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Abstracts Book - IMRC 2018

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• SB6-O025<br />

NOVEL POLYMERIC MATERIALS FOR SOLID- PHASE EXTRACTION<br />

OF SARCOSINE<br />

Soane Fernández Puig 1 , Miguel Alberto López Sánchez 1 , Jheny Adriana Rodríguez Mendez 2 ,<br />

Arístides Camilo Valdés González 3 , Abraham Ulises Chávez Ramírez 1<br />

1 Centro de Investigación y Desarrollo Tecnológico en Electroquímica, Electrochemistry, Mexico.<br />

2 Universidad Autónoma de Querétaro, Faculty of Medicine, Mexico. 3 Universidad de La<br />

Habana, LUCES, Cuba.<br />

Prostate cancer (PCa) is an important cause of mortality and morbidity of men.<br />

The prostate specific antigen (PSA) normally used as a marker can only be<br />

detected in blood with low sensitivity an specificity. Recently, several metabolites<br />

presented in body fluids such as serum or urine have been investigated as new<br />

putative biomarkers in relation to PCa [1]. Sarcosine [2]has received attention<br />

as a potential PCa biomarker, since it has found that its concentration levels<br />

increased with cancer progression. In this work, highly selective molecularly<br />

imprinted polymers (MIPs) for sarcosine pre-concentration were developed and<br />

its use as solid-phase extraction (SPE) sorbent material was demonstrated.<br />

These MIPs were prepared was prepared by a very simple procedure using<br />

metacrilic acid as funtional monomers, acetonitrile as porogen and ethylene<br />

glicol dimethacrylate as cross-linking agent. The synthetized materials were<br />

charaterized by SEM and irregular morphology was observed in both materials,<br />

particle size was in the range of 38 to 250 microns.<br />

The polymer was tested in batch experiment in order to evaluate its binding<br />

properties: the maximum extraction pH, the sorption capacity, as well as the<br />

sorption capacity of the MIP with respect to the non-printed one were<br />

determined. The developed polymer was able to detect low sarcosine<br />

concentrations in the range of 10 -1 to 1 ng/L in synthetic samples and these<br />

results support a potential material to be tested in biological samples for PCa<br />

diagnostics.<br />

[1] A.P. Khan, T.M. Rajendiran, A. Bushra, I.A. Asangani, J.N. Athanikar, A.K.<br />

Yocum, R. Mehra, J. Siddiqui, G. Palapattu, J.T. Wei, G. Michailidis, A. Sreekumar,<br />

A.M. Chinnaiyan, The Role of Sarcosine Metabolism in Prostate Cancer<br />

Progression, Neoplasia 15(5) (2013) 491-IN13.<br />

[2] A. Sreekumar, L.M. Poisson, T.M. Rajendiran, A.P. Khan, Q. Cao, J. Yu, B.<br />

Laxman, R. Mehra, R.J. Lonigro, Y. Li, Metabolomic profiles delineate potential

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