Establishment of gas chromatography for content determination of five volatile components in Qingxuan pills / 中国药房

OBJECTIVE To estab lish a meth od for the determination of 5 volatile components as menthone ，menthol， pulegone，piperitone and ligustilide in Qingxuan pills. METHODS Seven batches of Qingxuan pills were taken as test samples and determined by gas chromatography. The gas chromatographic column was DB- 5 sillica capillary column ，the carrier gas was nitrogen，the inlet temperature was 200 ℃. The sample size was 1 μL，and the split ratio was 10 ∶ 1. The temperature was programmed（the initial temperature was kept at 100 ℃ for 2 min，and then raised to 220 ℃ at 5 ℃/min for 2 min），and the temperature of the flame ionization detector was 250 ℃. RESULTS The chromatographic peaks of menthone ，menthol，pulegone， piperitone and ligustilide reached the baseline separation ；the linear ranges of the five components were 0.008-0.388，0.010-0.527， 0.006-0.327，0.006-0.312，0.053-2.672 mg/mL（all r＞0.999 0）；the average recoveries were 96.33％（RSD＝1.23％，n＝6）， 96.92％（RSD＝1.38％，n＝6），97.53％（RSD＝1.81％，n＝6），96.80％（RSD＝1.89％，n＝6）and 95.61％（RSD＝0.77％， n＝6）；the contents of the five components were 0.009-0.070，0.040-0.157，0.017-0.150，0.008-0.049 and 0.144-0.932 mg/g， respectively. CONCLUSIONS The gas chromatography method established in this study is simple and accurate ，which can simultaneously determine the contents of five volatile components in Qingxuan pills .

Simultaneous Determination of 5 Components in the Classical Formula Huaihua San by HPLC Wavelength Switching Method / 中国药房

OBJECTIVE：To develop a method for simultaneous determination of 5 components in classical formula Huaihua san，including rutin ，naringin，neohesperidin，quercetin and pulegone. METHODS ：HPLC wavelength switching method was adopted. The determination was performed on Cosmosil C 18 column with mobile phase consisted of acetonitrile- 0.05％ phosphoric acid solution （gradient elution ）at the flow rate of 1.0 mL/min. The detection wavelengths were set at 257 nm for rutin ，283 nm for naringin and neohesperidin ，254 nm for quercetin ，252 nm for pulegone ，respectively. The column temperature was set at 30 ℃， and sample size was 10 μL. RESULTS：The linear range was 21.7-2 170 μg/mL for rutin，46-4 600 μg/mL for naringin，22.3- 2 230 μg/mL for neohesperidin，0.96-96 μg/mL for quercetin，2.7-270 μg/mL for pulegone（all r＞0.999），respectively. RSDs of precision，stability（24 h）and reproducibility tests were all lower than 2％（n＝6）. Average recoveries were 100.70％，99.31％， 101.10％，100.03％ and 99.63％（all RSD ＜2％，n＝9）. Among 3 batches of Huaihua san samples ，the contents of above 5 components were 20.055-22.615，25.557-27.806，11.428-13.250，0.350-0.478，2.372-4.011 mg/g，respectively. CONCLUSIONS ： Established method is simple ，accurate and reproducible ，and could be used for the simultaneous determination of 5 components in Huaihua san.

Evaluation of key production processes of Schizonepetae Herba formula granules based on characteristic chromatogram and quantitative transfer relationship / 中国中药杂志

The aim of this paper was to evaluate the key production processes of Schizonepetae Herba formula granules based on the new model of combining characteristic chromatogram with quantitative transfer relationship. The rationality of production process design was evaluated by studying the intermediates in different processes of formula granules, analyzing the loss of index component pulegone in each step, and establishing the characteristic chromatogram. The content of pulegone in 10 batches of standard decoction ranged between 0.067% and 0.124%(70%-130% of the average value), and the transfer rate of pulegone was 44.58%-93.97%. After the improvement of the production process, the content of pulegone in Schizonepetae Herba formula granules was 0.093%, and the transfer rate of pulegone was 68.38%, which was consistent with the parameters range of standard decoction. This study emphasized the integrality of the research process of traditional Chinese medicine(TCM) formula granules, and provided a new idea for the quality control of TCM with content determination as the main evaluation index for a long time.

