The Influence of Viscosity and Surface Tension on Atomization of Water/Methanol and Diesel Emulsions

This paper shows the result of experimental studies of the influence of viscosities, surface tensions on atomization characteristics of water/methanol and diesel emulsions. Three emulsifying agents Y01, Y02 and Y03, with viscosity of 1.32 ～ 1.5 Pa·s and HLB values of 5.36, 4.83 and 4.51 respectively was produced by Span 80 and Tween 60. In the W/O emulsions, the aqueous phase is between 10% and 50%; the agent concentration added is 0.8 ～ 8.0%. The viscosity of the emulsions is 0.003 ～ 0.02 Pa·s, and the surface tension is 0.04 ～ 0.1 N/m. The types and concentrations of agents and the aqueous phase ( < 50%) significantly influence the viscosity of the emulsions and the Sauter Mean Diameter, measured by Malvern Particle Analyzer SERIES 2600.

Simultaneous determination of microcystin-LR and its glutathione conjugate in fish tissues by liquid chromatography-tandem mass spectrometry

A sensitive and selective liquid chromatography-tandem mass spectrometry method was developed and validated for the simultaneous quantitative determination of microcystin-LR (MC-LR) and its glutathione conjugate (MC-LR-GSH) in fish tissues. The analytes were extracted from fish liver and kidney using 0.01 M EDTA-Na-2-5% acetic acid, followed by a solid-phase extraction (SPE) on Oasis HLB and silica cartridges. High-performance liquid chromatography (HPLC) with electrospray ionization mass spectrometry, operating in selected reaction monitoring (SRM) mode, was used to quantify MC-LR and its glutathione conjugate in fish liver and kidney. Recoveries of analytes were assessed at three concentrations (0.2, 1.0, and 5 mu g g(-1) dry weight [DW]) and ranged from 91 to 103% for MC-LR, and from 65.0 to 75.7% for MC-LR-GSH. The assay was linear within the range from 0.02 to 5.0 mu g g(-1) DW, with a limit of quantification (LOQ) of 0.02 mu g g(-1) DW. The limit of detection (LOD) of the method was 0.007 mu g g(-1) DW in both fish liver and kidney. The overall precision was determined on three different days. The values for within- and between-day precision in liver and kidney were within 15%. This method was applied to the identification and quantification of MC-LR and its glutathione conjugate in liver and kidney of fish with acute exposure of MC-LR. (c) 2007 Elsevier B.V. All rights reserved.

Structure-activity relationship of surfactant for preparing DMFC anodic catalyst

Three kinds of surfactants as stabilizer were applied to the preparation of electrocatalysts for direct methanol fuel cell (DMFC). The catalysts have been characterized by examining their catalytic activities, morphologies and particle sizes by means of cyclic voltammetry, chronoamperometry, X-ray diffraction and transmission electron microscopy (TEM). It is found that the surfactants with different structures have a significantly influence on the catalyst shape and activity. The catalysts prepared with non-ionic surfactants as the stabilizer show higher activity for direct oxidation of methanol. The structure-activity relationship (SAR) analysis has been explored and the effect of hydrophile-lipophile balance (HLB value) has also been discussed.

