Detection Of Tetrabromobisphenol A Research Articles

Facile green synthesis of silver nanoparticles: Relevance in localized surface plasmon resonance and molecular imprinted polymer sensor for detection of Tetrabromobisphenol A in electronic waste

The present study demonstrates evocatively the interest in prioritizing an environmental friendly approach. Green synthesis of metallic nano-particles is carried out, which is further incorporated with a technique known as Molecular Imprinted Polymers (MIP) to develop a highly sensitive cuvette-based localized surface plasmon resonance (LSPR) probe for the selective detection of a Tetrabromobisphenol-A (TBBPA). TBBPA is a hazardous phenolic compound, mostly found in electronic waste (E-waste), that is abundant on earth. We have fabricated an LSPR probe with the help of a transparent glass substrate. A layer of Silver nanoparticles has been decorated over the glass substrate which further has an MIP overlayer on it. The glass slide dimensions are so chosen that it can fit inside the cuvette along its one side. The absorbance spectra are then recorded for a concentration range of 0–500 ng/ml of TBBPA. The sensitivity and limit of detection of the proposed sensor have been found to be 0.228 nm/ng ml−1 and 4.68 ng/ml respectively. Also, the probe showed quite promising recovery percentage greater than 85 % in real samples. Hence, with the findings and outcomes our fabricated probe can be represented as a potential candidate in selective detection of TBBPA along with the benefits of low cost of fabrication, portable, and real-time monitoring.

Functional Melanin Nanoparticles-Assisted Laser Desorption Ionization Mass Spectrometry for High-Sensitivity Detection of TBBPA and TBBPS Contaminations in Animal-Derived Foodstuffs.

Tetrabromobisphenol A (TBBPA) and tetrabromobisphenol S (TBBPS) have been widely used as additives in various products; however, their residues damage human health mainly via dietary ingestion. The current detection techniques remain challenging in directly and sensitively identifying TBBPA and TBBPS from food samples. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) has great potential as an alternative tool for the analysis of low-mass environmental pollution. Herein, we successfully screened and optimized COOH-MNP-COOH as a novel MALDI matrix to enhance deprotonation for the analysis of TBBPA and TBBPS from animal-derived food samples in negative-ion mode. Notably, COOH-MNP-COOH was synthesized by a facile self-assembly strategy and characterized by TEM, FT-IR, UV-vis, and zeta potential analysis. Compared with conventional and control matrices, the COOH-MNP-COOH matrix exhibited excellent performance of TBBPA and TBBPS with high chemical stability, favorable reproducibility, remarkable salt and protein tolerance, and high sensitivity owing to abundant active groups, stronger UV-vis absorption at 355 nm, and better hydrophilicity and biocompatibility. TBBPA and TBBPS were detected with the assistance of an internal standard with limits of detection (LODs) of 300 and 200 pg/mL, respectively. Moreover, this method was applied to directly identify the residues of TBBPA and TBBPS in milk products, followed by basa catfish and meat. This research may provide a promising approach for the analysis of environmental pollutants in foodstuffs.

Fabrication of well-aligned Co-MOF arrays through a controlled and moderate process for the development of a flexible tetrabromobisphenol A sensor.

Tetrabromobisphenol A (TBBPA) has attracted a great deal of attention due to its side effects and potential bioaccumulation properties. It is of great importance to construct and develop novel electrochemical sensors for the sensitive and selective detection of TBBPA. In the present study, cobalt (Co) based metal-organic frameworks (MOFs) were synthesized on carbon cloth (CC) by using cobalt nitrate hexahydrate and 2-methylimidazole. The morphological characterization was carried out by transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR). The results showed that Co-MOFs/CC have a leaf-like structure and abundant surface functional groups. The electrochemical properties of the sensor were investigated by differential pulse voltammetry (DPV). The effects of different ratios of metal ions to organic ligands, reaction temperature, time, concentration, pH value of the electrolyte, and incubation time on the oxidation peak current of TBBPA were studied. Under the optimal conditions, the linear range of the designed sensor was 0.1 μM-100 μM, and the limit of detection was 40 nM. The proposed sensor is simple, of low cost and efficient, which can greatly facilitate the detection tasks of environmental monitoring workers.

Biosynthesis of magnetosome-nanobody complex in Magnetospirillum gryphiswaldense MSR-1 and a magnetosome-nanobody-based enzyme-linked immunosorbent assay for the detection of tetrabromobisphenol A in water.

