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1.
Chem Pharm Bull (Tokyo) ; 56(1): 1-6, 2008 Jan.
Article in English | MEDLINE | ID: mdl-18175965

ABSTRACT

Basic hydrolysis procedure is often included in the sample preparation in order to quantify malonylglucosides or acetylglucosides of soy materials. However, it is preferable not to use NaOH as a hydrolytic reagent considering the effect of its alkalinity on the successive injection to HPLC and low acidity of soy isoflavones. This paper presents an improved method for basic hydrolysis using ammonia as a hydrolytic reagent without the additional neutralization step. Moreover, by means of HPLC and LC-MS methods, a systematic quality evaluation of natural soy materials from Chinese markets were established and discussed, inclusive of soybeans, black soybeans, defatted soy flours, as well as the distribution of isoflavones in the seed coat, hypocotyl and cotyledon. The results indicate that HPLC profiling patterns of originating various isoflavone constituents of Chinese soybeans was similar to those of Japanese ones, and those of Chinese black soybeans was similar to those of American ones. The average content level of total soy isoflavones of Chinese soybeans and black soybeans were a little lower than that of American and Japanese ones. Additionally, the thorough analysis for Semen Sojae Praeparatum, a Chinese herbal medicine made from fermented black soybeans or soybeans was done for the first time and the characteristic of its HPLC profiling patterns shows the higher content of isoflavone glucosides and aglycones than those of natural soy materials.


Subject(s)
Dietary Supplements/analysis , Drugs, Chinese Herbal/analysis , Food Analysis/methods , Glucosides/analysis , Glycine max/chemistry , Isoflavones/analysis , Seeds/chemistry , Soy Foods/analysis , Chromatography, High Pressure Liquid , Dietary Supplements/classification , Drugs, Chinese Herbal/chemistry , Drugs, Chinese Herbal/classification , Drugs, Chinese Herbal/isolation & purification , Glucosides/classification , Hydrolysis , Isoflavones/classification , Molecular Structure , Seeds/classification , Seeds/cytology , Soy Foods/classification
2.
Biol Pharm Bull ; 30(3): 527-31, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17329850

ABSTRACT

Chloroplast trnK gene sequences of Cnidium officinale and Ligusticum chuanxiong were determined to establish an effective method for identifying Japanese Senkyu and Chinese Chuanxiong, the two which have the same drug name in Chinese characters, similar external feature, but different botanical origins. Three sites of nucleotide differences were found between these 2 species at positions 767,924 and 964 from upstream in trnK gene sequence, allowing molecular identification of the two plants and crude drugs. Further, three kinds of specific primers of 14 mer, 23 mer and 30 mer long were designed to detect these 3 sites of marker nucleotides. By using multiplex single base extension (MSBE) analysis with the 3 specific primers, C. officinale and L. chuanxiong could be distinguished clearly by the electrophoretograms, where 3 peaks with different color of ddTMP, ddCMP and ddTMP were observed in case of C. officinale and those of ddGMP, ddAMP and ddGMP in L. chuanxiong. Moreover, trnK gene sequence of "Dongxiong," a kind of Chuanxiong cultivated in Northeast China, suggested that its botanical origin was C. officinale.


Subject(s)
Cnidium/genetics , DNA, Chloroplast/genetics , Drugs, Chinese Herbal/chemistry , Ligusticum/genetics , RNA, Transfer, Lys/genetics , Amino Acid Sequence , Base Sequence , Cnidium/chemistry , DNA, Chloroplast/chemistry , DNA, Plant/chemistry , DNA, Plant/genetics , Ligusticum/chemistry , Molecular Sequence Data , RNA, Ribosomal, 18S/genetics , Sequence Analysis, DNA/methods , Species Specificity
3.
Chem Pharm Bull (Tokyo) ; 53(9): 1204-6, 2005 Sep.
Article in English | MEDLINE | ID: mdl-16141600

ABSTRACT

Caragana tibetica KOM. (Fabaceae) is a medicinal plant that has been traditionally used in western part of China. In the course of our screening study on antioxidant activity of medicinal plants, the 70% acetone extract of the stems of C. tibetica was found to have a potent superoxide anion scavenging activity. Tibeticanol (1), a new piceatannol dimer possessing antioxidant activity, was isolated along with eleven known aromatic compounds. Their structures were elucidated on the basis of NMR and MS data. Enzyme oxidation of monomeric stilbene, piceatannol (3), with horseradish peroxidase and hydrogen peroxide yielded cassigarol E (5) and G (6) as major products. Most of the isolated compounds exhibited superoxide anion scavenging activity.


Subject(s)
Antioxidants/chemistry , Caragana/chemistry , Acetylation , Carbohydrate Conformation , Free Radical Scavengers/chemistry , Horseradish Peroxidase/chemistry , Hydrogen Peroxide/chemistry , Magnetic Resonance Spectroscopy , Oxidation-Reduction , Plant Stems/chemistry , Spectrometry, Mass, Fast Atom Bombardment , Stilbenes/chemistry , Superoxides/chemistry
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