1997
DOI: 10.1016/s0378-5173(96)04857-0
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Adsorption of ketotifen onto some pharmaceutical excipients

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Cited by 39 publications
(9 citation statements)
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“…Density influences pellet transit along the gastrointestinal tract. A critical density range to achieve a delay in gastric emptying and tentatively prolonged release of drug in the stomach from coated pellets was 2.4–2.8 g.cm – . The pellet densities produced with Prosolv SMCC 50 or Avicel PH101 according to the conditions in this study are found in the close range of 1.4 and 1.5 g.cm −3 (Table ).…”
Section: Resultsmentioning
confidence: 59%
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“…Density influences pellet transit along the gastrointestinal tract. A critical density range to achieve a delay in gastric emptying and tentatively prolonged release of drug in the stomach from coated pellets was 2.4–2.8 g.cm – . The pellet densities produced with Prosolv SMCC 50 or Avicel PH101 according to the conditions in this study are found in the close range of 1.4 and 1.5 g.cm −3 (Table ).…”
Section: Resultsmentioning
confidence: 59%
“…For instance, some studies had showed the sorption of drug molecules onto the surface of MCC fibers as well as chemical incompatibility between MCC and various drugs. Also, MCC powders originated from different suppliers were found to alter physicochemical properties of pellets . Thus, researchers have evaluated alternative spheronization aids such as k‐carrageenan, powdered cellulose, blend of starch plus dextrin, and even use of new grades of MCC, which is known as MCCII with the intention to overcome some of the limitations of standard MCC .…”
Section: Introductionmentioning
confidence: 99%
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“…There are few drugs, e.g. ketotifen [13], ampicilline and amoxycilline [14], fluphenazine dihydrochloride and promehazine hydrochloride [15] have been investigated to find out the adsorption capacity of MCC.…”
Section: Introductionmentioning
confidence: 99%
“…Some studies have indicated that adsorption increases when pH of the solution increases. [13][14][15]20] This is attributed to the reduction of the solubility of the drug with the increase in pH [13]. Franz and Peck suggested [15] that it is due to the ionization of carboxyl groups on the cellulose surface.…”
Section: Introductionmentioning
confidence: 99%