东营凹陷沙三中亚段湖相浊积岩储层特征及油气成藏规律研究

Turbidity sandstone reservoirs have been an important field of hydrocarbon exploration and development in the basins all over the world, as well as in China. Lithologic pools are composed of turbidity sandstones and other sandstones are frequently found in the Jiyang Depression that is a Mesozoic-Cenozoic non-marine oil-bearing basin. The Dongying Sag lies in the sedimentary center of the basin. The subtle traps with turbidity reservoirs are generally difficult to be predicted and described by using current techniques. The studies on turbidity reservoirs plays thus an important theoretical and theoretical practical role in exploration and development in the Jiyang Depression. The attention is, in this thesis, focused on the petrologic properties and oil accumulating behaviors in lake turbidity sedimentary systems in the middle part of the third section of Shahejie Formation in the Dongying Sag, especially in Dongxin area, which lies on the central uplift of the Sag. The paper has disclosed the origin types of turbidity sandstones, distribution pattern and controlling factors of turbidity sandstones, and set up hydrocarbon accumulation patterns of the middle part of the third section of Shahejie Formation in Dongxin, based on nonmarine high resolution sequence stratigraphy, event sedimentology and new theories of hydrocarbon forming. By studying prediction method and technology of turbidity sandstone reservoirs, using precise geological model developing, new techniques of high resolution seismic inversion constrained by logging, the paper has forecast low permeability turbidity sandstone reservoirs and pointed out advantage exploration aims to progressive exploration and development. The paper has obtained mainly many productions and acknowledges as follows: 1.Turbidity sandstone reservoirs of the third section of Shahejie Formationin Dongying Sag are formed in such specifical geological background as rift and extension of basin. The inherited Dongying delta and transgression make up many turbidity distribution areas by overlaying and joining together. The hydrocarbon migrates from depression area to adjacent turbidity sandstone continuously. Accumulation area which is sufficient in oil is formed. 2.The paper has confirmed distinguishable sign of sequence boundary , established stratigraphic framework of Dongying Sag and realized isotime stratigraphic correlation. Es3 of Dongying delta is divided into eleven stages. Among them, the second period of the lower section in Es3, the sixth period of the middle section in Es3, the third period of the upper section in Es3 correspond to eleven sedimentary isotime surface in seismic profile, namely Es3 is classified into eleven Formations. 3.According to such the features of turbidity sandstone as deep in burial, small in area, strong in subtle property, overlaying and joining together and occurring in groups, management through fault and space variations of restriction quantum are realized and the forecast precision of turbidity sandstone by using precise geological model developing, new techniques of high resolution seismic inversion constrained by logging, based on the analysis of all kinds of interwell seismic inversion techniques. 4.According to the features of low permeable turbidity sandstone reservoirs, new method of log interpretation model is put forward. At the same time, distinguish technology of familiar low resistivity oil layer in the turbidity sandstone reservoirs is studied based on petrophysical laboratory work and "four properties" interrelationship between lithological physical Jogging and bearing hydrocarbon properties. Log interpretation model and reservoir index interpretation model of low resistivity oil layer are set up. So the log interpretation precision is improved. 