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  1. Article ; Online: Efficacy and safety of Xiao-ai-ping injection add-on therapy to chemotherapy in patients with non-small cell lung cancer: A systematic review and meta-analysis.

    Li, Andong / Liu, Shilin / Zhang, Hui / Lin, Minghao / Guo, Lijiao / Yuan, Chengbo / Li, Zhenyu / Xu, Jianan / Wang, Tan

    Medicine

    2023  Volume 102, Issue 40, Page(s) e35483

    Abstract: Background: Xiao-ai-ping injection (XAPI) combined with chemotherapy has potential efficacy and ...

    Abstract Background: Xiao-ai-ping injection (XAPI) combined with chemotherapy has potential efficacy and less side effects in the treatment of non-small cell lung cancer (NSCLC). At present, there are many clinical studies on XAPI combined with chemotherapy in the treatment of NSCLC, but the results are different. The purpose of this study was to evaluate the efficacy and safety of XAPI combined with chemotherapy in the treatment of NSCLC by meta-analysis system.
    Methods: The databases to be searched include PubMed, Cochrane Library, Web of Science, Chinese National Knowledge Infrastructure, Chinese Biomedical Literature Database, Wanfang database, Chinese Scientific Journal Database, and so on. In addition, relevant journals and magazines will manually search in various fields as supplements. The search date is set from the establishment of the database until July 8, 2023. The 2 researchers will use Endnote X9 software for literature screening and data extraction and independently evaluate the quality. We then assessed the quality and risk of inclusion in the study and observed outcome indicators.
    Results: A total of 28 trials were included in this study, 1947 patients with NSCLC (974 receiving XAPI combined chemotherapy and 973 receiving chemotherapy alone). The results of meta-analysis showed that: Objective tumor response rate of NSCLC (P < .00001). Improvement in Karnofsky performance score of NSCLC (P < .00001). Quality of life score of NSCLC (P < .00001). The result of CD3 + (P < .00001). The result of CD4 + (P < .00001). The result of CD8 + (P < .00001). The result of CD4+/CD8 + (P = .0001). Leukopenia (P < .00001). Thrombocytopenia (P < .00001). Hemoglobin decrease (P < .00001). Liver function (P = .04). Nausea and vomiting (P < .00001).
    Conclusion: Our meta-analyses demonstrated that XAPI adjunct with chemotherapy can improve the patient quality of life, reduce adverse reactions, and enhanced immune function, the treatment is effective and high safety. Which suggests that it might be used for NSCLC. However, a large sample of randomized controlled trials are needed to further study the long-term efficacy of XAPI.
    MeSH term(s) Humans ; Carcinoma, Non-Small-Cell Lung/pathology ; Lung Neoplasms/pathology ; Quality of Life ; Drugs, Chinese Herbal/adverse effects ; Thrombocytopenia/chemically induced
    Chemical Substances Marsdeniae tenacissimae extract ; Drugs, Chinese Herbal
    Language English
    Publishing date 2023-10-06
    Publishing country United States
    Document type Meta-Analysis ; Systematic Review ; Journal Article
    ZDB-ID 80184-7
    ISSN 1536-5964 ; 0025-7974
    ISSN (online) 1536-5964
    ISSN 0025-7974
    DOI 10.1097/MD.0000000000035483
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: UPLC-MS/MS for the Herb-Drug Interactions of Xiao-Ai-Ping Injection on Enasidenib in Rats Based on Pharmacokinetics.

    Wang, Bo-Wen / Qiu, Cheng-Zheng / Tang, Chang-Qian / Zhang, Jia-Hui / Zhang, Yi / Du, Qi-Guang / Feng, Yi / Qiu, Xiang-Jun

    BioMed research international

    2021  Volume 2021, Page(s) 6636266

    Abstract: ... the effect of Xiao-ai-ping injection (XAPI) on the pharmacokinetics of enasidenib in rats.: Methods ...