Optimization of the Extraction Technology of Volatile Oil from Schizonepeta tenuifolia and Forsythia suspensa / 中国药房

OBJECTIVE： To establish the method for content determination of volatile oil of Schizonepeta tenuifolia and Forsythia suspensa， and to optimize the extraction technology of the volatile oil. METHODS： The contents of β-pinene and pulegone were determined by GC method. The determination was performed on Hp-5 capillary column. The detector was hydrogen flame ion detector with programmed temperature. The sample size was 0.5 μL， the split ratio was 70 ∶ 1， the carrier gas was nitrogen， the inlet temperature was 250 ℃， the detector temperature was 280 ℃， the air flow rate was 390 mL/min， the hydrogen flow rate was 36 mL/min， the tail flow rate was 15 mL/min， and the nitrogen flow rate was 1 mL/min. Based on single factor test， orthogonal test combined with information entropy method were used to optimize the extraction technology of S. tenuifolia and F. suspensa using soaking time， extraction time， material-liquid ratio and forsythia grain size as factors， with the extraction amount of volatile oil， the content of β-pinene and pulegone and their comprehensive score as indexes.  RESULTS： The linear range of β-pinene and pulegone 1.575-7.875（r＝0.999 9） and 1.892-9.46 μg（r＝0.999 7）， respectively. The limits of quantitation were 0.10 and 0.25 μg； the limits of detection were 0.03 and 0.08 μg； RSDs of precision， stability and reproducibility tests were less than 2％ （n＝6）； the recoveries were 97.77％-100.01％ （RSD＝0.93％，n＝9） and 96.47％-99.00％（RSD＝0.89％， n＝9）. The optimal extraction technology was soaking 2 h， extracting for 6 h， 10-fold water （mL/g）， half a clove of granularity. Under this condition， the extraction amount of volatile oil， the contents of β-pinene and pulegone were 3.6 mL， 1 450.4 mg， 127.6 mg， respectively. RSD were 1.62％， 0.20％， 1.42％. CONCLUSIONS： Established method is simple， accurate and reproducible， and the optimal extraction technology is stable and feasible.

Fingerprinting study on Niuhuang Shangqing Pills based on comprehensive two-dimensional liquid chromatography / 中草药

Objective: To develop a new three-dimensional fingerprinting method and its assessing Methods: based on comprehensive two-dimensional liquid chromatography using Niuhuang Shangqing Pills (NSP) as an example. The developed method could offer new method for the quality control of NSP. Methods: In first dimension, the separation was achieved with an Acquity UPLC HSS CYANO column (100 mm × 2.1 mm, 1.8 μm), methanol-0.1% formic acid in water were used as mobile phases, flow rates were 0.1 mL/min. In second dimension, the separation was achieved with a Kinetex Phenyl-Hexyl column (50 mm × 3 mm, 2.6 μm), acetonitrile-0.1% formic acid in water were used as mobile phases, flow rates were 1.5 mL/min, detection wavelength was set at 254 nm, and acquiring frequency was at 12.5 Hz. Column temperature for each dimension was 40 ℃ and volume of loop linking the two dimensions was 100 μL. Three similarity-calculating Methods:, Euclidean Distance, Cosine, and Correlation Coefficient, were employed to assess the similarities among the 21 samples on the market using medians with arithmetic means of peak volumes of the common peaks as control fingerprints. Results: The three-dimensional fingerprints of 21 batches of NSP samples on the market were developed; Eighteen common peaks were assigned and five of them were identified, which were geniposide (1), pulegone (8), baicalin (9), imperatorin (15), and wogonin (16). Conclusion: A three-dimensional fingerprinting method and its assessing Methods: based on comprehensive two-dimensional liquid chromatography using NSP as an example were successfully developed for the first time, suggesting that it is a feasible method for developing fingerprints for Chinese materia medica. This work improves and supplements the traditional liquid-chromatography fingerprints.

Pulegone Exhibits Anti-inflammatory Activities through the Regulation of NF-κB and Nrf-2 Signaling Pathways in LPS-stimulated RAW 264.7 cells

Pulegone is a naturally occurring organic compound obtained from essential oils from a variety of plants. The aim of this study was to investigate the anti-inflammatory effects through the inhibitory mechanism of inducible nitric oxide synthase (iNOS), cyclooxygenase (COX-2), nuclear factor kappa B (NF-κB), mitogen-activated protein kinases (MAPK) pathways and the activation of nuclear factor erythroid 2-related factor 2 (Nrf2)/ heme oxygenase (HO)-1 pathways in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. Results revealed that pulegone significantly inhibited NO production as well as iNOS and COX-2 expressions. Meanwhile, western blot analysis showed that pulegone down-regulated LPS-induced NF-κB and MAPKs activation in RAW 264.7 cells. Furthermore, the selected compound suppressed LPS-induced intracellular ROS production in RAW 264.7 cells, while the expression of stress response gene, HO-1, and its transcriptional activator, Nrf-2 was upregulated upon pulegone treatment. Taking together, these findings provided that pulegone inhibited the LPS-induced expression of inflammatory mediators via the down-regulation iNOS, COX-2, NF-κB, and MAPKs signaling pathways as well as up-regulation of Nrf-2/HO-1 indicating that pulegone has a potential therapeutic and preventive application in various inflammatory diseases.

