Nonionic surfactant
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Particle size is a key parameter when dealing with drug particle formation, delivery or dissolution. The correct measurement of particle size depends on various factors, such as sample preparation or dilution, but also on the choice of method for its characterization. In this work, we study the process of precipitation of poorly water-soluble drug Valsartan from supersaturated solution in the presence of nonionic surfactant Tween 20. Several techniques including dynamic light scattering (DLS) operated in several measuring modes, optical microscope (OM) and static light scattering (SLS) were used to analyze the kinetics of particle formation. As concluded by the results, the increase in turbidity of the solution seriously limits the application of classical DLS to properly measure the particle size and polydispersity. One way to get around this restriction is by dilution, which however results in a decrease in the size of Valsartan particles in the studied population. In contrast, here we present for a first time technique based on modulated 3D cross correlation DLS equipped with the sample goniometer to determine size of submicron particles of the drug in highly turbid solutions. Additionally, a modified OM was used to measure micron-sized particles for samples without any dilution in a continuous mode. Measured particle sizes combined with measured Valsartan concentration allowed us to identify mechanism responsible for the particle formation from supersaturated solutions. The main mechanism, as it is shown in this work, is covering surface of precipitate particles by the amount of used Tween 20.
Removal of nonionic surfactants from municipal wastewater using a constructed wetland with a horizontal subsurface flow was studied in 2009 and 2010. Extraction spectrophotometry with 3',3″,5',5″-tetrabromophenolphthalein ethyl ester and KCl served to determine the analyte concentrations. Triton(®) X-100 was used as a standard to express the nonionic-surfactant concentrations. Anionic and cationic surfactants were shown not to interfere during the determination. Nonionic surfactants were degraded (to products undeterminable by the method) with a high average efficiency that reached 98.1% in 2009 and 99.1% in 2010, respectively. The average concentration of nonionic surfactants at the inflow was 0.978 mg/l, while it was close to the limit of quantification at the outflow (0.014 mg/l). A significant fraction of nonionic surfactants (38.7%) was already degraded during the pretreatment, and only 14.0% of the nonionic surfactants remained in the interstitial H(2) O taken in the vegetation bed at a distance of 1 m from the inflow zone at a 50-cm depth. Nonionic surfactants were degraded both under aerobic and anaerobic conditions.
Surfactants have the potential to modify the environmental behavior of hydrophobic pesticides leading to an enhanced or reduced mobility risk. This risk is often overlooked in registration procedures due to a lack of suitable methodologies to quantify the transport potential of pesticides with surfactants. In this study we present a novel methodology designed to study the surfactant facilitated transport of pesticides under controlled equilibrium and dynamic hydrologic conditions. Using this methodology, we investigated the risk of chlorpyrifos enhanced mobility for two common surfactant application practices in agrosystems: pesticide spraying and irrigation with waste water. With the dynamic experiments we showed that a single irrigation event with artificial reclaimed water containing the nonionic surfactant Triton X100 at a concentration of 15 mg/L reduced the leaching of chlorpyrifos by 20% while the presence of the same surfactant in the chlopyrifos spraying formulation reduced the leaching amount by 60%. However, in the first case 90% of the chlropyrifos fraction remaining in soil was retained in the upper 3 cm while in the second cas, 72% was transported to the bottom layers. The presence of Triton X100 in irrigation water or spraying formulation retards the leaching of chlorpyrifos but enhances its downward transport.
