河北医科大学学报
河北醫科大學學報
하북의과대학학보
JOURNAL OF HEBEI MEDICAL UNIVERSITY
2014年
11期
1300-1303
,共4页
王茉莉%朱建平%张菁%庞文哲%郭丽
王茉莉%硃建平%張菁%龐文哲%郭麗
왕말리%주건평%장정%방문철%곽려
交沙霉素%色谱法,高压液相%质量控制
交沙黴素%色譜法,高壓液相%質量控製
교사매소%색보법,고압액상%질량공제
josamycin%chromatography,high pressure liquid%quality control
目的:建立高效液相色谱(high efficiency liquid chromatography,HPLC)法测定交沙霉素原料药中主组分的含量。方法采用十八烷基键合硅胶柱(C18)为固定相,以高氯酸溶液(取高氯酸钠-水合物119g,加水至1000 mL,用1mol/L的盐酸调节 pH 值为2.5)-乙腈(60∶40)为流动相。柱温为40℃,检测波长为231nm,进样量为20μL。结果交沙霉素主组分在考察的浓度范围内线性关系良好,线性范围为0.1255~0.8785g/L(r =1.0000),平均回收率为99.7%。定量限为2.51ng,最低检出限为0.84ng。结论 HPLC 可用于交沙霉素原料药中主组分含量的测定,快速简便,准确可靠,灵敏度高。
目的:建立高效液相色譜(high efficiency liquid chromatography,HPLC)法測定交沙黴素原料藥中主組分的含量。方法採用十八烷基鍵閤硅膠柱(C18)為固定相,以高氯痠溶液(取高氯痠鈉-水閤物119g,加水至1000 mL,用1mol/L的鹽痠調節 pH 值為2.5)-乙腈(60∶40)為流動相。柱溫為40℃,檢測波長為231nm,進樣量為20μL。結果交沙黴素主組分在攷察的濃度範圍內線性關繫良好,線性範圍為0.1255~0.8785g/L(r =1.0000),平均迴收率為99.7%。定量限為2.51ng,最低檢齣限為0.84ng。結論 HPLC 可用于交沙黴素原料藥中主組分含量的測定,快速簡便,準確可靠,靈敏度高。
목적:건립고효액상색보(high efficiency liquid chromatography,HPLC)법측정교사매소원료약중주조분적함량。방법채용십팔완기건합규효주(C18)위고정상,이고록산용액(취고록산납-수합물119g,가수지1000 mL,용1mol/L적염산조절 pH 치위2.5)-을정(60∶40)위류동상。주온위40℃,검측파장위231nm,진양량위20μL。결과교사매소주조분재고찰적농도범위내선성관계량호,선성범위위0.1255~0.8785g/L(r =1.0000),평균회수솔위99.7%。정량한위2.51ng,최저검출한위0.84ng。결론 HPLC 가용우교사매소원료약중주조분함량적측정,쾌속간편,준학가고,령민도고。
Objective A high efficiency liquid chromatography method was established for the determination of principal component crude drug josamycin.Methods A octadecyl bonded silica column was used as the stationary phase,with the mobile phase of mixture of perchloric acid solution-acetonitrile (60∶40)at the detection wavelength of 231nm.The column temperature was 40℃ and the injection volume was 20μL.Results The principal component of josamycin showed a linear range within 0.125 5- 0.878 5g/L (r = 1.000 0).The average recovery was 99.7%.The quantitation and detection limits were 2.51ng and 0.84ng,respectively.Conclusion The method was rapid,simple,accurate,sensitive,and suitable for the determination of principal component in crude drug josamycin.