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Naslov:Stabilnost in kontrolirano sproščanje vitamina D v simulacijskih raztopinah : magistrsko delo
Avtorji:ID Lavrič, Danijel (Avtor)
ID Kotnik, Petra (Mentor) Več o mentorju... Novo okno
ID Knez Marevci, Maša (Komentor)
Datoteke:.pdf MAG_Lavric_Danijel_2022.pdf (2,88 MB)
MD5: 1A7BCAB350960146A5458160A6CE3646
PID: 20.500.12556/dkum/48f4861e-9b47-4eb3-bcd1-c36125b9d045
 
Jezik:Slovenski jezik
Vrsta gradiva:Magistrsko delo/naloga
Tipologija:2.09 - Magistrsko delo
Organizacija:FKKT - Fakulteta za kemijo in kemijsko tehnologijo
Opis:Stabilnost in topnost vitamina D v raztopinah sta pomembni lastnosti, ki jih je potrebno dobro poznati pri pripravi različnih formulacij prehranskih dopolnil ali zdravil. Znano je, da je vitamin D slabo topen v vodnih raztopinah, prav tako pa vemo, da je občutljiv na pH, svetlobo, temperaturo ter hitro oksidira. Namen našega magistrskega dela je bil predvsem določiti stabilnost in topnost vitamina D v različnih simulacijskih raztopinah. S pomočjo stresnih testov smo preverjali vpliv temperature in pH na razpad vitamina D v raztopini. Analize dobljenih vzorcev smo opravili na napravi LC-MS in ugotovili, da razpad sicer najhitreje poteka pri temperaturi 60°C, vendar temperatura pri razpadanju, ni odločilni faktor. Bolj pomembna je namreč izbira raztopine oz. njen pH, saj so rezultati analiz pokazali, da se razpad v HCl začne zelo hitro, medtem ko prve razpadne produkte v primeru NaOH in H2O2, opazimo šele po 4 urah. Nizek pH in visoka temperatura torej najbolj negativno vplivata na stabilnost vitamina D v raztopinah. S pomočjo testov topnosti smo ugotovili, da v vodi dosežemo samo 1 % deleža topnosti vitamina D, kot se ga raztopi v MeOH. V raztopini 0,1 % SDS ta delež sicer znaša 7 %, vendar je tudi to dokaj malo. Z primerjavo topnosti različnih formulacij smo potrdili, da se tableta in kapsula v SDS v celoti raztopita, pri čemer pa je vitamin D v obliki kapsule bolj zaščiten pred vplivi okolice, kot v tableti. V zadnjem delu magistrskega dela smo opravili še teste v simuliranih gastrointestinalnih pogojih. Simulirane raztopine sline in želodčnih sokov smo pripravili s pomočjo encimov α-amilaze (slina) in pepsina (želodec). Rezultati analiz so pokazali, da α-amilaza odločilno vpliva na topnost vitamina D v ustih, medtem ko pepsin v želodcu na topnost nima vpliva. Najvišje koncentracije raztopljenega vitamina D smo dosegli v simuliranih oralnih pogojih, medtem ko je v kislih želodčnih koncentracija začela upadati oz. je vitamin D začel razpadati. Zaradi tega bi bilo smiselno narediti primerjavo uporabe ustnih pršil z klasičnimi trdnimi formulacijami, ki vsebujejo vitamin D. Sicer pa pri nadaljnjih raziskavah na tem področju, priporočamo uporabo manjših volumnov in nižjih koncentracij α-amilaze, ki naj bo pripravljena v vodni raztopini.
Ključne besede:Stabilnost vitamina D, topnost vitamina D, gastrointestinalni testi, pepsin, α-amilaza
Kraj izida:Maribor
Kraj izvedbe:Maribor
Založnik:[D. Lavrič]
Leto izida:2022
Št. strani:1 spletni vir (1 datoteka PDF (63 f.))
PID:20.500.12556/DKUM-81247 Novo okno
UDK:604.4:577.16(043.2)
COBISS.SI-ID:99477763 Novo okno
Datum objave v DKUM:02.03.2022
Število ogledov:1028
Število prenosov:155
Metapodatki:XML DC-XML DC-RDF
Področja:KTFMB - FKKT
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Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Začetek licenciranja:07.02.2022

Sekundarni jezik

Jezik:Angleški jezik
Naslov:Stability and controlled release of vitamin D in simulation solutions
Opis:Stability and solubility of vitamin D in solutions are properties that play very important role in preparation of different food supplements or drugs. It’s known that vitamin D has a very poor solubility in water solutions. Studies suggest that various factors such as temperature, pH, light and oxygen have big influence on stability of vitamin D in solutions. Therefore the main goal of our studies was to determine stability in solubility of vitamin D in different simulation solutions. Stress tests were carried out to determine the effect of temperature and pH on stability of vitamin D. Analysis were preformed with LC-MS method. We determined, that higher temperature had caused the fastest degradation of vitamin D in solution, but we have also noticed that it is not the most important factor regarding the speed of degradation. Results shoved that pH had far more bigger impact on the stability of vitamin D than temperature. Mass spectra shoved, that degradation of vitamin D occurred very fast when using HCl, meanwhile when we used NaOH and H2O2, degradation products started to form after 4 hours. With that we determined that vitamin D is least stable in low pH and at high temperatures. Solubility tests were preformed in order to determine how much vitamin D can be dissolved in our simulated solutions in comparison to solubility of it in MeOH. Results shoved that we could dissolve only 1% of vitamin D in water, compared to MeOH and the most we could dissolve was 7 % in SDS solution. For the effect of formulation of vitamin D we carried out solubility tests of tablet and capsule. As expected both formulation dissolved completely in solution and the only difference was that tablet was more prone to the effect of matrix, which was also expected. Last part of our studies was reserved for gastrointestinal tests, which simulated oral and gastro conditions. α-amylase and pepsin were used to prepare the simulated solutions of saliva and gastric juices. Results of analysis shoved that α-amylase has the most important role in the solubility of vitamin D, meanwhile pepsin doesn't effect solubility. The highest measured concentration of dissolved vitamin D were found in simulated saliva solution, while in gastric conditions vitamin D started to disintegrate. That means its possible that mouth spray solutions with vitamin D could have better effect than other solid oral doses. For the determination of that hypothesis it would be necessary to do more studies. However we can recommend the use of smaller volumes and lower concentrations of α-amylase which should be prepared in aqueous solution for further studies.
Ključne besede:Stability of vitamin D, solubility of vitamin D, gastrointestinal tests, pepsin, α-amylase


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