کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
702041 1460773 2015 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Nanodiamond-conjugated transferrin as chemotherapeutic drug delivery
ترجمه فارسی عنوان
انتقالنروی نانو دی آموند به عنوان داروی شیمیایی
موضوعات مرتبط
مهندسی و علوم پایه سایر رشته های مهندسی مهندسی برق و الکترونیک
چکیده انگلیسی


• The ND-(Tf-DOX) system can target drug delivery in vitro and inhibit tumor growth with low side effects in vivo.

Targeted therapy is considered to be a promising strategy of cancer treatments. Herein we demonstrate the potential of a nanotechnology strategy for special drug delivery based on nanodiamond (ND) functionalized by transferrin. Specifically, the transferrin–doxorubicin (Tf–DOX) complex is covalently coupled with carboxylated ND to prepare the targeted nanomedicine (ND-(Tf–DOX)). In vitro studies showed that ND-(Tf–DOX) can effectively deliver the drug inside living cells via a clathrin-dependent and transferrin receptor-mediate endocytosis pathway by flow cytometry analysis, and the ND-(Tf–DOX) nanomedicine located in the lysosomes through laser scanning confocal microscopy. In vivo, we found that tumor volume change of tumor-bearing mice treated with ND-(Tf–DOX) nanomedicine was lightly lower than that of DOX-treated. The results demonstrated that the targeting capability of ND-(Tf–DOX) nanomedicine relative drug alone is not significant, and it may be disturbed by proteins when they are placed in a complex biological environment. However, it can markedly decrease side effects compared to DOX alone in both the liver and spleen. This suggests that in vivo ND-(Tf–DOX) nanomedicine can effectively inhibit tumor growth as the same as DOX. More importantly, it can decrease side effects. This study attempts to endowed transferrin-functionalized and chemotherapeutic drug-loaded nanodiamond as a platform for drug delivery and therapy to cancer cells.

The drug system ND-(Tf–DOX) tends to selectively target tumor cells with overexpressed TfR and enter the cells by clathrin-dependent and transferrin receptor-mediated endocytosis. In addition, ND-(Tf–DOX) nanoparticles not only played a slow and sustained drug release profile, and but also had a tumor-targeted toxicity in vitro. In vivo ND-(Tf–DOX) nanomedicine can effectively inhibit tumor growth as the same as DOX. Much importantly, it can decrease side effects. This implies that ND-(Tf–DOX) can act as a nanodrug with promising chemotherapeutic efficacy and safety.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Diamond and Related Materials - Volume 58, September 2015, Pages 84–93
نویسندگان
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