Stable isotope values are reported separately (Bentzen et al., companion paper). The research project, CONACYT-SALUD 2010-C01-140272 ABT-888 ic50 (also known as “Antioxidant response in breast milk to the presence of chemical contamination”), was approved by the Baja California Sur Chapter of the National Mexican Academy for Bioethics. Demographic and epidemiological data were collected through a survey. The questionnaire requested information on age, parity (1st, 2nd or 3 or more), body weight, and height. Weight and height were used to calculate the body mass index [BMI = weight (kg)/height squared (m2)]. General food consumption data covered 30 days prior

to hair sample collection. No information was obtained about meal portion

size, recipes, or preparation methods. Finfish and shellfish intake frequency data were grouped into four categories: not consumed; consumed once a month; consumed once every two weeks; and consumed more than twice a week. Information about tobacco smoke exposure was also requested and categorized as: smoker; passive exposure; and non-smoker. Informed consent Fulvestrant price was obtained from all participants. Hair samples were prepared for [THg] segmental analyses to assess potential temporal variability (analysis of multiple segments per hair sample). The proximal end (segment) of the samples was identified and marked with thread. Each hair sample was tied with white thread every 3-4 cm to prevent tangling during 3-mercaptopyruvate sulfurtransferase washing. Samples were immersed in a 1% solution of Triton X-100® for 15 – 20 minutes to remove external contamination, then followed by an initial 10 minute immersion in ultra-pure water (NANOpure Model D4751, Barnstead International, Dubuque, Iowa); then a 5 minute immersion,

with 3 additional sequential immersions. Cleaned samples were placed in 4 oz polyethylene bags and freeze-dried for 48 hours. Each scalp hair specimen was subsampled in 3 locations (segments 3-4 cm long) along the length of the hair. Initial subsamples were 3 cm, but in some cases this did not result in sufficient sample mass for duplicate [THg] measurements. Consequently, sub-sample length was increased to 4 cm. Initially, sub-samples (3 cm) were cut from the proximal, middle, and distal segments of the intact hair samples. This resulted in three distinct periods of growth from each sample with the consistent proximal segment always representing recent hair growth (3 to 4 months). The growth time between the 2 distinct segments was variable depending on the initial length of the sample. Distal samples were occasionally of inadequate mass for replicate [THg] measurement as hair length was uneven. Most hair samples were at least 15 cm long, so subsequent segmental analysis included three 4-cm long segments starting at the proximal end, with 1 cm between each segment; thereby, incorporating the most recent 14 cm of hair growth (Fig. 1).