广东药学院学报
廣東藥學院學報
엄동약학원학보
ACADEMIC JOURNAL OF GUANGDONG COLLEGE OF PHARMACY
2014年
4期
395-398
,共4页
吉国辉%李勇%朱家校%江斌%何伟
吉國輝%李勇%硃傢校%江斌%何偉
길국휘%리용%주가교%강빈%하위
参芎滴丸%制备工艺%高效液相色谱法%人参皂苷Rg1%人参皂苷Re%含量测定
參芎滴汍%製備工藝%高效液相色譜法%人參皂苷Rg1%人參皂苷Re%含量測定
삼궁적환%제비공예%고효액상색보법%인삼조감Rg1%인삼조감Re%함량측정
Shenxiong dropping pills%preparation%HPLC%ginsenoside Rg1%ginsenoside Re%determination
目的:研究参芎滴丸的最佳成型工艺及有效成分的含量测定方法。方法以滴丸外观质量、溶散时限、丸质量差异为评价指标,在单因素试验的基础上,采用正交试验对基质组成、药物与基质配比、冷凝剂温度和滴距等进行筛选;采用高效液相色谱法测定滴丸中人参皂苷Rg1、Re的质量分数。结果滴丸最佳成型工艺为:PEG4000-PEG6000(质量比为2∶1)为基质,药物与基质质量比为1∶3,冷凝剂为液体石蜡,冷凝剂温度为8~10℃,滴距为8 cm。人参皂苷Rg1在0.2035~6.105μg、人参皂苷Re在0.2005~6.015μg范围内与峰面积呈良好线性关系( r=0.9999);人参皂苷Rg1平均回收率为100.79%,RSD为1.14%( n=6);人参皂苷Re平均回收率为99.93%,RSD为1.72%( n=6)。结论优选得到的参芎滴丸制备工艺合理可行,含量测定方法简便、准确、专属性强,可用于参芎滴丸的制备及质量控制。
目的:研究參芎滴汍的最佳成型工藝及有效成分的含量測定方法。方法以滴汍外觀質量、溶散時限、汍質量差異為評價指標,在單因素試驗的基礎上,採用正交試驗對基質組成、藥物與基質配比、冷凝劑溫度和滴距等進行篩選;採用高效液相色譜法測定滴汍中人參皂苷Rg1、Re的質量分數。結果滴汍最佳成型工藝為:PEG4000-PEG6000(質量比為2∶1)為基質,藥物與基質質量比為1∶3,冷凝劑為液體石蠟,冷凝劑溫度為8~10℃,滴距為8 cm。人參皂苷Rg1在0.2035~6.105μg、人參皂苷Re在0.2005~6.015μg範圍內與峰麵積呈良好線性關繫( r=0.9999);人參皂苷Rg1平均迴收率為100.79%,RSD為1.14%( n=6);人參皂苷Re平均迴收率為99.93%,RSD為1.72%( n=6)。結論優選得到的參芎滴汍製備工藝閤理可行,含量測定方法簡便、準確、專屬性彊,可用于參芎滴汍的製備及質量控製。
목적:연구삼궁적환적최가성형공예급유효성분적함량측정방법。방법이적환외관질량、용산시한、환질량차이위평개지표,재단인소시험적기출상,채용정교시험대기질조성、약물여기질배비、냉응제온도화적거등진행사선;채용고효액상색보법측정적환중인삼조감Rg1、Re적질량분수。결과적환최가성형공예위:PEG4000-PEG6000(질량비위2∶1)위기질,약물여기질질량비위1∶3,냉응제위액체석사,냉응제온도위8~10℃,적거위8 cm。인삼조감Rg1재0.2035~6.105μg、인삼조감Re재0.2005~6.015μg범위내여봉면적정량호선성관계( r=0.9999);인삼조감Rg1평균회수솔위100.79%,RSD위1.14%( n=6);인삼조감Re평균회수솔위99.93%,RSD위1.72%( n=6)。결론우선득도적삼궁적환제비공예합리가행,함량측정방법간편、준학、전속성강,가용우삼궁적환적제비급질량공제。
Objective To study the preparation of Shenxiong dropping pills and establish a method for the determination of ginsenoside Rg1 , ginsenoside Re. Methods On the basis of preliminary experiment, the formulation technology was selected among sort of the ratio of extractum to matrix, component of matrix, temperature of refrigerant and dropping distance,and all the procedure was evaluated by the appearance quality, disintegration time and weight variance of dropping pills as the evaluation indexes by means of orthogonal experimental method. Ginsenoside Rg1 ,and ginsenoside Re were determined by HPLC. Results The optimized preparation was as follows:PEG4000 to PEG6000(2∶1)was used as matrix with the extractum to matrix at 1∶3, the temperature of refrigerant was 8-10℃ and the dropping distance was 8 cm. The linear range of ginsenoside Rg1 was 0.203 5-6.105 μg,and the linear range of ginsenoside Re was 0.200 5-6.015 μg(r=0. 999 9). The average recovery of ginsenoside Rg1 was 100. 79%, RSD was 1. 14%( n=6 ) , and the average recovery of ginsenoside Re was 99.93%,RSD was 1.72%( n=6) . Conclusion The preparation is reasonable and feasible, and the determination method is sample,accurate and rapid with good reproducibility,which can be used in the preparation and the quality control of Shenxiong dropping pills.