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机构地区:[1]河南省食品药品检验所,河南郑州450003 [2]郑州大学药学院,河南郑州450003
出 处:《华西药学杂志》2013年第6期612-614,共3页West China Journal of Pharmaceutical Sciences
摘 要:目的采用顶空气相色谱法测定注射用利福霉素钠中的残留溶剂。方法采用DB—FFAP毛细管柱(30m×0.32mm,0.25μm),柱温采用程序升温:40℃保持5min,以10℃·min。升至50cC保持1min,再以50℃·min-1升至200℃保持5min,进样口温度200℃,FID检测器温度250℃,分流比20:1,N,流速0.7mL·min-1。结果3种残留溶剂各峰的分离度良好,异丙醇、乙醇、乙酸丁酯顶空进样检测的色谱峰面积与浓度的线性关系良好,线性范围分别为0.0100~4.0128(r=0.9999)、0.0100~4.0141(r=0.9999)、9.9×10~3.9766mg·mL-1(r=0.9999);最低检测限分别为0.9910、1.1968、1.3996μg·mL-1;平均加样回收率为97.9%~103.4%,RSO为0.9%~1.9%(n=3)。结论所用方法选择性强、重复性好、灵敏度高、操作方便,可作为注射用利福霉素钠中残留溶剂的质控方法。OBJECTIVE To establish a headspace GC method for the content determination of the residual organic solvents in Rifa- mycin sodium for injection. METHODS The determination were performed on a DB - FFAP (30 m - 0.32 mm,0.25 μm) capillary column, using temperature programming. The initial temperature was kept at 40 h2 for 5 min, then the temperature was raised to 50℃ at the rate of 10 ℃ .rain -j and kept for 1 rain. At last the temperature was raised to 200 ℃ at the rate of 50% .min-1 and kept for 5 min. FID was used as detector with a temperature of 250 ℃. The inlet temperature was 200 ℃, and the split ratio was 20 : 1. RESULTS All the peaks were completely separated. The method had good linearity with a range of 0.0100 -4. 0128 mg mL-1 for isopropyl alcohol ( r = 0. 9999 ), 0. 0100 - 4. 0141 mg mL-1 for ethanol ( r = 0. 9999 ) , and 9.9 x 10 -3 - 3. 9766 mg. mL- 1 for butyl acetate ( r = 0. 9999). The detection limits of them were 0. 9910 μg mL-1 , 1. 1968μg mL-1 and 1. 3996 μg mL-1 , respectively. The average recoveries were in the range of 97.9% - 103.4% with RSD of 0.9% - 1.9% ( n = 3 ). CONCLUSION The method is selective, repeatable, sensitive and convenient, and can be used to control the residual organic solvents in Rifamycin sodium for injection.
分 类 号:R917[医药卫生—药物分析学]
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