中国组织工程研究 ›› 2015, Vol. 19 ›› Issue (52): 8473-8479.doi: 10.3969/j.issn.2095-4344.2015.52.020

• 复合支架材料 composite scaffold materials • 上一篇    下一篇

骨碎补总黄酮/聚乳酸-羟基乙酸微囊的制备

陈虹舟1,马仕昆2,胡龙驹1,杨建东1   

  1. 1江苏省苏北人民医院骨科,江苏省扬州市  2250012武警江苏总队医院胸外科,江苏省扬州市 225003
  • 收稿日期:2015-09-23 出版日期:2015-12-17 发布日期:2015-12-17
  • 通讯作者: 杨建东,博士, 教授,主任医师,江苏省苏北人民医院骨科,江苏省扬州市 225001
  • 作者简介:陈虹舟,男,1990年生,江苏省宿迁市人,汉族,扬州大学医学院在读硕士,主要从事骨科脊柱研究。
  • 基金资助:

    江苏省十一五“科教兴卫”医学人才、重点人才项目(RC2011162)

The preparation of rhizoma drynariae total flavonoids/polylactic-co-glycolic acid microcapsules

Chen Hong-zhou1, Ma Shi-kun2, Hu Long-ju1, Yang Jian-dong1   

  1. 1Department of Orthopaedics, Subei People’s Hospital of Jiangsu Province, Yangzhou 225001, Jiangsu Province, China; 2Department of Thoracic Surgery, Jiangsu Armed Police General Hospital, Yangzhou 225003, Jiangsu Province, China
  • Received:2015-09-23 Online:2015-12-17 Published:2015-12-17
  • Contact: Yang Jian-dong, M.D., Professor, Chief physician, Department of Orthopaedics, Subei People’s Hospital of Jiangsu Province, Yangzhou 225001, Jiangsu Province, China
  • About author:Chen Hong-zhou, Studying for master’s degree, Department of Orthopaedics, Subei People’s Hospital of Jiangsu Province, Yangzhou 225001, Jiangsu Province, China
  • Supported by:

    the Medical Personnel and Key Talents Project for Health Scientific Development during the Eleventh Five-Year Period in Jiangsu Province, China, No. RC2011162

摘要:

背景:微囊是目前靶向治疗给药体系的主要方向之一,其大小为数微米到数百微米,可用于口服、注射、动脉给药及局部靶器官治疗等多种治疗途径。
目的:制备骨碎补总黄酮/聚乳酸-羟基乙酸共聚物微囊,并对微囊制备条件进行优化。
方法:采用乳化溶剂挥发法制备骨碎补总黄酮/聚乳酸-羟基乙酸共聚物微囊,单因素分析聚乳酸-羟基乙酸共聚物质量浓度(60,100,140,180 g/L)、搅拌速度(50,1 000,2 000,4 000 r/min)、初乳乳化时间(2,4,6,8 min)及水油比(1∶5、1∶10、1∶15、1∶20)对微囊大体形态、粒径分布宽度与微囊中总黄酮包封率的影响,筛选出微囊粒径较小、分散均匀、包封率较高的骨碎补总黄酮/聚乳酸-羟基乙酸共聚物微囊。
结果与结论:确定最佳工艺参数为:140 g/L 聚乳酸-羟基乙酸共聚物溶液,匀浆机2 000 r/min搅拌速度,初乳乳化时间6 min,水油比为1∶15。优化工艺下所制备的微囊分布均匀,平均粒径为(789.8±712.3) nm,粒径分布宽度较窄,基本小于5 μm;扫描电镜下观察所见微囊呈圆形,边缘较规则;微囊平均包封率为47.72%。 

关键词: 生物材料, 缓释材料, 骨碎补总黄酮, 聚乳酸-羟基乙酸共聚物, 微囊, 乳化溶剂挥发法, 包封率

Abstract:

BACKGROUND: Microcapsules is one of the main directions of targeted therapeutic dosing system. With a size of several microns to several hundred microns, it can be used for injection, oral, arterial administration and local treatment of targeted organs and other treatment approaches.
OBJECTIVE: To prepare rhizoma drynariae total flavonoids/polylactic-co-glycolic acid microcapsules and optimize the preparation conditions.
METHODS: The rhizoma drynariae total flavonoids/polylactic-co-glycolic acid microcapsules was prepared by ultrasonic emulsification. The effect of the mass concentration (60, 100, 140, 180 g/L), stirring speed (50, 1 000,  2 000, 4 000 r/minutes), colostrum emulsification time (2, 4, 6, 8 minutes), colostrum water oil ratio (1:5, 1:10, 1:15, 1:20) of rhizoma drynariae total flavonoids/polylactic-co-glycolic acid microcapsules on gross morphology, particle size distribution width and total flavonoids encapsulation efficiency of microcapsules was univariately analyzed. The rhizoma drynariae total flavonoids/polylactic-co-glycolic acid microcapsules with smaller particle size, uniform dispersion and higher encapsulation efficiency was filtered out.
RESULTS AND CONCLUSION: The optimum process parameters were as follows: 140 g/L polylactic acid-glycolic acid solution, the stirring speed of 2 000 r/min, the colostrum emulsification time of 6 minutes, and the colostrum water-oil ratio of 1:15. The microcapsules prepared in the optimized process displayed a uniform distribution and its average particle size was (789.8±712.3) nm, which distributed relative narrowly and basically less than 5 μm. Microcapsules presented round, with a regular edge under scanning electron microscope. The average encapsulation efficiency was 47.72%.
 

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