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Co-registered photoacoustic and fluorescent imaging of a switchable nanoprobe based on J-aggregates of indocyanine green

机译:基于吲哚菁绿J聚集体的可转换纳米探针的共配准光声和荧光成像

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We introduce a preclinical imaging platform - a 3D photoacoustic/fluorescence tomography (PAFT) instrument augmented with an environmentally responsive dual-contrast biocompatible nanoprobe. The PAFT instrument was designed for simultaneous acquisition of photoacoustic and fluorescence orthogonal projections at each rotational position of a biological object, enabling direct co-registration of the two imaging modalities. The nanoprobe was based on liposomes loaded with J-aggregates of indocyanine green (PAtrace). Once PAtrace interacts with the environment, a transition from J-aggregate to monomeric ICG is induced. The subsequent recovery of monomeric ICG is characterized by dramatic changes in the optical absorption spectrum and reinstated fluorescence. In the activated state, PAtrace can be simultaneously detected by both imaging modes of the PAFT instrument using 780 nm excitation and fluorescence detection at 810 nm. The fluorescence imaging component is used to boost detection sensitivity by providing low-resolution map of activated nanoprobes, which are then more precisely mapped in 3D by the photoacoustic imaging component. Activated vs non-activated particles can be distinguished based on their different optical absorption peaks, removing the requirements for complex image registration between reference and detection scans. Preliminary phantom and in vivo animal imaging results showed successful activation and visualization of PAtrace with high sensitivity and resolution. The proposed PAFT-PAtrace imaging platform could be used in various functional and molecular imaging applications including multi-point in vivo assessment of early metastasis.
机译:我们引入了临床前成像平台-增强了3D光声/荧光层析成像(PAFT)仪器,并增加了对环境敏感的双对比度生物相容性纳米探针。 PAFT仪器设计用于在生物物体的每个旋转位置同时采集光声和荧光正交投影,从而可以直接共配准这两种成像方式。纳米探针基于负载有吲哚菁绿(PAtrace)的J-聚集体的脂质体。一旦PAtrace与环境相互作用,就会引发从J聚集体到单体ICG的转变。单体ICG的后续回收的特征在于光吸收光谱和恢复的荧光的剧烈变化。在激活状态下,可以使用780 nm激发和810 nm荧光检测,通过PAFT仪器的两种成像模式同时检测PAtrace。荧光成像组件可通过提供低分辨率的活化纳米探针图来提高检测灵敏度,然后通过光声成像组件将其精确地映射到3D中。可以根据激活粒子与未激活粒子的不同光吸收峰来区分它们,从而消除了在参考扫描与检测扫描之间进行复杂图像配准的要求。初步的体模和体内动物成像结果表明,PAtrace成功激活并可视化,具有很高的灵敏度和分辨率。提出的PAFT-PAtrace成像平台可用于各种功能和分子成像应用,包括早期转移的多点体内评估。

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