Negatively charged carboxymethylated polyethersulfone (CMPES) and positively charged quaternized polyethersulfone (QAPES) ultrafiltration (UF) membranes were prepared by bulk chemical modification and non-solvent induced phase separation method. The effects of PES membrane interfacial electrokinetic property on the bovine serum albumin (BSA) membrane fouling behavior were studied with the aid of the membrane-modified colloidal atomic force microscopy (AFM) probe. Electrokinetic test results indicated that the streaming potential (ΔE) of QAPES membrane was not consistent with its expected IEC value, however, within the pH range of 3–10, the ζ potentials of two charged-modified PES membranes were more stable than the unmodified membrane. When pH value was 3, 4.7 or 9, the interaction behavior between charged PES membrane and BSA showed that there was significant linear correlation between the jump distance r0 of membrane-BSA adhesion force (F/R) and the ζ potential absolute value. Charged modification significantly reduced the adhesion of PES membrane-BSA, and the adhesion data was good linear correlated with the flux decline rate in BSA filtration process, especially reflected in the CMPES membrane. The above experimental facts proved that the charged membrane interfacial electric double layer structure and its electrokinetic property had strong ties with the protein membrane fouling behavior.
Humans are exposed to both lead (Pb) and methylmercury (MeHg), two chemicals known to affect the developing nervous system. It is therefore important to know whether these chemicals interact toxicologically to develop reliable estimates of human health risks. The nature of the potential interaction and how it may change with dose are also critical factors which need to be understood and considered in risk assessment. The available toxicological literature was reviewed and yielded five animal studies which involved combined exposure to both metals. None of these studies examined developmental neurotoxicity, the key endpoint of interest. Doses in these studies were also in the range of 1–100?mg?kg?1?day?1, which is far above average exposure levels for Pb and MeHg in the U.S. population. The combined exposure literature is therefore uninformative concerning the potential for Pb–MeHg interaction. A subsequent evaluation of the available mechanistic data was conducted, looking for similarities in proposed modes of action relevant at low doses. Shared biological targets suggesting a potential for low dose interaction include protein kinase C, calcium homeostasis, and apoptosis. Whether interaction actually occurs, and the form the interaction might take, remains to be studied. A phased research program is proposed that may provide data needed to address this significant data gap and permit more robust Pb and MeHg risk assessment. 相似文献
In this communication we present data on S-phenylcysteine (SPC) in human serum albumin in an Estonian cohort. A total of 112 human samples were collected from workers of a benzene processing plant in Kohtla-Järve, Estonia and another 56 samples from nearby countryside residents. Albumin was isolated using a sequential precipitation method designed for low volume plasma samples. The adducted cysteine derivatives were cleaved off from the albumin and subsequently derivatized to phenyl trifluorothioacetate (PTTA) derivatives. Derivatized adducts were subjected to GC/MS analysis utilizing negative chemical ionization and a selected ion monitoring (SIM) technique. The detection limit for the PTTA adduct was 0.2?pmol?g?1 albumin and the limit of quantification was 2?pmol?g?1 albumin. The method utilized deuterated SPC as an internal standard. The analysis revealed that adduct levels were also high in the population that was not occupationally exposed to benzene. The reason for this is unknown, but may cause problems if not of environmental origin, when one is attempting to monitor low level occupational or environmental benzene exposure. 相似文献
The complex capacity of different types of organic matters （OMs） for Cu was quantitatively studied by simulation experiments using different adsorbents prepared from the sediment in Taihu Lake. The free Cu was measured with ion selective electrode （ISE） and complex capacity was calculated using a conditional formation constant model. The result indicated that the complex capacity was 0.048 mmol·g-1, 0.009 and 0.005 mmol.g-1for raw sediment, sediment without DOM, sediment without insoluble organic matters but with DOM and sediment without OM. Insoluble organic matter played a major role in the sorption of Cu in sediment and it can adsorb most Cu from water column. In the solution, Cu mainly existed as a complex with DOM and the DOM-Cu complexation capacity was 327.87 mg. g-1. The change of TOC and pH indicated ion-exchange in the interaction between free Cu and DOM. When the Cu concentration in the experiment reached the complex capacity of DOM, precipitation was the major mechanism to remove Cu from water phase, which was observed from UV absorbance change of DOM, that is, its aromaticity increased while molecular weight decreased. The desorption result indi- cated that DOM was more capable of desorbing Cu from adsorbents without OM than adsorbent with OM. The desorbed quantity with DOM was 1.65, 1.78 and 2.25 times higher than that with water for adsorbents without OM, raw adsorbents （sediment） and adsorbents without DOM. 相似文献
The dynamics of accumulation and loss of different physico-chemical forms of 106Ru were measured in the euphausiid Meganyctiphanes norvegica. The accumulation of 106Ru was directly related to the concentration of the radioisotope in solution, as evidenced by similar concentration factors for euphausiids in the low and high activity 106Ru chloride solutions. The chemical form of the radioisotope in solution had a pronounced effect on the uptake, with 106Ru chloride fractions being accumulated at a faster rate than 106Ru nitrosyl-nitrato complexes. Euphausiids lost 106Ru, previously accumulated from the 106Ru chloride complexes, at a faster rate than 106Ru which had been accumulated from 106Ru nitrosyl-nitrato forms. Also, in the case of the 106Ru chloride complexes, the loss rate was inversely proportional to the time allowed for isotope accumulation. The process of molting greatly accelerated the loss of 106Ru from euphausiids, with first molts shed during the loss phase accounting for 70 to 80% of the total 106Ru body burden. When euphausiids accumulated 106Ru from the food chain, the initial-loss rate was rapid due to large amounts of the radioisotope associated with fecal pellets; however, no relationship was found between loss rate and the number of food rations received. Molts from these individuals did not contain 106Ru, thus, loss from euphausiids obtaining this radioisotope through the food chain is mainly due to fecal pellet deposition and other excretion or exchange processes. 相似文献
