Статті в журналах з теми "Sulfamerazine"
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Chuang, Li Chin, Chin Hsiang Luo, and Sing Wei Huang. "Degradation Mechanism of Aqueous Sulfamerazine by AOPs of O3 and UV/TiO2." Advanced Materials Research 396-398 (November 2011): 772–75. http://dx.doi.org/10.4028/www.scientific.net/amr.396-398.772.
Повний текст джерелаChen, Lei, Yean Kee Lee, Yanawut Manmana, Kheng Soo Tay, Vannajan Sanghiran Lee, and Noorsaadah Abd Rahman. "Synthesis, characterization, and theoretical study of an acrylamide-based magnetic molecularly imprinted polymer for the recognition of sulfonamide drugs." e-Polymers 15, no. 3 (May 1, 2015): 141–50. http://dx.doi.org/10.1515/epoly-2015-0017.
Повний текст джерелаMalla, Avirup, Koel Mukherjee, Mukulika Mandal, Aishwarya Mukherjee, Runa Sur, and Suvroma Gupta. "An Insight to the Toxic Effect of Sulfamerazine on Porcine Pancreatic Amylase and Lactate Dehydrogenase Activity: An In Vitro Study." Current Chemical Biology 15, no. 2 (August 9, 2021): 171–81. http://dx.doi.org/10.2174/2212796815666210216101221.
Повний текст джерелаHossain, G. M. Golzar. "A new polymorph of sulfamerazine." Acta Crystallographica Section E Structure Reports Online 62, no. 6 (May 5, 2006): o2166—o2167. http://dx.doi.org/10.1107/s1600536806014449.
Повний текст джерелаYao, Youru, Na Mi, Yongqing Zhu, Li Yin, Yong Zhang, and Shiyin Li. "Efficient removal of sulfamerazine (SMR) by ozonation in acetic acid solution after enrichment SMR from water using granular activated carbon." RSC Advances 9, no. 16 (2019): 9145–52. http://dx.doi.org/10.1039/c8ra10429h.
Повний текст джерелаZhang, Geoff G. Z., Chonghui Gu, Mark T. Zell, R. Todd Burkhardt, Eric J. Munson, and David J. W. Grant. "Crystallization and Transitions of Sulfamerazine Polymorphs." Journal of Pharmaceutical Sciences 91, no. 4 (April 2002): 1089–100. http://dx.doi.org/10.1002/jps.10100.
Повний текст джерелаSmallidge, Robert L., Elzbieta J. Kentzer, Kelly R. Stringham, Eun H. Kim, Connie Lehe, Rodger W. Stringham, and Elizabeth C. Mundell. "Sulfamethazine and Sulfathiazole Determination at Residue Levels in Swine Feeds by Reverse-Phase Liquid Chromatography with Post-Column Derivatization." Journal of AOAC INTERNATIONAL 71, no. 4 (July 1, 1988): 710–17. http://dx.doi.org/10.1093/jaoac/71.4.710.
Повний текст джерелаVosough, Maryam, Mahdieh Nazari Onilghi, and Amir Salemi. "Optimization of matrix solid-phase dispersion coupled with high performance liquid chromatography for determination of selected antibiotics in municipal sewage sludge." Analytical Methods 8, no. 24 (2016): 4853–60. http://dx.doi.org/10.1039/c6ay00112b.
Повний текст джерелаDeng, Fengxia, Jinyu Xie, Orlando Garcia-Rodriguez, Baojian Jing, Yingshi Zhu, Zhonglin Chen, Jyh-Ping Hsu, Jizhou Jiang, Shunwen Bai, and Shan Qiu. "Correction: A dynamic anode boosting sulfamerazine mineralization via electrochemical oxidation." Journal of Materials Chemistry A 10, no. 4 (2022): 2133. http://dx.doi.org/10.1039/d1ta90273c.
