Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/12789
Full metadata record
DC FieldValueLanguage
dc.contributor.authorQu, Changhai-
dc.contributor.authorLin, Longfei-
dc.contributor.authorYin, Xingbin-
dc.contributor.authorZhang, Xiaoyan-
dc.contributor.authorYang, Pei-
dc.contributor.authorZhang, Hui-
dc.contributor.authorKong, Hui-
dc.contributor.authorWu, Huangyan-
dc.contributor.authorNi, Jian-
dc.date.accessioned2022-10-07T10:25:43Z-
dc.date.available2022-10-07T10:25:43Z-
dc.date.issued2018-11-
dc.identifier.citationQu, C., Lin, L., Yin, X., Zhang, X., Yang, P., Zhang, H., ... & Ni, J. (2018). Preformulation study and initial determination of biological Properties of isopropylidene shikimic acid. Pakistan Journal of Pharmaceutical Sciences, 31(6), 2329-2332.en_US
dc.identifier.issn1011-601X-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/12789-
dc.description.abstractIsopropylidene shikimic acid (ISA), a new drug derviatived from Shikimic Acid, had been proved to be effective in the cerebral protection after cerebral ischemia and reperfusion. But there was little research on the physical pharmacy and biopharmaceutical properties about the drug. In order to provide some useful data for the pharmaceutical development of ISA, the solubility, stability and Oil/Water partition coefficient (LogP) were determined by the classic preformulation study method, and the transmembrane performance of ISA was studied by Franz -diffusion cell method in vitro. The results showed that ISA was water-soluble with a solubility 32.52mg/ml, which could be improved to 44.32 mg/ml by 1% (w/v) sodium dodecylsulfate; the LogP was -0.63; ISA was less stable in water but it was stable when pH greater than 6.0 and unstable when pH less than 6.0; the accumulated permeation rates at 1h were about 50% and more than 80% at 6h. Data obtained by the study indicated that the medium selection and pH control were important for liquid preparation of ISA, and avoiding dissolution and absorption in stomach was critical for the oral solid dosage forms. Mucosal drug delivery systems would be considered, according to the certain hydrophilic-lipophilic characters and good transmembrane capability.en_US
dc.language.isoen_USen_US
dc.publisherPakistan Journal of Pharmaceutical Sciences University of Karachien_US
dc.subjectPreformulation studyen_US
dc.subjectisopropylidene shikimic aciden_US
dc.subjectstabilityen_US
dc.subjectpartition coefficienten_US
dc.subjecttransmembraneen_US
dc.titlePreformulation study and initial determination of biological Properties of isopropylidene shikimic aciden_US
dc.typeArticleen_US
Appears in Collections:Issue 6

Files in This Item:
File Description SizeFormat 
Paper-2.htm130 BHTMLView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.