Tähkä Sari M, Bonabi Ashkan, Nordberg Maria-Elisa, Kanerva Meeri, Jokinen Ville P, Sikanen Tiina M
Division of Pharmaceutical Chemistry and Technology, Faculty of Pharmacy, FI-00014 University of Helsinki, Helsinki, Finland.
Department of Materials Science and Engineering, School of Chemical Technology, Aalto University, Aalto FI-00076, Finland.
J Chromatogr A. 2015 Dec 24;1426:233-40. doi: 10.1016/j.chroma.2015.11.072. Epub 2015 Nov 26.
Thiol-ene polymer formulations are raising growing interest as new low-cost fabrication materials for microfluidic devices. This study addresses their feasibility for microchip electrophoresis (MCE) via characterization of the effects of UV curing conditions and aging on the surface charge and wetting properties. A detailed comparison is made between stoichiometric thiol-ene (1:1) and thiol-ene formulations bearing 50% molar excess of allyls ("enes"), both prepared without photoinitiator or other polymer modifiers. Our results show that the surface charge of thiol-ene 1:1 increases along with increasing UV exposure dose until a threshold (here, about 200J/cm(2)), whereas the surface charge of thiol-ene 2:3 decreases as a function of increasing UV dose. However, no significant change in the surface charge upon storage in ambient air was observed over a period of 14 days (independent of the curing conditions). The water contact angles of thiol-ene 2:3 (typically 70-75°) were found to be less dependent on the UV dose and storing time. Instead, water contact angles of thiol-ene 1:1 slightly decrease (from initial 90 to 95° to about 70°) as a function of UV increasing exposure dose and storing time. Most importantly, both thiol-ene formulations remain relatively hydrophilic over extended periods of time, which favors their use in MCE applications. Here, MCE separation of biologically active peptides and selected fluorescent dyes is demonstrated in combination with laser-induced fluorescence detection showing high separation efficiency (theoretical plates 8200 per 4cm for peptides and 1500-2700 per 4cm for fluorescent dyes) and lower limits of detection in the sub-μM (visible range) or low-μM (near-UV range) level.
硫醇-烯聚合物配方作为微流控设备新型低成本制造材料正日益受到关注。本研究通过表征紫外光固化条件和老化对表面电荷及润湿性的影响,探讨了其用于微芯片电泳(MCE)的可行性。对化学计量比的硫醇-烯(1:1)和含50%摩尔过量烯丙基(“烯”)的硫醇-烯配方进行了详细比较,二者均在无光引发剂或其他聚合物改性剂的情况下制备。我们的结果表明,1:1硫醇-烯的表面电荷随紫外光照射剂量增加而增加,直至达到一个阈值(此处约为200J/cm²),而2:3硫醇-烯的表面电荷随紫外光剂量增加而降低。然而,在14天的时间内,在环境空气中储存时表面电荷未观察到显著变化(与固化条件无关)。发现2:3硫醇-烯的水接触角(通常为70 - 75°)对紫外光剂量和储存时间的依赖性较小。相反,1:1硫醇-烯的水接触角随紫外光照射剂量和储存时间增加而略有降低(从初始的90至95°降至约70°)。最重要的是,两种硫醇-烯配方在较长时间内都保持相对亲水性,这有利于它们在MCE应用中的使用。在此,结合激光诱导荧光检测展示了生物活性肽和选定荧光染料的MCE分离,显示出高分离效率(肽每4cm理论塔板数为8200,荧光染料每4cm为1500 - 2700)以及亚微摩尔(可见光范围)或低微摩尔(近紫外范围)水平的较低检测限。