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植物化学
Journal of Analytical Methods in Chemistry · 2022 ·Vol. 2022 ·期 1 ·2565494 · IF 2.594

Pharmacokinetic Study of Coadministration with Cefuroxime Sodium for Injection Influencing ReDuNing Injection-Derived Seven Phytochemicals and Nine Metabolites in Rats

Qiulong Zhao,Chunxue Wang,Jiaxin Cheng,Hui Yan,Ling Wang,Dawei Qian,Jinao Duan

According to the sixth edition of China’s “New Coronavirus Diagnosis and Treatment Plan (NCDTP),” ReDuNing injection (RDN) was firstly introduced to treat severe and critical COVID-19, whereas its combination with broad-spectrum antibiotics was suggested to take with extreme caution and full reasons. Therefore, we aim to describe the pharmacokinetics of seven active phytochemicals and semiquantification of nine relevant metabolites in ReDuNing injection (RDN) after combining with cefuroxime sodium (CNa) for injection in rat plasma. Male Sprague–Dawley rats were randomly assigned to six groups, and they were intravenously administered, respectively, with different prescriptions of RDN (2 mL/kg) and CNa (225 mg/kg). At different time points (0.03, 0.08, 0.17, 0.24, 0.33, 0.50, 0.67, 1, and 6 h) after administration, the drug concentrations of iridoids glycosides, organic acids, and metabolites in rat plasma were determined using ultrahigh-pressure liquid chromatography coupled with linear ion rap-orbitrap tandem mass spectrometry (UHPLC–LTQ–Orbitrap–MS), and main pharmacokinetic parameters were estimated by noncompartment model. The results showed that there were differences in pharmacokinetic parameters, AUC (0-t) , T 1/2 , C max , CL of iridoids glycosides, and organic acids, after the intravenous administration of the different combinations of RDN and CNa. Moreover, different combinations of the injections also resulted in different curves of relative changes of each metabolite. The obtained results suggested that RDN and CNa existed pharmacokinetic drug–herb interactions in rats. The findings not only lay the foundation for evaluating the safety of RDN injection combined with CNa but also make contributions to clinically applying RDN injection combined with CNa, which works potentially against severe forms of COVID-19.

研究领域: 药理学 · 药物代谢 · 中药学 · 临床药学 · 分析化学 · 病毒学 · 转化医学
✓ 已验证 DOI 高影响因子
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Biomed Research International · 2018 ·Vol. 2018 ·期 1 ·5314320 · IF 2.583

Antioxidant and Tyrosinase Inhibitory Activities of Seed Oils from Torreya grandis Fort. ex Lindl.

Hong-Xin Cui,Fang-Fang Duan,Shan-Shan Jia,Fang-Rong Cheng,Ke Yuan

Torreya grandis Fort. ex Lindl. is a plant belonging to the Taxaceae family and Torreya grandis cv. Merrillii is the only grafted and thoroughbred species belonging to this species. In this study, we extracted five different seed oils, including T. grandis seed oil (TGSO), T. grandis “Xiangyafei” seed oil (XYSO), T. grandis “Zhimafei” seed oil (ZMSO), T. grandis “Majus”seed oil (TGMSO), and T. grandis “cunguangfei” seed oil (CGSO) using physical pressure. The resulting extracts were analyzed to determine their fatty acid composition, antioxidant activity, and inhibitory activity towards tyrosinase. The results of the antioxidant activity assays revealed that XYSO and ZMSO exhibited much greater DPPH radical scavenging activity and ferric reducing power than TGSO. Notably, all five of the seed oils showed dose-dependent inhibitory activity towards tyrosinase. XYSO and TGSO gave the highest activities of all of the seed oils tested in the current study against monophenolase and diphenolase, with IC 50 values of 227.0 and 817.5 μ g/mL, respectively. The results of this study show that wild TGSOs exhibit strong antioxidant and tyrosinase inhibition activities. These results therefore suggest that wild TGSOs could be used as a potential source of natural antioxidant agents and tyrosinase inhibitors.

