Orthner M P, Lin G, Avula M, Buetefisch S, Magda J, Rieth L W, Solzbacher F
Department of Electrical and Computer Engineering, University of Utah, Salt Lake City, UT, USA.
Sens Actuators B Chem. 2010 Mar 19;145(2):807-816. doi: 10.1016/j.snb.2010.01.063.
This report details the first experimental results from novel hydrogel sensor array (2 × 2) which incorporates analyte diffusion pores into a piezoresistive diaphragm for the detection of hydrogel swelling pressures and hence chemical concentrations. The sensor assembly was comprised of three components, the active four sensors, HPMA/DMA/TEGDMA (hydroxypropyl methacrylate (HPMA), N,N-dimethylaminoethyl methacrylate (DMA) and crosslinker tetra-ethyleneglycol dimethacrylate (TEGDMA)) hydrogel, and backing plate. Each of the individual sensors of the array can be used with various hydrogels used to measure the presence of a number of stimuli including pH, ionic strength, and glucose concentrations. Ideally, in the future, these sensors will be used for continuous metabolic monitoring applications and implanted subcutaneously. In this paper and to properly characterize the sensor assembly, hydrogels sensitive to changes ionic strength were synthesized using hydroxypropyl methacrylate (HPMA), N,N-dimethylaminoethyl methacrylate (DMA) and crosslinker tetra-ethyleneglycol dimethacrylate (TEGDMA) and inserted into the sensor assembly. This hydrogel quickly and reversibly swells when placed environments of physiological buffer solutions (PBS) with ionic strengths ranging from 0.025 to 0.15 M, making it ideal for proof-of-concept testing and initial characterization. The assembly was wire bonded to a printed circuit board and coated with 3 ± 0.5 μm of Parylene-C using chemical vapor deposition (CVD) to protect the sensor and electrical connections during ionic strength wet testing. Two versions of sensors were fabricated for comparison, the first incorporated diffusion pores into the diaphragm, and the second used a solid diaphragm with perforated backing plate. This new design (perforated diaphragm) was shown to have slightly higher sensitivity than solid diaphragm sensors with separate diffuse backing plates when coupled with the hydrogel. The sensitivities for the 1 mm × 1 mm, 1.25 mm × 1.25 mm, 1.5 mm × 1.5 mm perforated diaphragm sensors were 53.3 ± 6.5, 171.7 ± 8.8, and 271.47 ± 27.53 mV/V-M, respectively. These results show that perforations in the diaphragm can be used not only to allow the diffusion of analyte into the cavity but to increase mechanical stress in the piezoresistive diaphragm, thereby increasing sensor output signal. The time constants for swelling () and contracting () were calculated by fitting the sensor output half cycles to an exponential growth function. We found that the sensors' response was initially retarded during the preliminary hydrogel conditioning period then improved after 3-5 cycles with values of approximately 9 and 7 min for and . For all sensors tested > . This may be due to the increased loading on the hydrogel from the diaphragm during the swelling process. During contraction the diaphragm aids the hydrogel by reversibly applying mechanical pressure and therefore reducing . Long term stability testing showed the sensors remained functional for upwards of 2 weeks in the test phosphate buffer solution (PBS).
本报告详细介绍了新型水凝胶传感器阵列(2×2)的首批实验结果,该阵列将分析物扩散孔整合到压阻式膜片中,用于检测水凝胶膨胀压力,进而检测化学浓度。传感器组件由三个部分组成:四个有源传感器、HPMA/DMA/TEGDMA(甲基丙烯酸羟丙酯(HPMA)、N,N-二甲基氨基乙基甲基丙烯酸酯(DMA)和交联剂四乙二醇二甲基丙烯酸酯(TEGDMA))水凝胶以及背板。该阵列中的每个单独传感器都可与多种水凝胶配合使用,以测量多种刺激因素的存在,包括pH值、离子强度和葡萄糖浓度。理想情况下,这些传感器未来将用于连续代谢监测应用,并皮下植入。在本文中,为了正确表征传感器组件,使用甲基丙烯酸羟丙酯(HPMA)、N,N-二甲基氨基乙基甲基丙烯酸酯(DMA)和交联剂四乙二醇二甲基丙烯酸酯(TEGDMA)合成了对离子强度变化敏感的水凝胶,并将其插入传感器组件中。当置于离子强度范围为0.025至0.15 M的生理缓冲溶液(PBS)环境中时,这种水凝胶会迅速且可逆地膨胀,这使其成为概念验证测试和初始表征的理想选择。该组件通过引线键合连接到印刷电路板上,并使用化学气相沉积(CVD)涂覆3±0.5μm的聚对二甲苯-C,以在离子强度湿法测试期间保护传感器和电气连接。制造了两种版本的传感器进行比较,第一种在膜片中加入了扩散孔,第二种使用带有穿孔背板的实心膜片。结果表明,这种新设计(穿孔膜片)与水凝胶结合使用时,比带有单独扩散背板的实心膜片传感器具有略高的灵敏度。1mm×1mm、1.25mm×1.25mm、1.5mm×1.5mm穿孔膜片传感器的灵敏度分别为53.3±6.5、171.7±8.8和271.47±27.53 mV/V-M。这些结果表明,膜片中的穿孔不仅可用于使分析物扩散到腔中,还可增加压阻式膜片中的机械应力,从而增加传感器输出信号。通过将传感器输出半周期拟合到指数增长函数来计算膨胀()和收缩()的时间常数。我们发现传感器的响应在初步水凝胶调节期最初会延迟,然后在3-5个周期后得到改善,和的值约为9分钟和7分钟。对于所有测试的传感器,>。这可能是由于膨胀过程中膜片对水凝胶的负载增加所致。在收缩过程中,膜片通过可逆地施加机械压力来辅助水凝胶,从而减小。长期稳定性测试表明,传感器在测试磷酸盐缓冲溶液(PBS)中可保持功能超过2周。