کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2010437 | 1066977 | 2016 | 4 صفحه PDF | دانلود رایگان |
BackgroundChronic pancreatitis (CP) is a progressive, irreversible disease causing damage of the gland. Abdominal pains are a typical symptom of pancreatitis both in the chronic and acute form. Paracetamol is one of analgesics used for treating mild or moderate pain. Functional and anatomical changes in the gastrointestinal tract caused by pancreatitis may influence on the pharmacokinetics of administered drugs.MethodsIn the present study we analysed the pharmacokinetics of paracetamol after oral and intravenous administration to patients with CP. The patients were allocated to one of the two groups of the drug under study: I iv, intravenous administration of paracetamol 1000 mg (n = 17; mean [SD] age, 46.18 [13.78] years; and BMI, 22.03 [2.62] kg/m2) and II po, oral administration of paracetamol 1000 mg (n = 17; mean [SD] age, 48.29 [10.08] years; and BMI, 22.50 [2.92] kg/m2. The plasma concentrations of paracetamol and its metabolite (glucuronide) were measured with the validated high-pressure liquid chromatography (HPLC) method with ultraviolet (UV) detection.ResultsThe main pharmacokinetic parameters for paracetamol after iv and po administration to patients with CP were as follows: Cmax, 19.00 [4.50] and Cmax, 9.26 [3.35] μg/ml; AUC0-t, 42.37 [13.92] and 36.68 [11.7] μg × h/mL, respectively. After iv and po administration the AUC ratio between the metabolite (glucuronide) and paracetamol was enhanced.ConclusionsThe research findings revealed that patients with chronic pancreatitis had lower concentrations of paracetamol. Therefore, it may be necessary to apply additional analgesic therapy. Moreover, we observed enhanced glucuronidation in our patients.
Journal: Pharmacological Reports - Volume 68, Issue 4, August 2016, Pages 733–736