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    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Iranian Journal of Pharmaceutical Research
    • Volume 18, Issue 3
    • مشاهده مورد
    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Iranian Journal of Pharmaceutical Research
    • Volume 18, Issue 3
    • مشاهده مورد
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    Novel Palladium Complex: Cytotoxicity against Cisplatin-resistant K562 Cells

    (ندگان)پدیدآور
    Jahanian, AliMirian, MinaRouhani, fatemehkarami, kazemHosseini kharat, MahboubehSadeghi-Aliabadi, Hojjat
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    اندازه فایل: 
    969.1کیلوبایت
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    نوع مدرک
    Text
    Research article
    زبان مدرک
    English
    نمایش کامل رکورد
    چکیده
    Today, development of resistance to anticancer drugs (including cisplatin) is noticed as a major problem. Recently several studies demonstrated that palladium complexes showed remarkable cytotoxic effects against K562 cell line and could be used efficiently for treatment of many human cancers including leukemia. Hereof, K562 cells were made resistant to cisplatin using increasing concentration of cisplatin up to 4.5 , and then cytotoxic effect of synthesized palladium complex was evaluated on this sub-line using MTT assay. Annexin V/PI staining using flow cytometry and scanning electron microscopy (SEM) were performed to find out the mechanism of the observed cytotoxicity. Results indicated that tested compounds had a noticeable cytotoxic effect on K562 cells 80 times more than cisplatin. Palladium complex also showed significant cytotoxicity on resistant K562 sub-line. Flow cytometry and SEM results revealed that these compounds exert their cytotoxic effect via apoptosis and it could be concluded that the novel synthesized palladium complex might be a good candidate for replacing cisplatin in case of treatment of cisplatin resistant tumors.
    کلید واژگان
    K562 cells
    Cisplatin Resistance
    Palladacyclic complex
    MTT assay
    Apoptosis assay
    Medicinal chemistry

    شماره نشریه
    3
    تاریخ نشر
    2019-07-01
    1398-04-10
    ناشر
    School of Pharmacy, Shahid Beheshti University of Medical Sciences
    سازمان پدید آورنده
    Department of Pharmaceutical Biotechnology, School of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran.
    Department of Pharmaceutical Biotechnology, School of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran.
    Department of Pharmaceutical Chemistry, School of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran.
    Department of Chemistry, Isfahan University of Technology, Isfahan, Iran.
    Department of Chemistry, Isfahan University of Technology, Isfahan, Iran.
    Department of Pharmaceutical Chemistry, School of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran.

    شاپا
    1735-0328
    1726-6890
    URI
    https://dx.doi.org/10.22037/ijpr.2019.1100714
    http://ijpr.sbmu.ac.ir/article_1100714.html
    https://iranjournals.nlai.ir/handle/123456789/313466

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