| Literature DB >> 29893047 |
Uma Keyal1, Qiong Luo2, Anil K Bhatta1, Hansen Luan3, Ping Zhang4, Qianqian Wu1, Haiyan Zhang1, Pei Liu1, Linglin Zhang1, Peiru Wang1, Degang Yang1, Guolong Zhang1, Jing Yao4, Xiuli Wang1, Lei Shi1.
Abstract
Zinc pthalocyanine (ZnPc) is a second-generation photodynamic therapy (PDT) sensitizer with sufficient PDT activity for squamous cell carcinoma (SCC). ZnPc is hydrophobic and insoluble in water, which creates hurdles in systemic administration and hence restricts its use in clinic. Here we have loaded ZnPc on chitosan/methoxy polyethylene glycol-polylactic acid (CPP) nanoparticles to form Z-CPP to enhance PDT efficacy. In vitro and in vivo studies were performed to see dark toxicity of the compounds ZnPc, CPP and Z-CPP. Then PDT was done and its growth inhibitory effect on SCC cells was evaluated. In addition, reactive oxygen species (ROS) formation and apoptosis of cancer cells following PDT were studied. The results showed that the tested compounds exhibit no dark toxicity and the effect of PDT was significantly better with Z-CPP when compared to free ZnPc (P < .05). Photoactivation of Z-CPP led to a dose-dependent growth inhibition of cancer cells of >50% at 1 μM to >80% at 10 μM concentration. Also Z-CPP-treated cells had highest number of apoptotic cells and produced more ROS compared to free ZnPc-treated cells (P < .05). Hence, this study suggests that Z-CPP is a suitable pharmaceutical compound to increase PDT efficacy.Entities:
Keywords: chitosan/mPEG-PLA; nanoparticles; photodynamic therapy; photosensitizer; squamous cell carcinoma; zinc pthalocyanine
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Year: 2018 PMID: 29893047 DOI: 10.1002/jbio.201800114
Source DB: PubMed Journal: J Biophotonics ISSN: 1864-063X Impact factor: 3.207