女性护理液抗炎止痒作用的实验研究

女性护理液为中药苦参醇提液加三氯羟基二苯醚复配而成，根据药理方法学以实验动物建立模型，观察护理液的抗炎、止痒作用。结果，单独使用三氯羟基二苯醚，有较好的抗菌消炎作用，但是止痒作用不明显。以苦参醇提液和三氯羟基二苯醚复配，其抗炎、止痒作用均接近地塞米松磷酸钠注射液。     

Enhanced transformation of triclosan by laccase in the presence of redox mediators

Triclosan (TCS), an antimicrobial agent, is an emerging and persistent environmental pollutant that is often found as a contaminant in surface waters and sediments; hence, knowledge of its degradability is important. In this study we investigated laccase-mediated TCS transformation and detoxification, using laccase (from the fungus Ganoderma lucidum) in the presence and absence of redox mediators. Transformation products were identified using HPLC, ESI-MS and GC-MS, and transformation mechanisms were proposed. In the absence of redox mediator, 56.5% TCS removal was observed within 24 h, concomitant with formation of new products with molecular weights greater than that of TCS. These products were dimers and trimers of TCS, as confirmed by ESI-MS analysis. Among the various mediators tested, 1-hydroxybenzotriazole (HBT) and syringaldehyde (SYD) significantly enhanced TCS transformation (∼90%). The presence of these mediators resulted in products with lower molecular weights than TCS, including 2,4-dichlorophenol (2,4-DCP; confirmed by GC-MS) and dechlorinated forms of 2,4-DCP. When SYD was used as the mediator, dechlorination resulted in 2-chlorohydroquinone (2-CHQ). Bacterial growth inhibition studies revealed that laccase-mediated transformation of TCS effectively decreased its toxicity, with ultimate conversion to less toxic or nontoxic products. Our results confirmed the involvement of two mechanisms of laccase-catalyzed TCS removal: (i) oligomerization in the absence of redox mediators, and (ii) ether bond cleavage followed by dechlorination in the presence of redox mediators. These results suggest that laccase in combination with natural redox mediator systems may be a useful strategy for the detoxification and elimination of TCS from aqueous systems.     

Development of an in-house method for the incorporation of model migrants in polyethylene films and determination of diffusion constants in food

Two methods were tested and compared for the additivation of low density polyethylene (LDPE). The aim was to obtain highly contaminated plastic films to enable the study of migration (diffusion and partition phenomena). One of the methods involved immersion of low density polyethylene (LDPE) films in a concentrated solution of the selected substances. The other method involved achieving close contact of plastic films with a polyethylene wax contaminated with the selected compounds. The PE-wax method provided better results as regards the final concentration and homogeneity of the contaminants in the plastic films (deviations between replicates for each plastic film was lower than 10% for both migrants tested). This method was therefore considered suitable for preparing a homogeneous additive release system. Finally, to test the applicability of the method, concentration profiles were studied in chocolate spread placed in contact with the contaminated films, and diffusion coefficients were estimated in this foodstuff. Estimated diffusion coefficients were 4.6 × 10⁻⁰⁷ cm²/s for DPBD and 3.2 × 10⁻⁰⁷ cm²/s for triclosan in the same conditions.     

Resistance and recovery of river biofilms receiving short pulses of Triclosan and Diuron

The effects of the herbicide Diuron (DIU) and the bactericide Triclosan (TCS) were assessed on laboratory-grown stream biofilms. Four week-old biofilms were exposed in mesocosms to 48-hours of short pulses of either DIU or TCS. The direct and indirect effects of each toxicant on the biofilms, and the subsequent recovery of the biofilms, were evaluated according to structural and functional biomarkers. These parameters were analyzed immediately before exposure, immediately after exposure, and 9 and 16 days post-exposure. DIU caused an increase in diatom mortality (+ 79%), which persisted until the end of the experiment. TCS also affected diatom mortality (+ 41%), although the effect did not appear until 1 week post-exposure. TCS caused an increase in bacterial mortality (+ 45%); however, this parameter returned to normal values 1 week post-exposure. TCS compromised the cellular integrity of the green alga Spirogyra sp., whereas DIU did not. TCS also strongly inhibited phosphate uptake (− 71%), which did not return to normal values until 2 weeks post-exposure. DIU directly affected algae, but barely affected the heterotrophs, whereas TCS seriously impaired bacteria (direct effect) as well as autotrophs (indirect effect). However, the biofilms recovered their normal structure and function within only a few days to a few weeks. These findings demonstrate the capacity of biofilms to cope with periodic inputs of toxicants, but also the risks associated to repeated exposure or multi-contamination in aquatic ecosystems.     

