Graduate School of Information Science and Electrical Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan.
Intelligent Sensor Technology, Inc., 5-1-1 Onna, Atsugi-shi 243-0032, Japan.
Sensors (Basel). 2021 Dec 14;21(24):8343. doi: 10.3390/s21248343.
The lipid phosphoric acid di-n-decyl ester (PADE) has played an important role in the development of taste sensors. As previously reported, however, the concentration of PADE and pH of the solution affected the dissociation of H+, which made the measurement results less accurate and stable. In addition, PADE caused deterioration in the response to bitterness because PADE created the acidic environment in the membrane. To solve these problems, our past study tried to replace the PADE with a completely dissociated substance called tetrakis [3,5-bis (trifluoromethyl) phenyl] borate sodium salt dehydrate (TFPB) as lipid. To find out whether the two substances can be effectively replaced, it is necessary to perform an in-depth study on the properties of the two membranes themselves. In this study, we fabricated two types of membrane electrodes, based on PADE or TFPB, respectively, using 2-nitrophenyl octyl ether (NPOE) as a plasticizer. We measured the selectivity to cations such as Cs+, K+, Na+ and Li+, and also the membrane impedance of the membranes comprising PADE or TFPB of the different concentrations. As a result, we found that any concentration of PADE membranes always had low ion selectivity, while the ion selectivity of TFPB membranes was concentration-dependent, showing increasing ion selectivity with the TFPB concentrations. The ion selectivity order was Cs+>K+>Na+>Li+. The hydration of ions was considered to participate in this phenomenon. In addition, the membrane impedance decreased with increasing PADE and TFPB concentrations, while the magnitudes differed, implying that there is a difference in the dissociation of the two substances. The obtained results will contribute to the development of novel receptive membranes of taste sensors.
双十二烷基磷酸二酯(PADE)在味觉传感器的发展中发挥了重要作用。然而,如前所述,PADE 的浓度和溶液的 pH 值会影响 H+的离解,这使得测量结果不够准确和稳定。此外,PADE 会导致对苦味的响应恶化,因为 PADE 在膜中产生了酸性环境。为了解决这些问题,我们之前的研究试图用一种称为四[3,5-双(三氟甲基)苯基]硼酸三钠盐脱水物(TFPB)的完全离解物质代替 PADE 作为脂质。为了确定这两种物质是否可以有效替代,有必要深入研究这两种膜本身的性质。在这项研究中,我们分别使用 2-硝基苯基辛基醚(NPOE)作为增塑剂,制备了基于 PADE 或 TFPB 的两种类型的膜电极。我们测量了对 Cs+、K+、Na+和 Li+等阳离子的选择性,以及不同浓度的 PADE 或 TFPB 膜的膜阻抗。结果发现,任何浓度的 PADE 膜的离子选择性总是很低,而 TFPB 膜的离子选择性则与浓度有关,随着 TFPB 浓度的增加而增加离子选择性。离子选择性顺序为 Cs+>K+>Na+>Li+。认为离子的水合作用参与了这一现象。此外,随着 PADE 和 TFPB 浓度的增加,膜阻抗降低,但幅度不同,这表明两种物质的离解程度不同。所得结果将有助于新型味觉传感器接收膜的开发。