期刊文献+
共找到994篇文章
< 1 2 50 >
每页显示 20 50 100
挠度法探究UV固化涂层内应力及附着力影响因素
1
作者 姚景耀 孙冠卿 《涂料工业》 北大核心 2026年第2期1-6,共6页
【目的】探究UV固化涂层内应力的产生机制、测量方法及其对附着力的影响,减少开裂、弯曲或剥落等缺陷,提高涂层的耐用性和外观质量。【方法】通过悬臂挠度法测量了不同配方下涂层的内应力,并研究了内应力与涂层附着力之间的关系。【结... 【目的】探究UV固化涂层内应力的产生机制、测量方法及其对附着力的影响,减少开裂、弯曲或剥落等缺陷,提高涂层的耐用性和外观质量。【方法】通过悬臂挠度法测量了不同配方下涂层的内应力,并研究了内应力与涂层附着力之间的关系。【结果】光引发剂的种类、树脂交联密度以及活性稀释剂的选择对涂层内应力的控制具有重要影响,合理调配配方能有效减小内应力积累,提升涂层的附着力,如TPO引发剂可提升涂层交联密度与硬度,但需控制用量以防应力过高;稀释剂存在最佳添加量,且其链长增加可降低内应力。【结论】为提升光固化涂层附着力、减少缺陷提供了具体方法。 展开更多
关键词 uv固化涂层 附着力 内应力 挠度法
在线阅读 下载PDF
DETERMINATION OF DISSOLVED ORGANIC CARBON IN SEAWATER USING UV/PERSULPHATE METHOD AND HTCO METHOD 被引量:9
2
作者 王江涛 张正斌 刘莲生 《Chinese Journal of Oceanology and Limnology》 SCIE CAS CSCD 1997年第1期25-31,共7页
A comparison between the high-temperature catalytic oxidation method (HTCO) and the UV/persulphate method for the determination of dissolved organic carbon (DOC)in seawater is presented in this paper. In seawater samp... A comparison between the high-temperature catalytic oxidation method (HTCO) and the UV/persulphate method for the determination of dissolved organic carbon (DOC)in seawater is presented in this paper. In seawater sample chloride ion can affect the oxidation efficiency of the UV/persulphate method if the asymptotic concentration of persulphate is not reached.During HTCO analysis, blanks that appear to originate mainly from the catalyst are high and far from constant.If the blanks are well estimated and correction is made, the difference of determined DOC values between the UV/persulphatemethod and the HTCO mehod is small, the HTCO values being slightly higher. 展开更多
关键词 DOC uv/persulphate method HTCO method
原文传递
COMPARISON OF HTC METHOD AND UV/PERSULPHATE METHOD TO DETERMINE COLLOIDAL ORGANIC CARBON IN SEAWATER 被引量:2
3
作者 王江涛 赵卫红 +1 位作者 谭丽菊 张正斌 《Chinese Journal of Oceanology and Limnology》 SCIE CAS CSCD 2000年第1期80-84,共5页
The application of cross flow ultrafiltration(CFF) techniques to separate colloidal organic carbon(COC) from truly dissolved organic carbon(TDOC) was investigated; COC and TDOC were determined by the high temperature ... The application of cross flow ultrafiltration(CFF) techniques to separate colloidal organic carbon(COC) from truly dissolved organic carbon(TDOC) was investigated; COC and TDOC were determined by the high temperature combustion method(HTC) and UV/persulphate method. It was found that CFF can quantitatively separate COC from seawater. The determination results by the HTC and UV/persulphate method for COC and TDOC showed little difference, which suggested that the oxidation efficiency of the two methods are identical. Colloidal particles have no remarkable influence on the oxidation efficiency of the UV/persulphate method. 展开更多
关键词 cross flow ULTRAFILTRATION COLLOIDAL organic carbon high temperature combustion method uv/persulphate method
原文传递
Development of an HPLC–UV assay method for the simultaneous quantification of nine antiretroviral agents in the plasma of HIV-infected patients 被引量:4
4
