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近红外量子点经皮下注射后行荧光成像及在小鼠体内的全身生物分布用于区域性淋巴结示踪。

Fluorescence imaging and whole-body biodistribution of near-infrared-emitting quantum dots after subcutaneous injection for regional lymph node mapping in mice.

机构信息

Centre de Recherche en Automatique de Nancy-Nancy-University-CNRS-Centre Alexis Vautrin, avenue de Bourgogne, 54511 Vandoeuvre-lès-Nancy Cedex, France.

出版信息

Mol Imaging Biol. 2010 Aug;12(4):394-405. doi: 10.1007/s11307-009-0288-y. Epub 2009 Nov 21.

DOI:10.1007/s11307-009-0288-y
PMID:19936843
Abstract

PURPOSE

This study compares fluorescence imaging to mass spectroscopy (inductively coupled plasma-mass spectroscopy, ICP-MS) for detection of quantum dots (QDs) in sentinel lymph node (LN) mapping of breast cancer.

PROCEDURES

We study the accumulation of near-infrared-emitting QDs into regional LNs and their whole-body biodistribution in mice after subcutaneous injection, using in vivo fluorescence imaging and ex vivo elemental analysis by ICP-MS.

RESULTS

We show that the QD accumulation in regional LNs is detectable by fluorescence imaging as early as 5 min post-delivery. Their concentration reaches a maximum at 4 h then decreases over a 10-day observation period. These data are confirmed by ICP-MS. The QD uptake in other organs, assessed by ICP-MS, increases steadily over time; however, its overall level remains rather low.

CONCLUSIONS

Fluorescence imaging can be used as a non-invasive alternative to ICP-MS to follow the QD accumulation kinetics into regional LNs.

摘要

目的

本研究比较了荧光成像与质谱(电感耦合等离子体质谱法,ICP-MS)在乳腺癌前哨淋巴结(SLN)示踪中检测量子点(QD)的效果。

方法

我们通过皮下注射,在体内荧光成像和 ICP-MS 体外元素分析中研究了近红外发射 QD 在后注射后在局部淋巴结中的积累及其全身生物分布。

结果

我们发现,在注射后 5 分钟即可通过荧光成像检测到 QD 在局部淋巴结中的积累。它们的浓度在 4 小时达到最大值,然后在 10 天的观察期内逐渐下降。这些数据通过 ICP-MS 得到了证实。通过 ICP-MS 评估,其他器官中的 QD 摄取量随时间稳定增加;然而,其整体水平仍然相当低。

结论

荧光成像可以作为 ICP-MS 的非侵入性替代方法,用于跟踪 QD 向局部淋巴结中的积累动力学。

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