药学研究
藥學研究
약학연구
JOURNAL OF PHARMACEUTICAL RESEARCH
2015年
5期
266-268,271
,共4页
陶鑫%焦丹丹%吴卫忠%张建军%余洛汀
陶鑫%焦丹丹%吳衛忠%張建軍%餘洛汀
도흠%초단단%오위충%장건군%여락정
高效液相色谱法%CZYS-201402-04%有关物质
高效液相色譜法%CZYS-201402-04%有關物質
고효액상색보법%CZYS-201402-04%유관물질
HPLC%CZYS-201402-04%Related substances
目的:采用高效液相色谱法测定新型丙型肝炎治疗药物CZYS-201402-04的有关物质。方法采用Zorbax Eclipse Plus C18(4.6 mm ×100 mm,3.5μm),用二元梯度洗脱的方式,流动相A为10 mmol·L-1磷酸二氢钾溶液( pH 3.0),流动相B为乙腈,检测波长为210 nm,柱温40℃,流速1.0 mL·min-1。结果 CZYS-201402-04的峰能与相邻杂质峰完全分离。CZYS-201402-04定量限为0.039 ng(0.0039μg·mL-1),最低检出限为0.013 ng(0.0013μg·mL-1)。重复性RSD=1.5%(n=6),中间精密度RSD=1.4%(n=9)。样品溶液在24 h内稳定。结论该方法为CZYS-201402-04的有关物质检查提供了方便、灵活、精确、可靠的方法。
目的:採用高效液相色譜法測定新型丙型肝炎治療藥物CZYS-201402-04的有關物質。方法採用Zorbax Eclipse Plus C18(4.6 mm ×100 mm,3.5μm),用二元梯度洗脫的方式,流動相A為10 mmol·L-1燐痠二氫鉀溶液( pH 3.0),流動相B為乙腈,檢測波長為210 nm,柱溫40℃,流速1.0 mL·min-1。結果 CZYS-201402-04的峰能與相鄰雜質峰完全分離。CZYS-201402-04定量限為0.039 ng(0.0039μg·mL-1),最低檢齣限為0.013 ng(0.0013μg·mL-1)。重複性RSD=1.5%(n=6),中間精密度RSD=1.4%(n=9)。樣品溶液在24 h內穩定。結論該方法為CZYS-201402-04的有關物質檢查提供瞭方便、靈活、精確、可靠的方法。
목적:채용고효액상색보법측정신형병형간염치료약물CZYS-201402-04적유관물질。방법채용Zorbax Eclipse Plus C18(4.6 mm ×100 mm,3.5μm),용이원제도세탈적방식,류동상A위10 mmol·L-1린산이경갑용액( pH 3.0),류동상B위을정,검측파장위210 nm,주온40℃,류속1.0 mL·min-1。결과 CZYS-201402-04적봉능여상린잡질봉완전분리。CZYS-201402-04정량한위0.039 ng(0.0039μg·mL-1),최저검출한위0.013 ng(0.0013μg·mL-1)。중복성RSD=1.5%(n=6),중간정밀도RSD=1.4%(n=9)。양품용액재24 h내은정。결론해방법위CZYS-201402-04적유관물질검사제공료방편、령활、정학、가고적방법。
Objective To establish an HPLC method for the determination of related substances of a novel anti-HCV drug CZYS-201402-04. Methods Zorbax Eclipse Plus C18(4. 6 mm × 100 mm,3. 5 μm)column was used. The mobile phase A was water solution containing 10 mmol·L-1 potassium dihydrogen phosphate(pH 3. 0)and the mobile phase B was acetonitrile. The UV detection wavelength was 210 nm,the column temperature was 40 ℃ and the flow rate was 1. 0 mL·min-1. Results CZYS -201402 -04 could be effectively separated with impurities. The LOQ was 0. 039 ng (0. 003 9 μg·mL-1 )and LOD was 0. 013 ng(0. 001 3μg·mL-1). RSD of repeatability was 1. 4% and RSD of interme-diate precision was 1. 5%. The solution was stable in 24 h. Conclusion The method was convenient,sensitive,accurate and reliable for the determination of assay and related substances of CZYS-201402-04.