CAJ | 학술논문

目的：通过改进药典标准中尼莫地平片溶出度方法及测定方法,以达到区分不同厂家尼莫地平片质量差异的目的。方法建立高效液相色谱法(HPLC)测定尼莫地平片的体外溶出度,以尼莫地平溶解度、稳定性和区分能力为评价指标,筛选溶出介质。结果与结论采用 HPLC 法,以 Kromasil KR100-5 C18(4.6 mm×150 mm,5μm)为色谱柱,以乙腈-四氢呋喃-水(1∶1∶3)为流动相,流速1.0 mL·min-1,柱温40℃,检测波长235 nm,以 pH4.5醋酸盐缓冲溶液(含0.1%十二烷基硫酸钠)为溶出介质,可良好区分不同厂家尼莫地平片溶出曲线的差异。
목적：통과개진약전표준중니막지평편용출도방법급측정방법,이체도구분불동엄가니막지평편질량차이적목적。방법건립고효액상색보법(HPLC)측정니막지평편적체외용출도,이니막지평용해도、은정성화구분능력위평개지표,사선용출개질。결과여결론채용 HPLC 법,이 Kromasil KR100-5 C18(4.6 mm×150 mm,5μm)위색보주,이을정-사경부남-수(1∶1∶3)위류동상,류속1.0 mL·min-1,주온40℃,검측파장235 nm,이 pH4.5작산염완충용액(함0.1%십이완기류산납)위용출개질,가량호구분불동엄가니막지평편용출곡선적차이。
Objective To distinguish the quality difference of nimodipine tablets by improving the dissolution test method and the assay method described in the pharmacopeial standard.Methods An HPLC method was established to determinate in vitro dissolution of nimodipine,and the appropriate dissolution medium was selected according to indexes of nimodipine solubility, stability and distinguishing ability. Results and Conclusion Kromasil KR100-5 C18 (4.6 mm × 150 mm,5 μm)was chosen as the column, acetonitrile-tetrahydrofuran-water (1 ∶ 1 ∶3)was used as the mobile phase.The flow rate,the column temperature and the detection wavelength were respectively set at 1.0 mL·min-1 ,40 ℃ and 235 nm. pH4.5 acetate buffer solution containing 0.1% sodium dodecyl sulfate was chosen as the appropriate dissolution medium.This HPLC method could well distinguish dissolution profiles of nimodipine tablets produced by different manufacturers.