Synthesization, characterization, and in vitro evaluation of cytotoxicity of biomaterials based on halloysite nanotubes
- Antonio Sánchez-Fernández,
- ,
- ,
- Rodrigo Cué-Sampedro,
- Ana Mendoza-Martínez,
- Viviana C. Zomosa-Signoret
- Instituto Tecnologico de Estudios Superiores de Monterrey,
- Universidad de,
- Hospital Universitario Dr. Jose Eleuterio Gonzalez
Research Output:
Contribution to journal
Article
Peer-reviewPublication metrics
Metrics
SciVal
FWCI
0.40
SciVal
Author count
8
SciVal
Citations
35
SciVal
Paper percentile
51
Abstract
Halloysite is an aluminosilicate clay that has been widely used for controlled drug delivery, immobilization of enzymes, and for the capture of circulating tumor cells (CTCs). Surface modification of halloysite by organosilanes has been explored to improve their properties. In this study halloysite clay nanotubes (HNTs) were functionalized by two different organosilanes: Trimethoxy(propyl)silane (TMPS), and Triethoxy(octyl)silane (EOS). Untreated and modified samples were characterized by scanning electron microscopy (SEM), X-ray diffractometry (XRD), thermogravimetrical analysis (TGA), and Fourier transform infrared spectroscopy (FTIR). Results showed a strong interaction of organosilanes with the chemical groups present in HNTs. Biocompatibility and cytotoxicity of these nanomaterials were determined using C6 rat glioblastoma cells. Our results indicate that prior to functionalization, HNTs show a high biocompatibility and low cytotoxicity. However, HNTs functionalized with EOS and TMPS showed high cytotoxicity by inducing apoptosis. These results allow the identification of potential applications in biomedical areas for HNTs.
Publication Information
Output type
Research Output:
Contribution to journal
Article
Peer-reviewOriginal language
EnglishPages from-to (Number of pages)
Pages 7770-7780 (11 pages)Journal (Volume, Issue Number)
Materials (Volume 7, Issue 12)Publication milestones
- Published - 01/01/2014
Publication status
Published - 01/01/2014
ISSN
1996-1944Publication IDs
- Scopus: 84921269989
- PubMed: 28788274
