摘要
研究药品中水溶性维生素含量的高效液相色谱测定方法。色谱柱:Micropak MCH-10;紫外检测器波长:254 nm;流速:1 mL.min^-1。柱温:40℃;用磷酸调整pH;色谱条件:先采用pH值为3.0的20%甲醇流动相淋洗,3分钟后改用pH为6.0的40%甲醇流动相淋洗。维生素C、维生素B2和烟酰胺的线性范围分别为9.0-45.1μg.mL^-1(r=0.9993)、3.3-16.7μg.mL^-1(r=0.9989)和5.0-25.0μg.mL-1(r=0.9996)。平均回收率分别为:99.5%(RSD=1.04%)、96.3%(RSD=1.37%)和100.8%(RSD=0.81%)。本方法同时测定三种维生素具有快速、简便、准确的特点。
To establish a HPLC method for determination of water-soluble vitamins in drug. A Micropak MCH-10 was used by HPLC and the Column temperature was 40℃. Detector wavelength. 254 nm; flow rate. 1 mL · min^-1. pH was adjusted by phosphate acid. Gradient elution conditions. 20M methanol in water (pH=3) for 3min, and then 40% methanol in water (pH=6) for the rest elution. The liner ranges of vitamin C, vitamin B2 and niacin amide were at 9.0-45.1μg·mL^-1 (r=0.9993), 3.3- 16.7μg·mL^-1 (r=0. 9989) and 5.0-25.0μg·mL^-1(r=0. 9996). The average recovery were 99.5% (RSD= 1.04%), 96.3% (RSD= 1.37%) and 100.8% (RSD= 0. 81%), respectively. This method is rapid, convenient and accurate for the simultaneous determination of three vitamins.
出处
《中国药事》
CAS
2007年第4期255-257,共3页
Chinese Pharmaceutical Affairs