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The formation of furfural compounds in selected saccharide- and polysaccharide-based pharmaceutical excipients
M. Douša, P. Gibala, J. Břicháč, J. Havlíček,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, validační studie
NLK
Medline Complete (EBSCOhost)
od 2005-06-01 do 2015-12-31
Wiley Online Library (archiv)
od 1996-01-01 do 2012-12-31
PubMed
22318787
DOI
10.1002/jps.23072
Knihovny.cz E-zdroje
- MeSH
- 2-furaldehyd chemická syntéza MeSH
- hmotnostní spektrometrie MeSH
- hydrolýza MeSH
- kinetika MeSH
- koncentrace vodíkových iontů MeSH
- léčivé přípravky chemie MeSH
- limita detekce MeSH
- magnetická rezonanční spektroskopie MeSH
- polysacharidy chemie MeSH
- pomocné látky MeSH
- reprodukovatelnost výsledků MeSH
- sacharidy chemie MeSH
- teplota MeSH
- vysokoúčinná kapalinová chromatografie MeSH
- Publikační typ
- časopisecké články MeSH
- validační studie MeSH
The acid hydrolysis of various selected saccharide- and polysaccharide-based pharmaceutical excipients under acid hydrolysis and the formation of degradation compounds were studied. New degradation products formed from these excipients were discovered. Liquid chromatography-mass spectrometry and nuclear magnetic resonance techniques were employed to identify and fully characterize these unknown compounds. The degradation products were identified as [(5-formylfuran-2-yl)methoxy]acetic acid, 5-[(propan-2-yloxy)methyl]furan-2-carbaldehyde, along with the previously identified 5-(methoxymethyl)furan-2-carbaldehyde. On the basis of the identification of these degradation products, a reasonable mechanism for their formation can be proposed. Temperature and pH affect the hydrolysis rates of saccharides and polysaccharides, which in turn affects the rate of formation of furfural compounds.
Citace poskytuje Crossref.org
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- $a The acid hydrolysis of various selected saccharide- and polysaccharide-based pharmaceutical excipients under acid hydrolysis and the formation of degradation compounds were studied. New degradation products formed from these excipients were discovered. Liquid chromatography-mass spectrometry and nuclear magnetic resonance techniques were employed to identify and fully characterize these unknown compounds. The degradation products were identified as [(5-formylfuran-2-yl)methoxy]acetic acid, 5-[(propan-2-yloxy)methyl]furan-2-carbaldehyde, along with the previously identified 5-(methoxymethyl)furan-2-carbaldehyde. On the basis of the identification of these degradation products, a reasonable mechanism for their formation can be proposed. Temperature and pH affect the hydrolysis rates of saccharides and polysaccharides, which in turn affects the rate of formation of furfural compounds.
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