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Md. Abdul Halim Ratan K. Majumder Syeda Afsarun Nessa Keita Oda Yoshinario Hiroshiro Kenji Jinno 《Environmental monitoring and assessment》2010,161(1-4):453-472
Probable sources and mechanisms of arsenic (As) release in shallow aquifer in eastern Bangladesh are evaluated using statistical analysis of groundwater compositions. Dissolved As in 39 samples ranged from 8.05 to 341.5 μg/L with an average of 95.14 μg/L. Ninety seven percent of wells exceed the WHO limit (10 μg/L) for safe drinking water. Principal component analysis is applied to reduce 16 measured compositional variables to five significant components (principal components—PCs) that explain 86.63% of the geochemical variance. Two component loadings, namely PC 1 and PC 2 (45.31% and 23.05%) indicate the natural processes within the aquifers in which organic matter is a key reactant in the weathering reactions. Four groups of wells are defined by the PCA and each group of wells represents distinct physicochemical characteristics. Among them, group III groundwater shows higher As concentration together with high concentrations of Fe, Mn, dissolved organic carbon, $\text{PO}_{4}^{3-}$ and $\text{HCO}_{3}^{-}$ than groups I and II. Speciation calculations suggest that only wells of group III are saturated with respect to siderite, and all groups of samples are supersaturated with respect of rhodochrosite. The relationship of As with these parameters in the different groups of wells of the study area suggests that reductive dissolution of Fe–Mn oxyhydroxides with microbially mediated degradation of organic matter is considered to be the dominant processes to release As in groundwater. 相似文献
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SAITOYoshihiro JINNOKiyokatsu 《环境化学》2003,22(3):241-245
1 IntroductionGaschromatography(GC)isoneofthemostpopularseparationmethodsfortheanalysisofvolatilecompounds,andawidevarietyofpolymericmaterialsasthestationaryphases,havebeendeveloped .Incontrasttothesuccessfulapplicationsandsubsequentcommercializationofth… 相似文献
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Hanioka N Takahara Y Takahara Y Tanaka-Kagawa T Jinno H Narimatsu S 《Chemosphere》2012,89(9):1112-1117
Diester phthalates are industrial chemicals used primarily as plasticizers to import flexibility to polyvinylchloride plastics. In this study, we examined the hydrolysis of di-n-butyl phthalate (DBP), butylbenzyl phthalate (BBzP) and di(2-ethylhexyl) phthalate (DEHP) in human liver microsomes. These diester phthalates were hydrolyzed to monoester phthalates (mono-n-butyl phthalate (MBP) from DBP, mono-n-butyl phthalate (MBP) and monobenzyl phthalate (MBzP) from BBzP, and mono(2-ethylhexyl) phthalate (MEHP)) by human liver microsomes. DBP, BBzP and DEHP hydrolysis showed sigmoidal kinetics in V-[S] plots, and the Hill coefficient (n) ranged 1.37-1.96. The S50, Vmax and CLmax values for DBP hydrolysis to MBP were 99.7 μM, 17.2 nmol min−1 mg−1 protein and 85.6 μL min−1 mg−1 protein, respectively. In BBzP hydrolysis, the values of S50 (71.7 μM), Vmax (13.0 nmol min−1 mg−1 protein) and CLmax (91.3 μL min−1 mg−1 protein) for MBzP formation were comparable to those of DBP hydrolysis. Although the S50 value for MBP formation was comparable to that of MBzP formation, the Vmax and CLmax values were markedly lower (<3%) than those for MBzP formation. The S50, Vmax and CLmax values for DEHP hydrolysis were 8.40 μM, 0.43 nmol min−1 mg−1 protein and 27.5 μL min−1 mg−1 protein, respectively. The S50 value was about 10% of DBP and BBzP hydrolysis, and the Vmax value was also markedly lower (<3%) than those for DBP hydrolysis and MBzP formation for BBzP hydrolysis. The ranking order of CLmax values for monoester phthalate formation in DBP, BBzP and DEHP hydrolysis was BBzP to MBzP ? DBP to MBP > DEHP to MEHP > BBzP to MBP. These findings suggest that the hydrolysis activities of diester phthalates by human liver microsomes depend on the chemical structure, and that the metabolism profile may relate to diester phthalate toxicities, such as hormone disruption and reproductive effects. 相似文献
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The effect of bisphenol A (BPA) on the kinetics of cytochrome P450 (P450)-dependent monooxygenases in rat liver microsomes was studied. Testosterone 16beta-hydroxylase (TS16BH) and testosterone 2alpha-hydroxylase (TS2AH) activities were extensively inhibited by BPA at 100 microM (69% and 74%, respectively). The inhibition type was mixed for both P450-dependent monooxyganases. The Ki of TS16BH and TS2AH from Lineweaver-Burk plots were 25.9 and 24.9 microM, respectively. The activities of acetanilide 4-hydroxylase (AA4H), 7-ethoxycoumarin O-deethylase (ECOD), bufuralol 1'-hydroxylase (BF1'H), chlorzoxazone 6-hydroxylase (CZ6H) and testosterone 6beta-hydroxylase (TS6BH) were also effectively inhibited by BPA at 100 microM (43-52%). The inhibition type of these P450-dependent monooxygenases was mixed or uncompetitive, and the K(i)s (50.5-88.5 microM) were higher than those of TS16BH and TS2AH. By contrast, the values of IC50 and Ki of testosterone 7alpha-hydroxylase (TS7AH) and lauric acid omega-hydroxylase (LAOH) for BPA were >1000 microM. These results suggest that BPA interacts with rat hepatic CYP1A2, CYP2A2, CYP2B2, CYP2C11, CYP2D1, CYP2E1 and CYP3A2 in vitro. 相似文献
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