    Abstract Objective: To develop and validate a sensitive and rapid ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the determination of enasidenib in rat plasma and to investigate the effect of Xiao-ai-ping injection (XAPI) on the pharmacokinetics of enasidenib in rats.
    Methods: The rat plasma was precipitated with acetonitrile, enasidenib and internal standard (IS) were separated on an Acquity UPLC BEH C18 column, and acetonitrile and 0.1% formic acid were used as the mobile phase in gradient mode. Enasidenib and IS were monitored and detected by multiple reaction monitoring (MRM) using tandem mass spectrometry in positive ion mode. 12 Sprague-Dawley (SD) rats were randomly divided into control group (group A) and experimental group (group B), 6 rats in each group. Group B was intramuscularly injected with XAPI (0.3 mL/kg) every morning, 7 days in a row. Group A was intramuscularly injected with normal saline, 7 days in a row. On the seventh day, enasidenib (10 mg/kg) was given to both groups 30 min after injection of normal saline (group A) or XAPI (group B), and the blood was collected at different time points such as 0.33, 0.67, 1, 1.5, 2, 3, 4, 6, 9, 12, 24, and 48 h. The concentration of enasidenib was detected by UPLC-MS/MS, and the main parameters of pharmacokinetic of enasidenib were calculated using the DAS 2.0 software.
    Results: Under the current experimental conditions, this UPLC method showed good linearity in the detection of enasidenib. Interday and intraday precision did not exceed 10%, the range of accuracy values were from -1.43% to 2.76%. The results of matrix effect, extraction recovery, and stability met the requirements of FDA approval guidelines of bioanalytical method validation. The
    Conclusion: An UPLC-MS/MS method for the determination of enasidenib in rat plasma was established. XAPI can inhibit the metabolism of enasidenib and increase the concentration of enasidenib in rats. It is suggested that when XAPI was combined with enasidenib, the herb-drug interaction and adverse reactions should be paid attention to, and the dosage should be adjusted if necessary.
    MeSH term(s) Aminopyridines/pharmacokinetics ; Aminopyridines/pharmacology ; Animals ; Chromatography, High Pressure Liquid ; Drugs, Chinese Herbal/pharmacokinetics ; Drugs, Chinese Herbal/pharmacology ; Herb-Drug Interactions ; Male ; Rats ; Rats, Sprague-Dawley ; Tandem Mass Spectrometry ; Triazines/pharmacokinetics ; Triazines/pharmacology
    Chemical Substances Aminopyridines ; Drugs, Chinese Herbal ; Marsdeniae tenacissimae extract ; Triazines ; enasidenib (3T1SS4E7AG)
    Language English
    Publishing date 2021-02-23
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2698540-8
    ISSN 2314-6141 ; 2314-6133
    ISSN (online) 2314-6141
    ISSN 2314-6133
    DOI 10.1155/2021/6636266
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Book: Wei xiao fei ai

    Zhang, Guozhen

    ying xiang zhen duan yu ying dui ce lüe = Micronodular lung cancer : imaging and management strategies

    2015  

    Title variant Micronodular lung cancer : imaging and management strategies
    Author's details chu bian Zhang Guozhen, Zheng Xiangpeng, Li Ming
    MeSH term(s) Lung Neoplasms/diagnostic imaging ; Lung Neoplasms/therapy
    Language Chinese
    Size 4, 320 pages :, illustrations, portrait
    Edition Di 1 ban.
    Document type Book
    ISBN 9787509186381 ; 7509186382
    Database Catalogue of the US National Library of Medicine (NLM)

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  4. Article ; Online: UPLC-MS/MS for the Herb-Drug Interactions of Xiao-Ai-Ping Injection on Enasidenib in Rats Based on Pharmacokinetics

    Bo-wen Wang / Cheng-zheng Qiu / Chang-qian Tang / Jia-hui Zhang / Yi Zhang / Qi-guang Du / Yi Feng / Xiang-jun Qiu

    BioMed Research International, Vol

    2021  Volume 2021

    Abstract: ... the effect of Xiao-ai-ping injection (XAPI) on the pharmacokinetics of enasidenib in rats. Methods. The rat ...