作者 Nitin Charbe Sara Baldelli +3 位作者 Valeria Cozzi Simone Castoldi Dario Cattaneo Emilio Clementi 《Journal of Pharmaceutical Analysis》 SCIE CAS 2016年第6期396-403,共8页
A new method using high-performance liquid chromatography coupled with ultra violet detection(HPLC–UV)was developed and validated for the simultaneous quantification of atazanavir,dolutegravir,darunavir,efavirenz,etr... A new method using high-performance liquid chromatography coupled with ultra violet detection(HPLC–UV)was developed and validated for the simultaneous quantification of atazanavir,dolutegravir,darunavir,efavirenz,etravirine lopinavir,raltegravir,rilpivirine and tipranavir in human plasma.For the first time we reported here the development and validation of an HPLC–UV assay to quantify the frequently administered 9antiretroviral compounds including dolutegravir and rilpivirine.A simple solid phase extraction procedure was applied to 500 μL aliquots of plasma.The chromatographic separation of the drugs and internal standard(quinoxaline) was achieved with a gradient of acetonitrile and sodium acetate buffer on a C_(18) reverse-phase analytical column with a 25 min analytical run time.Calibration curves were optimised according to the therapeutic range of drug concentrations in patients,and the coefficient of determination(r^2) was higher than0.99 for all analytes.Mean intraday and interday precisions(RSD) for all compounds were less than 15.0%,and the mean accuracy(% deviation from nominal concentration) was also found to be less than 15.0%.Extraction recovery range was between 80% and 120% for all drugs analysed.The solid phase extraction and HPLC–UV method enable a specific,sensitive,and reliable simultaneous determination of nine antiretroviral agents in plasma.Good extraction efficiency and low limit of HPLC–UV quantification make this method suitable for use in clinical trials and therapeutic drug monitoring. 展开更多
关键词 HPLC–uv ANTIRETROVIRALS BIOANALYTICAL method validation
暂未订购
Estimating Aluminum Leaching into Meat Baked with Aluminum Foil Using Gravimetric and UV-Vis Spectrophotometric Method 被引量:1
5
作者 Layla A. Al Juhaiman 《Food and Nutrition Sciences》 2015年第5期538-545,共8页
Baking meat by wrapping them in Aluminum (Al) foil is common in many countries. The excessive use of Al foil in baking and the disagreement about using Al foils were the motivation to do this study especially after th... Baking meat by wrapping them in Aluminum (Al) foil is common in many countries. The excessive use of Al foil in baking and the disagreement about using Al foils were the motivation to do this study especially after the 2007 WHO/FDA Report. In this investigation, a gravimetric and a UV-Vis spectrophotometric method are used to estimate Aluminum (Al) leaching into meat baked by wrapping in Al foil. Three kinds of meat were used fish, cow stakes and chicken. The importance of Al exposure area was neglected by many studies. Five factors affecting Al leaching into meat are studied (baking temperature, baking time, additives, Al exposure area and weight of meat). The effect of cooking times (20, 40, 60 minutes) at 