Industrial perspective of gastroretentive drug delivery systems: physicochemical, biopharmaceutical, technological and regulatory consideration

• Published in: Expert opinion on drug delivery Vol. 9; no. 5; p. 551
• Main Authors: Pawar, Vivek K, Kansal, Shaswat, Asthana, Shalini, Chourasia, Manish K
• Format: Journal Article
• Language: English
• Published: England 01.05.2012
• Subjects: Biological Availability; Biological Products - administration & dosage; Chemistry, Pharmaceutical; Delayed-Action Preparations - administration & dosage; Delayed-Action Preparations - chemistry; Delayed-Action Preparations - pharmacokinetics; Drug Carriers - administration & dosage; Drug Carriers - chemistry; Drug Carriers - pharmacokinetics; Drugs, Generic - administration & dosage; Drugs, Generic - chemistry; Drugs, Generic - pharmacokinetics; Duodenum - metabolism; Excipients - administration & dosage; Excipients - chemistry; Excipients - pharmacokinetics; Humans; Intestinal Absorption; Jejunum - metabolism; Pharmaceutical Preparations - administration & dosage; Pharmaceutical Preparations - chemistry; Product Surveillance, Postmarketing - economics; Product Surveillance, Postmarketing - standards; Stomach - metabolism; Technology, Pharmaceutical - legislation & jurisprudence; Technology, Pharmaceutical - standards
• ISSN: 1744-7593
• DOI: 10.1517/17425247.2012.677431

Gastroretentive drug delivery systems (GRDDS) can overcome drawbacks associated with oral drug delivery, by defeating natural physiological principles. Various gastroretentive technologies have been developed in the past, but few of them achieved success on the market. This review is focused on the key concepts required to make a high-quality drug product available in a timely and economical manner. Pharmacotherapy of various disease states can be amended by drug repurposing through GRDDS. Assessment of the effect of the fed and fasted condition on product performance should be necessary during initial development phases. Dual working technology would be a possible way to overcome drawbacks associated with different GRDDS. Before development of a drug product, the principles of scale up and process validation must be considered to improve the quality and market availability of GRDDS. Knowledge of all regulatory aspects will help to deliver a product to the market within a reasonable timeframe and in a cost-effective manner.