    Abstract Objective. To develop and validate a sensitive and rapid ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the determination of enasidenib in rat plasma and to investigate the effect of Xiao-ai-ping injection (XAPI) on the pharmacokinetics of enasidenib in rats. Methods. The rat plasma was precipitated with acetonitrile, enasidenib and internal standard (IS) were separated on an Acquity UPLC BEH C18 column, and acetonitrile and 0.1% formic acid were used as the mobile phase in gradient mode. Enasidenib and IS were monitored and detected by multiple reaction monitoring (MRM) using tandem mass spectrometry in positive ion mode. 12 Sprague-Dawley (SD) rats were randomly divided into control group (group A) and experimental group (group B), 6 rats in each group. Group B was intramuscularly injected with XAPI (0.3 mL/kg) every morning, 7 days in a row. Group A was intramuscularly injected with normal saline, 7 days in a row. On the seventh day, enasidenib (10 mg/kg) was given to both groups 30 min after injection of normal saline (group A) or XAPI (group B), and the blood was collected at different time points such as 0.33, 0.67, 1, 1.5, 2, 3, 4, 6, 9, 12, 24, and 48 h. The concentration of enasidenib was detected by UPLC-MS/MS, and the main parameters of pharmacokinetic of enasidenib were calculated using the DAS 2.0 software. Results. Under the current experimental conditions, this UPLC method showed good linearity in the detection of enasidenib. Interday and intraday precision did not exceed 10%, the range of accuracy values were from -1.43% to 2.76%. The results of matrix effect, extraction recovery, and stability met the requirements of FDA approval guidelines of bioanalytical method validation. The Cmax of enasidenib in the group A and the group B was (458.87±136.02) ng/mL and (661.47±107.32) ng/mL, t1/2 was (7.74±0.91) h and (8.64±0.42) h, AUC0−t was (4067.24±1214.36) ng·h/mL and (5645.40±1046.30) ng·h/mL, AUC0−∞ was (4125.79±1235.91) ng·h/mL and (5759.61±1078.59) ng·h/mL, ...
    Keywords Medicine ; R
    Subject code 630
    Language English
    Publishing date 2021-01-01T00:00:00Z
    Publisher Hindawi Limited
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article ; Online: Xiao-Ai-Ping Injection Enhances Effect of Paclitaxel to Suppress Breast Cancer Proliferation and Metastasis via Activating Transcription Factor 3.

    Chen, Junjun / Zhang, Xiangqi / Xiao, Xiao / Ding, Yawei / Zhang, Wei / Shi, Meizhi / Yang, Jiao / Liu, Ying / Han, Yonglong

    Integrative cancer therapies

    2020  Volume 19, Page(s) 1534735420906463

    Abstract: ... effects in the progress of treating breast cancer. Xiao-Ai-Ping (XAP) injection, composed of a traditional ...

    Abstract Chemotherapy is an effective treatment for invasive breast cancer. Paradoxically, many recently published findings showed that the first-line chemotherapeutic agent paclitaxel (PTX) showed pro-metastatic effects in the progress of treating breast cancer. Xiao-Ai-Ping (XAP) injection, composed of a traditional herbal medicine,
    MeSH term(s) Activating Transcription Factor 3/metabolism ; Animals ; Antineoplastic Agents/pharmacology ; Antineoplastic Agents, Phytogenic/pharmacology ; Apoptosis/drug effects ; Breast Neoplasms ; Cell Line, Tumor ; Cell Proliferation/drug effects ; Drugs, Chinese Herbal/pharmacology ; Female ; Humans ; Mice ; Neoplasm Invasiveness/prevention & control ; Paclitaxel/pharmacology ; Xenograft Model Antitumor Assays
    Chemical Substances Activating Transcription Factor 3 ; Antineoplastic Agents ; Antineoplastic Agents, Phytogenic ; Drugs, Chinese Herbal ; Marsdeniae tenacissimae extract ; Paclitaxel (P88XT4IS4D)
    Language English
    Publishing date 2020-04-04
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2182320-0
    ISSN 1552-695X ; 1534-7354
    ISSN (online) 1552-695X
    ISSN 1534-7354
    DOI 10.1177/1534735420906463
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Xiao-ai-ping injection adjunct with platinum-based chemotherapy for advanced non-small-cell lung cancer: a systematic review and meta-analysis.

