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A Molecular Imaging 'Skin' A Time-resolving Intraoperative Imager for Microscopic Residual Cancer Detection Using Enhanced Upconverting Nanoparticles

机译:分子成像“皮肤”的时间分辨术中成像仪用于使用增强的上转换纳米粒子的显微残留癌检测。

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Optimal cancer therapy requires targeted and individualized treatment of all tumor cells, including both gross and microscopic disease. Intraoperatively hard to visualize and often left behind, microscopic foci of residual cancer cells significantly increase the risk of cancer recurrence and treatment failure rates. Fluorescently-tagged targeted molecular labels are employed to guide surgery, but conventional fluorescent intraoperative imagers suffer from lack of sensitivity and maneuverability, limiting practicality in small tumor cavities owing to their cumbersome sizes driven by optics. This work does away with conventional lenses and filters and introduces an optics-free molecular imaging “skin” consisting of only a 25μm thin CMOS contact imager that synergistically integrates the long emission lifetimes of upconverting nanoparticles (UCNP) combined with upconversion to use a time domain approach to acquire the image coupled with infrared illumination allowing deep tissue penetration and elimination of autofluorescence. Using this strategy, we are able to visualize UCNPs at fluences (W/cm2) compatible with intraoperative use, opening the door to visualize targeted areas with microscopic sensitivity and facilitate residual microscopic disease detection during surgery, and laying the groundwork for precision post-operative radiation.
机译:最佳的癌症治疗需要对所有肿瘤细胞(包括肉眼疾病和微观疾病)进行有针对性的个性化治疗。术中难以观察到并且经常遗留下来的残留癌细胞的微观灶明显增加了癌症复发的风险和治疗失败率。带有荧光标签的靶向分子标记物被用于指导手术,但是常规的荧光术中成像仪由于缺乏灵敏性和可操作性而受到困扰,由于其光学器件驱动的笨重尺寸限制了其在小肿瘤腔中的实用性。这项工作消除了传统的透镜和滤光片,并引入了仅由25μm薄CMOS接触式成像器组成的无光学分子成像“皮肤”,该成像器协同整合了上转换纳米粒子(UCNP)的长发射寿命和上转换以使用时域。结合红外照明的图像采集方法,可实现深层组织穿透并消除自发荧光。使用此策略,我们可以可视化以通量(W / cm 2 )与术中使用兼容,可打开门以微观灵敏度可视化目标区域,并有助于在手术过程中检测残留的微观疾病,并为精确的术后放射奠定基础。

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