Method, Arrangement, Computer Program Product and Sensor Foil for Detecting Microorganisms on a Surface

Abstract

A method and an arrangement, for detecting microorganisms on a surface are disclosed. At least a portion of the surface is covered with a sensor foil in an airtight manner. An oxygen-permeable layer of the sensor foil is doped with an oxygen indicator dye, loaded with oxygen and faces the at least one portion of the surface. An excitation light passes through an oxygen-impermeable at least partially transparent read-out carrier layer of the foil to the dye in the oxygen-permeable layer which is then excited by the excitation light. An emission of the oxygen indicator dye) transmitted through the carrier layer is detected by a detection element over or after a period of time (t). The emission of the oxygen indicator dye from the oxygen-permeable layer is indicative of the amount of oxygen consumed by microorganisms from the oxygen-permeable layer covering the at least one portion of the surface.

Claims

1. A method for detecting microorganisms on a surface, the method comprising: attaching a sensor foil to at least a portion of the surface to be examined in an airtight manner, wherein an oxygen-permeable layer of the sensor foil is doped with an oxygen indicator dye, is loaded with oxygen and faces the at least one portion of the surface and placing a detection element in optical relation to the sensor foil; exciting the oxygen indicator dye in the oxygen-permeable layer with an excitation light through an oxygen-impermeable at least partially transparent read-out carrier layer of the sensor foil; and detecting an emission of the oxygen indicator dye transmitted through the oxygen-impermeable at least partially transparent read-out carrier layer of the sensor foil by the detection element over or after a period of time, wherein the emission of the oxygen indicator dye from the oxygen-permeable layer being indicative of an amount of oxygen consumed by the microorganisms from the oxygen-permeable layer covering the at least one portion of the surface.

2. The method as claimed in claim 1, wherein the detection element is a detector chip directly attached to the at least partially transparent read-out carrier layer for receiving the emission of the oxygen indicator dye.

3. The method as claimed in claim 1, wherein a detector chip is part of a detection element and the emission of the oxygen indicator dye is imaged on the detector chip for detecting the emission of the oxygen indicator dye.

4. The method as claimed in claim 1, further comprising: post-processing the detected emission to determine the presence and distribution of the microorganisms in situ with respect to the at least one portion of the surface; and displaying a graphical representation or a statistical evaluation of a concentration of the microorganisms on the at least a portion of the surface based on the detected emission.

5. The method as claimed in claim 4, wherein the graphical representation or the statistical evaluation of the concentration of the microorganisms is a 2-dimensional image of the distribution of the microorganisms on the at least a portion of the surface, a plot showing development of the concentration of the microorganisms over time, or a statistical interpretation on the microorganisms.

6. The method as claimed in claim 1, wherein the surface is an antimicrobial surface by being provided as antimicrobial or antimicrobially treated or coated for testing and wherein the antimicrobial surface is either directly examined and measured for presence and/or distribution of the microorganisms, or the antimicrobial surface is intentionally contaminated with germs or other microorganisms to monitor the effectiveness of the killing of germs or other microorganisms or the reduction of germination by the antimicrobial surface.

7. The method as claimed in claim 1, wherein a response of the microorganisms depends from the oxygen indicator dye or the oxygen indicator dye plus at least one reference dye in the oxygen-permeable layer of the sensor foil.

8. The method as claimed in claim 7, further comprising changing a temperature of at least a part of the at least one surface to be examined by infrared or an internal tempering system in the sensor foil, in order to change an activity of the microorganisms.

9. The method as claimed in claim 7, further comprising treating at least a part of the surface with UV radiation, so that the microorganisms are killed wherein the UV radiation is emitted from at least a part of the sensor foil.

10. The method as claimed in claim 7, further comprising placing at least one respiratory decoupler on the oxygen-permeable layer of the sensor foil, so that the microorganisms consume more oxygen and a faster response time is achieved, wherein the at least one respiratory decoupler is selected specifically to target specific types of microorganisms.

11. The method as claimed in claim 7, further comprising selecting specific antibiotics to detect specific microorganisms which are selectively killed or resistant microorganisms by the specific antibiotics.

12. An arrangement for detecting microorganisms on a surface, the arrangement comprising: a sensor foil having an oxygen-permeable layer doped with an oxygen indicator dye and loaded with oxygen and an oxygen-impermeable at least partially transparent read-out carrier layer carrying the oxygen-permeable layer, wherein the sensor foil is placed on at least a portion of the surface in an airtight manner; a detection element arranged in optical relation to the sensor foil for receiving an emission of the oxygen indicator dye when the dye is in an excited state, the emission being transmitted through the oxygen-impermeable at least partially transparent read-out layer; an evaluation unit for calculating a graphical or statistical representation of the received emission; and a display connected to the evaluation unit and adapted to display the graphical or statistical representation of a concentration of the microorganisms on the surface being indicative to a presence of the microorganisms on the at least one portion of the surface covered by the sensor foil.