180℃ and cooking temperatures (160℃, 180℃, 200℃) at 60 minutes on the amount of Al leaching were evaluated. It was found that Al leaching into meat increased with increasing temperature, baking time, additives and Al exposure area. Moreover, Al exposure area was more effective than the weight of the meat. The Al leaching was highest in fish and lowest in chicken. Comparing the present results with the Provisional Tolerance Weekly Intake of Al approved by WHO/FDA, it shows that Al leaching into meat baked by wrapping in Al foil may add considerable doses into the diet. Continuous monitoring of Al foil used for baking meat is recommended. 展开更多
关键词 AL FOIL AL LEACHING into MEAT Weight Loss uv-VIS method Provisional Tolerable WEEKLY Intake
暂未订购
Quality Control of Tramadol in Kisangani: Development, Validation, and Application of a UV-Vis Spectroscopic Method 被引量:4
6
作者 Marguerite Borive Amani Jérémie Mbinze Kindenge +4 位作者 Emile Tweni Baruti Elodie Nsasi Bakiantima Salomon Batina Agasa Philippe Hubert Roland Marini Djang’eing’a 《American Journal of Analytical Chemistry》 2021年第8期295-309,共15页
<strong>Context:</strong> Substandard and falsified medicines are circulating in low-income countries mostly without any control. We availed a simple and not expensive UV-Vis spectroscopic method to evalua... <strong>Context:</strong> Substandard and falsified medicines are circulating in low-income countries mostly without any control. We availed a simple and not expensive UV-Vis spectroscopic method to evaluate the quality of tramadol in Kisangani before and during the Covid-19 period. <strong>Methods:</strong> For the analytical quantitative method, an experimental design was applied to set up the optimal levels of the selected factors, namely, pH of dissolution medium, type of cuvette, and wavelength. Taking into account the capsule pharmaceutical formulation within 80 - 120 μg&middotmL<sup>-1</sup> concentration range, we analyzed 89 tramadol samples from pharmacies and hospitals of the six Kisangani municipalities. <strong>Results:</strong> pH showed a significant effect on absorbance, whereas quartz cuvette and wavelength did not. A typical 100 μg&middotmL<sup>-1</sup> tramadol solution gave an absorbance of 0.64 at 272 nm. Validation highlighted a matrix effect observed with a 6% bias. A correction factor of 0.9372 allowed to improve the accuracy profile, which were then totally included within the 10% acceptance limits. Quality control revealed that 25 samples out of 89 were not compliant in terms of manufacturing license, registration status in DRC and content as well. <strong>Conclusion:</strong> This study showed that the strengthening of analytical strategy in Kisangani is a need. 展开更多
关键词 TRAMADOL uv-Vis Spectroscopy method Development VALIDATION Quality Control
暂未订购
Application of Total Error Strategy in Validation of Affordable and Accessible UV-Visible Spectrophotometric Methods for Quality Control of Poor Medicines 被引量:1
7
