{"title":"Title Page","authors":"","doi":"10.1002/jps.3030491201","DOIUrl":"10.1002/jps.3030491201","url":null,"abstract":"","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Page I"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491201","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134818224","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Non-benzenoid aromatic compounds. Edited by David Ginsburg. Interscience Publishers, Inc., 250 Fifth Ave., New York 1, N. Y., 1959. xii + 543 pp. 15 × 23 cm. Price $18","authors":"","doi":"10.1002/jps.3030491216","DOIUrl":"10.1002/jps.3030491216","url":null,"abstract":"","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Page 787"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491216","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134818225","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Detoxication mechanisms. 2nd ed. By R. Tecwyn Williams. John Wiley & Sons, Inc., 440 Fourth Ave., New York 16, N. Y., 1960. x + 796 pp. 14 × 21 cm. Price $19","authors":"","doi":"10.1002/jps.3030491218","DOIUrl":"10.1002/jps.3030491218","url":null,"abstract":"","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Page 787"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491218","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134818227","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Handbuch der papierchromatographie. Vol. 1. Grundlagen und Technik. Vol. 2. Bibliographie und Anwendungen. Edited by I. M. Hais and K. Macek. Veb Gustav Fischer Verlag, Jena, Germany, 1960. Vol. 1, xxiv + 860 pp. and Vol. 2, xxiv + 728 pp. 16.5 × 24 cm. Price Vol. 1, DM 58.40; Vol. 2, DM 44","authors":"","doi":"10.1002/jps.3030491223","DOIUrl":"10.1002/jps.3030491223","url":null,"abstract":"","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Page 788"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491223","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134880776","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Determination of prednisolone in the presence of hydroxyzine and in formulations containing analgesics","authors":"J.D. Duerr , B.A. Pappas","doi":"10.1002/jps.3030491206","DOIUrl":"10.1002/jps.3030491206","url":null,"abstract":"<div><p>A colorimetric method for the determination of prednisolone in the presence of hydroxyzine [1-(<em>p</em>-chlorobenzhydryl)-4-2-(2-hydroxyethoxy) ethyl piperazine], acetylsalicylic acid, caffeine, and acetophenetidin is proposed. Samples of tablet formulations containing prednisolone and the above mentioned compounds were assayed by the addition of sulfuric acid and ferric chloride to alcoholic solutions of the active ingredient and subsequent measurement of the absorbance of the resulting colored solutions.</p></div>","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Pages 759-761"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491206","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"23317644","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Synthesis of some symmetrical aldehyde glycol monoether acetals","authors":"Arthur J. Getzkin , Werner M. Lauter","doi":"10.1002/jps.3030491203","DOIUrl":"10.1002/jps.3030491203","url":null,"abstract":"<div><p>Forty-two acetals of seven aldehydes and the mono-methyl, ethyl and <em>n</em>-butyl ethers of ethylene glycol and diethylene glycol were prepared, and their physical constants determined. An <em>in vitro</em> test was used to determine their hydrolysis in a slightly acidic medium, considered to be similar to the natural acidity of the human skin. It was shown that regeneration of the parent aldehydes proceeded with sufficient rapidity to warrant <em>in vivo</em> tests of these acetals in cosmetic formulas.</p></div>","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Pages 746-750"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491203","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86290725","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"New approach to the determination of vitamin a in pharmaceutical products","authors":"Real Tardif","doi":"10.1002/jps.3030491202","DOIUrl":"10.1002/jps.3030491202","url":null,"abstract":"<div><p>A modified analytical procedure for the determination of vitamin A in pharmaceutical preparations and its method of calculation based on geometric and trigonometric relationships is presented. Ether and isopropyl alcohol solvents are replaced by hexane, a more selective solvent, for the extraction of the unsaponifiable fraction. Absorbance readings of this latter are measured at one wavelength (325 mμ) before and after the destruction of vitamin A. A comparison study of the accuracy and precision of the U. S. P. XV method and of this proposed method was made on five characteristic polyvitamin preparations and on a cod liver oil sample. Statistical analysis of the results in per cent recovery of added vitamin A has shown a 100 per cent yield by the “hexane-destruction” method, and 82 to 96 per cent yield by the U. S. P. XV method. With this proposed method, the standard deviations were less than one-third as grdeat.</p></div>","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Pages 741-745"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491202","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84501820","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Acid hydrolysis of tetrahydropyranyl glycosides: Effects of 2-methylation and 3-hydroxylation on rate of hydrolysis","authors":"Robert V. Petersen","doi":"10.1002/jps.3030491204","DOIUrl":"10.1002/jps.3030491204","url":null,"abstract":"<div><p>A series of methyl glycosides (acetals and ketals) analogous to aldopyranosides, ketopyranosides, and their 3-hydroxy analogs (tetrahydropyran, 2-methyl-tetrahydropyran, and 3-hydroxyl derivatives of these compounds) were synthesized, subjected to acids of various concentrations, and their rates of hydrolysis determined spectrophotometrically.</p></div>","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Pages 750-755"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491204","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72999204","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Evan W. McChesney, Raymond F. Koss, James M. Shekosky, William H. Deitz
{"title":"Metabolism of dextrosulphenidol in several animal species","authors":"Evan W. McChesney, Raymond F. Koss, James M. Shekosky, William H. Deitz","doi":"10.1002/jps.3030491207","DOIUrl":"10.1002/jps.3030491207","url":null,"abstract":"<div><p>The <em>in vivo</em> metabolism of dextrosulphenidol has been studied using various test organisms. Differences are noted and comparisons are made as to the effect of biological variation on the absorption, distribution, and excretion of the drug.</p></div>","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Pages 762-766"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491207","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76433574","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Subsidia pharmaceutica i, 1960 supplement and index of names. Compiled and edited by the Scientific center of the Swiss Pharmaceutical Society, and Published by the Society, Zurich, 1960. 514 pp. 17 × 24 cm. Ring Binder, loose-leaf","authors":"","doi":"10.1002/jps.3030491219","DOIUrl":"10.1002/jps.3030491219","url":null,"abstract":"","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Page 787"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491219","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134818228","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}