13. The arrangement as claimed in claim 12, further comprising a light source providing excitation light and being placed in optical relation to the sensor foil so that excitation light can reach the oxygen-permeable layer.

14. The arrangement as claimed in claim 12, wherein the detection element is a sensor chip directly attached to the at least partially transparent read-out carrier layer for receiving the emission of the oxygen indicator dye, and wherein the sensor chip is in a communicative connection with the evaluation unit.

15. The arrangement as claimed in claim 12, wherein the detection element is a detection device having at least one detector chip and an optic held in position by a housing, wherein the optic images the emission of the oxygen indicator dye transmitted through the oxygen-impermeable at least partially transparent read-out layer of the sensor foil onto the detector chip and the detector chip is in a communicative connection with the evaluation unit.

16. The arrangement as claimed in claim 15, wherein the detection device encompasses at least one light source adapted to direct the excitation light through the oxygen-impermeable at least partially transparent read-out carrier layer to the oxygen-permeable layer to excite the oxygen indicator dye in the oxygen-permeable layer by the excitation light and to emit the emission.

17. The arrangement as claimed in claim 12, wherein the detection device is attached in a fixed or detachable manner to a second free surface side of the oxygen-impermeable at least partially transparent read-out layer of the sensor foil.

18. A computer program product disposed on a non-transitory computer readable medium for detecting microorganisms on a surface, the computer program product comprising computer executable process steps operable to control a computer to: read data from a detector chip which is placed in optical relation to a sensor foil attached in an airtight manner to at least a portion of the surface to be examined, wherein an oxygen-permeable layer of the sensor foil is doped with an oxygen indicator dye, is loaded with oxygen and faces the at least one portion of the surface, and wherein an oxygen-impermeable at least partially transparent read-out carrier layer of the sensor foil faces the detector chip; calculate from the data an amount of the microorganisms and their distribution on at least one portion of the surface; and control a display to show a graphical or statistical representation of a concentration of the microorganisms on the surface based on detected emission in or after defined time intervals.

19. A computer program product as defined in claim 18, wherein at least one image window is defined on the detector chip so that the data are only read from the at least one image window in order to calculate the amount of the microorganisms.

20. A sensor foil for detecting microorganisms on a surface, the sensor foil comprising: an oxygen-permeable layer which is doped with an oxygen indicator dye and loaded with oxygen, wherein the oxygen-permeable layer is adapted to be attached in an airtight manner to at least one portion of the surface; and an oxygen-impermeable at least partially transparent read-out carrier layer adapted to carry the oxygen-permeable layer.

21. The sensor foil as claimed in claim 20, wherein the sensor foil is flexible.

22. The sensor foil as claimed in claim 20, wherein a first free surface side of the oxygen-permeable layer of sensor foil carries a regular pattern of a plurality of fields, wherein each field, except one, contains a different type of an antibiotic.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0069] The present invention will become more fully understood from the detailed description given herein below and the accompanying drawings which are given by way of illustration only, and thus, are not limiting to the present invention, and wherein:

[0070] FIG. 1 is a flowchart of a method for detecting microorganisms according to an embodiment to the present invention;

[0071] FIG. 2 is a schematic view of an arrangement for detecting microorganisms according to an embodiment to the present invention;

[0072] FIG. 3 is a schematic view of an arrangement for detecting microorganisms according to a further embodiment to the present invention;

[0073] FIG. 4 is a detailed view of the sensor foil according to an embodiment to the present invention;

[0074] FIG. 5 is a schematic view of a detection element according to an embodiment of the present invention;

[0075] FIG. 6 is a schematic view of the first free surface side of the oxygen-permeable layer to be in contact with the possible microorganisms on the surface to be detected, according to an embodiment of the present invention;

[0076] FIG. 7 is a schematic view of an embodiment of an array with a series of samples to be detected for microorganisms;

[0077] FIG. 8 is a schematic view of an embodiment of the display for showing a 2-dimensional distribution of microorganisms on the series of samples in FIG. 7;

[0078] FIG. 9 is an exemplary time series of detection result images;

[0079] FIG. 10 shows the first and the last detection result images of an exemplary time series with 200 samples and detection result images;

[0080] FIG. 11 is a diagram with a graph showing the sensor foil response along the time axis for a first region of interest;

[0081] FIG. 12 is a diagram with a graph showing the sensor foil response along the time axis for a second region of interest;

[0082] FIG. 13 is a diagram with a graph showing the sensor foil response along the time axis for a third region of interest;

[0083] FIG. 14 is a schematic view of another example of a response of a sensor foil according an embodiment of the invention for a sample, wherein two exemplary regions of interest are selected; and

[0084] FIG. 15 is a diagram with two graphs regarding the two exemplary regions of interest in FIG. 14.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0085] Reference will now be made in detail to the subject matter disclosed, which is illustrated in the accompanying drawings. The scope of the invention is limited only by the claims; numerous alternatives, modifications and equivalents are encompassed. For the purpose of clarity, technical material that is known in the technical fields related to the embodiments has not been described in detail to avoid unnecessarily obscuring the description.