作者 Jérémie Kindenge Mbinze Jean Nsangu Mpasi +8 位作者 Elza Maghe Sébastien Kobo Rodrigue Mwanda Guy Mulumba Jacquie Bolavie Bolande Trésor Menanzambi Bayebila Maguy Borive Amani Philippe Hubert Roland Djang’eing’a Marini 《American Journal of Analytical Chemistry》 2015年第2期106-117,共12页
In the framework of fighting against the poor quality medicines sold in developing countries using classical analytical methods easily accessible in those countries, four UV-Visible spectrophotometric methods for one ... In the framework of fighting against the poor quality medicines sold in developing countries using classical analytical methods easily accessible in those countries, four UV-Visible spectrophotometric methods for one antimalarial (quinine) and two antibiotics (amoxicillin and metronidazole) have been developed and validated according to the total error strategy using the accuracy profiles as a decision tool. The dosing range was 2 - 10 μg/mL (for quinine sulfate in tablet), 4 - 12 μg/mL (for quinine bichlorhydrate in oral drop-metronidazole benzaote in oral suspension) and 15 - 35 μg/mL (for amoxicillin trihydrate in capsule). The validated methods were then applied in determining the content of some analogous medicines sold in the Democratic Republic of Congo. Thus, the proposed UV-Visible spectrophotometric methods are simple and suitable to quantify quinine, amoxicillin and metronidazole in different pharmaceutical forms. 展开更多
关键词 POOR Quality MEDICINES uv-VISIBLE Spectrophotometric methods QUININE Amoxicillin METRONIDAZOLE VALIDATION Total Error Accuracy Profiles
暂未订购
Development of simple HPLC/UV with a column-switching method for the determination of nicotine and cotinine in hair samples
8
作者 Masayoshi Tsuji Yayoi Mori +7 位作者 Hideyuki Kanda Teruna Ito Tomoo Hidaka Takeyasu Kakamu Tomohiro Kumagai Takehito Hayakawa Yoneatsu Osaki Tetsuhito Fukushima 《Health》 2013年第4期687-694,共8页
Nicotine and cotinine in hair are good biomarkers for assessing long-term exposure to smoking. However, analytical devices such as GC/MS are associated with high cost and are not widely used. HPLC/UV is used widely in... Nicotine and cotinine in hair are good biomarkers for assessing long-term exposure to smoking. However, analytical devices such as GC/MS are associated with high cost and are not widely used. HPLC/UV is used widely in laboratories, but is unsuitable for measurement of minor constituents, except when using the column-switching method. Thus, we aimed to establish a simple, inexpensive and sensitive method based on HPLC/UV with column switching for measuring nicotine and cotinine in hair. First, we compared the presence and absence of a column selection unit. We then measured amounts of nicotine and cotinine in hair samples collected from the general population, and compared both the corresponding levels and the detection limits with those in previous studies. Finally, initial and running costs of HPLC/UV were compared with other analytical methods. As one of the results, the areas of nicotine and cotinine measured by HPLC/UV with column-switching method were 12.9 and 16.9 times greater, respectively, than