Effects of different extraction methods on composition and antibacterial activity of volatile oil from Forsythiae Fructus, Schinzonepetae Herba, and Menthae Haplocalycis Herba / 中草药

Objective To compare the chemical composition and antibacterial activity of the volatile oils from Forsythiae Fructus (FF), Schizonepetae Herba (SH), Menthae Haplocalycis Herba (MH), and their compatibility, and to explore the influence of different extraction methods on components and antibacterial activity of volatile oil. Methods GC-MS was employed to analyze the composition of the volatile oil from FF, SH, and MH extracted separately, and their mixture extracted, as well as physical mixing volatile oil of FF, SH, and MH extracted separately. The diameter of the inhibition zone and the minimum inhibitory concentration (MIC) were measured using the paper agar diffusion method and micro dilution method. The antibacterial activities of volatile oil on four common pathogens of respiratory tract were evaluated. Results When FF, SH, and MH were mixed and extracted, the main obtained components and contents of volatile oil changed. Compared to separately extracted volatile oil, eight new components emerged, seven components from FF and seven components from SH disappeared in FF and SH mixture extracted volatile oil. In FF and MH mixture extracted volatile oil, compared with separately extracted, six components from FF and eight components from MH disappeared, and eight new components emerged. As to SH and MH mixture extracted volatile oil, four components from SH and seven components from MH disappeared, and seven new components emerged. In the three herbs mixture extracted volatile oil, six components from FF, four components from SH, and two components from MH disappeared, one commom component of FF and MH, two common components of SH and MH disappeared, however, nine new components emerged. The content of pulegone significantly decreased in the three herbs mixture extracted volatile oil compared with that in separately extracted. The antibacterial experiments showed that the antibacterial effects of the volatile oils obtained by different extraction methods were different. The antibacterial effects of volatile oil extracted separately and their physical mixing volatile oil on Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, and Candida albicans were better than that from mixture extracted. Conclusion Volatile oil is an important effective component of Chinese patent medicines with relieving exterior syndrome function. Different extraction methods have a certain influence on the yield and composition of volatile oil, which ultimately affects the efficacy of drugs. Therefore, we should pay more attention to extraction method and process of volatile oil in these prescriptions.

Uses of hazardous medicinal plants: composition of the essential oil of Clinopodium gilliesii (Benth. ) Kuntze (Lamiaceae), collected in Chile / Uso de plantas medicinales peligrosas: composición del aceite esencial de Clinopodium gilliesii (Benth. ) Kuntze (Lamiaceae), recolectada en Chile

Clinopodium gilliesii (Benth.) Kuntze, harvested in the Chilean highlands, contains a surprising 93.87% of the toxic monoterpene pulegone in the essential oil. These results show remarkable differences with studies of the same species carried out in Argentina and Peru. These dissimilarities in the monoterpene composition of essential oils should be associated with differences in toxicity and biological activity of this medicinal plant used in ethnomedicine in different countries for the treatment of similar discomforts and diseases. These results are discussed considering the risk of consuming C. gilliesii, without clear recommendations and control of at least pulegone content in essential oils.

Clinopodium gilliesii (Benth.) Kuntze, recolectada en el altiplano chileno, contiene un sorprendente 93,87% del monoterpeno toxico pulegona, en el aceite esencial. Estos resultados muestran diferencias notables con estudios de la misma especie realizados en Argentina y Perú. Estas disimilitudes, en la composición de los aceites esenciales deben estar asociadas con diferencias en la toxicidad y actividad biológica de esta especie medicinal que se utiliza en etnomedicina en diferentes lugares para el tratamiento de molestias y enfermedades similares. Estos resultados se discuten considerando el riesgo de consumir C. gilliesii, sin recomendaciones claras y control de al menos el contenido de pulegona en los aceites esenciales.