    Feng, Fanchao / Huang, Jingyi / Wang, Zhichao / Zhang, Jiarui / Han, Di / Wu, Qi / He, Hailang / Zhou, Xianmei

    BMC complementary medicine and therapies

    2020  Volume 20, Issue 1, Page(s) 3

    Abstract: Background: Xiao-ai-ping injection (XAPI), as patented Chinese medicine, has shown promising ...

    Abstract Background: Xiao-ai-ping injection (XAPI), as patented Chinese medicine, has shown promising outcomes in non-small-cell lung cancer (NSCLC) patients. This meta-analysis investigated the efficacy and safety of XAPI in combination with platinum-based chemotherapy.
    Methods: A comprehensive literature search was conducted to identify relevant studies in Pubmed, EMBASE, the Cochrane Library, Chinese National Knowledge Infrastructure, Wangfang Database, VIP Database, and Chinese Biology Medical Database from the date of their inception to September 2018. The RevMan 5.3 software was applied to calculate the risk ratio (RR) and mean difference (MD) with 95% confidence interval (CI).
    Results: We included and analyzed 24 randomized controlled trials. The meta-analysis showed that XAPI adjunctive to platinum-based chemotherapy had better outcomes in objective tumor response rate (ORR) (RR: 1.27, 95% CI, 1.14-1.40); improved Karnofsky performance scores (KPS) (RR: 1.70, 95% CI, 1.48-1.95); reduction in occurrence of grade 3/4 leukopenia (RR: 0.49, 95% CI, 0.38-0.64), anemia (RR: 0.63, 95% CI, 0.46-0.87) and thrombocytopenia (RR: 0.53, 95% CI, 0.38-0.73), nausea and vomiting (RR: 0.57, 95% CI, 0.36-0.90); and enhanced immune function (CD8
    Conclusions: Our meta-analyses demonstrated that XAPI in combination with platinum-based chemotherapy had a better tumor response, improved the quality of life, attenuated adverse side effects, and enhanced immune function, which suggests that it might be used for advanced NSCLC. Moreover, low dosage (< 60 ml/d) and long-term treatment of XAPI might be a choice for advanced NSCLC patients.
    MeSH term(s) Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Carcinoma, Non-Small-Cell Lung/drug therapy ; Drugs, Chinese Herbal/therapeutic use ; Humans ; Injections ; Karnofsky Performance Status ; Lung Neoplasms/drug therapy ; Medicine, Chinese Traditional ; Platinum Compounds/therapeutic use ; Randomized Controlled Trials as Topic
    Chemical Substances Drugs, Chinese Herbal ; Marsdeniae tenacissimae extract ; Platinum Compounds
    Language English
    Publishing date 2020-01-13
    Publishing country England
    Document type Journal Article ; Meta-Analysis ; Systematic Review
    ISSN 2662-7671
    ISSN (online) 2662-7671
    DOI 10.1186/s12906-019-2795-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: [Effects and mechanisms of Xiao-Ai-Ping injection on angiogenesis].

    Wang, Mei-jian / Du, Dan-yu / Fan, Wei / Zhang, Cang / Liu, Yang / Fan, Jia-hong / Yuan, Sheng-tao / Lin, Sen-sen

    Yao xue xue bao = Acta pharmaceutica Sinica

    2016  Volume 51, Issue 2, Page(s) 309–315

    Abstract: This study was designed to investigate the effect of Xiao-Ai-Ping injection on cancer angiogenesis ... CCK8 assay and Brd U incorporation immunofluorescence assay were used to detect the effect of Xiao-Ai ... the effect of Xiao-Ai-Ping injection on HUVECs migration. The anti-angiogenic effect of Xiao-Ai-Ping ...

