Facile synthesis of Ca2+-crosslinked sodium alginate/graphene oxide hybrids as electro- and pH-responsive drug carrier

The design of stimuli-responsive drug carrier for controlled drug release is of significant importance in pharmaceutics, medicine and biology. Here, sodium alginate (SA) was integrated with graphene oxide (GO) by using Ca2+ as the crosslinker. The resultant SA-Ca2+-GO composites were freeze-dried to...

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Veröffentlicht in:Materials Science & Engineering C 2020-03, Vol.108, p.110380-110380, Article 110380
Hauptverfasser: Yun, Yajing, Wu, Hongwei, Gao, Jun, Dai, Wei, Deng, Linhong, Lv, Ouyang, Kong, Yong
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Sprache:eng
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Zusammenfassung:The design of stimuli-responsive drug carrier for controlled drug release is of significant importance in pharmaceutics, medicine and biology. Here, sodium alginate (SA) was integrated with graphene oxide (GO) by using Ca2+ as the crosslinker. The resultant SA-Ca2+-GO composites were freeze-dried to produce SA-Ca2+-GO hybrids, which were then examined by Fourier transform infrared (FT-IR) spectrometry, field emission scanning electron microscopy (FESEM) and atomic force microscopy (AFM). The SA-Ca2+-GO hybrids were used as the drug carrier of methotrexate (MTX), and electro- and pH-responsive release of MTX was successfully achieved due to the excellent conductive ability of GO and the pH-sensitive property of SA. Finally, Higuchi model was employed to investigate the release kinetics of MTX from the SA-Ca2+-GO hybrids, and the results indicate that the release of MTX is controlled by Fickian diffusion. [Display omitted] •SA-Ca2+-GO hybrids are facilely synthesized by using Ca2+ as the crosslinker.•The release of MTX from the SA-Ca2+-GO hybrids is electro- and pH-responsive.•Release kinetics study shows the release of MTX is controlled by Fickian diffusion.•It opens a new avenue for the synthesis of smart and stimuli-responsive drug carrier.
ISSN:0928-4931
1873-0191
DOI:10.1016/j.msec.2019.110380