Search In this Thesis
   Search In this Thesis  
العنوان
Formulation and evaluation of transdermal ethosomal drug delivery of vancomycin hydrochloride /
الناشر
Mennatullah Mohammed Ahmed Abdellatif ,
المؤلف
Mennatullah Mohammed Ahmed Abdellatif
تاريخ النشر
2015
عدد الصفحات
225 P. :
الفهرس
Only 14 pages are availabe for public view

from 271

from 271

Abstract

Vancomycin hydrochloride is a glycopeptide antibiotic with a relatively high molecular weight of 1485.7 Da, used in the prophylaxis and treatment of infections caused by gram-positive bacteria. However ototoxicity and nephrotoxicity is seen to be associated with vancomycin administration, in addition to thrombophlebitis and infusion related reaction known as red man syndrome. Therefore designing a delivery system capable of providing sustained serum level of vancomycin hydrochloride above MIC of target pathogen for prolonged duration is a desirable target. Several attempts have been done in order to formulate and design a delivery system able to provide sustained vancomycin serum level such as biodegradable in situ gel-forming controlled drug delivery, biodegradable chitosan microspheres and scaffolds. Also several researchers noted that vancomycin encapsulation into liposomal or nano sized vehicle offered an enhancement in pharmacodynamics, pharmacokinetics characteristics of drug and decreased its toxicity compared to standard preparations