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Lipid nanoemulsion passive tumor accumulation dependence on tumor stage and anatomical location: a new mathematical model for in vivo imaging biodistribution studies

机译:脂质纳米乳液被动肿瘤积累依赖性对肿瘤阶段和解剖地点:体内成像生物分布研究的新数学模型

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摘要

Nanoparticle delivery to tumor tissue is one of the most important applications of nanomedicine. However, the literature shows that this pharmacological event is highly-affected by several tumor biology characteristics, including tumor size and maturation. Thus, the objective of the present study is to report on the investigation of the biodistribution of a lipid nanoemulsion (NE) in a breast cancer tumor model using in vivo imaging techniques. As highlights of this study, we can indicate that the biodistribution was measured in different tumor sites (primary and metastatic tumors) and in the same experimental mice for four subsequent weeks. With this approach it is possible to observe that the NE tumor delivery is significantly altered during tumor growth and metastasis progression. Furthermore, in the present report we introduce a phenomenological mathematical model that successfully explains the delivery behavior of a hydrophobic infrared fluorescent NE marker to both primary tumor and metastatic lesions. We believe that these data, in addition to the phenomenological mathematical model, are relevant to understanding how the stage of tumor development can alter macromolecule and/or nanoparticle delivery to tumor tissues, thus improving the efficacy of the passive delivery features promoted by tumor biology.
机译:纳米粒子递送至肿瘤组织是纳米胺的最重要应用之一。然而,文献表明,该药理学事件受几种肿瘤生物学特征的高度影响,包括肿瘤大小和成熟。因此,本研究的目的是报告使用体内成像技术的乳腺癌肿瘤模型中脂纳米乳液(NE)的生物分布的研究。作为本研究的亮点,我们可以表明生物分布在不同的肿瘤部位(原发性和转移性肿瘤)中测量,并且在同一实验小鼠中进行了四个周末。通过这种方法,可以观察到在肿瘤生长和转移过程中显着改变NE肿瘤递送。此外,在本报告中,我们介绍了一种现象学的数学模型,其成功解释了疏水性红外荧光NE标志物与原发性肿瘤和转移性病变的递送行为。我们认为,除了现象学的数学模型之外,这些数据与理解肿瘤发育的阶段如何改变大分子和/或纳米颗粒输送到肿瘤组织的阶段,从而提高了肿瘤生物学促进的被动递送特征的功效。

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