کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2483228 1556474 2015 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Regulation of bifurcated cytokine induction by surface charge of nanoparticles during interaction between CpG oligodeoxynucleotides and toll-like receptor 9
موضوعات مرتبط
علوم پزشکی و سلامت داروسازی، سم شناسی و علوم دارویی اکتشاف دارویی
پیش نمایش صفحه اول مقاله
Regulation of bifurcated cytokine induction by surface charge of nanoparticles during interaction between CpG oligodeoxynucleotides and toll-like receptor 9
چکیده انگلیسی

Toll-like receptor 9 recognizes CpG oligodeoxynucleotides (ODNs) and induces immune-mediator cytokines. Natural phosphodiester class B CpG ODNs induce interleukin-6 (IL-6), but not interferon-α (IFN-α). We prepared silicon nanoparticles (Si NPs) with different positive surface charge density and bound negatively charged class B CpG ODN molecules electrostatically. No significant differences in the amount of class B CpG ODN molecules or negative surface charge after binding of the molecules onto naked NPs was observed. However, the profile of cytokine induction from peripheral blood mononuclear cells was correlated with a positive surface charge density of naked NPs prior to binding of CpG ODN molecules. The level of IL-6 induction slightly decreased as the positive surface charge density was increased, while the IFN-α induction significantly increased as the positive surface charge density was increased. This observation demonstrates that the bifurcated cytokine induction can be regulated by the surface charge of naked NPs.

Dispersed silicon nanoparticles (Si NPs) with different positive charge densities are used for delivery of immunostimulatory CpG oligodeoxynucleotide (CpG ODN). Free CpG ODN induces interleukin-6 (IL-6), but not interferon-α (IFN-α). However, CpG ODN bound electrostatically onto Si NPs induce not only IL-6, but also IFN-α, at levels that are dependent on the surface charge of the naked Si NPs.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Drug Delivery Science and Technology - Volume 29, October 2015, Pages 251–260
نویسندگان
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