当代化工
噹代化工
당대화공
CONTEMPORARY CHEMICAL INDUSTRY
2013年
11期
1528-1531
,共4页
贺康洪%林阳%赵文军%侯佳宁
賀康洪%林暘%趙文軍%侯佳寧
하강홍%림양%조문군%후가저
利咽颗粒%蝙蝠葛碱%蝙蝠葛苏林碱%高相液相色谱法%含量测定
利嚥顆粒%蝙蝠葛堿%蝙蝠葛囌林堿%高相液相色譜法%含量測定
리인과립%편복갈감%편복갈소림감%고상액상색보법%함량측정
Liyan granules%Dauricine%Daurisoline%RP-HPLC%Determination
建立了利咽颗粒中蝙蝠葛碱、蝙蝠葛苏林碱的含量测定方法。采用DiamonsilTMC18色谱柱(250 mm ×4.6 mm,5μm),以乙腈-体积分数为0.05%三乙胺水溶液为流动相,流速为1.5 mL·min-1,检测波长为284 nm,进样量20μL,柱温为35℃。在上述色谱条件下,蝙蝠葛碱和蝙蝠葛苏林碱在1.106~8.848μg·mL-1(r=0.9995)、5.6~28μg·mL-1(r=0.9998)范围内线性关系良好,蝙蝠葛碱和蝙蝠葛苏林碱的平均加样回收率(n=9)均为98.7%;RSD分别为1.6%、1.5%。该法简便、准确、重复性好,可用于利咽颗粒中蝙蝠葛碱和蝙蝠葛林碱的含量测定。提高了利咽颗粒的质量控制标准,为其临床用药的安全性和有效性提供了质量保证。
建立瞭利嚥顆粒中蝙蝠葛堿、蝙蝠葛囌林堿的含量測定方法。採用DiamonsilTMC18色譜柱(250 mm ×4.6 mm,5μm),以乙腈-體積分數為0.05%三乙胺水溶液為流動相,流速為1.5 mL·min-1,檢測波長為284 nm,進樣量20μL,柱溫為35℃。在上述色譜條件下,蝙蝠葛堿和蝙蝠葛囌林堿在1.106~8.848μg·mL-1(r=0.9995)、5.6~28μg·mL-1(r=0.9998)範圍內線性關繫良好,蝙蝠葛堿和蝙蝠葛囌林堿的平均加樣迴收率(n=9)均為98.7%;RSD分彆為1.6%、1.5%。該法簡便、準確、重複性好,可用于利嚥顆粒中蝙蝠葛堿和蝙蝠葛林堿的含量測定。提高瞭利嚥顆粒的質量控製標準,為其臨床用藥的安全性和有效性提供瞭質量保證。
건립료리인과립중편복갈감、편복갈소림감적함량측정방법。채용DiamonsilTMC18색보주(250 mm ×4.6 mm,5μm),이을정-체적분수위0.05%삼을알수용액위류동상,류속위1.5 mL·min-1,검측파장위284 nm,진양량20μL,주온위35℃。재상술색보조건하,편복갈감화편복갈소림감재1.106~8.848μg·mL-1(r=0.9995)、5.6~28μg·mL-1(r=0.9998)범위내선성관계량호,편복갈감화편복갈소림감적평균가양회수솔(n=9)균위98.7%;RSD분별위1.6%、1.5%。해법간편、준학、중복성호,가용우리인과립중편복갈감화편복갈림감적함량측정。제고료리인과립적질량공제표준,위기림상용약적안전성화유효성제공료질량보증。
A HPLC method was established to determine contents of dauricine and daurisoline in Liyan Granules. Sample were analyzed on an DiamonsilTMC18(250 mm×4.6, 5 μm)column eluted with acetonitrile and water containing 0.05% triethy lamine as mobile phase in a gradient model; the flow rate was 1.5mL·min-1, the detective wavelength was set at 284 nm,and the column temperature was set at 35℃. The linear response ranges were 1.106~8.848μg·mL-1 (r=0.999 5) and 5.6~28μg·mL-1 (r=0.999 8) for dauricine and daurisoline ,respectively,The average recoveries (n=9) of these compounds all were 98.7%,and the RSDs were 1.8%and 1.5%, respectively. The method is simple,accurate and reproducible for determination of dauricine and dauri-soline in Liyan Granules simutaneously, and its quality standard can be improved, the method can provide a quality assurance for medicinal safety and clinical effectiveness of Liyan granules.