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引用本文:叶菲,楼雪芳,杜永忠.HPLC测定龙血竭脂质纳米粒中龙血素A的含量[J].中国现代应用药学,2013,30(1):69-72.
YE Fei,LOU Xuefang,DU Yongzhong.Determination of Loureirin A in Solid Lipid Nanoparticles Encapsulating Resina Draconis by HPLC[J].Chin J Mod Appl Pharm(中国现代应用药学),2013,30(1):69-72.
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HPLC测定龙血竭脂质纳米粒中龙血素A的含量
叶菲1, 楼雪芳2, 杜永忠3
1.浙江大学校医院,杭州 310058;2.浙江大学城市学院,杭州 310015;3.浙江大学药学院,杭州 310058
摘要:
目的 采用HPLC测定龙血竭脂质纳米粒中龙血素A的含量并计算其包封率。方法 采用DiamonsilTM C18(200 mm×4.6 mm,5 μm)色谱柱,以乙腈-1%冰醋酸水溶液(38∶62)为流动相,流速为1.3 mL·min-1,检测波长为260 nm,柱温为40 ℃,测定样品中龙血素A的含量并计算其包封率。结果 龙血素A 于0.135~5.4 μg·mL-1内有良好线性关系,Y=33.694X+1.589 8(r=0.999 9)。低、中、高3个浓度的日内RSD分别为2.70%,2.36%,1.48%;日间RSD分别为2.70%,2.61%,1.97%,该方法的平均回收率为99.2%,RSD为3.9%,平均包封率为89.59%。结论 本方法准确、简便、重复性好,可用于龙血竭脂质纳米粒中龙血素A含量的测定。
关键词:  高效液相色谱法  龙血竭  龙血素A  脂质纳米粒
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Determination of Loureirin A in Solid Lipid Nanoparticles Encapsulating Resina Draconis by HPLC
YE Fei1, LOU Xuefang2, DU Yongzhong3
1.Hospital of Zhejiang University, Hangzhou 310058, China;2.Zhejiang University City College, Hangzhou 310015, China;3.College of Pharmaceutial Sciences, Zhejiang University, Hangzhou 310058, China
Abstract:
OBJECTIVE To establish an HPLC method for determination of loureirin A content in solid lipid nanoparticles(SLN) of Resina Draconis. METHODS A DiamonsilTM C18(200 mm×4.6 mm, 5 μm) column was used for the determination of loureirin A with mobile phase of acetonitrile-1% acetic acid solution (38∶62). The flow rate was 1.3 mL·min-1, the detection wavelength was set at 260 nm, and the column temperature was 40 ℃. RESULTS The linear range of 1oureirin A was 0.135-5.4 μg·mL-1, Y=33.694X+1.589 8(r=0.999 9). The RSDs of within-day were 2.70%, 2.36%, 1.48%, and the RSDs of between-day were 2.70%, 2.61%, 1.97% in the high-, middle-, and low-dose Resina Draconis loaded SLN. The average recovery was 99.2%(RSD 3.9%), and the average drug encapsulation efficiency was 89.59%. CONCLUSION The method is simple and reliable for the determination of loureirin A in Resina Draconis loaded SLN.
Key words:  HPLC  Resina Draconis  loureirin A  solid lipid nanoparticle
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