Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13573
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dc.contributor.authorWiranidchapong C.
dc.contributor.authorKieongarm W.
dc.contributor.authorManagit C.
dc.contributor.authorPhrompittayarat W.
dc.date.accessioned2021-04-05T03:24:45Z-
dc.date.available2021-04-05T03:24:45Z-
dc.date.issued2016
dc.identifier.issn3639045
dc.identifier.other2-s2.0-84964330168
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13573-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84964330168&doi=10.3109%2f03639045.2015.1062513&partnerID=40&md5=a69af910a4750a6230542dc93fd81358
dc.description.abstractThe objective of this study was to investigate thermal and mechanical properties as well as in vitro drug release of Eudragit® RL (ERL) film using chlorpheniramine maleate (CPM) as either active pharmaceutical ingredient or non-traditional plasticizer. Differential scanning calorimeter was used to measure the glass transition temperature (Tg) of 0-100% w/w CPM in ERL physical mixture. Instron testing machine was used to investigate Young's modulus, tensile stress and tensile strain (%) of ERL film containing 20-60% w/w CPM. Finally, a Franz diffusion cell was used to study drug release from ERL films obtained from four formulations, i.e. CRHP0/0, CRHP0/5, CRHP2/0 and CRHP2/5. The Tg of ERL was decreased when the weight percentage of CPM increased. The reduction of the Tg could be described by Kwei equation, indicating the interaction between CPM and ERL. Modulus and tensile stress decreased whereas tensile strain (%) increased when weight percentage of CPM increased. The change of mechanical properties was associated with the reduction of the Tg when weight percentage of CPM increased. ERL films obtained from four formulations could release the drug in no less than 10 h. Cumulative amount of drug release per unit area of ERL film containing only CPM (CRHP0/0) was lower than those obtained from the formulations containing traditional plasticizer (CRHP0/5), surfactant (CRHP2/0) or both of them (CRHP2/5). The increase of drug release was a result of the increase of drug permeability through ERL film and drug solubility based on traditional plasticizer and surfactant, respectively. © 2015 Taylor & Francis.
dc.subjectchlorpheniramine maleate
dc.subjecteudragit
dc.subjectpolyacrylic acid
dc.subjectsurfactant
dc.subjecteudragit
dc.subjectplasticizer
dc.subjectpolymer
dc.subjectArticle
dc.subjectdifferential scanning calorimetry
dc.subjectdrug diffusion
dc.subjectdrug formulation
dc.subjectdrug penetration
dc.subjectdrug release
dc.subjectdrug solubility
dc.subjectglass transition temperature
dc.subjectin vitro study
dc.subjectinvestigative procedures
dc.subjectstress
dc.subjecttensile stress
dc.subjectYoung modulus
dc.subjectbiomechanics
dc.subjectchemistry
dc.subjectmedicinal chemistry
dc.subjectmetabolism
dc.subjecttensile strength
dc.subjectX ray diffraction
dc.subjectBiomechanical Phenomena
dc.subjectChemistry, Pharmaceutical
dc.subjectDrug Liberation
dc.subjectPlasticizers
dc.subjectPolymers
dc.subjectTensile Strength
dc.subjectX-Ray Diffraction
dc.titleThermal, mechanical and drug release characteristics of an acrylic film using active pharmaceutical ingredient as non-traditional plasticizer
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationDrug Development and Industrial Pharmacy. Vol 42, No.4 (2016), p.644-653
dc.identifier.doi10.3109/03639045.2015.1062513
Appears in Collections:Scopus 1983-2021

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