scholarly journals Bisphenol A (BPA) in human serum and urine :||exposure via dermal absorption from thermal paper receipts and oral ingestion after transfer from hand to food

2013 ◽  
Author(s):  
Annette M. Hormann
2018 ◽  
Vol 410 (7) ◽  
pp. 1885-1891 ◽  
Author(s):  
Yu Su ◽  
Chenggang Shao ◽  
Xielin Huang ◽  
Jinxia Qi ◽  
Renshan Ge ◽  
...  

Author(s):  
Elena Reale ◽  
David Vernez ◽  
Nancy B Hopf

Abstract Objectives Bisphenol A (BPA) is the most used colour developer in thermal paper for cashiers receipts, labels, and tickets. BPA can migrate onto the skin and be absorbed when handling these papers. BPA is a known endocrine disruptor and is therefore being replaced in thermal paper by some alternatives such as Bisphenol S (BPS), D-8, and Pergafast 201® (PF201). To our knowledge, no studies have characterized skin permeation of these BPA alternatives. Methods We measured/characterized skin absorption for BPA, BPS, D-8, and PF201 through ex vivo human skin using flow-through diffusion cells according to OECD guideline 428. Skin samples were 7–12 per test substance from three different skin donors. Skin metabolism was studied for BPA. Dermal absorption was expressed as the amount of the BPA alternatives in the receptor fluid over applied dose in percent (%). Results The absorbed dose after 24 h of exposure was 25% for BPA, 17% for D-8, 0.4% for BPS, and <LLOQ for PF201. The amount of BPA-glucuronide in the receptor fluid after 24 h was under the limit of quantification (LLOQ = 0.2 µg l−1). Despite the 10-fold lower concentration of the aq solution applied on the skin, D-8’s permeation rate JMAX was 5-fold higher than the one for BPS (0.032 versus 0.006 µg cm−2 h−1). Neither D-8 nor BPS permeated readily through the skin (tlag = 3.9 h for D-8, 6.4 h for BPS). None of PF201’s skin permeation kinetic parameters could be determined because this BPA analogue was not quantifiable in the receptor fluid in our test conditions. Conclusions Skin absorption was in decreasing order: BPA > D-8 >> BPS > PF201. These results are in agreement with their log Kow and molecular weights. We provided here the necessary data to estimate the extent of skin absorption of BPA analogues, which is a necessary step in risk assessment, and ultimately evaluate public health risks posed by D-8, BPS, and PF201.


1972 ◽  
Vol 18 (12) ◽  
pp. 1493-1497 ◽  
Author(s):  
L Fridhandler ◽  
J Edward Berk ◽  
M Ueda

Abstract We describe a sensitive quantitative procedure for separating isoamylases in human serum, urine, and tissue homogenates. Two components have been discerned with chromatographic characteristics resembling those of pancreatic and salivary amylases, respectively. Several lines of evidence—derived from studies in normal subjects, pancreatectomized patients, and patients with acute pancreatitis—indicate that the pancreas is probably the source of the component in serum and urine that exhibits characteristics of pancreatic amylase. The source of the component resembling salivary amylase has not yet been fully defined. Isoamylase analysis of extracts of fallopian tube and liver revealed two amylase components with chromatographic properties similar to pancreatic and salivary amylases, respectively.


2017 ◽  
Vol 106 ◽  
pp. 135-143 ◽  
Author(s):  
Rachel Rogers Worley ◽  
Susan McAfee Moore ◽  
Bruce C. Tierney ◽  
Xiaoyun Ye ◽  
Antonia M. Calafat ◽  
...  

2015 ◽  
Vol 78 (18) ◽  
pp. 1181-1188 ◽  
Author(s):  
Bruno Alves Rocha ◽  
Lara Ferreira Azevedo ◽  
Matheus Gallimberti ◽  
Andres Dobal Campiglia ◽  
Fernando Barbosa

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