食品与药品
食品與藥品
식품여약품
FOOD AND DRUG
2013年
4期
262-263,264
,共3页
刘彩霞%王长斌%杨海霞%邢玉仁
劉綵霞%王長斌%楊海霞%邢玉仁
류채하%왕장빈%양해하%형옥인
布南色林%气相色谱法%残留溶剂
佈南色林%氣相色譜法%殘留溶劑
포남색림%기상색보법%잔류용제
blonanserin%gas chromatography%residual solvent
目的建立气相色谱法测定布南色林中残留溶剂含量的方法。方法采用6%氰丙基苯基-94%二甲基聚硅氧烷为固定液的毛细管柱(DB-624,0.53 mm×30 m,3.0μm),程序升温,初始温度50℃,保持5 min,以20℃/min的速率升温至200℃,保持5 min;氢火焰离子化检测器(FID),检测器温度250℃,进样口温度220℃,载气为氮气,流速2 mL/min,进样体积1 mL。外标法计算残留溶剂的含量。结果5种有机溶剂进样浓度与峰面积呈良好线性关系,相关系数均大于0.9990,加样回收率在97.6%~102.9%之间。结论此法准确可靠,灵敏度高,可用于布南色林中残留溶剂的测定。
目的建立氣相色譜法測定佈南色林中殘留溶劑含量的方法。方法採用6%氰丙基苯基-94%二甲基聚硅氧烷為固定液的毛細管柱(DB-624,0.53 mm×30 m,3.0μm),程序升溫,初始溫度50℃,保持5 min,以20℃/min的速率升溫至200℃,保持5 min;氫火燄離子化檢測器(FID),檢測器溫度250℃,進樣口溫度220℃,載氣為氮氣,流速2 mL/min,進樣體積1 mL。外標法計算殘留溶劑的含量。結果5種有機溶劑進樣濃度與峰麵積呈良好線性關繫,相關繫數均大于0.9990,加樣迴收率在97.6%~102.9%之間。結論此法準確可靠,靈敏度高,可用于佈南色林中殘留溶劑的測定。
목적건립기상색보법측정포남색림중잔류용제함량적방법。방법채용6%청병기분기-94%이갑기취규양완위고정액적모세관주(DB-624,0.53 mm×30 m,3.0μm),정서승온,초시온도50℃,보지5 min,이20℃/min적속솔승온지200℃,보지5 min;경화염리자화검측기(FID),검측기온도250℃,진양구온도220℃,재기위담기,류속2 mL/min,진양체적1 mL。외표법계산잔류용제적함량。결과5충유궤용제진양농도여봉면적정량호선성관계,상관계수균대우0.9990,가양회수솔재97.6%~102.9%지간。결론차법준학가고,령민도고,가용우포남색림중잔류용제적측정。
Objective To establish a GC method for the determination of residual solvents in blonanserin. Methods DB-624 chromatographic column (coated with 6%cyanopropylphenyl-94%dimethylpolysiloxane, length 30 m, I.D. 0.53 mm, film 3.0μm) was adopted. The column temperature was programmed: kept at 50℃for 5 min, and then increased by 20℃/min to 200℃for 5 min, and kept for 5 min. The temperature of FID detector was 250℃and the temperature of inlet was 220℃. The carrier gas was nitrogen at a flow rate of 2 mL/min. The injection volume was 1 mL. Contents of residual solvents were calculated according to the external standard method. Results The calibration curves of five solvents all showed good linearity in a detected concentration range(r>0.9990), the range of average recovery was 97.6%~102.9%. Conclusion The method was accurate, reliable and sensitive, and can be used for assay of residual organic solvents in blonanserin.