Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/34804
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 18240/20438 (89%)
Visitors : 5455118      Online Users : 1320
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    CNU IR > Offices > 456 >  Item 310902800/34804
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/34804


    Title: Cytotoxic, Antibacterial, and Antioxidant Activities of the Leaf Extract of Sinningia bullata
    Authors: Chen, Pin-Jui
    Lin, En-Shyh
    Su, Hsin-Hui
    Huang, Cheng-Yang
    Contributors: Chung Shan Med Univ, Dept Biomed Sci
    Natl Taichung Univ Sci & Technol, Dept Beauty Sci
    Chia Nan Univ Pharm & Sci, Dept Pharm
    Chung Shan Med Univ Hosp, Dept Med Res
    Keywords: cytotoxic activities
    anticancer
    antioxidation
    antibacterial
    TPC
    TFC
    GC-MS analysis
    Sinningia bullata
    Date: 2023
    Issue Date: 2024-12-25 11:03:48 (UTC+8)
    Publisher: MDPI
    Abstract: Sinningia bullata is a tuberous member of the flowering plant family Gesneriaceae. Prior to this work, the antibacterial, antioxidant, and cytotoxic properties of S. bullata were undetermined. Here, we prepared different extracts from the leaf, stem, and tuber of S. bullata and investigated their pharmacological activities. The leaf extract of S. bullata, obtained by 100% acetone (Sb-L-A), had the highest total flavonoid content, antioxidation capacity, and cytotoxic and antibacterial activities. Sb-L-A displayed a broad range of antibacterial activities against Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa. The inhibition zones of Sb-L-A ranged from 8 to 30 mm and were in the following order: S. aureus > E. coli > P. aeruginosa. Incubation of B16F10 melanoma cells with Sb-L-A at a concentration of 80 mu g/mL caused deaths at the rate of 96%, reduced migration by 100%, suppressed proliferation and colony formation by 99%, and induced apoptosis, which was observed in 96% of the B16F10 cells. In addition, the cytotoxic activities of Sb-L-A were synergistically enhanced when coacting with the antitumor drug epothilone B. Sb-L-A was also used to determine the cytotoxic effects against 4T1 mammary carcinoma cells. Sb-L-A of 60 mu g/mL boosted the distribution of the G2 phase from 1.4% to 24.4% in the B16F10 cells. Accordingly, Sb-L-A might suppress melanoma cell proliferation by inducing G2 cell-cycle arrest. The most abundant compounds in Sb-L-A were identified using gas chromatography-mass spectrometry. The top two contents in this extract were adlupulone and villosin. Overall, the collective data in this study may indicate the pharmacological potentials of Sb-L-A for possible medical applications.
    Relation: Plants-Basel, v.12, n.4, Article 859
    Appears in Collections:[Offices] 456

    Files in This Item:

    File Description SizeFormat
    index.html0KbHTML1View/Open


    All items in CNU IR are protected by copyright, with all rights reserved.


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback