中国医药科学
中國醫藥科學
중국의약과학
CHINA MEDICINE AND PHARMACY
2013年
15期
63-64,142
,共3页
王洪江%王萌萌%王颖%康慧%孙洪刚%刘磊%王超众
王洪江%王萌萌%王穎%康慧%孫洪剛%劉磊%王超衆
왕홍강%왕맹맹%왕영%강혜%손홍강%류뢰%왕초음
顶空气相色谱法%布洛芬缓释胶囊%乙醇残留%质量控制
頂空氣相色譜法%佈洛芬緩釋膠囊%乙醇殘留%質量控製
정공기상색보법%포락분완석효낭%을순잔류%질량공제
Headspace GC%Ibuprofen sustained release capsule%Residual ethanol%Quality control
目的建立顶空气相色谱法测定布洛芬缓释胶囊中乙醇残留量。方法采用Agilent HP-FFAP(30 m×0.320 m,0.25μm )毛细管柱为色谱柱,柱温为40℃,进样口温度为150℃,FID检测器温度为250℃,顶空瓶平衡温度为85℃,平衡时间为30 min,进样量1 mL,载气为氮气,流速2.0 mL/min。结果乙醇在0.05036~2.0144 mg/mL范围内呈良好线性关系(r=0.9997,n=6),平均回收率(n=9)为100.9%(RSD为0.24%)。结论本法简便、准确,重复性好,专属性强,灵敏度高,可用于布洛芬缓释胶囊中乙醇残留量的测定。
目的建立頂空氣相色譜法測定佈洛芬緩釋膠囊中乙醇殘留量。方法採用Agilent HP-FFAP(30 m×0.320 m,0.25μm )毛細管柱為色譜柱,柱溫為40℃,進樣口溫度為150℃,FID檢測器溫度為250℃,頂空瓶平衡溫度為85℃,平衡時間為30 min,進樣量1 mL,載氣為氮氣,流速2.0 mL/min。結果乙醇在0.05036~2.0144 mg/mL範圍內呈良好線性關繫(r=0.9997,n=6),平均迴收率(n=9)為100.9%(RSD為0.24%)。結論本法簡便、準確,重複性好,專屬性彊,靈敏度高,可用于佈洛芬緩釋膠囊中乙醇殘留量的測定。
목적건립정공기상색보법측정포락분완석효낭중을순잔류량。방법채용Agilent HP-FFAP(30 m×0.320 m,0.25μm )모세관주위색보주,주온위40℃,진양구온도위150℃,FID검측기온도위250℃,정공병평형온도위85℃,평형시간위30 min,진양량1 mL,재기위담기,류속2.0 mL/min。결과을순재0.05036~2.0144 mg/mL범위내정량호선성관계(r=0.9997,n=6),평균회수솔(n=9)위100.9%(RSD위0.24%)。결론본법간편、준학,중복성호,전속성강,령민도고,가용우포락분완석효낭중을순잔류량적측정。
Objective To determine the residual ethanol in ibuprofen sustained release capsule by headspace gas chromatography.Methods Agilent HP-FFAP(30 m×0.320 m,0.25μm) was used.The column temperature was 40℃. The injection port temperature was 150 ℃ .The FID detector temperature was 250 ℃ .The equilibrium temperature of the headspace gas bottle was 85 ℃ .The equilibrium time was 30 minutes.The injection volume was 1 mL.The Carrier gas was nitrogen.The flow rate was 1.0 mL/min. Results A good linear correlation of ethanol was observed within the range of 0.05036-2.0144 mg/mL(r=0.9997,n=6). The average recovery was 100.9% with RSD 0.24%(n=9). Conclusion The method is simple,accurate and repeatable,with strong selectivity and high sensitivity.It can be applied to the determination of of residual ethanol in ibuprofen sustained release capsule.