Long-term and high-efficiency capture of Escherichia coli using cellulose acetate nanofiber membrane functionalized with reactive 19 dye and polyhexamethylene biguanide

IF 3.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Thi My Huong Dinh , Bing-Lan Liu , Penjit Srinophakun , Chi-Yun Wang , Chen-Yaw Chiu , Shen-Long Tsai , Kuei-Hsiang Chen , Yu-Kaung Chang
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Abstract

Cellulose acetate (CA) nanofibers have been popularly applied in various biomedical and textile products. In this work, a textile azo-dye Reactive Green 19 (RG19) was selected to be chemically coupled to the CA nanofiber membrane to form dyed CA nanofiber membrane (namely CA-RG19) and then poly(hexamethylene biguanide) (PHMB) as an antibacterial reagent was physically attached to the dyed CA nanofiber membrane, forming CA-RG19-PHMB nanofiber membrane. The nanofiber membranes were evaluated for their physical and mechanical properties, including functional group analysis, morphological characterization, and thermal stability assessment. To investigate the antibacterial properties of the nanofiber membrane, various concentrations of RG19 dye and PHMB were tested to evaluate the antibacterial efficiency (AE) against Escherichia coli of the membranes. It was found that the CA-RG19-PHMB nanofiber membrane exhibited an AE value of approximately 100 %, with the immobilization concentrations of RG19 dye and PHMB being 373.46 mg/g and 0.333 mg/g, respectively. The CA-RG19-PHMB nanofiber membrane showed 100 % antibacterial efficacy after 10 min against E. coli cells. Furthermore, the storage stability of the CA-RG19-PHMB nanofiber membrane remained at approximately 100 % of its initial antibacterial efficacy after 60 days, and it exhibited excellent antibacterial efficacy after five cycles.

使用活性 19 染料和聚六亚甲基双胍功能化的醋酸纤维素纳米纤维膜长期高效捕获大肠杆菌
醋酸纤维素(CA)纳米纤维已被广泛应用于各种生物医学和纺织产品中。本研究选择了一种纺织偶氮染料活性绿19(RG19)与CA纳米纤维膜进行化学耦合,形成染色CA纳米纤维膜(即CA-RG19),然后将抗菌试剂聚六亚甲基双胍(PHMB)物理附着在染色CA纳米纤维膜上,形成CA-RG19-PHMB纳米纤维膜。对纳米纤维膜的物理和机械性能进行了评估,包括官能团分析、形态特征和热稳定性评估。为了研究纳米纤维膜的抗菌性能,对不同浓度的 RG19 染料和 PHMB 进行了测试,以评估膜对大肠杆菌的抗菌效率(AE)。结果发现,CA-RG19-PHMB 纳米纤维膜的 AE 值约为 100%,RG19 染料和 PHMB 的固定浓度分别为 373.46 mg/g 和 0.333 mg/g。10 分钟后,CA-RG19-PHMB 纳米纤维膜对大肠杆菌细胞的抗菌效果达到 100%。此外,CA-RG19-PHMB 纳米纤维膜的贮存稳定性在 60 天后仍保持其初始抗菌效力的约 100%,并且在五个周期后表现出卓越的抗菌效力。
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来源期刊
Biochemical Engineering Journal
Biochemical Engineering Journal 工程技术-工程:化工
CiteScore
7.10
自引率
5.10%
发文量
380
审稿时长
34 days
期刊介绍: The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology. The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields: Biocatalysis (enzyme or microbial) and biotransformations, including immobilized biocatalyst preparation and kinetics Biosensors and Biodevices including biofabrication and novel fuel cell development Bioseparations including scale-up and protein refolding/renaturation Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells Bioreactor Systems including characterization, optimization and scale-up Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization Industrial Biotechnology including specialty chemicals, platform chemicals and neutraceuticals Biomaterials and Tissue Engineering including bioartificial organs, cell encapsulation, and controlled release Cell Culture Engineering (plant, animal or insect cells) including viral vectors, monoclonal antibodies, recombinant proteins, vaccines, and secondary metabolites Cell Therapies and Stem Cells including pluripotent, mesenchymal and hematopoietic stem cells; immunotherapies; tissue-specific differentiation; and cryopreservation Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis Protein Engineering including enzyme engineering and directed evolution.
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