5.The evolution law and its difference of the turbidity sandstone are embodies as follows: the source of sediments come from the south and east of the study area in the middle period of Es3. East source of sediments is pushed from west to east. However, the south source supply of sediments in the early and middle period of Es3 is in full, especially in Es3. subsequently, the supply is decreased gradually. Turbidity fan moves back toward the south and the size of fan is minished accordingly. The characteristic of turbidity sandstone in Dongying Sag is different in different structural positions. Dongxin in the middle-east of the central lift and Niuzhuang Sag He in Dongying delta front and prodelta deep lake subfacies. Although the turbidity sandstone of the two areas root in the Dongying delta sedimentary system, the sand body has different remarkably characteristic. 6.The sedimentary model of the turbiditys in study area have three types as follows: (1) collapse turbidity fan in respect of delta; (2) fault trench turbidity fan; (3) other types of microturbidity sandstone. Middle fan and outer fan, can be found mainly in sublacustrine fan. Middle fan includes braided channel microfacies, central microfacies and braided interchannel microfacies, which is main prospecting oil-bearing subfacies. The middle section of the third section of Shahejie Formation in study area (for example the central lift) can be divided into middle-lower and upper part. The middle-lower part is characteristic of turbidity fan. The upper part is sedimented mainly by delta-collapse fan. 7.The turbidity reservoirs of the middle part of the third section of Shahejie Formation in study area characterize by low maturity both in component and texture, strong in diagenesis and low in permeability. The reservoir can be classified into four types. Type III is the body of reservoir and comprises two types of H a and HI b. M a belongs to middle porosity - low permeability reservoir and distributes in the central lift. Hlb belongs to low porosity - low permeability and distributes in Haojia region. 8.A11 single sand body of lens turbidity reservoir of the middle part of the third section of Shahejie Formation in study area are surrounded by thick dark source rocks. The oil-water system is complex and behaves that every sandstone is single seal unit. The water body is 1/3-1-5 of the sand body. The edge water is not active. The gas exists in the top of reservoir in the form of mixed gas. For far-range turbidity fan with big scale channel, the area and volume of sand body is large and the gap is big in oil packing degree. There are lots of edge water and bottom water, and the latter increases rapidly during the course of development. 9.By exerting the modern hydrocarbon forming theories, the third section of Shahejie Formation in study area belongs to abnormally pressured fluid compartment. The lithological reservoir of the third section of Shahejie Formation is formed in the compartment. The reservoir-formed dynamic system belongs to lower self-source enclosed type. The result and the practice indicate that the form and accumulation of lithological oil reservoirs are controlled by the temperature and pressure of stratum, microfacies, thickness of sand body, fault and reservoir heterogeneity. 10. Based on studies above, the emphases focus on in south and north part of Dongying structure, west Dongxin region and south part Xinzhen structure in the application of production. The practice proves that the turbidity sandstone reservoirs in Ying 11 block and the fault-lithological reservoirs in Xin 133 block have been obtained significant breakthrough. The next target is still sandstone groups of the third section of Shahejie Formation in the bordering areas of Dongxin region for instance Xin 149 area, He 89 area, Ying 8 area etc.

