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  1. Article ; Online: Scissor-like Au

    Wu, Xue-Meng / Wang, Jin-Yun / Huang, Ya-Zi / Chen, Zhong-Ning

    Molecules (Basel, Switzerland)

    2023  Volume 28, Issue 7

    Abstract: Reaction of [Au(tht) ...

    Abstract Reaction of [Au(tht)
    Language English
    Publishing date 2023-04-05
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 1413402-0
    ISSN 1420-3049 ; 1431-5165 ; 1420-3049
    ISSN (online) 1420-3049
    ISSN 1431-5165 ; 1420-3049
    DOI 10.3390/molecules28073247
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Heteroctanuclear Au

    Xie, Pei / Wang, Jin-Yun / Huang, Ya-Zi / Wu, Xue-Meng / Chen, Zhong-Ning

    Molecules (Basel, Switzerland)

    2022  Volume 27, Issue 7

    Abstract: Two heteroctanuclear ... ...

    Abstract Two heteroctanuclear Au
    MeSH term(s) Ligands ; Luminescence
    Chemical Substances Ligands
    Language English
    Publishing date 2022-03-25
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 1413402-0
    ISSN 1420-3049 ; 1431-5165 ; 1420-3049
    ISSN (online) 1420-3049
    ISSN 1431-5165 ; 1420-3049
    DOI 10.3390/molecules27072127
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: A novel UHPLC‒MS/MS method for quantitative analysis of zanubrutinib in rat plasma: application to an in vivo interaction study between zanubrutinib and triazole antifungal.

    Tang, Peng-Fei / Bao, Su-Su / Xiao, Zhong-Xiang / Xie, Wei-Fei / Wu, Xue-Meng / Ge, Hong-Lei / Shao, Chuan-Feng

    BMC chemistry

    2023  Volume 17, Issue 1, Page(s) 107

    Abstract: Background: This study establishes a UHPLC‒MS/MS method for the detection of zanubrutinib and explores its interaction with fluconazole and isavuconazole in rats.: Methods: A protein precipitation method using acetonitrile was used to prepare plasma ... ...

    Abstract Background: This study establishes a UHPLC‒MS/MS method for the detection of zanubrutinib and explores its interaction with fluconazole and isavuconazole in rats.
    Methods: A protein precipitation method using acetonitrile was used to prepare plasma samples using ibrutinib as an internal standard. Chromatographic separation and mass spectrometric detection of the analytes and internal standards were performed on a Shimadzu 8040 UHPLC‒MS/MS equipped with a Shim-pack velox C18 column (2.1 × 50 mm, 2.7 µm). Methanol and 0.1% formic acid-water were used as mobile phases. Intraday and interday precision and accuracy, extraction recoveries, and matrix effects of this method were determined. The linearity and sample stability of the method were assessed. Eighteen male Sprague‒Dawley (SD) rats were randomly divided into three groups with zanubrutinib (30 mg/kg) alone, zanubrutinib in combination with fluconazole (20 mg/kg) or zanubrutinib in combination with isavuconazole (20 mg/kg). Blood samples (200 µL) were collected at designated time points (ten evenly distributed time points within 12 h). The concentration of zanubrutinib was determined using the UHPLC‒MS/MS method developed in this study.
    Results: The typical fragment ions were m/z 472.15 → 290.00 for zanubrutinib and m/z 441.20 → 138.10 for ibrutinib (IS). The range of the standard curve was 1-1000 ng/mL with a regressive coefficient (R
    Conclusion: This study provides information to understand the metabolism of zanubrutinib with concurrent use with isavuconazole or fluconazole, and further clinical trials are needed to validate the results in animals.
    Language English
    Publishing date 2023-08-30
    Publishing country Switzerland
    Document type Journal Article
    ISSN 2661-801X
    ISSN (online) 2661-801X
    DOI 10.1186/s13065-023-01017-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Development and Validation of a UHPLC-MS/MS Method for Quantitation of Almonertinib in Rat Plasma: Application to an

    Tang, Peng-Fei / Bao, Su-Su / Gao, Nan-Yong / Shao, Chuan-Feng / Xie, Wei-Fei / Wu, Xue-Meng / Zhao, Le-Ping / Xiao, Zhong-Xiang

    Frontiers in pharmacology

    2022  Volume 13, Page(s) 960311

    Abstract: Almonertinib was approved for the first-line treatment of advanced NSCLC patients with EGFR-TKI-sensitive genetic mutations by National Medical Products Administration (NMPA) in 2021.The purpose of this study was to establish and validate a fast, ... ...

    Abstract Almonertinib was approved for the first-line treatment of advanced NSCLC patients with EGFR-TKI-sensitive genetic mutations by National Medical Products Administration (NMPA) in 2021.The purpose of this study was to establish and validate a fast, accurate, stable and facile ultra-performance liquid chromatography-tandem mass spectrometry method for the quantification of almonertinib in rat plasma, it was employed to explore the effect of Paxlovid on the pharmacokinetics of almonertinib in rats. Zanubrutinib was used as an internal standard (IS), and the plasma samples were prepared by the protein precipitation method using acetonitrile. Chromatographic separation was carried out on a Shimadzu LC-20AT ultra-performance liquid chromatography system using a Shim-pack velox C18 (2.1× 50 mm, 2.7 μM) column. The mobile phase consisted of methanol and 0.1% formic acid-water. Mass spectrum analysis was executed using Shimadzu 8040 Triple quadrupole mass spectrometry. The precursor and product ions of the analyte and internal standard were detected in multiple reaction monitoring (MRM) mode. The typical fragment ions were
    Language English
    Publishing date 2022-07-22
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2587355-6
    ISSN 1663-9812
    ISSN 1663-9812
    DOI 10.3389/fphar.2022.960311
    Database MEDical Literature Analysis and Retrieval System OnLINE

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