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活体中循环肿瘤细胞、感染和其他病理特征的纳米示踪诊断。

Nanotheranostics of circulating tumor cells, infections and other pathological features in vivo.

机构信息

Bio/Nano Technology Laboratory, Institute for Nanoscience and Engineering, University of Arkansas, Fayetteville, Arkansas 72701, USA.

出版信息

Mol Pharm. 2013 Mar 4;10(3):813-30. doi: 10.1021/mp300577s. Epub 2013 Feb 25.

Abstract

Many life-threatening diseases are disseminated through biological fluids, such as blood, lymph, and cerebrospinal fluid. The migration of tumor cells through the vascular circulation is a mandatory step in metastasis, which is responsible for ∼90% of cancer-associated mortality. Circulating pathogenic bacteria, viruses, or blood clots lead to other serious conditions including bacteremia, sepsis, viremia, infarction, and stroke. Therefore, technologies capable of detecting circulating tumor cells (CTCs), circulating bacterial cells (CBCs), circulating endothelial cells (CECs), circulating blood clots, cancer biomarkers such as microparticles and exosomes, which contain important microRNA signatures, and other abnormal features such as malaria parasites in biological fluids may facilitate early diagnosis and treatment of metastatic cancers, infections, and adverse cardiovascular events. Unfortunately, even in a disease setting, circulating abnormal cells are rare events that are easily obscured by the overwhelming background material in whole blood. Existing detection methods mostly rely on ex vivo analyses of limited volumes (a few milliliters) of blood samples. These small volumes limit the probability of detecting CTCs, CECs, CBCs and other rare phenomena. In vivo detection platforms capable of continuously monitoring the entire blood volume may substantially increase the probability of detecting circulating abnormal cells and, in particular, increase the opportunity to identify exceedingly rare and potentially dangerous subsets of these cells, such as circulating cancer stem cells (CCSCs). In addition, in vivo detection technologies capable of destroying and/or capturing circulating abnormal cells may inhibit disease progression. This review focuses on novel therapeutic and diagnostic (theranostic) platforms integrating in vivo real-time early diagnosis and nano-bubble based targeted therapy of CTCs, CECs, CBCs and other abnormal objects in circulation. This critical review particularly focuses on nanotechnology-based theranostic (nanotheranostic) approaches, especially in vivo photoacoustic (PA) and photothermal (PT) nanotheranostic platforms. We emphasize an urgent need for in vivo platforms composed of multifunctional contrast nanoagents, which utilize diverse modalities to realize a breakthrough for early detection and treatment of harmful diseases disseminated through the circulation.

摘要

许多危及生命的疾病都是通过生物体液传播的,如血液、淋巴液和脑脊液。肿瘤细胞通过血管循环的迁移是转移的必要步骤,这是导致 90%癌症相关死亡的原因。循环中的病原体细菌、病毒或血栓会导致其他严重疾病,包括菌血症、败血症、病毒血症、梗死和中风。因此,能够检测生物体液中循环肿瘤细胞(CTCs)、循环细菌细胞(CBCs)、循环内皮细胞(CECs)、循环血液凝块、癌症生物标志物(如含有重要 microRNA 特征的微粒和外泌体)以及其他异常特征(如疟原虫)的技术,可能有助于早期诊断和治疗转移性癌症、感染和不良心血管事件。不幸的是,即使在疾病状态下,循环异常细胞也很少见,很容易被全血中的压倒性背景物质所掩盖。现有的检测方法大多依赖于对有限体积(几毫升)的血液样本进行离体分析。这些小体积限制了检测 CTCs、CECs、CBCs 和其他罕见现象的概率。能够连续监测整个血容量的体内检测平台可能会大大提高检测循环异常细胞的概率,特别是增加识别这些细胞中极其罕见且潜在危险亚群的机会,如循环肿瘤干细胞(CCSCs)。此外,能够破坏和/或捕获循环异常细胞的体内检测技术可能会抑制疾病的进展。本综述重点介绍了整合体内实时早期诊断和基于纳米气泡的靶向治疗循环中的 CTCs、CECs、CBCs 和其他异常物体的新型治疗和诊断(治疗诊断)平台。本综述特别关注基于纳米技术的治疗诊断(纳米治疗诊断)方法,特别是体内光声(PA)和光热(PT)纳米治疗诊断平台。我们强调需要开发由多功能对比纳米制剂组成的体内平台,这些制剂利用多种模式来实现通过循环传播的有害疾病的早期检测和治疗的突破。

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