儿童药物开发过程综述

Chetan Sushir, Vaishali A. Kilor, Ashika Rewatkar
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引用次数: 0

摘要

本文综述了提高儿童依从性的新制剂方法,如迷你片、3D打印、可分散膜、咀嚼片。改善患者依从性的各种策略,如“乳头护罩”给药系统,在给药点将干固体配方转化为液体,药丸吞咽杯,药物给药吸管。制定适合儿童年龄、体型、生理状况和治疗要求的儿科药物是很重要的。儿科配方立法,以确保治疗儿科患者的产品被适当授权用于儿科人群,最大限度地减少标签外药物的最坏影响,并改善这些产品在各种儿科人群中使用的可用信息。此外,审查还包括关于法规的立法义务和要求、现状、挑战和影响的资料。由于新的法规、额外的资助机会和合作研究倡议,儿科配方的开发最近取得了进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pediatric Drug Development Process: A Review
This review includes New Formulation approaches to improve Pediatric compliance such as Mini tablets, 3D printing, Orodispersible films, Chewable tablets. Various strategies to improve patient adherence such as ‘nipple shield’ delivery system, dry solid formulations to be converted to liquid at the point of administration, pill swallowing cups, Medicated dosing straw. It is important to formulate pediatric medicines that are tailored to a child’s age, size, physiological condition, and treatment requirements. Legislations for pediatric formulation to ensure that products to treat pediatric patients are appropriately authorized for use in the pediatric population, minimize the worst effect of Off-label medication and to improve the information available on the use of these products in the various pediatric populations. Also, the review consists of Information on legislative obligation and requirement, current State, challenges and effect of regulations. Recent progress has been made in the development of pediatric formulations due to new regulations, additional funding opportunities, and collaborative research initiatives.
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