Highly sensitive electrochemiluminescence detection of p53 protein using functionalized Ru–silica nanoporous@ gold nanocomposite

Highly sensitive electrochemiluminescence detection of p53 protein using functionalized Ru–silica nanoporous@ gold nanocomposite


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نویسندگان: محمدرضا رشیدی شاهگلی , بلال خلیل زاده

کلمات کلیدی: Electrochemiluminescence immunosensor; Gold nanoparticles; Graphene oxide; Human cancer cells; Ru–Si@Au nanocomposite; p53 Protein

نشریه: 0 , 80 , 80 , 2016

اطلاعات کلی مقاله
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نویسنده ثبت کننده مقاله محمدرضا رشیدی شاهگلی
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه دانشکده داروسازی
کد مقاله 61351
عنوان فارسی مقاله Highly sensitive electrochemiluminescence detection of p53 protein using functionalized Ru–silica nanoporous@ gold nanocomposite
عنوان لاتین مقاله Highly sensitive electrochemiluminescence detection of p53 protein using functionalized Ru–silica nanoporous@ gold nanocomposite
ناشر 7
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق) Biosensors and Bioelectronics
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت http://apps.webofknowledge.com/Search.do?product=WOS&SID=V1qhMvbwsQTKqjVgSRE&search_mode=GeneralSearch&prID=1aad572d-bc94-417c-8

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A simple, rapid response time and ultrahigh sensitive electrochemiluminescence (ECL) immunosensor based on Ru(bpy)3(2+)doped silica doped AuNPs (Ru-Si@Au nanocomposite) was developed for detection of p53 protein, a well-known tumor suppressor. The immunosensor was constructed using biotinylated capture antibody, immobilized on the glassy carbon electrode (GCE) using streptavidin modified-gold nanoparticles/thiolated graphene oxide, followed by its conjugation with the Ru-silica@Au nanocomposite labeled secondary antibody to form a sandwich-type immunocomplex. The use of Ru-Si@Au nanocomposites led to a remarkable increase in the ECL intensity and, thus, the sensitivity of the method. Under the optimized conditions, the linear range of the proposed p53 immunosensor was found between 0.2 and 200 pM with a calculated limit of detection of 22.8 fM. The selectivity and reproducibility of the immunosensor was also investigated and the results showed high specificity and great stability in detecting of p53. Moreover, the ECL immunosensor was successfully applied for quantification of p53 protein in the human spiked serum samples and more importantly in the human normal and cancer skin fibroblast cells showing much satisfactory result compared with the ELISA method. The proposed immunosensor reported herein offers a considerable potential in early detection of cancer and clinical diagnosis and provides a new platform for biomarker detection.

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نویسنده نفر چندم مقاله
محمدرضا رشیدی شاهگلیهفتم
بلال خلیل زادهسوم

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