固相萃取-色谱测定水、沉积物及土壤中氯霉素和3种四环素类抗生素

建立了固相萃取-高效液相色谱（UV）检测水、沉积物和土壤中的氯霉素、土霉素、四环素和金霉素4种抗生素的方法。水样、土壤和沉积物样品的前处理采用EDTA-McIlvaine缓冲溶液提取,用SAX-HLB串联小柱纯化和富集,用丙酮（含10%甲醇）洗脱进一步减小天然有机质的影响。采用乙腈和0.01mol/L草酸溶液作为流动相,8min内分离4种抗生素。测定了贵阳市阿哈湖、南明河和乌江渡水库的水样及沉积物,均有抗生素检出。

贵阳城市污水、河流及养鱼水域抗生素的地球化学行为

抗生素是广泛应用于人类和动物疾病治疗的药物，近年来在养殖业中抗生素更是常常作为动物催长剂。这些抗生素会通过人畜排泄物、药品的丢弃、污水排放、农业废物堆积等途径进入到环境中。环境中抗生素的残留会导致细菌耐药性的产生、微生态平衡的破坏，以及对生态环境和人类难以预知的影响。抗生素污染是近十年来才在国际上引起注意的新型环境问题，目前研究非常薄弱，要深入认识抗生素的环境影响特征就迫切需要对抗生素在环境中的迁移、归宿等地球化学行为进行针对性的研究。本文研究了贵阳城市污水、南明河及乌江渡水库中氯霉素（CAP）、土霉素（OTC）、四环素（TC）和金霉素（CTC）的环境地球化学特征，包括抗生素的分布、迁移特征及影响因素，并分析了贵阳市动物源性食品中抗生素的残留特征，探讨了环境因素对抗生素稳定性及吸附/解吸的影响，以期了解抗生素在环境中的降解、迁移等环境行为的特征，并据此评价抗生素的环境影响特点，为认识抗生素的污染特点、发展相应的控制、治理措施提供科学依据。主要内容包括： 1. 对环境样品中CAP和TCs的前处理过程和检测方法进行了优化。对水样的前处理采用固相萃取的方法，对土壤和沉积物的前处理采用EDTA-McIlvaine振荡萃取、SAX-HLB净化富集的方法；选择HPLC-UV作为分析的手段，对样品中的4种抗生素进行了检测，各化合物得到了很好的分离，该方法简便、快捷、重现性好。 2. 证实了抗生素在城市污水中的普遍存在。贵阳城市污水中以CAP的污染最为突出，其含量明显高于广州地区的城市污水；污水中四环素类药物（TCs）的含量和大多数欧美国家及地区城市污水中TCs的含量相当。这一结果证明，污水中抗生素的污染非常严重，对地表水环境形成严重的威胁。污水中抗生素的来源包括：人服用抗生素药物以及食用含有抗生素残留的食品之后的排泄物；食品中残留的抗生素随剩余食品的丢弃而进入污水。污水中抗生素的含量都具有明显的季节变化规律，冬春季含量明显高于夏秋季，我们认为这与各季节用水量和疾病特点有关。污水中抗生素的大量存在说明：1）抗生素存在滥用的现象，特别是CAP可能存在严重的违法使用，这一现象应当重视；2）污水中的抗生素会威胁水环境质量，应加强处理和控制技术。 3. 证明了城市河流受到多种来源的抗生素影响，其中城市污水是最重要的源，而且抗生素在河流中呈现一定的持久性。南明河上游河段中抗生素的来源包括郊区城镇污水、养鱼场、制药厂污水排放及地表垃圾。城市污水是抗生素的一大排放源，受其影响，排污口下游的河段受到的抗生素污染尤为严重，此外还有来自下游郊区城镇和农业污水的影响。对南明河中抗生素的来源及行为特点的剖析表明：1）抗生素在南明河的水和沉积物中具有不同的分布特征：河水中以CAP的污染最为严重，各水样中CAP的含量基本都高于TCs；而大部分沉积物中TCs的含量都高于CAP。CAP和TCs在水－沉积物之间的分布特征表明，它们在水环境中的地球化学行为明显受到吸附/解吸特点的影响，CAP的亲水性强，而TCs的亲粒性强。2）虽然在养殖业中已禁止使用CAP，但河水和污水中CAP的大量存在，这一结果揭露了CAP仍然存在大量违法使用的事实。3）河水中抗生素含量的季节差异明显，冬春季抗生素的含量高于夏秋季，其原因主要是夏秋季河水流量大，对河水中抗生素的稀释作用强。沉积物中抗生素的含量没有明显的季节变化规律，各季节抗生素的平均含量差异较小。4）受污水影响，各季节排污口下游的南明河水受到的抗生素污染尤为严重，污水口上下游之间的含量差异明显。