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醋酸戈舍瑞林预充式注射器中药物溶出相互作用产物的评价。

Drug-Leachable Interaction Product Evaluation in Prefilled Syringe of Ganirelix Acetate Injection.

机构信息

Department of Pharmaceutical Analysis, The National Institute of Pharmaceutical Education and Research-Ahmedabad (Ministry of Chemicals and Fertilizers, Government of India), Opposite Air force Station, Palaj, Gandhinagar, Gujarat 382355, India.

Department of Pharmaceutical Analysis, The National Institute of Pharmaceutical Education and Research-Ahmedabad (Ministry of Chemicals and Fertilizers, Government of India), Opposite Air force Station, Palaj, Gandhinagar, Gujarat 382355, India.

出版信息

J Pharm Sci. 2024 Aug;113(8):2023-2027. doi: 10.1016/j.xphs.2024.05.012. Epub 2024 May 23.

DOI:10.1016/j.xphs.2024.05.012
PMID:38796153
Abstract

The concept of extractables and leachable has introduced a new era for identifying potential impurities in drug products. Pharmaceutical packaging materials encompass a variety of polymers due to their appealing properties for storing the drug product. However, numerous chemical species may leach into the drug product from these polymers, posing significant health hazards in the public domain. Identifying such leachable is crucial for assessing safety and addressing toxicological concerns. Acrylic acids are commonly used materials for adhering needles to the barrel in pre-filled syringes. In this study, we identified acrylic acid leachable impurities in ganirelix drug products available in the market using mass spectrometry as an analytical technique. These impurities leached into the drug product during storage conditions. Characterization of the impurities was carried out through data obtained from HRMS and MS/MS analysis, revealing them as polyacrylic acid-ganirelix adduct impurities. This study offers valuable insights into identifying leachable and susceptible sites, providing a foundation for potential modifications in similar classes of drug products, thereby enhancing their safety and efficacy.

摘要

提取物和可浸出物的概念为识别药物产品中的潜在杂质引入了一个新时代。由于具有储存药物产品的诱人特性,药物包装材料包含各种聚合物。然而,这些聚合物中可能有许多化学物质会浸出到药物产品中,在公共领域构成重大健康危害。识别这些可浸出物对于评估安全性和解决毒理学问题至关重要。丙烯酸常用于将针头粘附到预填充注射器的桶上。在这项研究中,我们使用质谱法作为分析技术,在市场上可获得的加尼瑞克药物产品中鉴定出丙烯酸可浸出杂质。这些杂质在储存条件下浸出到药物产品中。通过 HRMS 和 MS/MS 分析获得的数据对杂质进行了表征,结果表明它们是聚(丙烯酸)-加尼瑞克加合物杂质。这项研究为识别可浸出和易受影响的部位提供了有价值的见解,为类似类别药物产品的潜在修饰提供了基础,从而提高了它们的安全性和疗效。

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