In this study, two mutant strains, TBC and TBC+, able to biosynthesize anovel functional magnetosome-nanobody (Nb), were derived from the magnetotactic bacteria Magnetospirillum gryphiswaldense MSR-1. The magnetosome-Nbs biosynthesized by TBC+ containing multi-copies of theNb gene had ahigher binding ability to an environmental pollutant, tetrabromobisphenol A (TBBPA), than those biosynthesized by TBC containing only one copy of theNb gene. The magnetosome-Nbs from TBC+ can effectively bind to TBBPA in solutions with high capacity without being affected by a broad range of NaCl and methanol concentrations as well as pH. Therefore, a magnetosome-Nb-based enzyme-linked immunosorbent assay (ELISA) was developed and optimized for the detection of TBBPA, yielding a half-maximum signal inhibition concentration of 0.23 ng/mL and a limit of detection of 0.025 ng/mL. The assay was used to detect TBBPA in spiked river water samples, giving average recoveries between 90 and 120% and coefficients of variation of2.5-6.3%. The magnetosome-Nb complex could be reused 4 times in ELISA without affecting the performance of the assay. Our results demonstrate the potential of magnetosome-Nbs produced by TBC+ as cost-effective and environment-friendly reagents for immunoassays to detect small molecules in environmental waters.

Sensitive method for simultaneous determination of TBBPA and its ten derivatives

Tetrabromobisphenol A (TBBPA) and its derivatives are regarded as new contaminants, raising much attention on their environmental occurrence and fates. However, the sensitive detection of TBBPA and its main derivatives is still a great challenge. This study investigated a sensitive method for simultaneous detection of TBBPA and its ten derivatives using high-performance liquid chromatography coupled with triple quadrupole mass spectrometry (HPLC-MS/MS) with atmospheric pressure chemical ionization (APCI) source. The method exhibited much better performance than previously reported methods. Furthermore, it was successfully applied in determining complicated environmental samples, including sewage sludge, river water and vegetable samples with concentration range from undetected (n.d.) to 25.8 ng g−1 dry weight (dw). For sewage sludge, river water and vegetable samples, the spiking recoveries of TBBPA and its derivatives ranged from 69.6 ± 7.0% to 86.1 ± 12.9%, 69.5 ± 13.9% to 87.5 ± 6.6%, and 68.2 ± 5.6% to 80.2 ± 8.3%, respectively; the accuracy ranged from 94.9 ± 4.6% to 113 ± 5%, 91.9 ± 10.9% to 112 ± 7%, and 92.1 ± 5.1% to 106 ± 6%, and the method quantitative limits ranged from 0.00801 to 0.224 ng g−1 dw, 0.0104–0.253 ng L−1, and 0.00524–0.152 ng g−1 dw, respectively. Moreover, the present manuscript describes for the first time the simultaneous detection of TBBPA and ten derivatives from various environmental samples, providing fundamental work for further research on their environmental occurrences, behaviors and fates.

Quantitative SERS Detection of TBBPA in Electronic Plastic Based on Hydrophobic Cu-Ag Chips.

Tetrabromobisphenol A (TBBPA) was one of the most widely used brominated flame retardants. However, it easily contaminates nature and harms the environment and human health during its production and use. Therefore, it is necessary to strictly control the content of TBBPA in electronics. Surface-enhanced Raman spectroscopy has the advantages of being fast and sensitive, but it is difficult to obtain the SERS spectra of TBBPA because the hydrophobic TBBPA molecule is difficult to approach with the hydrophilic surface of common noble metal SERS substrates. In the present work, a hydrophobic Cu-Ag chip was developed for the SERS detection of TBBPA. The integration of the hydrophobic interaction and the Ag-Br bonding promoted the adsorption of TBBPA on the Cu-Ag chip, allowing for SERS detection. It was observed that both the hydrophobicity and bimetallic composition of the Cu-Ag chip played important roles in the SERS detection of TBBPA. Under the optimized conditions, the low limit of detection of the established SERS method for TBBPA was 0.01 mg L−1, within a linear range of 0.1–10 mg L−1. Combined with ultrasonic-assisted extraction, the substrate could be used for the quantitative determination of TBBPA in electronic products. Compared with the HPLC-UV method used as a national standard, the relative error of the SERS method for quantifying the TBBPA content in a mouse cable and shell was ±3% and ±7.7%, respectively. According to the SERS results, the recovery of TBBPA in the spiked mouse shell was 95.6%.

