海峡药学
海峽藥學
해협약학
Strait Pharmaceutical Journal
2015年
9期
61-63
,共3页
颠茄合剂%硫酸阿托品%东莨菪碱%山莨菪碱%高效液相色谱法
顛茄閤劑%硫痠阿託品%東莨菪堿%山莨菪堿%高效液相色譜法
전가합제%류산아탁품%동랑탕감%산랑탕감%고효액상색보법
Belladonna mixture%Atropine sulfate%Scopolamine%anisodamine%RP-HPLC
目的:对颠茄合剂中托烷类生物碱进行定性与定量研究。方法利用反相高效液相色谱法对颠茄合剂中硫酸阿托品、东莨菪碱及山莨菪碱进行定性鉴别,同时对硫酸阿托品进行含量测定。色谱条件:色谱柱:ZORBAX SB-C18(4.6×150mm,5μm);流动相:乙腈-磷酸盐缓冲液(取磷酸二氢钾6.8g溶于1000mL水中,加三乙胺10mL,调pH至2.8)(13∶87),检测波长:210nm;流速为1mL· min -1,进样量20μL,柱温:30℃。结果样品溶液色谱图中显示与对照品溶液色谱图中相同的色谱峰。硫酸阿托品在15.06~120.5μg · mL -1范围内呈良好线性关系( r =0.9998);平均回收率(n=9)为98.27%,RSD为0.85%。结论该方法准确、可靠、专属性强,为建立颠茄合剂质量标准提供依据。
目的:對顛茄閤劑中託烷類生物堿進行定性與定量研究。方法利用反相高效液相色譜法對顛茄閤劑中硫痠阿託品、東莨菪堿及山莨菪堿進行定性鑒彆,同時對硫痠阿託品進行含量測定。色譜條件:色譜柱:ZORBAX SB-C18(4.6×150mm,5μm);流動相:乙腈-燐痠鹽緩遲液(取燐痠二氫鉀6.8g溶于1000mL水中,加三乙胺10mL,調pH至2.8)(13∶87),檢測波長:210nm;流速為1mL· min -1,進樣量20μL,柱溫:30℃。結果樣品溶液色譜圖中顯示與對照品溶液色譜圖中相同的色譜峰。硫痠阿託品在15.06~120.5μg · mL -1範圍內呈良好線性關繫( r =0.9998);平均迴收率(n=9)為98.27%,RSD為0.85%。結論該方法準確、可靠、專屬性彊,為建立顛茄閤劑質量標準提供依據。
목적:대전가합제중탁완류생물감진행정성여정량연구。방법이용반상고효액상색보법대전가합제중류산아탁품、동랑탕감급산랑탕감진행정성감별,동시대류산아탁품진행함량측정。색보조건:색보주:ZORBAX SB-C18(4.6×150mm,5μm);류동상:을정-린산염완충액(취린산이경갑6.8g용우1000mL수중,가삼을알10mL,조pH지2.8)(13∶87),검측파장:210nm;류속위1mL· min -1,진양량20μL,주온:30℃。결과양품용액색보도중현시여대조품용액색보도중상동적색보봉。류산아탁품재15.06~120.5μg · mL -1범위내정량호선성관계( r =0.9998);평균회수솔(n=9)위98.27%,RSD위0.85%。결론해방법준학、가고、전속성강,위건립전가합제질량표준제공의거。
ABSTRACT:OBJECTIVE To establish a method for qualitative and quantitative determination of the trapane al-kaloids in Inbelladonna mixtuxe.METHODS RP-HPLC methods was adopted for the atropine , scopolamine and anisodamine identification and the content of Atropine sulfate was also determined.The analyses were performed on a ZORBAX SB-C18(4.6 ×150mm,5μm) column with the mobile phase consisted of acetonitrile-phosphate buffer (pH 2.8)(13∶87)at a flow rate of 1.0mL· min-1,the detection wavelength was 210nm,the temperature of column was 30℃,and the injection volume was 20μL.RESULTS The chromatogram of the sample solution showed similarity to the reference solution.The linear range of Atropine sulfate was in the range of 15.06 ~120.5μg · mL -1 ( r =0.9998),the average recovery(n=9) was 98.27%and the RSD was 0.85%.CONCLUSION The method is ac-curate,reliable and specific ,which can be used for the quality contorl of Belladonna mixture.