Повний текст джерелаLiu, Chengxiang, Fengjuan Cao, Samir A. Kulkarni, Geoffrey P. F. Wood, and Erik E. Santiso. "Understanding Polymorph Selection of Sulfamerazine in Solution." Crystal Growth & Design 19, no. 12 (October 9, 2019): 6925–34. http://dx.doi.org/10.1021/acs.cgd.9b00576.
Повний текст джерелаKurotani, Masahiro, and Izumi Hirasawa. "Polymorph control of sulfamerazine by ultrasonic irradiation." Journal of Crystal Growth 310, no. 21 (October 2008): 4576–80. http://dx.doi.org/10.1016/j.jcrysgro.2008.08.002.
Повний текст джерелаLiu, Lingling, and Tao Zhu. "Emulsification liquid–liquid microextraction based on deep eutectic solvents: an extraction method for the determination of sulfonamides in water samples." Analytical Methods 9, no. 32 (2017): 4747–53. http://dx.doi.org/10.1039/c7ay01332a.
Повний текст джерелаLiang, Xiujuan, Dan Liu, Jingjing Zhou, Yuling Zhang, and Wenjing Zhang. "Effects of colloidal humic acid on the transport of sulfa antibiotics through a saturated porous medium under different hydrochemical conditions." Water Supply 18, no. 6 (February 20, 2018): 2199–207. http://dx.doi.org/10.2166/ws.2018.042.
Повний текст джерелаLee, Sun, Areum Choi, Woo-Sik Kim, and Allan S. Myerson. "Phase Transformation of Sulfamerazine Using a Taylor Vortex." Crystal Growth & Design 11, no. 11 (November 2, 2011): 5019–29. http://dx.doi.org/10.1021/cg200925v.
Повний текст джерелаLu, Jie, Yi-Ping Li, Jing Wang, Zhen Li, Sohrab Rohani, and Chi-Bun Ching. "Pharmaceutical cocrystals: a comparison of sulfamerazine with sulfamethazine." Journal of Crystal Growth 335, no. 1 (November 2011): 110–14. http://dx.doi.org/10.1016/j.jcrysgro.2011.09.032.
Повний текст джерелаAitipamula, Srinivasulu, Pui Shan Chow, and Reginald B. H. Tan. "The solvates of sulfamerazine: structural, thermochemical, and desolvation studies." CrystEngComm 14, no. 2 (2012): 691–99. http://dx.doi.org/10.1039/c1ce06095c.
Повний текст джерелаTalib Humeidy, Israa. "Spectrophotometric method for Determination of sulfamerazine Using 2,4-dinitrophenylhydrazineReagent." Journal of Physics: Conference Series 1294 (September 2019): 052022. http://dx.doi.org/10.1088/1742-6596/1294/5/052022.
Повний текст джерелаKawakami, Kohsaku, Yasuo Asami, and Itsuro Takenoshita. "Calorimetric investigation of solvent-mediated transformation of sulfamerazine polymorphism." Journal of Pharmaceutical Sciences 99, no. 1 (January 2010): 76–81. http://dx.doi.org/10.1002/jps.21837.
Повний текст джерелаDeng, Fengxia, Jinyu Xie, Orlando Garcia-Rodriguez, Baojian Jing, Yingshi Zhu, Zhonglin Chen, Jyh-Ping Hsu, Jizhou Jiang, Shunwen Bai, and Shan Qiu. "A dynamic anode boosting sulfamerazine mineralization via electrochemical oxidation." Journal of Materials Chemistry A 10, no. 1 (2022): 192–208. http://dx.doi.org/10.1039/d1ta08095d.
Повний текст джерелаQin, Shili, Fenglong Jin, Lidi Gao, Liqiang Su, Yingjie Li, Shuang Han, and Peng Wang. "Determination of sulfamerazine in aquatic products by molecularly imprinted capillary electrochromatography." Royal Society Open Science 6, no. 6 (June 2019): 190119. http://dx.doi.org/10.1098/rsos.190119.