In vitro activity of the essential oil from Hesperozygis myrtoides on Rhipicephalus (Boophilus) microplus and Haemonchus contortus

ABSTRACT Commercial antiparasitics have been the main tool to control parasites, but due to the resistance development, plant extracts have been widely investigated to find new molecules. The present study aimed to investigate the in vitro acaricide and anthelmintic activities of the essential oil from the aerial parts of Hesperozygis myrtoides (A.St.-Hil. ex Benth.) Epling, Lamiaceae. The essential oil was obtained by hydrodistillation analyzed by GC-FID and GC-MS. Four tests were conducted in vitro to screen the antiparasitic action of the essential oil. The evaluation on Rhipicephalus (Boophilus) microplus was performed with the adult immersion test at concentrations ranging from 0.391 to 25 mg/ml and the larval packet test from 3.125 to 100 mg/ml. For Haemonchus contortus the egg hatch test was performed from 0.012 to 25 mg/ml and the larval development test from 0.003 to 0.4 mg/ml. The LC50 and LC90 values were calculated by Probit. The main components identified in the essential oil were isomenthone (47.7%), pulegone (21.4%), limonene (7.7%), isomenthyl acetate (6.8%) and neoisomenthol (3.9%). In the larval packet test the LC50 and LC90 were 13.5 and 21.8 mg/ml, respectively. In egg hatch test, the LC50 and LC90 were 0.249 and 0.797 mg/ml, respectively, while in the larval development test were 0.072 and 0.167 mg/ml, respectively. This is the first report of the H. myrtoides evaluation against those parasites. The anthelmintic results proved its efficacy on H. contortus encouraging new research with a focus on their main bioactives.

HPLC fingerprint and determination of multi-components in Chitong Xiaoyanling Granules / 中草药

Objective To establish an HPLC fingerprint and to determine six compounds in Chitong Xiaoyanling Granules (CXG) for reference of the effective quality control. Methods The analysis was carried out on an analytical column Dikma Luster ODS (250 mm × 4.6 mm, 5 μm) with gradient elution by methanol (A)-0.1% phosphoric acid solution (B) (0-15 min, 20%-30% A; 15-30 min, 30% A; 30-40 min, 30%-60% A; 40-55 min, 60% A), at the detection wavelengths of 254, 283, 274, and 300 nm and a flow rate of 1.0 mL/min. The column temperature was 30 ℃. Similarity evaluation software was used to evaluate the fingerprint of 10 batches of CXG, and the six marker components were quantified. Results The common mode of the fingerprint was set up with 18 common peaks, and six of them were identified by comparison with the reference. The similar degrees of 10 batches of samples were over 0.9, they were prim-O-glucosylcimifugin, 4'-O-β-D-glucosyl-5-O-methylvisamminol, pulegone, hesperidin, paeonol, and isoimperatorin. The linear ranges were 0.013-0.505 mg/mL (r = 0.999 8), 0.052-2.097 mg/mL (r = 0.999 2), 0.019-0.772 mg/mL (r = 0.998 9), 0.025-1.003 mg/mL (r = 0.999 1), 0.006-0.251 mg/mL (r = 0.999 5), and 0.014-0.576 mg/mL (r = 0.999 4) for prim- O-glucosylcimifugin, 4'-O-β-D-glucosyl-5-O-methylvisamminol, pulegone, hesperidin, paeonol, and isoimperatorin, respectively. The contents of prim-O-glucosylcimifugin, 4'-O-β-D-glucosyl-5-O-methylvisamminol, pulegone, hesperidin, paeonol, and isoimperatorin were 7.267-7.333, 4.260-4.522, 2.033-2.093, 12.234-12.771, 19.023-19.334, and 11.152-11.291 mg/g in 10 batches of samples, respectively. Conclusion The established method has high sensitivity and specificity, and can be used for the quality control of CXG.

Seasonal variability of the essential oil of Hesperozygis ringens (Benth.) Epling. / Variabilidade sazonal do óleo essencial de Hesperozygis ringens (Benth.) Epling.

