This article details the construction of a multiplexed microneedle-based sensor. The device is being developed for in situ sampling and electrochemical analysis of multiple analytes in a rapid and selective manner. We envision clinical medicine and biomedical research uses for these microneedle-based sensors.
The development of a minimally invasive multiplexed monitoring system for rapid analysis of biologically-relevant molecules could offer individuals suffering from chronic medical conditions facile assessment of their immediate physiological state. Furthermore, it could serve as a research tool for analysis of complex, multifactorial medical conditions. In order for such a multianalyte sensor to be realized, it must be minimally invasive, sampling of interstitial fluid must occur without pain or harm to the user, and analysis must be rapid as well as selective.
Initially developed for pain-free drug delivery, microneedles have been used to deliver vaccines and pharmacologic agents (e.g., insulin) through the skin.1-2 Since these devices access the interstitial space, microneedles that are integrated with microelectrodes can be used as transdermal electrochemical sensors. Selective detection of glucose, glutamate, lactate, hydrogen peroxide, and ascorbic acid has been demonstrated using integrated microneedle-electrode devices with carbon fibers, modified carbon pastes, and platinum-coated polymer microneedles serving as transducing elements.3-7,8
This microneedle sensor technology has enabled a novel and sophisticated analytical approach for in situ and simultaneous detection of multiple analytes. Multiplexing offers the possibility of monitoring complex microenvironments, which are otherwise difficult to characterize in a rapid and minimally invasive manner. For example, this technology could be utilized for simultaneous monitoring of extracellular levels of, glucose, lactate and pH,9 which are important metabolic indicators of disease states7,10-14 (e.g., cancer proliferation) and exercise-induced acidosis.15
1. Microneedle Fabrication
2. Fabrication of Carbon Paste Electrode Arrays
3. Synthesis of Functional Carbon Pastes and Packing of Electrode Cavities
4. Detection and sensor calibration
5. Representative Results
When obtaining chronoamperometric curves (e.g., for glucose detection or lactate detection) in quiescent solutions with modified carbon paste-filled microneedles, the current will immediately decrease upon application of the respective detection potential. It will eventually decay to a steady state value. A representative result is shown in Figure 6; this result was obtained from 2 mM additions of lactate and recording at the lactate microneedle. The solution must be briefly stirred after each lactate addition. The current after 15 seconds rises upon increasing the concentration of lactate; the current response can then be used to determine the concentration of lactate in an unknown solution. Alternatively, continuous monitoring can be used in a stirred solution (or in a flowing solution) as demonstrated for a solution with an increasing glucose concentration (Figure 5). Again, the increase in current upon increasing the concentration of glucose can be used to standardize the glucose response to an unknown solution. Sufficient time must be allowed after each spike in order to allow the solution to stabilize. Cyclic voltammograms at the pH sensitive microneedle in 0.1 M phosphate buffer are shown over four different pH solutions from 5 to 8 in 1 pH unit increments in Figure 6. The oxidative peak potential shifts with increasing pH; this phenomenon is used as an indicator of the pH value.
Figure 1. Images of the STL file of the microneedle array created in Solidworks (A) and of the print screen, which shows the support structure (B).
Figure 2. Scanning electron micrographs of the microneedle array (A) and a single microneedle within this array (B).
Figure 3. Schematic of flat flexible cable assembly. The steps involved include modifying the flat flexible cable (A), ablating the patterned circles (B), adding the initially ablated Melinex layer, which is filled with carbon paste (C), as well as adding the second ablated Melinex layer and mating the microneedle array (D). Click here to view larger figure.
Figure 4. Calibration of lactate-sensitive paste with 15 second chronoamperometric scans at -0.15 V in 0.1 M phosphate buffer (pH=7.5). Each increase in current corresponds to a 2 mM addition of lactate.
Figure 5. Calibration of glucose-sensitive paste running chronoamperometric scans at -0.05 V. Each decrease in the response corresponds to a 2 mM addition of glucose. The 0.1 M phosphate buffer solution (pH=7.0) was stirred during calibration. External Ag/AgCl and Pt reference and counter electrodes were used in this study.
