Variability in urinary concentrations of primary aromatic amines.
Sridhar Chinthakindi1, Kurunthachalam Kannan2
1Department of Pediatrics and Department of Environmental Medicine, New York University School of Medicine, New York, NY 10016, USA.
The Science of the Total Environment
|March 28, 2022
Summary
Human exposure to primary aromatic amines (AAs) is concerning. This study measured urinary AA levels over five weeks, finding moderate variability and significant gender/ethnicity differences, but low daily intakes.
Area of Science:
- Environmental Health
- Toxicology
- Analytical Chemistry
Background:
- Primary aromatic amines (AAs) are chemicals with known carcinogenic potential, frequently found in consumer products.
- Human exposure to AAs is a significant public health concern.
- Understanding the temporal variability of urinary AA concentrations is crucial for accurate exposure assessment.
Purpose of the Study:
- To determine the concentrations and temporal variability of 30 AAs in urine samples.
- To investigate potential sources of AA exposure and correlations with oxidative stress biomarkers.
- To assess human exposure levels relative to tolerable daily intakes.
Main Methods:
- Longitudinal collection of 213 first morning void (FMV) urine samples over five weeks from 15 participants.
- Quantification of 30 AAs, nicotine, and cotinine using analytical techniques.
- Statistical analysis including intraclass correlation coefficients (ICCs) and Spearman's correlations.
Main Results:
- Eight AAs were detected in 68-100% of samples, with aniline and 2,6-dimethylaniline being predominant.
- Urinary AA concentrations exhibited moderate to poor temporal predictability (ICCs 0.248-0.697), except for 4-chloroaniline.
- Significant gender and ethnicity variations were observed in total AA concentrations; exposure sources were unrelated to tobacco smoke.
Conclusions:
- Urinary AA concentrations show considerable within- and between-individual variability, complicating exposure assessment.
- Observed AA exposure levels were substantially lower than established tolerable daily intakes.
- Further research is needed to elucidate specific exposure sources and long-term health implications.
More Related Videos
Related Concept Videos
Physical Properties of Amines
3.5K
Amines with low molecular weight are usually gaseous at room temperature, while those with high molecular weight are liquid or solids in nature. Usually, low molecular weight amines have a rotten fish-like smell. Diamines typically have a pungent smell. For instance, cadaverine and putrescine, depicted in Figure 1, are two molecules responsible for decaying tissue.
3.5K
Basicity of Aromatic Amines
7.4K
The basicity of aromatic amines is much weaker than that of aliphatic amines due to the involvement of the lone pair of electrons over the N atom in resonance with the aryl rings. Generally, the electron-donating ability of any substituents on the aryl ring of aromatic amines increases the basicity of the amine by increasing electron density, and hence the availability of lone pair on the nitrogen. On the other hand, electron-withdrawing functional groups on the aryl ring of amines decrease the...
7.4K
Basicity of Heterocyclic Aromatic Amines
6.3K
Heterocyclic amines, where the N atom is a part of an alicyclic system, are similar in basicity to alkylamines. Interestingly, the heterocyclic amine having a nitrogen atom as part of an aromatic ring has much less basicity than its corresponding alicyclic counterpart. For this reason, as presented in Figure 1, piperidine (pKb = 2.8) is significantly more basic than pyridine (pKb = 8.8).
6.3K
Urine Studies I: Urinalysis
253
Urinalysis is a widely used diagnostic test that analyzes urine's physical, chemical, and microscopic characteristics. Healthcare providers use it to detect and monitor various health conditions, including renal disease, urinary tract infections (UTIs), diabetes, and metabolic or systemic disorders.Components of UrinalysisUrinalysis consists of three primary components: physical, chemical, and microscopic examination. Each provides unique insights into the urine sample and, by extension, the...
253
Nomenclature of Aryl and Heterocyclic Amines
2.6K
The simplest aromatic amine is phenylamine, which contains an –NH2 functionality directly attached to an aromatic ring. The name aniline is designated for this skeleton. As shown in Figure 1, the common names of the functionalized anilines involve prefixes ortho-, meta-, and para- to indicate the substitution position. Different functionalized aniline derivatives also have notable trivial names.
2.6K
2° Amines to N-Nitrosamines: Reaction with NaNO2
4.6K
Secondary amines react with nitrous acid to form N-nitrosamines, as depicted in Figure 1. Nitrous acid, a weak and unstable acid, is formed in situ from an aqueous solution of sodium nitrite and strong acids, such as hydrochloric acid or sulfuric acid, in cold conditions. In the presence of an acid, the nitrous acid gets protonated. The subsequent loss of water results in the formation of the electrophile known as nitrosonium ion.
4.6K


