Institute for Biotechnology and Bioengineering, Centre of Biological Engineering, Campus de Gualtar, University of Minho, Braga 4710-05, Portugal.
Institute of Molecular and Cell Biology, Rua Campo Alegre, Porto 4099-003, Portugal.
Eur J Pharm Sci. 2017 Jun 15;104:102-113. doi: 10.1016/j.ejps.2017.03.045. Epub 2017 Apr 4.
We have, in previous work developed, characterized and evaluated the biocompatibility of an engineered hyaluronic acid nanogel. Here we assess the targetability of a hyaluronic acid nanogel towards CD44 overexpressing cells, in vitro and in vivo. Results obtained by flow cytometry and confocal fluorescence microscopy shows that nanogel is greatly internalized by non-small cancer lung cells (A549 cells), that overexpress CD44 receptors. The biodistribution and tumor targetability of the nanogel labelled with a near-infrared (NIR) probe were performed, in mice, through a non-invasive imaging system. Results revealed nanogel high targetability towards an induced subcutaneous A549 tumor. Nanogels pharmacokinetics was evaluated also in healthy animals, and Alexa Fluor 680 labelled nanogel exhibited higher accumulation in liver, kidneys and skin. Also, a comparative biodistribution study was performed, using two NIR imaging probes, Cy5.5 and Alexa Fluor 680.
我们之前已经开发、表征和评估了一种工程化透明质酸纳米凝胶的生物相容性。在这里,我们评估了透明质酸纳米凝胶对体外和体内过表达 CD44 受体的细胞的靶向性。流式细胞术和共聚焦荧光显微镜的结果表明,纳米凝胶被过表达 CD44 受体的非小细胞肺癌细胞(A549 细胞)大量内化。通过非侵入性成像系统,对用近红外(NIR)探针标记的纳米凝胶进行了体内分布和肿瘤靶向性研究。结果表明,纳米凝胶对诱导的皮下 A549 肿瘤具有很高的靶向性。还在健康动物中评估了纳米凝胶的药代动力学,结果表明,Alexa Fluor 680 标记的纳米凝胶在肝脏、肾脏和皮肤中的积累更高。此外,还使用两种 NIR 成像探针 Cy5.5 和 Alexa Fluor 680 进行了比较生物分布研究。