Examination of Imprinting Process with Molsidomine as a Template

Eight different functional monomers were used with ethylene glycol dimethacrylate as a cross-linker and molsidomine as a template to obtain molecularly imprinted polymers (MIPs). Non-covalent interactions between molsidomine and each functional monomer in DMSO prior to thermal bulk polymerization we...

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Main Authors: Dorota Maciejewska, Piotr Luliński
Format: Article
Language:English
Published: MDPI AG 2009-06-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/14/6/2212/
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spelling doaj-c8884676852045e4a879c6190963aab42020-11-24T23:38:58ZengMDPI AGMolecules1420-30492009-06-011462212222510.3390/molecules14062212Examination of Imprinting Process with Molsidomine as a TemplateDorota MaciejewskaPiotr LulińskiEight different functional monomers were used with ethylene glycol dimethacrylate as a cross-linker and molsidomine as a template to obtain molecularly imprinted polymers (MIPs). Non-covalent interactions between molsidomine and each functional monomer in DMSO prior to thermal bulk polymerization were utilized. On the basis of calculated imprinting factors, MIP prepared with N,N’-diallyltartaramide was chosen for further investigations. Examination of interactions in the prepolymerization complex between molsidomine and N,N’-diallyltartaramide was performed using the Job method. The absorbance of isomolar solutions reaching a maximum for the molar ratio of template to monomer equal to 1:4. Scatchard analysis was used for estimation of the dissociation constants and the maximum amounts of binding sites. The polymer based on N,N’-diallyltartaramide has two classes of heterogeneous binding sites characterized by two values of Kd and two Bmax: Kd(1) = 1.17 mM-1 and Bmax(1) = 0.8 μmol/mg for the higher affinity binding sites, and Kd(2) = 200 μM-1 and Bmax(2) = 2.05 μmol/mg for the lower affinity binding sites. Furthermore, effects of pH and organic solvent on binding properties of MIP and NIP were investigated, together with release of molsidomine from both MIP and NIP. http://www.mdpi.com/1420-3049/14/6/2212/molsidominemolecularly imprinted polymerssustained release
collection DOAJ
language English
format Article
sources DOAJ
author Dorota Maciejewska
Piotr Luliński
spellingShingle Dorota Maciejewska
Piotr Luliński
Examination of Imprinting Process with Molsidomine as a Template
Molecules
molsidomine
molecularly imprinted polymers
sustained release
author_facet Dorota Maciejewska
Piotr Luliński
author_sort Dorota Maciejewska
title Examination of Imprinting Process with Molsidomine as a Template
title_short Examination of Imprinting Process with Molsidomine as a Template
title_full Examination of Imprinting Process with Molsidomine as a Template
title_fullStr Examination of Imprinting Process with Molsidomine as a Template
title_full_unstemmed Examination of Imprinting Process with Molsidomine as a Template
title_sort examination of imprinting process with molsidomine as a template
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2009-06-01
description Eight different functional monomers were used with ethylene glycol dimethacrylate as a cross-linker and molsidomine as a template to obtain molecularly imprinted polymers (MIPs). Non-covalent interactions between molsidomine and each functional monomer in DMSO prior to thermal bulk polymerization were utilized. On the basis of calculated imprinting factors, MIP prepared with N,N’-diallyltartaramide was chosen for further investigations. Examination of interactions in the prepolymerization complex between molsidomine and N,N’-diallyltartaramide was performed using the Job method. The absorbance of isomolar solutions reaching a maximum for the molar ratio of template to monomer equal to 1:4. Scatchard analysis was used for estimation of the dissociation constants and the maximum amounts of binding sites. The polymer based on N,N’-diallyltartaramide has two classes of heterogeneous binding sites characterized by two values of Kd and two Bmax: Kd(1) = 1.17 mM-1 and Bmax(1) = 0.8 μmol/mg for the higher affinity binding sites, and Kd(2) = 200 μM-1 and Bmax(2) = 2.05 μmol/mg for the lower affinity binding sites. Furthermore, effects of pH and organic solvent on binding properties of MIP and NIP were investigated, together with release of molsidomine from both MIP and NIP.
topic molsidomine
molecularly imprinted polymers
sustained release
url http://www.mdpi.com/1420-3049/14/6/2212/
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