Doshi Mona, Copik Alicja, Gesquiere Andre J
NanoScience Technology Center, Department of Chemistry, Department of Materials Science and Engineering, and CREOL, The College of Optics and Photonics, University of Central Florida, 12424 Research Parkway Suite 400, Orlando, FL 32826, USA.
Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, 6900 Lake Nona Boulevard, Orlando, FL 32827, USA.
Photodiagnosis Photodyn Ther. 2015 Sep;12(3):476-89. doi: 10.1016/j.pdpdt.2015.04.010. Epub 2015 May 11.
Conducting polymer nanoparticles (CPNPs), composed of the conducting polymer poly[2-methoxy-5-(2-ethylhexyl-oxy)-p-phenylenevinylene] (MEH-PPV) were studied for applications in biophotonics and therapeutics. The extent of cellular uptake, cytotoxicity, and effectiveness of these nanoparticles in photodynamic therapy (PDT) was investigated for four cell lines, namely TE-71, MDA-MB-231, A549 and OVCAR3. Confocal fluorescence imaging and flow cytometry show that CPNPs are taken up only in limited quantities by TE-71, while they are taken up extensively by the cancer cell lines. The uptake among the cancer cell lines was observed to vary with cell line, with CPNPs uptake increasing from MDA-MB-231 to A549 to OVCAR3. Fluorescence imaging experiments show that the CPNPs have high brightness and appear stable in the intracellular environment. No cytotoxicity of non-photoactivated CPNPs (in dark) was observed from MTT assay. After completion of PDT, the quantitative data on cell viability suggest that cell death scales across the cell lines with CPNP uptake, is light dose dependent, and is complete for OVCAR3. In addition, for OVCAR3 apoptotic cell death is observed after PDT. The reported work illustrates the potential of the intrinsically fluorescent and photoactivateable CPNPs for application in biophotonics and therapeutics.
对由导电聚合物聚2-甲氧基-5-(2-乙基己氧基)-对苯撑乙烯撑组成的导电聚合物纳米颗粒(CPNPs)进行了生物光子学和治疗应用研究。针对四种细胞系,即TE-71、MDA-MB-231、A549和OVCAR3,研究了这些纳米颗粒在细胞摄取程度、细胞毒性以及光动力疗法(PDT)中的有效性。共聚焦荧光成像和流式细胞术表明,TE-71对CPNPs的摄取量有限,而癌细胞系对其摄取广泛。观察到癌细胞系之间的摄取情况因细胞系而异,CPNPs的摄取量从MDA-MB-231到A549再到OVCAR3逐渐增加。荧光成像实验表明,CPNPs具有高亮度,并且在细胞内环境中表现稳定。MTT分析未观察到非光活化CPNPs(在黑暗中)的细胞毒性。PDT完成后,关于细胞活力的定量数据表明,细胞死亡程度随CPNP摄取量在各细胞系中变化,与光剂量有关,并且OVCAR3细胞系的细胞死亡完全。此外,对于OVCAR3细胞系,PDT后观察到凋亡性细胞死亡。所报道的工作说明了具有内在荧光和可光活化的CPNPs在生物光子学和治疗应用中的潜力。