A Low Cost Fe3O4-Activated Biochar Electrode Sensor by Resource Utilization of Excess Sludge for Detecting Tetrabromobisphenol A.

Owing to its ubiquity in natural water systems and the high toxicity of its accumulation in the human body, it is essential to develop simple and low-cost electrochemical sensors for the determination of 3,3′,5,5′-tetrabromobisphenol A (TBBPA). In this work, Fe3O4–activated biochar, which is based on excess sludge, was prepared and characterized using scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR) and BET analysis to analyze its basic features. Subsequently, it was used to fabricate an electrochemical sensor for the detection of TBBPA. The electrochemical test results revealed that the Fe3O4–activated biochar film exhibited a larger active surface area, a lower charge transfer resistance and a higher accumulation efficiency toward TBBPA. Consequently, the peak current of TBBPA was significantly enhanced on the surface of the Fe3O4–activated biochar. The TBBPA sensing platform developed using the Fe3O4–activated biochar composite film, with relatively a lower detection limit (3.2 nM) and a wider linear range (5–1000 nM), was successfully utilized to determine TBBPA levels in water samples. In summary, the effective application of Fe3O4–activated biochar provided eco-friendly and sustainable materials for the development of a desirable high-sensitivity sensor for TBBPA detection.

Molecularly imprinted photoelectrochemical sensor for detecting tetrabromobisphenol A in indoor dust and water.

The gradual emissions of tetrabromobisphenol A (TBBPA) from the primitive recycling of E-waste createhuman health threats, which urgently require to develop an efficient, rapid yet simple detection method. The present study conducts a highly sensitive molecularly imprinted photoelectrochemical sensor (MIPES) containingmolecularly imprinted (MI)-TiO2, Au, and reduced graphene oxide for the trace detection of TBBPA in indoor dust and surface water from an E-waste recycling area. The photocurrent response is used to evaluate the sensing performance of the MIPES toward TBBPA detection. The working potential for amperometry is 0.48V. The wavelength range for photoelectrochemical detection is 320-780nm. The sensorshows a detection range of1.68 to 100nM with a low limit of detection of 0.51nM (LOD = 3 sb/S) and a limit of quantification of 1.68nM (LOQ = 3.3 LOD). In addition, the MIPES sensor exhibits rapid, excellent reproducibility, selectivity, and long-term stability toward TBBPA detection. The relative standarddeviation of three measurements for real samples is less than 7.0%, and the recovery range is 90.0-115%. The surface of molecular imprinting contributes to the high charge separation and sensing photocurrent response of TBBPA, which is confirmed by single-particle photoluminescence spectroscopy. The present study provides a new facile sensorwith highly sensitive yet rapid responseto detect environmental pollutants in E-waste by using the MIPES.

Indirect competitive-structured electrochemical immunosensor for tetrabromobisphenol A sensing using CTAB-MnO2 nanosheet hybrid as a label for signal amplification.

Tetrabromobisphenol A (TBBPA) is a kind of brominated flame retardant that is usually added to products to reduce their flame retardancy. However, its extensive use has resulted in their residues being found in the environment, which is very harmful. Herein, an indirect competitive immunosensor has been established for TBBPA detection based on the signal amplification system. Pd nanospheres in situ reduced on the surface of MnO2 nanosheet hybrid (MnO2/Pd) was used as the label for the secondary antibody through the Pd-N bond, and gold-toluidine blue composite was loaded onto MWCNTs (MWCNTs/Au-TB), which functioned as the platform for the immunosensor. The spherical structure of Pd had abundant catalytic active sites, which enhanced the catalytic activity of MnO2/Pd as the label, hence amplifying the signal response. Besides, MWCNTs/Au-TB improved electron transfer and produced a strong signaling pathway for immobilizing antigens through the Au-NH2 bond, which can specifically recognize primary antibodies to improve sensitivity. The immunosensor had a linear concentration range of 0-81ng/mL, a low detection limit of 0.17ng/mL (S/N = 3), with good stability, selectivity, and reproducibility based on the above advantages. Additionally, the acceptable accuracy and recoveries (recoveries, 92-124%; CV, 3.3-8.8%) in the real water sample analysis indicated that this strategy is promising for emerging pollutant analysis.

