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...
Saved in:
Main Author: | |
---|---|
Format: | Final Project |
Language: | Indonesia |
Online Access: | https://digilib.itb.ac.id/gdl/view/45398 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
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 |
_version_ |
1822927083444109312 |