کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5859087 | 1562324 | 2015 | 11 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Dose metric considerations in in vitro assays to improve quantitative in vitro-in vivo dose extrapolations
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کلمات کلیدی
median effect concentrationPBBKOrganisation of Economic Cooperation and DevelopmentOECDSPMETWAHAHEC50NRCPAHPDMSAUC - AUCDMSO - DMSOIn vitro assay - آزمایش درون آزمایشگاهیBED - بسترsolid-phase microextraction - بیوفیزیک جامد فازRegistration, Evaluation, Authorisation and Restriction of Chemicals - ثبت، ارزیابی، مجوز و محدودیت مواد شیمیاییDose - دوز Biologically effective dose - دوز موثر زیستیDimethylsulfoxide - دیمتیل سولفواکسیدREACH - رسیدنFree concentration - غلظت آزادarea under the curve - منطقه تحت منحنیMechanism of action - مکانیسم عملTime weighted average - میانگین وزنی زمانPolycyclic aromatic hydrocarbons - هیدروکربن آروماتیک چندحلقهایHalogenated aromatic hydrocarbons - هیدروکربن های معطر هالوژنیPolydimethylsiloxane - پلیمتیلسیلوکسانKow - کوه
موضوعات مرتبط
علوم زیستی و بیوفناوری
علوم محیط زیست
بهداشت، سم شناسی و جهش زایی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Challenges to improve toxicological risk assessment to meet the demands of the EU chemical's legislation, REACH, and the EU 7th Amendment of the Cosmetics Directive have accelerated the development of non-animal based methods. Unfortunately, uncertainties remain surrounding the power of alternative methods such as in vitro assays to predict in vivo dose-response relationships, which impedes their use in regulatory toxicology. One issue reviewed here, is the lack of a well-defined dose metric for use in concentration-effect relationships obtained from in vitro cell assays. Traditionally, the nominal concentration has been used to define in vitro concentration-effect relationships. However, chemicals may differentially and non-specifically bind to medium constituents, well plate plastic and cells. They may also evaporate, degrade or be metabolized over the exposure period at different rates. Studies have shown that these processes may reduce the bioavailable and biologically effective dose of test chemicals in in vitro assays to levels far below their nominal concentration. This subsequently hampers the interpretation of in vitro data to predict and compare the true toxic potency of test chemicals. Therefore, this review discusses a number of dose metrics and their dependency on in vitro assay setup. Recommendations are given on when to consider alternative dose metrics instead of nominal concentrations, in order to reduce effect concentration variability between in vitro assays and between in vitro and in vivo assays in toxicology.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicology - Volume 332, 5 June 2015, Pages 30-40
Journal: Toxicology - Volume 332, 5 June 2015, Pages 30-40
نویسندگان
Floris A. Groothuis, Minne B. Heringa, Beate Nicol, Joop L.M. Hermens, Bas. J. Blaauboer, Nynke I. Kramer,