Modeling the Semicontinuous Heterophase Polymerization for Synthesizing Poly(n -butyl methacrylate) Nanoparticles

2013 ◽  
Vol 7 (9) ◽  
pp. 440-452 ◽  
Author(s):  
María G. Pérez-García ◽  
Lourdes A. Pérez-Carrillo ◽  
Eduardo Mendizábal ◽  
Jorge E. Puig ◽  
Francisco López-Serrano
Molecules ◽  
2014 ◽  
Vol 20 (1) ◽  
pp. 52-69 ◽  
Author(s):  
Dalia Sosa ◽  
Lourdes Guillén ◽  
Hened Saade ◽  
Eduardo Mendizábal ◽  
Jorge Puig ◽  
...  

2007 ◽  
Vol 45 (8) ◽  
pp. 1463-1473 ◽  
Author(s):  
Raquel Ledezma ◽  
M. Esther Treviño ◽  
Luis E. Elizalde ◽  
Lourdes A. Pérez-Carrillo ◽  
Eduardo Mendizábal ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-7 ◽  
Author(s):  
Abraham G. Alvarado ◽  
Andres Ortega ◽  
Lourdes A. Pérez-Carrillo ◽  
Israel Ceja ◽  
Martin Arellano ◽  
...  

Temperature- and pH-responsive core/shell nanoparticles were prepared by semicontinuous heterophase polymerization of N-isopropylacrylamide (NIPA) in the presence of chitosan micelles for drug delivery purposes. Micelles of chitosan, formed in an acetic acid aqueous solution at 70°C containing potassium persulfate, were fed with N-isopropylacrylamide (NIPA) at a controlled rate, to produce PNIPA/chitosan core/shell nanoparticles of about 350 nm. Then, the crosslinking agent, glutaraldehyde, was added to crosslink the nanoparticles. These nanocomposites were temperature- and pH-responsive, which make them suitable as controlled drug releasing agents. The nanoparticles exhibit thermoreversibility to heating-and-cooling cycles and show different responses depending on the releasing medium’s pH. Drug delivery tests were performed, employing as a model drug, doxycycline hyclate.


2018 ◽  
Vol 2018 ◽  
pp. 1-8
Author(s):  
J. A. Balleño ◽  
A. P. Mendizábal-Ruiz ◽  
H. Saade ◽  
R. Díaz de León-Gómez ◽  
E. Mendizábal ◽  
...  

Ibuprofen-loaded poly(ethyl cyanoacrylate) nanoparticles were prepared by semicontinuous heterophase polymerization of ethyl cyanoacrylate in the presence of ibuprofen; different surfactant concentration, pH, and temperature were used. Particle size was measured by quasi-light scattering and transmission electron microscopy, while the amount of drug released was determined by UV spectroscopy. Nanoparticles with diameters between 10 and 58 nm, loaded with ibuprofen, were obtained. The smallest particles and the higher drug loading were obtained at the highest pH tested. The analysis of the release data showed that the drug release profiles correspond to the Weibull model. Moreover, it was found that most of the ibuprofen is released within the first 80–120 min; initially the release rate is slow, but then it increases to finally decrease. This behavior contrasts with the reported burst of drug concentration in the plasma after oral administration of IB.


NANO ◽  
2014 ◽  
Vol 09 (06) ◽  
pp. 1450060 ◽  
Author(s):  
HENED SAADE ◽  
JESUS CEPEDA GARZA ◽  
MARIA LUISA LOPEZ-QUINTANILLA ◽  
FRANCISCO ENRIQUEZ-MEDRANO ◽  
SALVADOR FERNANDEZ ◽  
...  

Ibuprofen-loaded poly(methyl methacrylate) nanoparticles with mean diameters smaller than 20 nm were prepared by a novel method. This consists in carrying out a semicontinuous heterophase polymerization, in which a solution of drug-monomer is added on a micellar solution at an appropriate dosing rate. Scanning transmission electron microscopy (STEM) measurements showed number-average diameters in the range 16–19 nm with 1.14–1.15 in polydispersity, determined as the ratio of weight-average to number-average diameter. Drug contents in nanoparticles close to 24% were determined by UV-Vis spectrophotometry, confirming the results obtained from a procedure that combines latex filtration and quasielastic light scattering (QLS) measurements. Differential scanning calorimetry (CDSC) determinations suggest that at the ibuprofen contents attained in this study, crystals and dispersed molecules of the drug coexist inside the nanoparticles. Based on the relative simplicity of the process it is expected that its use will be adopted to prepare ultrafine nanoparticles composed of different hydrophobic polymers and water insoluble drugs.


2014 ◽  
Vol 51 (2) ◽  
pp. 144-155 ◽  
Author(s):  
M. G. Pérez-García ◽  
A. G. Alvarado ◽  
M. Rabelero ◽  
M. Arellano ◽  
L. A. Pérez-Carrillo ◽  
...  

2019 ◽  
Vol 60 (2) ◽  
pp. 223-232
Author(s):  
Abraham G. Alvarado ◽  
Rosaura Hernández‐Montelongo ◽  
Martin Rabelero ◽  
Lourdes A. Pérez‐Carrillo ◽  
Jorge E. Puig ◽  
...  

2010 ◽  
Vol 67 (2) ◽  
pp. 217-226 ◽  
Author(s):  
O. Esquivel ◽  
M. E. Treviño ◽  
H. Saade ◽  
J. E. Puig ◽  
E. Mendizábal ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-11 ◽  
Author(s):  
H. Saade ◽  
C. Barrera ◽  
R. Guerrero ◽  
E. Mendizábal ◽  
J. E. Puig ◽  
...  

We report the preparation of poly(ethyl cyanoacrylate) (PECA) nanoparticles by semicontinuous heterophase polymerization carried out at monomer starved conditions at three monomer addition rates. Particles in the nanometer range were obtained, the size of which diminishes with decreasing monomer addition rate as shown by the fact that particles with mean diameters of ca. 42 and 30 nm were obtained at the faster and intermediate dosing rates, respectively, whereas two populations of particles, one of 15.5 and the other of 36 nm in mean diameters, were produced at the slower dosing rate. The obtained molecular weights were from 2,200 to 3,500 g/mol, depending on the addition rate, which are typical of the anionic polymerizations of cyanoacrylates in aqueous dispersions at low pHs. The rifampicin (RIF) loading into the nanoparticles was successful since the entire drug added was incorporated. The drug release study carried out at pH of 7.2 indicated a faster release from the free RIF at intermediate and larger release times as expected since, in the nanoparticles, first the drug has to diffuse through the nanoparticle structure. The comparison of several drug release models indicates that the RIF release from PECA nanoparticles follows that of Higuchi.


2015 ◽  
Vol 9 (2) ◽  
pp. 114-124 ◽  
Author(s):  
María G. Pérez García ◽  
Abraham G. Alvarado ◽  
Lourdes A. Pérez-Carrillo ◽  
Jorge E. Puig ◽  
Francisco López-Serrano ◽  
...  

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