those without the column-switching method. The amount of nicotine and cotinine in hair was significantly correlated to number of cigarettes smoked per day (r = 0.228, p = 0.040). In addition, the HPLC/UV method showed similar sensitivity and detection limit (nicotine, 0.10 ng/mg;cotinine, 0.08 ng/mg) as reported in previous studies. The cost of the HPLC/UV method is lower than that of other analytical methods. We were able to establish a low-cost method with good sensitivity for measuring nicotine and cotinine in hair. The HPLC/UV with a column-switching method will be useful as a first step in screening surveys in order to better understand the effects of smoking exposure. 展开更多
关键词 HPLC/uv COLUMN-SWITCHING method NICOTINE HAIR COTININE
暂未订购
STUDY ON THE ASSAY QUALITY OF FOOD GRADE GPR BY UV—VIS METHOD
9
作者 刘雄亚 张大厚 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 1993年第2期50-60,共11页
In this paper, the kind of remanent small molecules in unsaturated polyester res(?) (UP resin) , the best extractant and the best suitalbe extractive time for measuring the content of these small molecules were studie... In this paper, the kind of remanent small molecules in unsaturated polyester res(?) (UP resin) , the best extractant and the best suitalbe extractive time for measuring the content of these small molecules were studied using ultraviolet- visible spectrophotometry ( UV-VIS method). According to the principle of additivity lightness absorption for mixid solution, the contents of samll molecules in several kinds of cured UP resin were measured. It is pointed out that the UV-VIS method in the assay quality of food grade GRP products is more suitable to China. 展开更多
关键词 ultraviolet- visible spectrophotometry ( uv- VIS ) method food grade GRP cured UP resin extractant remanent small molecules
在线阅读 下载PDF
Determination of Fenofibrate and the Degradation Product Using Simultaneous UV-Derivative Spectrometric Method and HPLC
10
作者 Fathy M. M. Salamaa Mohamed W. I. Nassar +2 位作者 Mohie M. K. Sharaf El-Din Khalid A. M. Attia Mohamed Yousri Kaddah 《American Journal of Analytical Chemistry》 2011年第3期332-343,共12页
Two new selective, precise, and accurate methods were developed for the determination of fenofibrate in the presence of its basic degradation product. In the first method fenofibrate was determined using an algorithm ... Two new selective, precise, and accurate methods were developed for the determination of fenofibrate in the presence of its basic degradation product. In the first method fenofibrate was determined using an algorithm bivariate calibration derivative method, in which an optimum pair of wavelengths was chosen for the determination of different binary mixtures. In the second method (HPLC), separation was achieved on RESTEK Pinnacle II phenyl column (5 μm, 250 × 4.6 mm) and Pinnacle II phenyl (5 μm, 10 × 4 mm) guard cartridge using a mobile phase consisting of methanol –0.1% phosphoric acid (60:40, v/v) at a flow rate 2 mL●min–1, and the column oven temperature was set at 50°C. The UV detector was time programmed at 302 nm and 289 nm for the internal standard (I.S.) and fenofibrate, respectively. The proposed methods were successfully applied for the determination of fenofibrate and its degradation product in the laboratory-prepared mixture and in pharmaceutical formulation. The assay results obtained using the bivariate method were statistically compared to those of the HPLC method and good agreement was observed. 展开更多