[0086] FIG. 1 is a flowchart of an embodiment of a method for detecting microorganisms 3 consuming oxygen 4. In step S1, at least a portion of the surface 2 to be detected or examined is covered with a sensor foil 20 in an airtight manner, wherein an oxygen-permeable layer 21 of the sensor foil 20 is doped with an oxygen indicator dye 26, loaded with oxygen 4 and faces the at least one portion of the environment 2.

[0087] In step S2, a detection element 30 is placed in optical relation to the sensor foil 20.

[0088] In step S3, an excitation light 32 is sent through an oxygen-impermeable transparent read-out carrier layer 24 of the sensor foil 20 to the oxygen-permeable layer 21 of the sensor foil 20, to the oxygen indicator dye 26 in the oxygen-permeable layer 21 which oxygen indicator dye 26 is then excited by the excitation light 32.

[0089] In step S4, an emission 27 of the oxygen indicator dye 26 transmitted through the oxygen-impermeable transparent read-out carrier layer 24 of the sensor foil 20 is detected by the detection element 30 over or after a period of time t, wherein the emission 27 of the oxygen indicator dye 26 from the oxygen-permeable layer 21 is indicative to the amount of oxygen 4 consumed by microorganisms 3 from the oxygen-permeable layer 21 covering the at least one portion of the surface 2.

[0090] In an optional step S5, the detected emission 27 is imaged or recorded, for example with a sensor chip 34 of the detection element 30 for detecting the emission 27.

[0091] In an optional query Q1, it is determined whether a next or another portion of the surface 2 should be examined; if so, step S1 to S4 and optionally S5 are repeated; if not, the method is terminated, or in an optional step S6, the detected emission 27 is post-processed, so that the amount and/or the distribution of the microorganisms 3 is/are determined in situ with respect to the at least one (current) portion on the surface 2 and based on the detected emission 27. The post-processing can be done, for example, by a computer-implemented software. Such a query Q1 can be useful in case more than one sample as portion of the surface 2 shall be examined for possible microorganisms 3.

[0092] During step S4 or thereafter, for example the minimum inhibitory concentration (MIC) based on the detected emission 27 can be determined.

[0093] FIG. 2 shows a schematic view of an arrangement 1 for detecting microorganisms 3 consuming oxygen 4 according to an embodiment to the present invention.

[0094] The arrangement 1 provides a sensor foil 20 for covering at least a portion of the environment 2 to be detected. The sensor foil 20 is essentially composed of a first layer 11 and a second layer 12. The first layer 11 is an oxygen-permeable layer 21 doped with an oxygen indicator dye 26 and loaded with oxygen 4. The oxygen-permeable layer 21 loads oxygen (O.sub.2) 4 from the environment and thus represents an oxygen reservoir inside the sensor foil 20 due to oxygen solubility in the polymer used. A second layer 12 is an oxygen-impermeable transparent read-out carrier layer 24 for carrying the oxygen-permeable layer 21.

[0095] The sensor foil 20 has a first free surface side 22 and a second free surface side 25. The first free surface side 22 is a free surface side of the oxygen-permeable layer 21 and is used to contact at least a portion of the surface 2. The second free surface side 25 is a free surface side of the oxygen-impermeable transparent read-out carrier layer 24.

[0096] A read-out surface side 23 of the oxygen-permeable layer 21 is covered with the oxygen-impermeable transparent read-out carrier layer 24. The read-out surface side 23 is opposite to the second free surface side 25 with regard to the oxygen-impermeable transparent read-out carrier layer 24.

[0097] In an embodiment of the invention, the arrangement 1 comprises a detection element 30 adapted to illuminate at least a portion of the sensor foil 20 attached to at least a portion of the surface 2 to excite the oxygen indicator dye 26 in the oxygen-permeable layer 21 and to detect an emission 27 transmitted through the oxygen-impermeable transparent read-out layer 24.

[0098] Hence, the first free surface side 22 of the oxygen-permeable layer 21 is an oxygen-permeable contact side towards the possible microorganisms 3, and the second free surface side 25 of the oxygen-impermeable transparent read-out carrier layer 24 is an oxygen-impermeable transparent read-out side towards the detection element 30.

[0099] In an embodiment of the invention, the arrangement 1 shown here, comprises a display 42 adapted to show a distribution of microorganisms 3, for example a 2-dimensional distribution, on the at least one portion of the sample 2. A statistical analysis of microorganisms per area on the surface is possible with the use of an evaluation unit 40 in communicative connection with the display 42. The detected emission 27 is indicative to a presence of microorganisms 3 on the at least one portion of the surface 2.

