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On-chip cell lysis by antibacterial non-leaching reusable quaternary ammonium monolithic column

机译:抗菌非浸出可重复使用的季铵整体柱在芯片上的细胞裂解

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摘要

Reusable antibacterial non-leaching monolithic columns polymerized in microfluidic channels designed for on-chip cell lysis applications were obtained by the photoinitiated free radical copolymerization of diallyldimethylammonium chloride (DADMAC) and ethylene glycol diacrylate (EGDA) in the presence of a porogenic solvent. The microfluidic channels were fabricated in cross-linked poly(methyl methacrylate) (X-PMMA) substrates by laser micromachining. The monolithic columns have the ability to inhibit the growth of, kill and efficiently lyse gram-positive Micrococcus luteus (Schroeter) (ATCC 4698) and Kocuria rosea (ATCC 186), and gram-negative bacteria Pseudomonas putida (ATCC 12633) and Escherichia coli (ATCC 35218) by mechanically shearing the bacterial membrane when forcing the cells to pass through the narrow pores of the monolithic column, and simultaneously disintegrating the cell membrane by physical contact with the antibacterial surface of the column. Cell lysis was confirmed by off-chip PCR without the need for further purification. The influence of the cross-linking monomer on bacterial growth inhibition, leaching, lysis efficiency of the monolithic column and its mechanical stability within the microfluidic channel were investigated and analyzed for three different cross-linking monomers: ethylene glycol dimethacrylate (EGDA), ethylene glycol dimethacrylate (EGDMA) and 1,6-hexanediol dimethacrylate (1,6-HDDMA). Furthermore, the bonding efficiency of two X-PMMA substrates with different cross-linking levels was studied. The monolithic columns were shown to be stable, non-leaching, and reusable for over 30 lysis cycles without significant performance degradation or DNA carryover when they were back-flushed between lysis cycles.
机译:在成孔溶剂存在下,通过二烯丙基二甲基氯化铵(DADMAC)和乙二醇二丙烯酸酯(EGDA)的光引发自由基共聚,获得了设计用于芯片上细胞裂解应用的在微流体通道中聚合的可重复使用的抗菌非浸出整体柱。通过激光微加工在交联的聚甲基丙烯酸甲酯(X-PMMA)基板中制造微流通道。整体式色谱柱具有抑制,消灭革兰氏阳性微球菌(Schroeter)(ATCC 4698)和玫瑰科库里亚(Kocuria rosea)(ATCC 186)以及革兰氏阴性细菌恶臭假单胞菌(Pseudomonas putida)(ATCC 12633)和大肠杆菌的生长,杀死并有效裂解的能力。 (ATCC 35218),当迫使细胞通过整体柱的狭窄孔时,通过机械剪切细菌膜,并通过与柱的抗菌表面物理接触同时分解细胞膜。通过片外PCR证实细胞裂解,而无需进一步纯化。对于三种不同的交联单体:乙二醇二甲基丙烯酸酯(EGDA),乙二醇,研究并分析了交联单体对整体生长柱的细菌生长抑制,浸出,裂解效率及其机械稳定性的影响。二甲基丙烯酸酯(EGDMA)和1,6-己二醇二甲基丙烯酸酯(1,6-HDDMA)。此外,研究了两种具有不同交联度的X-PMMA基材的粘合效率。整体柱显示稳定,不浸出,可重复使用30多个裂解周期,而在裂解周期之间反吹时,不会造成明显的性能下降或DNA残留。

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