Transdermal delivery of vancomycin hydrochloride using combination of nano-ethosomes and iontophoresis: in vitro and in vivo study.

Autor: Mohammed MI; a Department of Pharmaceutics and Industrial Pharmacy , College of Pharmacy, Cairo University , Cairo , Egypt .; b Department of Pharmaceutics and Industrial Pharmacy ., Makky AM; a Department of Pharmaceutics and Industrial Pharmacy , College of Pharmacy, Cairo University , Cairo , Egypt .; b Department of Pharmaceutics and Industrial Pharmacy ., Teaima MH; a Department of Pharmaceutics and Industrial Pharmacy , College of Pharmacy, Cairo University , Cairo , Egypt ., Abdellatif MM; b Department of Pharmaceutics and Industrial Pharmacy ., Hamzawy MA; c Department of Pharmacology , and., Khalil MA; d Department of Microbiology and Immunology , College of Pharmacy, Misr University for Science and Technology , Giza , Egypt.
Jazyk: angličtina
Zdroj: Drug delivery [Drug Deliv] 2016 Jun; Vol. 23 (5), pp. 1558-64. Date of Electronic Publication: 2015 Mar 02.
DOI: 10.3109/10717544.2015.1013200
Abstrakt: This study aimed to evaluate transdermal delivery of vancomycin hydrochloride using the combination of ethosomes as an encapsulating vesicle and iontophoresis. Ethosomes were prepared and evaluated in terms of electrochemical stability. Cathodal iontophoresis of negatively charged ethosomes and anodal iontophoresis of free drug solution and positively charged vesicles were conducted. The effect of current mode, density, concentration of drug and ionic strength was studied. In vivo study was performed by inducing mediastinitis in Sprague-Dawley rats using methicillin-resistant Staphylococcus aureus as infected pathogen, the mean bacterial count was compared between groups of rats, one of the treated groups received drug intramuscularly while the other group received vancomycin using iontophoretic delivery of optimized ethosomal formula. Ethosomes showed efficient electrochemical stability, cathodal iontophoresis of negatively charged vesicle (F2) showed maximum transdermal flux (550 µg/cm(2)/h) compared to free drug solution and other ethosomal formulae, transdermal flux was reduced by altering current mode from continuous to ON/OFF mode, reducing current density and by using normal saline as drug solvent; on the other hand, flux was potentiated by increasing drug concentration from 25 to 75 mg/ml. In vivo study revealed that there was a significant difference in terms of bacterial count between untreated and treated groups, while there was no statistically significant difference between the I.M. vancomycin treatment and treatment conducted by iontophoretic delivery of vancomycin encapsulated in ethosomal formula. Combination between ethosomes and iontophoresis had succeeded in delivering vancomycin transdermally.
Databáze: MEDLINE
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