Activated soil filters (bio filters) for the elimination of xenobiotics (micro-pollutants) from storm- and waste waters

A technical scale (0.12 m³) activated soil filter (bio filter) has been used to eliminate diverse xenobiotics (organic micro-pollutants) such as organophosphate flame retardants, and -plasticisers, musk fragrances, DEHP, benzothiazoles and triclosan from water. Model experiments to treat combined sewer overflow, storm water and a post treatment of waste water were performed in controlled laboratory experiments. The indicator compounds were typical for waste water. Diverse chemical compound groups and a wide spectrum from the lipophilic (pK_ow = 5.9) to the hydrophilic (pK_ow = 2.6) were included. The system consisted of a layer with high organic content (with vegetation to prevent clogging), a sand filter and a gravel drainage layer. The organic layer was spiked with activated sludge to enhance biomass and biodegradation potential. Usually the elimination rates varied from 64% to 99%, with only one compound reaching as little as 17%. For a technical suitability assessment it was calculated how long these filters would be stable in eliminating organic compounds from water. The estimated operating times for such systems was found to be about 100 years for a stack height of 2 m a year in regard to most compounds in this study.     

Bactericidal Low Density Polyethylene (LDPE) urinary catheters: Microbiological characterization and effectiveness

This study investigated the antimicrobial efficacy of Low Density Polyethylene (LDPE) catheters containing triclosan at 0.10 wt.%, 0.50 wt.%, 1.00 wt.% and 1.50 wt.%. The catheters were characterized with the Minimum Inhibitory Concentration (MIC) and Agar Diffusion Tests. They were evaluated in terms of incrustation, biofilm formation and the efficiency of inhibition of bacterial growth after thirty days of lab tests with artificial urine. This research demonstrated the effectiveness of triclosan for inhibiting the growth of microorganisms when incorporated into long-term catheters. The antimicrobial efficiency and genotoxicity results demonstrate that 0.5 wt.% triclosan is the optimal concentration. The genotoxicity test results indicate that triclosan did not result in any significant alterations in the cellular DNA compared to the catheter without triclosan.     

Synthesis and characterization of novel antimicrobial polymers containing pendent triclosan moieties

Novel antimicrobial copolymers were produced by first converting the commodity biocide, triclosan (TCS), to an epoxy-functional derivative, 2-((5-chloro-2-(2,4-dichlorophenoxy)phenoxy) methyl)oxirane (ETCS), and then reacting ETCS with polyethylenimine (PEI). While neither ETCS or PEI showed high antimicrobial activity toward either the Gram-positive bacterium, Staphylococcus epidermidis, or the Gram-negative bacterium, Escherichia coli, some the copolymers showed very high activity toward both bacteria. Antimicrobial activity for these copolymers was found to be highly dependent on both the molecular weight of the PEI utilized and the concentration of pendent groups derived from ETCS. In general, decreasing PEI molecular weight and increasing TCS pendent group concentration increased antimicrobial activity. Surface tension measurements showed that the molecular parameters affecting antimicrobial activity also affected surface activity in a similar fashion. Thus, it was speculated that the mechanism of antimicrobial activity associated with these copolymers involves interaction of the copolymers with the bacterial cell wall. A comparison of the antimicrobial activity of the most effective copolymers to TCS showed that the copolymers were more effective toward E. coli than pure TCS when compared using an equivalent TCS content (i.e. TCS pendent group content for the copolymers). This characteristic coupled with the fact that the TCS-containing copolymers are highly aqueous soluble liquids as opposed to a crystalline solid of limited solubility may afford utility of these copolymers for a variety of applications.     

