Silver(I)-imidazole cyclophane gem-diol complexes encapsulated by electrospun tecophilic nanofibers: Formation of nanosilver particles and antimicrobial activity

被引:511
作者
Melaiye, A
Sun, ZH
Hindi, K
Milsted, A
Ely, D
Reneker, DH
Tessier, CA
Youngs, WJ [1 ]
机构
[1] Univ Akron, Dept Chem, Akron, OH 44325 USA
[2] Univ Akron, Dept Polymer Sci, Akron, OH 44325 USA
[3] Univ Akron, Dept Biol, Akron, OH 44325 USA
关键词
D O I
10.1021/ja040226s
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Silver(I)-imidazole cyclophane gem-diol complex, 3 [Ag2C36N10O4](2+)2(x)(-), where x = OH- or CO32-, was synthesized and well characterized. The minimum inhibition concentration tests showed that the aqueous form of 3 is 2 times less effective as an antibiotic than 0.5% AgNO3, with about the same amount of silver. The antimicrobial activity of 3 was enhanced when encapsulated into Tecophilic polymer by electrospinning to obtain mats made of nano-fibers. The fiber mats released nanosilver particles, which in turn sustained the antimicrobial activity of the mats over a long period of time. The rate of bactericidal activity of 3 was greatly improved by encapsulation, and the amount of silver used was much reduced. The amount of silver contained in the fiber mat of 3, with 75% of 3 and 25% Tecophilic, was 8 times less than that in 0.5% AgNO3 and 5 times lower than that in silver sulfadiazine cream 1%. The fiber mat was found to kill S. aureus at the same rate as 0.5% AgNO3, with zero colonies on an agar plate, and about 6 times faster than silver sulfadiazine cream. The silver mats were found effective against E coli, P. aeruginosa, S. aureus, C. albicans, A. niger, and S. cerevisiae. Transmission electron microscopy and scanning electron microscopy were used to characterize the fiber mats. The acute toxicity of the ligand (imidazolium cyclophane gem-diol dichloride) was assessed by intravenous administration to rats, with an LID 50 of 100 mg/kg of rat.
引用
收藏
页码:2285 / 2291
页数:7
相关论文
共 39 条
[1]  
ANSELL CA, 1971, J CHEM SOC B, P443
[2]  
ANSELL CB, 1969, CHEM COMMUN, P1300
[3]   HOMOLEPTIC CARBENE SILVER(I) AND CARBENE COPPER(I) COMPLEXES [J].
ARDUENGO, AJ ;
DIAS, HVR ;
CALABRESE, JC ;
DAVIDSON, F .
ORGANOMETALLICS, 1993, 12 (09) :3405-3409
[4]  
Atiyeh Bishara S., 2002, Current Pharmaceutical Biotechnology, V3, P179, DOI 10.2174/1389201023378283
[5]  
ATIYEH BS, 2003, J BURNS WOUND CARE, V2, P1
[6]   CRYSTAL-STRUCTURE OF 2-SULFANILAMIDOPYRIMIDINESILVER(I) [J].
BAENZIGER, NC ;
STRUSS, AW .
INORGANIC CHEMISTRY, 1976, 15 (08) :1807-1809
[7]   Imidazolium-linked cyclophanes [J].
Baker, MV ;
Bosnich, MJ ;
Williams, CC ;
Skelton, BW ;
White, AH .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1999, 52 (09) :823-825
[8]  
Bitter I, 2001, EUR J ORG CHEM, V2001, P2861
[9]  
Bognitzki M, 2000, ADV MATER, V12, P637, DOI 10.1002/(SICI)1521-4095(200005)12:9<637::AID-ADMA637>3.0.CO
[10]  
2-W