Literature DB >> 20872634

Quantification of deuterated bisphenol A in serum, tissues, and excreta from adult Sprague-Dawley rats using liquid chromatography with tandem mass spectrometry.

Nathan C Twaddle1, Mona I Churchwell, Michelle Vanlandingham, Daniel R Doerge.   

Abstract

Bisphenol A (BPA) is an important industrial chemical used in the manufacture of polycarbonate plastic products, epoxy resin-based food can liners, and paper products. The presence of BPA in urine of >90% of Americans aged 6-60 suggests ubiquitous and frequent exposure and is problematic because of the potential for endocrine disruption. The ubiquity of environmental BPA in common laboratory supplies used for sample collection, storage, and analysis greatly increases the likelihood of false positive determinations, particularly at trace levels. The current study validated using liquid chromatography/tandem mass spectrometry (LC/MS/MS) in conjunction with deuterated BPA as the dosing material to circumvent contamination for high sensitivity quantifications in rat serum, tissues, urine, and feces. The methods described provided measurements of both estrogen receptor-active aglycone and metabolically deactivated conjugated forms of BPA, a distinction that is critical to assessing toxicological potential. The adequacy of the described methodology was substantiated by its utility in analyzing samples from rats treated orally with a 100 µg/kg body weight dose of d6-BPA. These results emphasize the challenges inherent in measuring BPA in biological samples and how employing stable isotope labeled dosing can facilitate pharmacokinetic studies needed to understand BPA metabolism and disposition. Such studies conducted in experimental animal models, in conjunction with properly validated human biomonitoring data, will be the basis for PBPK modeling of BPA in environmentally exposed humans. Published in 2010 by John Wiley & Sons, Ltd.

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Year:  2010        PMID: 20872634     DOI: 10.1002/rcm.4733

Source DB:  PubMed          Journal:  Rapid Commun Mass Spectrom        ISSN: 0951-4198            Impact factor:   2.419


  15 in total

Review 1.  Bisphenol A, obesity, and type 2 diabetes mellitus: genuine concern or unnecessary preoccupation?

Authors:  Priyadarshini Mirmira; Carmella Evans-Molina
Journal:  Transl Res       Date:  2014-03-13       Impact factor: 7.012

2.  Pharmacokinetics of bisphenol A in humans following a single oral administration.

Authors:  Kristina A Thayer; Daniel R Doerge; Dawn Hunt; Shepherd H Schurman; Nathan C Twaddle; Mona I Churchwell; Stavros Garantziotis; Grace E Kissling; Michael R Easterling; John R Bucher; Linda S Birnbaum
Journal:  Environ Int       Date:  2015-06-24       Impact factor: 9.621

3.  Toxicity evaluation of bisphenol A administered by gavage to Sprague Dawley rats from gestation day 6 through postnatal day 90.

Authors:  K Barry Delclos; Luísa Camacho; Sherry M Lewis; Michelle M Vanlandingham; John R Latendresse; Greg R Olson; Kelly J Davis; Ralph E Patton; Gonçalo Gamboa da Costa; Kellie A Woodling; Matthew S Bryant; Mani Chidambaram; Raul Trbojevich; Beth E Juliar; Robert P Felton; Brett T Thorn
Journal:  Toxicol Sci       Date:  2014-02-04       Impact factor: 4.849

4.  Comparison of life-stage-dependent internal dosimetry for bisphenol A, ethinyl estradiol, a reference estrogen, and endogenous estradiol to test an estrogenic mode of action in Sprague Dawley rats.

Authors:  Mona I Churchwell; Luísa Camacho; Michelle M Vanlandingham; Nathan C Twaddle; Estatira Sepehr; K Barry Delclos; Jeffrey W Fisher; Daniel R Doerge
Journal:  Toxicol Sci       Date:  2014-02-04       Impact factor: 4.849

5.  The concentration of bisphenol A in urine is affected by specimen collection, a preservative, and handling.

Authors:  M P Longnecker; K Harbak; G E Kissling; J A Hoppin; M Eggesbo; T A Jusko; J Eide; H M Koch
Journal:  Environ Res       Date:  2013-07-27       Impact factor: 6.498

6.  Sex specific impact of perinatal bisphenol A (BPA) exposure over a range of orally administered doses on rat hypothalamic sexual differentiation.

Authors:  Katherine A McCaffrey; Brian Jones; Natalie Mabrey; Bernard Weiss; Shanna H Swan; Heather B Patisaul
Journal:  Neurotoxicology       Date:  2013-03-13       Impact factor: 4.294

7.  Bisphenol A (BPA) and bisphenol S (BPS) alter the promoter activity of the ABCB1 gene encoding P-glycoprotein in the human placenta in a haplotype-dependent manner.

Authors:  Jordan T Speidel; Meixiang Xu; Sherif Z Abdel-Rahman
Journal:  Toxicol Appl Pharmacol       Date:  2018-09-19       Impact factor: 4.219

Review 8.  Evidence that bisphenol A (BPA) can be accurately measured without contamination in human serum and urine, and that BPA causes numerous hazards from multiple routes of exposure.

Authors:  Frederick S vom Saal; Wade V Welshons
Journal:  Mol Cell Endocrinol       Date:  2014-10-07       Impact factor: 4.102

Review 9.  Critical evaluation of key evidence on the human health hazards of exposure to bisphenol A.

Authors:  J G Hengstler; H Foth; T Gebel; P-J Kramer; W Lilienblum; H Schweinfurth; W Völkel; K-M Wollin; U Gundert-Remy
Journal:  Crit Rev Toxicol       Date:  2011-04       Impact factor: 5.635

10.  Pharmacokinetics of bisphenol A in humans following dermal administration.

Authors:  Alan F Sasso; Ralph Pirow; Syam S Andra; Rebecca Church; Rebecca M Nachman; Susanne Linke; Dustin F Kapraun; Shepherd H Schurman; Manish Arora; Kristina A Thayer; John R Bucher; Linda S Birnbaum
Journal:  Environ Int       Date:  2020-08-13       Impact factor: 13.352

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