02140 2200181 4500001002100000005001500021035002000036007000300056008003900059082001500098084001500113100001900128245014400147260004500291300000700336650004200343520157300385INLIS00000000001921320240911014951 a0010-0924000292ta240911 | | |  aARTVET2418 aARTVET24180 aWardhana AH1,21 aPengembangan Biosensor Penyakit Surra (Trypanosoma evansi) Berbasis Protein dengan Metode Differential Pulse Voltammetry /cWardhana AH1,2 a1Balai Besar Penelitian Veteriner,c2020 a37 4aPengembangan Biosensor Penyakit Surra aTrypanosoma evansi remains a major cause of Trypanosomiasis in Indonesia, called Surra. However, the lack of accessibility and affordability for diagnostic tests: Card Agglutination Test for Trypanosomiasis/T. evansi – CATT/T. evansi; ELISA and PCR lead to unsuccessful control of Surra in the field. Accordingly, the accurate, rapid and applicable kit for alternative Surra diagnosis is needed, for example biosensor. The study aimed to investigate the performance of protein-based biosensor of Surra (Trypanosoma evansi) for distinguishing positive and negative sera. Herein, protein was obtained from the T. evansi propagation. This protein was immobilized by carbodiimide reaction on the surface of carbon screen printed electrode as the lowest interaction material with serum/antibody (% I < 90%). The sensor method used in this present study was differential pulse voltammetry (DPV). Data were normalized and analyzed using PSTrace 5.8 program. The results demonstrated that false negative and false positive of sensor were observed at 64 and 2 dilution times respectively. The positive serum analyzed using DVP (potential range -0.2 - +1.0 V, scan rate 0.1 Vs-1) revealed that the slope of positive serum (1.84) was higher than those of the negative serum (1.01) indicating the sensitivity of the produced biosensor for Surra (T. evansi). Similarly, these results were confirmed by serological test (CATT/T. evansi). From this study, the obtained protein-based biosensor is a promising tool for Surra detection in livestock.