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Formulation and Evaluation of Mouth Disintegrating Tablets of Atenolol and Atorvastatin

TLDR
Sublimation method is found to be the best among three methods of preparation used to study the effect of manufacturing processes, nature and concentration of superdisintegrants on various features of mouth-disintegrating tablets.
Abstract
In this study, mouth-disintegrating tablets of atenolol and atorvastatin combination were formulated using superdisintegrants to impart fast disintegration. Fifteen formulations were prepared based on different concentrations of two superdisintegrants, croscarmellose sodium and Kyron-T134. Three different techniques such as direct compression, effervescent and sublimation were used to study the effect of manufacturing processes, nature and concentration of superdisintegrants on various features of these tablets. Five formulations were made using each method. Precompression studies like bulk density, tapped density, angle of repose, Carr's compressibility index, Hausner's ratio and compatibility studies such as Fourier transform infrared spectroscopy and differential scanning calorimetry were performed. Various features such as hardness, thickness, diameter, weight variation, friability, disintegration time, dissolution studies, wetting time, wetting volume, water absorption ratio, modified disintegration, uniformity of contents and stability were evaluated. Finally results were statistically analyzed by the application of one way ANOVA test. Formulation F13 containing Kyron-T134 (6%) and croscarmellose sodium (2%) was found to be the best among all fifteen formulations prepared in all aspects evaluated. Sublimation method is found to be the best among three methods of preparation used.

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Patent

Fast dissolving drug delivery systems

TL;DR: The present invention discloses the administration of biological active agent via the oral sokbun dispersible / soluble in the drug delivery system for the medical treatment of a patient suffering from dysphagia and /or swallowing whole and / or aspiration hazard.
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Fast Dissolving Tablets

TL;DR: Loratadine fast dissolving tablets were prepared by solid dispersion and using croscarmellose sodium, sodium starch glycolate and polyplasdone XL as super disintegrants and showed quick disintegration and higher dissolution.
Journal ArticleDOI

Fabrication and Characterization of Diclofenac Sodium Loaded Hydrogels of Sodium Alginate as Sustained Release Carrier

TL;DR: In this paper, the authors used free radical polymerization to fabricate naturally derived polymer based hydrogels for controlled release of diclofenac sodium (DS) for a long duration of time.
Journal ArticleDOI

Using Carbomer-Based Hydrogels for Control the Release Rate of Diclofenac Sodium: Preparation and In Vitro Evaluation

TL;DR: Different kinetics such as zero- order, first-order, the Higuchi model and the Korsmeyer–Peppas model were applied to know the mechanism of release order of drugs from the hydrogels.
Journal ArticleDOI

Development of β-cyclodextrin-based hydrogel microparticles for solubility enhancement of rosuvastatin: an in vitro and in vivo evaluation.

TL;DR: A potential approach for solubility enhancement of RST calcium and other hydrophobic moieties was successfully developed and better results regarding pharmacokinetic parameters were seen in the case of hydrogel microparticles.
References
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Book

The Theory and Practice of Industrial Pharmacy

TL;DR: The theoty and practice of industrial pharmacacy as mentioned in this paper, Thetheory and Practice of Industrial Pharmacy, Thetheology and the Practice of industrial pharmacy, and Thethety and the practice of Industrial pharmacacy.
Journal ArticleDOI

Drug-delivery products and the Zydis fast-dissolving dosage form.

TL;DR: Many patients find it difficult to swallow tablets and hard gelatin capsules and do not take their medication as prescribed, but such problems can be resolved by means of the Zydis dosage form which does not require water to aid swallowing.
Journal ArticleDOI

Preparation and Evaluation of a Compressed Tablet Rapidly Disintegrating in the Oral Cavity

TL;DR: In order to make a compressed tablet which can rapidly disintegrate in the oral cavity, microcrystalline cellulose and low-substituted hydroxypropylcellulose were used as disintegrants, and ethenzamide and ascorbic acid were chosen as poorly and easily water soluble model drugs, respectively.
Journal ArticleDOI

Predictors of medication adherence in the elderly

TL;DR: It is indicated that there remains some uncertainty about the reasons for noncompliant medication-taking in the elderly, and the current knowledge should be considered when designing and implementing disease-management programs for the elderly.
Journal Article

Fast-dissolving tablets

TL;DR: This artide describes existing fast-dissolving technologies and discusses several techniques used to formulate such tablets, namely tablet molding, freeze-drying, spray-Drying, sublimation, disintegrant addition, and the use of sugar-based excipients.
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