Повний текст джерелаGarden, Scott W., and Peter Sporns. "Development and Evaluation of an Enzyme Immunoassay for Sulfamerazine in Milk." Journal of Agricultural and Food Chemistry 42, no. 6 (June 1994): 1379–91. http://dx.doi.org/10.1021/jf00042a026.
Повний текст джерелаHossain, G. M. Golzar, A. J. Amoroso, A. Banu, and K. M. A. Malik. "Syntheses and characterisation of mercury complexes of sulfadiazine, sulfamerazine and sulfamethazine." Polyhedron 26, no. 5 (March 2007): 967–74. http://dx.doi.org/10.1016/j.poly.2006.09.056.
Повний текст джерелаDelgado, Daniel R., and Fleming Martínez. "Solution Thermodynamics and Preferential Solvation of Sulfamerazine in Methanol + Water Mixtures." Journal of Solution Chemistry 44, no. 2 (February 2015): 360–77. http://dx.doi.org/10.1007/s10953-015-0317-1.
Повний текст джерелаKurotani, Masahiro, and Izumi Hirasawa. "Effect of ultrasonic irradiation on the selective polymorph control in sulfamerazine." Chemical Engineering Research and Design 88, no. 9 (September 2010): 1272–78. http://dx.doi.org/10.1016/j.cherd.2010.02.014.
Повний текст джерелаGu, Chong-Hui, Koustuv Chatterjee, Victor Young, and David J. W. Grant. "Stabilization of a metastable polymorph of sulfamerazine by structurally related additives." Journal of Crystal Growth 235, no. 1-4 (February 2002): 471–81. http://dx.doi.org/10.1016/s0022-0248(01)01784-5.
Повний текст джерелаGoyal, R. N., N. C. Mathur, and S. Bhargava. "Mechanism of electrochemical oxidation of sulfamerazine at a pyrolytic graphite electrode." Electroanalysis 2, no. 1 (January 1990): 57–62. http://dx.doi.org/10.1002/elan.1140020111.
Повний текст джерелаLiu, Xinghao, Wenxiu Zhu, Zhaoguang Yang, Ying Yang, and Haipu Li. "Efficient ozone catalysis by manganese iron oxides/activated carbon for sulfamerazine degradation." Journal of Water Process Engineering 49 (October 2022): 103050. http://dx.doi.org/10.1016/j.jwpe.2022.103050.
Повний текст джерелаZhuang, Xiaoxuan, Xing Li, Yanling Yang, Nan Wang, Yi Shang, Zhiwei Zhou, Jiaqi Li, and Huiping Wang. "Enhanced Sulfamerazine Removal via Adsorption–Photocatalysis Using Bi2O3–TiO2/PAC Ternary Nanoparticles." Water 12, no. 8 (August 13, 2020): 2273. http://dx.doi.org/10.3390/w12082273.
Повний текст джерелаAday, Burak, Pınar Sola, Ferdağ Çolak, and Muharrem Kaya. "Synthesis of novel sulfonamide analogs containing sulfamerazine/sulfaguanidine and their biological activities." Journal of Enzyme Inhibition and Medicinal Chemistry 31, no. 6 (August 31, 2015): 1005–10. http://dx.doi.org/10.3109/14756366.2015.1079183.
Повний текст джерелаDatta, Sharmistha, and David J. W. Grant. "Computing the Relative Nucleation Rate of Phenylbutazone and Sulfamerazine in Various Solvents." Crystal Growth & Design 5, no. 4 (July 2005): 1351–57. http://dx.doi.org/10.1021/cg0342462.
Повний текст джерелаRuss Christenson, W., Vijayapal R. Reddy, and Walter N. Piper. "Reversal of sulfamerazine inhibition of rat hepatic uroporphyrinogen synthesis by folic acid." Life Sciences 38, no. 18 (May 1986): 1679–84. http://dx.doi.org/10.1016/0024-3205(86)90412-1.
