In this work, polyacrylic acid-functionalized MCM-41 was synthesized, which was made to interact with calcium ions, in order to realize enhanced pH-responsive nanocarriers for sustained drug release. First, mesoporous silica nanoparticles (MSNs) were prepared by the sol-gel method. Afterward, a (3-trimethoxysilyl)propyl methacrylate (TMSPM) modified surface was prepared by using the post-grafting method, and then the polymerization of the acrylic acid was performed. After adding a calcium chloride solution, polyacrylic acid-functionalized MSNs with calcium-carboxyl ionic bonds in the polymeric layer, which can prevent the cargo from leaking out of the mesopore, were prepared. The structure and morphology of the modified nanoparticles (PAA-MSNs) were characterized by X-ray diffraction (XRD), Fourier-transform infrared (FT-IR) spectroscopy, transmission electron microscopy (TEM), and N2 adsorption–desorption analysis, etc. The controlled release of guest molecules was studied by using 5-fluorouracil (5-FU). The drug molecule-incorporated nanoparticles showed different releasing rates under different pH conditions. It is considered that our current materials have the potential as pH-responsive nanocarriers in the field of medical treatment.
In this work, polyacrylic acid-functionalized MCM-41 was synthesized, which was further interacted with calcium ions, to realize enhanced pH-responsive nanocarrier for sustained drug release. First, mesoporous silica nanoparticles (MSNs) were prepared by the sol-gel method. Afterward, (3-trimethoxysilyl)propyl methacrylate (TMSPM) modified surface was prepared by using the post-grafting method, then polymerization of acrylic acid was proceeded. After adding calcium chloride solution, polyacrylic acid-functionalized MSNs with calcium-carboxyl ionic bonds in the polymeric layer, which can prevent the cargo from leaking out of the mesopore, were prepared. The structure and morphology of the modified nanoparticles (PAA-MSNs) were characterized by X-ray diffraction (XRD), Fourier-transform infrared (FT-IR) spectroscopy, transmission electron microscopy (TEM), and N2 adsorption-desorption analysis, etc. The controlled release of guest molecules was studied by using 5-fluorouracil (5-FU). The drug molecules-incorporated nanoparticles showed different releasing rates under different pH conditions. It is considered that our current materials have the potential as pH-responsive targeted nanocarriers in the field of medical treatment.
In this study, we examined the highly selective sensing of Fe3+ ions in water using metal complex-functionalized mesoporous silica materials. Metal complex-functionalized mesoporous silica materials were synthesized on the mesoporous surface of SBA-15 via complexation process
between Eu3+ and aminosilane groups. Mesoporous silica, SBA-15, and the Eu3+-complex functionalized SBA-15 were characterized using X-ray diffraction (XRD), transmittance electron microscopy (TEM), nitrogen sorption behavior, and Fourier transform infrared (FTIR) spectroscopy.
The sensing behavior of the Eu3+-complex functionalized SBA-15 was studied using various metal ions (Fe3+, Cu2+, Cr3+, Co2+, Hg2+, Pb2+, and Zn2+) aqueous solutions. Photoluminescence intensity (λ
= 612 nm) of the Eu3+-complex functionalized SBA-15 was dependent on the different interactions between metal ions and Eu3+-complexes. Photoluminescence intensity at λ = 612 nm of the Eu3+-complex functionalized SBA-15 decreased to near zero and
proved the highly selective sensing effect of Fe3+. Therefore, the Eu3+-complex functionalized SBA-15 can be considered an excellent candidate for sensing iron ions in water.
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