Efthimiadou Eleni K, Fragogeorgi Eirini, Palamaris Lazaros, Karampelas Theodoros, Lelovas Pavlos, Loudos George, Tamvakopoulos Constantin, Kostomitsopoulos Nikolaos, Kordas George
Institute for Nanoscience and Nanotechnology, NCSR "Demokritos", 15310 Aghia Paraskevi, Attikis, Greece.
Radiochemical/Radiopharmacological Quality Control Laboratory, Institute of Nuclear and Radiological Sciences and Technology, Energy & Safety, N.C.S.R. 'Demokritos', 15310 Aghia Paraskevi, Greece; Department of Medical Instruments Technology, Technological Educational Institute, GR 12210 Athens, Greece.
Mater Sci Eng C Mater Biol Appl. 2017 Oct 1;79:605-612. doi: 10.1016/j.msec.2017.05.082. Epub 2017 May 13.
Nanostructured delivery and diagnostic systems that induces specific targeting properties by exploiting the local physicochemical tumour characteristics will be evaluated is the present work. It is well known that cancer cells have specific physicochemical characteristics, which can be taken into consideration for the design of a broad spectrum of drug delivery systems (DDS). Some of those characteristics including the different temperature environment their susceptibility when temperature ranges between 40 and 43°C where cell apoptosis is induced, the intra- and extra-cellular pH which varies from 6.0 to 6.8, for cancer cells, and 6.5 to 7.4 for normal cells respectively, (lysosomes acidic pH ranges 4-5). Additional significant factors are the overexpressed receptors on the tumour surface. Loading and release studies were carried out by using the anthracycline drug Doxorubicin and their cytotoxicity was evaluated by using the MTT assay in healthy and diseased cell lines. The highlight of this work is the in vitro and in vivo studies which were performed in order to evaluate different nanostructures as for their biodistribution, pharmacokinetic and toxicity per se.
本研究将评估通过利用肿瘤局部物理化学特性诱导特定靶向特性的纳米结构递送和诊断系统。众所周知,癌细胞具有特定的物理化学特性,在设计广泛的药物递送系统(DDS)时可予以考虑。其中一些特性包括不同的温度环境,当温度在40至43°C之间时它们的敏感性会诱导细胞凋亡,癌细胞的细胞内和细胞外pH值分别在6.0至6.8之间,正常细胞的pH值在6.5至7.4之间,(溶酶体酸性pH值范围为4-5)。其他重要因素是肿瘤表面过度表达的受体。使用蒽环类药物阿霉素进行了负载和释放研究,并通过MTT法在健康和患病细胞系中评估了它们的细胞毒性。这项工作的亮点是进行了体外和体内研究,以评估不同纳米结构的生物分布、药代动力学和本身的毒性。