[0100] In the embodiment shown here, the detection element 30 is a detection device 38. The detection device 38 has at least one detector chip 34. The detector chip 34 and an optic 35 are held in position by a housing 33. The detector chip 34 is used to detect the emission 27 of the oxygen indicator dye 26 which is transmitted through the oxygen-impermeable transparent read-out carrier layer 24 of the sensor foil 20. The optic 35 can as well be held in position by the housing 33. The optic 35 images the emission 27 of the oxygen indicator dye 26, which emission 27 is transmitted through the oxygen-impermeable transparent read-out layer 24 of the sensor foil 20, onto the detector chip 34. In the embodiment shown here, the detector chip 34 is in a communicative connection 39 with an evaluation unit 40. In the embodiment shown here, the evaluation unit 40 is a laptop with a display 42. It should be noted the laptop does not limit the present invention, but any mobile device (evaluation unit 40 with display 42) can be used to practice the invention.

[0101] In FIG. 2 the housing 33 comprises at least one light source 31 (light emitting element) adapted to direct an excitation light 32 through the oxygen-impermeable transparent read-out carrier layer 24 of the sensor foil 20 to the oxygen-permeable layer 21 of the sensor foil 20. The oxygen indicator dye 26 in the oxygen-permeable layer 21 is excited by the excitation light 32 and emits the emission 27. However, the detection element 30 can encompass more than one light source 31 (not shown in drawings). In the embodiment shown here, the at least one light source 31 is a part of the housing 33 which is not limiting the invention, since another construction of a light source 31 can be used.

[0102] In an embodiment of the invention, the detection element 30 is connected with the evaluation unit 40 by a connection 35. A transmission circuitry 36 can be assigned to the detector chip 34. The evaluation unit 40 is used to evaluate the amount of oxygen 4 detected by the detection element 30 over or after a period of time t. By way of non-limiting example, the evaluation unit 40 illustrated in FIG. 2 is configured with the above-mentioned display 42 adapted to show a distribution of microorganisms 3. It is obvious to a person skilled in the art that the display 42 can be provided as a separate device or integrated in the detection element 30 (see FIG. 4) or integrated in any other separate device, for example a smart device as mentioned above. The connection 35 between the detection element 30 and the evaluation unit 40 can comprise at least one cable or can be a wireless connection.

[0103] In an embodiment of the invention, the oxygen-permeable layer 21 of the sensor foil 20 for determining at least one parameter of the microorganisms 3 is doped with at least one reference dye 28 so that an emission 29 of the at least one reference dye 28 is transmitted through the oxygen-impermeable transparent read-out carrier layer 24 and is detected by the detection element 30.

[0104] FIG. 3 shows a schematic view of an alternative embodiment of the arrangement 1 of the present invention. The detection element 30 is a sensor chip 34. The sensor chip 34 is directly attached to the second free surface side 25 of the transparent read-out carrier layer 24. The sensor chip 34 receives the emission 27 of the oxygen indicator dye 26. The sensor chip 34 is in a communicative connection 39 with the evaluation unit 40. The evaluation unit 40, shown here, is a mobile device with an integrated display 42. No optic 35, as necessary in the embodiment of FIG. 2, is needed. The detected emission 27 of the oxygen indicator dye 26 in the first layer 11 (oxygen-permeable layer 21) is projected onto the sensor chip 34. The composition of the sensor foil 20 is already described in FIG. 2.

[0105] FIG. 4 shows a detailed view of the sensor foil 20 according to an embodiment to the present invention. According to an embodiment of the present invention, the oxygen-permeable layer 21 (first layer 11) of the sensor foil 20 comprises polyvinyl chloride.

[0106] In an embodiment of the invention, the oxygen-impermeable transparent read-out carrier layer 24 (second layer) of the sensor foil 20 comprises polyester.

[0107] In an embodiment of the invention, at least one oxygen indicator dye 26 or at least one oxygen indicator dye 26 plus at least one reference dye 28 are fluorescent, phosphorescent, luminescent, colorimetric and/or have another optical property changing over time t with respiration of oxygen 4 by the microorganisms 3.

[0108] FIG. 5 shows a schematic view of a detection element 30 according to another embodiment to the present invention. In comparison to FIG. 2, in the detection element 30 according to the embodiment of FIG. 5, the evaluation unit 40 with the display 42 is communicatively attached to the detection element 30. The design of the detection element 30 is already described in FIG. 2. The evaluation unit 40, which can be, for example, a smart phone, is used as an embedded system for carrying out the evaluations of the data and information detected by the sensor foil 20. According to the evaluation, it is possible to show a 2-dimensional distribution of microorganisms 3 on the display 42 or carry out a statistical analysis of the microorganisms present on the at least one portion of the surface 2. The evaluation unit 40 can be an integrated part of the detection element 30.

