Development of Biodegradable GQDs-hMSNs for Fluorescence Imaging and Dual Cancer Treatment via Photodynamic Therapy and Drug Delivery.
Sarah ReagenYingfen WuDi SunCarlos MunozNuri OncelColin CombsJulia Xiaojun ZhaoPublished in: International journal of molecular sciences (2022)
Recently, nano-based cancer therapeutics have been researched and developed, with some nanomaterials showing anticancer properties. When it comes to cancer treatment, graphene quantum dots (GQDs) contain the ability to generate 1 O 2 , a reactive oxidative species (ROS), allowing for the synergistic imaging and photodynamic therapy (PDT) of cancer. However, due to their small particle size, GQDs struggle to remain in the target area for long periods of time in addition to being poor drug carriers. To address this limitation of GQDs, hollow mesoporous silica nanoparticles (hMSNs) have been extensively researched for drug delivery applications. This project investigates the utilization and combination of biomass-derived GQDs and Stöber silica hMSNs to make graphene quantum dots-hollow mesoporous silica nanoparticles (GQDs-hMSNs) for fluorescent imaging and dual treatment of cancer via drug delivery and photodynamic therapy (PDT). Although the addition of hMSNs made the newly synthesized nanoparticles slightly more toxic at higher concentrations, the GQDs-hMSNs displayed excellent drug delivery using fluorescein (FITC) as a mock drug, and PDT treatment by using the GQDs as a photosensitizer (PS). Additionally, the GQDs retained their fluorescence through the surface binding to hMSNs, allowing them to still be used for cell-labeling applications.
Keyphrases
- photodynamic therapy
- fluorescence imaging
- drug delivery
- quantum dots
- papillary thyroid
- cancer therapy
- squamous cell
- high resolution
- drug release
- single cell
- lymph node metastasis
- emergency department
- small molecule
- quality improvement
- oxidative stress
- carbon nanotubes
- bone marrow
- single molecule
- childhood cancer
- fluorescent probe
- living cells
- adverse drug