2016
DOI: 10.4172/1920-4159.1000209
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Formulation and Evaluation of Floating Osmotic Tablets of Nizatidine

Abstract: This study was conducted to develop floating osmotic tablets of Nizatidine, a H2 receptor antagonist, to release the drug as two distinct pulses separated by a lag time that achieve plasma concentration profiles varying in a circadian rhythm fashion, for the chronotherapy of ulcer. Floating osmotic tablets were developed using effervescence method consisted of three different steps viz, preparation of floating sustained release drug containing tablets followed by time-lagged (4 hrs) coating with hydrophobic ru… Show more

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Cited by 10 publications
(11 citation statements)
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“…Twenty tablets from both of the brands of enalapril maleate were weighed individually with the mentioned analytical balance and average weight and the percent deviation was determined for each brand 10 .…”
Section: Determination Of Weight Variationmentioning
confidence: 99%
See 1 more Smart Citation
“…Twenty tablets from both of the brands of enalapril maleate were weighed individually with the mentioned analytical balance and average weight and the percent deviation was determined for each brand 10 .…”
Section: Determination Of Weight Variationmentioning
confidence: 99%
“…The tablets were placed in 900 mL of Phosphate buffer (pH 6.8) at 37 ± 0.1°C. At appropriate intervals (5,10,15,30, and 60 min), 5 mL of the samples were taken and filtered. The dissolution medium was then replaced by 5 mL of fresh dissolution fluid to maintain a constant volume.…”
Section: Dissolution Studies Of Enalapril Maleate Tabletsmentioning
confidence: 99%
“…It decreases the amount of acid produced in the stomach. Esomeprazole is used to treat and prevent stomach and intestinal ulcers, erosive esophagitis (damage to the esophagus from stomach acid), and other conditions involving excessive stomach acid such as Zollinger-Ellison syndrome 4 . In Peptic ulcer patients, gastric distress occurs is most likely in the late night and early morning hours.…”
Section: Introductionmentioning
confidence: 99%
“…More often, the drug absorption is unsatisfactory and highly variable among and between individuals, despite excellent in vitro release patterns. The reasons for this are essentially physiological and usually affected by the GI transit of the form, especially its gastric residence time, which appears to be one of the major causes of the overall transit time variability [2].…”
Section: Introductionmentioning
confidence: 99%