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pH 控制的发光铕涂层纳米颗粒向血小板的递送。

pH-controlled delivery of luminescent europium coated nanoparticles into platelets.

机构信息

Physical Sciences of Imaging in the Biomedical Sciences (PSIBS) Doctoral Training Centre, University of Birmingham, Edgbaston, Birmingham, B15 2TT, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2012 Feb 7;109(6):1862-7. doi: 10.1073/pnas.1112132109. Epub 2012 Jan 20.

Abstract

Water soluble, luminescent gold nanoparticles are delivered into human platelets via a rapid, pH-controlled mechanism using a pH low insertion peptide, pHLIP. The approach introduces cocoating of gold nanoparticles with a europium luminescent complex, EuL and the pHLIP peptide to give pHLIP•EuL•Au. The 13-nm diameter gold nanoparticles act as a scaffold for the attachment of both the luminescent probe and the peptide to target delivery. Their size allows delivery of approximately 640 lanthanide probes per nanoparticle to be internalized in human platelets, which are not susceptible to transfection or microinjection. The internalization of pHLIP•EuL•Au in platelets, which takes just minutes, was studied with a variety of imaging modalities including luminescence, confocal reflection, and transmission electron microscopy. The results show that pHLIP•EuL•Au only enters the platelets in low pH conditions, pH 6.5, mediated by the pHLIP translocation across the membrane, and not at pH 7.4. Luminescence microscopy images of the treated platelets show clearly the red luminescence signal from the europium probe and confocal reflection microscopy confirms the presence of the gold particles. Furthermore, transmission electron microscopy gives a detailed insight of the internalization and spatial localization of the gold nanoparticles in the platelets. Thus, we demonstrate the potential of the design to translocate multimodal nanoparticle probes into cells in a pH dependent manner.

摘要

水溶性、发荧光的金纳米颗粒通过一种快速、pH 控制的机制被递送人血小板,这种机制使用了一种低 pH 插入肽,pHLIP。该方法引入了金纳米颗粒的共包被,共包被物是一种铕发光络合物 EuL 和 pHLIP 肽,得到 pHLIP•EuL•Au。13nm 直径的金纳米颗粒作为附着发光探针和肽以靶向递药的支架。它们的大小允许每个纳米颗粒内吞大约 640 个镧系探针,这些探针不会被转染或微注射所影响。pHLIP•EuL•Au 在血小板中的内化只需几分钟,研究人员使用了多种成像方式,包括发光、共聚焦反射和透射电子显微镜。结果表明,pHLIP•EuL•Au 仅在 pH6.5 的低 pH 条件下通过 pHLIP 跨膜转运进入血小板,而在 pH7.4 时则不会。处理过的血小板的发光显微镜图像清楚地显示了铕探针的红色发光信号,共聚焦反射显微镜证实了金颗粒的存在。此外,透射电子显微镜详细地观察到了金纳米颗粒在血小板中的内化和空间定位。因此,我们证明了这种设计能够以 pH 依赖的方式将多模态纳米颗粒探针转运到细胞中。

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