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co-condensation synthesis of salicylaldimine calcium complex containing mesoporous silica nanoparticles as carriers for drug release

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Abstract

A series of functional mesoporous silica nanoparticles(MSNs) was synthesized by a one-step simple synthesis approach involving co-condensation of tetraethoxysilane(TEOS) and salicylaldimine ligand(Sal-Si) in the presence of cetyltrimethylammonium chloride(CTAC) under basic conditions. The target MSNs with different sizes (50, 100 and 200 nm, respectively) were obtained. Furthermore, the Ca2+ cations were also introduced into MSNs. The prepared nanoparticles were characterized by means of infrared(IR) spectra, thermogravimetric analysis(TGA), inductively coupled plasma(ICP), CHN elemental analysis, nitrogen adsorption-desorption, scanning electron microscope( SEM) and transmission electron microscope(TEM). Ibuprofen(IBU) which contains carboxyl groups was selected as a model drug. The results of drug loading and release reveal that the loading capacities and release behaviors of the model drug are highly dependent on the Ca2+ cations in MSNs. The release of IBU from the MSNs functionalized by Ca2+ cations is found to be effectively controlled when compared to the release from the MSNs without the functionalization of Ca2+ cations, which is due to the ionic interaction between carboxyl groups in IBU and Ca2+ cations in MSNs.

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Correspondence to Lirong Zhang.

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Supported by the National Natural Science Foundation of China(Nos. 21371067, 21171064).

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Tang, D., Zhang, W., Wang, Y. et al. co-condensation synthesis of salicylaldimine calcium complex containing mesoporous silica nanoparticles as carriers for drug release. Chem. Res. Chin. Univ. 30, 531–537 (2014). https://doi.org/10.1007/s40242-014-4097-8

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  • DOI: https://doi.org/10.1007/s40242-014-4097-8

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