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ISSN 2063-5346
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A detailed review on methods, evaluation and limitations of Pastillation process

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Amit Kumar# , Seema# , Neha S.L. # , Satyender Kumar#1
» doi: 10.48047/ecb/2023.12.Si12.145

Abstract

This article introduces a brand new technique known as "Pastillation," which, for the first time in the history of the pharmaceutical industry, may be utilized to produce lipid-based oral multiparticulate controlled release dosage forms. This multiparticulate system is able to keep the drug release constant for a period of twenty-four hours, it has very good flow qualities, and it is extremely uniform in terms of size, weight, and drug content. This process of pastille formation is opted on either small scale or large scale in which various processes are discussed. The fact that the chemical industry already has well-established large-scale equipment for pastillation is likely the most significant advantage that this technique offers. Because of this, the application of this one-of-a-kind dosage form has the potential to throw open a new door in the sector of the pharmaceutical industry that deals with the delivery of medications

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