Physical Characterization of the Hydrates of Urapidil
Three hydrates of urapidil were prepared and characterized by means of differential scanning calorimetry, thermogravimetric analysis, infrared spectroscopy, X-ray powder diffraction, intrinsic dissolution rates, and solution calorimetry. The stoichiometry of the urapidil hydrates was found to be 1:5...
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Veröffentlicht in: | Journal of pharmaceutical sciences 1988-05, Vol.77 (5), p.444-451 |
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container_title | Journal of pharmaceutical sciences |
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creator | Botha, S.A. Caira, M.R. Guillory, J.K. Lötter, A.P. |
description | Three hydrates of urapidil were prepared and characterized by means of differential scanning calorimetry, thermogravimetric analysis, infrared spectroscopy, X-ray powder diffraction, intrinsic dissolution rates, and solution calorimetry. The stoichiometry of the urapidil hydrates was found to be 1:5, 1:3, and 1:1 (urapidiliwater). The crystal and molecular structures of urapidil pentahydrate were determined from three-dimensional X-ray data. The stability of the pentahydrate and monohydrate under different storage conditions was also determined. |
doi_str_mv | 10.1002/jps.2600770518 |
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The stoichiometry of the urapidil hydrates was found to be 1:5, 1:3, and 1:1 (urapidiliwater). The crystal and molecular structures of urapidil pentahydrate were determined from three-dimensional X-ray data. The stability of the pentahydrate and monohydrate under different storage conditions was also determined.</description><identifier>ISSN: 0022-3549</identifier><identifier>EISSN: 1520-6017</identifier><identifier>DOI: 10.1002/jps.2600770518</identifier><identifier>PMID: 3411469</identifier><identifier>CODEN: JPMSAE</identifier><language>eng</language><publisher>Washington: Elsevier Inc</publisher><subject>Biological and medical sciences ; Chemical Phenomena ; Chemistry, Physical ; Crystallography ; Differential Thermal Analysis ; Drug Stability ; General pharmacology ; Medical sciences ; Microscopy, Electron, Scanning ; Pharmacology. Drug treatments ; Physicochemical properties. 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Pharm. Sci</addtitle><description>Three hydrates of urapidil were prepared and characterized by means of differential scanning calorimetry, thermogravimetric analysis, infrared spectroscopy, X-ray powder diffraction, intrinsic dissolution rates, and solution calorimetry. The stoichiometry of the urapidil hydrates was found to be 1:5, 1:3, and 1:1 (urapidiliwater). The crystal and molecular structures of urapidil pentahydrate were determined from three-dimensional X-ray data. The stability of the pentahydrate and monohydrate under different storage conditions was also determined.</description><subject>Biological and medical sciences</subject><subject>Chemical Phenomena</subject><subject>Chemistry, Physical</subject><subject>Crystallography</subject><subject>Differential Thermal Analysis</subject><subject>Drug Stability</subject><subject>General pharmacology</subject><subject>Medical sciences</subject><subject>Microscopy, Electron, Scanning</subject><subject>Pharmacology. Drug treatments</subject><subject>Physicochemical properties. 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Drug treatments</topic><topic>Physicochemical properties. Structure-activity relationships</topic><topic>Piperazines - analysis</topic><topic>Solubility</topic><topic>Spectrophotometry, Infrared</topic><topic>Stereoisomerism</topic><topic>X-Ray Diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Botha, S.A.</creatorcontrib><creatorcontrib>Caira, M.R.</creatorcontrib><creatorcontrib>Guillory, J.K.</creatorcontrib><creatorcontrib>Lötter, A.P.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Botha, S.A.</au><au>Caira, M.R.</au><au>Guillory, J.K.</au><au>Lötter, A.P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Physical Characterization of the Hydrates of Urapidil</atitle><jtitle>Journal of pharmaceutical sciences</jtitle><addtitle>J. Pharm. Sci</addtitle><date>1988-05</date><risdate>1988</risdate><volume>77</volume><issue>5</issue><spage>444</spage><epage>451</epage><pages>444-451</pages><issn>0022-3549</issn><eissn>1520-6017</eissn><coden>JPMSAE</coden><abstract>Three hydrates of urapidil were prepared and characterized by means of differential scanning calorimetry, thermogravimetric analysis, infrared spectroscopy, X-ray powder diffraction, intrinsic dissolution rates, and solution calorimetry. The stoichiometry of the urapidil hydrates was found to be 1:5, 1:3, and 1:1 (urapidiliwater). The crystal and molecular structures of urapidil pentahydrate were determined from three-dimensional X-ray data. The stability of the pentahydrate and monohydrate under different storage conditions was also determined.</abstract><cop>Washington</cop><pub>Elsevier Inc</pub><pmid>3411469</pmid><doi>10.1002/jps.2600770518</doi><tpages>8</tpages></addata></record> |
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source | Wiley Online Library - AutoHoldings Journals; MEDLINE; Alma/SFX Local Collection |
subjects | Biological and medical sciences Chemical Phenomena Chemistry, Physical Crystallography Differential Thermal Analysis Drug Stability General pharmacology Medical sciences Microscopy, Electron, Scanning Pharmacology. Drug treatments Physicochemical properties. Structure-activity relationships Piperazines - analysis Solubility Spectrophotometry, Infrared Stereoisomerism X-Ray Diffraction |
title | Physical Characterization of the Hydrates of Urapidil |
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