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首页> 外文期刊>Journal of innovative optical health sciences >QUANTIFYING NANOPARTICLE TRANSPORT IN VIVO USING HYPERSPECTRAL IMAGING WITH A DORSAL SKINFOLD WINDOW CHAMBER
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QUANTIFYING NANOPARTICLE TRANSPORT IN VIVO USING HYPERSPECTRAL IMAGING WITH A DORSAL SKINFOLD WINDOW CHAMBER

机译:使用高光谱成像和背鳍窗腔室对体内的纳米颗粒运输进行定量

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摘要

We have developed a noninvasive imaging method to quantify in vivo drug delivery pharmacokinetics without the need for blood or tissue collection to determine drug concentration. By combining the techniques of hyperspectral imaging and a dorsal skinfold window chamber, this method enabled the real-time monitoring of vascular transport and tissue deposition of nanoparticles labeled with near-infrared (NIR) dye. Using this imaging method, we quantified the delivery pharmacokinetics of the native high-density lipoprotein (HDL) and epidermal growth factor receptor (EGFR)-targeted HDL nanoparticles and demonstrated these HDLs had long circulation time in blood stream (half-life 12 h). These HDL nanoparticles could efficiently carry cargo DiR-BOA to extravasate from blood vessels, diffuse through extracellular matrix, and penetrate and be retained in the tumor site. The EGFR targeting specificity of EGFR-targeted HDL (EGFR-specific peptide conjugated HDL) was also visualized in vivo by competitive inhibition w...
机译:我们已经开发出一种无创成像方法,可以定量体内药物传递的药代动力学,而无需收集血液或组织来确定药物浓度。通过结合高光谱成像技术和背部皮褶窗腔室技术,该方法可以实时监测血管注射和近红外(NIR)染料标记的纳米颗粒的组织沉积。使用这种成像方法,我们量化了天然高密度脂蛋白(HDL)和表皮生长因子受体(EGFR)靶向的HDL纳米颗粒的递送药代动力学,并证明了这些HDL在血流中的循环时间长(半衰期> 12 h) )。这些HDL纳米颗粒可以有效地携带货物DiR-BOA从血管中渗出,通过细胞外基质扩散,并渗透并保留在肿瘤部位。 EGFR靶向的HDL(EGFR特异性肽结合的HDL)的EGFR靶向特异性也可以通过竞争性抑制在体内观察到。

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