dc.contributor.author
Mohylyuk, Valentyn
dc.contributor.author
Goldoozian, Seyedreza
dc.contributor.author
Andrews, Gavin P.
dc.contributor.author
Dashevskiy, Andriy
dc.date.accessioned
2021-01-15T15:25:20Z
dc.date.available
2021-01-15T15:25:20Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/29280
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-29027
dc.description.abstract
Purpose When establishing IVIVC, a special problem arises by interpretation of averagedin vivoprofiles insight of considerable individual variations in term of time and number of mechanical stress events in GI-tract. The objective of the study was to investigate and forecast the effect of mechanical stress onin vivobehavior in human of hydrophilic matrix tablets. Methods Dissolution profiles for the marketed products were obtained at different conditions (stirring speed, single- or repeatable mechanical stress applied) and convoluted into C-t profiles. Vice versa, publishedin vivoC-t profiles of the products were deconvoluted into absorption profiles and compared with dissolution profiles by similarity factor. Results Investigated hydrophilic matrix tablets varied in term of their resistance against hydrodynamic stress or single stress during the dissolution. Different scenarios, including repeatable mechanical stress, were investigated on mostly prone Seroquel (R) XR 50 mg. None of the particular scenarios fits to the publishedin vivoC-t profile of Seroquel (R) XR 50 mg representing, however, the average of individual profiles related to scenarios differing by number, frequency and time of contraction stress. When different scenarios were combined in different proportions, the profiles became closer to the originalin vivoprofile including a burst between 4 and 5 h, probably, due to stress-events in GI-tract. Conclusion For establishing IVIVC of oral dosage forms susceptible mechanical stress, a comparison of the deconvoluted individualin vivoprofiles within vitroprofiles of different dissolution scenarios can be recommended.
en
dc.format.extent
10 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
extended release
en
dc.subject
gastrointestinal contraction
en
dc.subject
hydrophilic matrix tablet
en
dc.subject
pharmacokinetic profile
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften
dc.title
IVIVC for Extended Release Hydrophilic Matrix Tablets in Consideration of Biorelevant Mechanical Stress
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
227
dcterms.bibliographicCitation.doi
10.1007/s11095-020-02940-7
dcterms.bibliographicCitation.journaltitle
Pharmaceutical Research
dcterms.bibliographicCitation.number
11
dcterms.bibliographicCitation.volume
37
dcterms.bibliographicCitation.url
https://doi.org/10.1007/s11095-020-02940-7
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Pharmazie
refubium.funding
Springer Nature DEAL
refubium.note.author
Die Publikation wurde aus Open Access Publikationsgeldern der Freien Universität Berlin gefördert.
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.issn
0724-8741
dcterms.isPartOf.eissn
1573-904X
refubium.resourceType.provider
WoS-Alert