Biodegradation of triclosan by a wastewater microorganism

Triclosan, a synthetic antimicrobial agent, has been considered as an emerging environmental contaminant. Here we reported a triclosan-degrading wastewater bacterial isolate, Sphingopyxis strain KCY1, capable of dechlorinating triclosan with a stoichiometric release of chloride. The stain can degrade diphenyl ether but not 2,4,4′-tribromodiphenyl ether and 2,2′,4,4′-tetrabromodiphenyl ether, despite all these three compounds are structurally similar to triclosan. While strain KCY1 was unable to grow on triclosan and catechol, it could grow with glucose, sodium succinate, sodium acetate, and phenol. When grown with complex nutrient medium containing a trace amount of triclosan (as low as 5 μg/L), the strain could retain its degradation ability toward triclosan. The maximum-specific triclosan degradation rate (q_m) and the half-velocity constant (K_m) are 0.13 mg-triclosan/mg-protein/day and 2.8 mg-triclosan/L, respectively. As triclosan degradation progressed, five metabolites were identified and these metabolites continue to transform into non-chlorinated end products, which was supported by a sharp drop in androgenic potential. The activity of catechol 2,3-dioxygenase in the cell extract was detected. No triclosan degradation was observed in the presence of 3-fluorocatechol, an inhibitor of meta-cleavage enzyme, suggesting that triclosan degradation proceed via meta-cleavage pathway. Based on all the observations, a degradation pathway for triclosan by strain KCY1 was proposed.     

Formation of bromo-substituted triclosan during chlorination by chlorine in the presence of trace levels of bromide

The side reactions of triclosan (2,4,4'-trichloro-2'-hydroxydiphenyl ether, TC) and chlorine in the presence of sodium chloride were investigated. In the absence of sodium chloride, three chloro-derivatives of TC, 2',3,4,4'-tetrachloro-2-hydroxydiphenyl ether (3-Cl-TC), 2',4,4',5-tetrachloro-2-hydroxydiphenyl ether (5-Cl-TC), and 2',3,4,4',5-pentachloro-2-hydroxydiphenyl ether (3,5-Cl(2)-TC) were formed, whereas in the presence of sodium chloride, 3-bromo-2',4,4'-trichloro-2-hydroxydiphenyl ether (3-Br-TC), 5-bromo-2',4,4'-trichloro-2-hydroxydiphenyl ether (5-Br-TC), (3 or 5)-bromo-2',4,4',(5 or 3)-chloro-2-hydroxydiphenyl ether ((3,5)-(BrCl)-TC), and 3,5-dibromo-2',4,4'-trichloro-2-hydroxydiphenyl ether (3,5-Br(2)-TC) were additionally formed. Radiochemical neutron activation analysis indicated that 1g of commercially available sodium chloride contained 73 microg of bromide and the bromide ion was determined to be the source of the side reactions. The rate of decrease of TC due to reaction with chlorine was greatly accelerated by the presence of bromide ion in the system: the rate with only 1 x 10(-5) M bromide ion was three times the rate in the absence of bromide.     

Microwave activation of electrochemical processes: High temperature phenol and triclosan electro-oxidation at carbon and diamond electrodes

The electrochemical oxidation of phenolic compounds in aqueous media is known to be affected by the formation of electro-polymerized organic layers which lead to partial or complete electrode blocking. In this study the effect of high intensity microwave radiation applied locally at the electrode surface is investigated for the oxidation of phenol and triclosan in alkaline solution at a 500 μm diameter glassy carbon or at a 500 μm × 500 μm boron-doped diamond electrode. The temperature at the electrode surface and mass transport enhancement are determined by calibration with the Fe(CN)₆^3−/4− redox system in aqueous 0.3 M NaOH and 0.2 NaCl (pH 12) solution. The calibration shows that strong thermal and mass transport effects occur at both glassy carbon and boron-doped diamond electrodes. The average electrode temperature reaches up to 390 K and mass transport enhancements of more than 20-fold are possible. For the phenol electro-oxidation at glassy carbon electrodes and at a concentration below 2 mM a multi-electron oxidation (ca. 4 electrons) occurs in the presence of microwave radiation. For the electro-oxidation of the more hydrophobic triclosan only the one-electron oxidation occurs. Although currents are enhanced in presence of microwave radiation, rapid blocking of the electrode surface in particular at high phenol concentrations still occurs.