沉积物在冬季受城市污水的影响大，在排污口下游的抗生素的含量明显高于上游，而春、夏、秋季受污水影响不明显。这可能是因为在春、夏和秋季其它污染源的影响较大，因此污水的影响强度减弱。夏季上游沉积物中CAP的含量甚至高于下游，原因一方面是因为夏季城市污水中抗生素含量低，对南明河的影响减小，另一方面可能因为夏季雨水多、水量大，将上游的地表垃圾以及积累在小河沟中的垃圾冲刷到南明河中，而这些工业及生活垃圾通常是抗生素的一大来源。 抗生素在河流中呈现了一定的持久性，在20 km的范围内水和沉积物显示了明显的污染水平，可能会对水生生态以及流域的环境造成一定的影响。此外，贵阳市南明河两岸的农田通常是用河水进行灌溉的，从而可能使抗生素的污染危及到食物链，对人体的健康有潜在的威胁。 4. 由于食品（如鱼肉、猪肉等）中残留的抗生素是污水中抗生素的重要来源，因此我们研究了养殖业（水产养殖区）中抗生素的环境行为特点，还研究了常见动物源性食品中抗生素的残留特点。对养鱼区的研究表明，养鱼饲料中含有大量的抗生素，是养鱼区水环境中抗生素的来源。由于饲料的颗粒大，且河水流速快，因此饲料中的抗生素不会对水体造成很大的影响，但是在网箱区的沉积物中形成了高含量的残留，除此以外，在乌江渡主航道的河心沉积物中抗生素的含量也相当可观。这说明该区水产养殖的抗生素主要影响沉积物，且相应的污染不是局部的，而会影响到整个养鱼区。从沉积物中抗生素平均含量的季节差异来看，各季TCs的用药量可能不同，秋季的用量可能最大，而其它季节用量相当；CAP在每个季节的用量可能相当。尽管分析的饲料中CAP的含量高于TCs，但在各季节乌江渡水库主航道沉积物中TCs的含量几乎都远高于CAP，这是由于TCs比CAP更易存在于沉积物中。乌江渡水库上下游主航道沉积物中抗生素的含量差异日益减小，说明了乌江渡水库的污染已日益严重。这些抗生素虽然暂时被固定在了沉积物中，活性相对较小，但是在外界条件的影响下，它们的吸附/解吸作用是可以改变的。因此，乌江渡沉积物中高含量的抗生素残留对水生生态环境具有潜在的威胁。 对贵阳市动物源性食品（鱼肉、猪肉和牛奶）中抗生素的残留特征的分析表明，这些食品中普遍残留有高含量的抗生素，被人食用后，其中的抗生素也会被人体摄入，一部分抗生素会随着人的排泄物而进入到污水中，并最终进入环境中；另一部分抗生素会积蓄在人体中，到一定浓度后就会对人体造成伤害。鲩鱼、鲫鱼、鲤鱼、鳙鱼和鲢鱼中CAP、OTC、TC和CTC的平均含量范围分别在57.1～365.5 µg/kg、37.0～60.7µg/kg、34.3～72.4 µg/kg和22.3～68.0 µg/kg之间。秋季的长吻鲍、团头鲂、鲈鱼、长江洄鱼、对虾、黄鳝、泥鳅和猪肉中CAP、OTC、TC和CTC的平均含量分别为88.1 µg/kg、76.8 µg/kg、343.7 µg/kg和34.2 µg/kg；牛奶中的含量分别为4.2 µg/L、1.6 µg/L和2.5 µg/L和22.0 µg/L。 5. 确定了抗生素的稳定性、吸附/解吸作用与各因素的关系，据此可以探讨环境中抗生素的行为特点及机理，并为环境中抗生素的污染防治提供依据。在短时的加热中，TCs发生了部分降解，而CAP却几乎没有发生分解，说明烹饪过程中的加热不能去除食品中的抗生素，这些抗生素则会进入到人体和污水中。当pH在2～8之间时，TCs的性质较稳定；CAP在pH＝1～10的范围内性质都比较稳定。地表和地下水体的pH一般为7左右，说明了水环境中TCs受pH的影响小，而CAP几乎不受影响。在6个月的时间内，TCs在3种介质中都发生了不同程度的降解，但仍有大部分残留；CAP几乎没有发生明显的降解，这说明CAP和TCs的污染具有一定的持久性。TCs的吸附/解吸受颗粒物粒径的影响大，粒径越小，吸附越强；CAP不受影响。这证明了在环境中CAP更易以水溶态的形式存在，而TCs更易吸附在沉积物中。颗粒物中CaCO3含量越高，TC和CTC的吸附越强，证明CaCO3可以用来增强TC、CTC的吸附，这为环境中抗生素的治理提供了一条思路。

