摘要
目的:考察白术经超微粉碎后的粒度和体外溶出变化。方法:用粒度分析仪分析白术超微粉碎前后的粒径差异;以白术内酯Ⅲ、白术内酯Ⅰ含量为指标,采用高效液相色谱法测定其含量,以此反映溶出情况。结果:超微粉碎后样品粒径明显变小,约为白术细粉的30%;与白术细粉比较,白术内酯Ⅲ、白术内酯Ⅰ的含量提高约27%。结论:超微粉碎可以明显降低粒径,增加比表面积,有助于白术药材中白术内酯Ⅲ、白术内酯Ⅰ的溶出。
OBJECTIVE: To study the change in grain size and in vitro dissolution ratio of Atractylodes macrocephala after ultramicronization. METHODS: The particle size before and after ultramicronization was analyzed using particle size analyzer. The content of the sample was determined by HPLC using atractylenolide Ⅲ and atractylenolide Ⅰ as indexes to reflect the dissolution ratio. RESULTS: After ultramicronization, the particle size of the sample became thinner obviously, about 30% that of the common fine powder, and the content increased by 27% as compared with the common fine powder. CONCLUSION: The ultramicronization can significantly decrease the particle size, increase specific surface area and contribute to the dissolution of atractylenolide Ⅲ and atractylenolide Ⅰ from Atractylodes macrocephala.
出处
《中国药房》
CAS
CSCD
北大核心
2009年第9期653-655,共3页
China Pharmacy
基金
"十五"国家科技攻关计划重大项目(2004BA721A)
浙江省科研院所优秀青年科技人才资助计划(2008R20007)
关键词
白术
超微粉碎
白术内酯Ⅲ
白术内酯Ⅰ
粒度分析
高效液相色谱法
Atractylodes macrocephala
Ultramicronization
Atractylenolide Ⅲ
Atractylenolide Ⅰ
Particle size analysis
HPLC