药学与临床研究
藥學與臨床研究
약학여림상연구
PHARMACEUTICAL AND CLINICAL RESEARCH
2014年
5期
416-418
,共3页
符映均%张莉%胡浩彬%吴迪
符映均%張莉%鬍浩彬%吳迪
부영균%장리%호호빈%오적
强力枇杷露%薄荷脑%磷酸可待因%吗啡%盐酸罂粟碱%含量测定%气相色谱法
彊力枇杷露%薄荷腦%燐痠可待因%嗎啡%鹽痠罌粟堿%含量測定%氣相色譜法
강력비파로%박하뇌%린산가대인%마배%염산앵속감%함량측정%기상색보법
Qianlipipa syrup%Menthol%Codeine Phosphate%Morphine%Papaverine hydrochloride%Gas Chromatography
目的:建立气相色谱法同时测定强力枇杷露中薄荷脑、磷酸可待因、吗啡、盐酸罂粟碱四种成分含量的方法。方法:试样用乙酸乙酯振摇提取,色谱柱为100%二甲基聚硅氧烷固定液的毛细管柱,柱温从100℃程序升温至270℃,保持20 min,检测器为 FID。结果:薄荷脑、磷酸可待因、吗啡、盐酸罂粟碱在各自测定范围内有良好线性关系,各成分平均回收率(n=6)在96.76%~113.34%,RSD<6.0%。结论:本方法准确可靠,重现性好,可有效地控制强力枇杷露的质量。
目的:建立氣相色譜法同時測定彊力枇杷露中薄荷腦、燐痠可待因、嗎啡、鹽痠罌粟堿四種成分含量的方法。方法:試樣用乙痠乙酯振搖提取,色譜柱為100%二甲基聚硅氧烷固定液的毛細管柱,柱溫從100℃程序升溫至270℃,保持20 min,檢測器為 FID。結果:薄荷腦、燐痠可待因、嗎啡、鹽痠罌粟堿在各自測定範圍內有良好線性關繫,各成分平均迴收率(n=6)在96.76%~113.34%,RSD<6.0%。結論:本方法準確可靠,重現性好,可有效地控製彊力枇杷露的質量。
목적:건립기상색보법동시측정강력비파로중박하뇌、린산가대인、마배、염산앵속감사충성분함량적방법。방법:시양용을산을지진요제취,색보주위100%이갑기취규양완고정액적모세관주,주온종100℃정서승온지270℃,보지20 min,검측기위 FID。결과:박하뇌、린산가대인、마배、염산앵속감재각자측정범위내유량호선성관계,각성분평균회수솔(n=6)재96.76%~113.34%,RSD<6.0%。결론:본방법준학가고,중현성호,가유효지공제강력비파로적질량。
Objective: To establish a GC method for the determination of menthol, codeine phosphate, morphine, papaverine hydrochloride in Qiangli Pipa syrup. Methods: The syrup was extracted by ethyl acetate and determined by gas chromatography with a flame ionization detector. The compounds were separated on an Agilent HP -1MS capillary column by using temperature programming. Results: The menthol, codeine phosphate, morphine, papaverine hydrochloride showed a good linear relationship, respectively, in their own detecting ranges. The average recoveries were between 96.76% and 113.34%,with RSD<6.0%. Conclusions: This method is accurate and suitable for the determination of menthol, codeine phosphate, morphine, papaverine hydrochloride in Qianli Pipa syrup.