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在含有橡胶的包装中储存的药物制剂中多环芳烃的瓶内固相萃取

In-vial solid-phase extraction of polycyclic aromatic hydrocarbons in drug formulations stored in packaging containing rubber.

作者信息

Yang Hao, Ding Yinmeng, Ding Ya, Liu Jing

机构信息

Department of Pharmaceutical Analysis, China Pharmaceutical University 24 Tongjiaxiang Nanjing 210009 China

Key Laboratory of Drug Quality Control and Pharmacovigilance, Ministry of Education, China Pharmaceutical University 24 Tongjiaxiang Nanjing 210009 China

出版信息

RSC Adv. 2023 Mar 9;13(12):7848-7856. doi: 10.1039/d2ra07582b. eCollection 2023 Mar 8.

Abstract

Polycyclic aromatic hydrocarbons (PAHs) are a class of ubiquitous and persistent organic compounds that are significantly teratogenic, carcinogenic and mutagenic. Rubber stoppers commonly used in sterile formulation packaging materials often contain carbon black as the additive to enhance mechanical strength. However, PAHs may be formed during the production of carbon black, which could cause the drug formulations to be contaminated when contacting with the rubber stopper, and then enter the patient's body. The determination of PAHs in drug formulations is challenging, due to their trace amounts and matrix interference. Therefore, sample pretreatment is necessary and important. In this work, a novel technique, named in-vial solid-phase extraction (IVSPE), was developed for the selective extraction and enrichment of 16 PAHs in pharmaceuticals. The coated sample vial was directly used as the container for the whole process of sample pretreatment. As the solid-phase adsorbent, the coating was prepared by successively modifying the inner surface of a sample vial with polydopamine film and octadecylamine. PAHs could be selectively extracted through π-π stacking interaction and hydrophobic interaction, and then desorbed and enriched by a small amount of organic solvent. After systematic optimization of the coating preparation and the extraction process, the limits of detection and quantification of 16 PAHs were in the range of 0.002-0.60 ng mL and 0.007-2.00 ng mL, respectively. Good linearities and precision of six repeated injections were obtained. The recoveries at three spiked concentration levels in normal saline were in the range of 62.72-106.90% with the relative standard deviation between 0.83% and 6.78%. Finally, PAHs in normal saline and powders for injection were extracted by established IVSPE, followed by separation and detection with high-performance liquid chromatography with a fluorescence detector and diode array detector (HPLC-FLD/DAD). It is worth noting that the preparation conditions of the adsorbent in the IVSPE method are mild, simple and green. Moreover, IVSPE has the advantages of having few work steps and avoiding the risk of contamination, because no special instrumentation or sample transfer is required. IVSPE could also be used for the pretreatment of multiple samples at the same time, which is beneficial to practical applications.

摘要

多环芳烃(PAHs)是一类普遍存在且持久的有机化合物,具有显著的致畸、致癌和致突变性。无菌制剂包装材料中常用的橡胶塞通常含有炭黑作为增强机械强度的添加剂。然而,在炭黑生产过程中可能会形成多环芳烃,当与橡胶塞接触时,可能会导致药物制剂受到污染,进而进入患者体内。由于药物制剂中多环芳烃含量痕量且存在基质干扰,对其进行测定具有挑战性。因此,样品预处理是必要且重要的。在本工作中,开发了一种名为瓶内固相萃取(IVSPE)的新技术,用于选择性萃取和富集药物中的16种多环芳烃。涂覆的样品瓶直接用作样品预处理全过程的容器。作为固相吸附剂,通过依次用聚多巴胺膜和十八烷基胺修饰样品瓶的内表面来制备涂层。多环芳烃可通过π-π堆积相互作用和疏水相互作用被选择性萃取,然后用少量有机溶剂解吸并富集。在对涂层制备和萃取过程进行系统优化后,16种多环芳烃的检测限和定量限分别在0.002 - 0.60 ng/mL和0.007 - 2.00 ng/mL范围内。获得了良好的线性关系和六次重复进样的精密度。在生理盐水三个加标浓度水平下的回收率在62.72% - 106.90%范围内,相对标准偏差在0.83% - 6.78%之间。最后,通过建立的IVSPE方法萃取生理盐水和注射用粉末中的多环芳烃,然后用配备荧光检测器和二极管阵列检测器的高效液相色谱(HPLC - FLD/DAD)进行分离和检测。值得注意的是,IVSPE方法中吸附剂的制备条件温和、简单且绿色环保。此外,IVSPE具有工作步骤少且避免污染风险的优点,因为不需要特殊仪器或样品转移。IVSPE还可同时用于多个样品的预处理,有利于实际应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6720/9996413/7b2955946378/d2ra07582b-f1.jpg

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