Preparation of thermo and pH-responsive polymer@Au/ Fe3O4 core/shell nanoparticles as a carrier for delivery of anticancer agent

Preparation of thermo and pH-responsive polymer@Au/ Fe3O4 core/shell nanoparticles as a carrier for delivery of anticancer agent


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دانشگاه علوم پزشکی تبریز
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نویسندگان: مرجان قربانی , حامد همیشه کار

کلمات کلیدی: Dual stimuli-responsive  Core/shell  Au/Fe3O4  Targeted drug delivery  Doxorubicin  Chemotherapy  Nanomedicine

نشریه: 0 , 17 , 17 , 2015

اطلاعات کلی مقاله
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نویسنده ثبت کننده مقاله مرجان قربانی
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز سلولهای بنیادی
کد مقاله 69531
عنوان فارسی مقاله Preparation of thermo and pH-responsive polymer@Au/ Fe3O4 core/shell nanoparticles as a carrier for delivery of anticancer agent
عنوان لاتین مقاله Preparation of thermo and pH-responsive polymer@Au/ Fe3O4 core/shell nanoparticles as a carrier for delivery of anticancer agent
ناشر 4
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ خیر
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت

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In this work, a thermo and pH-responsive poly-N-isopropylacrylamide-co-itaconic acid containing thiol side groups were successfully synthesized to prepare Doxorubicin-loaded polymer@Au/ Fe3O4 core/shell nanoparticles (DOX-NPs). Copolymer and NPs were fully characterized by FT-IR, HNMR, photo-correlation spectroscopy, SEM, X-ray diffraction, vibrating-sample magnetometer, thermal gravimetric analysis, and UV–Vis spectroscopy. The stimuli-responsive characteristics of NPs were evaluated by in vitro release study in simulated cancerous environment. The biocompatibility and cytotoxic properties of NPs and DOX-NPs are explored by MTT method. The prepared NPs with the size of 50 nm showed paramagnetic characteristics with suitable and stable dispersion at physiological medium and high loading capacity (up to 55 %) of DOX. DOX-NPs yielded a pH- and temperaturetriggered release of entrapped drugs at tumor tissue environment (59 % of DOX release) compared to physiological condition (20 % of DOX release) during 48 h. In vitro cytotoxicity studies indicated that the NPs showed no cytotoxicity on A549 cells at different amounts after incubation for 72 h confirming its suitability as a drug carrier. DOX-NPs, on the other hand, caused an efficient anticancer performance as verified by MTT assay test. It was concluded that developed NPs by us in this study may open the possibilities for targeted delivery of DOX to the cancerous tissues.

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نویسنده نفر چندم مقاله
مرجان قربانیاول
حامد همیشه کاردوم

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نام فایل تاریخ درج فایل اندازه فایل دانلود
Ghorbani 2015 1.pdf1398/08/041720271دانلود