Contribution to journalArticle

Harvard

Chang, ED, Hogstrand, C, Miller, TH, Owen, SF & Bury, NR 2019, 'The use of molecular descriptors to model pharmaceutical uptake by a fish primary gill cell culture epithelium', Environmental science & technology, vol. 53, no. 3, pp. 1576-1584. https://doi.org/10.1021/acs.est.8b04394

APA

Chang, E. D., Hogstrand, C., Miller, T. H., Owen, S. F., & Bury, N. R. (2019). The use of molecular descriptors to model pharmaceutical uptake by a fish primary gill cell culture epithelium. Environmental science & technology, 53(3), 1576-1584. https://doi.org/10.1021/acs.est.8b04394

Vancouver

Chang ED, Hogstrand C, Miller TH, Owen SF, Bury NR. The use of molecular descriptors to model pharmaceutical uptake by a fish primary gill cell culture epithelium. Environmental science & technology. 2019 Feb 5;53(3):1576-1584. https://doi.org/10.1021/acs.est.8b04394

Author

Chang, Elisabeth D. ; Hogstrand, Christer ; Miller, Thomas H. ; Owen, Stewart F. ; Bury, Nic R. / The use of molecular descriptors to model pharmaceutical uptake by a fish primary gill cell culture epithelium. In: Environmental science & technology. 2019 ; Vol. 53, No. 3. pp. 1576-1584.

Bibtex Download

@article{b4bde8ab800a41a3bab24945088b22ff,
title = "The use of molecular descriptors to model pharmaceutical uptake by a fish primary gill cell culture epithelium",
abstract = "Modelling approaches, such as Quantitative Structure-Activity Relationships (QSARs) use molecular descriptors to predict the bioavailable properties of a compound in biota. However, these models have mainly been derived based on empirical data for lipophilic neutral compounds and may not predict the uptake of ionizable compounds. The majority of pharmaceuticals are ionizable and freshwaters can have a range of pH values that will affect speciation. In this study we assessed the uptake of 10 pharmaceuticals (acetazolamide, beclomethasone, carbamazepine, diclofenac, gemfibrozil, ibuprofen, ketoprofen, norethindrone, propranolol and warfarin) with differing modes-of action and physicochemical properties (pKa, logS, logD, logKow, molecular weight (MW) and polar surface area (PSA)) by an in vitro primary fish gill cell culture system (FIGCS) for 24 h in artificial freshwater. Principal component analysis (PCA) and partial least squares (PLS) regression was used to determine the molecular descriptors that influence the uptake rates. Ionizable drugs were taken up by FIGCS and a strong positive correlation was observed between logS and a negative correlation observed between pKa, logD, MW and the uptake rate. This approach shows that models can be derived based on physicochemical properties of pharmaceuticals and using an in vitro gill system to predict uptake of other compounds. There is a need for a robust and validated model for gill uptake that could be used in a tiered risk assessment to prioritize compounds for experimental testing.",
author = "Chang, {Elisabeth D.} and Christer Hogstrand and Miller, {Thomas H.} and Owen, {Stewart F.} and Bury, {Nic R.}",
year = "2019",
month = "2",
day = "5",
doi = "10.1021/acs.est.8b04394",
language = "English",
volume = "53",
pages = "1576--1584",
journal = "Environmental science & technology",
issn = "0013-936X",
publisher = "American Chemical Society",
number = "3",

}

RIS (suitable for import to EndNote) Download

TY - JOUR

T1 - The use of molecular descriptors to model pharmaceutical uptake by a fish primary gill cell culture epithelium

AU - Chang, Elisabeth D.

AU - Hogstrand, Christer

AU - Miller, Thomas H.

AU - Owen, Stewart F.

AU - Bury, Nic R.

PY - 2019/2/5

Y1 - 2019/2/5

N2 - Modelling approaches, such as Quantitative Structure-Activity Relationships (QSARs) use molecular descriptors to predict the bioavailable properties of a compound in biota. However, these models have mainly been derived based on empirical data for lipophilic neutral compounds and may not predict the uptake of ionizable compounds. The majority of pharmaceuticals are ionizable and freshwaters can have a range of pH values that will affect speciation. In this study we assessed the uptake of 10 pharmaceuticals (acetazolamide, beclomethasone, carbamazepine, diclofenac, gemfibrozil, ibuprofen, ketoprofen, norethindrone, propranolol and warfarin) with differing modes-of action and physicochemical properties (pKa, logS, logD, logKow, molecular weight (MW) and polar surface area (PSA)) by an in vitro primary fish gill cell culture system (FIGCS) for 24 h in artificial freshwater. Principal component analysis (PCA) and partial least squares (PLS) regression was used to determine the molecular descriptors that influence the uptake rates. Ionizable drugs were taken up by FIGCS and a strong positive correlation was observed between logS and a negative correlation observed between pKa, logD, MW and the uptake rate. This approach shows that models can be derived based on physicochemical properties of pharmaceuticals and using an in vitro gill system to predict uptake of other compounds. There is a need for a robust and validated model for gill uptake that could be used in a tiered risk assessment to prioritize compounds for experimental testing.

AB - Modelling approaches, such as Quantitative Structure-Activity Relationships (QSARs) use molecular descriptors to predict the bioavailable properties of a compound in biota. However, these models have mainly been derived based on empirical data for lipophilic neutral compounds and may not predict the uptake of ionizable compounds. The majority of pharmaceuticals are ionizable and freshwaters can have a range of pH values that will affect speciation. In this study we assessed the uptake of 10 pharmaceuticals (acetazolamide, beclomethasone, carbamazepine, diclofenac, gemfibrozil, ibuprofen, ketoprofen, norethindrone, propranolol and warfarin) with differing modes-of action and physicochemical properties (pKa, logS, logD, logKow, molecular weight (MW) and polar surface area (PSA)) by an in vitro primary fish gill cell culture system (FIGCS) for 24 h in artificial freshwater. Principal component analysis (PCA) and partial least squares (PLS) regression was used to determine the molecular descriptors that influence the uptake rates. Ionizable drugs were taken up by FIGCS and a strong positive correlation was observed between logS and a negative correlation observed between pKa, logD, MW and the uptake rate. This approach shows that models can be derived based on physicochemical properties of pharmaceuticals and using an in vitro gill system to predict uptake of other compounds. There is a need for a robust and validated model for gill uptake that could be used in a tiered risk assessment to prioritize compounds for experimental testing.

UR - http://www.scopus.com/inward/record.url?scp=85061042818&partnerID=8YFLogxK

U2 - 10.1021/acs.est.8b04394

DO - 10.1021/acs.est.8b04394

M3 - Article

VL - 53

SP - 1576

EP - 1584

JO - Environmental science & technology

JF - Environmental science & technology

SN - 0013-936X

IS - 3

ER -

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