关键词 FENOFIBRATE Stability Degradation Product uv DERIVATIVE Spectrometric method HPLC
在线阅读 下载PDF
Preparation and UV property of size-controlled monodisperse nickel nanoparticles (<10 nm) by reductive method 被引量:1
11
作者 Xiao Guo Feng Zheng +2 位作者 Min Guo Mei Zhang Kuo-Chih Chou 《Rare Metals》 SCIE EI CAS CSCD 2013年第2期179-185,共7页
Nickel nanoparticles (〈10 nm) were success fully synthesized using a reductive method of nickel chloride with sodium borohydride in the ethanol/poly vinylpyrrolidone (PVP) system. The effects of three fac tors, s... Nickel nanoparticles (〈10 nm) were success fully synthesized using a reductive method of nickel chloride with sodium borohydride in the ethanol/poly vinylpyrrolidone (PVP) system. The effects of three fac tors, such as the concentration of the nickel ions, the time of reaction, and the amount of PVP (surfactant), were discussed. The possible growth process of the particles and optimum reactive conditions was also investigated. The result of transmission electron microscopy (TEM) reveals that these nickel nanoparticles are spherical. The average diameter could be controlled as 25 nm under selected conditions. Highresolution TEM and energydispersive spectroscopy results indicates that the nickel nanoparticles are pure. The UVvisible light absorption spectrum shows that the peaks of nickel nanoparticles moves toward the short wavelength along with the decrease of sizes. 展开更多
关键词 Reductive method Nickel nanoparticles Size controllable uv-visible light absorption
在线阅读 下载PDF
Analytical Method Development and Validation of Filgrastim by UV and RP-UFLC Methods 被引量:1
12
作者 Husna Kanwal Qureshi Ciddi Veeresham Chinta Srinivas 《American Journal of Analytical Chemistry》 2021年第10期333-346,共14页
The research work was carried out for establishing a new Ultra Violet (UV)— Visible spectroscopy and Reverse phase-Ultra Fast Liquid Chromatography (RP-UFLC) method for the analysis and quantification of a biosimilar... The research work was carried out for establishing a new Ultra Violet (UV)— Visible spectroscopy and Reverse phase-Ultra Fast Liquid Chromatography (RP-UFLC) method for the analysis and quantification of a biosimilar drug, Filgrastim. Filgrastim or recombinant methionyl granulocyte colony stimulating factor (rGCSF) is a glycoprotein. It has a biological action essential for proliferation and differentiation of hematopoetic and progenitor cells. The UV and RP-UFLC work was carried on a Shimadzu UV1800 Spectrophotometer and Shimadzu Prominence LC-20AD UFLC systems, respectively. The <i>λ</i><sub>max</sub> of filgrastim was found to be 215 nm. The correlation coefficient