研究目的
To develop a novel electrochemiluminescence (ECL) method for the detection and determination of caspase-3 activity based on reduced graphene oxide sheets decorated by gold nanoparticles as signal amplification element and horseradish peroxidase enzyme (HRP) as ECL intensity enhancing agent.
研究成果
The prepared peptide based biosensor could be considered as an excellent candidate for early detection of apoptosis, cell turnover, and cancer related diseases, with a linear dynamic range of 0.5-100 fM and a lower limit of quantification of 0.5 fM.
研究不足
The study does not explicitly mention limitations, but potential areas for optimization could include further enhancing the sensitivity and selectivity of the biosensor, reducing the complexity of the biosensor fabrication process, and expanding the range of detectable caspase-3 activities.
1:Experimental Design and Method Selection:
The study employed a novel electrochemiluminescence (ECL) method for caspase-3 activity detection, utilizing reduced graphene oxide (RGO) decorated with gold nanoparticles (AuNPs) and horseradish peroxidase (HRP) enzyme.
2:Sample Selection and Data Sources:
A549 epithelial cell line was used as real samples for validation.
3:List of Experimental Equipment and Materials:
Equipment included Autolab PGSTAT302N, Hamamatsu photomultiplier, FE-SEM, Siemens D 5000 XRD, Shimadzu FT-IR spectrophotometer. Materials included GO, MPTMS, sodium borohydride, trisodium citrate, tetrachloroaurate, hydrogen peroxide, MCH, luminol, biotinylated peptide, biotinylated HRP, streptavidin coated magnetic beads.
4:Experimental Procedures and Operational Workflow:
Functionalization of GO, cell culture, apoptosis induction, biosensor preparation including electrode cleaning and modification steps, ECL characterization, optimization of operation parameters, and real sample analysis.
5:Data Analysis Methods:
Electrochemical measurements were analyzed using CV and EIS techniques; ECL intensity was measured and analyzed for caspase-3 activity determination.
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