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Journal articles on the topic 'Carbinoxamina'

Author: Grafiati

Published: 4 June 2021

Last updated: 17 February 2022

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1

El-Masry, Soha M., and Rasha M. El-Morsi. "Simple HPLC Method for Quantitative Determination of Carbinoxamine in Human Plasma: Application in Pharmacokinetic Studies and Therapeutic Drug Monitoring." Drug Research 69, no. 06 (2019): 342–47. http://dx.doi.org/10.1055/a-0787-1302.

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AbstractA sensitive, specific and cost-effective HPLC method was developed for quantitative determination of carbinoxamine in human plasma using liquid chromatography with ultraviolet detection. A simple liquid–liquid extraction by ethyl acetate was used to extract carbinoxamine from human plasma. Satisfactory separation was achieved by a mobile phase consisting of 20 mM ammonium dihydrogen orthophosphate containing 0.01% triethyl amine (pH adjusted to 3 by using phosphoric acid) and acetonitrile in ratio of (75:25, v/v) at a flow rate of 0.9 mL/min on Hypersil® BDS C18 column (250×4.6 mm, 5 μ

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2

Ault, Alicia. "Carbinoxamine Products Targeted." Family Practice News 36, no. 14 (2006): 60. http://dx.doi.org/10.1016/s0300-7073(06)73554-x.

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3

Aly, Fatma Ahmed, Nahed EL-Enany, Heba Elmansi, and Amany Nabil. "A fast spectrofluorimetric method for determination of carbinoxamine maleate in the nano-molar range. Application to pharmaceutical preparations, biological fluids and stability studies." Analytical Methods 10, no. 31 (2018): 3851–58. http://dx.doi.org/10.1039/c8ay01202d.

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Carbinoxamine maleate (CBX), which is a common ingredient of cold and cough treatment preparations, is determined by a sensitive, simple and convenient spectrofluorimetric method in its pure form, pharmaceutical preparations and spiked human plasma.

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4

Cockrell, Janice L. "Acute Hallucinogenic Reaction to Carbinoxamine Maleate." Journal of Toxicology: Clinical Toxicology 25, no. 1-2 (1987): 161–67. http://dx.doi.org/10.3109/15563658708992621.

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5

AULT, ALICIA. "FDA Demands Approval Data on Carbinoxamine." Pediatric News 40, no. 7 (2006): 50. http://dx.doi.org/10.1016/s0031-398x(06)71185-7.

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6

Abbirami, E., та M. Selvakumar. "Identification of Novel Drug-Like Compounds from Momordica cymbalaria as PPAR-γ Agonists: A Molecular Docking Study". Asian Journal of Engineering and Applied Technology 8, № 2 (2019): 71–74. http://dx.doi.org/10.51983/ajeat-2019.8.2.1135.

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Peroxisome Proliferator-Activated Receptor – γ (PPARγ) is a ligand-activated transcription factor, has become a main target for the treatment of diabetes. It is a member of the nuclear receptor superfamily that regulate the gene expression of proteins involved in glucose, lipid metabolism, adipocyte proliferation and differentiation and insulin sensitivity. Thiazolidinediones (TZDs) are one important class of synthetic agonists of PPAR-γ. TZDs are antidiabetic agents that target adipose tissue and improve insulin sensitivity, and they are currently being used in the treatment of type 2 diabete

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7

Yen, Yao-Te, Yin-Jue Chang, Pin-Jung Lai, Chi-Lun Chang, Ting-Yueh Chen, and San-Chong Chyueh. "A Study of Opiate, Opiate Metabolites and Antihistamines in Urine after Consumption of Cold Syrups by LC-MS/MS." Molecules 25, no. 4 (2020): 972. http://dx.doi.org/10.3390/molecules25040972.