by UV spectroscopy was found to be 0.9994 for the concentration range of 1 to 3 μg/ml in double distilled water. The Reverse phase UFLC was done by using Phenomenex C4 (25 cm × 0.46 cm internal diameter) 15 μ, 300 A° analytical column. The optimized mobile phase for binary elution was Acetonitrile and double distilled water (80:20) with a flow rate of 1 ml/min. The retention time of drug was at 3.2 min. It was observed that the response of the detector was linear in the range of 5 - 15 μg/ml with correlation coefficient value of 0.999. After developing the methods, it was assured for the intended use by validation of the analytical parameters like linearity, accuracy, precision, limit of detection, limit of quantitation, ruggedness and robustness. The results of all the parameters for both the methods were found to be within the acceptance criteria as per the International Council for Harmonisation (ICH) guidelines. 展开更多
关键词 BIOSIMILARS Filgastim method Development RP-UFLC uv Visible Spectroscopy VALIDATION
暂未订购
采用UV-Vis法建立党参中总皂苷及总黄酮含量测定方法 被引量:1
13
作者 杨超 薛春龙 +3 位作者 张玺雅 王雅婷 段青青 段秀俊 《广州化工》 2025年第13期56-59,70,共5页
建立党参药材中总皂苷与总黄酮的UV-Vis含量测定方法。总皂苷采用香草醛-浓硫酸显色,总黄酮采用硝酸铝显色,单因素结合正交实验优化显色条件,并通过方法学考察进行验证。得出党参总皂苷的最佳显色条件为浓硫酸加入量0.2 mL、显色温度50... 建立党参药材中总皂苷与总黄酮的UV-Vis含量测定方法。总皂苷采用香草醛-浓硫酸显色,总黄酮采用硝酸铝显色,单因素结合正交实验优化显色条件,并通过方法学考察进行验证。得出党参总皂苷的最佳显色条件为浓硫酸加入量0.2 mL、显色温度50℃,显色时间30 min;总黄酮最佳显色条件为加5%NaNO_(2)溶液2.5 mL、10%Al(NO_(3))_(3)溶液2.5 mL、10%NaOH溶液1 mL,显色温度60℃。在上述显色条件下,党参总皂苷与总黄酮的UV-Vis测定方法满足药典分析方法验证指导原则相关规定。本实验建立的UV-Vis法操作简便,显色稳定,准确度高,重复性好,可用于党参中总皂苷与总黄酮的含量测定。 展开更多
关键词 党参 总皂苷 总黄酮 uv-Vis法 含量测定
暂未订购
重铬酸钾法和UV法测污水中COD值的实验分析
14
作者 温娟 《山西化工》 2025年第12期149-150,184,共3页
为更好地对污水中COD值进行检测,实验分析了重铬酸钾法与UV法测定污水中COD值的效果。研究发现:重铬酸钾法测定结果极差为2.43 mg/L,重铬酸钾-UV法测定结果极差为0.19 mg/L,UV法测定结果极差为4.72 mg/L,三种方法对应的RE值依次是0.84%... 为更好地对污水中COD值进行检测,实验分析了重铬酸钾法与UV法测定污水中COD值的效果。研究发现:重铬酸钾法测定结果极差为2.43 mg/L,重铬酸钾-UV法测定结果极差为0.19 mg/L,UV法测定结果极差为4.72 mg/L,三种方法对应的RE值依次是0.84%、0.53%与1.36%。重铬酸钾-UV法的线性范围为0~280 mg/L,UV法的线性范围为0~400 mg/L。三种方法中,重铬酸钾-UV法的测定结果更加精确,且检测周期较短。UV法虽然测定结果精度低,但操作较为简单,检测周期较短,成本相对较低,检测人员可根据实际需求选择检测污水COD值的最佳方法。 展开更多
关键词 重铬酸钾 uv 污水 COD
在线阅读 下载PDF
微波辅助构筑SnO_(2)/rGO复合材料及其UV光的敏感特性
15
作者 崔乐 王博林 +2 位作者 李春 南宁 于灵敏 《西安工业大学学报》 2025年第1期27-34,共8页
由于光生电子-空穴对的快速复合,使得纯SnO_(2)对UV光的敏感性较弱。本文采用微波辅助法成功制备了SnO_(2)/rGO复合材料,并采用悬涂工艺将SnO_(2)/rGO浆料涂覆到叉指电极上,制成厚膜型光敏传感器器件,通过SEM、XRD和Raman分析了样品的... 由于光生电子-空穴对的快速复合,使得纯SnO_(2)对UV光的敏感性较弱。本文采用微波辅助法成功制备了SnO_(2)/rGO复合材料,并采用悬涂工艺将SnO_(2)/rGO浆料涂覆到叉指电极上,制成厚膜型光敏传感器器件,通过SEM、XRD和Raman分析了样品的形貌、物相及缺陷类型,并研究其对紫外(UV)光的敏感特性。结果表明:rGO较为均匀地分布在SnO_(2)颗粒之间,有效抑制了SnO_(2)纳米颗粒的团聚,同时SnO_(2)/rGO复合材料中的空位缺陷增多。随着工作温度的升高或UV光强度的降低,其响应值均减小。较纯SnO_(2),SnO_(2)/rGO复合纳米材料对UV光的响应值提高了153.39%,响应时间由51 s缩短至28 s。SnO_(2)/rGO复合材料对UV光响应的增强是基于样品中空位缺陷浓度的增大以及rGO对SnO_(2)能级的改变和提供的载流子传输通道。 展开更多
关键词 SnO_(2)/rGO复合材料 微波辅助法 光敏性能 uv 响应值
在线阅读 下载PDF
被动采样-UV法测定环境空气中的臭氧浓度 被引量:5
16
作者 汤灿 曾清如 +2 位作者 蒋朝晖 周细红 钟宁 《安全与环境学报》 CAS CSCD 2004年第4期13-16,共4页