[0109] Regardless of the embodiment, whether the evaluation unit 40 is an integrated part of the detection element 30 or not, the detection element 30 can be attached in a fixed or detachable manner to the second free surface side 25 of the oxygen-impermeable transparent read-out layer 24 of the sensor foil 20. This design provides a particularly compact detector element 30.

[0110] All further elements in FIG. 5 have already been described with reference to FIG. 2 in detail. The connection 39 between the detector element 30 and the evaluation unit 40 can be a hard wire connection or wireless connection.

[0111] For rather large surfaces 2 to be inspected for possible microorganisms 3, the sensor foil 20 can have respective similar extensions.

[0112] FIG. 6 is a schematic view onto the first free surface side 22 of the oxygen-permeable layer 21 of the sensor foil 20 according to an embodiment of the present invention. The first free surface side 22 is in contact with the microorganisms 3 on the surface 2 to be detected. The first free surface side 22 of the oxygen-permeable layer 21 of sensor foil 20 carries a regular pattern of a plurality of fields 15.sub.1, 15.sub.2, . . . , 15.sub.N, wherein each field 15.sub.1, 15.sub.2, . . . , 15.sub.N, except at least one reference field 14, carries a substance which is antimicrobial and/or antibiotic. The arrangement of the fields 15.sub.1, 15.sub.2, . . . , 15.sub.N and the at least one reference field 14 shows only one possible embodiment and does not limit the arrangement of the fields 15.sub.1, 15.sub.2, . . . , 15.sub.N and the reference field 14 on the first free surface side 22 of the sensor foil 20. For example, each field 15.sub.1, 15.sub.2, . . . , 15.sub.N can carry a different type of antibiotic in order to determine their effect on the microorganisms 3.

[0113] FIG. 7 is a schematic view of a further embodiment of an arrangement 1 according to the present invention. A plate 5 is provided with an array 6 of a series of samples 7.sub.i, i=1, . . . , j, . . . , k, . . . , m. The individual samples 7.sub.i represent individual environments 2 to be examined for possible microorganisms 3 by the method of the present invention. Each sample 7.sub.i contains a probing solution with microorganisms 3, for example bacteria and/or fungi to be tested. For example, but not limited to, the samples 7.sub.i contain immobilized antimicrobial substances of different concentration. A sensor foil 20 is configured so that it can cover a portion of the plate 5 with all the samples 7.sub.i in an airtight manner and so that the microorganisms breathe directly into the oxygen-permeable layer 21 of the sensor foil 20.

[0114] A detection element 30, for example having a CMOS, is configured so that it illuminates at least a portion of the sensor foil 20 when attached to the plate 5 to excite the oxygen indicator dye 26 in the oxygen-permeable layer 21, to detect an emission 27 transmitted through the oxygen-impermeable transparent read-out layer 24 (see FIG. 2), and to read the sensor response of the sensor foil 20. Through this arrangement extremely small volumes (Picoliter respiratory chambers) of samples 7.sub.i can be produced and a time series of the response of the sensor foil 20 can be recorded, so that an oxygen consumption kinetics can be determined. For example, the minimum inhibitory concentration (MIC) based on the detected emission 27 and kinetics can be determined. This arrangement is useful for sensitivity tests and detection of resistance mechanisms in clinically relevant bacteria and yeasts.

[0115] In further embodiments, the oxygen-permeable layer 21 of the sensor foil 20 is treated and/or functionalized.

[0116] In one embodiment, the oxygen-permeable layer 21 of the sensor foil 20 is coated or soaked with antibiotics in order to determine the degree of effectiveness of the antibiotics in a series of samples 7.sub.i covered with the thus treated sensor foil 20.

[0117] The antibiotics should cause reduced respiration of the microorganisms (bacteria, fungi etc.). In case the microorganisms are sensitive to the antibiotics, the detected O.sub.2 values remain high over time. In case the microorganisms are less sensitive to the antibiotics, the microorganisms alter their breathing and the O.sub.2 values change by consumption. In case the microorganisms are resistant to the antibiotics, the microorganisms do not change their breathing and the O.sub.2 values greatly decrease by O.sub.2 consumption over time.

[0118] Each sample 7.sub.i is connected via a wire, cable or wireless connection 8.sub.i with a circuitry 9 for sending the data to a remote or local evaluation unit (not shown).

[0119] FIG. 8 is a schematic view of an embodiment of a display 42 for showing a 2-dimensional distribution of microorganisms 3 on the series of samples 7.sub.i in FIG. 5. Each sample 7.sub.i is represented by a respective result image 43.sub.i, i=1, . . . , j, . . . , k, . . . , m. Each result image 43.sub.i shows, for example, a representative image taken by the detection element 30, which can be configured as a CCD-camera. When activating a single image icon 43.sub.i, for example, further results details and/or a magnified image 43.sub.i, are shown on display 42.