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Studying the origin of opiate and/or opiate metabolites in individual urine specimens after consumption of cold syrups is vital for patients, doctors, and law enforcement. A rapid liquid chromatography–tandem mass spectrometry method using “dilute-and-shoot” analysis without the need for extraction, hydrolysis and/or derivatization has been developed and validated. The approach provides linear ranges of 2.5–1000 ng mL−1 for 6-acetylmorphine, codeine, chlorpheniramine, and carbinoxamine, 2.5–800 ng mL−1 for morphine and morphine-3-β-d-glucuronide, and 2.5–600 ng mL−1 for morphine-6-β-d-glucuron

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8

&NA;. "Abbreviated New Drug Application approved for carbinoxamine in US." Inpharma Weekly &NA;, no. 1628 (2008): 17. http://dx.doi.org/10.2165/00128413-200816280-00072.

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9

Mansour, Ali M. "Determination of Pseudoephedrine Hydrochloride and Carbinoxamine Maleate in Combination Drug Formulation by Liquid Chromatography." Journal of AOAC INTERNATIONAL 81, no. 5 (1998): 958–62. http://dx.doi.org/10.1093/jaoac/81.5.958.

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Abstract An isocratic, reversed-phase liquid chromatographic (LC) method was developed for simultaneous determination of pseudoephedrine hydrochloride (I) and carbinoxamine maleate (II) in a pharmaceutical dosage form. Analysis was conducted on a CN column (10μm), with a mobile phase consisting of acetonitrile-methanol-phosphate buffer (pH 5.3)-water (140 + 170 + 40 + 100) and at a detection wavelength of 262 nm. The method was validated for linearity, precision, system reproducibility, and accuracy. Recoveries at 80-120% of labeled claim ranged from 97.4 to 100.7% and from 98.5 to 100.2% for

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10

Bhavani, B. Geeta, B. M. Gurupadayya, and S. Sharfuddin. "LC-MS/MS method for the quantification of carbinoxamine in human plasma." IOSR Journal of Applied Chemistry 6, no. 6 (2014): 46–51. http://dx.doi.org/10.9790/5736-0664651.

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11

Tang, Yi-Fen, Hsin-Lung Wu, Shou-Mei Wu, Su-Hwei Chen, and Hwang-Shang Kou. "Quantitative chiral analysis of carbinoxamine, doxylamine, and orphenadrine by capillary zone electrophoresis." Journal of Microcolumn Separations 12, no. 6 (2000): 366–70. http://dx.doi.org/10.1002/1520-667x(2000)12:6<366::aid-mcs5>3.0.co;2-c.

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12

Corey, E. J., and Christopher J. Helal. "Asymmetric synthesis of (S)-carbinoxamine. New aspects of oxazaborolidine-catalyzed enantioselective carbonyl reduction." Tetrahedron Letters 37, no. 32 (1996): 5675–78. http://dx.doi.org/10.1016/0040-4039(96)01198-7.

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13

Ioutsi, Anna, Elena Shapovalova, Aleksandra Prokhorova, and Oleg Shpigun. "Layer-by-Layer Assembly of Polysaccharides and 6,10-Ionene for Separation of Nitrogen-Containing Pharmaceuticals and Their Enantiorecognition by Capillary Electrophoresis." Journal of Chemistry 2015 (2015): 1–9. http://dx.doi.org/10.1155/2015/836076.

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Two silica capillaries modified layer-by-layer with 6,10-ionene and N-(3-sulfo-3-carboxy)-propionylchitosan (SCPC) and with 6,10-ionene and dextran sulfate (DS) were prepared and investigated. Dynamic coating of the capillary efficiently reduces the adsorption of the background electrolyte, sample matrix components, and analytes on its inner wall. Such coatings effect good reproducibility and sensitivity of determination. We demonstrate that separation of betablockers, calcium channel blockers, alpha-adrenergic agonists, H1-blockers, and diuretics was the most efficient and rapid separation wi

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14

Bastos, Carina de A., and Marcone A. L. de Oliveira. "Quantitative determination of acetaminophen, phenylephrine and carbinoxamine in tablets by high-performance liquid chromatography." Química Nova 32, no. 7 (2009): 1951–55. http://dx.doi.org/10.1590/s0100-40422009000700044.

