Basic Considerations for Container Closure Selection of Parenteral DrugProducts

L. Kolluru
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引用次数: 1

Abstract

By definition, container closure system encompasses all components of the packaging system that hold and protect the drug product. It includes primary packaging system (components with which the drug product comes in direct contact) and secondary packaging system (components that offer additional protection to the system but do not come in direct contact with the drug product). This article focuses on primary packaging components as they have a significant effect on the critical quality attributes of the drug product throughout the product shelf-life. Selection of an appropriate container closure system for a parenteral drug product is of utmost importance as Food and Drug Administration (FDA) classified that the probability of interaction of the drug product with the packaging component is high and the risks associated from such interactions are highest for injections administered via parenteral route [1]. Impeachment of container closure integrity leads to compromised sterility of the drug product system, which in turn is one of the major reasons for FDA drug product recalls in 2016 [2].
肠外药品容器封闭选择的基本考虑
根据定义,容器封闭系统包括保存和保护药品的包装系统的所有组成部分。它包括初级包装系统(与药品直接接触的组件)和二级包装系统(为系统提供额外保护但不与药品直接接触的组件)。本文主要关注主要包装成分,因为它们在整个产品保质期内对药品的关键质量属性有重大影响。为肠外药物选择合适的容器封闭系统至关重要,因为美国食品和药物管理局(FDA)认为,药物与包装成分相互作用的可能性很高,而通过肠外途径进行注射的药物与包装成分相互作用的相关风险最高[1]。容器封闭完整性的弹劾导致药品系统的无菌性受损,这反过来又是2016年FDA召回药品的主要原因之一[2]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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