Formulation and optimization of effervescent tablet containing bismuth sub-citrate

(2019) Formulation and optimization of effervescent tablet containing bismuth sub-citrate. Journal of Reports in Pharmaceutical Sciences. pp. 236-244. ISSN 23221232 (ISSN)

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Abstract

Objective: The objective of this study was to design, evaluate and optimize effervescent tablets containing bismuth sub-citrate with sufficient hardness and friability in treatment of peptic ulcer. Materials and Methods: Effervescent tablets were prepared by direct compression method and were optimized using irregular factorial design. Amount of citric acid, sodium bicarbonate to citric acid molar ratio, polyvinyl pyrrolidone K 30 (PVP k30), polyethylene glycol 6000 (PEG 6000) were selected as independent variables, whereas disintegration time, amount of carbon dioxide (CO2), friability, pH, and hardness were selected as dependent variables. All the batches were assessed for various pre and post compression characteristics such as flowability, hardness, friability, effervescent time, pH, and content uniformity. For the enhancement of tablets' palatability, the components of optimized formulation were mixed with same amounts of different flavoring agents. Results: The best results obtained from effervescent tablets prepared by 500 mg citric acid, 5 PEG 6000 and 3 PVP k30 while the molar ratio of the sodium bicarbonate to citric acid was 3. The disintegration time, amount of CO2, friability, pH, and hardness of optimized formulation were confirmed to be 95.33 ± 1.15sec, 398.73 ± 1.46 mg, 0.73, 6.0 ± 0.06 and 72.3 ± 5.5 N, respectively. The most pleasant taste according to volunteers' acceptability was the taste of cherry. Conclusion: These results suggest that developed effervescent tablets may be promising for delivery of bismuth sub-citrate in peptic ulcers therapy. © 2019 Journal of Reports in Pharmaceutical Sciences | Published by Wolters Kluwer-Medknow.

Item Type: Article
Keywords: Bismuth sub-citrate direct compression method effervescent tablet polyvinylpyrrolidone k 30 bicarbonate bismuth citrate carbon dioxide citric acid flavoring agent macrogol 6000 mannitol povidone sucrose angle of repose Article berry bulk density chemical composition cherry controlled study flavor human human experiment normal human palatability particle size pH process optimization raspberry sour cherry tablet compression tablet disintegration time tablet formulation tablet friability tablet hardness tablet weight tapped density tutti frutti
Subjects: QV Pharmacology
Divisions: Faculty of Pharmacy and Pharmaceutical Sciences > Department of Pharmacotherapy
Novel Drug Delivery Systems Research Center
Page Range: pp. 236-244
Journal or Publication Title: Journal of Reports in Pharmaceutical Sciences
Journal Index: Scopus
Volume: 8
Number: 2
Identification Number: https://doi.org/10.4103/jrptps.JRPTPS₁₁₁₉
ISSN: 23221232 (ISSN)
Depositing User: Zahra Otroj
URI: http://eprints.mui.ac.ir/id/eprint/11997

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