研究领域: 植物化学 · 食品科学 · 药用植物学 · 生物活性成分 · 天然产物化学
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INDUSTRIAL CROPS AND PRODUCTS · 2015 · IF 2.837

Green and efficient extraction of bioactive flavonoids from Equisetum palustre L. by deep eutectic solvents-based negative pressure cavitation method combined with macroporous resin enrichment

Xiao-Lin Qi,Xiao Peng,Yu-Yan Huang,Lu Li,Zuo-Fu Wei,Yuan-Gang Zu,Yu-Jie Fu

In the present study, deep eutectic solvents (DESs) as new extraction solvents, are proposed for the green and efficient extraction and separation of bioactive flavonoids from Equisetum palustre L. with negative pressure cavitation-assisted extraction (NPCE) combined with macroporous resin enrichment. A series of different DES systems were investigated for the extraction of bioactive flavonoids in E. palustre. Compared with conventional extraction solvents, DES composed of choline chloride/betaine hydrochloride-ethylene glycol possessed a more effective extraction yields. In addition, the DES-NPCE extraction procedures were also optimized systematically. The optimal conditions were obtained as follows: choline chloride-betaine hydrochloride-ethylene glycol formed a DES with the mole ratio of 1:1:2, 20% water content, extraction pressure −0.07   MPa, extraction temperature 60°C, solvent to solid ratio 25:1   mL/g, and the extraction time 20   min. Furthermore, the direct enrichment of nine flavonoids in DES extraction solution were efficiently achieved using macroporous resin HPD-826. The contents of the nine target flavonoids separated by HPD-826 resin were from 0.17% to 3.37%, and the recovery yields from 57.14% to 89.25%. In conclusion, the developed DES-NPCE combined with macroporous resin enrichment can be an alternative procedure for the green and efficient extraction and separation of bioactive flavonoids from plant sample matrices.

研究领域: 天然产物化学 · 植物化学 · 分析化学 · 药物分离与纯化 · 绿色化学
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Horticultural Plant Journal · 2017 ·Vol. 3 ·期 4 ·165-171 · IF 0

The Contents of Terpene Trilactone and Flavonoid in Leaves of Seedlings from Ancient Female Ginkgo Trees in China

Yanhui ZHANG,Peiying LIU,Qianqian KONG,Shiyan XING,Xiaojing LIU,Limin SUN

Flavonoids and terpene trilactones, especially, ginkgo flavonglycosides, ginkgolides and bilobalides in leaves of ginkgo trees, need to be studied for effective application of these active components with high medical and health-care values. This study was aimed to provide scientific bases for genealogies selection and harvest season confirmation for Ginkgo biloba . A high-performance liquid chromatographic method (HPLC-ELSD) was developed to determine the contents of terpene trilactone and flavonoid of 36 ancient G. biloba genealogies from 19 provinces in China. The study indicated that the content gradually increased from April to August, and thereafter declined. Analysis of variance indicated that the contents of terpene trilactone, flavonoids, and their respective components had significant difference among 36 genealogies. The cluster analysis showed that No. 72 (Xing'an, Guangxi), No. 58 (Youyang, Chongqing), No. 82 (Rugao, Jiangsu), No. 123 (Huixian, Gansu), No. 99 (Dujun, Guizhou), No. 10 (Tai'an, Shandong) and No. 133 (Mentougou, Beijing) genealogies have higher content of terpene trilactone and flavonoid. These results can help us to select superior variety containing high content of terpene trilactone and flavonoid.

研究领域: 植物化学 · 药用植物学 · 天然产物化学 · 林木遗传育种 · 药物代谢
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TheScientificWorldJOURNAL · 2014 ·Vol. 2014 ·期 1 ·857982 · IF 1.219

Antioxidative Activities and Active Compounds of Extracts from Catalpa Plant Leaves

