中国药业
中國藥業
중국약업
CHINA PHARMACEUTICALS
2015年
12期
19-20,21
,共3页
王柏强%刘福%江承平%何效平%曾芝兰
王柏彊%劉福%江承平%何效平%曾芝蘭
왕백강%류복%강승평%하효평%증지란
杜仲叶提取物滴丸%质量标准%薄层色谱法%高效液相色谱法%稳定性
杜仲葉提取物滴汍%質量標準%薄層色譜法%高效液相色譜法%穩定性
두중협제취물적환%질량표준%박층색보법%고효액상색보법%은정성
Folium Eucommiae Extract Dropping Pills%quality standards%TLC%HPLC%stability
目的:建立杜仲叶提取物滴丸的质量标准并考察其在室温和加速条件下的稳定性。方法采用薄层色谱(TLC)法定性鉴别滴丸中的绿原酸;采用高效液相色谱(HPLC)法测定滴丸中绿原酸的含量,色谱柱为Hypersic C18柱(250 mm ×4.6 mm,5μm),流动相为乙腈-0.4%磷酸溶液(13:87),流速为1.0 mL/min,检测波长为327 nm,柱温为室温。结果薄层色谱法色谱斑点清晰,专属性强,重复性好。绿原酸进样量在1.3~130μg/mL范围内与峰面积线性关系良好( r=0.9999),平均回收率为99.81%,RSD=1.28%( n=9);3批滴丸中试样品经6个月加速试验和12个月长期试验考察,各项指标均符合质量标准要求。结论杜仲叶提取物滴丸稳定性好,建立的鉴别方法专属性强,定量方法简便、准确,可用于其质量控制。
目的:建立杜仲葉提取物滴汍的質量標準併攷察其在室溫和加速條件下的穩定性。方法採用薄層色譜(TLC)法定性鑒彆滴汍中的綠原痠;採用高效液相色譜(HPLC)法測定滴汍中綠原痠的含量,色譜柱為Hypersic C18柱(250 mm ×4.6 mm,5μm),流動相為乙腈-0.4%燐痠溶液(13:87),流速為1.0 mL/min,檢測波長為327 nm,柱溫為室溫。結果薄層色譜法色譜斑點清晰,專屬性彊,重複性好。綠原痠進樣量在1.3~130μg/mL範圍內與峰麵積線性關繫良好( r=0.9999),平均迴收率為99.81%,RSD=1.28%( n=9);3批滴汍中試樣品經6箇月加速試驗和12箇月長期試驗攷察,各項指標均符閤質量標準要求。結論杜仲葉提取物滴汍穩定性好,建立的鑒彆方法專屬性彊,定量方法簡便、準確,可用于其質量控製。
목적:건립두중협제취물적환적질량표준병고찰기재실온화가속조건하적은정성。방법채용박층색보(TLC)법정성감별적환중적록원산;채용고효액상색보(HPLC)법측정적환중록원산적함량,색보주위Hypersic C18주(250 mm ×4.6 mm,5μm),류동상위을정-0.4%린산용액(13:87),류속위1.0 mL/min,검측파장위327 nm,주온위실온。결과박층색보법색보반점청석,전속성강,중복성호。록원산진양량재1.3~130μg/mL범위내여봉면적선성관계량호( r=0.9999),평균회수솔위99.81%,RSD=1.28%( n=9);3비적환중시양품경6개월가속시험화12개월장기시험고찰,각항지표균부합질량표준요구。결론두중협제취물적환은정성호,건립적감별방법전속성강,정량방법간편、준학,가용우기질량공제。
Objective To establish the quality standard of Folium Eucommiae Extract Dropping Pills and to investigate the stability un-der the condition of the room temperature and accelerated testing. Methods Chlorogenic acid in Folium Eucommiae Extract Dropping Pills was qualitatively identified by TLC;its content was determined by adopting HPLC. The chromatographic column was the Hypersic C18(250 mm × 4. 6 mm,5 μm),acetonitrile-0. 4% phosphoric acid solution(13 :87) was used as the mobile phase at the rate of 1. 0 mL/min. The detection wavelength was 327 nm and the column temperature was the room temperature. Results The chromato-graphic spots of samples were distinct with strong specificity and good reproducibility. The sample size of chlorogenic acid in the range of 1. 3 -130 μg/mL showed good linear relation with the peak area( r=0. 999 9 );the average recovery rate was 99. 81%( RSD=1. 28%,n=9);after the accelerated testing and the long-term testing,the various indexes of 3 batches of pilot test samples accorded with the quality standard of Folium Eucommiae Extract Dropping Pills. Conclusion Folium Eucommiae Extract Dropping Pills is excellent in stability;the established identification method is simple,accurate and reliable,and can be used for quality control of Foli-um Eucommiae Extract Dropping Pills.