[0120] Function keys 44.sub.n, n=1, . . . , o, enable the user to call various sub-routines in order to carry out different evaluations and/or graphical representations of the detected data. Additionally, the detection element 30 not shown can be controlled via specific function keys 44.sub.n.

[0121] Thus, a time series of samples 7.sub.i, i=1, j, . . . , k, . . . , m, as to detecting microorganisms 3 on these samples 7.sub.i can be recorded with the detection element 30 and displayed via a respective time series of result images 43.sub.i. For example, a surface partially colonized with microorganisms 3 is covered with a sensor foil 20 and read-out in fixed time intervals, for example 2 sec, as shown in FIG. 9. Hence, FIG. 9 is a time series of detection result images 43.sub.i.

[0122] FIG. 10 shows the first last detection result image 43.sub.1 and the last detection result image 43.sub.200 of an exemplary time series with 200 samples 7.sub.i, i=1, . . . , 200 (see FIG. 7), and therefrom resulting m=200 detection result images 43.sub.i, i=1, . . . , 200, as for example, shown in FIGS. 8 and 9.

[0123] In the exemplary series of samples 7.sub.i, each sample 7.sub.i, i=1, . . . , 200, is provided with the same amount of microorganisms 3, a maximum amount of antibiotics or a maximum strong antibiotics is added to the first sample 7.sub.i, the last sample 7.sub.200 contains no antibiotics, and with increasing index i=2, . . . , 199, an increasing amount of antibiotics or increasingly stronger antibiotics have been added to the respective samples 7.sub.i. Then the method according to the invention is applied to each of the samples 7.sub.i, for example as described with regard to FIG. 7, for detecting the remaining amounts of microorganisms 3 on the samples 7.sub.i after the have been treated with the different amounts and/or strengths of antibiotics. At least one detection result image 43.sub.i is taken of each sample 7.sub.i. The content of a result image 43.sub.i depends on the amount of antibiotics added to the respective sample 7.sub.i as will be described in the following.

[0124] In an embodiment of the invention, each O.sub.2 value detected and indicating the presence or absence of microorganisms 3 by the method and/or arrangement 1 is assigned to a specific color 50, 51, . . . , 55. Thus, the quantification, i.e. the amounts, of O.sub.2 consumption across the respective sample 7.sub.i can be visualized by means of the result images 43.sub.k. The colors can be, but are not limited to, a range of greys or a range of any other colors of the known continuous color spectrum. The sensor foil 20 should provide ratiometric properties accordingly. For mere explanation, in the example of FIG. 10, six distinctive separate colors 50, 51, . . . , 55 have been chosen. However, in reality, the number of microorganisms 3 and hence the amount of O.sub.2 usually changes across the sample to be detected in a continuous manner. Therefore, the colors selected for representation of the diverse O.sub.2 amounts across the pixels of any single image 43.sub.i can be taken from a continuous interval of the maximal O.sub.2 value and the minimum O.sub.2 value detected.

[0125] In the exemplary case of FIG. 10, light regions 45 in the last result image 43.sub.200 represent surface portions of the respective last sample 7.sub.200 where a maximum of microorganisms 3 are present, and hence, O.sub.2 presence is low due to O.sub.2 consumption of the microorganisms 3, represented, for example by the lightest color 55 in the chosen range of colors. Dark regions 46 in the last result image 43.sub.200 represent other surface portions of the respective last sample 7.sub.200 where the presence of microorganisms 3 is at its minimum, maybe even absent, and hence, O.sub.2 presence is high, represented, for example by the darkest color 50 in the chosen range of colors. The series of result images 43.sub.i thus visualize the degree of effectiveness of an antibiotic and the amounts of the antibiotic needed for reducing or even eliminating the microorganisms on the samples 7.sub.i of an environment 2.

[0126] In the last result image 43.sub.200, three regions of interest 56, 57, 58 are marked which are examined and described in more detail in FIGS. 11, 12, 13.

[0127] Reference sign 47 in the result images 43.sub.i represents boundary lines of the surface 2 or boundaries of the sensor foil 20.

[0128] A person skilled in the art knows that any other range of colors can be chosen suitable for visualizing the amounts of O.sub.2 and hence visualizing the amounts of microorganisms 3 on a sample 7.sub.i, without departing from the scope of the invention. A person skilled in the art also knows that in the series of samples 7.sub.i and result images 43.sub.i, i=1, . . . , m, the total number m can be less or more than 200 and/or the total number m of result images 43.sub.i can be equal or greater than the total number m of samples 7.sub.i and/or the number of regions of interest 56, 57, 58 can be different from three without departing from the scope of the invention.

[0129] Description data 48, such as, but not limited to, the index i of a respective result image (slide) 43.sub.i (for example 1 and 200), the total number of result images (slides) 43.sub.i (for example 200), the date and time of the result images 43.sub.i, the path where the file of the result image (slide) 43.sub.i is saved, and the and file name of the result image (slide) 43.sub.i, can be added to each result image 43.sub.i automatically by a respective software.

