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本文引用的文献

1
Biomimetic membranes designed from amphiphilic block copolymers.由两亲性嵌段共聚物设计的仿生膜。
Soft Matter. 2006 Aug 16;2(9):751-759. doi: 10.1039/b605165k.
2
Quantitative membrane loading of polymer vesicles.聚合物囊泡的定量膜负载
Soft Matter. 2006 Oct 17;2(11):973-980. doi: 10.1039/b604212k.
3
Bioresorbable Vesicles Formed through Spontaneous Self-Assembly of Amphiphilic Poly(ethylene oxide)-block-polycaprolactone.通过两亲性聚(环氧乙烷)-嵌段-聚己内酯的自发自组装形成的生物可吸收囊泡。
Macromolecules. 2006 Mar 7;39(5):1673-1675. doi: 10.1021/ma0519009.
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Controlling Bulk Optical Properties of Emissive Polymersomes Through Intramembranous Polymer-Fluorophore Interactions.通过膜内聚合物-荧光团相互作用控制发光聚合物囊泡的整体光学性质
Chem Mater. 2007 Mar 20;19(6):1309-1318. doi: 10.1021/cm062427w.
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Leuko-polymersomes.白细胞聚合物囊泡
Faraday Discuss. 2008;139:129-41; discussion 213-28, 419-20. doi: 10.1039/b717821b.
6
Ultrafast excited-state dynamics of nanoscale near-infrared emissive polymersomes.纳米级近红外发光聚合物囊泡的超快激发态动力学
J Am Chem Soc. 2008 Jul 30;130(30):9773-84. doi: 10.1021/ja711497w. Epub 2008 Jul 9.
7
Initial studies of in vivo absorbing and scattering heterogeneity in near-infrared tomographic breast imaging.近红外断层乳腺成像中体内吸收和散射异质性的初步研究。
Opt Lett. 2001 Jun 1;26(11):822-4. doi: 10.1364/ol.26.000822.
8
Polymeric nanoparticles as imaging probes for protein kinase activity in cells.用于细胞中蛋白激酶活性成像检测的聚合物纳米颗粒
Angew Chem Int Ed Engl. 2007;46(46):8744-6. doi: 10.1002/anie.200702853.
9
Fluorescence imaging in vivo: recent advances.体内荧光成像:最新进展
Curr Opin Biotechnol. 2007 Feb;18(1):17-25. doi: 10.1016/j.copbio.2007.01.003. Epub 2007 Jan 17.
10
A review of the formation and classification of amphiphilic block copolymer nanoparticulate structures: micelles, nanospheres, nanocapsules and polymersomes.两亲性嵌段共聚物纳米颗粒结构的形成与分类综述:胶束、纳米球、纳米胶囊和聚合物囊泡。
Eur J Pharm Biopharm. 2007 Mar;65(3):259-69. doi: 10.1016/j.ejpb.2006.11.009. Epub 2006 Nov 23.

体内荧光成像:个人视角。

In vivo fluorescence imaging: a personal perspective.

机构信息

Department of Medicine, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.

出版信息

Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2009 Mar-Apr;1(2):156-67. doi: 10.1002/wnan.7.

DOI:10.1002/wnan.7
PMID:20049787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3091504/
Abstract

In vivo fluorescence imaging with near-infrared (NIR) light holds enormous potential for a wide variety of molecular diagnostic and therapeutic applications. Because of its quantitative sensitivity, inherent biological safety, and relative ease of use (i.e., with respect to cost, time, mobility, and its familiarity to a diverse population of investigators), fluorescence-based imaging techniques are being increasingly utilized in small-animal research. Moreover, there is substantial interest in the translation of novel optical techniques into the clinic, where they will prospectively aid in noninvasive and quantitative screening, disease diagnosis, and post-treatment monitoring of patients. Effective deep-tissue fluorescence imaging requires the application of exogenous NIR-emissive contrast agents. Currently, available probes fall into two major categories: organic and inorganic NIR fluorophores (NIRFs). In the studies reviewed herein, we utilized polymersomes (50 nm to 50 microm diameter polymer vesicles) for the incorporation and delivery of large numbers of highly emissive oligo (porphyrin)-based, organic NIRFs.

摘要

体内近红外(NIR)光荧光成像是各种分子诊断和治疗应用的巨大潜力。由于其定量灵敏度、固有生物安全性以及相对易用性(即成本、时间、移动性以及对不同研究人群的熟悉程度),基于荧光的成像技术在小动物研究中得到了越来越多的应用。此外,人们对将新型光学技术转化为临床应用非常感兴趣,因为它们有望在临床上用于非侵入性和定量筛查、疾病诊断以及对患者的治疗后监测。有效的深层组织荧光成像需要应用外源 NIR 发射对比剂。目前,可用的探针分为两大类:有机和无机 NIR 荧光团(NIRFs)。在本文综述的研究中,我们利用聚合物囊泡(50nm 至 50μm 直径的聚合物囊泡)来掺入和递增大数量的高发光寡(卟啉)基有机 NIRFs。