Ammoniated MOF-74(Zn) derivatives as luminescent sensor for highly selective detection of tetrabromobisphenol A

In this study, a porous framework MOF-74(Zn) (Zn2 (DHBDC)(DMF)(H2O)2, H4dondc = 1, 5-dioxido-2, 6-naphthalenedicarboxylic acid) with open metal sites was successful synthesized. MOF-74(Zn) as a template was grafted on the open metal sites with ethylenediamine (en) named MOF-74(Zn)-en to develop a highly selective and sensitive fluorescence detector for rapid determination of tetrabromobisphenol A (TBBPA). The obtained MOF-74(Zn)-en was well characterized by Fourier Transform Infrared (FT-IR), Scanning Electron Microscopy (SEM) and showed ideal properties of photoluminescence. The fluorescence enhancement showed a good linear relationship with the concentrations of TBBPA in the range of 50–400 μg/L, and its limit of detection could reach to 0.75 μg/L. Furthermore, the possible sensing mechanism of the fluorescence enhancement could be attributed to Förster resonance energy transfer (FRET). The results will provide a convenient and quick method for detection of TBBPA. To the best of my knowledge, this is the first case to detect TBBPA by fluorescence enhancement with MOF derivatives.

Expanded graphite decorated with PdO@C nanoparticles for individual and simultaneous sensing of multiple phenols

Sensitive, selective, and reproducible monitoring of multiple phenols simultaneously needs an electrochemical interface with a large surface area and a big amount of active sites. Herein, expanded graphite (EG) as the supporter is decorated with the sensing material of carbon-coated palladium oxide (PdO@C) nanoparticles. After its characterization using transmission electron microscopy, X-ray photoelectron spectroscopy, and electrochemical techniques, this composite based electrochemical interface has been utilized for the voltammetric sensing of tetrabromobisphenol A (TBBPA), hydroquinone (HQ), and catechol (CC). Compared with either EG or PdO@C based interfaces, this one delivers much enhanced redox currents for three phenols. Individual and simultaneous detection of TBBPA, HQ, and CC has been realized at nano-molar levels. The calculated detection limits are 1.3, 26, and 17 nM for TBBPA, HQ, and CC, respectively. Such an interface thus owns great prospect in constructing a universal platform for individual and simultaneous detection of multiple phenols in different samples.

An Ultrasensitive Real-time Immuno-polymerase Chain Reaction Assay for Detection of Tetrabromobisphenol A in PM2.5 Particles Using Functionalized Nanoprobes

Abstract Tetrabromobisphenol A (TBBPA), a type of brominated flame retardant, is widely distributed in the environment. In this work, different TBBPA antigens and polyclonal anti-TBBPA antibody (pAb-TBBPA) were prepared, and on the basis of this, an ultrasensitive real-time immuno-polymerase chain reaction for TBBPA detection using functionalized nanoprobes (FNPs-IPCR) was developed. Gold nanoparticles modified with thiol-capped DNA and pAb-TBBPA were prepared as antibody-DNA conjugates, and the signal intensity of the immunoassay was greatly enhanced. Under optimal conditions, the proposed immunoassay was used to detect TBBPA with a linearity ranging from 1 pg L−1 to 10 ng L−1, and the limit of detection was 0.62 pg L−1. The recovery was 89.2%–107.4% and the coefficient of variation was 3.17%–7.73%. The FNPs-IPCR assay was highly selective and sensitive. Finally, the detection results of TBBPA in PM2.5 samples were consistent with those from high performance liquid chromatography, indicating that the FNPs- IPCR method is suitable for trace TBBPA screening in environmental samples.

Electrochemical sensor based on electropolymerized dopamine molecularly imprinted film for tetrabromobisphenol A

This work reported the simple and direct detection of 3,3′,5,5′‑tetrabromobisphenol A (TBBPA) by a polydopamine imprinted electrochemical sensor. The imprinted film was directly prepared by electropolymerization of dopamine on a glassy carbon electrode in the presence of template molecule, and then characterized using electrochemical probe of potassium ferricyanide, scanning electron microscopy and atomic force microscopy. It was found that the obtained sensing film greatly enhanced the oxidation signals of TBBPA due to strong accumulation ability. The influences of electropolymerization conditions (e.g. template concentration, scan cycles and scan rates), accumulation time and pH value were studied. The developed sensing platform exhibited good reproducibility, excellent sensitivity and selectivity, offering a low detection limit (0.27 nM) and a linear range from 1 to 50 nM. It was applied for TBBPA detection in plastic e-waste samples, and the results were consistent with those obtained by high-performance liquid chromatography.

