Author/Authors :
ashrafi, hajar shiraz university of medical sciences - school of pharmacy - department of pharmaceutics, Shiraz, Iran , azadi, amir shiraz university of medical sciences - pharmaceutical sciences research center, school of pharmacy - department of pharmaceutics, Shiraz, Iran , mohammadi-samani, soliman shiraz university of medical sciences - pharmaceutical sciences research center, school of pharmacy - department of pharmaceutics, Shiraz, Iran , ghasemi, younes shiraz university of medical sciences - school of pharmacy, pharmaceutical sciences research center - department of pharmaceutical biotechnology, Shiraz, Iran , daneshamouz, saeid shiraz university of medical sciences - school of pharmacy - department of pharmaceutics, Shiraz, Iran
Abstract :
In the present study, the mixing behavior of different surfactants and fatty acid bioconjugated L-asparaginase was investigated. The amphiphilic macromolecules were achieved by covalent linkage of fatty acids with different chain lengths (C12, C16, and C22) to the native enzyme, L-asparaginase. The amino group of L-asparaginase lysine residue was conjugated to the carboxylic group of fatty acids, using a carbodiimide activator. The particle sizes of resulted micellar nanocarrier before and after lyophilization and enzyme activity was investigated. Among all surfactants, pluronic F-127 with fatty acid bioconjugated L-asparaginase presented more plasma and PBS half-life and Higher activity value after lyophilization. These findings from L-asparaginase modification by fatty acid and surfactants indicate a promising stabilized product that may serve as a new candidate for medical purposes.
Keywords :
L , asparaginase , Lipid , protein conjugation , Micellar Nanocarrier , Pluronic F , 127