Huanglongbing (ex-greening): um alerta aos citricultores da Bahia.

A produção de citros no Brasil é uma das principais atividades do agronegócio nacional, apresentando significativa importância econômica e social devido aos números vultosos de produção. A Bahia destaca-se como o segundo produtor nacional de laranja. Para manter esse desempenho, cuidados devem ser empregados a fim de garantir a sanidade dos pomares do estado. Dentre as doenças que afetam os citros, o huanglongbing (HLB), comumente chamado de ?greening? é altamente devastador e amplamente distribuído no mundo. Essa doença tornou-se importante no cenário brasileiro desde 2004, quando ocorreram os primeiros registros no estado de São Paulo. O HLB é causado pela bactéria Candidatus Liberibacter, que no Brasil está associada às formas Ca. L. asiaticum e Ca. L. americans. A disseminação do HLB pode ocorrer por enxertia de material contaminado ou pelo inseto vetor da bactéria, o psilídeo Diaphorina citri Kuwayama (Hemyptera: Psyllidae). Além dos citros, o D. citri também utiliza como hospedeiro a espécie Murraya paniculata, popularmente conhecida como murta.

Utilização de práticas culturais na citricultura frente ao huanglongbing.

A citricultura é uma das principais atividades do agronegócio brasileiro, estando presente em todas as regiões do país em diferentes ambientes de produção. A presença da doença huanglongbing (HLB), constatada no Brasil em 2004, vem provocando perdas expressivas em importantes regiões produtoras e colocando em cheque a sustentabilidade da cadeia citrícola. Estratégias de controle atual se baseiam no uso de mudas sadias, inspeção e erradicação sistemática de plantas sintomáticas e controle químico do inseto vetor. Pesquisas vêm sendo conduzidas pela Embrapa e outras instituições brasileiras com o objetivo de alcançar a resistência ao HLB por melhoramento genético via biotecnologia. Contudo, as limitações inerentes a essas ações determinam que proposições adicionais e não-excludentes sejam consideradas para a mitigação de efeitos do HLB. Práticas horticulturais com possibilidade de emprego imediato na citricultura são apresentadas de forma a contribuir com o enfrentamento a essa doença. As proposições a seguir são discutidas: seleção de materiais tolerantes de ocorrência natural, mudança geográfica da produção, conceitos não usuais de mudas protegidas, plantas repelentes e atrativas, sistemas de produção de baixo ingresso, uso de elicitores de resistência, cultivo protegido, consorciação e ultra-adensamento.

Development and validation of a dried blood spot-LC-APCI-MS assay for estimation of canrenone in paediatric samples

A selective and sensitive liquid chromatography (LC)-atmospheric pressure chemical ionisation (APCI)-mass spectroscopic (MS) assay of canrenone has been developed and validated employing Dried Blood Spots (DBS) as the sample collection medium. DBS samples were prepared by applying 30 mu l of spiked whole blood onto Guthrie cards. A 6 mm disc was punched from the each DBS and extracted with 2 ml of methanolic solution of 17 alpha-methyltestosterone (Internal Standard). The methanolic extract was evaporated to dryness and reconstituted in acetonitrile:water (1:9, v/v). The reconstituted solution was further subjected to solid phase extraction using HLB cartridges. Chromatographic separation was achieved using Waters Sunfire C18 reversed-phase column using isocratic elution, followed by a high organic wash to clear late eluting/highly retained components. The mobile phase consisted of methanol:water (60:40, v/v) pumped at a flow rate of 0.3 ml/min. LC-APCI-MS detection was performed in the selected-ion monitoring (SIM) mode using target ions at m/z 341.1 and 303.3 for canrenone and internal standard respectively. The selectivity of the method was established by analysing DBS samples from 6 different sources (individuals). The calibration curve for canrenone was found to be linear over 25-1000 ng/ml (r >0.994). Accuracy (% RE) and precision (% CV) values for within and between day were

A simple bioanalytical method for the quantification of antiepileptic drugs in dried blood spots

An increasing number of publications on the dried blood spot (DBS) sampling approach for the quantification of drugs and metabolites have been spurred on by the inherent advantages of this sampling technique. In the present research, a selective and sensitive high-performance liquid chromatography method for the concurrent determination of multiple antiepileptic drugs (AEDs) [levetiracetam (LVT), lamotrigine (LTG), phenobarbital (PHB)], carbamazepine (CBZ) and its active metabolite carbamazepine-10,11 epoxide (CBZE)] in a single DBS has been developed and validated. Whole blood was spotted onto Guthrie cards and dried. Using a standard punch (6. mm diameter), a circular disc was punched from the card and extracted with methanol: acetonitrile (3:1, v/v) containing hexobarbital (Internal Standard) and sonicated prior to evaporation. The extract was then dissolved in water and vortex mixed before undergoing solid phase extraction using HLB cartridges. Chromatographic separation of the AEDs was achieved using Waters XBridge™ C18 column with a gradient system. The developed method was linear over the concentration ranges studied with r=0.995 for all compounds. The lower limits of quantification (LLOQs) were 2, 1, 2, 0.5 and 1. µg/mL for LVT, LTG, PHB, CBZE and CBZ, respectively. Accuracy (%RE) and precision (%CV) values for within and between day were

Validation and application of a reporter gene assay for the determination of estrogenic endocrine disruptor activity in milk

