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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Türkes, Cüneyt Söyüt, Hakan Beydemir, Sükrü |
| Description | Country affiliation: Turkey Author Affiliation: Türkes C ( Department of Chemistry, Faculty of Science, Atatürk University, 25240, Erzurum, Turkey.); Söyüt H ( Department of Primary Education, Faculty of Education, Bayburt University, 69000, Bayburt, Turkey.); Beydemir S ( Department of Chemistry, Faculty of Science, Atatürk University, 25240, Erzurum, Turkey. Electronic address: beydemir@atauni.edu.tr.) |
| Abstract | In this study, we investigated the effects of the drugs, palonosetron hydrochloride, bevacizumab and cyclophosphamide, on human serum paraoxonase-I (hPON1) enzyme activity in in vitro conditions. The enzyme was purified â¼231-fold with 34.2% yield by using ammonium sulphate precipitation, DEAE-Sephadex A-50 ion-exchange chromatography and Sephadex G-200 gel-filtration chromatography from human serum. hPON1 exhibited a single protein band on the SDS polyacrylamide gel electrophoresis. The inhibition studies were performed on paraoxonase activity of palonosetron hydrochloride, bevacizumab and cyclophosphamide. Ki constants were found as 0.033±0.001, 0.054±0.003 mM and 3.419±0.518 mM, respectively. Compared to the inhibition rates of the drugs, palonosetron hydrochloride has the maximum inhibition rate. However, inhibition mechanisms of the drugs were determined as noncompetitive by Lineweaver-Burk curves. |
| File Format | HTM / HTML |
| ISSN | 13826689 |
| Journal | Environmental Toxicology and Pharmacology |
| Volume Number | 42 |
| e-ISSN | 18727077 |
| Language | English |
| Publisher | Elsevier |
| Publisher Date | 2016-03-01 |
| Publisher Place | Netherlands |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Discipline Environmental Health Discipline Pharmacology |
| Content Type | Text |
| Resource Type | Article |
| Subject | Health, Toxicology and Mutagenesis Medicine Toxicology Pharmacology |
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