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波棱内酯A纳米混悬剂冻干粉的制备及其抗乙肝病毒活性评价
引用本文:钟雨佶,刘青川,张婷,刘肖,王立强,袁海龙.波棱内酯A纳米混悬剂冻干粉的制备及其抗乙肝病毒活性评价[J].中国中药杂志,2020(5):1076-1081.
作者姓名:钟雨佶  刘青川  张婷  刘肖  王立强  袁海龙
作者单位:华侨大学;空军特色医学中心药学部;解放军总医院第五医学中心
基金项目:国家自然科学基金项目(81873092,81573697);国家“重大新药创制”科技重大专项(2016ZX09101073)。
摘    要:制备波棱内酯A纳米混悬剂冻干粉(HPA-NS-LP),考察其体外溶出和抗乙肝病毒活性。采用超声沉淀法制备波棱内酯A纳米混悬剂(HPA-NS),单因素试验优化其处方及工艺;冷冻干燥法制备HPA-NS-LP。扫描电镜(SEM)观察形态;桨法测定其溶出度。以HepG2.2.15细胞模型评价HPA-NS-LP体外抗乙肝病毒活性,并与波棱内酯A普通混悬剂冻干粉(HPA-CS-LP)进行比较。结果显示,优化后的HPA-NS的粒径为(173.46±4.36)nm,PDI为0.110±0.012;制备所得的HPA-NS-LP复溶后平均粒径和PDI均有所增加,但变化值均在合理范围之内;SEM下观察HPA-NS-LP呈圆球状;体外溶出度试验发现HPA-NS-LP在2 h内累积溶出度达到90%以上,显著高于HPA-CS-LP;HPA-CS-LP与HPA-NS-LP均可有效抑制HepG2.2.15细胞抗原(HBsAg和HBeAg)的分泌,但HPA-NS-LP的抑制作用显著强于HPA-CS-LP(P<0.05)。高、中、低剂量(50,25,12.5 mg·kg-1)的HPA-NS-LP可显著抑制HepG2.2.15细胞HBV-DNA的复制(P<0.05);且效果优于同剂量的HPA-CS-LP(P<0.05)。结果表明波棱内酯A(HPA)制备成纳米混悬剂冻干粉后抗乙肝病毒活性明显增强。

关 键 词:波棱内酯A  纳米混悬剂  冻干粉  抗乙肝病毒  HEPG2.2.15

Preparation of herpetolide A nanosuspension lyophilized powder and evaluation of its anti-hepatitis B virus activity
ZHONG Yu-ji,LIU Qing-chuan,ZHANG Ting,LIU Xiao,WANG Li-qiang,YUAN Hai-long.Preparation of herpetolide A nanosuspension lyophilized powder and evaluation of its anti-hepatitis B virus activity[J].China Journal of Chinese Materia Medica,2020(5):1076-1081.
Authors:ZHONG Yu-ji  LIU Qing-chuan  ZHANG Ting  LIU Xiao  WANG Li-qiang  YUAN Hai-long
Institution:(Huaqiao University,Quanzhou 362021,China;Department of Pharmacy,Air Force Medical Center,PLA,Beijing 100142,China;Fifth Medical Center of Chinese PLA General Hospital,Beijing 100039,China)
Abstract:To prepare the herpetolide A nanosuspension lyophilized powder(HPA-NS-LP),in order to investigate its anti-hepatitis B virus(HBV)activity and the dissolution in vitro.Herpetolide A nanosuspension(HPA-NS)was prepared by ultrasonic precipitation method.The formulation and process of HPA-NS were optimized by the single factor experiment.Lyophilized powder(HPA-NS-LP)was prepared by freeze-drying method.Scanning electron microscopy was used to observe morphology of HPA-NS-LP.Paddle method was used to determinate the dissolution of HPT-NS-LP in vitro.The anti-HBV activity of herpetolide A coarse suspension lyophilized powder(HPA-CS-LP)and HPA-NS-LP was evaluated by HepG2.2.15 cell model.The mean particle size of optimized HPA-NS was(173.46±4.36)nm,with a polydispersity index of 0.110±0.012.After redispersion,the mean particle size and the polydispersity index of HPA-NS-LP increased,with changes within a rational range.Scanning electron microscopy showed that HPA-NS-LP was spherical in shape.Cumulative dissolution rate of HPA-NS-LP was more than 90%in 2 hours,which was higher than that of HPA-CS-LP.Both HPA-CS-LP and HPA-NS-LP could effectively inhibit the secretion of HepG2.2.15 cell antigens(HBsAg and HBeAg),and the inhibitory effect of HPA-NS-LP was significantly higher than that of HPA CS-LP(P<0.05).HBV-DNA test showed that high,medium and low-dose HPA-NS-LP(50,25,12.5 mg·kg-1)significantly decreased the level of HBV-DNA(P<0.05),and the effect was better than that of the same dose of HPA-CS-LP(P<0.05).The results revealed that HPA-NS-LP exhibited anti-HBV activity in vitro,and its effect was superior to that of HPA-CS-LP.
Keywords:herpetolide A  nanosuspension  lyophilized powder  anti-hepatitis B  HepG2  2  15
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