Hongyu Xu,Gege Hu,Juane Dong,Qin Wei,Hongbo Shao,Ming Lei

In order to screen the Catalpa plant with high antioxidant activity and confirm the corresponding active fractions from Catalpa ovata G. Don, C. fargesii Bur., and C. bungei C. A. Mey., total flavonoid contents and antioxidant activities of the extracts/fractions of Catalpa plant leaves were determined. The determined total flavonoid content and antioxidant activity were used as assessment criteria. Those compounds with antioxidant activity were isolated with silica gel column chromatography and ODS column chromatography. Our results showed that the total flavonoid content in C. bungei C. A. Mey. (30.07 mg/g·DW) was the highest, followed by those in C. fargesii Bur. (25.55 mg/g·DW) and C. ovata G. Don (24.96 mg/g·DW). According to the determination results of total flavonoid content and antioxidant activity in 3 clones of leaves of C. bungei C. A. Mey., the total flavonoid content and antioxidant activity in crude extracts from C. bungei C. A. Mey. 6 (CA6) leaves were the highest. Moreover, the results showed that the total flavonoid content and antioxidant activities of ethyl acetate (EA) fraction in ethanol crude extracts in CA6 leaves were the highest, followed by n -butanol, petroleum ether (PE), and water fractions. Two flavonoid compounds with antioxidant activity were firstly isolated based on EA fraction. The two compounds were luteolin ( 1 ) and apigenin ( 2 ), respectively.

研究领域: 植物化学 · 天然产物化学 · 药用植物学 · 抗氧化研究 · 分子生物学
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JOURNAL OF ETHNOPHARMACOLOGY · 2019 · IF 3.414

Seven new veratramine-type alkaloids with potent analgesic effect from Veratrum taliense

Qiong Li,Yun-Li Zhao,Cheng-Bo Long,Pei-Feng Zhu,Ya-Ping Liu,Xiao-Dong Luo

Ethnopharmacological relevance Veratrum taliense is traditionally used TCMs in Yunnan province of China for pain and inflammation. Previous research and clinical applications have shown that V. taliense had significant analgesic activity. Jevine-type alkaloids were shown to be one of the anti-inflammatory and analgesic agents from V. taliense . However, other types of compounds from V. taliense related to its traditional use remains unknown. Aim of the study To identify veratramine-type steroidal alkaloids with analgesic effects from the roots and rhizomes of V. taliense . Materials and methods Compounds were isolated from the roots and rhizomes of V. taliense by chromatographic separation. Their structures were elucidated based on UV, IR, NMR and MS spectra data. Analgesic activity was assessed with acetic acid-induced writhing in mice model. Results Seven new veratramine-type alkaloids were isolated from the roots and rhizomes of V. taliense . They all exhibited significant analgesic activity, of which alkaloids 1 and 4 were more potent antalgic than the well-known analgesic drug, pethidine . Conclusions The veratramine-type alkaloids from V. taliense may serve as new leads for the discovery of analgesic drugs.

研究领域: 民族药理学 · 天然产物化学 · 植物化学 · 疼痛研究 · 药用植物
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JOURNAL OF FOOD QUALITY · 2018 ·Vol. 2018 ·期 1 ·7673652 · IF 0.841

Determination of Free Amino Acids in Three Species of Duckweed (Lemnaceae)

Xiaolong Zhang,Hongyan Chen,Dawei Wu,Wei Gu,Xiao Sun,Jian Chen,Qinan Wu

In this study, a fast, simple, precise, and sensitive hydrophilic interaction liquid chromatography (HILIC) method was established for simultaneous determination of free amino acids in three different varieties of duckweed including Spirodela polyrhiza (L.) Schleid., Landoltia punctata (G. Mey.) Les & D. J. Crawford, and Lemna aequinoctialis Welwitsch by ultrahigh performance liquid chromatography coupled with tandem mass spectrometry (UHPLC-MS/MS). Method validation was processed in terms of linearity, precision, stability, repeatability, and accuracy as well as limits of detection and quantification. The developed method was applied for quantification of 59 batches of samples. Then chemometric analysis was used to evaluate different duckweeds by principle component analysis (PCA) and orthogonal partial least squares-discriminant analysis (OPLS-DA). The results demonstrated that there was no significant difference in FAAs’ profile among three varieties of duckweed.

