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MIP synthesis <strong>of</strong> 4-vinylpyridine<br />
Author<br />
Ilse van Kessel<br />
Academy <strong>of</strong> Technology for Health and Environment<br />
Avans Hogeschool, Breda<br />
Avans Lectorate<br />
Sonny van Seeters<br />
Abstract<br />
MIP synthesis <strong>of</strong> 4-vinylpyridine<br />
Taxol is a medicine used against different kinds <strong>of</strong> cancer. For the production <strong>of</strong> Taxol mostly used is 10 -DAB (10-<br />
deacetylbaccatin III, this compound can be extracted from the Taxus Baccata L.. To simplify the extraction <strong>of</strong> 10 -DAB from<br />
the Taxus Baccata L. a MIP (Molecular Imprinted Polymer) can be used. A MIP is an highly selective polymer whereby the<br />
synthesis <strong>of</strong> a MIP uses a template <strong>of</strong> the molecule, a monomer and a cross linker. [1] The result is a high cross-linked<br />
polymer because <strong>of</strong> the new bonds between the template and the cross -linked polymer during the curing process. The<br />
template is removed and the permanent pores stay in the polymer. The polymer is highly selective for the template<br />
molecule (10-DAB). In figure 1 is the schematic representation <strong>of</strong> the synthesis <strong>of</strong> the MIP shown.[2] The goal <strong>of</strong> this study<br />
is the synthesis <strong>of</strong> a MIP with another functional monomer than used in earlier investigations. This MIP has to be specific<br />
for 10-DAB, the analysis that are used are HPLC, DSC, TGA and FTIR. 4 -VP (4-vinylpyridine) is used as functional monomer.<br />
The expectation <strong>of</strong> this study is that a MIP with 4-VP can be synthesised. The MIP will also be selective for 10-DAB and has<br />
a recovery higher than 80%.<br />
Keywords: Taxol, 10-DAB, MIP<br />
Table <strong>of</strong> content<br />
Figure 1: Schematic representation <strong>of</strong> MIP synthesis.<br />
[1] M. J. M. E.-M. R. D. &. F. A. Fatemeh Azizi Ishkuh, „Synthesis and characterization <strong>of</strong> paclitaxel-imprinted nanoparticles<br />
for recognition and controlled release <strong>of</strong> an anticancer drug,” Journal <strong>of</strong> materials science, vol. 48, nr. 68, pp. 6343-6352,<br />
2014.<br />
[2] B. v. d. Velde, „Synthesis <strong>of</strong> molecularly imprinted polymers (MIPs) <strong>of</strong> 10-DAB III particles using a magnetite core-shell<br />
approach,” Breda, 2017.<br />
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