Endocrine disruptors (EDs) are compounds known to interfere with the endocrine system by disturbing the action or pathways of natural hormones which may lead to infertility or cancer.Our diet is considered to be one of the main exposure routes to EDs. Since milk and dairy products are major components of our diet they should be monitored for ED contamination. Most assays developed to date utilise targeted, chromatography based methods which lack information on the biological activity and mixture effects of the monitored compounds.A biological reporter gene assay (RGA) was developed to assess the total estrogen hormonal load in milk. It has been validated according to EU decision 2002/657/EC. Analytes were extracted by liquid-liquid extraction with acetonitrile followed by clean up on a HLB column which yielded good recovery and small matrix effects. The method has been shown to be estrogen specific, repeatable and reproducible, with covariance values below 20%. In conclusion, this method enables the detection of low levels of estrogen hormonal activity in milk with a detection capability of 36pgg EEQ and has been successfully applied in testing a range of milk samples. © 2014 Elsevier Ltd.

Desenvolvimento e validação de um método analítico para a determinação de clorpromazina em sangue por extracção em fase sólida e cromatografia gasosa/espectometria de massa

O objectivo deste trabalho foi o desenvolvimento e validação de uma metodologia analítica para a determinação de clorpromazina em sangue total, tendo a protriptilina sido usada como padrão interno. A extracção e purificação dos analitos foi efectuada por extracção em fase sólida com colunas Oasis® HLB, e análise posterior por cromatografia gasosa com detector de espectrometria de massa de impacto electrónico (GC/EI-MS). Para a preparação das curvas de calibração foram fortificadas diariamente amostras de sangue branco com concentrações crescentes de clorpromazina entre 0,01 e 5 µg/mL. Foi utilizado um modelo de regressão linear, sendo os coeficientes de correlação superiores a 0,998. Os coeficientes de variação e os erros relativos foram respectivamente inferiores a 12 e 13%, cumprindo assim critérios internacionalmente aceites para a validação de métodos bioanalíticos. Foram também estudados os limites de detecção e quantificação, sendo de 3 e 10 ng/mL respectivamente. A interferência de outras substâncias foi excluída por análise de dez amostras brancas de sangue. O rendimento médio do método foi de 81%. Em virtude da sua simplicidade e rapidez, este método pode ser aplicado na determinação deste antipsicótico em amostras de sangue total, sendo adequado para análises de rotina no âmbito da toxicologia clínica e forense.

Polymorphism, crystallinity and hydrophilic-lipophilic balance of stearic acid and stearic acid-capric/caprylic triglyceride matrices for production of stable nanoparticles

There is an increasing interest in lipid nanoparticles because of their suitability for several administration routes. Thus, it becomes even more relevant the physicochemical characterization of lipid materials with respect to their polymorphism, lipid miscibility and stability, as well as the assessment of the effect of surfactant on the type and structure of these nanoparticles. This work focuses on the physicochemical characterization of lipid matrices composed of pure stearic acid or of mixtures of stearic acid-capric/caprylic triglycerides, for drug delivery. The lipids were analyzed by Differential Scanning Calorimetry (DSC), Wide Angle X-ray Diffraction (WAXD), Polarized Light Microscopy (PLM) and hydrophilic-lipophilic balance (HLB) in combination with selected surfactants to determine the best solid-to-liquid ratio. Based on the results obtained by DSC and WAXD, the selected qualitative and quantitative composition contributed for the production of stable nanoparticles, since the melting and the tempering processes provided important information on the thermodynamic stability of solid lipid matrices. The best HLB value obtained for stearic acid-capric/caprylic triglycerides was 13.8, achieved after combining these lipids with accepted surfactants (trioleate sorbitan and polysorbate 80 in the ratio of 10:90). The proposed combinations were shown useful to obtain a stable emulsion to be used as intermediate form for the production of lipid nanoparticles. (C) 2011 Elsevier B.V. All rights reserved.

