Hector Ivan Melendez-Ortiz

Dr. Hector Ivan Melendez-Ortiz

Center for Research in Applied Chemistry, Blvd. Enrique Reyna Hermosillo 140, Saltillo 25294, Mexico
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Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

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

Representative Publications

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1 February 2019 in Carbohydrate Polymers
Verified
Journal Article
Closed access
ALAngélica Lumbreras-Aguayo
Angélica Lumbreras-Aguayo
Hector Ivan Melendez-OrtizHector Ivan Melendez-Ortiz
Hector Ivan Melendez-Ortiz
BPBertha Puente-Urbina
Bertha Puente-Urbina
CACarmen Alvarado-Canché
Carmen Alvarado-Canché
ALAntonio Ledezma
Antonio Ledezma
RBRebeca Betancourt-Galindo
Rebeca Betancourt-Galindo

Verified
Journal Article
Open access
PDF file
LGLluvia Azhalea Guerrero
Lluvia Azhalea Guerrero
Hector Ivan Melendez-OrtizHector Ivan Melendez-Ortiz
Hector Ivan Melendez-Ortiz
GMGladis Y Cortez Mazatan
Gladis Y Cortez Mazatan
SVSandra Sandra Vaillant-Sánchez
Sandra Sandra Vaillant-Sánchez
René D. PeraltaRené D. Peralta
René D. Peralta
The use of surfactants in polymerization reactions is particularly important, mainly in emulsion polymerizations. Further, micelles from biocompatible surfactants find use in pharmaceutical dosage forms. This paper reviews recent developments in the synthesis of novel gemini and bicephalous surfactants, micelle formation, and their applications in polymer and nanoparticle synthesis, oil recovery, catalysis, corrosion, protein binding, and biomedical area, particularly in drug delivery.

17 January 2019 in International Journal of Applied Ceramic Technology
Verified
Journal Article
Closed access
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Hector Ivan Melendez-OrtizHector Ivan Melendez-Ortiz
Hector Ivan Melendez-Ortiz
BPBertha Puente‐Urbina
Bertha Puente‐Urbina
JMJesus Alfonso Mercado‐Silva
Jesus Alfonso Mercado‐Silva
Lorena Garcia UriosteguiLorena Garcia Uriostegui
Lorena Garcia Uriostegui

1 February 2022 in International Journal of Biological Macromolecules
Verified
Journal Article
Closed access
Hector Ivan Melendez-OrtizHector Ivan Melendez-Ortiz
Hector Ivan Melendez-Ortiz
RBRebeca Betancourt-Galindo
Rebeca Betancourt-Galindo
BPBertha Puente-Urbina
Bertha Puente-Urbina
JOJorge Luis Sánchez Orozco
Jorge Luis Sánchez Orozco
ALAntonio Ledezma
Antonio Ledezma

25 August 2022 in Antibiotics
Verified
Journal Article
Open access
PDF file
ANAlberto Antonio Neira-Vielma
Alberto Antonio Neira-Vielma
Hector Ivan Melendez-OrtizHector Ivan Melendez-Ortiz
Hector Ivan Melendez-Ortiz
JLJosué López
Josué López
SSSaul Sanchez
Saul Sanchez
Mario CruzMario Cruz
Mario Cruz
SBSonia Noemí Ramírez Barrón
Sonia Noemí Ramírez Barrón
Nowadays, the increase in bacteria resistant to multiple antibiotics has become a real threat to the human health, forcing researchers to develop new strategies. Silver nanoparticles (AgNPs) may be a viable solution to this problem. The green synthesis of AgNPs is considered a green, ecological and low-priced process that provides small and biocompatible nanostructures with antimicrobial activity with a potential application in medicine. In this work, pecan nut shell extracts were analyzed in order to determine their viability for the production of AgNPs. These NPs were synthesized using an extract rich in bioactive molecules, varying the reaction time and silver nitrate (AgNO3) concentration. AgNPs production was confirmed by FT-IR, UV-Vis and EDX spectroscopy, while their morphology and size were determined by transmission electron microscopy (TEM) and dynamic light scattering (DLS). The antibacterial activity of AgNPs was evaluated by the agar diffusion method against Salmonella typhi, Staphylococcus aureus and Proteus mirabilis. The results showed that it is possible to obtain nanoparticles from an extract rich in antioxidant molecules with a size between 39.9 and 98.3 nm with a semi-spherical morphology. In addition, it was shown that the reaction time and the concentration of the precursor influence the final nanoparticles size. Antimicrobial tests showed that there is greater antimicrobial inhibition against Gram-negative than Gram-positive microorganisms, obtaining inhibition zone from 0.67 to 5.67 mm.

16 December 2020 in International Journal of Polymeric Materials and Polymeric Biomaterials
Verified
Journal Article
Closed access
DDDaniela Díaz-Zepeda
Daniela Díaz-Zepeda
RPRené D. Peralta-Rodríguez
René D. Peralta-Rodríguez
BPBertha Puente-Urbina
Bertha Puente-Urbina
GCGladis Cortez-Mazatan
Gladis Cortez-Mazatan
Hector Ivan Melendez-OrtizHector Ivan Melendez-Ortiz
Hector Ivan Melendez-Ortiz
Oil-in-water microemulsions (o/w MEs) were coated with chitosan to obtain new curcumin delivery systems. First, ternary phase diagrams were constructed using mixtures of Tween 20, Tween 80, ethanol, and monopropyleneglycol (MPG) to determine the macroscopic phase region of MEs and their capacity to incorporate clove oil. Particularly, MEs with size less than 20 nm could be formed using low amount of the surfactant Tween 20. The prepared MEs were subjected to diverse stability tests and characterized by dynamic light scattering (DLS), zeta potential (Z potential), conductivity, pH, and transmission electron microscopy (TEM). Stable, spherical uncoated and polymer-coated MEs were obtained with low droplet size (Dp), <50 nm, for the water/Tween 20/clove oil/ and water/Tween80/MPG/clove oil systems using a chitosan solution of 1 mg/mL. For all polymer-coated MEs, an increase of Z potential (17–54 mV) was observed due to the presence of chitosan. The loading with curcumin did not affect the Dp of MEs (e.g., for ME with Tween 20, Dp unloaded 12.35 ± 1.86 nm and Dp loaded 11.13 ± 0.32 nm) but Z potential and conductivity values were increased (typically for coated ME prepared with Tween 20 17.00 ± 0.36 mV ≤Z potential ≤41.5 mV, 162.20 ± 8.95 μS/cm ≤ conductivity ≤183.8 ± 0.56 μS/cm). Drug delivery studies for the chitosan-coated MEs were carried out at different pH (7.4, 6.5, and 5.8). The release of curcumin from the chitosan-coated MEs, formed with Tween 20, showed a dependence of the pH with a maximum release at the acidic pH of 5.8 (58%). The release of curcumin from all MEs was best described by the Korsmeyer- Peppas model with a Fickian transport mechanism. Graphical Abstract