Electrochemically Reduced Carboxyl Graphene Modified Electrode for Simultaneous Determination of Guanine and Adenine

<div><p>An electrochemically reduced carboxyl graphene modified glassy carbon electrode (ERCGr/GCE) was prepared from a carboxyl graphene modified glassy carbon electrode (CGr/GCE) and employed for the simultaneous determination of guanine and adenine. The ERCGr/GCE showed an enhanced voltammetric response toward the oxidation of guanine and adenine compared with the CGr/GCE because the conductivity and electrochemical active surface area increased during the reduction process. The voltammetric peak current was linearly dependent on guanine and adenine concentration over the ranges of 0.5–10 and 2.5–50 µmol L⁻¹, respectively. The detection limits were 0.15 µmol L⁻¹ for guanine and 0.10 µmol L⁻¹ for adenine in 50 µmol L⁻¹ phosphate buffer at pH 6.86. Determination of guanine and adenine in thermally denatured herring sperm DNA showed that the ratio of guanine/adenine was 0.758 demonstrating practical application of the ERCGr/GCE.</p></div

Small Molecule-Initiated Light-Activated Semiconducting Polymer Dots: An Integrated Nanoplatform for Targeted Photodynamic Therapy and Imaging of Cancer Cells

Photodynamic therapy (PDT) is a noninvasive and light-activated method for cancer treatment. Two of the vital parameters that govern the efficiency of PDT are the light irradiation to the photosensitizer and visual detection of the selective accumulation of the photosensitizer in malignant cells. Herein, we prepared an integrated nanoplatform for targeted PDT and imaging of cancer cells using folic acid and horseradish peroxidase (HRP)-bifunctionalized semiconducting polymer dots (FH-Pdots). In the FH-Pdots, meta-tetra­(hydroxyphenyl)-chlorin (m-THPC) was used as photosensitizer to produce cytotoxic reactive oxygen species (ROS); fluorescent semiconducting polymer poly­[2-methoxy-5-((2-ethylhexyl)­oxy)-<i>p</i>-phenylenevinylene] was used as light antenna and hydrophobic matrix for incorporating m-THPC, and amphiphilic Janus dendrimer was used as a surface functionalization agent to conjugate HRP and aminated folic acid onto the surface of FH-Pdots. Results indicated that the doped m-THPC can be simultaneously excited by the on-site luminol–H₂O₂–HRP chemiluminescence system through two paths. One is directly through chemiluminescence resonance energy transfer (CRET), and the other is through CRET and subsequent fluorescence resonance energy transfer. In vitro PDT and specificity studies of FH-Pdots using a standard transcriptional and translational assay against MCF-7 breast cancer cells, C6 glioma cells, and NIH 3T3 fibroblast cells demonstrated that cell viability decreased with increasing concentration of FH-Pdots. At the same concentration of FH-Pdots, the decrease in cell viability was positively relevant with increasing folate receptor expression. Results from in vitro fluorescence imaging exhibited that more FH-Pdots were internalized by cancerous MCF-7 and C6 cells than by noncancerous NIH 3T3 cells. All the results demonstrate that the designed semiconducting FH-Pdots can be used as an integrated nanoplatform for targeted PDT and on-site imaging of cancer cells