A sensitive microextraction by packed sorbent-based methodology combined with ultra-high pressure liquid chromatography as a powerful technique for analysis of biologically active flavonols in wines

A new approach based on microextraction by packed sorbent (MEPS) and reversed-phase high-throughput ultra high pressure liquid chromatography (UHPLC) method that uses a gradient elution and diode array detection to quantitate three biologically active flavonols in wines, myricetin, quercetin, and kaempferol, is described. In addition to performing routine experiments to establish the validity of the assay to internationally accepted criteria (selectivity, linearity, sensitivity, precision, accuracy), experiments are included to assess the effect of the important experimental parameters such as the type of sorbent material (C2, C8, C18, SIL, and C8/SCX), number of extraction cycles (extract-discard), elution volume, sample volume, and ethanol content, on the MEPS performance. The optimal conditions of MEPS extraction were obtained using C8 sorbent and small sample volumes (250 μL) in five extraction cycle and in a short time period (about 5 min for the entire sample preparation step). Under optimized conditions, excellent linearity View the MathML source(Rvalues2>0.9963), limits of detection of 0.006 μg mL−1 (quercetin) to 0.013 μg mL−1 (myricetin) and precision within 0.5–3.1% were observed for the target flavonols. The average recoveries of myricetin, quercetin and kaempferol for real samples were 83.0–97.7% with relative standard deviation (RSD, %) lower than 1.6%. The results obtained showed that the most abundant flavonol in the analyzed samples was myricetin (5.8 ± 3.7 μg mL−1). Quercetin (0.97 ± 0.41 μg mL−1) and kaempferol (0.66 ± 0.24 μg mL−1) were found in a lower concentration. The optimized MEPSC8 method was compared with a reverse-phase solid-phase extraction (SPE) procedure using as sorbent a macroporous copolymer made from a balanced ratio of two monomers, the lipophilic divinylbenzene and the hydrophilic N-vinylpyrrolidone (Oasis HLB) were used as reference. MEPSC8 approach offers an attractive alternative for analysis of flavonols in wines, providing a number of advantages including highest extraction efficiency (from 85.9 ± 0.9% to 92.1 ± 0.5%) in the shortest extraction time with low solvent consumption, fast sample throughput, more environmentally friendly and easy to perform.

A fast method using a new hydrophilic–lipophilic balanced sorbent in combination with ultra-high performance liquid chromatography for quantification of significant bioactive metabolites in wines

This manuscript describes the development and validation of an ultra-fast, efficient, and high throughput analytical method based on ultra-high performance liquid chromatography (UHPLC) equipped with a photodiode array (PDA) detection system, for the simultaneous analysis of fifteen bioactive metabolites: gallic acid, protocatechuic acid, (−)-catechin, gentisic acid, (−)-epicatechin, syringic acid, p-coumaric acid, ferulic acid, m-coumaric acid, rutin, trans-resveratrol, myricetin, quercetin, cinnamic acid and kaempferol, in wines. A 50-mm column packed with 1.7-μm particles operating at elevated pressure (UHPLC strategy) was selected to attain ultra-fast analysis and highly efficient separations. In order to reduce the complexity of wine extract and improve the recovery efficiency, a reverse-phase solid-phase extraction (SPE) procedure using as sorbent a new macroporous copolymer made from a balanced ratio of two monomers, the lipophilic divinylbenzene and the hydrophilic N-vinylpyrrolidone (Oasis™ HLB), was performed prior to UHPLC–PDA analysis. The calibration curves of bioactive metabolites showed good linearity within the established range. Limits of detection (LOD) and quantification (LOQ) ranged from 0.006 μg mL−1 to 0.58 μg mL−1, and from 0.019 μg mL−1 to 1.94 μg mL−1, for gallic and gentisic acids, respectively. The average recoveries ± SD for the three levels of concentration tested (n = 9) in red and white wines were, respectively, 89 ± 3% and 90 ± 2%. The repeatability expressed as relative standard deviation (RSD) was below 10% for all the metabolites assayed. The validated method was then applied to red and white wines from different geographical origins (Azores, Canary and Madeira Islands). The most abundant component in the analysed red wines was (−)-epicatechin followed by (−)-catechin and rutin, whereas in white wines syringic and p-coumaric acids were found the major phenolic metabolites. The method was completely validated, providing a sensitive analysis for bioactive phenolic metabolites detection and showing satisfactory data for all the parameters tested. Moreover, was revealed as an ultra-fast approach allowing the separation of the fifteen bioactive metabolites investigated with high resolution power within 5 min.