Novel Carboxymethyl Cellulose-Based Hydrogel with Core-Shell Fe 3 O 4 @SiO 2 Nanoparticles for Quercetin Delivery.
Mohammad Mahdi EshaghiMehrab PourmadadiAbbas RahdarAna Maria Diez-PascualPublished in: Materials (Basel, Switzerland) (2022)
A nanocomposite composed of carboxymethyl cellulose (CMC) and core-shell nanoparticles of Fe 3 O 4 @SiO 2 was prepared as a pH-responsive nanocarrier for quercetin (QC) delivery. The nanoparticles were further entrapped in a water-in-oil-in-water emulsion system for a sustained release profile. The CMC/Fe 3 O 4 @SiO 2 /QC nanoparticles were characterized using dynamic light scattering (DLS), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), a field emission scanning electron microscope (FE-SEM), and a vibrating sample magnetometer (VSM) to obtain insights into their size, stability, functional groups/chemical bonds, crystalline structure, morphology, and magnetic properties, respectively. The entrapment and loading efficiency were slightly improved after the incorporation of Fe 3 O 4 @SiO 2 NPs within the hydrogel network. The dialysis method was applied for drug release studies. It was found that the amount of QC released increased with the decrease in pH from 7.4 to 5.4, while the sustained-release pattern was preserved. The A549 cell line was chosen to assess the anticancer activity of the CMC/Fe 3 O 4 @SiO 2 /QC nanoemulsion and its components for lung cancer treatment via an MTT assay. The L929 cell line was used in the MTT assay to determine the possible side effects of the nanoemulsion. Moreover, a flow cytometry test was performed to measure the level of apoptosis and necrosis. Based on the obtained results, CMC/Fe 3 O 4 @SiO 2 can be regarded as a novel promising system for cancer therapy.
Keyphrases
- drug delivery
- drug release
- cancer therapy
- magnetic nanoparticles
- flow cytometry
- electron microscopy
- high throughput
- magnetic resonance imaging
- oxidative stress
- ionic liquid
- chronic kidney disease
- walled carbon nanotubes
- endoplasmic reticulum stress
- hyaluronic acid
- magnetic resonance
- wound healing
- quantum dots
- reduced graphene oxide
- tissue engineering
- fatty acid
- signaling pathway
- cell cycle arrest
- room temperature
- contrast enhanced