000 02432nam a2200193Ia 4500
005 20151006154114.0
008 150525s2013xx 000 0 und d
041 _aeng
082 _a1788,T
100 _aMuhammad Zeeshan Saleem
_98683
110 _cProf. Dr. Muhammad Ashraf
_94840
245 _aPharmacokinetic Study Of Different Dosage Forms Of Potassium Iodide (Renessans) In Healthy Human Volunteers
260 _c2013
502 _aThis project was designed to determine the pharmacokinetic parameters of different dosage forms of potassium iodide in healthy human volunteers and also to compare the pharmacokinetic parameters of potassium iodide in healthy male and female volunteers. For this study 36 healthy volunteers were selected (Divided into three groups, 6 male and 6 female in each group). Only those volunteers who were between ages 20-35 were selected, not suffering from any disease. Volunteers were clearly informed about the objectives of study and written consent was taken. Healthy volunteers were divided in to three equal groups and were given capsule, solution, powder dosage form of potassium iodide respectively through oral route. 5ml blood samples were collected at 0, 0.25, 0.5, 1.0, 1.5, 2.0, 2.5, 3.0, 4.0, 6.0, 8.0, 10, 12, and 24 hours from vein of either arm with I/v branula. Plasma was separated by centrifugation at 3000 RPM for 10 minutes and was stored at -80 0C till analysis. Method for the determination of potassium iodide was validated appropriately and analysis of samples was performed on HPLC. All pharmacokinetic parameters were calculated by entering plasma concentration-time data in excel based software PK solutions version 2.0. Pharmacokinetic parameters of potassium iodide in healthy individuals were studied by using statistical tests mean ± SD (standard deviation) and One Way ANOVA. Pharmacokinetic comparison of different dosage forms of potassium iodide in healthy male and female volunteers was studied by unpaired t-test. Results were summarized in tables. Between the dosage forms there is significant difference in the pharmacokinetic parameters of healthy human volunteers but there was no significant difference found in pharmacokinetic parameters between healthy male and female volunteers in each dosage form.
650 _aDepartment of Pharmaoclogy & Toxicology
_95037
700 _aDr. Aualeha Riffat
_98684
700 _aDr. Mateen
_95138
942 _cTH
999 _c3496
_d3496