Development of antibacterial coating on silicone surface via chlorhexidine-loaded nanospheres

被引:49
作者
Phuengkham, Hathaichanok [1 ,2 ,3 ]
Nasongkla, Norased [1 ,2 ,3 ]
机构
[1] Mahidol Univ, Fac Engn, Dept Biomed Engn, 25-25 Puttamonthon 4 Salaya, Nakhon Pathom 73170, Thailand
[2] Mahidol Univ, Dept Chem, Fac Sci, Bangkok 10400, Thailand
[3] Mahidol Univ, Ctr Excellence Innovat Chem, Fac Sci, Bangkok 10400, Thailand
关键词
URINARY-TRACT-INFECTION; IN-VITRO; PLGA NANOPARTICLES; POLYMERIC MICELLES; CATHETER; DEVICES; POLY(EPSILON-CAPROLACTONE); CIPROFLOXACIN; COMBINATION; PREVENTION;
D O I
10.1007/s10856-015-5418-2
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Urinary tract infections (UTIs) are the most common type of hospital-acquired infection which cause significant morbidity and mortality. Antibacterial urinary devices to prevent UTIs are in great demand, while the problem of releasing antibacterials is still limited by duration of antibacterial release and hinders their clinical applications. This study investigated a new approach to sustain release of chlorhexidine (CHX) from urinary devices by coating of chlorhexidine-loaded nanospheres (CHX-NPs) on the surface. CHX-NPs were prepared by high-pressure emulsification-solvent evaporation technique that provided the size of nanospheres at 198.8 nm and the drug loading content at 5.6 %. These nanospheres were spray-coated on silicone surface with reproducible and predictable amount of CHX. Release studies conducted in artificial urine to mimic in vivo condition showed that suitable dose of CHX was released in a sustained manner within a couple of weeks. Additionally, CHX-NPs showed antibacterial activity against common bacteria causing UTIs up to 15 days, which is threefold longer than that of physical mixing between CHX and polymer. Results from this study suggest possible applications of CHX-NPs in coating the surface of ureteral-relating devices for sustained antibacterial release.
引用
收藏
页码:1 / 11
页数:11
相关论文
共 34 条
[1]   Initial inappropriate urinary catheters use in a tertiary-care center: Incidence, risk factors, and outcomes [J].
Apisarnthanarak, Anucha ;
Rutjanawech, Sasinuj ;
Wichansawakun, Sanit ;
Ratanabunjerdkul, Hataiwan ;
Patthranitima, Patarawin ;
Thongphubeth, Kanokporn ;
Suwannakin, Akeruetai ;
Warren, David K. ;
Fraser, Victoria J. .
AMERICAN JOURNAL OF INFECTION CONTROL, 2007, 35 (09) :594-599
[2]   Furanones as potential anti-bacterial coatings on biomaterials [J].
Baveja, JK ;
Wilcox, MDP ;
Hume, EBH ;
Kumar, N ;
Odell, R ;
Poole-Warren, LA .
BIOMATERIALS, 2004, 25 (20) :5003-5012
[3]   Haloperidol-loaded PLGA nanoparticles: Systematic study of particle size and drug content [J].
Budhian, Avinash ;
Siegel, Steven J. ;
Winey, Karen I. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2007, 336 (02) :367-375
[4]   A novel drug-eluting stent spray-coated with multi-layers of collagen and sirolimus [J].
Chen, MC ;
Liang, HF ;
Chiu, YL ;
Chang, Y ;
Wei, HJ ;
Sung, HW .
JOURNAL OF CONTROLLED RELEASE, 2005, 108 (01) :178-189
[5]   Effect of Daily Chlorhexidine Bathing on Hospital-Acquired Infection [J].
Climo, Michael W. ;
Yokoe, Deborah S. ;
Warren, David K. ;
Perl, Trish M. ;
Bolon, Maureen ;
Herwaldt, Loreen A. ;
Weinstein, Robert A. ;
Sepkowitz, Kent A. ;
Jernigan, John A. ;
Sanogo, Kakotan ;
Wong, Edward S. .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 368 (06) :533-542
[6]   Bacterial biofilms: A common cause of persistent infections [J].
Costerton, JW ;
Stewart, PS ;
Greenberg, EP .
SCIENCE, 1999, 284 (5418) :1318-1322
[7]   Efficacy of combination of chlorhexidine and protamine sulphate against device-associated pathogens [J].
Darouiche, Rabih O. ;
Mansouri, Mohammad D. ;
Gawande, Purushottam V. ;
Madhyastha, Srinivasa .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2008, 61 (03) :651-657
[8]   A scoping review of important urinary catheter induced complications [J].
Dellimore, K. H. ;
Helyer, A. R. ;
Franklin, S. E. .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2013, 24 (08) :1825-1835
[9]   Just spray it - LbL assembly enters a new age [J].
Dierendonck, Marijke ;
De Koker, Stefaan ;
De Rycke, Riet ;
De Geest, Bruno G. .
SOFT MATTER, 2014, 10 (06) :804-807
[10]   In vitro studies on the release of isoniazid incorporated in poly(ε-caprolactone) [J].
Duran, N. ;
De Oliveira, A. F. ;
De Azevedo, M. M. M. .
JOURNAL OF CHEMOTHERAPY, 2006, 18 (05) :473-479