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首页> 外文期刊>Biomaterials >Near infrared photoacoustic detection of sentinel lymph nodes with gold nanobeacons.
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Near infrared photoacoustic detection of sentinel lymph nodes with gold nanobeacons.

机译:金纳米信标近红外光声检测前哨淋巴结。

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Detection of sentinel lymph node (SLN) using photoacoustic imaging is an emerging technique for noninvasive axillary staging of breast cancer. Due to the absence of intrinsic contrast inside the lymph nodes, exogenous contrast agents are used for photoacoustic detection. In this work, we have demonstrated near infrared detection of SLN with gold nanobeacons (GNBs) providing the photoacoustic contrast in a rodent model. We found that size dictates the in vivo characteristics of these nanoparticles in SLN imaging. Larger nanobeacons with high payloads of gold were not as efficient as smaller size nanobeacons with lower payloads for this purpose. Colloidal GNBs were designed as a nanomedicine platform with "soft" nature that is amenable to bio-elimination, an essential feature for in vivo efficacy and safety. The GNBs were synthesized as lipid- or polymer-encapsulated colloidal particles incorporating tiny gold nanoparticles (2-4 nm) in three tunable sizes (90 nm, 150 nm and 290 nm). Smaller GNBs were noted trafficking through the lymphatic system and accumulating more efficiently in the lymph nodes in comparison to the bigger nanoagents. At 20 min, the GNBs reached the SLN and were no longer observed within the draining lymphatic vessel. Within 1 h post-injection, the contrast ratio of the lymph nodes with the surrounding blood vessels was 9:1. These findings were also supported by analytical measurements of the ex vivo tissue samples. Results indicate that cumulative nanoparticle deposition in lymph nodes is size dependent and that high payloads of gold, although offering greater contrast in vitro, may yield nanoagents with poor intradermal migration and lymphatic transport characteristics.
机译:使用光声成像检测前哨淋巴结(SLN)是一种用于乳腺癌的非侵入性腋窝分期的新兴技术。由于在淋巴结内部不存在内在的对比,因此将外源性对比剂用于光声检测。在这项工作中,我们证明了用金纳米信标(GNB)在啮齿动物模型中提供光声对比的SLN的近红外检测。我们发现大小决定了SLN成像中这些纳米粒子的体内特征。为此,具有高黄金有效载荷的较大纳米信标的效率不及具有较低有效载荷的较小尺寸纳米信标的效率。胶体GNBs被设计为具有“软”性质的纳米药物平台,该性质适于生物消除,这是体内功效和安全性的基本特征。将GNB合成为脂质或聚合物包封的胶体颗粒,并掺入三种可调尺寸(90 nm,150 nm和290 nm)的微小金纳米颗粒(2-4 nm)。与较大的纳米剂相比,较小的GNB被注意到通过淋巴系统运输,并在淋巴结中更有效地积累。在20分钟时,GNB到达了SLN,并且在引流淋巴管中不再观察到。注射后1小时内,淋巴结与周围血管的对比度为9:1。这些发现也得到离体组织样品的分析测量的支持。结果表明,累积的纳米颗粒在淋巴结中的沉积取决于大小,尽管在体外可提供更高的对比度,但高的金有效负载量可能会产生真皮内迁移和淋巴运输特性较差的纳米剂。

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