Biomaterials Science
Biomaterials Science
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DOI:
10.1039/2047-4849/2013
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发表时间:
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通讯作者:
Ziyuan Song;Yee Ming Khaw;Lazaro A Pacheco;Kuan-Ying Tseng;Zhengzhong Tan;Kaimin Cai;Ettigounder Ponnusamy;Jianjun Cheng;Makoto Inoue
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作者:
Ziyuan Song;Yee Ming Khaw;Lazaro A Pacheco;Kuan-Ying Tseng;Zhengzhong Tan;Kaimin Cai;Ettigounder Ponnusamy;Jianjun Cheng;Makoto Inoue
In the last decades, non-thermal plasma has been extensively investigated as a relevant tool for various biomedical applications, ranging from tissue decontamination to regeneration and from skin treatment to tumor therapies. This high versatility is due to the di ff erent kinds and amount of reactive oxygen and nitrogen species that can be generated during a plasma treatment and put in contact with the biological target. Some recent studies report that solutions of biopolymers with the ability to generate hydrogels, when treated with plasma, can enhance the generation of reactive species and in fl uence their stability, resulting thus in the ideal media for indirect treatments of biological targets. The direct e ff ects of the plasma treatment on the structure of biopolymers in water solution, as well as the chemical mechanisms responsible for the enhanced generation of RONS, are not yet fully understood. In this study, we aim at fi lling this gap by investigating, on the one hand, the nature and extent of the modi fi cations induced by plasma treatment in alginate solutions, and, on the other hand, at using this information to explain the mechanisms responsible for the enhanced generation of reactive species as a consequence of the treatment. The approach we use is twofold: (i) investigating the e ff ects of plasma treatment on alginate solutions, by size exclusion chromatography, rheology and scanning electron microscopy and (ii) study of a molecular model (glucuro-nate) sharing its chemical structure, by chromatography coupled with mass spectrometry and by molecular dynamics simulations. Our results point out the active role of the biopolymer chemistry during direct plasma treatment. Short-lived reactive species, such as OH radicals and O atoms, can modify the polymer structure, a ff ecting its functional groups and causing partial fragmentation. Some of these chemical modi fi cations, like the generation of organic peroxide, are likely responsible for the secondary generation of long-lived reactive species such as hydrogen peroxide and nitrite ions. This is relevant in view of using biocompatible hydrogels as vehicles for storage and delivery reactive species for targeted therapies.