This review highlights current developments, challenges, and future directions for the use of invasive and noninvasive biosample-based small biosensors for early diagnosis of Alzheimer’s disease (AD) with biomarkers to incite a conceptual idea from a broad number of readers in this field. We provide the most promising concept about biosensors on the basis of detection scale (from femto to micro) using invasive and noninvasive biosamples such as cerebrospinal fluid (CSF), blood, urine, sweat, and tear. It also summarizes sensor types and detailed analyzing techniques for ultrasensitive detection of multiple target biomarkers (i.e., amyloid beta (Aβ) peptide, tau protein, Acetylcholine (Ach), microRNA137, etc.) of AD in terms of detection ranges and limit of detections (LODs). As the most significant disadvantage of CSF and blood-based detection of AD is associated with the invasiveness of sample collection which limits future strategy with home-based early screening of AD, we extensively reviewed the future trend of new noninvasive detection techniques (such as optical screening and bio-imaging process). To overcome the limitation of non-invasive biosamples with low concentrations of AD biomarkers, current efforts to enhance the sensitivity of biosensors and discover new types of biomarkers using non-invasive body fluids are presented. We also introduced future trends facing an infection point in early diagnosis of AD with simultaneous emergence of addressable innovative technologies.
Polydimethylsiloxane (PDMS)-based elastomers have become the de facto platform for various biomedical applications. But the stable attachment of biomolecules to PDMS for more robust and long-term performance of the PDMS-based devices has been a significant challenge, owing to its unique physical properties (e.g. hydrophobicity, dynamic molecular mobility). Herein, the PDMS membrane with tunable surface porosity is developed via high-pressure saturated steam technology in order to promote a strong and lasting bioadhesion to the PDMS membrane without additional processing steps. The resulting porous PDMS membranes demonstrate enhanced physical properties (e.g. Young’s modulus, roughness, and air permeability), which is dependent on the membrane thickness. The bioactivity of porous PDMS membranes, evaluated by measuring the adhesion of various biomolecules and bioactivity of cells, shows significant improvement over conventional non-porous control. This effect can be attributed to the strong physical adsorption on the porous PDMS membrane by increased surface roughness and stiffness. In sum, the porous PDMS membrane provides a simple and yet highly effective platform to create bioactive surface for various biomedical devices.
A femtosecond laser can be used for single or multiple writing processes to create sub 10-µm lines or holes directly without the use of masks. In this study, we characterized the depth and width of micro-channels created by femtosecond laser micro-scribing in polydimethylsiloxane (PDMS) under various energy doses (1%, 5%, 10%, 15% and 20%) and laser beam passes (5, 10 and 15). Based on a microfluidic simulation in a bio-application, a DNA distributor was designed and fabricated based on an energy dose of 5% and a laser beam pass of 5. The simulated depth and width of the micro-channels was 3.58 and 5.27 µm, respectively. The depth and width of the micro-channels were linearly proportional to the energy dose and the number of laser beam passes. In a DNA distribution experiment, a brighter fluorescent intensity for YOYO-1 Iodide with DNA was observed in the middle channels with longer DNA. In addition, the velocity was the lowest as estimated in the computational simulation. The polymer processability of the femtosecond laser and the bio-applicability of the DNA distributor were successfully confirmed. Therefore, a promising technique for the maskless fabrication of sub 10-µm bio-microfluidic channels was demonstrated.
The three-dimensional volumetric application of conductive poly (3,4-ethylenedioxythiophene)/poly (4-styrenesulfonate) (PEDOT:PSS) to multiwalled carbon nanotubes (MWCNTs) has not been widely reported. In this study, the applicability of the 3D PEDOT:PSS-MWCNT composite for a gas sensor was investigated with different PEDOT:PSS concentrations. The gas-sensing performance of the 3D PEDOT:PSS-MWCNT composites was investigated using ethanol and carbon monoxide (CO) gas. Overall, in comparison with the pristine MWCNTs, as the PEDOT:PSS concentration increased, the 3D PEDOT:PSS-MWCNT composites exhibited increased conductivity and enhanced gas sensing performances (fast response and recovery times) to both ethanol and CO gases. Importantly, although the PEDOT:PSS coating layer reduced the number of sites for the adsorption and desorption of gas molecules, the charge-carrier transport between the gas molecules and MWCNTs was significantly enhanced. Thus, PEDOT:PSS can be chemically grafted to MWCNTs to enhance the connectivity and conductivity of a 3D network, leading to possible applications in gas sensors.
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