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dc.contributor.authorMesut, Burcu
dc.contributor.authorErginer, Yıldız
dc.contributor.authorPirinçci Tok, Yağmur
dc.date.accessioned2021-12-10T13:01:47Z
dc.date.available2021-12-10T13:01:47Z
dc.identifier.citationPirinçci Tok Y., Mesut B., Erginer Y., "Design, Preparation and Evaluation of Taste-Masked Dexketoprofen of Orally Disintegrating Tablet By Using QbD Approach", The 1st International Electronic Conference on Pharmaceutics, Basel, İsviçre, 1 - 03 Aralık 2020, ss.1
dc.identifier.othervv_1032021
dc.identifier.otherav_e9cf8b0a-3407-48ad-8d70-acae4c7d6402
dc.identifier.urihttp://hdl.handle.net/20.500.12627/175264
dc.identifier.urihttps://sciforum.net/paper/view/conference/8675
dc.identifier.urihttps://doi.org/10.3390/iecp2020-08675
dc.description.abstractThe present investigation was carried out to develop a taste-masked orally disintegrating tablet containing Dexketoprofen for evaluating the effect of the coating amount on the product’s quality attributes via Quality by Design (QbD) systematically roadmap.Dexketoprofen, S(+)-enantiomer of bitter taste ketoprofen, involves in arylalkil group which is the most frequently used analgesic in the management of acute and chronic pain.Bitter-taste active pharmacological ingredients should involve taste masking approach. For this purpose, the bitter taste dexketoprofen particles were coated pH-dependent methacrylates polymer in which one of the methods of taste-masking as a taste-masking agent.The experimental design was enforced with the four-factor three-level Box-Behnken method within the framework of response surface modeling (RSM). Ready to use matrix excipient, Eudragit RS 30D, dextrates, aroma, tablet pressing force was chosen as independent factors and were assessed on four dependent factors dissolution rate, disintegration time, tablet hardness, and friability.Our findings indicate that when tablet pressing force is applied as 250 PSI, the tablets disintegrate below 1 minute and friability values is under 1%. Disintegration time increases as the coating amount increases. However the Pareto charts shows engrossingly that the dissolution rate is affected mostly by tablet pressing force in first, third, fifth time points, and by matrix excipient and coating in tenth, fifteenth, twentieth, thirtieth-time points.It was concluded that QbD study helped to understand how coating amount and process variables impacting the dissolution rate, disintegration time, tablet hardness and friability of Dexketoprofen orally disintegrating tablet (ODT) finished product.
dc.language.isoeng
dc.subjectFarmasötik Teknoloji
dc.subjectPharmacology
dc.subjectGeneral Pharmacology, Toxicology and Pharmaceutics
dc.subjectPharmacology, Toxicology and Pharmaceutics (miscellaneous)
dc.subjectPharmacology (medical)
dc.subjectPharmacy
dc.subjectDrug Guides
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectEczacılık
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectKlinik Tıp (MED)
dc.subjectEczacılık Teknolojisi
dc.subjectSağlık Bilimleri
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.titleDesign, Preparation and Evaluation of Taste-Masked Dexketoprofen of Orally Disintegrating Tablet By Using QbD Approach
dc.typeBildiri
dc.contributor.departmentİstanbul Üniversitesi , Eczacılık Fakültesi , Eczacılık Teknolojisi Bölümü
dc.contributor.firstauthorID2532986


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