Wu Gaoyi, Shi Wei, Liu Moran, Liang Lixin, Wang Tao, Zhang Jinyong, Chen Jing, Liang Yongsheng, Tang Wei, Li Hui
College of Big Data and Internet, Shenzhen Technology University, 3002 Lantian Road, Shenzhen, Guangdong 518118, China.
Key Laboratory of Human-Machine-Intelligence Synergic System, Research Center for Neural Engineering, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, 1068 Xueyuan Road, Shenzhen, Guangdong 518055, China.
ACS Appl Mater Interfaces. 2025 Feb 12;17(6):9879-9890. doi: 10.1021/acsami.4c20994. Epub 2025 Feb 2.
Hydrogels have emerged as promising candidates for flexible sensors due to their softness, biocompatibility, and tunable physicochemical properties. However, achieving synchronous satisfaction of conformality, conductivity, and diverse biological functions in hydrogel sensors remains a challenge. Here, we proposed a multifunctional hydrogel sensor by incorporating silver-loaded polydopamine nanoparticles (Ag@PDA) into a thermally cross-linked methacrylamide chitosan (CSMA) and acrylamide network, namely, Ag@PDA/(CSMA-PAM). The Ag@PDA/(CSMA-PAM) hydrogel showed the capability to respond effectively to both strain and pressure, enabling its independent application as either a strain sensor or a pressure sensor. The sensitivity of the hydrogel can reach 2.13 within the strain range of 65 to 150%, exhibiting a response and recovery time of 550 ms when utilized as a strain sensor. In contrast, its sensitivity was 0.07 kPa during pressures ranging from 0 to 2.15 kPa, with a response and recovery time of 136 ms when employed as a pressure sensor. Additionally, the hydrogel sensor demonstrated high linearity (0.998 for strain and 0.98 for pressure), stable cycling ability (500 cycles), and low detection limit (0.5% for strain and 150 Pa for pressure). Moreover, the Ag@PDA/(CSMA-PAM) hydrogel exhibited good stability and reliability for a variety of practical applications, including the detection of subtle and large deformations, as well as real-time physiological activity monitoring. Further, owing to the bioactive components of chitosan and Ag@PDA present in the hydrogel, the Ag@PDA/(CSMA-PAM) sensor exhibited satisfactory biocompatibility along with excellent antioxidant and antibacterial activities, making it highly promising for applications as wearable sensors in personalized healthcare.
水凝胶因其柔软性、生物相容性和可调节的物理化学性质,已成为柔性传感器的理想候选材料。然而,要使水凝胶传感器同时满足保形性、导电性和多种生物功能,仍然是一项挑战。在此,我们通过将载银聚多巴胺纳米颗粒(Ag@PDA)掺入热交联的甲基丙烯酰胺壳聚糖(CSMA)和丙烯酰胺网络中,制备了一种多功能水凝胶传感器,即Ag@PDA/(CSMA-PAM)。Ag@PDA/(CSMA-PAM)水凝胶显示出对应变和压力都能有效响应的能力,使其能够独立用作应变传感器或压力传感器。该水凝胶在65%至150%的应变范围内灵敏度可达2.13,用作应变传感器时响应和恢复时间为550毫秒。相比之下,在0至2.15千帕的压力范围内,其灵敏度为0.07千帕,用作压力传感器时响应和恢复时间为136毫秒。此外,该水凝胶传感器具有高线性度(应变线性度为0.998,压力线性度为0.98)、稳定的循环能力(500次循环)和低检测限(应变检测限为0.5%,压力检测限为150帕)。此外,Ag@PDA/(CSMA-PAM)水凝胶在各种实际应用中表现出良好的稳定性和可靠性,包括对细微和大变形的检测以及实时生理活动监测。此外,由于水凝胶中存在壳聚糖和Ag@PDA等生物活性成分,Ag@PDA/(CSMA-PAM)传感器表现出令人满意的生物相容性以及出色的抗氧化和抗菌活性,使其在个性化医疗中作为可穿戴传感器的应用前景广阔。