Separation and purification of furanocoumarins from Toddalia asiatica (L.) Lam. using microwave-assisted extraction coupled with high-speed counter-current chromatography

被引:30
作者
Qiu, Heyuan [2 ]
Xiao, Xiaohua [1 ]
Li, Gongke [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem & Chem Engn, Guangzhou 510275, Guangdong, Peoples R China
[2] Hanshan Normal Univ, Dept Chem, Chaozhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Furanocoumarin; High-speed counter-current chromatography; Microwave-assisted extraction; Toddalia asiatica (L; ) Lam; CHEMICAL-CONSTITUENTS; CNIDIUM-MONNIERI; MEDICINAL-PLANT; COUMARINS; ISOPIMPINELLIN;
D O I
10.1002/jssc.201100995
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A method of microwave-assisted extraction coupled with high-speed counter-current chromatography was established for separation and purification of isopimpinellin, pimpinellin and phellopterin from Toddalia asiatica (L.) Lam. The conditions of MAE including the extraction solvent, size of sample, solid/liquid ratio, extraction temperature and extraction time were optimized by a mono-factor test. That is, 2.0 g dried powder of T. asiatica (L.) Lam of 0.30-0.15 mm size was extracted with 20 mL (solid/liquid ratio of 1:10, g/mL) methanol under 50 degrees C for 1 min. The crude extract was separated and purified by high-speed counter-current chromatography with hexaneethyl acetatemethanolwater (5:5:5.5:4.5, v/v/v/v) solvent system. 0.85 mg/g of isopimpinellin, 2.55 mg/g of pimpinellin and 0.95 mg/g of phellopterin were obtained from original sample in one-step within 240 min, the purity determined by high performance liquid chromatography was 95.0%, 99.1% and 96.4%, respectively. Their chemical structures were further identified by mass spectroscopy and nuclear magnetic resonance spectroscopy. The results demonstrated that microwave-assisted extraction coupled with high-speed counter-current chromatography was a feasible, economical and efficient technique for rapid extraction, separation and purification of effective compounds from natural products.
引用
收藏
页码:901 / 906
页数:6
相关论文
共 27 条
[11]   Tumor-selective cytotoxicity of benzo[c]phenanthridine derivatives from Toddalia asiatica Lam. [J].
Iwasaki, Hironori ;
Okabe, Takafumi ;
Takara, Kensaku ;
Toda, Takayoshi ;
Shimatani, Masayuki ;
Oku, Hirosuke .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2010, 65 (04) :719-726
[12]   Oral administration of the citrus coumarin, isopimpinellin, blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[a]anthracene in SENCAR mice [J].
Kleiner, HE ;
Vulimiri, SV ;
Starost, MF ;
Reed, MJ ;
DiGiovanni, J .
CARCINOGENESIS, 2002, 23 (10) :1667-1675
[13]   Spasmolytic activity of Toddalia asiatica var. floribunda [J].
Lakshmi, V ;
Kapoor, S ;
Pandey, K ;
Patnaik, GK .
PHYTOTHERAPY RESEARCH, 2002, 16 (03) :281-282
[14]   Simultaneous separation and purification of five bioactive coumarins from the Chinese medicinal plant Cnidium monnieri by high-speed countercurrent chromatography [J].
Li, HB ;
Chen, F .
JOURNAL OF SEPARATION SCIENCE, 2005, 28 (03) :268-272
[15]   Preparative isolation and purification of coumarins from Cnidium monnieri (L.) Cusson by high-speed counter-current chromatography [J].
Liu, RM ;
Feng, L ;
Sun, AL ;
Kong, LY .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1055 (1-2) :71-76
[16]   Oviposition stimulants for the tropical swallowtail butterfly, Papilio polytes, feeding on a rutaceous plant, Toddalia asiatica [J].
Nakayama, T ;
Honda, K ;
Omura, H ;
Hayashi, N .
JOURNAL OF CHEMICAL ECOLOGY, 2003, 29 (07) :1621-1634
[17]   Redetermination and comparative structural study of isopimpinellin: a new inhibitor against the Leishmania APRT enzyme [J].
Napolitano, HB ;
Silva, M ;
Ellena, J ;
Rocha, WC ;
Vieira, PC ;
Thiemanna, OH ;
Oliva, G .
ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2003, 59 :O1506-O1508
[18]   The use of Toddalia asiatica (L) Lam. (Rutaceae) in traditional medicine practice in East Africa [J].
Orwa, J. A. ;
Jondiko, I. J. O. ;
Minja, R. J. A. ;
Bekunda, A. .
JOURNAL OF ETHNOPHARMACOLOGY, 2008, 115 (02) :257-262
[19]  
Rajkumar M., 2008, PHARMACOL REV, V4, P386
[20]  
Sundararajan G, 2001, J ENVIRON BIOL, V22, P11