高风险头孢菌素粉针剂包装材料兼容性研究及指标成分评价方法的建立

IF 0.7 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Chao Chen, Yan Wang, Yue Chen, Aijing Zhang, Zhiwei Cai, Lei Cheng, Bingyong Xu, Xinyou Bao, Jianmou Liang
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引用次数: 0

摘要

目的建立测定注射用头孢曲松钠瓶塞中可萃取物质的气相色谱-质谱法;建立测定注射用头孢曲松钠瓶塞中硫化剂和抗氧剂的高效液相色谱法,并分析橡胶瓶塞中挥发性物质与溶液澄清度的相关性:建立测定注射用头孢曲松钠瓶塞中可萃取物质的气相色谱-质谱法;建立测定注射用头孢曲松钠瓶塞中硫化剂和抗氧化剂的高效液相色谱法,并分析橡胶瓶塞中挥发性物质与溶液澄清度的相关性:采用毛细管色谱柱 Rtx-5MS(30.0 m×0.25 mm, 0.25 µm),载气为 He,流速为 1.8mL-min-1,进样口温度为 200 ℃,分流比为 10∶l,柱温为程序温度(初始柱温为 40 ℃,保持 15 min,以 10 ℃升温至 100 ℃,保持 2 min,以 25 ℃升温至 100 ℃,保持 2 min)、以 25 ℃升温至 230 ℃,保持 10 分钟),界面温度为 250 ℃,扫描范围为 29 至 600(m-z-1),挥发性物质采用全扫描。采用 inertsil ODS-3 色谱柱(250 mm×4.6 mm, 5 µm)进行高效液相色谱分析。流动相 A 为含 0.04% 三氟乙酸的水,流动相 B 为含 0.04% 三氟乙酸的乙腈,梯度洗脱,流速为 1.0 mL-min-1。柱温为 30 ℃,检测波长为 210 nm,进样量为 10 µL:通过气相色谱-质谱检测,橡胶塞中的抗氧化剂 BHT(264)、硅油和其他有机化合物随着时间的加速而渗透并迁移到样品中。在 0.5-100 μg-mL-1 范围内线性关系良好(r>0.999)。硫化剂和抗氧化剂的检出限约为 0.03 μg-mL-1,定量限约为 0.1 μg-mL-1。通过添加标准回收率实验,抗氧化剂(168、264、330、1076、1010)和硫化剂(二硫化碳、硫磺)的平均回收率(低、中、高)在 90.0% 至 110.0% 之间,相应的 RSD 均小于 5%(n=9)。稳定性实验表明,抗氧剂和硫化剂溶液具有良好的稳定性,在 24 小时内稳定。结论:GC-MS/HPLC 法可用于注射用头孢曲松钠胶塞的质量控制,初步形成了注射用头孢曲松钠包装材料的相容性研究和综合评价体系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Research on Compatibility of Packaging Materials of High-Risk Cephalosporin Powder Injection and Establishment of Indicator Component Evaluation Method
aims: To establish a GC-MS method for the determination of extractable substances in the stoppers of Ceftriaxone sodium bottles for injection; To establish a HPLC method for the determination of vulcanizing agent and antioxidant in Ceftriaxone sodium for injection bottle stopper and to analyze the correlation between the volatile substances of rubber stopper and the clarity of solution. objective: To establish a GC-MS method for the determination of extractable substances in the stoppers of Ceftriaxone sodium bottles for injection; To establish a HPLC method for the determination of vulcanizing agent and antioxidant in Ceftriaxone sodium for injection bottle stopper and to analyze the correlation between the volatile substances of rubber stopper and the clarity of solution. method: GC-MS method was used with capillary column Rtx-5MS (30.0 m×0.25 mm, 0.25 µm), the carrier gas was He at the flow rate of 1.8mL·min-1, the temperature of injection port was 200 ℃, shunt ratio was 10∶l, the column temperature was programmed temperature(initial column temperature was 40 ℃ and kept for 15 min, and with the speed of 10 ℃ upping to 100 ℃ and kept for 2 min, and with the speed of 25 ℃ upping to 230 ℃ and kept for 10 min), the interface temperature was 250 ℃, and the scanning range was from 29 to 600(m·z-1), and the volatile substances were using full scan. An inertsil ODS-3 column(250 mm×4.6 mm, 5 µm) was used for the HPLC analysis. The mobile phase A consisted of water containing 0.04% trifluoroacetic and the mobile phase B consisted of acetonitrile containing 0.04% trifluoroacetic acid, the gradient elution was used and the flow rate was set as 1.0 mL·min-1. The column temperature was 30 ℃, the detection wavelength was 210 nm and the injection volume was 10 µL. result: Antioxidant BHT(264), silicone oil and other organic compounds in rubber stopper permeated and migrated to the sample with acceleration time by GC-MS. A good linearity was observed over the range of 0.5-100 μg·mL-1(r>0.999). The detection limits of vulcanizing agent and antioxidant were about 0.03 μg·mL-1, and the quantitation limits were about 0.1 μg·mL-1. The average recoveries (low, medium and high) of antioxidant (168, 264, 330, 1076, 1010) and vulcanizing agents (carbon disulfide, sulfur) were between 90.0% and 110.0%, and the corresponding RSD were less than 5% (n=9) by adding standard recovery experiments. The stability test showed that the antioxidant and the vulcanizing agent solution had good stability and was stable within 24 hours. conclusion: the GC-MS/HPLC method can be used for the quality control of rubber stopper of cefuroxime Sodium for Injection.The compatibility study and comprehensive evaluation system of Ceftriaxone sodium for injection packaging materials have been initially formed.
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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
85
审稿时长
3 months
期刊介绍: Aims & Scope Current Pharmaceutical Analysis publishes expert reviews and original research articles on all the most recent advances in pharmaceutical and biomedical analysis. All aspects of the field are represented including drug analysis, analytical methodology and instrumentation. The journal is essential to all involved in pharmaceutical, biochemical and clinical analysis.
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