Comparative Pharmacokinetics Of Levofloxacin In Healthy Volunteers & Patients Suffering From Typhoid Fever
By: Muhammed Usman | Prof.Dr.Muhammad Ashraf.
Contributor(s): Dr. Muhammad Imran Khokhar | Dr. Shehryar.
Material type: BookPublisher: 2008Subject(s): Department of Pharmaoclogy & ToxicologyDDC classification: 1027,T Dissertation note: This study was designed to compare the pharmacokinetic parameters of Levofloxacin in healthy volunteers and in human patients suffering from typhoid fever (target individuals). The study was conducted in six healthy male volunteers and six male patients suffering from typhoid fever in Services Institute of Medical Sciences (SIMS) Lahore. Only those patients were selected who were suffering from typhoid (confirmed after widal test) between the age of 25-40 years. Healthy volunteers were also between age of 25-40 years. The patients were considered as group A and healthy volunteers were considered as group B. Both groups were treated with Levofloxacin 5 00mg tab orally per individual. 5m1 Blood samples were collected at 0, 0.25, 0.5, 1, 2, 3, 6, 12, 24, 36 & 72 hr from vein through 5m1 B.D syring of 23guage needle after oral administration of Levofloxacin. Plasma was separated by centrifugation at 5000 RPM and stored at -20°C until assayed. Levofloxacin concentrations in plasma were measured by previously described HPLC method. Calculation of all the pharmacokinetic parameters was done by entering plasma concentration-time data in software APO pharmacological analysis MW/PHARM version 3.02 by assuming bio-availability of levofloxacin after oral administration as 1. Pharmacokinetic parameters of Levofloxacin in healthy volunteers and in typhoid patients were compared. Data was analyzed by appropriate statistical methods and it was observed that there is no significant difference in pharmacokinetic parameters of Levofloxacin in healthy volunteers and in typhoid patients after oral administration and there is no need for dose adjustment of Levofloxacin in typhoid patients.Item type | Current location | Collection | Call number | Status | Date due | Barcode | Item holds |
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Thesis | UVAS Library Thesis Section | Veterinary Science | 1027,T (Browse shelf) | Available | 1027,T |
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This study was designed to compare the pharmacokinetic parameters of Levofloxacin in healthy volunteers and in human patients suffering from typhoid fever (target individuals). The study was conducted in six healthy male volunteers and six male patients suffering from typhoid fever in Services Institute of Medical Sciences (SIMS) Lahore. Only those patients were selected who were suffering from typhoid (confirmed after widal test) between the age of 25-40 years. Healthy volunteers were also between age of 25-40 years. The patients were considered as group A and healthy volunteers were considered as group B. Both groups were treated with Levofloxacin 5 00mg tab orally per individual. 5m1 Blood samples were collected at 0, 0.25, 0.5, 1, 2, 3, 6, 12, 24, 36 & 72 hr from vein through 5m1 B.D syring of 23guage needle after oral administration of Levofloxacin. Plasma was separated by centrifugation at 5000 RPM and stored at -20°C until assayed. Levofloxacin concentrations in plasma were measured by previously described HPLC method. Calculation of all the pharmacokinetic parameters was done by entering plasma concentration-time data in software APO pharmacological analysis MW/PHARM version 3.02 by assuming bio-availability of levofloxacin after oral administration as 1. Pharmacokinetic parameters of Levofloxacin in healthy volunteers and in typhoid patients were compared. Data was analyzed by appropriate statistical methods and it was observed that there is no significant difference in pharmacokinetic parameters of Levofloxacin in healthy volunteers and in typhoid patients after oral administration and there is no need for dose adjustment of Levofloxacin in typhoid patients.
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