Reusable Boron-Doped Diamond Electrodes for the Semi-Continuous Detection of Tetrabromobisphenol A

It is of great importance to measure tetrabromobisphenol A (TBBPA) owing to its high toxicity and wide existence in the environment. In this paper, an electrochemical sensor based on boron-doped diamond (BDD) thin film was developed for the detection of TBBPA. The diamond thin film was deposited on Si substrate via filament-assisted chemical vapor deposition. Due to the great electrochemical properties, the BDD electrode could be reactivated after a pretreatment process after each measurement, which realized a continuous detection of TBBPA and solved the problem of renewal. The electrochemical pretreatment procedure was studied in order to achieve better performance. The peak current of the BDD electrode displayed a good linearity toward TBBPA concentrations ranging from 50 nM to $10~\mu \text{M}$ , and the detection limit was 27 nM (S/N = 3).

Legacy and novel brominated flame retardants in indoor dust from Beijing, China: Occurrence, human exposure assessment and evidence for PBDEs replacement

Levels of legacy brominated flame retardants (BFRs), including tetrabromobisphenol A (TBBPA), hexabromocyclododecane isomers (HBCDs) and polybrominated diphenyl ethers (PBDEs), and six currently used novel BFRs were determined in house dust and office dust collected from a community in Beijing, China. This is the first study where the three kinds of legacy BFRs and novel BFRs were all measured in dust samples from China. HPLC-MS/MS was used for the detection of TBBPA and HBCDs, and the other BFRs were tested on a GC-NCI/MS. Decabromodiphenyl ethane (DBDPE), PBDEs, HBCD and TBBPA were found to be the main BFRs in the dust samples, with median levels of 709, 241, 199 and 26.7ng/g dust, respectively. Due to the high density of electronic equipment used in offices, levels of BFRs in office dust were found to be higher than those in house dust. DBDPE, as a replacement of PBDEs, was the predominant BFR, and the median level of DBDPE was not only several orders of magnitude higher than that of other novel BFRs but also 3 to 27 times higher than that of the three legacy BFRs, indicating that the consumption pattern of BFRs in the Chinese market has shifted from PBDEs to PBDE alternatives. Median estimated daily intakes (EDIs) of BFRs through dust ingestion for adults (>20years) and toddlers (<2years) were in the range of 2.8×10−5–0.201ng/kg body weight (bw)/day and 5.7×10−4–2.52ng/kg bw/day, respectively. The body burden of BFRs for toddlers was far higher than that for adults; however, a comparison between EDIs and threshold values suggested that daily intakes of BFRs for both adults and toddlers were unlikely to raise significant health concerns.

Synergetic signal amplification of multi-walled carbon nanotubes-Fe3O4 hybrid and trimethyloctadecylammonium bromide as a highly sensitive detection platform for tetrabromobisphenol A.

In this work, we fabricated an electrochemical sensor based on trimethyloctadecylammonium bromide and multi-walled carbon nanotubes-Fe3O4 hybrid (TOAB/MWCNTs-Fe3O4) for sensitive detection of tetrabromobisphenol A (TBBPA). The nanocomposite was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy (FT-IR) techniques. The electrochemical behaviors of TBBPA on TOAB/MWCNTs-Fe3O4 composite film modified glassy carbon electrode (GCE) were investigated by cyclic voltammetry (CV), differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS) method. The experimental results indicated that the incorporation of MWCNTs-Fe3O4 with TOAB greatly enhanced the electrochemical response of TBBPA. This fabricated sensor displayed excellent analytical performance for TBBPA detection over a range from 3.0 nM to 1000.0 nM with a detection limit of 0.73 nM (S/N = 3). Moreover, the proposed electrochemical sensor exhibited good reproducibility and stability, and could be successfully applied to detect TBBPA in water samples with satisfactory results.

