Emulsion Copolymerization of Vinyl Acetate and Vinyl Silanes: Kinetics and Development of Microstructure

2020 ◽  
Vol 14 (2) ◽  
pp. 1900043 ◽  
Author(s):  
Aitor Barquero ◽  
Amaia Agirre ◽  
María Jesús Barandiaran ◽  
Jose Ramon Leiza
2020 ◽  
Vol 11 (13) ◽  
pp. 2390-2398
Author(s):  
Aitor Barquero ◽  
Fernando Ruipérez ◽  
María Jesús Barandiaran ◽  
Jose Ramon Leiza

Radical entry affected by alkoxysilane monomers in free radical emulsion copolymerization with vinyl acetate.


1991 ◽  
Vol 29 (2) ◽  
pp. 169-186 ◽  
Author(s):  
Belen Urquiola ◽  
Gurutze Arzamendi ◽  
José R. Leiza ◽  
Aranzazu Zamora ◽  
José M. Asua ◽  
...  

1998 ◽  
Vol 35 (10) ◽  
pp. 1741-1751 ◽  
Author(s):  
Dan Donescu ◽  
Sever Serban ◽  
Liana Fusulan ◽  
Cristian Petcu

1996 ◽  
Vol 28 (10) ◽  
pp. 851-859 ◽  
Author(s):  
Young-Je Kwark ◽  
Won Seok Lyoo ◽  
Wan Shik Ha

2007 ◽  
Vol 57 (4) ◽  
pp. 429-439
Author(s):  
Bistra Kostova ◽  
Dimitar Rachev

New co-polymer zwitterionic matrices for sustained release of verapamil hydrochlorideStable co-polymer [vinyl acetate-co-3-dimethyl(methacryloyloxyethyl) ammonium propane sulfonate, p(VA-co-DMAPS)] latex of different compositions has been synthesized for the first time by emulsifier-free emulsion copolymerization. The unusual >>overshooting<< behavior of the co-polymer tablets has been explained by the formation of specific clusters from the opposite oriented dipoles-zwitterionic species. The change of their concentration with the DMAPS unit fraction (mDMAPS), pH and ionic strength has been considered responsible for the differences observed in the swelling kinetics. The results obtained prove that mDMAPSand ionic strength could be used to control the swelling degree of the p(VA-co-DMAPS) matrices and their sustained drug delivery. In this way, p(VA-co-DMAPS) matrices could be effectively used to control the sustained release of drugs with basic properties like verapamil hydrochloride from model tablets.


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