N-type polymer based electrochemical device for direct enzymatic metabolite sensing and methods of making and using
N-type polymer based electrochemical devices include one or more source electrodes, one or more drain electrodes, one or more channels, a gate electrode, and an electrolyte solution are disclosed. The channels include one or more n-type polymers and one or more enzymes. The gate electrode includes one or more n-type polymers and one or more enzymes. The source and the drain electrodes are electrically connected by the corresponding channel. The electrolyte solution contains one or more metabolites capable of reacting with the one or more enzymes in the channel and the gate electrode and is in electrical contact with the channel and the gate electrode. Saturation current that flows through the channel increases when the metabolites react with the enzymes to produce electrons, which are directly transferred to the n-type polymers at the gate electrode and the channel. Methods of making and using the n-type electrochemical device are also disclosed.
1. An n-type polymer based electrochemical device for metabolite sensing comprising:
one or more source electrodes;
one or more drain electrodes;
one or more channels which comprise (a) one or more n-type polymers and (b) one or more enzymes; and
a gate electrode formed of an electrode material capable of conducting an electric current, wherein the gate electrode further comprises (a) one or more n-type polymers and (b) one or more enzymes, wherein the one or more n-type polymers and one or more enzymes are coated on a surface of the electrode material, and wherein the one or more n-type polymers are in physical contact with the one or more enzymes, allowing direct electron transfer therebetween;
wherein the source electrodes and drain electrodes are electrically connected by the one or more channels, and
wherein the electrochemical device is an organic electrochemical transistor.
2. The electrochemical device of claim 1 further comprising:
(a) a supporting substrate, wherein the one or more source electrodes, the one or more drain electrodes, and the gate electrode are patterned on the supporting substrate; or (b) an electron mediator, or a combination thereof.
3. The electrochemical device of claim 2 , wherein the supporting substrate is glass, polyethylene terephthalate, polyethylene naphthalene dicarboxylate, polyethylene, polypropylene, polycarbonate, paper, coated paper, resin-coated paper, paper laminates, paperboard, or corrugated board.
4. The electrochemical device of claim 1 , wherein: (a) the one or more source electrodes, the one or more drain electrodes, and the gate electrode are in planar configuration, (b) the one or more n-type polymer is a structure-modified n-type polymer to introduce polar groups; or (c) the electrochemical device comprises a plurality of independently addressable source and drain electrodes, a common gate electrode, and corresponding channels, or a combination thereof.
5. The electrochemical device of claim 4 , wherein the polar group is lysine.
6. The electrochemical device of claim 5 , wherein the one or more n-type polymer is P90.
7. The electrochemical device of claim 4 , wherein the corresponding channels each comprise a different enzyme.
8. The electrochemical device of claim 1 , wherein the one or more n-type polymer is selected from the group consisting of N2300, P (NDI-T2), poly (diketopyrrolopyrrole) (DPP), poly(benzimidazobenzophenanthroline), poly(2,5-di(3,7-dimethyloctyloxy) cyanoterephthalylidene), poly(2,5-di(hexyloxy) cyanoterephthalylidene), poly(5-(3,7-dimethyloctyloxy)-2-methoxy-cyanoterephthalylidene), poly(2,5-di(octyloxy) cyanoterephthalylidene), and poly(5-(2-ethylhexyloxy)-2-methoxy-cyanoterephthalylidene).
9. The electrochemical device of claim 1 , wherein the one or more enzymes are selected from the group consisting of glucose oxidase, glucose dehydrogenase, alcohol dehydrogenase, aldehyde dehydrogenase, formate dehydrogenase, formaldehyde dehydrogenase, lactic dehydrogenase, lactose dehydrogenase, lactate oxidase, cholesterol oxidase, tyrosinase, and pyruvate dehydrogenase.
10. The electrochemical device of claim 1 , wherein the gate electrode has a dimension between 100 μm 2 and 250000 μm 2 ; the length of the one or more channels are is between 1 μm and 1000 μm; the width of the one or more channels are is between 1 μm and 1000 μm; or a dimension of the electrochemical device is between 1000 and 1000000 μm 2 , or a combination thereof.
11. The electrochemical device of claim 1 , wherein the electrochemical device is stable for 6 months.
12. The electrochemical device of claim 1 , wherein the electrochemical device does not contain a reference electrode.
13. A method of detecting one or more metabolites using the electrochemical device of claim 1 , comprising contacting the electrochemical device with an electrolyte solution, wherein the electrolyte solution is in electrical contact with the one or more channels and the gate electrode, and wherein the electrolyte solution comprises the one or more metabolites: (a) applying a gate potential (V G ); and (b) monitoring changes of a source-drain current (I D ) that flows through the one or more channels that connect the one or more source electrodes and the one or more drain electrodes.
14. The electrochemical device of claim 13 , wherein the electrolyte solution is a buffer, a biological fluid, or a combination thereof.
15. The method of claim 13 , wherein: (a) the I D increases with increasing concentration of the metabolites; (b) the gate potential equal to or higher than a threshold voltage; or (c) wherein the reaction between the one or more enzymes on the one or more channels and/or the gate electrode and the one or more metabolites produces electrons which are directly transferred to the one or more n-type polymers, or a combination thereof.
16. The method of claim 15 , wherein the threshold voltage is 0.5 V.
17. The method of claim 13 , wherein the one or more metabolites are capable of reacting with the enzymes on the one or more channels and/or the gate electrode.
18. The method of claim 17 , wherein the one or more metabolites are selected from the group consisting of glucose, glucose-1, D-glucose, L-glucose, glucose-6-phosphate, ammonia, methanol, ethanol, propanol, isobutanol, butanol and isopropanol, allyl alcohols, aryl alcohols, glycerol, cholesterol, propanediol, mannitol, glucoronate, aldehyde, carbohydrates, lactate, lactate-6-phosphate, D-lactate, L-lactate, fructose, galactose-1, galactose, aldose, sorbose, mannose, glycerate, coenzyme A, acetyl Co-A, malate, isocitrate, formaldehyde, acetaldehyde, acetate, citrate, L-gluconate, beta-hydroxysteroid, alpha-hydroxysteroid, lactaldehyde, testosterone, gluconate, fatty acids, lipids, phosphoglycerate, retinal, estradiol, cyclopentanol, hexadecanol, long-chain alcohols, coniferyl-alcohol, cinnamyl-alcohol, formate, long-chain aldehydes, pyruvate, butanal, acryl-CoA, steroids, amino acids, favin, NADH, NADH 2 , NADPH, NADPH 2 , and hydrogen.
19. The method of claim 13 further comprising applying a drain voltage.