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15

Gil-Agustí, Mayte, Llorenç Monferrer-Pons, Josep Esteve-Romero, and María Celia García-Alvarez-Coque. "Quantitation of Antihistamines in Pharmaceutical Preparations by Liquid Chromatography with a Micellar Mobile Phase of Sodium Dodecyl Sulfate and Pentanol." Journal of AOAC INTERNATIONAL 84, no. 6 (2001): 1687–94. http://dx.doi.org/10.1093/jaoac/84.6.1687.

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Abstract A reversed-phase liquid chromatographic procedure with a micellar mobile phase of sodium dodecyl sulfate (SDS), containing a small amount of pentanol, was developed for the control of 7 antihistamines of diverse action in pharmaceutical preparations (tablets, capsules, powders, solutions, and syrups): azatadine, carbinoxamine, cyclizine, cyproheptadine, diphenhydramine, doxylamine, and tripelennamine. The retention times of the drugs were &lt;9 min with a mobile phase of 0.15M SDS–6% (v/v) pentanol. The recoveries with respect to the declared compositions were in the range of 93–1

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16

COREY, E. J., and C. J. HELAL. "ChemInform Abstract: Asymmetric Synthesis of (S)-Carbinoxamine. New Aspects of Oxazaborolidine-Catalyzed Enantioselective Carbonyl Reduction." ChemInform 27, no. 45 (2010): no. http://dx.doi.org/10.1002/chin.199645055.

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17

Monferrer-Pons, Li, J. S. Esteve-Romero, G. Ramis-Ramos, and M. C. Garcia-Alvarez-Coque. "Spectrophotometric Determination of the Antihistamines, Carbinoxamine Maleate and Doxylamine Succinate, in anN-Cetylpyridinium Chloride Micellar Medium." Analytical Letters 29, no. 8 (1996): 1399–413. http://dx.doi.org/10.1080/00032719608001490.

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18

Moustafa, Azza A., Maha A. Hegazy, Dalia Mohamed, and Omnia Ali. "Novel Approach for the Simultaneous Determination of Carbinoxamine Maleate, Pholcodine, and Ephedrine Hydrochloride Without Interference from Coloring Matter in an Antitussive Preparation Using Smart Spectrophotometric Methods." Journal of AOAC INTERNATIONAL 101, no. 2 (2018): 414–26. http://dx.doi.org/10.5740/jaoacint.17-0078.

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Abstract The presence of coloring matters in syrups usually interferes with the spectrophotometric determination of active pharmaceutical ingredients. A novel approach was introduced to eliminate the interference of sunset yellow (coloring matter) in Cyrinol syrup. Smart, simple, accurate, and selective spectrophotometric methods were developed and validated for the simultaneous determination of a ternary mixture of carbinoxamine maleate, pholcodine, and ephedrine hydrochloride in syrup. Four of the applied methods used ratio spectra: successive derivative subtraction coupled with constant mul

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19

Palabiyik, Ismail Murat, and Feyyaz Onur. "Simultaneous spectrophotometric and liquid chromatographic determination of dextromethorphan hydrobromide, phenylephrine hydrochloride, and carbinoxamine maleate in pharmaceutical preparations." Journal of Analytical Chemistry 67, no. 1 (2011): 56–63. http://dx.doi.org/10.1134/s1061934812010066.

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20

Ramadan, A. A., and H. Mandil. "Spectrophotometric determination of carbinoxamine maleate in pharmaceutical formulations by ternary complex formation with Cu(II) and eosin." Analytical Biochemistry 353, no. 1 (2006): 133–37. http://dx.doi.org/10.1016/j.ab.2006.02.020.

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21

Deng, Yaxin, Tiantian Wang, Jinlong Li, et al. "Studies on the in vitro ion exchange kinetics and thermodynamics and in vivo pharmacokinetics of the carbinoxamine-resin complex." International Journal of Pharmaceutics 588 (October 2020): 119779. http://dx.doi.org/10.1016/j.ijpharm.2020.119779.

