邻苯二甲醛柱前衍生化-HPLC测定复方氨基酸注射液中蛋氨酸亚砜的含量

    Determination of Methionine Sulfoxide in Compound Amino Acid Injection by HPLC with OPA Pre-column Derivatization

    • 摘要: 目的 建立测定复方氨基酸注射液中蛋氨酸亚砜含量的方法。方法 采用邻苯二甲醛(O-phthaladehyde,OPA)柱前衍生HPLC。色谱柱为Agilent ZORBAX Eclipse AAA C18柱(150 mm×4.6 mm,5µm),检测波长为338 nm,流动相A为0.04 mol·L-1磷酸二氢钠溶液(调节pH至7.8),流动相B为乙腈-甲醇-水(45:45:10),梯度洗脱,流速为2.0 ml·min-1,柱温为40℃,供试品溶液与OPA衍生剂及硼酸盐缓冲液按设定程序自动混匀后进样。结果 蛋氨酸亚砜的质量浓度线性范围为0.000 5~0.050 0 mg·mL-1R=0.999 9);定量限为0.250 5 μg·mL-1,检测限为0.083 5 μg·mL-1;精密度、稳定性、重复性试验的RSD<3.0%;平均回收率为99.1%(RSD=1.33%,n=9)。结论 该方法操作简便,可用于复方氨基酸注射液中蛋氨酸亚砜的含量测定。

       

      Abstract: OBJECTIVE To establish a method for the content determination of methionine sulfoxide in Compound Amino Acid injection. METHODS O-phthaladehyde(OPA) pre-column derivatization HPLC was performed on the column of Agilent ZORBAX Eclipse AAA C18(150 mm×4.6 mm, 5 µm) with mobile phase A 0.04 mol·L-1 sodium dihydrogen phosphate solution (adjust pH to 7.8), mobile phase B acetonitrile-methanol-water (45:45:10)(gradient elution) at the flow rate of 2.0 ml·min-1, the detection wavelength was 338 nm and the column temperature was 40℃. The sample solution was automatic mixed with OPA agent and borate buffer according to set procedure. RESULTS The linear range of methionine sulfoxide was 0.000 5-0.050 0 mg·mL-1(R=0.999 9). The limit of quantitation was 0.250 5 μg·mL-1, and the limit of detection was 0.083 5 μg·mL-1. RSDs of precision, stability and repetitive test were all <3.0%. The average recovery was 99.1%(RSD=1.33%, n=9). CONCLUSION The method is simple, rapid and suitable for the content determination of methionine sulfoxide in Compound Amino Acid injection.

       

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