[0130] FIG. 11 is a diagram with a graph 62 showing the response of the sensor foil 20 as a function of time t along the X-axis X for the first region of interest 56 (ROI) in the last detection result image 43.sub.200 of FIG. 10. Graph 62 shows a strong decrease of oxygen O.sub.2 which means a high O.sub.2 respiration rate which reaches a saturation after a certain period of time, which in turn means a high number of microorganisms in average present in the first region of interest 56. The scale of the Y-axis Y is in arbitrary units.

[0131] FIG. 12 is a diagram with a graph 63 showing the response of the sensor foil 20 of FIG. 10 as a function of time t along the X-axis X for the second region of interest 57 in the last detection result image 43.sub.200 of FIG. 10. Graph 63 shows a mediate decrease of oxygen O.sub.2 which means a mediate O.sub.2 respiration rate. The scale of the Y-axis is in arbitrary units and the range of the Y-axis Y of FIG. 12 is lower than the range of the Y-axis Y in FIG. 11. This means in turn that a mediate number of microorganisms in average is present in the second region of interest 57.

[0132] FIG. 13 is a diagram with a graph 64 showing the response of the sensor foil 20 of FIG. 10 as a function of time t along the X-axis X for the third region of interest 58 in the last detection result image 43.sub.200 of FIG. 10. Graph 64 shows a low decrease of oxygen O.sub.2 which means a low O.sub.2 respiration rate. The scale of the Y-axis is in arbitrary units and the range of the Y-axis Y of FIG. 13 is lower than the range of the Y-axis Y in FIG. 12. This means that a low number of microorganisms in average is present in the third region of interest 58.

[0133] For example, in FIGS. 11, 12 and 13 a ratiometric sensor foil 20 can be used which, for example ratiometric with regard to the colors red and green.

[0134] In another embodiment of the inventive arrangement and method, bacteria as microorganisms are detected on a surface via determining pH value changes. In general, most bacteria generate acids or protons during metabolism. Acids and protons influence the pH value of an aqueous phase. Bacterial growth is a spatially diverged phenomenon. Therefore 2-dimensional information has to be gained, which is achieved in the present invention through the result images 43 as response of the sensor foil 20. For example, pH changes caused by bacterial metabolism can be observed via optical pH sensor foils 20.

[0135] For example, bacteria can be detected via determining pH value changes by using a planar optical sensor foil 20. A surface of a sample that is suspicious to contain (a relevant amount of) bacteria is covered with a planar optical pH sensor foil 20. The planar optical pH sensor foil 20 can consist of at least one fluorescent or colorimetric pH indicator that results in a pH dependent signal change. Further the planar optical pH sensor foil 20 can consist of a referencing element that enables referenced signal read out. Planar optical pH sensor foils 20 should comprise a certain amount of humidity for enabling a bacteria dependent pH-change. The signal change is read out in a spatially derived manner, e.g. with an array detector or a camera. pH changes can be monitored either as signal change after a certain period of time or in a time dependent experiment.

[0136] Spatially and time dependent signal changes in the response of the sensor foil 20 enable to locate regions in a region of interest in a sample with pH changes by bacterial presence or growth. Signal thresholds of recorded pH changes can be used to determine positive and negative results. A color system can be used for the result images 43 resulting from the response of the sensor foil 20 as described above in order to visualize the results, i.e. the degree of presence or absence of bacteria in the sample. Metabolism activators can be used in the oxygen-permeable layer 21 of sensor foil 20 to enhance pH changes caused by bacterial growth and metabolism.

[0137] In another embodiment of the inventive arrangement and method, bacteria as microorganisms are detected on a surface via determining pCO2 levels by using a pCO2 sensitive sensor foil analogous to the respiration described above.

[0138] FIG. 14 is a schematic view of another example of a response of a sensor foil 20 according an embodiment of the invention for a sample, wherein two exemplary regions of interest 56, 57 are selected in a result image 43. FIG. 15 is a diagram with two graphs 61, 62 regarding the two exemplary regions 56, 57 of interest in FIG. 14. The first graph 61 shows the progress of the response of the exemplary sensor foil 20 as to the first region of interest 56, and thereby the progress of oxygen O.sub.2 amounts in the first region of interest 56 in the sample as a function of time t along the X axis X. The first region of interest 56 is an area of the surface which is covered by the sensor foil where the population of microorganisms is high. Accordingly, the second graph 62 shows the progress of the response of the exemplary sensor foil 20 as to the second region of interest 57, and thereby the progress of oxygen O.sub.2 amounts in the second region of interest 57 in the sample as a function of time t along the X axis X. In a time series, the result image 43 depicted in FIG. 14 is repeatedly recorded at certain time intervals and is represented in the two graphs 61, 62 in FIG. 15.

