TY - JOUR
T1 - Development of electrode carbon paste modified by molecularly imprinted polymer as sensor for analysis of creatinine by potentiometric
AU - Darmokoesoemo, Handoko
AU - Khasanah, Miratul
AU - Sari, Nunung Mareta
AU - Kadmi, Yassine
AU - Elmsellem, Hicham
AU - Kusuma, Heri Septya
N1 - Publisher Copyright:
© 2017 The Author
PY - 2017
Y1 - 2017
N2 - This research aims to develop an electrode carbon paste/molecularly imprinted polymer (MIP) as a sensor for the analysis of creatinine by potentiometric. The preparation of a non-imprinted polymer (NIP) is done by mixing aniline, creatinine, and potassium peroxodisulfate with mole ratio of 2:0.1:1. Creatinine is extracted from the polymer using hot water to form mold creatinine, this so-called MIP. In this study, the optimum electrode has a composition made of activated carbon, paraffin, and MIP of 40:35:25 (mass ratio), pH of working solution 6, and response time of 91–192 s. The Nernst factor obtained from this study was 23.2 mV/decade, the measuring range of 10−6–10−3 M, lower detection limit of 5.49 × 10−6 M, and the upper detection limit of 1.07 × 10−3 M. The accuracy of methods for concentration of 10−6–10−3 M was 76.40–165.80%, and the precision expressed by the coefficient of variation for the concentration is 0.05–0.32%. The electrodes have up to 83 times of usage. Urea does not interfere with the performance of the electrode carbon paste MIP on the analysis of creatinine.
AB - This research aims to develop an electrode carbon paste/molecularly imprinted polymer (MIP) as a sensor for the analysis of creatinine by potentiometric. The preparation of a non-imprinted polymer (NIP) is done by mixing aniline, creatinine, and potassium peroxodisulfate with mole ratio of 2:0.1:1. Creatinine is extracted from the polymer using hot water to form mold creatinine, this so-called MIP. In this study, the optimum electrode has a composition made of activated carbon, paraffin, and MIP of 40:35:25 (mass ratio), pH of working solution 6, and response time of 91–192 s. The Nernst factor obtained from this study was 23.2 mV/decade, the measuring range of 10−6–10−3 M, lower detection limit of 5.49 × 10−6 M, and the upper detection limit of 1.07 × 10−3 M. The accuracy of methods for concentration of 10−6–10−3 M was 76.40–165.80%, and the precision expressed by the coefficient of variation for the concentration is 0.05–0.32%. The electrodes have up to 83 times of usage. Urea does not interfere with the performance of the electrode carbon paste MIP on the analysis of creatinine.
KW - Carbon paste
KW - Creatinine
KW - Molecularly imprinted polymer
KW - Potentiometric
UR - http://www.scopus.com/inward/record.url?scp=85020163804&partnerID=8YFLogxK
U2 - 10.1016/j.rinp.2017.05.012
DO - 10.1016/j.rinp.2017.05.012
M3 - Article
AN - SCOPUS:85020163804
SN - 2211-3797
VL - 7
SP - 1808
EP - 1817
JO - Results in Physics
JF - Results in Physics
ER -