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Formulation design and optimization of mouth dissolve tablets of nimesulide using vacuum drying technique.

TLDR
Results of multiple linear regression analysis revealed that for obtaining a rapidly disintegrating dosage form, tablets should be prepared using an optimum concentration of camphor and a higher percentage of crospovidone.
Abstract
The purpose of this research was to develop mouth dissolve tablets of nimesulide. Granules containing nimesulide, camphor, crospovidone, and lactose were prepared by wet granulation technique. Camphor was sublimed from the dried granules by exposure to vacuum. The porous granules were then compressed. Alternatively, tablets were first prepared percentage friability, wetting time, and disintegration time. In the investigation, a 32 full factorial design was used to investigate the joint influence of 2 formulation variables: amount of camphor and crospovidone. The results of multiple linear regression analysis revealed that for obtaining a rapidly disintegrating dosage form, tablets should be prepared using an optimum concentration of camphor and a higher percentage of crospovidone. A contour plot is also presented to graphically represent the effect of the independent variables on the disintegration time and percentage friability. A checkpoint batch was also prepared to prove the validity of the evolved mathematical model. Sublimation of camphor from tablets resulted in superior tablets as compared with the tablets prepared from granules that were exposed to vacuum. The systematic formulation approach helped in understanding the effect of formulation processing variables.

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Journal ArticleDOI

Orodispersible tablets: An overview

TL;DR: This review describes the various formulation aspects, disintegrants employed and technologies developed for ODTs, along with various excipients, evaluation tests, marketed formulations, and drugs explored in this field.
Journal ArticleDOI

Optimizing drug delivery systems using systematic "design of experiments." Part II: retrospect and prospects.

TL;DR: A vast account of various DoE reports on optimization of diverse drug delivery system and processes along with the critical graphical analysis of various designs, input, and response variables have been presented here in a categorical form.
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Formulation and optimization of mouth dissolve tablets containing rofecoxib solid dispersion.

TL;DR: The potential of experimental design in understanding the effect of the formulation variables on the quality of mouth dissolve tablets containing solid dispersion of a hydrophobic drug is demonstrated.
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Taste masking of ondansetron hydrochloride by polymer carrier system and formulation of rapid-disintegrating tablets.

TL;DR: Results conclusively demonstrated successful masking of taste and rapid disintegration of the formulated tablets in the oral cavity.
Journal ArticleDOI

Formulation and Evaluation of Rapidly Disintegrating Fenoverine Tablets: Effect of Superdisintegrants

TL;DR: Direct compressible rapidly disintegrating tablets of fenoverine with lower friability, acceptable taste, and shorter disintegration times were obtained using crospovidone and other excipients at optimum concentrations.
References
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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 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.
Journal ArticleDOI

Solubility enhancement of Cox-2 inhibitors using various solvent systems.

TL;DR: Physico-chemical properties of the solvent such as polarity, intermolecular interactions, and the ability of the liquid to form a hydrogen bond with the drug molecules were found to be the major factors involved in the dissolution of drugs by pure solvents.
Journal ArticleDOI

New method of preparing high-porosity rapidly saliva soluble compressed tablets using mannitol with camphor, a subliming material

TL;DR: In this article, the authors developed a direct compression method for the preparation, using mannitol and camphor, of a meclizine tablet with high porosity which dissolves rapidly in saliva.
Journal ArticleDOI

Statistics (2nd Ed.)

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