Development of an immunochromatographic test strip and ic-ELISA for tetrabromobisphenol: a detection in lake water and rice pudding samples

ABSTRACTA sensitive and selective indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) and an immunochromatographic test strip were developed for the detection of tetrabromobisphenol A (TBBPA), an important brominated flame retardant. A monoclonal antibody (mAb) against TBBPA was produced and the half inhibition concentration (IC50) was 0.44 ng/ml, with the linear range 0.15–1.32 ng/ml. TBBPA recovery by ic-ELISA was 70.7–108.8% from rice pudding samples and 110.2–119.8% from lake water samples. A sensitive and rapid immunochromatographic test strip was developed using this specific mAb, with a good cut-off value of 25 and 50 ng/ml in lake water and rice pudding samples, respectively. The results of this study revealed that the ic-ELISA and immunochromatographic test strip represent useful methods of TBBPA detection in lake water and rice pudding samples.

Direct detection of brominated flame retardants from plastic e-waste using liquid extraction surface analysis mass spectrometry.

The worldwide generation of plastic electronic waste (e-waste) is reaching epic proportions. The presence of toxic brominated flame retardants (BFRs) within these materials limits their ability to be recycled, resulting in large amounts of e-waste reaching landfills. Liquid extraction surface analysis mass spectrometry (LESA-MS) employing a chip-based nanoelectrospray coupled to a triple quadrupole mass spectrometer represents a novel control technology for directing e-waste streams for recycling. LESA-MS allows direct sampling and analysis of solid material, capable of detecting BFRs including polybrominated diphenyl ethers (PBDEs) and tetrabromobisphenol A (TBBP-A), the two most common flame retardant additives currently in circulation. Authentic PBDE congeners and TBBP-A were deposited on glass and characterised by LESA-MS analysis. PBDEs are notoriously difficult to detect via electrospray; however, they were detected with ease by utilising a combination of nanoelectrospray and solvent doped with ammonium acetate. In situ detection of TBBP-A within plastic e-waste was also possible by performing LESA-MS on the surface of granulated material provided by a commercial waste depot. E-waste sample analysis was completely automated, with each sample analysed in less than 1 min. LESA-MS is fast, simple, and robust allowing unambiguous detection of a range of additives through tandem mass spectrometry. LESA-MS does not require dissolution of the solid matrix nor the sample to be present under vacuum and the use of separative techniques prior to analysis is not necessary.

Molecularly imprinted electrochemical sensor based on a reduced graphene modified carbon electrode for tetrabromobisphenol A detection

A simple strategy for the indirect detection of 3,3',5,5'-tetrabromobisphenol A (TBBPA) was developed with a surface imprinted sensor based on an electrochemical reduced graphene modified carbon electrode. The preparation procedure of imprinted electrode and the response mechanism of the imprinted electrode toward TBBPA are discussed in detail. The electrochemical characteristics of the imprinted sensor were investigated using cyclic voltammetry and their morphologies were characterized using scanning electron microscopy. The indirect detection for TBBPA was successfully implemented by monitoring the peak current of Fe(CN)6(3-/4-)-TBBPA complex. The response currents of the imprinted sensor exhibited a linear relationship toward the TBBPA concentration range from 0.5 to 4.5 nM with a detection limit of 0.23 nM (S/N = 3). The fabricated electrochemical imprinted sensor was successfully applied to the detection of TBBPA in rain and lake water samples using the standard addition method. With the advantages of high sensitivity and simple operation, the determination methodology is a promising candidate for TBBPA detection in real water samples.

A rapid method to determine tetrabromobisphenol a in rat serum and urine by liquid chromatography-tandem mass spectrometry

Tetrabromobisphenol A (TBBPA), one of the most widely used brominated flame retardants in the world, is used to improve fire safety of laminates in electrical and electronic equipment. A liquid chromatography-tandem mass spectrometry was developed for the determination of TBBPA in rat serum and urine, and applied to the toxicokinetic study of TBBPA in rats. Acceptable linearity was observed over the concentration ranges of 0.25-50 and 0.01-5 μg/mL in serum and urine, respectively. The limits of detection of TBBPA were 0.04 μg/mL in serum, and 0.0025 μg/mL in urine. The precisions for the assay in serum and urine were below 13 and 14%, respectively, and the accuracies ranged 95-111% and 98-101% for intraday and 97-107% and 97-102% for inter-day, respectively. Serum and urine concentrations of TBBPA were successfully monitored following oral administrations at the dose of 200 mg/kg in male Sprague Dawley rats. Toxic signs were not observed at 200 mg/kg of TBBPA. The present results suggest that the rapid method developed in the present study affords sensitivity, accuracy and precision necessary for quantitative measurements in toxicokinetic studies of TBBPA in vivo.