Повний текст джерелаZhuang, Shuting, Yong Liu, and Jianlong Wang. "Covalent organic frameworks as efficient adsorbent for sulfamerazine removal from aqueous solution." Journal of Hazardous Materials 383 (February 2020): 121126. http://dx.doi.org/10.1016/j.jhazmat.2019.121126.
Повний текст джерелаEsrafili, Mehdi D., Hadi Behzadi, Javad Beheshtian, and Nasser L. Hadipour. "Theoretical 14N nuclear quadrupole resonance parameters for sulfa drugs: Sulfamerazine and sulfathiazole." Journal of Molecular Graphics and Modelling 27, no. 3 (October 2008): 326–31. http://dx.doi.org/10.1016/j.jmgm.2008.05.007.
Повний текст джерелаOthman, Rasha M., Wasfi A. Al-Masoudi, Adil A. Hama, and Sara M. Hussain. "Antimicrobial Activity and Molecular Modeling Study of Schiff Base Derived from Sulfamerazine." Indian Journal of Forensic Medicine & Toxicology 13, no. 4 (2019): 694. http://dx.doi.org/10.5958/0973-9130.2019.00374.8.
Повний текст джерелаMacfhionnghaile, Pól, Yun Hu, Katarzyna Gniado, Sinead Curran, Patrick Mcardle, and Andrea Erxleben. "Effects of Ball-Milling and Cryomilling on Sulfamerazine Polymorphs: A Quantitative Study." Journal of Pharmaceutical Sciences 103, no. 6 (June 2014): 1766–78. http://dx.doi.org/10.1002/jps.23978.
Повний текст джерелаHossain, G. M. Golzar, та A. J. Amoroso. "Bis[4-amino-N-(4-methylpyrimidin-2-yl-κN3)benzenesulfonamidato-κN](2,2′-bipyridine-κ2N,N′)mercury(II)". Acta Crystallographica Section E Structure Reports Online 70, № 4 (8 березня 2014): m127—m128. http://dx.doi.org/10.1107/s1600536814004760.
Повний текст джерелаDelgado, Daniel R., María Á. Peña, and Fleming Martínez. "Extended Hildebrand solubility approach applied to some structurally related sulfonamides in ethanol + water mixtures." Revista Colombiana de Química 45, no. 1 (August 11, 2016): 34. http://dx.doi.org/10.15446/rev.colomb.quim.v45n1.57201.
Повний текст джерелаNose, Norihide, Youji Hoshino, Yoshinori Kikuchi, Masakazu Horie, Kouichi Saitoh, Takashi Kawachi, and Hiroyuki Nakazawa. "Simultaneous Liquid Chromatographic Determination of Residual Synthetic Antibacterials in Cultured Fish." Journal of AOAC INTERNATIONAL 70, no. 4 (July 1, 1987): 714–17. http://dx.doi.org/10.1093/jaoac/70.4.714.
Повний текст джерелаde Moraes, Nicolas Perciani, Robson da Silva Rocha, Abner de Siervo, Caio César Achiles do Prado, Teresa Cristina Brazil de Paiva, Tiago Moreira Bastos Campos, Gilmar Patrocinio Thim, Marcos Roberto de Vasconcelos Lanza, and Liana Alvares Rodrigues. "Resorcinol-based carbon xerogel/ZnO composite for solar-light-induced photodegradation of sulfamerazine." Optical Materials 128 (June 2022): 112470. http://dx.doi.org/10.1016/j.optmat.2022.112470.
Повний текст джерелаWang, Bingqing, Tao Fu, Baohua An, and Yong Liu. "UV light-assisted persulfate activation by Cu0-Cu2O for the degradation of sulfamerazine." Separation and Purification Technology 251 (November 2020): 117321. http://dx.doi.org/10.1016/j.seppur.2020.117321.
