Quantitative determination of atractylon in Atractylodis Rhizoma and Atractylodis Lanceae Rhizoma by 1H-NMR spectroscopy

被引:26
作者
Hasada, Keiko [1 ,2 ]
Yoshida, Takamitsu [1 ]
Yamazaki, Takeshi [3 ]
Sugimoto, Naoki [3 ]
Nishimura, Tetsuji [3 ]
Nagatsu, Akito [2 ]
Mizukami, Hajime [1 ]
机构
[1] Nagoya City Univ, Grad Sch Pharmaceut Sci, Mizuho Ku, Nagoya, Aichi 4678603, Japan
[2] Kinjo Gakuin Univ, Coll Pharm, Moriyama Ku, Nagoya, Aichi 4638521, Japan
[3] Natl Inst Hlth Sci, Setagaya Ku, Tokyo 1588501, Japan
关键词
Quantitative H-1-NMR; qHNMR; Atractylon; Atractylodis Rhizoma; Atractylodis Lanceae Rhizoma; ATRACTYLENOLIDE-III; BYAKU-JUTSU; SESQUITERPENOIDS; PLANTS; OVATA; RDNA;
D O I
10.1007/s11418-010-0393-x
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
H-1-NMR spectroscopy was successfully applied to the quantitative determination of atractylon in Atractylodis Rhizoma (dried rhizomes of Atractylodes ovata and A. japonica) and Atractylodis Lanceae Rhizoma (dried rhizomes of Atractylodes lancea and A. chinensis). The analysis was carried out by comparing the integral of the H-12 singlet signal of atractylon, which was well separated in the range of delta 6.95-7.05 ppm in the NMR spectrum, with the integral of a hexamethyldisilane (HMD) signal at delta 0 ppm. The atractylon contents obtained by the H-1-NMR spectroscopy were consistent with those obtained by the conventional HPLC analysis. The present method requires neither reference compounds for calibration curves nor sample pre-purification. It also allows simultaneous determination of multiple constituents in a crude extract. Thus, it is applicable to chemical evaluation of crude drugs as a powerful alternative to various chromatographic methods.
引用
收藏
页码:161 / 166
页数:6
相关论文
共 15 条
[1]  
[Anonymous], 2002, ANNU REP NMR SPECTRO, DOI DOI 10.1016/S0066-4103(02)47039-1
[2]   DNA authentication of So-jutsu (Atractylodes lancea rhizome) and Byaku-jutsu (Atractylodes rhizome) obtained in the market based on the nucleotide sequence of the 18S-5.8S rDNA internal transcribed spacer region [J].
Guo, Yahong ;
Kondo, Kenji ;
Terabayashi, Susumu ;
Yamamoto, Yutaka ;
Shimada, Hiroshi ;
Fujita, Masao ;
Kawasaki, Takeshi ;
Maruyama, Takuro ;
Goda, Yukihiro ;
Mizukami, Hajime .
JOURNAL OF NATURAL MEDICINES, 2006, 60 (02) :149-156
[3]   Toxicity of atractylon and atractylenolide III identified in Atractylodes ovata rhizome to Dermatophagoides farinae and Dermatophagoides pteronyssinus [J].
Kim, Hyun-Kyung ;
Yun, Yeon-Kyeong ;
Ahn, Young-Joon .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2007, 55 (15) :6027-6031
[4]  
Kohda Hiroshi, 1994, Natural Medicines, V48, P58
[5]  
*MIN HLTH WELF, 2000, JAP PHARM, P11
[6]  
Mizukami H, 1996, BIOL PHARM BULL, V19, P577, DOI 10.1248/bpb.19.577
[7]   Quantitative 1H NMR:: Development and potential of a method for natural products analysis [J].
Pauli, GF ;
Jaki, BU ;
Lankin, DC .
JOURNAL OF NATURAL PRODUCTS, 2005, 68 (01) :133-149
[8]   Influence of traditional Chinese anti-inflammatory medicinal plants on leukocyte and platelet functions [J].
Prieto, JM ;
Recio, MC ;
Giner, RM ;
Máñez, S ;
Giner-Larza, EM ;
Ríos, JL .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2003, 55 (09) :1275-1282
[9]   A new traceability scheme for the development of international system-traceable persistent organic pollutant reference materials by quantitative nuclear magnetic resonance [J].
Saito, Takeshi ;
Ihara, Toshihide ;
Koike, Masayoshi ;
Kinugasa, Shinichi ;
Fujimine, Yoshinori ;
Nose, Kazutoshi ;
Hirai, Tetsuya .
ACCREDITATION AND QUALITY ASSURANCE, 2009, 14 (02) :79-86
[10]   Specific inhibition of Na+,K+-ATPase activity by atractylon, a major component of Byaku-jutsu, by interaction with enzyme in the E(2) state [J].
Satoh, K ;
Nagai, F ;
Ushiyama, K ;
Kano, I .
BIOCHEMICAL PHARMACOLOGY, 1996, 51 (03) :339-343