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使用量子点介导的荧光测温法监测消融治疗中的热剂量。

Monitoring of thermal dose during ablation therapy using quantum dot-mediated fluorescence thermometry.

机构信息

Department of Urology, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9110, USA.

出版信息

J Endourol. 2010 Dec;24(12):1903-8. doi: 10.1089/end.2010.0110. Epub 2010 Sep 21.

DOI:10.1089/end.2010.0110
PMID:20858063
Abstract

PURPOSE

The objective of this study was to demonstrate the feasibility of quantum dot (QD)-mediated fluorescence thermometry to monitor thermal dose in an in-vitro thermal ablation zone generated by laser-heated gold nanoshells (LGNS).

MATERIALS AND METHODS

Hyperthermic cell death of human prostate cancer cell line (PC-3) was determined after various heating settings and correlated to the thermal conditions using an Arrhenius model prior to LGNS ablation. PC-3 cells with gold nanoshells (GNS) and QDs were exposed to a near-infrared laser and QD excitation light. When the cells were heated by GNS, local temperature was measured using the temperature-dependent fluorescence intensity of QDs. Using the predetermined Arrhenius model, the thermal dose (i.e., cell death of PC-3 cells) by LGNS was estimated with local temperatures measured with QD-mediated thermometry. The estimated thermal dose was confirmed with calcein-acetoxy-methylester viability assay.

RESULTS

For PC-3 cell line, the activation energy and frequency factor of the Arrhenius model were 86.78 kcal/mol and 6.35 × 10(55) Hz, respectively. During LGNS ablation of PC-3 cells, QD-mediated temperature measurement showed that the temperature of the laser spot increased rapidly to ∼58 °C ± 4 °C. The estimated thermal dose showed that cell death reached to ∼90% in 120 seconds. The death cell zone observed after staining corresponded to a peak area of the temperature profile generated after analysis of the QD fluorescence intensity.

CONCLUSIONS

This study shows that the QD fluorescence thermometry can accurately monitor the PC-3 cell death by LGNS ablation. This approach holds promises for a better monitoring of thermal ablation procedures in clinical practice.

摘要

目的

本研究旨在展示利用量子点(QD)介导的荧光测温法监测激光加热金壳纳米球(LGNS)产生的体外热消融区热剂量的可行性。

材料与方法

在进行 LGNS 消融之前,通过 Arrhenius 模型确定不同加热条件下人类前列腺癌细胞系(PC-3)的过热细胞死亡,并将其与热条件相关联。用近红外激光和 QD 激发光照射载金纳米壳(GNS)和 QD 的 PC-3 细胞。当 GNS 加热细胞时,使用 QD 荧光强度与温度相关的特性来测量局部温度。利用预先确定的 Arrhenius 模型,通过 QD 介导的测温法测量的局部温度来估计 LGNS 的热剂量(即 PC-3 细胞的死亡)。用 calcein-acetoxy-methylester 活力测定法验证估计的热剂量。

结果

对于 PC-3 细胞系,Arrhenius 模型的活化能和频率因子分别为 86.78 kcal/mol 和 6.35×10(55) Hz。在 LGNS 消融 PC-3 细胞期间,QD 介导的温度测量显示激光点的温度迅速升高至约 58°C±4°C。估计的热剂量显示,细胞死亡在 120 秒内达到约 90%。染色后观察到的死亡细胞区与分析 QD 荧光强度后生成的温度曲线的峰值区域相对应。

结论

本研究表明,QD 荧光测温法可准确监测 LGNS 消融导致的 PC-3 细胞死亡。这种方法有望更好地监测临床实践中的热消融程序。

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