A flexible,
biocompatible, nitrile butadiene rubber (NBR)-based
strain sensor with high stretchability, good sensitivity, and excellent
repeatability is presented for the first time. Carbon black (CB) particles
were embedded into an NBR matrix via a dissolving-coating technique,
and the obtained NBR/CB composite was coated with polydopamine (PDA)
to preserve the CB layer. The mechanical properties of the NBR films
were found to be significantly improved with the addition of CB and
PDA, and the produced composite films were noncytotoxic and highly
biocompatible. Strain-sensing tests showed that the uncoated CB/NBR
films possess a high sensing range (strain of ∼550%) and good
sensitivity (gauge factor of 52.2), whereas the PDA/NBR/CB films show
a somewhat reduced sensing range (strain of ∼180%) but significantly
improved sensitivity (gauge factor of 346). The hysteresis curves
obtained from cyclic strain-sensing tests demonstrate the prominent
robustness of the sensor material. Three novel equations were developed
to accurately describe the uniaxial and cyclic strain-sensing behavior
observed for the investigated strain sensors. Gloves and knee/elbow
covers were produced from the films, revealing that the signals generated
by different finger, elbow, and knee movements are easily distinguishable,
thus confirming that the PDA/NBR/CB composite films can be used in
a wide range of wearable strain sensor applications.
A novel epitope molecularly imprinted polymer on the surface of magnetic carbon nanotubes (MCNTs@EMIP) was successfully fabricated to specifically recognize target protein cytochrome c (Cyt C) with high performance. The peptides sequences corresponding to the surface-exposed C-terminus domains of Cyt C was selected as epitope template molecule, and commercially available zinc acrylate and ethylene glycol dimethacrylate (EGDMA) were employed as functional monomer and cross-linker, respectively, to synthesize MIP via free radical polymerization. The epitope was immobilized via metal chelation and six-membered ring formed between the functional monomer and the hydroxyl and amino groups of the epitope. The resulting MCNTs@EMIP exhibited specific recognition ability toward target Cyt C including more satisfactory imprinting factor (about 11.7) than that of other reported imprinting methods. In addition, the MCNTs@EMIP demonstrated a high adsorption amount (about 780.0 mg g(-1)) and excellent selectivity. Besides, the magnetic property of the support material made the processes easy and highly efficient by assistance of an external magnetic field. High-performance liquid chromatography analysis of Cyt C in bovine blood real sample and protein mixture indicated that the specificity was not affected by other competitive proteins, which forcefully stated that the MCNTs@EMIP had potential to be applied in bioseparation area. In brief, this study provided a new protocol to detect target protein in complex sample via epitope imprinting approach and surface imprinting strategy.
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