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OBJECTIVE: To establish a method for simultaneous detection of 16 kinds of gas and particle-phase polycyclic aromatic hydrocarbons(PAHs) in workplace air by high performance liquid chromatography with ultraviolet and fluorescence detector(HPLC-UV-FLD).METHODS: PAHs in workplace air were collected by polytetrafluoroethlene filter with XAD-2 tube. The samples were added with 5 mL of acetonitrile. The samples were extracted by ultrasound and eluted with acetonitrile-water gradient. Ultraviolet with tandem fluorescence detector was used for determination.RESULTS: Eleven kinds of PAHs showed a good linear range of 1.0-400.0 μg/L. Five kinds of PAHs showed a good linear range of 10.0-2 000.0 μg/L and the linear correlation coefficient was greater than 0.999 0. The minimum detection concentration was 0.000 01-0.000 67 mg/m~3 (75 L air sample). The average elution efficiency of filter on granular PAHs except for naphthalene and acenaphthene ranged from 71.0% to 99.0%. The average desorption efficiencies of adsorbent tube was 43.0%-90.0%. The within-run relative standard deviations(RSD) was 0.3%-8.3%, and the between-run RSD was 0.0%-9.2%.CONCLUSION: This method is simple, sensitive, has good linear range and precise. It is suitable for simultaneous detection of PAHs in workplace air.
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OBJECTIVE: To establish a method for detection of 2-methylpropanal,2-methyl butanal and 3-methyl butanal in workplace air by portable gas chromatography-mass spectrometry( GC-MS). METHODS: The workplace air was collected by portable GC-MS sampling probe. After enrichment by Tri-bed tube,the thermal desorption sample was analyzed by retention time and characteristic ion characterization. The characteristic ion peak area was quantified. RESULTS: The linear ranges of 2-methylpropanal,2-methyl butanal and 3-methyl butanal were 0. 079-15. 880,0. 080-16. 080 and 0. 161-32. 120 mg/m~3,respectively. All the correlation coefficients were greater than 0. 999. The detection limits were 0. 012,0. 007 and0. 013 mg/m~3,and the quantitation limits were 0. 041,0. 023 and 0. 044 mg/m~3,respectively. The recovery rates of2-methylpropanal,2-methyl butanal and 3-methyl butanal were 92. 2%-104. 4%. The within-run relative standard deviation( RSD) was 5. 8%-9. 1%. The between-run RSD of different batches samples was 9. 3%-19. 6%. CONCLUSION: This method has high accuracy and is precise,which is suitable for rapid qualitative and quantitative detection of2-methylpropanal,2-methyl butanal and 3-methyl butanal in workplace air.
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OBJECTIVE: To explore the interference correction reduction method for the determination of cadmium(Cd), chromium(Cr), manganese(Mn), nickel(Ni) and lead(Pb) concentration in workplace air by inductively coupled plasma-atomic emission spectrometry(ICP-AES). METHODS: The interference sources in the determination of metals in workplace air with ICP-AES was analyzed. The results before and after the background correction or the internal standard calibration were compared. Linear regression is performed on the interference element mass concentration by interference error to obtain a table of interference factors. The measurement results of actual samples were corrected using background subtraction, internal standard correction, and interference factor method. RESULTS: The relative deviation of results and theoretical values without background subtraction were 219.5% and 131.5% for Cd and Pb, respectively. The relative deviation between the measured values and theoretical values was less than 10.0% after background subtraction. When the total metal ion concentration was >800.00 mg/L, the relative deviation between measured result and the theoretical values was-21.0%--11.0% without internal standard correction, and the absolute value of them were less than 10.0% after internal standard correction. The interference correction method was used to correct the concentration of Cd, Cr, Mn, Ni, Pb in welding smoke. The mass concentrations of Cd before and after interference correction were 3.90-32.50 and 1.20-7.10 μg/L, respectively. The mass concentrations of nickel before and after interference correction were 111.00-1 220.00 and 99.00-1 120.00 μg/L, respectively. The mass concentration of Cr,Mn and Pb remained unchanged before and after the interference correction. CONCLUSION: The background correction, internal standard correction and interference factor table can eliminate the interference for determination of metals in workplace air by ICP-AES and ensure the accuracy of results.
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This study was conducted to establish an in vitro 3D liver model and apply it to the drug liver toxicity evaluation. The 3D multicellular sphere model of HepaRG cells was established by hanging-drop technique for evaluation of liver function. The 3D liver model was used to test the hepatotoxicity of isoniazid and amiodarone hydrochloride compared to the 2D cell culture model. Our results showed that HepaRG cells formed a compact spheriod, and the level of cell albumin, urea and the CYP3A4 activity were significantly higher than that of 2D model. With the treatment of amiodarone hydrochloride in 2D and 3D model, the IC50 were 50 and 100 μmol·L-1, respectively. When the dose was less than 1 000 μmol·L-1, isoniazid had no hepatocyte toxicity in 2D model, while the IC50 in 3D model was 700 μmol·L-1. The LDH activities of both drugs in 3D model showed time-and dose-dependent correlation. The results suggest that this in vitro 3D hanging-drop liver model is good for testing liver functions with a high hepatic drug-metabolizing enzyme activity. Compared with the 2D model, the 3D liver model can accurately evaluate the liver toxicity of drugs. Our results demonstrated the importance of in vitro cell culture models for detection of in vivo-relevant adverse effects of drugs.
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OBJECTIVE: To establish a MDCK/L02 co-culture model and investigate the effect of intestinal absorption on triptolide (TP) induced liver toxicity. METHODS: Transwell was used to establish the MDCK/L02 model. The paracellular permeability was measured using fluorescein sodium (FS). The effect of TP on the paracellular pathway was also studied. The cytotoxicity of TP on MDCK was investigated by CCK-8. TP induced reactive oxygen species (ROS) in L02 cells was studied using high content analysis (HCA). RESULTS: The MDCK/L02 co-culture model was established with Papp of FS (4.10 ±0.36) × 10-8 cm · -1. After 1, 2 and 4 h treatment of TP, the IC50 on MDCK were 14, 8 and 7 μg · mL-1, respectively. After 1 h treatment of TP using the MDCK/L02 model, the paracellular permeability of MDCK was significantly increased. After intestinal absorption, TP toxicity on L02 was significantly decreased measured by ROS induction using HCA. CONCLUSION: The MDCK/L02 co-culture model is established. TP significantly increases the MDCK permeability. After intestinal absorption (across the MDCK), TP induced liver toxicity is significantly decreased.
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Metabolomics, a branch of systems biology, has gained extensive attention and profound achievements in the plant. Although plant metabolomics is to be explored, it has been one of the most effective methods to study the physiological and biochemical process and gene modification in pattern plants. We herein summarized the concept, development, and application of metabolomics and prospected the potentials in the metabolite profiling for plant. Metabolomics provides an omics' methodology to elucidate the whole biological process, identify and quantify the complex components in the plant. A number of metabolites present in the plant are active components of traditional Chinese medicine, and these bioactive components are influenced by the multi-factors such as environment, species, and processing methods etc. Therefore, it is of great importance to analyze a wide spectrum of compositions with diverse chemical characteristics and varied concentration, which is the foundation to quality control, allowing the elucidation of the pharmacological effectiveness, and further exploiting of traditional Chinese medicine.