Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/106489
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dc.titleUptake of water by excipients in tablets
dc.contributor.authorWan, L.S.C.
dc.contributor.authorPrasad, K.P.P.
dc.date.accessioned2014-10-29T02:00:45Z
dc.date.available2014-10-29T02:00:45Z
dc.date.issued1989-03-01
dc.identifier.citationWan, L.S.C.,Prasad, K.P.P. (1989-03-01). Uptake of water by excipients in tablets. International Journal of Pharmaceutics 50 (2) : 147-153. ScholarBank@NUS Repository.
dc.identifier.issn03785173
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/106489
dc.description.abstractDisintegrants such as sodium starch glycolate (NaSt glycolate), crospovidone (PVPP) and silicon dioxide (SiO2) play an active part in influencing water uptake and disintegration time (DT) of sulphanilamide tablets containing methylcellulose (MC) of varying viscosity grade as a binder. The disintegrants used were at the 1.25%, 2.50% and 5% level. The DT of tablets containing NaSt glycolate decreased with an increase in the viscosity of MC due to enhanced water uptake. Tablets without MC but only the drug and NaSt glycolate were observed to have a higher DT and lower water uptake at higher concentrations of the disintegrant. With PVPP, the DT increased with increasing viscosity of MC. This occurs despite an increase in water uptake by tablets containg higher viscosity MC. For tablets containing SiO2 and MC, DT is extremely high. In the absence of MC, water uptake is slightly higher with the higher concentration of SiO2 but DT still remained high. Water uptake alone does not determine the disintegration process. The choice of excipients, especially binders such as methylcellulose, plays a crucial role in influencing disintegrant action. © 1989.
dc.sourceScopus
dc.subjectColloidal silicon dioxide
dc.subjectCrospovidone
dc.subjectDisintegration
dc.subjectMethylcellulose
dc.subjectSodium starch glycolate
dc.subjectWater penetration
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.description.sourcetitleInternational Journal of Pharmaceutics
dc.description.volume50
dc.description.issue2
dc.description.page147-153
dc.description.codenIJPHD
dc.identifier.isiutNOT_IN_WOS
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