实用药物与临床
實用藥物與臨床
실용약물여림상
Practical Pharmacy and Clinical Remedies
2015年
9期
1090-1092
,共3页
王晓青%贾燕花%高磊%马静%刘皈阳
王曉青%賈燕花%高磊%馬靜%劉皈暘
왕효청%가연화%고뢰%마정%류귀양
咳喘宁%吗啡%氨茶碱%HPLC
咳喘寧%嗎啡%氨茶堿%HPLC
해천저%마배%안다감%HPLC
Kechuanning%Morphine%Aminophylline%HPLC
目的 建立咳喘宁合剂中氨茶碱和吗啡含量测定的HPLC方法. 方法 采用高效液相色谱法,色谱柱为资生堂C8 色谱柱,流动相为0.1 mol/L 磷酸二氢钾溶液 -0.005 mol/L 庚烷磺酸钠水溶液 -乙腈(47. 5:47. 5:5). 氨茶碱检测波长为271 nm,进样量为10 μL;吗啡检测波长为207 nm,进样量为20 μL. 结果茶碱在8. 62~68. 96 μg/mL范围内具有良好的线性关系,平均回收率为99. 2%;吗啡在1. 03 ~51. 60 μg/mL范围内具有良好的线性关系,平均回收率为101. 5%. 结论 该方法具有良好的准确度、精密度、专属性,能良好地控制咳喘宁合剂的质量.
目的 建立咳喘寧閤劑中氨茶堿和嗎啡含量測定的HPLC方法. 方法 採用高效液相色譜法,色譜柱為資生堂C8 色譜柱,流動相為0.1 mol/L 燐痠二氫鉀溶液 -0.005 mol/L 庚烷磺痠鈉水溶液 -乙腈(47. 5:47. 5:5). 氨茶堿檢測波長為271 nm,進樣量為10 μL;嗎啡檢測波長為207 nm,進樣量為20 μL. 結果茶堿在8. 62~68. 96 μg/mL範圍內具有良好的線性關繫,平均迴收率為99. 2%;嗎啡在1. 03 ~51. 60 μg/mL範圍內具有良好的線性關繫,平均迴收率為101. 5%. 結論 該方法具有良好的準確度、精密度、專屬性,能良好地控製咳喘寧閤劑的質量.
목적 건립해천저합제중안다감화마배함량측정적HPLC방법. 방법 채용고효액상색보법,색보주위자생당C8 색보주,류동상위0.1 mol/L 린산이경갑용액 -0.005 mol/L 경완광산납수용액 -을정(47. 5:47. 5:5). 안다감검측파장위271 nm,진양량위10 μL;마배검측파장위207 nm,진양량위20 μL. 결과다감재8. 62~68. 96 μg/mL범위내구유량호적선성관계,평균회수솔위99. 2%;마배재1. 03 ~51. 60 μg/mL범위내구유량호적선성관계,평균회수솔위101. 5%. 결론 해방법구유량호적준학도、정밀도、전속성,능량호지공제해천저합제적질량.
Objective To establish a method for the content determination of aminophylline and morphine in kechuanning mixture. Methods The determination was performed on Shisheido C8 column with the mobile phases of 0.1 mol/L potassium dihydrogen phosphate solution-0.005 mol/L sodium heptanesulfonate solution-acetonitrile (47. 5:47. 5:5). The detection wavelength for aminophylline was 271 nm and the sample volume was 10 μL;the detec-tion wavelength for morphine was 207 nm and the sample volume was 20 μL. Results The linear range of the theo-phylline was 8. 62~68. 96 μg/mL with an average recovery of 99. 2%;The linear range of the morphine was 1. 03~51. 60 μg/mL with an average recovery of 101. 5%. Conclusion The method is accurate,precise and specific for the quality control of aminophylline and morphine in kechuanning mixture.