FARMAKOKINETIK GLIKLAZID DAN SIPROFLOKSASIN PADA PEMBERIAN BERSAMA DI TIKUS WISTAR JANTAN

Diabetes Mellitus (DM) is a disease characterized by a decrease in body’s metabolism ability, which could be caused by a decrease in insulin secretion and/or increase in cellular resistance to insulin. The prevalence of DM is increasing, which could further impair other organs, one of which is re...

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Main Author: Leo, Margaretha
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/45398
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:45398
spelling id-itb.:453982019-12-18T13:30:48ZFARMAKOKINETIK GLIKLAZID DAN SIPROFLOKSASIN PADA PEMBERIAN BERSAMA DI TIKUS WISTAR JANTAN Leo, Margaretha Indonesia Final Project - INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/45398 Diabetes Mellitus (DM) is a disease characterized by a decrease in body’s metabolism ability, which could be caused by a decrease in insulin secretion and/or increase in cellular resistance to insulin. The prevalence of DM is increasing, which could further impair other organs, one of which is renal dysfunction. This condition could be worsened by the occurrence of urinary tract infection. The most commonly treatment used to treat urinary tract infection in nephropathy diabetic patients is ciprofloxacin. This research was aimed to evaluate the pharmacokinetic interactions of gliclazide and ciprofloxacin. Wistar male rats divided into four groups (each n = 5). Group I and II received gliclazide and ciprofloxacin respectively. Group III received both gliclazide and ciprofloxacin with gliclazide induction for 10 days, and group IV received both gliclazide and ciprofloxacin with ciprofloxacin induction for 10 days. Blood samples were collected at pre-determined sampling points, then analyzed by HPLC. Pharmacokinetic parameters for both drugs were determined. Clearance of gliclazide showed a significant increase (p<0.05) in group IV (268,18 ± 53,74 mL/h/kg) compared to group I (172,36 ± 39,39 mL/h/kg). Pharmacokinetics parameters of ciprofloxacin with concomitant administration of gliclazide, both single and multiple doses, showed a significant increase (p<0.05) in biological half life (2.70 ± 0.95 to 7.47 ± 3.10 and 9.24 ± 4.74 h), AUC0-24 (3.95 ± 0.83 to 11.75 ± 4.55 and 8.45 ± 0.66 µg.h/mL), AUC0- ?(4.13 ± 0.89 to 12.57 ± 4.92 and 10.37 ± 2.26 µg.h/mL) and a significant decrease in clearance (20717.21 ± 4591.26 to 7648.18 ± 3722.45 and 8448.23 ± 1492.35 mL/h.kg). Administration of gliclazide with multiple dose of ciprofloxacin increased the clearance of gliclazide. Ciprofloxacin when given with gliclazide, either by single or multiple doses caused a significant impacts on pharmacokinetics of ciprofloxacin. text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
description Diabetes Mellitus (DM) is a disease characterized by a decrease in body’s metabolism ability, which could be caused by a decrease in insulin secretion and/or increase in cellular resistance to insulin. The prevalence of DM is increasing, which could further impair other organs, one of which is renal dysfunction. This condition could be worsened by the occurrence of urinary tract infection. The most commonly treatment used to treat urinary tract infection in nephropathy diabetic patients is ciprofloxacin. This research was aimed to evaluate the pharmacokinetic interactions of gliclazide and ciprofloxacin. Wistar male rats divided into four groups (each n = 5). Group I and II received gliclazide and ciprofloxacin respectively. Group III received both gliclazide and ciprofloxacin with gliclazide induction for 10 days, and group IV received both gliclazide and ciprofloxacin with ciprofloxacin induction for 10 days. Blood samples were collected at pre-determined sampling points, then analyzed by HPLC. Pharmacokinetic parameters for both drugs were determined. Clearance of gliclazide showed a significant increase (p<0.05) in group IV (268,18 ± 53,74 mL/h/kg) compared to group I (172,36 ± 39,39 mL/h/kg). Pharmacokinetics parameters of ciprofloxacin with concomitant administration of gliclazide, both single and multiple doses, showed a significant increase (p<0.05) in biological half life (2.70 ± 0.95 to 7.47 ± 3.10 and 9.24 ± 4.74 h), AUC0-24 (3.95 ± 0.83 to 11.75 ± 4.55 and 8.45 ± 0.66 µg.h/mL), AUC0- ?(4.13 ± 0.89 to 12.57 ± 4.92 and 10.37 ± 2.26 µg.h/mL) and a significant decrease in clearance (20717.21 ± 4591.26 to 7648.18 ± 3722.45 and 8448.23 ± 1492.35 mL/h.kg). Administration of gliclazide with multiple dose of ciprofloxacin increased the clearance of gliclazide. Ciprofloxacin when given with gliclazide, either by single or multiple doses caused a significant impacts on pharmacokinetics of ciprofloxacin.
format Final Project
author Leo, Margaretha
spellingShingle Leo, Margaretha
FARMAKOKINETIK GLIKLAZID DAN SIPROFLOKSASIN PADA PEMBERIAN BERSAMA DI TIKUS WISTAR JANTAN
author_facet Leo, Margaretha
author_sort Leo, Margaretha
title FARMAKOKINETIK GLIKLAZID DAN SIPROFLOKSASIN PADA PEMBERIAN BERSAMA DI TIKUS WISTAR JANTAN
title_short FARMAKOKINETIK GLIKLAZID DAN SIPROFLOKSASIN PADA PEMBERIAN BERSAMA DI TIKUS WISTAR JANTAN
title_full FARMAKOKINETIK GLIKLAZID DAN SIPROFLOKSASIN PADA PEMBERIAN BERSAMA DI TIKUS WISTAR JANTAN
title_fullStr FARMAKOKINETIK GLIKLAZID DAN SIPROFLOKSASIN PADA PEMBERIAN BERSAMA DI TIKUS WISTAR JANTAN
title_full_unstemmed FARMAKOKINETIK GLIKLAZID DAN SIPROFLOKSASIN PADA PEMBERIAN BERSAMA DI TIKUS WISTAR JANTAN
title_sort farmakokinetik gliklazid dan siprofloksasin pada pemberian bersama di tikus wistar jantan
url https://digilib.itb.ac.id/gdl/view/45398
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