Chitosan-functionalized Fe3O4@SiO2 nanoparticles as a potential drug delivery system
This study developed and characterized the chitosan-functionalized Fe 3 O 4 @SiO 2 nanoparticles (Fe 3 O 4 @SiO 2 @CS NP) as a drug delivery system. Fe 3 O 4 NP were first synthesized by co-precipitation method, followed by coating with SiO 2 , and functionalized with chitosan via glutaraldehyde cro...
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Veröffentlicht in: | Chemical papers 2022-07, Vol.76 (7), p.4561-4570 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | This study developed and characterized the chitosan-functionalized Fe
3
O
4
@SiO
2
nanoparticles (Fe
3
O
4
@SiO
2
@CS NP) as a drug delivery system. Fe
3
O
4
NP were first synthesized by co-precipitation method, followed by coating with SiO
2
, and functionalized with chitosan via glutaraldehyde crosslinking bridges. The newly synthesized Fe
3
O
4
@SiO
2
@CS NP possessed an octagonal shape with a diameter of ~ 20 nm. In the FT-IR spectrum, the Fe
3
O
4
@SiO
2
@CS NP demonstrated the appearances of C–O, N–H, and C–H peaks, indicating the presence of chitosan in their structures. The Fe
3
O
4
@SiO
2
@CS NP could preserve the Fe
3
O
4
magnetic property with a magnetization value of 52.43 emu/g, a magnetization remanence of almost 0 emu/g, and minimal residual coercivity. Utilizing curcumin as a drug model, the Fe
3
O
4
@SiO
2
@CS NP could adsorb the drug rapidly, to more than 71% within 20 min, with an adsorption capacity of 6.54 mg/g and an adsorption energy of 0.2029 kJ/mol (following the Dubinin–Radushkevich model). The curcumin adsorption process was in good agreement with the pseudo-second-order kinetics (
R
2
= 0.9975). Interestingly, in the simulated body fluid, the curcumin-loaded Fe
3
O
4
@SiO
2
@CS NP could retain the curcumin release, with no detectable drug release, in the first hour, followed by a burst release within the next hour. This confirms the contribution of CS in the system. Conclusively, the Fe
3
O
4
@SiO
2
@CS NP could be further developed to potentially become a controlled-release drug delivery system. |
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ISSN: | 0366-6352 1336-9075 2585-7290 |
DOI: | 10.1007/s11696-022-02189-x |