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Formulation and Evaluation of Sintered Floating Tablets of Cefpodoxime Proxetil

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Specialty Pharmacology
Date 2020 May 27
PMID 32454671
Citations 1
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Abstract

Objectives: To develop sintered floating tablets of CP using locust bean gum as a release-controlling material. CP is an orally- administered, extended-spectrum, semi-synthetic antibiotic of the cephalosporin class.

Materials And Methods: CP has a short elimination half-life, possesses high solubility, chemical, enzymatic stability and absorption profiles in acidic pH, which makes it a suitable candidate for formulation in a gastro-retentive dose form for improved bioavailability. Camphor was used to get the desired floating properties. The prepared CP floating tablets were subjected to sintering, where the cross linkage within the polymeric structure was increased by exposing the tablets to acetone vapors. The advantage with sintering is that prolonged drug release can be attained at low hardness and low concentrations of polymers.

Results: The prepared tablets were evaluated and found to have acceptable physicochemical properties. Formulation S2 containing locust bean gum: drug (0.3:1.0) and camphor (10% w/w), which was exposed to acetone vapors for a period of 6 hrs showed optimum floating properties and a better dissolution profile i.e. 97.3% in 12 hrs. Hence, formulation S2 was considered as the optimized formulation. The release data of the optimized formulation was treated with mathematical equations and the drug release followed zero-order kinetics (0.9599) with an anomalous transport mechanism (0.5331).

Conclusion: Based on the results, it can be concluded that sintered floating matrix tablets of CP containing locust bean provides a better choice for controlled release.

Citing Articles

Polymeric Excipients in the Technology of Floating Drug Delivery Systems.

Blynskaya E, Tishkov S, Vinogradov V, Alekseev K, Marakhova A, Vetcher A Pharmaceutics. 2022; 14(12).

PMID: 36559272 PMC: 9786229. DOI: 10.3390/pharmaceutics14122779.

References
1.
Alonso-Sande M, Teijeiro-Osorio D, Remunan-Lopez C, Alonso M . Glucomannan, a promising polysaccharide for biopharmaceutical purposes. Eur J Pharm Biopharm. 2008; 72(2):453-62. DOI: 10.1016/j.ejpb.2008.02.005. View

2.
Beneke C, Viljoen A, Hamman J . Polymeric plant-derived excipients in drug delivery. Molecules. 2009; 14(7):2602-20. PMC: 6255379. DOI: 10.3390/molecules14072602. View

3.
Laurienzo P . Marine polysaccharides in pharmaceutical applications: an overview. Mar Drugs. 2010; 8(9):2435-65. PMC: 2953395. DOI: 10.3390/md8092435. View

4.
Khan F, Katara R, Ramteke S . Enhancement of bioavailability of cefpodoxime proxetil using different polymeric microparticles. AAPS PharmSciTech. 2010; 11(3):1368-75. PMC: 2974107. DOI: 10.1208/s12249-010-9505-x. View

5.
Oh T, Kim J, Ha J, Chi S, Rhee Y, Park C . Preparation of highly porous gastroretentive metformin tablets using a sublimation method. Eur J Pharm Biopharm. 2012; 83(3):460-7. DOI: 10.1016/j.ejpb.2012.11.009. View