Figure 6. Cyclic voltammogram (CV) of pH sensitive carbon paste in 0.1 M phosphate buffer over pH 5-8 in 1 pH unit increments (teal=pH 8.0, green=pH 7.0, purple=pH 6.0, red=pH 5.0). A fifth CV was used for analysis versus Ag/AgCl reference and Pt wire counter electrodes.
Multiple aspects of the design of this microneedle-based sensor were considered prior to device fabrication. In order to use this sensor for real-time detection, the response time of the sensor must be low; in this protocol, each tested sensor exhibited a response time below fifteen seconds. Pastes used in this protocol were also chosen for their selectivity within in vivo environments, which contain electroactive biomolecules that can interfere with electrode response. In addition to paste composition, the operating potentials were chosen to minimize the influence of interfering electroactive species. Successful fabrication of the microneedle array involves the selection of a suitable microneedle design and microneedle material. These two aspects will determine if the microneedle can puncture the skin, protect the electrodes from physical damage, and preclude electrode-tissue contact. It should be noted that an external Ag/AgCl and Pt reference and counter electrodes were used during measurements; in vivo use of this device with human or animal subjects would require that these electrodes be incorporated within the device.
Each component of the microneedle-based sensor has features that must be validated to ensure proper functionality. Quality control during modification of the flat flexible cable (Figure 3 B) involves ensuring that the insulating layer is completely removed from the surface of the tin-plated copper wires after laser ablation (Figure 3). Failure to remove the insulating layer from the surface of the copper wire after laser ablation can cause irregular responses due to incomplete electrical contact. The laser-ablated Melinex tape needs to be examined with a microscope to ensure that the diameter of each opening is consistent as it defines the working area of the electrode. When applying carbon paste to the laser-ablated Melinex tape cavities, the paste must conform to the exact hole diameter with no excess in order to avoid signal variations due to differences in surface area. During chronoamperometric measurements with modified carbon pastes, the signal must stabilize to a limiting value before current is recorded. These results can slightly vary due to mixing effects. Mechanical testing of the microneedle arrays was performed prior to sensor incorporation; in a previous study, our group showed these arrays were capable of puncturing porcine skin, which was used as an analog for human skin.3 Microneedle arrays should not undergo deformation or fracture during skin penetration since these processes could lead to electrode damage.
This protocol has detailed the construction of a novel transdermal device for electrochemical monitoring. We envision future efforts involving microneedle sensors with an even greater number of individually addressable microneedles and a greater variety of transducers. This device was designed for analysis of interstitial fluid in humans; use with animals is also possible with appropriate species-specific modifications to microneedle design. Future directions with this technology include but are not limited to remote patient monitoring as well as coupling with a drug delivery device for automated sensing-drug delivery.
The authors have nothing to disclose.
Sandia is multiprogram laboratory operated by Sandia Corporation, a Lockheed Martin Company, for the United Stated Department of Energy’s National Nuclear Security Administration under Contract DE-AC04-94AL85000. The authors acknowledge funding from Sandia National Laboratories’ Laboratory Directed Research & Development (LDRD) program.
Name of the reagent | Company | Catalogue number |
Flat flexible cable | Molex | 3302/10SF |
0.003″ Side sided tape | Melinex | |
0.004″ Double sided tape | Melinex | |
Lactate oxidase | Sigma | L0638 |
Glucose oxidase | Sigma | G7141 |
Rhodium on carbon | Sigma | 206164 |
Graphite powder | Sigma | 385031000 |
poly(ethylenimine) | Acros | 178570010 |
Mineral oil | Sigma | M5904 |
Glucose | Sigma | G8270 |
Lactate | Sigma | L1750 |
Fast Blue RR salt | Sigma | F0500 |
e-Shell 300 | EnvisionTEC | |
e-Shell 200 | EnvisionTEC | |
Ag/AgCl reference electrode | Basi | MF-2052 |
Pt wire | Basi | |
PGSTAT12 AutolabPotentiostat | EcoChemie | |
Perfactory RP | EnvisionTEC | |
Ottoflash Postcuring system | EnvisionTEC | |
Phosphoric acid | Fisher | A366-4 |
60W Model 6.75 CO2 raster/vector laser system | Universal Laser Systems | PLS6.75 |
CorelDraw | Corel | |
Solidworks | Dassault Systemes | 2009 |
Magics RP13 | Materialise |