[0139] As described before, the sensor foil 20 is charged in ambient air before it is applied to the surface (oxygen partial pressure is identical to the environment inside the sensor and thus high). In regions where microorganisms 3 are not present, the oxygen partial pressure remains high, i.e. no breathing and no O.sub.2 consumption occur, which can be represented, for example, by the color 50 blue or the darkest grey in the result image 43. In regions where microorganisms 3 are present, the oxygen partial pressure is reduced by breathing after a short time, i.e. respiration and consumption O.sub.2 consumption occur, which can be represented, for example, by the color 55 yellow or white in the result image 43. If the above-described embodiment of an arrangement 1 with an OLED is used directly on the sensor foil 20, the user sees this colored result image 43 directly via the OLED. Therefore, in this embodiment, no optical read-out system, like for example a camera, is required to visualize microorganisms on the surface of the sample 7 to be tested.

[0140] Evaluating the mean value over the entire sensor foil 20, i.e. essentially over the second region of interest 57, results in little change if only a few (microscopic small) microorganisms are present within this large region of interest 57. The partial strong change in small regions, like for example in the small region of interest 56, has little effect on the average value of a large region of interest, like for example of the large region of interest 57. This type of detection is typical for point measurements in which millimeter-sized points or spots are read average with an optical fiber.

[0141] If, however, the response of the sensor foil 20 is only evaluated around the spots emerging from oxygen consumption in small regions of interest like region 56, the oxygen partial pressure change at microscopically small regions can be evaluated with a significant change in the sensor response. For example, one uses the core property of a sensor, i.e. detecting at very high spatial resolution due to individual dyes, and of a camera, i.e. detecting two-dimensionally resolved sensor responses due to single pixels.

[0142] It is believed that the present disclosure and many of its attendant advantages will be understood by the foregoing description, and it will be apparent that various changes may be made in the form, construction and arrangement of the components without departing from the disclosed subject matter or without sacrificing all of its material advantages. The form described is merely explanatory, and it is the intention of the following claims to encompass and include such changes. Furthermore, it is to be understood that the invention is defined by the appended claims.

LIST OF REFERENCE NUMERALS

[0143] 1 arrangement [0144] 2 surface [0145] 3 microorganism [0146] 4 oxygen (O.sub.2) [0147] 5 plate [0148] 6 array [0149] 7.sub.i sample, i=1, . . . , j, . . . , k, . . . , m [0150] 8.sub.i wire, cable or wireless connection, i=1, . . . , j, . . . , k, . . . , m [0151] 9 circuitry [0152] 11 first layer [0153] 12 second layer [0154] 14 reference field [0155] 15.sub.1, 15.sub.2, . . . , 15.sub.N field [0156] 20 sensor foil [0157] 21 oxygen-permeable layer (sensitive layer, polymer layer) [0158] 22 first free surface side (oxygen-permeable contact side to microorganisms) [0159] 23 read-out surface side [0160] 24 oxygen-impermeable at least partially transparent read-out carrier layer (polyester support) [0161] 25 second free surface side (oxygen-impermeable and at least partially transparent read-out side) [0162] 26 oxygen indicator dye [0163] 27 emission of oxygen indicator dye [0164] 28 reference dye [0165] 29 emission of reference dye [0166] 30 detection element [0167] 31 light source (light emitting element) [0168] 32 excitation light [0169] 33 housing [0170] 34 detector chip, sensor chip [0171] 35 optic [0172] 36 transmission circuitry [0173] 38 detection device [0174] 39 connection [0175] 40 evaluation unit [0176] 42 display [0177] 43.sub.i result image (slide), i=1, . . . , j, . . . , k, . . . , m [0178] 44.sub.n function key, n=1, . . . , o [0179] 45 image region with microorganisms present [0180] 46 image region with microorganisms absent [0181] 47 boundary line [0182] 48 description data [0183] 50 color [0184] 51 color [0185] 52 color [0186] 53 color [0187] 54 color [0188] 55 color [0189] 56 first region of interest [0190] 57 second region of interest [0191] 58 third region of interest [0192] 60 graph [0193] 61 graph [0194] 62 graph [0195] 63 graph [0196] 64 graph [0197] Q1 query of examining next portion of environment [0198] S1 step of covering at least a portion of the environment to be detected with a sensor foil in an airtight manner [0199] S2 step of placing a detection element in relation to the sensor foil [0200] S3 step of sending an excitation light through an oxygen-impermeable at least partially transparent read-out carrier layer of the sensor foil to the oxygen-permeable layer of the sensor foil [0201] S4 step of detecting an emission of the oxygen indicator dye transmitted through the oxygen-impermeable at least partially transparent read-out carrier layer of the sensor foil by the detection element over a period of time [0202] S5 step of imaging the detected emission [0203] S6 step of post-processing the detected emission [0204] t time [0205] X X-axis [0206] Y X-axis