Preparation, characterization and in vitro release study of drug-loaded sodium carboxy-methylcellulose/chitosan composite sponge.
Baoyi CaiTian ZhongPeizhou ChenJia FuYuanbao JinYinglei LiuRan HuangLianjiang TanPublished in: PloS one (2018)
A sodium carboxy-methylcellulose (CMC)/chitosan (CS) composite sponge as drug carrier was prepared, and its structure and functions were investigated. Samples with different CMC/chitosan ratios and under different pH conditions were synthesized via a freeze-drying method. The microstructure of the dried sponges was analyzed by Scanning Electron Microscope (SEM). Molecule interactions between polymers were confirmed by Fourier transform infrared (FTIR) spectra and Thermal gravimetric analyze (TGA). The swelling degree, weight loss, in vitro drug release behavior and antibacterial property of the sponges were determined as well. The results showed that the CMC/chitosan ratio and the pH value significantly affected the appearance of the blending solution and the microstructure of the final product, and also affected the sponge's degradation behavior, drug-loading capacity and the antibacterial activity. Gentamicin (GEN) as a hydrophilic model drug was remarkably superior to the other two hydrophobic drugs, ibuprofen (IBU) and roxithromycin (ROX), with respect to in vitro releasing. Moreover, higher CMC content and lower pH value of the sponge were confirmed to lead a larger loading for GEN. The bacteriostatic experiment showed a strong antimicrobial ability of GEN-loaded sponges on inhibiting Escherichia coli.
Keyphrases
- drug delivery
- drug release
- wound healing
- escherichia coli
- cancer therapy
- weight loss
- white matter
- adverse drug
- bariatric surgery
- type diabetes
- staphylococcus aureus
- signaling pathway
- emergency department
- cystic fibrosis
- multidrug resistant
- roux en y gastric bypass
- molecular dynamics
- electron microscopy
- mass spectrometry
- pseudomonas aeruginosa
- molecularly imprinted
- high speed
- density functional theory
- aqueous solution
- tandem mass spectrometry