研究领域: 分析化学 · 植物化学 · 代谢组学 · 植物生物化学
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Revista Brasileira de Farmacognosia-Brazilian Journal of Pharmacognosy · 2019 ·Vol. 29 ·期 1 ·46-53 · IF 1.754

Anti-allergic rhinitis effects of caffeoylquinic acids from the fruits of Xanthium strumarium in rodent animals via alleviating allergic and inflammatory reactions

Peng Wei,Han Ping,Yu Luyao,Chen Ying,Ye Bingzhu,Qin Luping,Xin Hailiang,Han Ting

The fruits of Xanthium strumarium L., Asteraceae, have been used for various diseases in Chinese folk medicine, including allergic rhinitis, tympanitis, arthritis, ozena etc. The current study was aimed to investigate the therapeutic effects of caffeoylquinic acids from fruits of X. strumarium on allergic rhinitis in animals. The toxicity test indicated that the caffeoylquinic acids have no obvious toxicity. By using HPLC assays combined with reference standards, ten caffeoylquinic acids were identified as the predominant constituents. Anti-allergic activities of the caffeoylquinic acids were evaluated using passive cutaneous anaphylaxis test and Schultz-Dale test; dimethylbenzene induced ear edema test was performed to evaluate its anti-inflammatory effect. Then, the allergic rhinitis model in rats was established to evaluate the therapeutic effects of the caffeoylquinic acids against allergic rhinitis with the following indexes: allergic rhinitis symptom scores, serum levels of pro-inflammatory cytokines, histopathological examination, and histamine release. Our study revealed that the caffeoylquinic acids showed obvious anti-allergic and anti-inflammatory properties, and its treatments were beneficial for ameliorating the nasal symptoms, decreasing pro-inflammatory cytokines, and inhibiting the releases of histamine. Collectively, the caffeoylquinic acids might be utilized as effective and safe disease therapeutic agents for allergic rhinitis.

CAS / MDL: 79794-75-5
研究领域: 药理学 · 免疫学 · 过敏 · 植物化学
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CHEMISTRY & BIODIVERSITY · 2019 ·Vol. 16 ·期 3 ·e1800581 · IF 1.449

Chromane Enantiomers from the Flower Buds of Tussilago farfara L. and Assignments of Their Absolute Configurations

Jia Sun,Jin-Hai Yu,Jun-Sheng Zhang,Xiu-Qing Song,Jie Bao,Hua Zhang

Fourteen chromane derivatives of seven pairs of enantiomers ( 1 – 14 ) have been obtained from the ethanolic extract of the flower buds of Tussilago farfara L. Their structures with absolute configurations have been elucidated by detailed spectroscopic analyses, chemical methods, and particularly comparison of experimental ECD spectra with theoretically computed ones. Biological evaluations revealed that they did not show cytoprotective, antimicrobial, and α - glucosidase inhibitory activities. Graphical

CAS / MDL: 56180-94-0 2492-87-7
研究领域: 植物化学 · 药理学 · 药物化学
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CHEMISTRY AND PHYSICS OF LIPIDS · 2019 · IF 2.536

Characterization of lignans in Schisandra chinensis oil with a single analysis process by UPLC-Q/TOF-MS

Yuan Gao,Shimin Wu,Renhuai Cong,Junyong Xiao,Fangli Ma

Schisandra chinensis is a medicinal and edible plant that contains various bioactive compounds. Among these, lignans are the major functional compounds. Nevertheless, detailed information about lignans in Schisandra chinensis oil remains scarce. A powerful UPLC-Q/TOF-MS method was established for the rapid identification of the lignan constituents of Schisandra chinensis oils. The results showed that 21 lignans have been unambiguously identified, and four lignans have been tentatively identified in the Schisandra chinensis oils. In addition, semi-quantitative analysis indicated that the total lignan content in the Schisandra chinensis oils was distributed from 67.73 ± 0.06 to 87.61 ± 1.83 mg/g. Schisandrin and schisandrin B were the most abundant lignans in the Schisandra chinensis oils, their content ranging from 15.85 ± 0.09 to 20.57 ± 0.38 mg/g. Additionally, this study provided a systematic characterization of lignans in Schisandra chinensis oil and indicated that the oil might be used as lignan-related functional foods.

CAS / MDL: 61281-37-6
研究领域: 植物化学 · 分析化学 · 药理学
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