Conţinutul numărului revistei |
Articolul precedent |
Articolul urmator |
1482 1 |
Ultima descărcare din IBN: 2023-03-15 19:59 |
SM ISO690:2012 DRANKA, I., POVAR, Igor, LUPASCU, Tudor. Pharmaceutical amorphous organic materials
characterization by using the differential scanning calorimetry and dynamic mechanical analysis
. In: Chemistry Journal of Moldova, 2011, nr. 2(6), pp. 91-95. ISSN 1857-1727. |
EXPORT metadate: Google Scholar Crossref CERIF DataCite Dublin Core |
Chemistry Journal of Moldova | ||||||
Numărul 2(6) / 2011 / ISSN 1857-1727 /ISSNe 2345-1688 | ||||||
|
||||||
Pag. 91-95 | ||||||
|
||||||
Descarcă PDF | ||||||
Rezumat | ||||||
This research has been carried out in order to demonstrate the use of differential scanning calorimetry (DSC)
in detecting and measuring α- and β-relaxation processes in amorphous pharmaceutical systems. DSC has been employed
to study amorphous samples of poly (vinylpyrrolidone) (PVP), indomethacin (InM), and ursodeoxycholic acid (UDA)
that are annealed at temperature (Ta) around 0.8 of their glass transition temperature (Tg). Dynamic mechanical analysis
(DMA) is used to measure β- relaxation in PVP. Yet, the DSC has been used to study the glassy indomethacin aged at
0 and -10 oC for periods of time up to 109 and 210 days respectively. The results demonstrate the emergence of a small
melting peak of the α-polymorph after aging for 69 days at 0°C and for 147 days at -10°C (i.e., ~55°C below the glass
transition temperature) that provides evidence of nucleation occurring in the temperature region of the β-relaxation.
The evolution of an endothermic recovery peak temperature features a plateau at longer annealing times, suggesting
that the glass has made a significant progress toward reaching the supercooled liquid state. It has been found that the
melting peaks become detectable after the recovery peak reaches the plateau. The results highlight the importance of
studying physical aging in the temperature region of the β – relaxation as a means of evaluating the physical stability of
amorphous pharmaceutical materials.
|
||||||
Cuvinte-cheie DSC – differential scanning calorimetry; DMA – dynamic mechanical analysis; drugs; excipients; glass transition; α- and β – relaxations; crystallization; kinetics |
||||||
|
DataCite XML Export
<?xml version='1.0' encoding='utf-8'?> <resource xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance' xmlns='http://datacite.org/schema/kernel-3' xsi:schemaLocation='http://datacite.org/schema/kernel-3 http://schema.datacite.org/meta/kernel-3/metadata.xsd'> <creators> <creator> <creatorName>Drancă, I.V.</creatorName> <affiliation>Institutul de Chimie al AŞM, Moldova, Republica</affiliation> </creator> <creator> <creatorName>Povar, I.G.</creatorName> <affiliation>Institutul de Chimie al AŞM, Moldova, Republica</affiliation> </creator> <creator> <creatorName>Lupaşcu, T.G.</creatorName> <affiliation>Institutul de Chimie al AŞM, Moldova, Republica</affiliation> </creator> </creators> <titles> <title xml:lang='en'>Pharmaceutical amorphous organic materials characterization by using the differential scanning calorimetry and dynamic mechanical analysis </title> </titles> <publisher>Instrumentul Bibliometric National</publisher> <publicationYear>2011</publicationYear> <relatedIdentifier relatedIdentifierType='ISSN' relationType='IsPartOf'>1857-1727</relatedIdentifier> <subjects> <subject>DSC – differential scanning calorimetry; DMA – dynamic mechanical analysis; drugs; excipients; glass transition; α- and β – relaxations; crystallization; kinetics</subject> </subjects> <dates> <date dateType='Issued'>2011-06-01</date> </dates> <resourceType resourceTypeGeneral='Text'>Journal article</resourceType> <descriptions> <description xml:lang='en' descriptionType='Abstract'>This research has been carried out in order to demonstrate the use of differential scanning calorimetry (DSC) in detecting and measuring α- and β-relaxation processes in amorphous pharmaceutical systems. DSC has been employed to study amorphous samples of poly (vinylpyrrolidone) (PVP), indomethacin (InM), and ursodeoxycholic acid (UDA) that are annealed at temperature (Ta) around 0.8 of their glass transition temperature (Tg). Dynamic mechanical analysis (DMA) is used to measure β- relaxation in PVP. Yet, the DSC has been used to study the glassy indomethacin aged at 0 and -10 oC for periods of time up to 109 and 210 days respectively. The results demonstrate the emergence of a small melting peak of the α-polymorph after aging for 69 days at 0°C and for 147 days at -10°C (i.e., ~55°C below the glass transition temperature) that provides evidence of nucleation occurring in the temperature region of the β-relaxation. The evolution of an endothermic recovery peak temperature features a plateau at longer annealing times, suggesting that the glass has made a significant progress toward reaching the supercooled liquid state. It has been found that the melting peaks become detectable after the recovery peak reaches the plateau. The results highlight the importance of studying physical aging in the temperature region of the β – relaxation as a means of evaluating the physical stability of amorphous pharmaceutical materials. </description> </descriptions> <formats> <format>application/pdf</format> </formats> </resource>