Development of Solid lipid nanoparticles as Eschar delivery system for Nitrofurazone Using Taguchi Design Approach

Behzad Sharif Makhmal Zadeh (1) , Nastaran Barati (2) , Mohammad Hossin Hassani (3) , Fakher Rahim (4)
(1) Nanotechnology Research Center, Jundishapur University of Medical Sciences, Ahvaz, Iran / School of Pharmacy, Jundishapur University of Medical Sciences, Ahvaz, Iran, Iran, Islamic Republic of ,
(2) School of Pharmacy, Jundishapur University of Medical Sciences, Ahvaz, Iran, Iran, Islamic Republic of ,
(3) School of Pharmacy, Jundishapur University of Medical Sciences, Ahvaz, Iran, Iran, Islamic Republic of ,
(4) Physiology Research Center, Jundishapur University of Medical Sciences, Ahvaz, Iran, Iran, Islamic Republic of

Abstract

Effective topical antimicrobial agents decrease bacterial colonization and infection. Localization of nitrofurazone into the eschar using vehicle such as solid lipid nanoparticles (SLN) improves antimicrobial efficiency in treatment of the infection in burn patients. This study was undertaken to develop solid lipid nanoparticles (SLN) of nitrofura-zone using cold homogenization technique and study the permeability of the drug through rat skin. Results show type and percentage of surfactant, type of lipid and drug/lipid ratio can influence SLN character Drug release from SLN was the rate limiting step for drug permeation across rat skin and so prepared formulations can act as a drug reservoir.

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Authors

Behzad Sharif Makhmal Zadeh
bsharifmakhmalzadeh@yahoo.com (Primary Contact)
Nastaran Barati
Mohammad Hossin Hassani
Fakher Rahim
Behzad Sharif Makhmal Zadeh, Nastaran Barati, Mohammad Hossin Hassani, & Fakher Rahim. (2010). Development of Solid lipid nanoparticles as Eschar delivery system for Nitrofurazone Using Taguchi Design Approach. International Journal of Research in Pharmaceutical Sciences, 1(4), 466–472. Retrieved from https://ijrps.com/home/article/view/2974

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