研究被动采样 -UV法测定臭氧浓度。以 Na NO2 作为诱捕试剂 ,用被动采样器吸收 O3,然后在紫外分光光度计上进行测定。通过测定所生成的 NO- 3浓度 ,间接计算出臭氧浓度。结果表明 ,测得臭氧浓度范围在 2 0~ 10 0 μg/m3,NO- 3浓度线性... 研究被动采样 -UV法测定臭氧浓度。以 Na NO2 作为诱捕试剂 ,用被动采样器吸收 O3,然后在紫外分光光度计上进行测定。通过测定所生成的 NO- 3浓度 ,间接计算出臭氧浓度。结果表明 ,测得臭氧浓度范围在 2 0~ 10 0 μg/m3,NO- 3浓度线性范围在 0~ 0 .6mmol/L。在测定 NO- 3浓度时 ,NO- 2 会造成很大的干扰 ,但在实验中 ,NO- 2 浓度在 0~ 0 .8mmol/L,氨基磺酸都能有效地去除其干扰。该方法是简单、灵敏。 展开更多
关键词 环境工程 被动采样-uv 臭氧 硝酸根离子 亚硝酸根离子
在线阅读 下载PDF
HPLC-UV法测定人血浆中替考拉宁药物浓度的方法学研究及其临床应用 被引量:3
17
作者 王彦改 沈芊 +3 位作者 苏甦 王雪梅 姜德春 闫素英 《中国药物应用与监测》 CAS 2020年第4期226-230,共5页
目的:建立测定人血浆中替考拉宁浓度的高效液相色谱-紫外检测(HPLC-UV)法,为临床个体化给药提供依据。方法:以哌拉西林钠为内标,将400μL血浆样本采用600μL乙腈沉淀蛋白后,再用二氯甲烷萃取,采用HPLC测定,色谱柱为kromasil柱(150 mm... 目的:建立测定人血浆中替考拉宁浓度的高效液相色谱-紫外检测(HPLC-UV)法,为临床个体化给药提供依据。方法:以哌拉西林钠为内标,将400μL血浆样本采用600μL乙腈沉淀蛋白后,再用二氯甲烷萃取,采用HPLC测定,色谱柱为kromasil柱(150 mm×4.6 mm,5μm),流动相为水(含0.01 mol·L-1磷酸二氢钾,用磷酸调pH至2.84)-乙腈(75∶25,v/v),流速1.0 mL·min^-1,柱温35℃,进样量20μL,检测波长为240 nm。结果:替考拉宁在3.12~100.00μg·mL-1范围内线性关系良好(R2=0.9999),定量下限为3.12μg·mL-1;日内、日间精密度的RSD为0.39%~8.54%,相对偏差为–7.19%~7.00%。血浆样品在经历3次冻融(–20℃到室温)循环、4℃放置6 d和冷冻(–40℃)放置21 d等条件下均稳定,处理后样品在自动进样器中(4℃)放置24 h均稳定(RSD<15%)。测定9例应用替考拉宁患者的血药浓度,仅有2例在有效血药浓度范围。结论:该法操作简便、灵敏、准确,适用于替考拉宁血药浓度的测定。 展开更多
关键词 替考拉宁 HPLC-uv 方法学评价 血药浓度监测 临床应用
暂未订购
HPLC-UV测定人血清中伏立康唑药物浓度的方法学研究及其临床应用 被引量:2
18
作者 王彦改 沈芊 +1 位作者 王雪梅 闫素英 《中国药学杂志》 CAS CSCD 北大核心 2023年第12期1117-1122,共6页
目的建立测定人血清中伏立康唑(voriconazole,VRCZ)浓度的高效液相色谱-紫外检测(HPLC-UV)方法。方法200μL血清样本采用400μL二氯甲烷萃取,采用HPLC测定,以硝西泮为内标,色谱柱为kromasil(4.6 mm×150 mm,5μm),流动相为水-乙腈(... 目的建立测定人血清中伏立康唑(voriconazole,VRCZ)浓度的高效液相色谱-紫外检测(HPLC-UV)方法。方法200μL血清样本采用400μL二氯甲烷萃取,采用HPLC测定,以硝西泮为内标,色谱柱为kromasil(4.6 mm×150 mm,5μm),流动相为水-乙腈(体积比60∶40),流速1.0 mL·min^(-1),柱温35℃,进样量20μL,检测波长为254 nm。结果VRCZ在0.2~16μg·mL^(-1)内线性关系良好(Y=0.073X+0.0019,r=0.9992),定量下限(LLOQ)为0.2μg·mL^(-1);日内、日间精密度为1.23%~5.51%,准确度为88.5%~102.36%,提取回收率为92.0%~106.5%,RSD<15%。血清样品在经历3次冻融(-20℃到室温)循环、冷藏放置2周和冷冻放置30 d等条件下均稳定,处理后样品在室温和自动进样器中(4℃)各放置24 h均稳定(RSD<15%),VRCZ储备液于-20℃和工作液于4℃放置10个月,内标储备液于-20℃放置1.5个月稳定(RSD<15%)。测定9个临床样本,范围在0.81~7.96μg·mL^(-1)之间,结论该法操作简便、灵敏、准确,适用于VRCZ血药浓度的测定。 展开更多
关键词 伏立康唑 高效液相色谱-紫外检测法 方法学评价 人血清药物浓度
原文传递
HPLC-UV法用于人血浆中罗红霉素的浓度测定及药代动力学和生物等效性研究 被引量:2
19
作者 张娟 张红 +3 位作者 隋双明 刘建明 王萍 熊玉卿 《实用临床医学(江西)》 CAS 2009年第6期4-7,共4页
目的建立HPLC-UV法测定人血浆中罗红霉素的方法,并探讨罗红霉素的药代动力学和生物等效性。方法采用Diamonsil C18柱(150mm×4.6mm,5μm),流动相为乙腈:0.01mool磷酸二氢铵=39:61(v/v),流速1mL/min;以卡马西平为内... 目的建立HPLC-UV法测定人血浆中罗红霉素的方法,并探讨罗红霉素的药代动力学和生物等效性。方法采用Diamonsil C18柱(150mm×4.6mm,5μm),流动相为乙腈:0.01mool磷酸二氢铵=39:61(v/v),流速1mL/min;以卡马西平为内标,检测波长为210nm。血浆样品用正己烷(含5%的异丙醇)液-液萃取后经C18分离。结果罗红霉素在0.25~16.0mg/L线性关系良好,r=0.999,最低检测限为0.25mg/L。萃取回收率〉70%,方法回收率99.8%~110.5%,批内、批间精密度均〈15%。结论HPLC—UV方法结果准确、灵敏度高,适用于罗红霉素药代动力学和生物等效性研究。 展开更多
关键词 罗红霉素 HPLC-uv 生物等效性 药代动力学
暂未订购
UV固化有机硅/SiO_2杂化涂料的制备及性能 被引量:10
20
作者 林金娜 侯有军 曾幸荣 《华南理工大学学报(自然科学版)》 EI CAS CSCD 北大核心 2007年第6期76-80,共5页
以正硅酸乙酯和常用的有机硅为原料,采用溶胶-凝胶法制备了可紫外光(UV)固化的有机硅/SiO2杂化涂料.研究了有机硅用量对杂化漆膜性能的影响,并用FTIR和固体29Si-NMR对杂化涂料进行了表征,测定了UV固化C C的转化率和硅氧烷的缩聚度.结果... 以正硅酸乙酯和常用的有机硅为原料,采用溶胶-凝胶法制备了可紫外光(UV)固化的有机硅/SiO2杂化涂料.研究了有机硅用量对杂化漆膜性能的影响,并用FTIR和固体29Si-NMR对杂化涂料进行了表征,测定了UV固化C C的转化率和硅氧烷的缩聚度.结果表明:杂化涂料的有机与无机网络间以共价键的方式结合,在UV固化240 s时双键转化率可达81.0%,硅氧烷的平均缩聚度为89.5%;由于采用了改进的溶胶-凝胶法,在高度交联的SiO2网络结构中引入线性Si O Si链段,使得漆膜既有高硬度又有良好的柔韧性,当TEOS/MPTMS/DDS摩尔比为6∶2∶3时膜的综合性能最佳. 展开更多
关键词 有机硅 杂化涂料 溶胶-凝胶法 uv固化
在线阅读 下载PDF
上一页 1 2 50 下一页 到第
使用帮助 返回顶部