William Talavera-Pech

Dr. William Talavera-Pech

Corrosion Research Center, Autonomous University of Campeche, Campeche, Mexico
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Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 April 2021 in Materials
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Journal Article
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WTWilliam Talavera-Pech
William Talavera-Pech
DMDiana Montiel-Rodríguez
Diana Montiel-Rodríguez
JEJOSEFA PAAT ESTRELLA
JOSEFA PAAT ESTRELLA
RLRUTH LOPEZ
RUTH LOPEZ
JPJosé Trinidad Pérez-Quiroz
José Trinidad Pérez-Quiroz
TPTezozomoc Pérez
Tezozomoc Pérez
In this work, sugarcane bagasse fiber, a waste product of agroindustry, was added to mortar mixes at different proportions looking to seal porosities so as to improve the resistance of concrete to carbonation and to improve its mechanical properties. To evaluate the behavior of bagasse fibers in the alkaline media typical of mortars, bagasse fibers were subjected to solutions with alkaline pH values, and their chemical structure and morphological behavior was evaluated using FTIR (Fourier transform infrared spectroscopy) and SEM (Scanning Electron Microscopy). Using mortar cylinders in an accelerated carbonation chamber to obtain results in short lapses, the compressive strength and the carbonation were evaluated. The FTIR analysis results indicate that pH values of 11 and 12 causes a delignification, while at pH 9 and 10, a swelling of the molecule occurs because of the addition of hydroxyl ions, behavior that is confirmed with SEM images. A clear effect of the fiber addition on the performance of concrete was observed as the carbonation front of 35 mm for the sample without fibers was reduced to 2 mm for the sample with 2% fiber addition, resulting in an increase of 5 MPa in compressive strength. These results indicate that in the range of mortar pH, chemical changes occured over the sugarcane surface that could cause the growth of fibers and could partially seal the porosity in the mortars, thus enhancing its performance.

26 September 2022 in Journal of Coatings Technology and Research
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Journal Article
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EUErik Uc-Fernández
Erik Uc-Fernández
JGJorge González-Sánchez
Jorge González-Sánchez
AÁAlejandro Ávila-Ortega
Alejandro Ávila-Ortega
YPYamile Pérez-Padilla
Yamile Pérez-Padilla
JCJ. Manuel Cervantes-Uc
J. Manuel Cervantes-Uc
WTWilliam Talavera-Pech
William Talavera-Pech

27 October 2020 in Current Drug Delivery
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AAAlejandro Avila-Ortega
Alejandro Avila-Ortega
LCLeydi Carrillo
Leydi Carrillo
COChristofer Enmanuel Olán-Noverola
Christofer Enmanuel Olán-Noverola
GNGeovanny I. Nic-Can
Geovanny I. Nic-Can
AVAlfredo Rafael Vilchis-Nestor
Alfredo Rafael Vilchis-Nestor
WTWilliam Talavera-Pech
William Talavera-Pech
Background: The encapsulation of anti-cancer drugs in stimulus-sensitive release systems may provide advantages such as enhanced drug toxicity in tumour tissue cells due to increased intracellular drug release. Encapsulation may also improve release in targeted tissue due to the response to a stimulus such as pH, which is lower in the tumour tissue microenvironment. Here, we evaluated the in vitro toxicity of the Drug Doxorubicin (DOX) loaded into a release system based on poly(β-amino ester)- modified MCM-41 silica nanoparticles. Methods: The MCM-41-DOX-PbAE release system was obtained by loading DOX into MCM-41 nanoparticles amino-functionalized with 3-aminopropyltriethoxysilane (APTES) and then coated with a pH-responsive poly(β-amino ester) (PbAE). The physicochemical characteristics of the release system were evaluated through TEM, FTIR and TGA. Cytotoxicity assays were performed on the MCM-41- DOX-PbAE system to determine their effects on the inhibition of human MCF-7 breast cancer cell proliferation after 48 h of exposure through crystal violet assay; the investigated systems included MCF-7 cells with MCM-41, PbAE, and MCM-41-PbAE alone. Additionally, the release of DOX and the change in pH in vitro were determined. Results: The physicochemical characteristics of the synthesized MCM-41-PbAE system were confirmed, including the nanoparticle size, spherical morphology, mesoporous ordered structure, and presence of PbAE on the surface of the MCM-41 nanoparticles. Likewise, we demonstrated that the release of DOX from the MCM-41-DOX-PbAE system promoted an important reduction in MCF-7 cell viability (~ 70%) compared to the values obtained with MCM-41, PbAE, and MCM-41-PbAE, as well as a reduction in the viability under treatment with just DOX (~ 50%). Conclusions: The results suggest that all the components of the release system are biocompatible and that the encapsulation of DOX in MCM-41-PbAE could allow better intracellular release, which would probably increase the availability and toxic effect of DOX.

30 November 2022 in Pharmaceutics
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MAMartín Aguirre-Pulido
Martín Aguirre-Pulido
JGJorge Antonio Gonzalez-Sanchez
Jorge Antonio Gonzalez-Sanchez
LPLuis Román Dzib Pérez
Luis Román Dzib Pérez
MSMontserrat Soria-Castro
Montserrat Soria-Castro
AAAlejandro Avila-Ortega
Alejandro Avila-Ortega
WTWilliam Talavera-Pech
William Talavera-Pech
In this paper, a controlled-release system of caffeine as a corrosion inhibitor was obtained by encapsulating it in MCM-41 silica nanoparticles coated with a poly(β-amino ester) (PbAE), a pH-sensible polymer. Encapsulation was verified using Fourier transform infrared spectroscopy (FTIR) and thermogravimetry (TGA). The release of caffeine from the nanocontainers was analyzed in electrolytes with pH values of 4, 5, and 7 using UV–Vis, showing a 21% higher release in acidic electrolytes than in neutral electrolytes, corroborating its pH sensitivity. Electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization were used to determine the inhibition mode and efficiency of the encapsulated and free caffeine. The caffeine released from the nanocontainers showed the highest efficiency, which was 85.19%. These results indicate that these nanocontainers could have potential use in smart anticorrosion coating applications.

3 November 2022 in Silicon
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MRMarina S. Ramírez-Arévalo
Marina S. Ramírez-Arévalo
TPTezozomoc Pérez-López
Tezozomoc Pérez-López
PQPatricia Quintana-Owen
Patricia Quintana-Owen
GMGerardo del J. Fajardo-San Miguel
Gerardo del J. Fajardo-San Miguel
WTWilliam Talavera-Pech
William Talavera-Pech

3 June 2024 in ChemistrySelect
Verified
Journal Article
Closed access
VAValentina Aguilar‐Melo
Valentina Aguilar‐Melo
IPIldefonso E. Pech‐Pech
Ildefonso E. Pech‐Pech
ÁBÁngel A. Bacelis‐Jiménez
Ángel A. Bacelis‐Jiménez
WTWilliam Talavera-Pech
William Talavera-Pech