| Literature DB >> 34900967 |
Shimin Yu1,2, Zhongqi Sun3, Zhanxiang Zhang2,4, Haoran Sun2, Lina Liu2, Wuyi Wang2, Mu Li1, Qingsong Zhao5, Tianlong Li2.
Abstract
With the development of designed materials and structures, a wide array of micro/nanomachines with versatile functionalities are employed for specific sensing applications. Here, we demonstrated a magnetic propelled microdimer-based point-of-care testing system, which can be used to provide the real-time data of plasma glucose and lipids relying on the motion feedback of mechanical properties. On-demand and programmable speed and direction of the microdimers can be achieved with the judicious adjustment of the external magnetic field, while their velocity and instantaneous postures provide estimation of glucose, cholesterol, and triglycerides concentrations with high temporal accuracy. Numerical simulations reveal the relationship between motility performance and surrounding liquid properties. Such technology presents a point-of-care testing (POCT) approach to adapt to biofluid measurement, which advances the development of microrobotic system in biomedical fields.Entities:
Keywords: angle of procession; magnetic microdimer; peak velocity; plasma glucose; plasma lipids; point-of-care testing
Year: 2021 PMID: 34900967 PMCID: PMC8660689 DOI: 10.3389/fbioe.2021.779632
Source DB: PubMed Journal: Front Bioeng Biotechnol ISSN: 2296-4185
FIGURE 1Conceptual schematic illustration of the estimation of plasma glucose and lipids using magnetic propelled microdimers.
FIGURE 2Actuation mechanisms of magnetic-propelled microdimers. (A) Schematic of a microdimer with permanent magnetization. The applied field is of strength H R rotating at angular velocity ω (frequency f = ω/2π). (B) Velocity and angle of precession (α p) varied with the driving frequency in 10% glycerol–water solution (1.74 cp). (C) The peak velocity of microdimers in glycerol–water solution of different viscosities. (D) Schemes of microdimers in tumbling, rolling, and wobbling modes at different α p under a rotating magnetic field. Scale bar 20 μm. (E) Simulation of the section view from one side of the microdimer shows the fluid flow velocity near a microdimer on the substrate at different α p.
FIGURE 3Estimating the strategy of plasma glucose levels. (A) Controllable motion of the microdimers in plasma with different glucose concentrations. (B) Variation in the velocity of the microdimers upon changing magnetic frequency and glucose concentration. (C) The step-out frequency at different glucose concentrations. (D) Function of the α p at step-out frequency as increasing glucose concentration.
FIGURE 4Estimating strategy of plasma cholesterol level. (A) Controllable motion of the microdimers in plasma with different cholesterol concentrations. (B) Time-lapse optical microscopy images of locomotion trajectories of microdimers propelled by rotating magnetic field in cholesterol concentrations of 200, 500, and 900 mg/dl. Scale bar: 20 μm. (C) Dependence of the translational speed of microdimer on the frequency of the external rotating magnetic and cholesterol concentration. (D) The step-out frequency at different cholesterol concentrations. (E) The peak velocity of microdimer was dependent on cholesterol concentration.
FIGURE 5Estimating strategy of plasma triglyceride level. (A) Controllable motion of the microdimer in plasma with different triglyceride concentrations. (B) The velocity of microdimers varied with the drive frequency and triglyceride concentrations. (C) Snapshots of the moving microdimer and corresponding measured α p at different triglyceride concentrations. Scale bar: 20 μm. (D) “Z” decreasing trend of precession angle with the increase in driving frequency. (E) Linear relationship of the α p at 9, 10, and 11 Hz with triglyceride concentration.