2021
DOI: 10.1016/j.colsurfb.2021.111597
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Synthesis and characterization of an injectable microparticles integrated hydrogel composite biomaterial: In-vivo biocompatibility and inflammatory arthritis treatment

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Cited by 17 publications
(9 citation statements)
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“…After incubating in media containing different concentrations of gels for 72 h, no morphology changes of MRC-5 cells were observed (Figure 4a), and the cell viability was high (>93%) even at a strong concentration of 0.5 wt% (Figure 4b), highlighting the non-toxicity to human normal cells. [51,52] Furthermore, the mineral hydrogels reported here are synthesized in a water-based setting with essential elements for life (Fe, Mo). Such excellent biocompatibility stems from its bio-essential components of Fe and Mo, and by its strictly water-based medium.…”
Section: Biocompatibility and Swelling Resistance Studymentioning
confidence: 99%
“…After incubating in media containing different concentrations of gels for 72 h, no morphology changes of MRC-5 cells were observed (Figure 4a), and the cell viability was high (>93%) even at a strong concentration of 0.5 wt% (Figure 4b), highlighting the non-toxicity to human normal cells. [51,52] Furthermore, the mineral hydrogels reported here are synthesized in a water-based setting with essential elements for life (Fe, Mo). Such excellent biocompatibility stems from its bio-essential components of Fe and Mo, and by its strictly water-based medium.…”
Section: Biocompatibility and Swelling Resistance Studymentioning
confidence: 99%
“…The polymer has the advantages of low toxicity and good biocompatibility, so it has a wide range of applications in pharmacology. 26 For example, Piotto et al 27 loaded clofazimine into a hydrogel prepared from nanocellulose and Tween-20 for drug release. It was found that the hydrogel was formed by ionic action, and its drug loading was as high as 37%, which can increase the solubility of the drug in water by about 50 times without requiring complicated preparation steps.…”
Section: Introductionmentioning
confidence: 99%
“…In the FTIR spectrum of OSA, the absorption peak at 1737 cm −1 attributed to aldehyde groups indicated the forming of OSA by oxidation of the SA 30 . As the FTIR spectrum of CMCS/OSA hydrogel, the aldehyde peak locked at 1735 cm −1 was disappeared, while a new peak appeared at 1625 cm −1 attributed to imine group, indicating the amino group of CMCS reacted with the aldehyde group of OSA 31 . Furthermore, the absorption peaks at 3445 cm −1 were split into two peaks, usually a sign of crosslinking occurred between amino group and dialdehyde group.…”
Section: Resultsmentioning
confidence: 96%
“…30 As the FTIR spectrum of CMCS/OSA hydrogel, the aldehyde peak locked at 1735 cm À1 was disappeared, while a new peak appeared at 1625 cm À1 attributed to imine group, indicating the amino group of CMCS reacted with the aldehyde group of OSA. 31 Furthermore, the absorption peaks at 3445 cm À1 were split into two peaks, usually a sign of crosslinking occurred between amino group and dialdehyde group. In spectrum of the MPs/CMCS/OSA hydrogel, the peaks ascribed to bending and stretching vibrations of CH 2 at 1325 and 2932 cm À1 were moved to 1322 and 2926 cm À1 , respectively.…”
Section: Sample Characterizationmentioning
confidence: 99%