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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/12907
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dc.contributor.authorUncu, Livia-
dc.contributor.authorCarmazan, Sabina-
dc.contributor.authorValica, Vladimir-
dc.contributor.authorPodgornîi, Ana-
dc.contributor.authorVîslouh, Oxana-
dc.contributor.authorDonici, Elena-
dc.date.accessioned2020-11-11T17:10:48Z-
dc.date.available2020-11-11T17:10:48Z-
dc.date.issued2020-10-
dc.identifier.urihttps://stiinta.usmf.md/ro/manifestari-stiintifice/zilele-universitatii-
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/12907-
dc.descriptionDepartment of Pharmaceutical and Toxicological Chemistry Nicolae Testemitanu State University of Medicine and Pharmacy of Republic of Moldova, Congresul consacrat aniversării a 75-a de la fondarea Universității de Stat de Medicină și Farmacie „Nicolae Testemițanu” din Republica Moldova, Ziua internațională a științei pentru pace și dezvoltareen_US
dc.description.abstractINTRODUCTION. The combined ear drops represent an advantage over the monocomponent ones due to their polyvalent action. The thin layer chromatography (TLC) method is used to separate the active principles. The purpose. Separation and identification of isohydrafural and methyluracil in mechanical combination and pharmaceutical form by TLC. MATERIAL AND METHODS. Experimental series of isohydrafural (IHF), methyluracil (MU) (Sigma Aldrich, USA), chromatographic plates "Silufol", chromatography chamber, solvents, reagents according to the European Pharmacopoeia. RESULTS. Mobile phases were used: chloroform-acetone (70:30), 1-butanol-diethyl ether-acetone (10:85:5), ethyl acetatehexane (2:1), glacial acetic acid-water-butanol (1:1) 1:4), chloroform-methanol-glacial acetic acid (90:8:8 and 95:10:2). During the analyzes, 4 working techniques were used with the detection of spots in UV light at different wavelengths, spraying with pyridine and pdimethylaminobenzaldehyde solutions. The mobile phase ethyl acetate-hexane (2:1) was selected for the qualitative analysis of the compounds in mechanical mixture (I) and the pharmaceutical form (II). The values of the retention factors are: I-IHF-Rf = 0,37; MU-Rf = 0,72 and II-IHF-Rf = 0,35; MU-Rf = 0,70. CONCLUSIONS. The elaborated working technique will be included in the quality specification of the combined ear drops for the identification of IHF and MU.en_US
dc.language.isoenen_US
dc.publisherUniversitatea de Stat de Medicină şi Farmacie "Nicolae Testemiţanu"en_US
dc.subjectthin layer chromatographyen_US
dc.subjectisohydrafuralen_US
dc.subjectmethyluracilen_US
dc.titleThin layer chromatographic separation of isohydrafural and methyluracyl in mechanical combination and ear dropsen_US
dc.typeOtheren_US
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