Flusitex

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F l u s i Te x Fluorescence sensing integrated into medical textiles Markus Bannwarth


Current Wound Monitoring

Current Methods  Full or partial removal of wound pad  Visual Observation  Skin Irritation  Increased chances of infection  Only qualitative information  Collecting biochemical information  Highly invasive  Expensive


The Business Case

Frost and Sullivan, Medtech insights 2009 $12bn worldwide market aimed solely at wound care Wound monitoring consists less than 1% of this industry 6 weeks treatment of a chronical wound

35.000 CHF


Working Principle

Non-invasive TOF camera

One fluorescence signal per sensing parameter per wound area

Sensing layer

Wound

pH, metabolites, oxygen,‌


The Team

Dr. Luciano Boesel

Sensing chemistry and matrix development Dr. Michael Richter

Enzyme engineering and coupling Dr. Stefano Cattaneo

Fluorescent lifetime camera development Prof. Bradley Nelson

Coating/microfabrication of wound pad Prof. Brigitte von Rechenberg

In vivo evaluation of wound pad


The Matrix Biocompatibility

Facile Processing

Alginate or agarose

Modification On the market


pH Sensing

Non-invasive TOF camera

One fluorescence signal per sensing parameter per wound area

Sensing layer

pH Wound


pH Sensing

Healing process of

Acute wound

Chronic wound 8 pH-values of wound

pH-values of wound

8

7 Injury

6 Inflammation

5

Granulation

7 Injury

6

Spontaneous reepithelisation

Time

Dargaville, T. R.; Farrugia, B. L.; Broadbent, J. A.; Pace, S.; Upton, Z.; Voelcker, N. H., Biosens. Bioelectron. 2013, 41, 30-42.

Acute phase

5

Chronic phase

Time


Fluorescence intensity / a.u.

Fluorescent pH-marker 700 pH = 8

600

pH = 7.7

500

pH = 7.3

400

pH = 7

300

pH = 6.7 pH = 6.3

200

pH = 6

100

pH = 5.5 pH = 5

0 620

670

720

pka ≈ 7

Fluorescence Intensity / a.u.

Wavelength / nm 700 600 500 400 300 200 100 0 5

6

7

pH

8


Biomarker Sensing

Non-invasive TOF camera

One fluorescence signal per sensing parameter per wound area

Sensing layer

Wound

Metabolites, Enzymes,..


Biomarker Sensing

material proteins and enzymes

E

E metabolites and enzymes

Several detection spots on the pad (microfabricated): • Various metabolites / enzymes • pH • Oxygen • etc.


Biomarker Sensing Metabolite/compound Calcium

detection Cameleon

A

Bicarbonate

Bicarbonate-dependent

A

Iron

Ferritin

A

Glucose

Fluorescent glucose

A

binding protein

B

Glucose oxidase Uric acid

Urate oxidase

B

Xanthine oxidase

B

Lactate oxidase

B

Lactate monooxygenase

B

Histamine

Diamine oxidase

B

Bilirubin

Bilirubin oxidase

B

Cholesterol

Cholesterol oxidase

B

Amino acids

Amino acid oxidases

B

Lactate dehydrogenase

Resazurin

C

Alkaline phosphatase

Fluorescein diphosphate

C

Metalloproteases

Fluorescent fusion

D

Lactate

protein Neutrophil elastase

Fluorescent fusion protein

D

B Coupled enzyme assay

C Commercial fluorescent substrate enzyme sensing

superoxide dismutase

metabolite sensing

A Intrinsic protein fluorescence

E

D Designed fluorescent substrates E


Protease Sensing S2 S1

S0

YFP fluorescence

donor

528 nm

S1

485 nm

CFP fluorescence

FRET absorbance

YFP: em = 528 nm

S0

acceptor 485 nm

528 nm

200

fluorescence intensity (a.u.)

CFP: ex = 428 nm em = 485 nm

180

before cleavage after cleavage

160 140 120 100 80 60 40 20 0 460

480

500

520

540

(nm)

560

580

600


Metabolite Sensing

Lactate oxidase

Lactate, glucose,‌


Oxygen Sensing

Non-invasive TOF camera

One fluorescence signal per sensing parameter per wound area

Sensing layer

Oxygen Wound


Oxygen Sensor System

Excitation band

Emission band

PtOEP

Quenching through

O2


Oxygen Sensor System

Correlate lifetime change with amount of oxygen


Oxygen Sensor Fabrication

Nanopillar formation

Electrodeposition

2 Îźm


The Lifetime Camera

Non-invasive TOF camera

One fluorescence signal per sensing parameter per wound area

Sensing layer

Wound

pH, metabolites, oxygen,‌


The Setup

Objective

Pinholes

Focusing lens Diffuser

Mirrors

Laser diode 450 nm


First Sample Measurements


In Vivo Evaluation

Non-invasive TOF camera

One fluorescence signal per sensing parameter per wound area

Sensing layer

Wound

pH, metabolites, oxygen,‌


In Vivo Evaluation  Standardized deep wounds  Wound parameters recorded until closure (pO2, pH, metabolites)  Wound healing semi-quantitative evaluation and tracking (Epithelialisation, wound surface area, granulation tissue)

 Infected deep wounds       

Inoculation with Staphylococcus Aureus or Pseudomonas Aeruginosa Tracking infection progress (sampling, swabs) Sensing wound parameters (pH, pO2, metabolites, glucose) Antibiotic therapy after infection establishment Tracking wound healing (Semi-quantitatively) and recording parameters Comparing infected and non-infected wound environments Correlating wound healing and monitored parameters

WP5 Sensing: in vitro and in vivo 5.1 Testing wound parameter monitoring (in vitro)

5.2

Design of in vivo analysis (non-infected and infected)

5.3

Medical correlation of sensed wound healing parameters

Year 2

Year 3


Achievements and Future Efforts Achievements •

Development of:

o o o

pH sensor biomarker sensors oxygen sensor

Coupling or integration of the sensor systems to/into the coating matrix

Development of optical setup for fluorescence lifetime imaging in the nanosecond range

Future Efforts •

Microfabrication of the functional matrix on a wound pad

Lifetime imaging of pH values, biomarker concentrations and oxygen content with the lifetime camera

In vitro and in vivo analysis of the monitor pads


Prof. Bradley Nelson Dr. Selman Sakar Dr. Chen Xiangzhong

Dr. Luciano Boesel Dr. Markus Bannwarth

Thanks! Dr. Stefano Cattaneo Christoph Hofer

Dr. Michael Richter Dr. Dagmara Jankowska Dr. Greta Faccio

Prof. Brigitte von Rechenberg Dr. Salim Darwiche


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