首页> 外文会议>Conference on Multiphoton Microscopy in the Biomedical Sciences >Multiphoton and FLIM imaging in quantifying ex vivo and in vivo body organ kinetics of solutes
【24h】

Multiphoton and FLIM imaging in quantifying ex vivo and in vivo body organ kinetics of solutes

机译:多光子和Flim成像在量化的earVivo和体内体内器官动力学中的溶质

获取原文

摘要

Traditionally, destructive sampling and analysis are used to determine the fate, kinetics and effects of exogenousmaterials in the body. Minimally invasive confocal and multiphoton microscopy (MPM) in 3D space over in time todeep tissue depths has enabled us to quantify endogenous fluorescent species in the body as well as exogenousfluorescent molecules, cells and nanoparticles that have been administered into the body and/or are applied to the skin,kidney and liver ex vivo and in vivo. Of particular importance has been the ability to get specificity in drug, metaboliteand endogenous solute measurement in tissues in vivo by using specific spectral excitation and emission wavelengths,the use of fluorescence lifetime and the measurement of fluorescence anisotropy.We have applied MPM to characterise physiologically based pharmacokinetics of solutes, mesenchymal stem cells andnanoparticles in various organs. More recently, we have used MPM to examine stem cell and nanoparticle – tissueinteractions directly in acute liver and kidney injury models, tumor models and inflammatory models. MPM has alsobeen used to measure changes in the redox state of cells, as well the use of photochemical probes to measure adversebiochemical events such as the formation of reactive oxygen species.Sun-induced skin damage, with its sequelae of photoaging, actinic keratosis and various skin cancers is a particular issuefor many of us in subtropical and temperate climates. Our group has therefore also used MPM to quantify the metabolicchanges seen in melanoma lesions, the safety of nanoparticle sunscreens, whose use may prevent these lesions, and to aidin the mechanistic and regulatory evaluation of topical product efficacy, bioequivalence and safety. In conclusion, MPMfluorescence lifetime imaging microscopy (FLIM) is a promising technology to aid in product characterization anddevelopment as well as in the translational diagnosis of skin related pathologies in the clinic.
机译:传统上,破坏性取样和分析用于确定外源的命运,动力学和效果体内的材料。在时间内,在3D空间中微创共焦和多光子显微镜(MPM)深度组织深度使我们能够量化体内的内源性荧光物质以及外源性已经施用于身体和/或施用于皮肤的荧光分子,细胞和纳米颗粒,肾脏和肝脏exvivo和体内。特别重要的是能够在药物,代谢物中获得特异性通过使用特定的光谱激发和发射波长在体内组织中的内源性溶质测量,使用荧光寿命和荧光各向异性的测量。我们已施用MPM以表征生理基础的溶质药代动力学,间充质干细胞和各种器官中的纳米颗粒。最近,我们使用MPM来检查干细胞和纳米颗粒 - 组织直接在急性肝癌和肾损伤模型中的相互作用,肿瘤模型和炎症模型。 MPM也有用于测量细胞氧化还原状态的变化,也可以使用光化学探头来测量不利生物化学事件,如反应性氧物种的形成。阳光诱导的皮肤损伤,用其光学手册的后遗症,光化角瘤和各种皮肤癌是一个特定的问题对于我们许多人在亚热带和温带气候中。因此,我们的小组也使用MPM来量化代谢在黑色素瘤病变中看到的变化,纳米粒子阳膜的安全性,其用途可能会阻止这些病变,并帮助在机械和监管评估局部产品疗效,生物等效和安全性。总之,MPM荧光寿命成像显微镜(FLIM)是有助于有助于产品表征和的有助于的技术开发以及临床中皮肤相关病理的翻译诊断。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号