Detailed Information on Publication Record
2013
Microfluidic chip coupled with modified paramagnetic particles for sarcosine isolation in urine
ZITKA, Ondrej, Natalia CERNEI, Zbynek HEGER, Miroslav MATOUSEK, Pavel KOPEL et. al.Basic information
Original name
Microfluidic chip coupled with modified paramagnetic particles for sarcosine isolation in urine
Authors
ZITKA, Ondrej (203 Czech Republic), Natalia CERNEI (203 Czech Republic), Zbynek HEGER (203 Czech Republic), Miroslav MATOUSEK (203 Czech Republic), Pavel KOPEL (203 Czech Republic), Jindrich KYNICKY (203 Czech Republic), Michal MASAŘÍK (203 Czech Republic, guarantor, belonging to the institution), Rene KIZEK (203 Czech Republic) and Vojtech ADAM (203 Czech Republic)
Edition
Electrophoresis, Hoboken, Wiley-Blackwell, 2013, 0173-0835
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10600 1.6 Biological sciences
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 3.161
RIV identification code
RIV/00216224:14110/13:00070631
Organization unit
Faculty of Medicine
UT WoS
000327590900006
Keywords in English
Ion exchange chromatography; Magnetic nanoparticles; Microfluidic separation; Prostate cancer; Surface modification
Tags
International impact, Reviewed
Změněno: 13/4/2014 12:34, Ing. Mgr. Věra Pospíšilíková
Abstract
V originále
Carcinoma of prostate (CaP) is the second most frequent malignant tumor occurring in men in Europe. Currently there is discussion on a wide range of potential CaP markers. One of them-nonprotein amino acid sarcosine, also known as N-methylglycine was chosen as a challenge for the development of microfluidic system with isolation by modified paramagnetic microparticles. Therefore, the aim of this study was to design a low-cost, simple, and rapid microfluidic system based on sarcosine isolation with modified paramagnetic microparticles and subsequent analysis on the ion exchange LC. We modified Dowex microparticles with Fe2O3 nanoparticles. Our paramagnetic microparticles were able to establish the binding with sarcosine. Moreover, we designed microfluidic device for sarcosine determination. Analysis of samples was carried out with LOD of 1 uM of a sarcosine that is sufficient because it is similar to concentrations of a sarcosine observed in the CaP patients.