USMF logo

Institutional Repository in Medical Sciences
of Nicolae Testemitanu State University of Medicine and Pharmacy
of the Republic of Moldova
(IRMS – Nicolae Testemitanu SUMPh)

Biblioteca Stiintifica Medicala
DSpace

University homepage  |  Library homepage

 
 
Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/12890
Full metadata record
DC FieldValueLanguage
dc.contributor.authorȘtefaneț, Tatiana
dc.contributor.authorVîslouh, Oxana
dc.contributor.authorValica, Vladimir
dc.date.accessioned2020-11-11T14:06:34Z
dc.date.available2020-11-11T14:06:34Z
dc.date.issued2020-10
dc.identifier.urihttps://stiinta.usmf.md/ro/manifestari-stiintifice/zilele-universitatii
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/12890
dc.descriptionUniversitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”, Catedra de chimie farmaceutică şi toxicologică, Chișinău, Republica 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. One of the most common mental diseases is depression, which is the leading cause of diseases and disability worldwide, according to the WHO. Thus, the researches on new compounds used in treating depression is very current, as well as the development of methods for their analysis. Dioxoindolinone – (1'-(2-oxo-propil)-spiro[[1,3]dioxolane-2',3'-indolin]-2'-one) – is a new native compound of the isatin group, synthesized in the Organic Synthesis and Biopharmaceutical Laboratory of the Institute of Chemistry. Purpose. To develop thin layer chromatographic method of analysis (TLC) in order to determine the specific impurities of Dioxoindolinone (fig.2). Material and methods. Dioxoindolinone and specific impurities possible (isatin – the starting substance, ketal izatin – intermediate and acetonide – decomposition product) served as object of study (fig. 3). Results. TLC conditions, development systems and development reagents were selected. The solvent system that achieved an optimal separation of specific impurities and Dioxoindolinone was the mixture of benzene: methanol (90:10). Chromatographic plate development was performed with iodine vapor. Rf values were obtained (fig. 4). Conclusion. The developed TLC method allowed the determination of specific impurities in Dioxoindolinone and will serve as a support for the preparation of the AND for this substance.en_US
dc.language.isoenen_US
dc.publisherUniversitatea de Stat de Medicină şi Farmacie "Nicolae Testemiţanu" din Republica Moldovaen_US
dc.subjectdioxoindolinoneen_US
dc.subjectTLCen_US
dc.subjectspecific impuritiesen_US
dc.titleDetermination of the purity of dioxoindolinone by thin layer chromatographyen_US
dc.typeOtheren_US
Appears in Collections:Culegere de postere

Files in This Item:
File Description SizeFormat 
DETERMINATION_OF_THE_PURITY_OF_DIOXOINDOLINONE_BY_THIN_LAYER_CHROMATOGRAPHY.pdf240.19 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

Valid XHTML 1.0! DSpace Software Copyright © 2002-2013  Duraspace - Feedback