electrochemical biosensors modern and future approaches to medical diagnostics j. f. rusling dept....

32
ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health Center

Post on 21-Dec-2015

220 views

Category:

Documents


0 download

TRANSCRIPT

Page 1: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

ELECTROCHEMICAL BIOSENSORS

Modern and future approaches to medical diagnostics

J. F. Rusling

Dept. of Chemistry

Dept. of Pharmacology, Univ. of CT Health Center

Page 2: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Medical Diagnostics

• Doctors increasingly rely on testing

• Needs: rapid, cheap, and “low tech”

• Done by technicians or patients

• Some needs for in-vivo operation, with feedback

Page 3: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

electrode

substrate product

Figure 9

Enzyme(label)

Apply voltage Measure current prop.to concentration of substrate

Principle of Electrochemical Biosensors

Page 4: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

E, V

time

E-t waveform

potentiostat

Electrochemical cell

counter

working electrode

N2

inlet

Protein film

reference

insulator electrodematerial

Equipment for developing electrochemical biosensors

Cyclic voltammetry

Page 5: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Electrode

enzyme

A lipid-enzyme film

Page 6: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

-2

-1.5

-1

-0.5

0

0.5

1

1.5

2

-0.8-0.6-0.4-0.200.20.40.60.8

I , μA

, E V vs SCE

Cyclic voltammogram (CV) at 100 mV s-1 and 25 oC of Mycobacterium Tuberculosis KatGcatalase-peroxidase in a thin film of dimyristoylphosphatidylcholine on basal plane PG electrode,in anaerobic pH 6.0 buffer.

OxidationOf FeII

ReductionOf FeIII

Reversible Peaks for

Direct electronTransfer

(not all proteins do this)

Page 7: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Electrode

enzyme

A lipid-enzyme film

Page 8: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Catalytic enzyme electrochemistry a basis for biosensor - glucose oxidase

oxidation

Fc mediator

Fc + glucose + enzyme

I = f [glucose]

A. Cass, G. Davis, G. D. Francis, H. O. A. Hill, W. J. Aston, I. J. Higgins, E. V. Plotkin, L. D. L.Scott, A. P. F. Turner, Anal. Chem. 56, 667-671 (1984).

Mediator shuttlesElectrons between Enzyme and electrode

Page 9: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Scheme 2

Glucose + GO(FAD) + 2 H+ Ÿ gluconolactone + GO(FADH2) (1)

GO(FADH2) + 2 Fc+ Ÿ GO(FAD) + 2 Fc + 2 H+ (4)

Fc Ÿ Fc+ + 2 e- (at electrode) (5)

Mechanism for catalytic oxidation of glucoseWith Glucose oxidase (GO) and Fc mediator

Signal can also be measured by amperometry:Hold const. E where oxidation occurs, measure I vs

time

Fc = ferrocenecarboxylate

Page 10: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Commercial Glucose Sensors • Biggest biosensor success story!

• Diabetic patients monitor blood glucose at home

• First made by Medisense (early 1990s), now 5 or more commercial test systems

• Rapid analysis from single drop of blood

• Enzyme-electrochemical device on a slide

Page 11: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Patient Diabetes Management

• Insulin secretion by pancreas regulated by blood glucose, 4.4 to 6.6 mM normal

• In diabetes, regulation breaks down

• Wide swings of glucose levels

• Glucose tests tell patient how much insulin to administer

Page 12: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

• Most sensors use enzyme called glucose oxidase (GO)• Most sensors are constructed on electrodes, and use a mediator to carry electrons from enzyme to GOFc = mediator, ferrocene, an iron complex

These reactions occur in the sensor:

Fc Fc+ + e- (measured)

GOR + 2 Fc + --> GOox + 2 Fc

GOox + glucose --> GOR + gluconolactone

Reach and Wilson, Anal. Chem. 64, 381A (1992)G. Ramsay, Commercial Biosensors, J. Wiley, 1998.

Page 13: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Glucose biosensor test strips (~$0.50-1.00 ea.)

MeterRead glucose

Dry coating of GO + Fc

Patient adds drop of blood,then inserts slide into meter

Output: Amperometry

Constant E

I

t

Patient reads glucose level on meter(B.B. King

e’selectrodes

http://www.bbking.com/)

Page 14: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Research on glucose sensors

• Non-invasive biosensors - skin, saliva

• Implantable glucose sensors to accompany artificial pancreas - feedback control of insulin supply

• Record is 3-4 weeks for implantable sensor in humans

Page 15: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Other biosensors

• Cholesterol - based on cholesterol oxidase• Antigen-antibody sensors - toxic

substances, pathogenic bacteria• Small molecules and ions in living things:

H+, K+, Na+, CO2, H2O2

• DNA hybridization and damage• Micro or nanoarrays, optical abs or

fluor.

Page 16: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Negativesurface

Polycation soln.,then wash

+ + + + + + + + + + + +

soln. of negative proteinthen wash

+ + + + + + + + + + + +

+ + + + + + + + + + + +

+ + + + + + + + + + + +

Repeat steps for desired number of layers

Proteinlayer

Polycation layersProteinlayer

Polycation soln.,then wash

Figure 19

Layer by layerFilm construction:

Page 17: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

PSS layer

SPAN layer

Enzyme

layer

Detection of hydrogen peroxideConductive polymers efficiently wire

peroxidase enzymes to graphite

Xin Yu, G. A. Sotzing, F. Papadimitrakopoulos, J. F. Rusling, Highly Efficient Wiring of Enzymes to Electrodes by Ultrathin Conductive Polyion Underlayers: Enhanced Catalytic Response to Hydrogen Peroxide, Anal. Chem., 2003, 75, 4565-4571.

