DC Field | Value | Language |
dc.contributor.author | Ștefaneț, Tatiana | |
dc.contributor.author | Vîslouh, Oxana | |
dc.contributor.author | Valica, Vladimir | |
dc.date.accessioned | 2020-11-11T14:06:34Z | |
dc.date.available | 2020-11-11T14:06:34Z | |
dc.date.issued | 2020-10 | |
dc.identifier.uri | https://stiinta.usmf.md/ro/manifestari-stiintifice/zilele-universitatii | |
dc.identifier.uri | http://repository.usmf.md/handle/20.500.12710/12890 | |
dc.description | Universitatea 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 dezvoltare | en_US |
dc.description.abstract | Introduction. 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.iso | en | en_US |
dc.publisher | Universitatea de Stat de Medicină şi Farmacie "Nicolae Testemiţanu" din Republica Moldova | en_US |
dc.subject | dioxoindolinone | en_US |
dc.subject | TLC | en_US |
dc.subject | specific impurities | en_US |
dc.title | Determination of the purity of dioxoindolinone by thin layer chromatography | en_US |
dc.type | Other | en_US |
Appears in Collections: | Culegere de postere
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