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本文引用的文献

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Nanoparticle clearance is governed by Th1/Th2 immunity and strain background.纳米颗粒的清除受 Th1/Th2 免疫和品系背景的控制。
J Clin Invest. 2013 Jul;123(7):3061-73. doi: 10.1172/JCI66895. Epub 2013 Jun 17.
2
Automated non-rigid registration and mosaicing for robust imaging of distinct retinal capillary beds using speckle variance optical coherence tomography.使用散斑方差光学相干断层扫描对不同视网膜毛细血管床进行稳健成像的自动非刚性配准和拼接
Biomed Opt Express. 2013 May 7;4(6):803-21. doi: 10.1364/BOE.4.000803. Print 2013 Jun 1.
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Two-photon luminescence properties of gold nanorods.金纳米棒的双光子发光特性
Biomed Opt Express. 2013 Apr 1;4(4):584-95. doi: 10.1364/BOE.4.000584. Epub 2013 Mar 21.
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In vivo photothermal optical coherence tomography of gold nanorod contrast agents.金纳米棒造影剂的体内光热光学相干断层扫描
Biomed Opt Express. 2012 Nov 1;3(11):2881-95. doi: 10.1364/BOE.3.002881. Epub 2012 Oct 17.
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A comparison of Doppler optical coherence tomography methods.多普勒光学相干断层扫描方法的比较
Biomed Opt Express. 2012 Oct 1;3(10):2669-80. doi: 10.1364/BOE.3.002669. Epub 2012 Sep 26.
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Fast three-dimensional imaging of gold nanoparticles in living cells with photothermal optical lock-in Optical Coherence Microscopy.利用光热光学锁相光学相干显微镜对活细胞中的金纳米颗粒进行快速三维成像。
Opt Express. 2012 Sep 10;20(19):21385-99. doi: 10.1364/OE.20.021385.
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Overcoming limitations in nanoparticle drug delivery: triggered, intravascular release to improve drug penetration into tumors.克服纳米药物传递的局限性:触发式血管内释放以提高药物渗透进入肿瘤。
Cancer Res. 2012 Nov 1;72(21):5566-75. doi: 10.1158/0008-5472.CAN-12-1683. Epub 2012 Sep 4.
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Optical detection of indocyanine green encapsulated biocompatible poly (lactic-co-glycolic) acid nanoparticles with photothermal optical coherence tomography.光热光相干断层扫描法对吲哚菁绿包封的生物相容性聚(乳酸-共-乙醇酸)纳米粒子的光学检测。
Opt Lett. 2012 Mar 1;37(5):981-3. doi: 10.1364/ol.37.000981.
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Dual-modality photothermal optical coherence tomography and magnetic-resonance imaging of carbon nanotubes.碳纳米管的双模态光热光学相干断层扫描和磁共振成像。
Opt Lett. 2012 Mar 1;37(5):872-4. doi: 10.1364/OL.37.000872.
10
Depth profiling of photothermal compound concentrations using phase sensitive optical coherence tomography.使用相敏光学相干断层扫描技术对光热化合物浓度进行深度剖析。
J Biomed Opt. 2011 Dec;16(12):126003. doi: 10.1117/1.3659211.

利用多模态光学相干断层扫描对纳米颗粒递送和肿瘤微血管进行体内成像。

In vivo imaging of nanoparticle delivery and tumor microvasculature with multimodal optical coherence tomography.

作者信息

Tucker-Schwartz Jason M, Beavers Kelsey R, Sit Wesley W, Shah Amy T, Duvall Craig L, Skala Melissa C

机构信息

Department of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.

Interdisciplinary Graduate Program in Materials Science, Vanderbilt University, Nashville, TN 37235, USA.

出版信息

Biomed Opt Express. 2014 May 1;5(6):1731-43. doi: 10.1364/BOE.5.001731. eCollection 2014 Jun 1.

DOI:10.1364/BOE.5.001731
PMID:24940536
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4052907/
Abstract

Current imaging techniques capable of tracking nanoparticles in vivo supply either a large field of view or cellular resolution, but not both. Here, we demonstrate a multimodality imaging platform of optical coherence tomography (OCT) techniques for high resolution, wide field of view in vivo imaging of nanoparticles. This platform includes the first in vivo images of nanoparticle pharmacokinetics acquired with photothermal OCT (PTOCT), along with overlaying images of microvascular and tissue morphology. Gold nanorods (51.8 ± 8.1 nm by 15.2 ± 3.3 nm) were intravenously injected into mice, and their accumulation into mammary tumors was non-invasively imaged in vivo in three dimensions over 24 hours using PTOCT. Spatial frequency analysis of PTOCT images indicated that gold nanorods reached peak distribution throughout the tumors by 16 hours, and remained well-dispersed up to 24 hours post-injection. In contrast, the overall accumulation of gold nanorods within the tumors peaked around 16 hours post-injection. The accumulation of gold nanorods within the tumors was validated post-mortem with multiphoton microscopy. This shows the utility of PTOCT as part of a powerful multimodality imaging platform for the development of nanomedicines and drug delivery technologies.

摘要

目前能够在体内追踪纳米颗粒的成像技术,要么提供大视野,要么提供细胞分辨率,但无法两者兼顾。在此,我们展示了一种光学相干断层扫描(OCT)技术的多模态成像平台,用于纳米颗粒的高分辨率、大视野体内成像。该平台包括通过光热OCT(PTOCT)获得的纳米颗粒药代动力学的首张体内图像,以及微血管和组织形态的叠加图像。将金纳米棒(长51.8±8.1纳米,宽15.2±3.3纳米)静脉注射到小鼠体内,并使用PTOCT在24小时内对其在乳腺肿瘤中的积累进行三维无创体内成像。PTOCT图像的空间频率分析表明,金纳米棒在16小时时在整个肿瘤中达到分布峰值,并在注射后24小时内保持良好分散。相比之下,肿瘤内金纳米棒的总体积累在注射后约16小时达到峰值。注射后通过多光子显微镜在死后验证了肿瘤内金纳米棒的积累情况。这表明PTOCT作为强大的多模态成像平台的一部分,对于纳米医学和药物递送技术的发展具有实用性。