MATERIALS TRANSACTIONS
Online ISSN : 1347-5320
Print ISSN : 1345-9678
ISSN-L : 1345-9678
TiO2@SiO2 Nanoparticles Functionalized with Para-Aminobenzoic Acid (PABA) by Fisher Esterification Reaction
María L. Carrera-JotaMargarita García-HernándezErnesto Rivera-BecerrilJorge H. Luna-DomínguezÁngel de J. Morales-RamírezArturo López-MarurePerla Y. López-CamachoBrenely González-Penguelly
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2019 年 60 巻 9 号 p. 2033-2040

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In this work, hybrid TiO2 nanoparticles embedded in SiO2 were obtained by means of sol-gel process, testing different proportions of the silicon and titanium oxides to obtain TiO2 particles with a high surface content of hydroxyl groups. Anatase crystalline form of TiO2 is a widely used material in active-substance release studies, due to its optimal properties for the transport, distribute and release of different molecules into biological systems. According to the X-ray diffraction analysis, all the proportions of evaluated hybrid systems presented the anatase phase, however, the molar proportion (20:80, TiO2:SiO2) contains a high quantity of hydroxyl groups according to infrared spectroscopy. The spherical morphology of the particles were observed by scanning electron microscopy forming agglomerates. The functionalization of these surfaces was carried out using para-aminobenzoic acid as a drug-binding model that generated a covalent bond between the TiO2@SiO2 system, likewise, thermogravimetric analysis identified the content of functionalized PABA. Dynamic light scattering showed particles and agglomerates around 25–609 nm and negative value of zeta (ζ)-potential in the molar ratio TiO2:SiO2 20:80-PABA. Finally, we demonstrated that PABA hydrolyzes in the presence of human plasma, recovering the nanoparticularized systems with the hydroxyl groups. The hydroxyl groups on the particle surface promote the incorporation of organic molecules that contain carboxyl groups in their structure.

Fig. 1 General scheme of TiO2@SiO2 functionalized with para-aminobenzoic acid (PABA) by Fisher esterification. Fullsize Image
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© 2019 The Japan Institute of Metals and Materials
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