4.8 Article

Organic Semiconducting Nanoparticles as Efficient Photoacoustic Agents for Lightening Early Thrombus and Monitoring Thrombolysis in Living Mice

Journal

ACS NANO
Volume 11, Issue 3, Pages 3298-3310

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.7b00594

Keywords

PDI nanoparticles; photoacoustic imaging; contrast agent; early thrombus; NIR absorption

Funding

  1. National Natural Science Foundation of China [21674048, 21574064, 61378081, 81501535]
  2. Natural Science Foundation of Jiangsu Province of China [NY211003, BM2012010]
  3. International Cooperation Project of Hubei Province [2015BHE018]
  4. Hubei Province's Outstanding Medical Academic Leader Program, Wuhan's Huanghe Talents Program
  5. Zhongnan Hospital of Wuhan University Science, Technology and Innovation Seed Fund [cxpy20160045]

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Acute venous thrombosis is prevalent and potentially fatal. Accurate diagnosis of early thrombus is needed for patients in timely clinical intervention to prevent life-threatening conditions. Photoacoustic imaging (PM) with excellent spatial resolution and high optical contrast shows more promise for this purpose. However, its application is dramatically limited by its signal-off effect on thrombus because of the ischemia in thrombus which lacks the endogenous photoacoustic (PA) signal of hemoglobin. To address this dilemma, we herein report the feasibility of using organic semiconducting nanoparticles (NPs) for contrast enhanced PM of thrombus in living mice. An organic semiconducting NP, self-assembled by amphiphilic perylene-3,4,9,10-tetracarboxylic diimide (PDI) molecules, is chemically modified with cyclic Arg-Gly-Asp (cRGD) peptides as a PA contrast agent (cRGD-PDI NPs) for selectively lightening early thrombus. cRGD-PDI NPs presents high PA intensity, good stability in light and serum, and sufficient blood-circulating half-life. In living mice, PA intensity of early thrombus significantly increases after tail vein injection of cRGD-PDI NPs, which is 4-fold greater than that of the control, blocking, and old thrombus groups. Pathological and inununohisto chemical findings show that glycoprotein I1b/Illa abundant in early thrombus is a good biomarker targeted by cRGD-PDI NPs for distinguishing early thrombus from old thrombus by PM. Such a lightening PAI effect by cRGD-PDI NPs successfully provides accurate information including the profile, size and conformation, and spatial distribution of early thrombus, which may timely monitor the obstructive degree of thrombus in blood vessels and the thrombolysis effect.

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