    Abstract This study was designed to investigate the effect of Xiao-Ai-Ping injection on cancer angiogenesis. CCK8 assay and Brd U incorporation immunofluorescence assay were used to detect the effect of Xiao-Ai-Ping injection on HUVECs proliferation; wound healing assay and transwell assay were employed to test the effect of Xiao-Ai-Ping injection on HUVECs migration. The anti-angiogenic effect of Xiao-Ai-Ping injection was examined by tube formation assay, rat aortic ring assay and chicken chorioallantoic membrane(CAM) assay. ELISA assay was used to measure the secretion of vascular endothelial growth factor(VEGF); and the activation of vascular endothelial growth factor receptor 2(VEGFR2) protein and its downstream signaling pathways were examined by Western blot. Our data demonstrated that Xiao-Ai-Ping injection inhibited HUVECs proliferation in a time- and dose-dependent manner, and the IC(50) (mg·m L(-1)) values for 24, 48 and 72 h were 48.7 ± 7.14, 29.1 ±2.25 and 22.0 ± 4.53, individually. Xiao-Ai-Ping injection inhibited HUVECs DNA synthesis and migration. Xiao-Ai-Ping injection suppressed HUVECs tube formation, and reduced microvessel sprouting from rat aortic rings and vessel growth in CAMs. Furthermore, Xiao-Ai-Ping injection attenuated the secretion of VEGF, and inhibited the expression of p-VEGFR2 and phosphorylation of protein kinase B(p-AKT). We conclude that Xiao-Ai-Ping injection inhibits angiogenesis by down-regulation of VEGF signaling and AKT pathway.
    MeSH term(s) Angiogenesis Inhibitors/pharmacology ; Animals ; Cell Movement ; Chickens ; Chorioallantoic Membrane ; Drugs, Chinese Herbal/pharmacology ; Human Umbilical Vein Endothelial Cells/drug effects ; Humans ; Neovascularization, Pathologic/drug therapy ; Phosphorylation ; Proto-Oncogene Proteins c-akt/metabolism ; Rats ; Signal Transduction ; Vascular Endothelial Growth Factor A/metabolism ; Vascular Endothelial Growth Factor Receptor-2/metabolism ; Wound Healing
    Chemical Substances Angiogenesis Inhibitors ; Drugs, Chinese Herbal ; Marsdeniae tenacissimae extract ; Vascular Endothelial Growth Factor A ; KDR protein, human (EC 2.7.10.1) ; Vascular Endothelial Growth Factor Receptor-2 (EC 2.7.10.1) ; Proto-Oncogene Proteins c-akt (EC 2.7.11.1)
    Language Chinese
    Publishing date 2016
    Publishing country China
    Document type Journal Article
    ZDB-ID 788758-9
    ISSN 0513-4870
    ISSN 0513-4870
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Xiao-ai-ping injection adjunct with platinum-based chemotherapy for advanced non-small-cell lung cancer

    Fanchao Feng / Jingyi Huang / Zhichao Wang / Jiarui Zhang / Di Han / Qi Wu / Hailang He / Xianmei Zhou

    BMC Complementary Medicine and Therapies, Vol 20, Iss 1, Pp 1-

    a systematic review and meta-analysis

    2020  Volume 15

    Abstract: Abstract Background Xiao-ai-ping injection (XAPI), as patented Chinese medicine, has shown ...

