摘要
为研究水溶性茯苓多糖提取方法,分别采用热水提取法及超声提取法提取水溶性茯苓多糖,并以杂多糖的得率为指标设计正交试验,采用BSTFA(双(三甲基硅烷基)三氟乙酰胺)和DM F(N,N-二甲基甲酰胺)对杂多糖进行衍生化,采用D-果糖作内标进行气相色谱-质谱联用(GC-M S)定量分析.实验表明:热水浸提的最佳条件为固液比1∶40,提取时间3 h,提取温度90℃;超声波法最佳条件为固液比1∶40,提取时间60 m in,超声功率为100 W.热水提取和超声提取水溶性茯苓多糖的平均提取率分别为13.0%,8.6%,热水浸提法的多糖得率较高.均高于现有文献值报道.
This work has inverstigated the extraction methods of water soulble pachymaran and qualitatively and quantitatively determined poly sacchairide components of Poria cocos F. A. Wolf by gas chromatography-mass spectrometry(GC-MS). Water-soluble pachymaran was extracted by hot water and ultrasound,respectively. The optimum extraction conditions were obtained by a series of orthogonal tests in which heteropolysaccharide yield was used as an indicator. STFA (bis-(trimethylsilyl)trifluoroacetamide) was used as the derivative agents to react with extracted polysaccharides for better volatility and stability, before the GC-MS quantitative analysis. D- fructose was used as the internal standard for quantitative analysis. Experimental results show that the optimum conditions of hot water extraction are follows: solid-liquid ratio 1 : 40, extraction time 3h, extraction temperature 90 ℃ ; whereas optimum conditions of ultrasound are solid-liquid ratio 1 : 40, extraction time 60 mint ultrasonic power 100 W. The average on rates of water-soluble pachymaran by hot water and ultrasonic extractions were 13.0% and 8.6%, respectively, In this study, whicht is higher than previously reported value.
出处
《中南民族大学学报(自然科学版)》
CAS
2010年第1期28-31,共4页
Journal of South-Central University for Nationalities:Natural Science Edition
基金
国家自然科学基金资助项目(20705041)
教育部留学回国人员科研启动基金资助项目(BZY07018)
武汉市晨光计划资助项目(SZY08003)
中南民族大学自然科学基金资助项目(YZZ07003)
关键词
气-质联用
热水浸提法
超声波提取法
水溶性茯苓多糖
gas chromatography-mass spectrometry(GC-MS)
hot water extraction
ultrasonic extraction
watersoluble pachymaranl