Abstract This study was developed to evaluate the effect of seasonality on the yield and chemical composition of the essential oil (EO) of Hesperozygis ringens (Benth.) Epling, a native species from the Brazilian Pampa. Leaves were collected from four specimens of a single population in each of the four seasons for a year and were extracted in triplicate by hydro-distillation for 2 hours. The yield of EO (% w/w) was calculated on fresh weight basis (FWB), and the 16 oil samples were analyzed by gas chromatography coupled to mass spectrometry (GC-MS) and gas chromatography with flame ionization detector (GC-FID). Hierarchical Cluster Analysis (HCA) and Principal Component Analysis (PCA) were used as statistical tools to evaluate differences in chemical composition. The highest yields were obtained in autumn, spring and summer (2.32-4.38%), while the lowest yields were detected in winter, ranging from 1.15 to 1.91%. Oxygenated monoterpenoids were the predominant class of chemical constituents in the EO obtained in all seasons, showing the highest contents in autumn and summer, and pulegone was identified as a major compound, whose contents varied between 54.13 and 81.17%. The EO samples were divided into three chemical groups by HCA and PCA and were assigned to the same group, except for the three samples gathered in winter. The results showed a seasonal influence on the yield and chemical composition of the EO.

Resumo Este estudo foi desenvolvido a fim de avaliar o efeito da sazonalidade no rendimento e composição química do óleo essencial (OE) de Hesperozygis ringens (Benth.) Epling., uma espécie nativa do Pampa brasileiro. Folhas foram coletadas de quatro indivíduos de uma mesma população, em cada uma das quatro estações de um ano, e foram extraídas em triplicada por hidrodestilação durante 2 horas. O rendimento do OE (% m/m) foi calculado considerando a base fresca (BF) e as 16 amostras de óleo foram analisadas por cromatografia gasosa acoplada à espectrometria de massas (CG-EM) e cromatografia gasosa com detector de ionização de chamas (CG-DIC). Análise Hierárquica de Cluster (AHC) e Análise de Componentes Principais (ACP) foram utilizadas como ferramentas estatísticas para avaliar as diferenças na composição química. Os maiores rendimentos foram obtidos no outono, primavera e verão (2,32-4,38%), enquanto que os menores foram detectados no inverno, variando de 1,15 até 1,91%. Os monoterpenoides oxigenados foram a classe predominante dos constituintes do OE obtido em todas as estações, apresentando os maiores teores no outono e no verão, e a pulegona foi identificada como o constituinte majoritário, cujos teores variaram entre 54,13 e 81,17%. As amostras de OE foram divididas em três grupos químicos por AHC e ACP e foram classificadas no mesmo grupo, com exceção de três amostras coletadas no inverno. Os resultados demonstraram influência sazonal no rendimento e na composição química dos OE.

Identification of volatile compounds of Clinopodium odorum (Lamiaceae):A comparison between HS-SPME and classic hydrodistillation / Identificación de compuestos volátiles de Clinopodium odorum (Lamiaceae): Una comparación entre HS-SPME ehidrodestilación clásica

In the present work an analytical methodology to micro scale based on the use of the HS-SPME/GC-MS to determine volatile compounds present in Clinopodium odorum (Griseb.) Harley (Lamiaceae)was optimized and settled differences and similarities with itsessential oil. A systematic description of the volatile components of flowers, stems, leaves and combined aerial parts (whole plant) was constructed via GC-MS analyses of HS-SPME adsorbed compounds and of essential oils obtained through hydrodistillation of the same tissues. Pulegone was the main component of both the HS-SPME analysis and essential oil analysis. In addition, piperitenone oxide andpiperitone oxide were the other main components in the essential oil whereas in the HS-SPME analysis cis-isopulegone and menthone prevailed. The HS-SPME method can achieve comparable results to those obtained by essential oil analysis, by using very fewer samples, ashorter extraction time and a much simpler procedure.

En el presente trabajo se ha optimizado una metodología analítica a micro-escala basada en HS-SPME/GC-MS para determinar los compuestos volátiles presentes en Clinopodium odorum (Griseb.) Harley (Lamiaceae), y se establecieron diferencias y similitudes con su aceite esencial. Se realizó una descripción sistemática de los componentes volátiles de flores, tallos, hojas y partes aéreas combinadas(planta entera) a partir de los análisis por GC-MS a través del sistema HS-SPME y de los aceites esenciales. Pulegona fue el componenteprincipal tanto del análisis por HS-SPME, como del aceite esencial. Además, el óxido de piperitenona y el óxido de piperitona eran los otroscomponentes principales en el aceite esencial mientras que en el análisis por HS-SPME, prevalecieron cis-isopulegona y mentona. El método de HS-SPME puede lograr resultados comparables a los obtenidos por el análisis de aceite esencial, mediante el uso de muestras de menor tamaño, un tiempo de extracción más corto y un procedimiento más simple.

