中国药业
中國藥業
중국약업
CHINA PHARMACEUTICALS
2014年
14期
64-65,66
,共3页
刘坚初%林丽%强姣%童国勇
劉堅初%林麗%彊姣%童國勇
류견초%림려%강교%동국용
连芩软膏%正交试验%盐酸小檗碱%黄芩苷
連芩軟膏%正交試驗%鹽痠小檗堿%黃芩苷
련금연고%정교시험%염산소벽감%황금감
Lianqin Ointment%orthogonal test%berberine hydrochloride%baicalin
目的:优选连芩软膏乙醇渗漉提取工艺。方法采用正交试验法,以盐酸小檗碱、黄芩苷的提取率和浸膏得率为评价指标,考察溶剂种类、溶剂用量、药材粉碎粒度及渗漉速率对连芩软膏提取工艺效果的影响。结果渗漉最佳工艺条件为,将黄连、黄芩、黄柏等药材粉碎过二号筛,以70%乙醇润湿、混匀,密闭放置30 min 后装入渗漉装置,加少量70%乙醇浸渍24 h,以12倍量70%乙醇进行渗漉,渗漉速率为9 mL /(min·kg),收集渗漉液。结论该优选工艺稳定、合理,可为连芩软膏的生产提供实验室依据。
目的:優選連芩軟膏乙醇滲漉提取工藝。方法採用正交試驗法,以鹽痠小檗堿、黃芩苷的提取率和浸膏得率為評價指標,攷察溶劑種類、溶劑用量、藥材粉碎粒度及滲漉速率對連芩軟膏提取工藝效果的影響。結果滲漉最佳工藝條件為,將黃連、黃芩、黃柏等藥材粉碎過二號篩,以70%乙醇潤濕、混勻,密閉放置30 min 後裝入滲漉裝置,加少量70%乙醇浸漬24 h,以12倍量70%乙醇進行滲漉,滲漉速率為9 mL /(min·kg),收集滲漉液。結論該優選工藝穩定、閤理,可為連芩軟膏的生產提供實驗室依據。
목적:우선련금연고을순삼록제취공예。방법채용정교시험법,이염산소벽감、황금감적제취솔화침고득솔위평개지표,고찰용제충류、용제용량、약재분쇄립도급삼록속솔대련금연고제취공예효과적영향。결과삼록최가공예조건위,장황련、황금、황백등약재분쇄과이호사,이70%을순윤습、혼균,밀폐방치30 min 후장입삼록장치,가소량70%을순침지24 h,이12배량70%을순진행삼록,삼록속솔위9 mL /(min·kg),수집삼록액。결론해우선공예은정、합리,가위련금연고적생산제공실험실의거。
Objective To optimize the ethanol percolation extraction technology of Lianqin Ointment. Methods With the extraction rate and the extract yield of baicalin and berberine hydrochloride as the evaluation indexes,the influence the solvent type,dosage of solvent, crushing granularity and percolation speed on the extraction technological effect were investigated. Results The optimum percolation technological conditions were as follows:Rhizoma coptidis,Scutellaria baicalensis georgi,Cortex phellodendri,etc. were shattered by No. 2 sieve,wetted and blent with 70% ethanol and placed in airtight for 30 min,then loaded into the percolation equipment,adding a small amount of 70% ethanol to immerse for 24 h,the percolation was performed with 12 times the amount of 70% ethanol and the percola-tion speed of 9 mL / (min·kg). Conclusion The optimized process is stable and reasonable,and provides an experimental basis for the production of Lianqin Ointment.