- MeSH
- látky znečišťující půdu analýza chemie MeSH
- pesticidy analýza chemie MeSH
- povrchově aktivní látky chemie MeSH
- Publikační typ
- časopisecké články MeSH
Horseradish peroxidase (HRP)/H2O2-mediated crosslinking of polypeptides in inverse miniemulsion is a promising approach for the development of next-generation biocompatible and biodegradable nanogels. Herein, we present a fundamental investigation of the effects of three surfactants and their different concentrations on the (HRP)/H2O2-mediated nanogelation of poly[N5-(2-hydroxyethyl)-l-glutamine-ran-N5-propargyl-l-glutamine-ran-N5-(6-aminohexyl)-l-glutamine]-ran-N5-[2-(4-hydroxyphenyl)ethyl)-l-glutamine] (PHEG-Tyr) in inverse miniemulsion. The surfactants sorbitan monooleate (SPAN 80), polyoxyethylenesorbitan trioleate (TWEEN 85), and dioctyl sulfosuccinate sodium salt (AOT) were selected and their influence on the nanogel size, size distribution, and morphology was evaluated. The most effective nanogelation stabilization was achieved with 20 wt% nonionic surfactant SPAN 80. The diameter of the hydrogel nanoparticles was 230 nm (dynamic light scattering, DLS) and was confirmed also by nanoparticle tracking analysis (NTA) which showed the diameters ranging from 200 to 300 nm. Microscopy and image analyses showed that the nanogel in the dry state was spherical in shape and had number-average diameter Dn = 26 nm and dispersity Ð = 1.91. In the frozen-hydrated state, the nanogel appeared porous and was larger in size with Dn = 182 nm and Ð = 1.52. Our results indicated that the nanogelation of the polymer precursor required a higher concentration of surfactant than classical inverse miniemulsion polymerization to ensure effective stabilization. The developed polypeptide nanogel was radiolabeled with 125I, and in vivo biodistribution and blood clearance evaluations were performed. We found that the 125I-labeled nanogel was well-biodistributed in the bloodstream, cleared from mouse blood during 48 h by renal and hepatic pathways and did not provoke any sign of toxic effects.
- MeSH
- myši MeSH
- nanogely MeSH
- peptidy MeSH
- peroxid vodíku * MeSH
- polyethylenglykoly MeSH
- polyethylenimin MeSH
- povrchově aktivní látky * MeSH
- tkáňová distribuce MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- MeSH
- chemické bojové látky škodlivé účinky MeSH
- dekontaminace metody MeSH
- finanční podpora výzkumu jako téma MeSH
- krysa rodu rattus MeSH
- organothiofosforové sloučeniny antagonisté a inhibitory MeSH
- povrchově aktivní látky farmakologie MeSH
- soman antagonisté a inhibitory MeSH
- techniky in vitro MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- zvířata MeSH
- Publikační typ
- srovnávací studie MeSH
Degradation of anionic and nonionic surfactants in a constructed wetland with horizontal subsurface flow was studied using high performance liquid chromatography and extraction spectrophotometry. The ratio of individual homologues of linear alkylbenzene sulfonates (LAS) and the efficiency of their removal were studied. Tridecyl-, dodecyl-, undecyl-, and decylbenzene sulfonates were removed with efficiencies of 92.9%, 84.3%, 64.7%, and 41.1%, respectively. These differences are due to sequential shortening of the alkyl chain in homologues during degradation (the higher homologue can provide the lower one). The formation of sulfophenyl carboxylic acids during ω-oxidation of the alkyl chain followed by successive α- and/or β-oxidation is also a possible mechanism for removal of LAS. Solid phase extraction using Chromabond® HR-P columns was used for preconcentration of the analytes prior to their determination by HPLC. Methylene blue active compounds were determined using extraction spectrophotometry. The average efficiency of their removal was 84.9% in this case. The efficiency of nonionic surfactant removal (98.2%) was significantly higher in comparison to that for anionic surfactants. The concentration of the endocrine disruptor nonylphenol (a product of nonylphenol polyethoxylate surfactant degradation) determined in the profile of the wetland was beneath the limit of detection (0.4 μg/L). The average outflow concentrations of anionic and nonionic surfactants determined by spectrophotometry were 0.54 and 0.021 mg/L, respectively. The average outflow concentrations of decyl- and tridecylbenzene sulfonates determined by HPLC were 0.195 and 0.015 mg/L. Efficiencies of 86.4% and 92.2% were obtained for removal of organic compounds as indicated by chemical and biochemical oxygen demand (COD(Cr) and BOD(5)). These results demonstrate the suitability of the constructed wetland for degrading surface-active compounds.
The hydrolytic efficacy of foam-making blends on the basis of cationic and nonionic surfactants and hydrogen peroxide was tested against the organophosphate Fenitrothion. The length of alkyl chains in both classes of surfactants and their mutual ratios are not parameters which significantly influenced the reactivity of blends. On the other hand an increase in the hydrogen peroxide concentration induced a significant increase in the velocity of hydrolysis of Fenitrothion.
