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适用于注射用和眼用药品的模型容器-密封系统的模拟浸出(迁移)研究。

Simulated Leaching (Migration) Study for a Model Container-Closure System Applicable to Parenteral and Ophthalmic Drug Products.

作者信息

Jenke Dennis, Egert Thomas, Hendricker Alan, Castner James, Feinberg Tom, Houston Christopher, Hunt Desmond G, Lynch Michael, Nicholas Kumudini, Norwood Daniel L, Paskiet Diane, Ruberto Michael, Smith Edward J, Holcomb Frank, Markovic Ingrid

机构信息

Baxter Healthcare Corporation, Round Lake, IL, USA;

Boehringer Ingelheim Pharmaceuticals, Inc., Ingelheim/Rhein, Germany.

出版信息

PDA J Pharm Sci Technol. 2017 Mar-Apr;71(2):68-87. doi: 10.5731/pdajpst.2016.007229. Epub 2016 Dec 14.

Abstract

A simulating leaching (migration) study was performed on a model container-closure system relevant to parenteral and ophthalmic drug products. This container-closure system consisted of a linear low-density polyethylene bottle (primary container), a polypropylene cap and an elastomeric cap liner (closure), an adhesive label (labeling), and a foil overpouch (secondary container). The bottles were filled with simulating solvents (aqueous salt/acid mixture at pH 2.5, aqueous buffer at pH 9.5, and 1/1 v/v isopropanol/water), a label was affixed to the filled and capped bottles, the filled bottles were placed into the foil overpouch, and the filled and pouched units were stored either upright or inverted for up to 6 months at 40 °C. After storage, the leaching solutions were tested for leached substances using multiple complementary analytical techniques to address volatile, semi-volatile, and non-volatile organic and inorganic extractables as potential leachables.The leaching data generated supported several conclusions, including that (1) the extractables (leachables) profile revealed by a simulating leaching study can qualitatively be correlated with compositional information for materials of construction, (2) the chemical nature of both the extracting medium and the individual extractables (leachables) can markedly affect the resulting profile, and (3) while direct contact between a drug product and a system's material of construction may exacerbate the leaching of substances from that material by the drug product, direct contact is not a prerequisite for migration and leaching to occur. The migration of container-related extractables from a model pharmaceutical container-closure system and into simulated drug product solutions was studied, focusing on circumstances relevant to parenteral and ophthalmic drug products. The model system was constructed specifically to address the migration of extractables from labels applied to the outside of the primary container. The study demonstrated that (1) the extractables that do migrate can be correlated to the composition of the materials used to construct the container-closure systems, (2) the extent of migration is affected by the chemical nature of the simulating solutions and the extractables themselves, and (3) even though labels may not be in direct contact with a contained solution, label-related extractables can accumulate as leachables in those solutions.

摘要

对一种与注射用和眼用药品相关的模型容器密封系统进行了模拟浸出(迁移)研究。该容器密封系统由线性低密度聚乙烯瓶(内包装容器)、聚丙烯瓶盖和弹性体瓶盖内衬(密封件)、不干胶标签(标签)以及铝箔外袋(外包装容器)组成。向瓶中装入模拟溶剂(pH值为2.5的盐水/酸混合水溶液、pH值为9.5的缓冲水溶液以及体积比为1/1的异丙醇/水),在装满并加盖的瓶子上贴上标签,将装满的瓶子放入铝箔外袋中,然后将装满并装入外袋的单元直立或倒置存放于40℃下长达6个月。储存后,使用多种互补分析技术对浸出溶液中的浸出物质进行检测,以分析挥发性、半挥发性和非挥发性有机及无机可提取物作为潜在浸出物的情况。所生成的浸出数据支持了几个结论,包括:(1)模拟浸出研究揭示的可提取物(浸出物)概况在定性上可与构成材料的成分信息相关联;(2)提取介质和单个可提取物(浸出物)的化学性质均可显著影响最终的概况;(3)虽然药品与系统的构成材料直接接触可能会加剧药品从该材料中浸出物质的情况,但直接接触并非迁移和浸出发生的先决条件。研究了与注射用和眼用药品相关情况下,容器相关可提取物从模型药品容器密封系统迁移至模拟药品溶液中的情况。该模型系统专门构建用于研究从贴在内包装容器外部的标签中迁移出的可提取物。研究表明:(1)确实发生迁移的可提取物与用于构建容器密封系统的材料成分相关;(2)迁移程度受模拟溶液和可提取物本身化学性质的影响;(3)即使标签可能未与所装溶液直接接触,与标签相关的可提取物也可能作为浸出物在那些溶液中积累。

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