• ثبت نام
    • ورود به سامانه
    مشاهده مورد 
    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Asian Pacific Journal of Cancer Prevention
    • Volume 20, Issue 1
    • مشاهده مورد
    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Asian Pacific Journal of Cancer Prevention
    • Volume 20, Issue 1
    • مشاهده مورد
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Anticancer Effect of Cisplatin-Loaded Poly (Butylcyanoacrylate) Nanoparticles on A172 Brain Cancer Cells Line

    (ندگان)پدیدآور
    Chiani, MohsenToofani Milani, AttabakNemati, MahdiehRezaeidian, JalalEhsanbakhsh, HosseinAhmadi, ZohreMazloomi, EbrahimSadeghi, VahidehAkbarzadeh Khiyavi, Azim
    Thumbnail
    دریافت مدرک مشاهده
    FullText
    اندازه فایل: 
    571.5کیلوبایت
    نوع فايل (MIME): 
    PDF
    نوع مدرک
    Text
    Research Articles
    زبان مدرک
    English
    نمایش کامل رکورد
    چکیده
    Background: Drug delivery systems have been designed to achieve targeted delivery and control the release rateof the drugs. A serious challenge associated with drug delivery systems is the presence of the blood-brain barrier whichlimits drugs penetration. In the current study, the effects of cisplatin nanoparticles on A172 brain cancer cell line wereinvestigated. Methods: Cisplatin nanoparticles were produced by miniemulsion polymerization technique and theirproperties were evaluated. Drug release assay was performed to characterize the nanoparticles' properties. Here, weexamined the effects of cisplatin nanoparticles and free form of cisplatin on A172 cancer cell line. MTT assay wasperformed for different concentrations of the drug. To measure the apoptosis rate in A172 cell line in the presenceof cisplatin nanoparticles or its free from, Annexin V staining method was used. Results: Our results indicated thatloading type of cisplatin was physical loading and only 4.7% of cisplatin was released after 68 h. Furthermore, MTTassay showed that cisplatin nanoparticles in all concentrations had more cytotoxic effects on the cells comparing withthe free form of cisplatin and control groups. We also showed that cisplatin nanoparticles could increase apoptosisin cancer cells more than the drug in the free form by using flow cytometry technique. Conclusion: Overall, thesefindings proved that cisplatin loaded on poly (Butylcyanoacrylate) nanoparticles, was more efficient than the free formof cisplatin in treating A172 cancer cell line.
    کلید واژگان
    Cisplatin
    poly (Butylcyanoacrylate) nanoparticles
    Apoptosis
    A172 Cells
    Drug delivery

    شماره نشریه
    1
    تاریخ نشر
    2019-01-01
    1397-10-11
    ناشر
    West Asia Organization for Cancer Prevention (WAOCP)
    سازمان پدید آورنده
    Department of Nanobiotechnology, Pasteur Institute of Iran, Tehran, Iran.
    Department of Biochemistry, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
    Department of Medical Nanotechnology, Faculty of Advanced Medical Science, Tabriz University of Medical Sciences, Tabriz, Iran.
    Department of Biology, Parand Branch, Islamic Azad University, Parand, Iran.
    Department of Biology, Science and Research Branch, Islamic Azad University , Tehran, Iran.
    Faculty of Health, Qom University of Medical Sciences, Qom, Iran.
    Cellular and Molecular Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Urmia, Iran.
    Department of Genetics, Tehran Medical Sciences Branch, Islamic Azad University, Tehran, Iran.
    Department of Nanobiotechnology, Pasteur Institute of Iran, Tehran, Iran.

    شاپا
    1513-7368
    2476-762X
    URI
    https://dx.doi.org/10.31557/APJCP.2019.20.1.303
    http://journal.waocp.org/article_80262.html
    https://iranjournals.nlai.ir/handle/123456789/30483

    مرور

    همه جای سامانهپایگاه‌ها و مجموعه‌ها بر اساس تاریخ انتشارپدیدآورانعناوینموضوع‌‌هااین مجموعه بر اساس تاریخ انتشارپدیدآورانعناوینموضوع‌‌ها

    حساب من

    ورود به سامانهثبت نام

    آمار

    مشاهده آمار استفاده

    تازه ترین ها

    تازه ترین مدارک
    © کليه حقوق اين سامانه برای سازمان اسناد و کتابخانه ملی ایران محفوظ است
    تماس با ما | ارسال بازخورد
    قدرت یافته توسطسیناوب