Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/75535
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dc.contributor.authorKarnkamol Trisoponen_US
dc.contributor.authorNisit Kittipongpatanaen_US
dc.contributor.authorPhanphen Wattanaarsakiten_US
dc.contributor.authorOrnanong Suwannapakul Kittipongpatanaen_US
dc.date.accessioned2022-10-16T07:00:34Z-
dc.date.available2022-10-16T07:00:34Z-
dc.date.issued2021-10-01en_US
dc.identifier.issn14248247en_US
dc.identifier.other2-s2.0-85117899248en_US
dc.identifier.other10.3390/ph14101047en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85117899248&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/75535-
dc.description.abstractA co-processed, rice starch-based excipient (CS), previously developed and shown to exhibit good pharmaceutical properties, is investigated as an all-in-one excipient for direct compression (DC). An SeDeM-ODT expert system is applied to evaluate the formulation containing CS, in comparison with those containing the physical mixture and the commercial DC excipients. The results revealed that CS showed acceptable values in all six incidence factors of the SeDeM-ODT diagram. In addition, the comprehensive indices (IGC and IGCB) were higher than 5.0, which indicated that CS could be compressed with DC technique without additional blending with a disintegrant in tablet formulation. The formulation study suggested that CS can be diluted up to 60% in the formulation to compensate for unsatisfactory properties of paracetamol. At this percentage, CS-containing tablets exhibited narrow weight variation (1.5%), low friability (0.43%), acceptable drug content (98%), and rapid disintegration (10 s). The dissolution profile of CS displayed that more than 80% of the drug content was released within 2 min. The functionality of CS was comparable to that of high functionality excipient composite (HFEC), whereas other excipients were unsuccessful in formulating the tablets. These results indicated that CS was a suitable all-in-one excipient for application in DC of tablets.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleFormulation study of a co-processed, rice starch-based, all-in-one excipient for direct compression using the sedem-odt expert systemen_US
dc.typeJournalen_US
article.title.sourcetitlePharmaceuticalsen_US
article.volume14en_US
article.stream.affiliationsChulalongkorn Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
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