Action mechanism of the monoterpenes (+)-pulegone and 4-terpinyl acetate in isolated guinea pig ileum / Mecanismo de accion de los monoterpenos (+)-pulegona y acetato de 4-terpinil en íleon aislado de cobayo

Recent studies have shown the spasmolytic activity of p-menthane monoterpenes (+)-pulegone and 4-terpinyl acetate (4-T) in guinea pig ileum. Since the action mechanism of these monoterpenes in intestinal smooth muscle is unknown, the present study was conducted to characterize their relaxant mechanism in isolated guinea pig ileum. We tested the involvement of voltage-dependent calcium and potassium channels and muscarinic antagonism. Both the monoterpenes caused a shift in the calcium curve to the right with reduction in the maximum effect. Pretreatment with tetraethylammonium chloride partially inhibited relaxation produced by both 4-T and (+)-pulegone. Both compounds caused a shift in the bethanechol curve to the right with reduction in the maximum effect. The results of this study indicate that the mechanisms of action of the smooth muscle relaxant monoterpenes (+)-pulegone and 4-T possibly involve the partial blockade of calcium channels, the activation of potassium channels, and the non-competitive antagonism of muscarinic receptors.

Estudios recientes han demostrado la actividad espasmolítica de los monoterpenos p-mentano de (+)-pulegona y acetato de 4-terpinilo (4-T) en el íleon de cobayo. Dado que el mecanismo de acción de estos monoterpenos en el músculo liso intestinal es desconocido, el presente estudio se llevó a cabo para caracterizar su mecanismo relajante en íleon aislado de conejillo de indias. Hemos probado la participación de tanto los canales calcio dependiente de voltaje como los canales de potasio y antagonistas muscarínicos. Ambos monoterpenos causaron un desplazamiento en la curva de calcio a la derecha con la reducción en el efecto máximo. El tratamiento previo con cloruro de tetraetilamonio inhibe parcialmente la relajación producida por tanto 4-T y (+)-pulegona. Ambos compuestos causaron un cambio en la curva de betanecol a la derecha con la reducción en el efecto máximo. Los resultados de este estudio indican que los mecanismos de acción de los monoterpenos relajantes del músculo liso (+)-pulegona y 4-T posiblemente implican el bloqueo parcial de los canales de calcio, la activación de los canales de potasio, y el antagonismo no competitivo de los receptores muscarínicos.

HPLC fingerprint analysis on Wei Medicine Ziziphora tenuior and Ziziphora clinopodioides / 中草药

Objective: To establish HPLC fingerprint for the analysis on Ziziphora tenuior and Z. clinopodioides and the determination of hyperin, rutine, and pulegone in eight batches of Z. tenuior and 22 batches of Z. clinopodioides synchronously. Methods: The HPLC method was used with Kromasil C18 column (250 mm × 4.6 mm, 5 μm), and a mixture of methanol-0.08% HCOOH was used as mobile phase with gradient elution. The HPLC fingerprint for eight batches of Z. tenuior and 22 batches of Z. clinopodioides was established. Results: The HPLC fingerprints of the two species were obviously different, so two modes were established for two species, respectively. The eight batches of Z. tenuior and 22 batches of Z. clinopodioides were classified into two groups based on the result of principal component, hierarchical cluster, and similarity analyses. Hyperin and pulegone were the common compositions; quercetin (161.06-213.22 μg/g) was founded in Z. tenuior, but not in Z. clinopodioides; the contents of hyperin (174.15-802.24 μg/g), pulegone (77.43-353.45 μg/g) of Z. clinopodioides were higher than those of Z. tenuior (49.72-204.33 and 36.19-93.29 μg/g). Conclusion: Z. tenuior and Z. clinopodioides have the different fingerprint, which could provide the evidence for their quality control, species identification, and classification.

Study on determination method of menthone and pulegone in Herba Schizonepetae / 中华中医药杂志

Objective: To establish a method for determination of methone and pulegone in Herba Schizonepetae. Methods: The contents of menthone and pulegone were determined by GC (equipped with FID) with HP-5 fused capillary column (5% phenyl methyl siloxane 30m?0.32mm?0.25?m) after the samples were extracted by the solvents. Results: The linear ranges were 0.002-5.0g/L (r=0.9999) for menthone and 0.002-5.0g/L (r=0.9996) for pulegone, the recoveries of menthone and pulygone were 96.30%-103.9% and 95.7%-102.5%, respectively. Conclusion: The method was simple and accurate, which could be applied to the determination of menthone and pulegone in Herba Schizonepetae.