Повний текст джерелаAloisio, Carolina, Anselmo Gomes de Oliveira, and Marcela Longhi. "Solubility and release modulation effect of sulfamerazine ternary complexes with cyclodextrins and meglumine." Journal of Pharmaceutical and Biomedical Analysis 100 (November 2014): 64–73. http://dx.doi.org/10.1016/j.jpba.2014.07.008.
Повний текст джерелаPark, Sun-Ah, Sun Lee, and Woo-Sik Kim. "Polymorphic Crystallization of Sulfamerazine in Taylor Vortex Flow: Polymorphic Nucleation and Phase Transformation." Crystal Growth & Design 15, no. 8 (July 10, 2015): 3617–27. http://dx.doi.org/10.1021/acs.cgd.5b00002.
Повний текст джерелаDelgado, Daniel R., and Fleming Martínez. "Solubility and solution thermodynamics of sulfamerazine and sulfamethazine in some ethanol+water mixtures." Fluid Phase Equilibria 360 (December 2013): 88–96. http://dx.doi.org/10.1016/j.fluid.2013.09.018.
Повний текст джерелаBarnabas, Mary Jenisha, Surendran Parambadath, Saravanan Nagappan, and Chang-Sik Ha. "Sulfamerazine Schiff-base complex intercalated layered double hydroxide: synthesis, characterization, and antimicrobial activity." Heliyon 5, no. 4 (April 2019): e01521. http://dx.doi.org/10.1016/j.heliyon.2019.e01521.
Повний текст джерелаQiao, Feng Xia, and Meng Ge Wang. "Synthesis of RAFT Molecularly Imprinting Polymer Based on Ionic Liquid." Advanced Materials Research 668 (March 2013): 246–49. http://dx.doi.org/10.4028/www.scientific.net/amr.668.246.
Повний текст джерелаLi, Bingyu, Cun Li, Haiyang Jiang, Zhahnui Wang, Xingyuan Cao, Sijun Zhao, Suxia Zhang, and Jianzhong Shen. "Purification of Nine Sulfonamides from Chicken Tissues by Immunoaffinity Chromatography Using Two Monoclonal Antibodies." Journal of AOAC INTERNATIONAL 91, no. 6 (November 1, 2008): 1488–93. http://dx.doi.org/10.1093/jaoac/91.6.1488.
Повний текст джерелаReimer, Gerry J., and Agripina Suarez. "Liquid Chromatographic Confirmatory Method for Five Sulfonamides in Salmon Muscle Tissue by Matrix Solid-Phase Dispersion." Journal of AOAC INTERNATIONAL 75, no. 6 (November 1, 1992): 979–81. http://dx.doi.org/10.1093/jaoac/75.6.979.
Повний текст джерелаMooser, Andrê E., and Herbert Koch. "Confirmatory Method for Sulfonamide Residues in Animal Tissues by Gas Chromatography and Pulsed Positive Ion-Negative Ion-Chemical Ionization Mass Spectrometry." Journal of AOAC INTERNATIONAL 76, no. 5 (September 1, 1993): 976–82. http://dx.doi.org/10.1093/jaoac/76.5.976.
Повний текст джерелаBeigizadeh, Hana, Mohammad Reza Ganjali, and Parviz Norouzi. "Voltammetric Sensors Based on Various Nanomaterials for the Determination of Sulfonamides." Current Analytical Chemistry 15, no. 2 (February 19, 2019): 124–30. http://dx.doi.org/10.2174/1573411014666180313114313.
Повний текст джерелаBui, Lap V. "Liquid Chromatographic Determination of Six Sulfonamide Residues in Animal Tissues Using Postcolumn Derivatization." Journal of AOAC INTERNATIONAL 76, no. 5 (September 1, 1993): 966–76. http://dx.doi.org/10.1093/jaoac/76.5.966.
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