海峡药学
海峽藥學
해협약학
STRAIT PHARMACEUTICAL JOURNAL
2014年
6期
54-56
,共3页
毛细管气相色谱法%联苯双酯%有机溶剂
毛細管氣相色譜法%聯苯雙酯%有機溶劑
모세관기상색보법%련분쌍지%유궤용제
GC%Bifendate%Residual organic
目的:建立气相色谱法测定联苯双酯中3种有机溶剂的残留量的方法。方法采用DB-624毛细管色谱柱(30.0m ×0.53mm ×3μm);进样口温度为200℃;FID检测器温度为260℃;柱温:程序升温,60℃保持5min,然后以20℃/min的速率升温220℃,保持5min;以氮气为载气,恒压模式,载气压力为2.4psi;直接进样,进样量为1μL;以二甲基亚砜为溶解介质,测定了联苯双酯中乙醇、二氯甲烷和N,N-二甲基甲酰胺的残留量。结果乙醇、二氯甲烷和N,N-二甲基甲酰胺及溶剂峰彼此均能良好分离,线性范围分别为0.90~401.72μg· mL -1(r=0.9999),2.51~50.20μg· mL -1(r=0.9999),1.43~75.36μg· mL -1(r=0.9998);方法重复性良好,回收率也符合规定。结论该法适用于联苯双酯中这3种有机溶剂残留量的测定。
目的:建立氣相色譜法測定聯苯雙酯中3種有機溶劑的殘留量的方法。方法採用DB-624毛細管色譜柱(30.0m ×0.53mm ×3μm);進樣口溫度為200℃;FID檢測器溫度為260℃;柱溫:程序升溫,60℃保持5min,然後以20℃/min的速率升溫220℃,保持5min;以氮氣為載氣,恆壓模式,載氣壓力為2.4psi;直接進樣,進樣量為1μL;以二甲基亞砜為溶解介質,測定瞭聯苯雙酯中乙醇、二氯甲烷和N,N-二甲基甲酰胺的殘留量。結果乙醇、二氯甲烷和N,N-二甲基甲酰胺及溶劑峰彼此均能良好分離,線性範圍分彆為0.90~401.72μg· mL -1(r=0.9999),2.51~50.20μg· mL -1(r=0.9999),1.43~75.36μg· mL -1(r=0.9998);方法重複性良好,迴收率也符閤規定。結論該法適用于聯苯雙酯中這3種有機溶劑殘留量的測定。
목적:건립기상색보법측정련분쌍지중3충유궤용제적잔류량적방법。방법채용DB-624모세관색보주(30.0m ×0.53mm ×3μm);진양구온도위200℃;FID검측기온도위260℃;주온:정서승온,60℃보지5min,연후이20℃/min적속솔승온220℃,보지5min;이담기위재기,항압모식,재기압력위2.4psi;직접진양,진양량위1μL;이이갑기아풍위용해개질,측정료련분쌍지중을순、이록갑완화N,N-이갑기갑선알적잔류량。결과을순、이록갑완화N,N-이갑기갑선알급용제봉피차균능량호분리,선성범위분별위0.90~401.72μg· mL -1(r=0.9999),2.51~50.20μg· mL -1(r=0.9999),1.43~75.36μg· mL -1(r=0.9998);방법중복성량호,회수솔야부합규정。결론해법괄용우련분쌍지중저3충유궤용제잔류량적측정。
OBJECTIVE To establish a method for determination of residual organic solvents in Bifen-date.METHODS The determination was carried out with DB-624 capillary column ( 30.0 m ×0.53 mm ×3μm ) and FID detector.The inlet temperature was 200℃and the detector temperature was 260℃.The column temperature rose by program:the initial temperature was 60℃,maintained for 5min,raise to 220℃with a rate of 20℃/min,main-tained for 5min,The carries gas was nitrogen and the pressure of carries gas was 2.4psi,the direct injection was used and the injection volume was 1μL.The dissolved medium used was Dimethylsulfoxide.RESULTS Ethanol ,dichlo-romethane and N ,N-dimethylformamide could be separated from solvent peak in chromatogram obtained from system suitability test.Their calibration curves were linear in the range of 0.90~401.72μg · mL -1 ( r=0.9999 ) ,2.51~50.20μg· mL-1 ( r=0.9999 ) ,1.43~75.36μg · mL -1 ( r=0.9998 ) , respectively.The repeatability and recovery met requirements.CONCLUSION The method can be applied in determination of three residual organic solvents in Bifendate.