    Abstract Abstract Background Xiao-ai-ping injection (XAPI), as patented Chinese medicine, has shown promising outcomes in non-small-cell lung cancer (NSCLC) patients. This meta-analysis investigated the efficacy and safety of XAPI in combination with platinum-based chemotherapy. Methods A comprehensive literature search was conducted to identify relevant studies in Pubmed, EMBASE, the Cochrane Library, Chinese National Knowledge Infrastructure, Wangfang Database, VIP Database, and Chinese Biology Medical Database from the date of their inception to September 2018. The RevMan 5.3 software was applied to calculate the risk ratio (RR) and mean difference (MD) with 95% confidence interval (CI). Results We included and analyzed 24 randomized controlled trials. The meta-analysis showed that XAPI adjunctive to platinum-based chemotherapy had better outcomes in objective tumor response rate (ORR) (RR: 1.27, 95% CI, 1.14–1.40); improved Karnofsky performance scores (KPS) (RR: 1.70, 95% CI, 1.48–1.95); reduction in occurrence of grade 3/4 leukopenia (RR: 0.49, 95% CI, 0.38–0.64), anemia (RR: 0.63, 95% CI, 0.46–0.87) and thrombocytopenia (RR: 0.53, 95% CI, 0.38–0.73), nausea and vomiting (RR: 0.57, 95% CI, 0.36–0.90); and enhanced immune function (CD8+ [MD: 4.96, 95% CI, 1.16–8.76] and CD4+/CD8+ [MD: 2.58, 95% CI, 1.69–3.47]). However, it did not increase dysregulated liver and kidney function, diarrhea, constipation, and fatigue. Subgroup analysis of ORR and KPS revealed that dosage, treatment duration, and methodological quality did not affect the outcome significantly. Conclusions Our meta-analyses demonstrated that XAPI in combination with platinum-based chemotherapy had a better tumor response, improved the quality of life, attenuated adverse side effects, and enhanced immune function, which suggests that it might be used for advanced NSCLC. Moreover, low dosage (< 60 ml/d) and long-term treatment of XAPI might be a choice for advanced NSCLC patients.
    Keywords Xiao-ai-ping injection ; Platinum-based chemotherapy ; Advanced non-small cell lung cancer ; Objective tumor response ; Adverse side effects ; Meta-analysis ; Other systems of medicine ; RZ201-999
    Subject code 610
    Language English
    Publishing date 2020-01-01T00:00:00Z
    Publisher BMC
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: Xiao-ai-ping injection adjunct with platinum-based chemotherapy for advanced non-small-cell lung cancer: a systematic review and meta-analysis

    Feng, Fanchao / Huang, Jingyi / Wang, Zhichao / Zhang, Jiarui / Han, Di / Wu, Qi / He, Hailang / Zhou, Xianmei

    BMC Complement Med Ther. 2020 Dec., v. 20, no. 1 p.3-3

    2020  

    Abstract: BACKGROUND: Xiao-ai-ping injection (XAPI), as patented Chinese medicine, has shown promising ...

    Abstract BACKGROUND: Xiao-ai-ping injection (XAPI), as patented Chinese medicine, has shown promising outcomes in non-small-cell lung cancer (NSCLC) patients. This meta-analysis investigated the efficacy and safety of XAPI in combination with platinum-based chemotherapy. METHODS: A comprehensive literature search was conducted to identify relevant studies in Pubmed, EMBASE, the Cochrane Library, Chinese National Knowledge Infrastructure, Wangfang Database, VIP Database, and Chinese Biology Medical Database from the date of their inception to September 2018. The RevMan 5.3 software was applied to calculate the risk ratio (RR) and mean difference (MD) with 95% confidence interval (CI). RESULTS: We included and analyzed 24 randomized controlled trials. The meta-analysis showed that XAPI adjunctive to platinum-based chemotherapy had better outcomes in objective tumor response rate (ORR) (RR: 1.27, 95% CI, 1.14–1.40); improved Karnofsky performance scores (KPS) (RR: 1.70, 95% CI, 1.48–1.95); reduction in occurrence of grade 3/4 leukopenia (RR: 0.49, 95% CI, 0.38–0.64), anemia (RR: 0.63, 95% CI, 0.46–0.87) and thrombocytopenia (RR: 0.53, 95% CI, 0.38–0.73), nausea and vomiting (RR: 0.57, 95% CI, 0.36–0.90); and enhanced immune function (CD8⁺ [MD: 4.96, 95% CI, 1.16–8.76] and CD4⁺/CD8⁺ [MD: 2.58, 95% CI, 1.69–3.47]). However, it did not increase dysregulated liver and kidney function, diarrhea, constipation, and fatigue. Subgroup analysis of ORR and KPS revealed that dosage, treatment duration, and methodological quality did not affect the outcome significantly. CONCLUSIONS: Our meta-analyses demonstrated that XAPI in combination with platinum-based chemotherapy had a better tumor response, improved the quality of life, attenuated adverse side effects, and enhanced immune function, which suggests that it might be used for advanced NSCLC. Moreover, low dosage (< 60 ml/d) and long-term treatment of XAPI might be a choice for advanced NSCLC patients.
    Keywords Oriental traditional medicine ; anemia ; complement ; computer software ; confidence interval ; constipation ; databases ; diarrhea ; drug therapy ; immune response ; leukopenia ; liver ; lung neoplasms ; meta-analysis ; nausea ; patents ; quality of life ; relative risk ; renal function ; systematic review ; thrombocytopenia
    Language English
    Dates of publication 2020-12
    Size p. 3.
    Publishing place BioMed Central
    Document type Article ; Online
    Note Resource is Open Access
    ISSN 2662-7671
    DOI 10.1186/s12906-019-2795-y
    Database NAL-Catalogue (AGRICOLA)

