RESUMO
In this study, we present a dimension-controllable 3D biomedical microelectrode based on low melting point metals (Bi/In/Sn/Zn alloy) applied using the phase transition method. We have established a process, in which the liquid metal is pumped through a syringe needle of the dispensing system to form a needle shape after cooling at room temperature. PDMS (polydimethylsiloxane) was chosen as the substrate of the electrode as it is amenable to micro-molding and has excellent flexibility. Several key factors, including lifting velocity of the syringe needle and sample temperature were examined as to how they would affect the height, width and depth-width ratio of the electrode, to realize size control of the electrode. Afterwards, the skin-electrode impedance was tested and the results were compared with those of an Ag/AgCl (wet) electrode. The impedance at 10â¯Hz is 2.357⯱â¯0.198â¯MΩ for the 3D microelectrode. From data, the impedance of 3D microelectrode is found to be at the same level as the Ag/AgCl electrode at the frequency of 10â¯Hz. By increasing the size of the array, the impedance of the low melting point metal electrode and the wet electrode converge. The resistance of the electrode was also measured to describe its stretchability. The electrode can be stretched to a maximum of 42% before it becomes non-conducting. In addition to acquisition of bio-electric signals, our method has strong prospects in the field of bio-sensing.
Assuntos
Metais/química , Transição de Fase , Temperatura de Transição , Microeletrodos , Agulhas , MaleabilidadeRESUMO
Dissolving microneedles have been employed as a safe and convenient transdermal delivery system for drugs and vaccines. To improve effective drug delivery, a multilayered pyramidal dissolving microneedle patch, composed of silk fibroin tips with the ability of robust mechanical strength, rapid dissolution and drug release supported on a flexible polyvinyl alcohol (PVA) pedestal is reported. To show the utility of this approach the ability of the fabricated microneedles to deliver insulin is demonstrated. The dissolving microneedles have sufficient mechanical strength to be inserted into abdomen skin of mice to a depth of approximately 150µm, and release their encapsulated insulin into the skin to cause a hypoglycemic effect. The fabrication of microneedles avoids high temperature which benefits storage stability at room temperature for 20d. This result indicates >99.4% of insulin remained in the microneedles. In comparison to traditional needle-based administration, the proposed multilayered pyramidal dissolving microneedle patches enable self-administration, miniaturization, pain-free administration, drug delivery and drug stability, all being important features in needle free drug delivery.