e’s

(sulfonated polyaniline)

Page 18: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Horseradish Peroxidase (HRP)

100nm

50nm

Tapping mode atomic force microscopy (AFM) image of HRP film

Page 19: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

O

2

H

2

O

2

P F e

I I I

P F e

I I

P F e

I I

- O

2

O

2

H

2

O

2

Possible reduced species in red

Electrochemical Response of Peroxidases

Page 20: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

-10

0

10

20

30

40

50

60

-0.8-0.6-0.4-0.200.2

I,μA

, E V vs SCE

with SPAN

a

00.5

2

4

67.5

μ M H202

Catalytic reduction of H2O2 by peroxidase filmsCatalytic cycles increase current

FeIII/FeII

reduction

Page 21: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

0

0.5

1

0 100 200 300 400

, t s

with PAPSA

without PAPSA

Rotating electrode amperometry at 0 VHRP, 50 nmol H2O2 additions

span

No span

reduction

Page 22: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

0

0.2

0.4

0.6

0.8

1

1.2

0 0.1 0.2 0.3 0.4 0.5 0.6

[H2O

2], μM

PAPSA/HRPPAPSA/Mb

Mb

HRP

Rotating electrode amperometry at 0 V

Sensitivity much higher with conductive polymer (SPAN);Electrically wires all the protein to electrode

Span/HRPSpan/Mb

Page 23: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Single-Walled Carbon Nanotube Forests: Antigen-Antibody Sensing

SPAN orNafion

Chattopadhyay, Galeska, Papadimitrakopoulos, J. Am. Chem. Soc. 2001, 123, 9451.

End COOH groups allow chemical attachment to proteins (antibodies)

High conductivity to conduct signal (e’s) from enzyme label to meas. circuit

~1.4 nm diameter, high conductivity

Page 24: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

AFM of SWNT forest with and without anti-HSA attached

SWNT forest on Si waferSWNT forest with anti-human serum albumin (HSA) attached by amide links

• Also linked enzymes to SWNT forests:X. Yu, D. Chattopadhyay, I. Galeska, F. Papadimitrakopoulos, and J. F. Rusling, “Peroxidase activity of enzymes bound to the ends of single-wall carbon nanotubeforest electrodes”, Electrochem. Commun., 2003, 5, 408-411.

Page 25: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Sandwich Electrochemical Immunosensor Proteins

H2O2

Ab1

Ag

HRPHRP

HRP HRPHRP

Ab1

Ag

HRP

HPR

Ab2

Apply E measure ISWNT forest Conductive polymer

(SPAN)

protein

Page 26: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Amperometry Detection of Human Serum albumin

-2

0

2

4

6

8

10

12

0 500 1000 1500

I, μA

, t s

1.5

7.5

15

45

600 / pmol mL HSA

300

140

140 300140

controls

a0

bc d

no SWNT bare PG

0.4 ;mM hydroquinone0.4 mM H

2O

2

• SWNTs provide 10-20 fold signal enhancement• Nanotubes aged in DMF fewer defects denser forests. Xin Yu, Sang Nyon Kim, Fotios Papadimitrakopoulos, and James F. Rusling,

"Protein Immunosensor Using Single-Wall Carbon Nanotube Forests with ElectrochemicalDetection of Enzyme Labels", Molecular Biosystems, 2005, 1, 70-78.

Page 27: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Initial Target: Prostate Specific Antigen

PSA - Single chain glycoprotein , MW 33 kDa

Sensitive, specific biomarker for detection of prostate cancer up to 5 years before clinical signs of disease

Detection of PSA in serum: clinical method for detection of prostate cancer

Led to less invasive treatment protocols, avoid surgery

Adapted From Brookhaven Protein Databank

Page 28: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Nanotube Strategies for PSA detection

~170 labels per PSA

Page 29: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Washing with 2% BSA/0.05% Tween 20 to control non-specific bindingLOD - 4 pg/mL; 100-fold enhancement over HRP-Ab2

Amperometric response at –0.3 V and 3000 rpm for SWNT immunosensors incubated with PSAin 10 μL undilut ed ne wborn calf serum for 1.25 hr using t he Ab2-CNT-HRP bioconjugate

Mediator + H2O2

Using HRP-Ab2-nanotube

Xin Yu, Bernard Munge, Vyo mesh Patel, Gary Jensen, Ashwin Bhirde, Joseph D. Gong, Sang-Nyon Kim, John Gillespie, J. Silvio Gutkind, Fotios Papadimitrakopoulos and James F. Rusling,"Carbon Nanotube Amplification Strategies for Highly Sensitive Immunosensing of CancerBiomarkers in Serum and Tissue", J. Am. Chem. Soc., 2006, 128, 11199-11205.

Page 30: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Amperometric current at –0.3 V and 3000 rpm for human serum samples and PSA standards incalf serum

Accurate results obtained for cancer patient serum

Good correlation with ELISA!

Using conventional HRP-Ab2

Page 31: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Future - arrays to detect many biomolecules at once

SWNT forest grown on 10 μm Au Array elements

Prototype 8-electrode Array, Univ. Edinburgh

Page 32: ELECTROCHEMICAL BIOSENSORS Modern and future approaches to medical diagnostics J. F. Rusling Dept. of Chemistry Dept. of Pharmacology, Univ. of CT Health

Biosensors

• Promising approach to medical diagnostics by patients or in doctors offices

• Other important applications: pH, CO2, cancer biomarkers, DNA, peroxide, etc.

• Method of choice for blood glucose in diabetics• Rapid diagnostics may lead to more timely and

effective treatment