Preučevanje fizikalno-kemijskih lastnosti nekaterih farmacevtskih učinkovin

Garmut, Ana

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Title:	Preučevanje fizikalno-kemijskih lastnosti nekaterih farmacevtskih učinkovin
Authors:	ID Garmut, Ana (Author) ID Kotnik, Petra (Mentor) More about this mentor... ID Knez Marevci, Maša (Comentor)
Files:	MAG_Garmut_Ana_2023.pdf (2,83 MB) MD5: 5E01190F996507FE9D04D6448B791ED6
Language:	Slovenian
Work type:	Master's thesis/paper
Typology:	2.09 - Master's Thesis
Organization:	FKKT - Faculty of Chemistry and Chemical Engineering
Abstract:	Aktivna farmacevtska učinkovina (API) je izraz, ki se uporablja za biološko aktivno sestavino zdravila. API v telesu povzročijo zahtevani učinek za zdravljenje določene bolezni. Stresno testiranje API lahko pomaga identificirati verjetne produkte razgradnje. S stresnim testiranjem lahko določimo tudi poti razgradnje in notranjo stabilnost molekule. Farmacevtske učinkovine lahko ločimo in jih razlikujemo od nečistot. Ugotavljanje stabilnosti je lahko sestavljeno iz kombinacije kromatografskega ločevanja in spektroskopskih tehnik. Za raziskovanje smo si izbrali tri farmacevtske učinkovine: fenofibrat, febuksostat in esomeprazol. Preverili smo njihovo stabilnost v raztopini metanola in jih izpostavili različnim stresnim pogojem ter prisilnemu staranju. Za kvantifikacijo smo uporabili tekočinsko kromatografijo z masno spektrometrijo (LC-MS/MS) in tankoplastno kromatografijo visoke ločljivosti (HPTLC). V raztopini metanola se je kot najbolj stabilen izkazal febuksostat. Koncentracija febuksostata je po 24 h ostala nespremenjena. S pomočjo stresnih testov smo določili razgradnjo posamezne farmacevtske učinkovine. Največji odstotek razgradnje je pri fenofibratu in febuksostatu povzročil dodatek 1 M NaOH. Po 48 h pri 60 °C je v vzorcu ostalo le še 2,36 % začetne mase fenofibrata. Pri enakih pogojih smo pri febuksostatu dosegli 83,09 % razgradnjo učinkovine. Do razgradnje esomeprazola je prišlo ob prisotnosti močne kisline in baze. Pri dodatku 1 M HCl je bila vsebnost esomeprazola po 24 h pri sobni temperaturi praktično nezaznavna. Shranjevanje vseh treh farmacevtskih učinkovin pri višjih temperaturah povzroča njihovo razgradnjo in posledično zmanjševanje koncentracije.
Keywords:	fenofibrat, febuksostat, esomeprazol, stresni testi, HPTLC, LC-MS/MS
Place of publishing:	Maribor
Publisher:	[A. Garmut]
Year of publishing:	2023
PID:	20.500.12556/DKUM-84021
UDC:	615.45:57.013(043.2)
COBISS.SI-ID:	152291331
Publication date in DKUM:	05.05.2023
Views:	752
Downloads:	103
Metadata:
Categories:	KTFMB - FKKT
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Licences

License:	CC BY-NC-ND 4.0, Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International

Link:	http://creativecommons.org/licenses/by-nc-nd/4.0/
Description:	The most restrictive Creative Commons license. This only allows people to download and share the work for no commercial gain and for no other purposes.
Licensing start date:	29.03.2023

Secondary language

Language:	English
Title:	Study of the physicochemical properties of certain active pharmaceutical ingredients
Abstract:	Active pharmaceutical ingredient (API) is the term used for the biologically active component of a medicinal product. APIs produce the required effect in the body to treat a specific disease. Stress testing of APIs can help identify likely degradation products. Stress testing can also determine the degradation pathways and internal stability of a molecule. Active pharmaceutical ingredients can be separated and distinguished from impurities. Stability determination may consist of a combination of chromatographic separation and spectrometric techniques. Three active pharmaceutical ingredients were chosen for investigation: fenofibrate, febuxostat and esomeprazole. Their stability in methanol solution was tested and they were exposed to different stress conditions and forced ageing. Liquid chromatography-mass spectrometry (LC-MS/MS) and high-performance thin-layer chromatography (HPTLC) were used for quantification. In methanol solution, febuxostat proved to be the most stable. The concentration of febuxostat remained unchanged after 24 h. The degradation of each active pharmaceutical ingredient was determined by stress tests. The highest percentage of degradation for fenofibrate and febuxostat was caused by the addition of 1 M NaOH. After 48 h at 60 °C, only 2,36 % of the initial mass of fenofibrate remained in the sample. Under the same conditions, 83,09 % degradation of the active substance was obtained with febuxostat. The degradation of esomeprazole occurred in the presence of strong acid and base. After 24 h at room temperature, the addition of 1 M HCl made the esomeprazole content practically undetectable. Storage of all three active pharmaceutical ingredients at elevated temperatures causes their degradation and consequent decrease in concentration.
Keywords:	fenofibrate, febuxostat, esomeprazole, stress testing, HPTLC, LC-MS/MS

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