首页|复方麝香黄芪滴丸成型工艺优选及挥发性成分含量测定

复方麝香黄芪滴丸成型工艺优选及挥发性成分含量测定

扫码查看
目的 优选复方麝香黄芪滴丸成型工艺,并完善该复方的质量标准。方法 通过单因素实验筛选复方麝香黄芪滴丸的基质种类、基质和药液比例、滴距的最佳考察范围;以外观性状、丸重差异、溶散时限等作为评价指标,采用星点设计-效应面法优选复方麝香黄芪滴丸最佳成型工艺条件;以3批复方麝香黄芪滴丸为检测样品,采用气相色谱法测定龙脑、麝香酮和藁本内酯含量;色谱柱为HP-5石英毛细管柱,进样口温度260 ℃,程序升温,检测器温度300 ℃,分流比10∶1,载气为氮气,流速为1。0 mL·min-1。结果 复方麝香黄芪滴丸的最佳成型工艺条件为基质∶基质=0。99、药物∶基质=0。55、滴距=6。00,综合评分为0。845 2;龙脑、麝香酮和藁本内酯与相邻成分色谱峰均达到基线分离;3种成分的线性范围依次为0。327~1。962、0。140~0。840、0。710 5-4。263 μg(均 r>0。999);平均加样回收率依次为 92。30%(RSD=1。65%,n=6)、101。28%(RSD=0。81%,n=6)、98。99%(RSD=0。65%,n=6);3 种成分的平均含量依次为 0。201 7、0。084 7、1。382 9 mg·g-1。结论 该成型工艺稳定可行,可为复方麝香黄芪滴丸的开发及应用提供参考;建立的气相色谱法能同时测定复方麝香黄芪滴丸中龙脑、麝香酮和藁本内酯的含量,可用于复方麝香黄芪滴丸的质量控制。
Optimization of Molding Process and Determination of Volatile Components Assay in Compound Shexiang Huangqi Dropping Pills by A Central Composite Design-Response Surface Method
Objective The molding process of compound Shexiang Huangqi dropping pills was optimized by central composite design and response surface method,the determination of volatile components in the compound by gas chromatography was established in order to improve the quality standard of the compound.Methods Single factor method was used to select the optimum range of matrix type,the ratio of matrix to liquid,and drop distance of compound Shexiang Huangqi dropping pills;Appearance traits,a difference of pill weight,and dissolution time were used as evaluation indexes,the optimum forming process conditions of compound Shexiang Huangqi dropping pills were optimized by central composite design and response surface method;Three batches of compound Shexiang Huangqi dropping pills were taken as test samples and determined by gas chromatography;The gas chromatographic column was HP-5 sillica capillary column,the inlet temperature was 260 ℃,the temperature was programmed,and the detector temperature was 300 ℃,the split ratio was 10∶1,nitrogen was selected as the carrier gas with a flow rate of 1.0 mL·min-1.Results The optimum forming process conditions of compound Shexiang Huangqi dropping pills were selected by central composite design and response surface method as a matrix:matrix=0.99,drug:matrix=0.55,drop distance=6.00,and the comprehensive score were 0.845 2.Under these conditions,the quality of the prepared dropping pills was the best;The chromatographic peaks of borneol,muscone,and ligustilide reached the baseline separation;the linear ranges of the three components were 0.327-1.962,0.140-0.840,0.710 5-4.263 μg(all r>0.999);The average recoveries were 92.30%(RSD=1.65%,n=6),101.28%(RSD=0.81%,n=6)and 98.99%(RSD=0.65%,n=6);The average contents of the three components were 0.201 7,0.084 7 and 1.382 9 mg·g-1,respectively.Conclusions The forming process is stable and feasible,which can provide a reference for the development and application of compound Shexiang Huangqi dropping pills;The gas chromatography method established can simultaneously determine the contents of borneol,muscone,and ligustilide in compound Shexiang Huangqi dropping pills,which can be used for quality control of compound Shexiang Huangqi dropping pills.

Compound Shexiang Huangqi dropping pillsCentral composite design and response surface methodMolding processGas chromatographyContent determination

邵梦迪、张舒彦、郑淇、常春辉、李家豪、张运克、贾永艳

展开 >

河南中医药大学药学院,郑州 450046

河南中医药大学康复医学院,郑州 450046

河南省中药特色炮制技术工程研究中心,郑州 450046

复方麝香黄芪滴丸 星点设计-效应面法 成型工艺 气相色谱法 含量测定

2025

医药导报
中国药理学会 华中科技大学同济医学院附属同济医院 中国医药商业协会

医药导报

北大核心
影响因子:1.042
ISSN:1004-0781
年,卷(期):2025.44(1)