中药新药与临床药理
中藥新藥與臨床藥理
중약신약여림상약리
TRADITIONAL CHINESE DRUG RESEARCH&CLINICAL PHARMACOLOGY
2010年
2期
202-205
,共4页
杨小催%柯雪红%陈锦富%王淑英
楊小催%柯雪紅%陳錦富%王淑英
양소최%가설홍%진금부%왕숙영
石菖蒲挥发油%包合工艺%稳定性%均匀设计%HPLC
石菖蒲揮髮油%包閤工藝%穩定性%均勻設計%HPLC
석창포휘발유%포합공예%은정성%균균설계%HPLC
Volatile oil from Rhizoma Acori Tatarinowii%Inclusion process%Stability%Uniform Design%HPLC
目的 探讨石菖蒲挥发油包合工艺,并对其包合物稳定性进行研究.方法 应用U7(7~6)均匀试验设计对影响包合的因素进行考察,筛选出最佳包合工艺;采用HPLC法,以β-细辛醚含量为指标研究包合前后石菖蒲挥发油稳定性.结果 石菖蒲挥发油的最佳包合工艺为:β-CD:挥发油=3:1,β-CD:水=1:15,包合温度为30℃,搅拌时间为3 h;包合后,在考察时间范围内石菖蒲挥发油中β-细辛醚含量变化较小,RSD<5%.结论 筛选出的包合工艺稳定可行,采用β-CD包合可有效提高石菖蒲挥发油的稳定性.
目的 探討石菖蒲揮髮油包閤工藝,併對其包閤物穩定性進行研究.方法 應用U7(7~6)均勻試驗設計對影響包閤的因素進行攷察,篩選齣最佳包閤工藝;採用HPLC法,以β-細辛醚含量為指標研究包閤前後石菖蒲揮髮油穩定性.結果 石菖蒲揮髮油的最佳包閤工藝為:β-CD:揮髮油=3:1,β-CD:水=1:15,包閤溫度為30℃,攪拌時間為3 h;包閤後,在攷察時間範圍內石菖蒲揮髮油中β-細辛醚含量變化較小,RSD<5%.結論 篩選齣的包閤工藝穩定可行,採用β-CD包閤可有效提高石菖蒲揮髮油的穩定性.
목적 탐토석창포휘발유포합공예,병대기포합물은정성진행연구.방법 응용U7(7~6)균균시험설계대영향포합적인소진행고찰,사선출최가포합공예;채용HPLC법,이β-세신미함량위지표연구포합전후석창포휘발유은정성.결과 석창포휘발유적최가포합공예위:β-CD:휘발유=3:1,β-CD:수=1:15,포합온도위30℃,교반시간위3 h;포합후,재고찰시간범위내석창포휘발유중β-세신미함량변화교소,RSD<5%.결론 사선출적포합공예은정가행,채용β-CD포합가유효제고석창포휘발유적은정성.
Objective To prepare the inclusion compound of volatile oil from Rhizoma Acori Tatarinowii and to study the stability of the compound . Methods U7 (7~6) uniform design was used for the optimization of conditions for the inclusion compound of Rhizoma Acori Tatarinowii . With β-asarone content as the evaluation index, the stability of inclusion compound was examined by HPLC. Results The optimal condition for the inclusion compound of Rhizoma Acori Tatarinowii was as follows: the ratio of β-CD and volatile oil being 3:1, β-CD : water being 1 : 15, inclusion temperature at 30 ℃, and stirring for 3 h. The stability of the inclusion compound wasis excellent and the RSD < 5 %. Conclusion The optimized process is stable and highly efficient. Inclusion with β-CD promotes the stability of volatile oil from Rhizoma Acori Tatarinowii.