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  10. Article ; Online: Simultaneous determination of six C21 steroids of Xiao-Ai-Ping injection in rat plasma by LC-MS/MS.

    Zeng, Qinghua / Zhang, Feng / Gao, Shouhong / Sun, Liang / Jiang, Bo / Chen, Wansheng

    Biomedical chromatography : BMC

    2014  Volume 28, Issue 2, Page(s) 223–230

    Abstract: Xiao-Ai-Ping injection (XAPI) is a traditional Chinese medicine that has been widely used to treat ...

    Abstract Xiao-Ai-Ping injection (XAPI) is a traditional Chinese medicine that has been widely used to treat cancer. Modern pharmacological studies have demonstrated that C21 steroids are the main active compounds in XAPI. In this study, a sensitive and specific liquid chromatography tandem mass spectrometry (LC-MS/MS) method was developed and validated the first time for simultanenous determination of three isomeric pregnane genins (17β-tenacigenin B, tenacigenin B and tenacigenin A) and their corresponding glycosides (tenacigenoside A, tenacissoside F and marsdenoside I) from XAPI in rat plasma. A simple liquid-liquid extraction technique was used after the addition of dexamethasone acetate as internal standard. The chromatography separation of analytes was achieved on an Agilent Zorbax Eclipse XDB-C18 column (3.5 µm, 150 × 3 mm i.d.) using methanol-water as mobile phase in a gradient elution program. Detection was performed in multiple reaction monitoring mode using electrospray ionization in the negative ion mode. The method showed satisfactory linearity over a concentration range 5.00-2000.00 ng/mL for tenacigenin B, tenacigenin A, marsdenoside I and tenacissoside F (r(2) > 0.99), 10.00-4000.00 ng/mL for 17β-tenacigenin B and tenacigenoside A (r(2) > 0.99). Intra- and inter-day precisions (valued as relative standard deviation) were <9.00% and accuracies (as relative error) in the range -6.31 to 7.23%. Finally, this validated method was successfully applied to the pharmacokinetic study of XAPI after intravenous administration to rats.
    MeSH term(s) Animals ; Chromatography, Liquid/methods ; Drug Stability ; Drugs, Chinese Herbal/chemistry ; Linear Models ; Liquid-Liquid Extraction ; Male ; Pregnanes/blood ; Pregnanes/chemistry ; Pregnanes/pharmacokinetics ; Rats ; Rats, Sprague-Dawley ; Reproducibility of Results ; Sensitivity and Specificity ; Steroids/blood ; Steroids/chemistry ; Steroids/pharmacokinetics ; Tandem Mass Spectrometry/methods
    Chemical Substances Drugs, Chinese Herbal ; Pregnanes ; Steroids ; tenacigenin B
    Language English
    Publishing date 2014-02
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 632848-9
    ISSN 1099-0801 ; 0269-3879
    ISSN (online) 1099-0801
    ISSN 0269-3879
    DOI 10.1002/bmc.3009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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