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22

Li, Meng, Junyuan Zhang, Siman Ma, Zhen Jiang, Xin Di, and Xingjie Guo. "Chiral separation of five antihistamine drug enantiomers and enantioselective pharmacokinetic study of carbinoxamine in rat plasma by HPLC-MS/MS." New Journal of Chemistry 44, no. 15 (2020): 5819–27. http://dx.doi.org/10.1039/d0nj00095g.

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23

Moustafa, Azza Aziz, Hesham Salem, Maha Hegazy, and Omnia A. Mahmoud. "Simultaneous Determination of Carbinoxamine, Pholcodine, and Ephedrine in Antitussive Preparation by High-Performance Liquid Chromatography and Thin-Layer Chromatography–Densitometry." Journal of Planar Chromatography – Modern TLC 28, no. 4 (2015): 307–15. http://dx.doi.org/10.1556/1006.2015.28.4.7.

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24

Abdelrahman, Maha Mohamed, Eglal Abdelhameed Abdelaleem, Nouruddin Wageih Ali, and Raghda Abdelmoneim Emam. "Simultaneous determination of carbinoxamine maleate and pseudoephedrine HCl in their pure form and in their pharmaceutical formulation by HPTLC-densitometric method." European Journal of Chemistry 7, no. 1 (2016): 37–41. http://dx.doi.org/10.5155/eurjchem.7.1.37-41.1355.

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25

Harikrishnan, Adhikesavan, Jayakumar Sanjeevi, and Chinnasamy Ramaraj Ramanathan. "The cooperative effect of Lewis pairs in the Friedel–Crafts hydroxyalkylation reaction: a simple and effective route for the synthesis of (±)-carbinoxamine." Organic & Biomolecular Chemistry 13, no. 12 (2015): 3633–47. http://dx.doi.org/10.1039/c4ob02597k.

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26

Liu, Yali, Peng Li, Rong Qian, et al. "A novel and discriminative method of in vitro disintegration time for preparation and optimization of taste-masked orally disintegrating tablets of carbinoxamine maleate." Drug Development and Industrial Pharmacy 44, no. 8 (2018): 1317–27. http://dx.doi.org/10.1080/03639045.2018.1449854.

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27

Li, Pei, Jie Xiao, Jing Liu, Ran Liu, Kaishun Bi, and Qing Li. "Development and full validation of a liquid chromatography-tandem mass spectrometry method for determination of carbinoxamine in beagle plasma and its application to a pharmacokinetic study." Journal of Chromatography B 1093-1094 (September 2018): 183–89. http://dx.doi.org/10.1016/j.jchromb.2018.05.002.

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28

"Clock Ticks for Carbinoxamine Products Targeted in FDA Crackdown." Skin & Allergy News 37, no. 8 (2006): 8. http://dx.doi.org/10.1016/s0037-6337(06)71442-5.

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29

"Caffeine/carbinoxamine/dihydrocodeine/guaifenesin/methylephedrine-hydrochloride/muramidase/paracetamol/riboflavin/sulbutiamine." Reactions Weekly 1606, no. 1 (2016): 40. http://dx.doi.org/10.1007/s40278-016-18444-2.

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30

Tadiboyina, Sirisha, B. M. Gurupadayya, and Bharath Kumar Inturi. "Bio-analytical chiral chromatography method for the enantioselective separation of carbinoxamine maleate in human plasma." Journal of Analytical Science and Technology 6, no. 1 (2015). http://dx.doi.org/10.1186/s40543-015-0072-3.

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31

Xu, Wei, Shuai Xia, Jing Pu, et al. "The Antihistamine Drugs Carbinoxamine Maleate and Chlorpheniramine Maleate Exhibit Potent Antiviral Activity Against a Broad Spectrum of Influenza Viruses." Frontiers in Microbiology 9 (November 6, 2018). http://dx.doi.org/10.3389/fmicb.2018.02643.

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