Synthesis, characterization and modification of Gum Arabic microgels for hemocompatibility and antimicrobial studies

被引:73
作者
Farooq, Muhammad [1 ]
Sagbas, Selin [2 ,3 ]
Sahiner, Mehtap [4 ]
Siddiq, Mohammad [1 ]
Turk, Mustafa [5 ]
Aktas, Nahit [6 ]
Sahiner, Nurettin [2 ,3 ]
机构
[1] Quaid I Azam Univ, Dept Chem, Islamabad 45320, Pakistan
[2] Canakkale Onsekiz Mart Univ, Dept Chem, Fac Sci & Arts, Terzioglu Campus, TR-17100 Canakkale, Turkey
[3] Canakkale Onsekiz Mart Univ, Nanosci & Technol Res & Applicat Ctr NANORAC, Terzioglu Campus, TR-17100 Canakkale, Turkey
[4] Ege Univ, Leather Engn Dept, TR-35080 Izmir, Turkey
[5] Kirikkale Univ, Bimomed Engn, TR-06450 Kirikkale, Turkey
[6] Yuzuncu Yil Univ, Dept Chem Engn, TR-65080 Van, Turkey
关键词
Gum Arabic microgels/nanogels; Modifiable GA particle; Degradable/biocompatible GA microgel; Antimicrobial GA microgel; IN-VITRO; CELLULOSE; PARTICLES; TAURINE; DIETHYLENETRIAMINE; NANOPARTICLES; OPTIMIZATION; MICROSPHERES; ADSORPTION; POLYMERS;
D O I
10.1016/j.carbpol.2016.09.052
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Gum Arabic (GA) microgels were successfully prepared via reverse micellization method with high yield (78.5 +/- 5.0%) in 5-100 mu m size range using divinyl sulfone (DVS) as a crosslinker. The GA microgels were degraded hydrolytically 22.8 +/- 3.5% at pH 1 in 20 days, whereas no degradation was observed at pH 7.4 and pH 9 at 37 degrees C. By using diethylenetriamine (DETA), and taurine (TA) as chemical modifying agents, GA microgels were chemically modified as GA-DETA and GA-TA, and the zeta potential values of 5.2 +/- 4.1 and -24.8 +/- 1.3 mV were measured, respectively in comparison to -27.3 +/- 4.2 mV for GA. Moreover, blood compatibility of GA, GA-TA, and GA-DETA microgels was tested via in vitro protein adsorption, % hemolysis ratio, and blood clotting index. All the microgels were hemocompatible with% hemolysis ratio between 0.23 to 2.05, and the GA microgels were found to be highly compatible with a blood clotting index of 81 +/- 40. The biocompatibility of GA, GA-DETA and GA-Taurine microgels against L929 fibroblast cells also revealed 84.4, 89.1, and 67.0% cell viability, respectively, at 25.0 mu g/mL concentration, suggesting great potential in vivo biomedical applications up to this concentration. In addition, 5 and 10 mgImL minimum inhibition concentrations of protonated GA-DETA microgels (GA-DETA-HCl) were determined against E. coli and S. aureus, respectively. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:380 / 389
页数:10
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