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. 2023 Feb 14;9(3):e13705.
doi: 10.1016/j.heliyon.2023.e13705. eCollection 2023 Mar.

pH-responsive gelatin polymer-coated silica-based mesoporous composites for the sustained-release of indomethacin

Affiliations

pH-responsive gelatin polymer-coated silica-based mesoporous composites for the sustained-release of indomethacin

Bo Yu et al. Heliyon. .

Abstract

This paper prepared drug-loaded mesoporous silica composites with a pH-responsive type. These composites were prepared by using three-dimensional caged silica (SBA-16) as the carrier, 3-aminopropyl trimethoxysilane (APTMS) as the silane coupling agent, and indomethacin (IMC) as the loaded drug, respectively. The drug-loaded precursor NH2-SBA-16@IMC was prepared by solution diffusion adsorption. Finally, the pH-responsive drug-loaded composites NH2-SBA-16@IMC@GA were synthesized by wrapping the NH2-SBA-16@IMC with a condensation polymer of gelatin and glutaraldehyde. The composition and structure of the drug-loaded composites were characterized by FT-IR, XRD, TG, SEM, TEM, and N2 adsorption-desorption. The in vitro simulated release performance of the drug-loaded composites was investigated at 37 °C under three pH conditions. The results show that the NH2-SBA-16@IMC@GA can be released in response to specific pH environment, which can effectively control the release speed of the indomethacin.

Keywords: Drug carrier; Gelatin coating; In vitro release; Mesoporous; SBA-16; pH-responsive.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Image 1
Graphical abstract
Scheme 1
Scheme 1
Schematic representation of the preparation process of NH2-SBA-16@IMC@GA drug-loaded composite.
Fig. 1
Fig. 1
The FT-IR spectra of IMC, SBA-16, NH2-SBA-16, SBA-16@IMC, NH2-SBA-16@IMC, SBA-16@IMC@GA and NH2-SBA-16@IMC@GA composites.
Fig. 2
Fig. 2
The small-angle XRD patterns of IMC, SBA-16, NH2-SBA-16, SBA-16@IMC, NH2-SBA-16@IMC, SBA-16@IMC@GA and NH2-SBA-16@IMC@GA.
Fig. 3
Fig. 3
The wide-angle XRD patterns of IMC, SBA-16, NH2-SBA-16, SBA-16@IMC, NH2-SBA-16@IMC, SBA-16@IMC@GA, and NH2-SBA-16@IMC@GA.
Fig. 4
Fig. 4
The Nitrogen adsorption–desorption isotherms of IMC, SBA-16, NH2-SBA-16, SBA-16@IMC, NH2-SBA-16@IMC, SBA-16@IMC@GA, and NH2-SBA-16@IMC@GA.
Fig. 5
Fig. 5
The Pore size distribution of IMC, SBA-16, NH2-SBA-16, SBA-16@IMC, NH2-SBA-16@IMC, SBA-16@IMC@GA, and NH2-SBA-16@IMC@GA.
Fig. 6
Fig. 6
The thermogravimetric curves of IMC, SBA-16, NH2-SBA-16, SBA-16@IMC, NH2-SBA-16@IMC, SBA-16@IMC@GA and NH2-SBA-16@IMC@GA.
Fig. 7
Fig. 7
The electron microscope photos of SBA-16 (A and B), NH2-SBA-16 (C and D), NH2-SBA-16@IMC (E and F), and NH2-SBA-16@IMC@GA (G and H).
Fig. 8
Fig. 8
Cumulative release of SBA-16@IMC, NH2-SBA-16@IMC, SBA-16@IMC@GA, and NH2-SBA-16@IMC@GA at pH = 2.0.
Fig. 9
Fig. 9
Cumulative release of SBA-16@IMC, NH2-SBA-16@IMC, SBA-16@IMC@GA, and NH2-SBA-16@IMC@GA at pH = 7.4.
Fig. 10
Fig. 10
Drug release of NH2-SBA-16@IMC@GA under different pH conditions.
Scheme 2
Scheme 2
Schematic diagram of the pH-responsive slow release of the NH2-SBA-16@IMC@GA drug-loaded composite.

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