文章摘要
王建,陈志鹏,蔡宝昌.载马钱子碱纳米粒的微球系统的制备与初步评价[J].南京中医药大学学报(社会科学版),2013,29(1):56-59.
载马钱子碱纳米粒的微球系统的制备与初步评价
Preliminary Evaluation and Preparation of Brucine Nanoparticles-in-microsphere System
投稿时间:2012-09-28  修订日期:2012-10-30
DOI:
中文关键词: 马钱子碱  纳米粒-微球系统  喷雾干燥
英文关键词: brucine  nanoparticles-in-microsphere system  spray drying technique
基金项目:
作者单位
王建1,2,陈志鹏1,2,蔡宝昌1,2,3* 1.南京中医药大学药学院江苏 南京 
210023
2.南京中医药大学国家教育部中药炮制规范化及标准化工程研究中心江苏 南京 
210029
3.南京海昌中药集团江苏 南京 
210061
 
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中文摘要:
      目的 制备包载马钱子碱纳米粒的壳聚糖微球系统(Brucine nanoparticles-in-microsphere system,Brucine-NiMS),以期获得一种降低突释作用用于关节腔注射的长效制剂。方法 以牛血清白蛋白(BSA)为材料,采用去溶剂化法制备载马钱子碱的纳米粒(Brucine nanoparticles, Brucine-Nps)。再以壳聚糖(CS)为载体,利用喷雾干燥法将纳米粒包载于壳聚糖微球系统中。在电镜下观察Brucine-NiMS的外观,并测定其体外释放特性。结果 Brucine-NiMS的处方为:CS的型号为600 kDa,CS醋酸溶液的浓度为1%,BSA与CS的比例为1∶5。喷雾干燥的条件为:蠕动泵速度为20%,进口温度为120 ℃,Q-Flow为40 mL/h。在此条件下制备的Brucine-NiMS的包封率、载药量和粒径分别为97.35%、3.17%和1.48 μm。Brucine-NiMS外观圆整,性质稳定。结论 Brucine-NiMS制备方法稳定可控,为开发药物新剂型提供了新的思路。
英文摘要:
      OBJECTIVE To find a long-acting preparation which can reduce the burst effect in intra-articular injection by preparing the brucine nanoparticles-in-microsphere system (Brucine-NiMS).METHODS Brucine nanoparticles (Brucine-Nps) were prepared by desolvation of BSA. Chitosan was used as an carrier and the nanoparticles were contained in the microsphere system by the spray drying method. The appearances of Brucine-NiMS were observed under the electron microscope and then the in vitro release characteristics were determined.RESULTS The formulation of Brucine-NiMS was as follows: BSA/CS (600KDA) 1∶5 (w/w) and the concentration of CS in the acetic acid was 1%. The spry drying conditions were as follows: The speed of the peristaltic pump was adjusted to 20%, the temperature of inlet was 120 ℃, and Q-Flow was 40 mL/h. The envelop rate, drug loading and particle sizes of Brucine-NiMS were 97.35%, 3.17% and 1.48 μm respectively. The appearance of Brucine-NiMS was rounding and the nature was stable.CONCLUSION The preparation method of Brucine-NiMS is stable and controllable, providing a new way to develop new dosage forms of drugs.
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