中国医药
中國醫藥
중국의약
CHINA MEDICINE
2013年
6期
842-844
,共3页
刘秀霞%钱瑞瑛%崔猛%顾孝红
劉秀霞%錢瑞瑛%崔猛%顧孝紅
류수하%전서영%최맹%고효홍
盐酸格拉司琼%反相高效液相色谱法%含量测定%有关物质
鹽痠格拉司瓊%反相高效液相色譜法%含量測定%有關物質
염산격랍사경%반상고효액상색보법%함량측정%유관물질
Granisetron hydrochloride%Reverse phase high-performance liquid chromatography%Determination%Related substances
目的 建立盐酸格拉司琼葡萄糖注射液含量及有关物质的反相高效液相色谱(RP-HPLC)测定法.方法 采用C18色谱柱,磷酸盐缓冲液(pH值2.0)(取无水磷酸二氢钠15.6g溶解于900 ml水中,用磷酸调节pH值至2.0,加水稀释至1000 ml)-甲醇-四氢呋喃(75∶24∶ 1.1)为流动相,流速1.2 ml/min,检测波长300 nm.结果 盐酸格拉司琼与杂质A、B、C、D及5-羟甲基糠醛的分离度均符合要求,系统适用性良好,盐酸格拉司琼在0.4426 ~2.213 μg范围内线性关系良好,方法平均回收率为100.1%(相对标准偏差=0.26%).结论 该法简便、准确,可用于盐酸格拉司琼葡萄糖注射液的主药含量及有关物质测定.
目的 建立鹽痠格拉司瓊葡萄糖註射液含量及有關物質的反相高效液相色譜(RP-HPLC)測定法.方法 採用C18色譜柱,燐痠鹽緩遲液(pH值2.0)(取無水燐痠二氫鈉15.6g溶解于900 ml水中,用燐痠調節pH值至2.0,加水稀釋至1000 ml)-甲醇-四氫呋喃(75∶24∶ 1.1)為流動相,流速1.2 ml/min,檢測波長300 nm.結果 鹽痠格拉司瓊與雜質A、B、C、D及5-羥甲基糠醛的分離度均符閤要求,繫統適用性良好,鹽痠格拉司瓊在0.4426 ~2.213 μg範圍內線性關繫良好,方法平均迴收率為100.1%(相對標準偏差=0.26%).結論 該法簡便、準確,可用于鹽痠格拉司瓊葡萄糖註射液的主藥含量及有關物質測定.
목적 건립염산격랍사경포도당주사액함량급유관물질적반상고효액상색보(RP-HPLC)측정법.방법 채용C18색보주,린산염완충액(pH치2.0)(취무수린산이경납15.6g용해우900 ml수중,용린산조절pH치지2.0,가수희석지1000 ml)-갑순-사경부남(75∶24∶ 1.1)위류동상,류속1.2 ml/min,검측파장300 nm.결과 염산격랍사경여잡질A、B、C、D급5-간갑기강철적분리도균부합요구,계통괄용성량호,염산격랍사경재0.4426 ~2.213 μg범위내선성관계량호,방법평균회수솔위100.1%(상대표준편차=0.26%).결론 해법간편、준학,가용우염산격랍사경포도당주사액적주약함량급유관물질측정.
Objective To establish a reverse phase high-performance liquid chromatography (RP-HPLC) method for determination of granisetron hydrochloride and related substances in granisetron hydrochloride and glucose injection.Methods A eclipse XDB-C18 column was used with mobile phase of phosphate buffer (pH 2.0) (measure sodium dihydrogen phosphate anhydride 15.6g dissolved in water of 900 ml,then regulated pH to 2.0 with phosphoric acid and diluted to 1000 ml with water)-methanol-tetrahydrofuran(75:24:1.1).The flow rate was 1.2 ml/min and the detection wavelength was 300 nm.Results There was a good resolution between the granisetron hydrochloride and all the impurities(A,B,C,D) as well as the 5-HMF,and the system suitability was fine.It had a good linearity over the concertration range of 0.4426-2.213 μg.The average recovery was 100.1% with RSD of 0.26%.Conclusions The method is accurate and convenient.It can be used for determination of granisetron hydrochloride and related substances in granisetron hydrochloride and glucose injection.