Surface-Catalyzed Nitric Oxide Release via a Metal Organic Framework Enhances Antibacterial Surface Effects

被引:47
作者
Garren, Mark [1 ]
Maffe, Patrick [1 ]
Melvin, Alyssa [2 ]
Griffin, Lauren [1 ]
Wilson, Sarah [1 ]
Douglass, Megan [1 ]
Reynolds, Melissa [2 ,3 ]
Handa, Hitesh [1 ,4 ]
机构
[1] Univ Georgia, Coll Engn, Sch Chem Mat & Biomed Engn, Athens, GA 30602 USA
[2] Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
[3] Colorado State Univ, Sch Biomed Engn & Chem & Biol Engn, Ft Collins, CO 80523 USA
[4] Univ Georgia, Coll Pharm, Dept Pharmaceut & Biomed Sci, Athens, GA 30602 USA
基金
美国国家卫生研究院;
关键词
metal organic framework; nitric oxide; infection; catalysis; S-nitrosothiols; NITROSO-N-ACETYLPENICILLAMINE; S-NITROSOGLUTATHIONE; GENERATION; INFECTIONS; POLYMERS; NANOPARTICLES; BIOMATERIALS; PREVENTION; REACTIVITY; CATHETERS;
D O I
10.1021/acsami.1c17248
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
It has been previously demonstrated that metal nano-particles embedded into polymeric materials doped with nitric oxide (NO) donor compounds can accelerate the release rate of NO for therapeutic applications. Despite the advantages of elevated NO surface flux for eradicating opportunistic bacteria in the initial hours of application, metal nanoparticles can often trigger a secondary biocidal effect through leaching that can lead to unfavorable cytotoxic responses from host cells. Alternatively, copper-based metal organic frameworks (MOFs) have been shown to stabilize Cu-2+(/)1+ via coordination while demonstrating longer-term catalytic performance compared to their salt counterparts. Herein, the practical application of MOFs in NO-releasing polymeric substrates with an embedded NO donor compound was investigated for the first time. By developing composite thermoplastic silicon polycarbonate polyurethane (TSPCU) scaffolds, the catalytic effects achievable via intrapolymeric interactions between an MOF and NO donor compound were investigated using the water-stable copper-based MOF H-3[(Cu4Cl)(3) (BTTri)(8)-(H2O)(12)]center dot 72H(2)O (CuBTTri) and the NO donor S-nitroso-N-acetyl-penicillamine (SNAP). By creating a multifunctional triple-layered composite scaffold with CuBTTri and SNAP, the surface flux of NO from catalyzed SNAP decomposition was found tunable based on the variable weight percent CuBTTri incorporation. The tunable NO surface fluxes were found to elicit different cytotoxic responses in human cell lines, enabling application-specific tailoring. Challenging the TSPCU-NO-MOF composites against 24 h bacterial growth models, the enhanced NO release was found to elicit over 99% reduction in adhered and over 95% reduction in planktonic methicillin-resistant Staphylococcus aureus, with similar results observed for Escherichia coli. These results indicate that the combination of embedded MOFs and NO donors can be used as a highly efficacious tool for the early prevention of biofilm formation on medical devices.
引用
收藏
页码:56931 / 56943
页数:13
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