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一种新型抗菌羊毛织物的制备 被引量:2

Preparation of a novel anti-bacterial wool fabrics
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摘要 将β-环糊精(β-CD)磺化改性后接枝于羊毛织物上,利用"锚固"在羊毛织物上的β-CD空腔充载抗菌剂硝酸咪康唑,制备一种新型的抗菌羊毛织物。磺化β-CD接枝羊毛织物最佳工艺条件为:磺化β-CD 60 g/L,无水硫酸钠5 g/L,pH值2-3,于90-100℃的整理浴中保温50-60 min。经磺化β-CD接枝改性后再充载硝酸咪康唑的羊毛织物,其抗菌性能好于未经磺化β-CD改性直接充载硝酸咪康唑的织物。改性织物抗菌性能的耐水性明显优于未经改性的织物。未经改性的织物水洗5次后,抗菌性能基本消失,而改性织物水洗10次后,其抗菌性能仍保持在60%~70%。 β- cyclodextrins(β- CDs) modified by sulfonation were grafted onto wool fabrics and a novel kind of anti-bacterial fabrics was prepared by filling the anti-bacterial agent(miconazole nitrate) into β- CDs' caves fixed onto the fabrics. The optimum conditions for sulfonated-β - CD grafting onto wool fabrics were: sulfonated-β- CD 60 g/L, Na2SO4 5 g/L, pH = 2 - 3, dipping the fabrics into solution at 90 - 95 ℃ for 50 - 60 min. Compared with the unmodified fabrics, the fabrics modified with sulfonated-β- CD increased the uptake of antibacterial agent, miconazole nitrate, enhancing the antibacterial properties of the modified fabrics. The binding of β - CD onto the wool fabrics improved the resistance of the entrapped antibacterial agents to washing cycles, prolonging the antibacterial effect. The anti-bacterial abilities of the unmodified fabrics was almost lost when washing 5 times, while sulfonated-β - CD fabrics kept 60% -70% even after washing 10 times.
出处 《毛纺科技》 CAS 北大核心 2009年第9期5-10,共6页 Wool Textile Journal
关键词 硝酸咪康唑 Β-环糊精 包合物 抗菌 羊毛织物 miconazole nitrate β- cyclodextrin inclusion anti-bacteria wool fabrics
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  • 1Bibby D C, Davies N M. Mechanism by which cyclodextrins modify drug release from polymeric drug delivery systems[J], Int J Pham, 2000,197:1 - 11.
  • 2Bibby D C, Davies N M. Poly(acrylic acid) microspheres containing β-cyclodextrin: loading and in vitro release of two dyes [J]. Int J Pharm, 1999,187 : 243 - 250.
  • 3Baille W E, Huang W Q. Functionalized β-cyclodextfin polymers for the sorption of bile salts[J]. J Macromol Sci-Pure Appl Chem, 2000 (7) : 677 - 690.
  • 4Loftsson M. Pharmaceutical application of cyclodextrin. 1. Drug solubilization and stabilization [ J ]. J Pharm Sci, 1996,85 : 1017 - 1025.
  • 5Liu Y Y, Fan X D. A cyclodextrin microgel for controlled release driven by inclusion effects[J]. Macromol Rapid Commum,2004,25: 729 - 736.
  • 6Vaios T, Karathanos M. Study of the solubility, antioxidant activity and structure of inclusion complex of vanillin with β-cyclodextrin[ J]. Food Chemistry,2007,101(3) : 652 - 653.
  • 7Jimenez S. A new method for determining the composition and stability constant of complex of the form AmBn [ J ]. J Anal Chem Acta,1997,90:223 - 231.
  • 8Nakajuma T, Hirobasbi M. Complex between cyclodextrins and bencylane in aqueous solution[ J]. J Chem Pharm Bull, 1984,32(2) : 383 - 389.
  • 9Nostro P, Frantoni L. Surface treatment on tencel fabric: grafting with β-cyclodextfin[J]. J. Appl. Polym. Sci ,2003,88 : 706 - 715.
  • 10Buschmann H J, Denter U, Knittel D. Removal of residual surfaetant deposits from textile materials with the aid of cyelodextrins [ J ]. Melliand Textiberichte, 1995(9) : 216 - 218.

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