中国药师
中國藥師
중국약사
CHINA PHARMACIST
2015年
4期
687-689
,共3页
金丽%周建丽%张晓丹%伍小勇%卜莹%古卓良
金麗%週建麗%張曉丹%伍小勇%蔔瑩%古卓良
금려%주건려%장효단%오소용%복형%고탁량
扑麻滴鼻液%高效液相色谱法%盐酸麻黄碱%马来酸氯苯那敏
撲痳滴鼻液%高效液相色譜法%鹽痠痳黃堿%馬來痠氯苯那敏
복마적비액%고효액상색보법%염산마황감%마래산록분나민
Chlorphenamine maleate and ephedrine nasal drops%HPLC%Ephedrine hydrochloride%Chlorphenamine maleate
目的:建立同时测定扑麻滴鼻液中盐酸麻黄碱和马来酸氯苯那敏含量的HPLC方法。方法:采用:Purospher STAR RP18色谱柱(150 mm ×4.6 mm,5μm),以磷酸盐缓冲液( pH 3.0±0.1)-乙腈(82:18)为流动相,流速为1.0 ml·min-1,在210 nm波长处同时检测盐酸麻黄碱和马来酸氯苯那敏,柱温35℃,进样量20μl。结果:盐酸麻黄碱和马来酸氯苯那敏分别在19.81~118.85μg·ml-1和6.21~37.25μg·ml-1浓度范围内线性关系良好,r分别为0.9996和0.9998。平均回收率分别为100.39%(RSD=0.69%,n=9)和100.11%(RSD=0.60%,n=9)。结论:该方法快速简便、重复性、准确性好,可用于该制剂中盐酸麻黄碱和马来酸氯苯那敏的含量测定。
目的:建立同時測定撲痳滴鼻液中鹽痠痳黃堿和馬來痠氯苯那敏含量的HPLC方法。方法:採用:Purospher STAR RP18色譜柱(150 mm ×4.6 mm,5μm),以燐痠鹽緩遲液( pH 3.0±0.1)-乙腈(82:18)為流動相,流速為1.0 ml·min-1,在210 nm波長處同時檢測鹽痠痳黃堿和馬來痠氯苯那敏,柱溫35℃,進樣量20μl。結果:鹽痠痳黃堿和馬來痠氯苯那敏分彆在19.81~118.85μg·ml-1和6.21~37.25μg·ml-1濃度範圍內線性關繫良好,r分彆為0.9996和0.9998。平均迴收率分彆為100.39%(RSD=0.69%,n=9)和100.11%(RSD=0.60%,n=9)。結論:該方法快速簡便、重複性、準確性好,可用于該製劑中鹽痠痳黃堿和馬來痠氯苯那敏的含量測定。
목적:건립동시측정복마적비액중염산마황감화마래산록분나민함량적HPLC방법。방법:채용:Purospher STAR RP18색보주(150 mm ×4.6 mm,5μm),이린산염완충액( pH 3.0±0.1)-을정(82:18)위류동상,류속위1.0 ml·min-1,재210 nm파장처동시검측염산마황감화마래산록분나민,주온35℃,진양량20μl。결과:염산마황감화마래산록분나민분별재19.81~118.85μg·ml-1화6.21~37.25μg·ml-1농도범위내선성관계량호,r분별위0.9996화0.9998。평균회수솔분별위100.39%(RSD=0.69%,n=9)화100.11%(RSD=0.60%,n=9)。결론:해방법쾌속간편、중복성、준학성호,가용우해제제중염산마황감화마래산록분나민적함량측정。
Objective:To establish a method for the simultaneous determination of chlorphenamine maleate and ephedrine hydro-chloride in chlorphenamine maleate and ephedrine nasal drops by HPLC. Methods:An HPLC method was performed on a column of Purospher STAR RP18(150 mm × 4. 6 mm,5 μm)with the mobile phase of acetonitrile -potassium dihydrogen phosphate buffer(pH 3. 0 ± 0. 1)(18:82 v/v)at the detection wavelength of 210 nm(adjusting the flow rate and column temperature to 1. 0 ml·min-1 and 35℃,respectively). The injection volume was 20 μl. Results:A good linear relationship was established between the peak response and the concentration of ephedrine hydrochloride and chlorphenamine maleate over the range of 19. 81-118. 85μg·ml-1(r=0. 999 6) and 6. 21-37. 25 μg·ml-1(r=0. 999 8),respectively. The mean recovery of ephedrine hydrochloride and chlorphenamine maleate was 100. 39%(RSD=0. 69%,n=9)and 100. 11%(RSD=0. 60%,n=9),respectively. Conclusion:The proposed method shows high repeatability,good durability and promising accuracy. It can be employed for the determination of two components in chlorphena-mine maleate and ephedrine nasal drops.