SELF-REFERENCED SENSOR

Abstract

The present invention provides a sensor comprising at least one whispering gallery mode resonator, wherein the resonator comprises a Bragg grating arranged over at least a portion of the perimeter of the resonator and wherein the resonator is selectively functionalized for the attachment of analyte receptors.

Claims

1. A sensor comprising at least one whispering gallery mode resonator, wherein the resonator comprises a Bragg grating arranged over at least a portion of the perimeter of the resonator and wherein the resonator is selectively functionalized for the attachment of analyte receptors.

2. The sensor according to claim 1, wherein the grating is functionalized for the attachment of analyte receptors.

3. The sensor according to any of the previous claims, wherein the resonator is made of a first material and the grating is made of a second material different to the first material.

4. The sensor according to any of the previous claims, wherein the grating is a grating of analyte receptors directly arranged over a surface of the resonator.

5. The sensor according to any of the previous claims, wherein the resonator is made of at least a material selected from Al.sub.2O.sub.3, Si.sub.3N.sub.4, SiO.sub.2, SiOn, TiO.sub.2, Ta.sub.2O.sub.5, Te.sub.2O.sub.5, phosphate glass, KY(WO.sub.4).sub.2, YAG, ZBLAN.

6. The sensor according to any of the previous claims, wherein the grating is made of a material comprising at least one of a polymer, preferably PMMA, SiO.sub.2, SiOn, SiN or TiO.sub.2.

7. The sensor according to any of the previous claims, wherein the period of the grating is substantially half the operating wavelength.

8. The sensor according to any of the previous claims, wherein the resonator material is doped with a material providing laser gain, preferably a rare-earth material, a semiconductor material, or a transition metal ion doped material.

9. The sensor according to any of the previous claims, wherein the sensor is functionalized over only a part of its perimeter, preferably over a quarter of the perimeter or over a half of the perimeter.

10. The sensor according to any of the previous claims, wherein: the resonator is a ring resonator embodied as a looped optical waveguide and the sensor further comprises a coupling mechanism to access the looped optical waveguide, or the resonator is shaped as a disk and the sensor further comprises a coupling mechanism to access the disk.

11. The sensor according to any of the previous claims, wherein the resonator has a closed loop configuration comprising a plurality of sections, each section being configured for coupling with an optical waveguide at a wavelength.

12. The sensor according to any of the previous claims, wherein the resonator is fabricated in rare-earth doped Al.sub.2O.sub.3, wherein the rare-earth ions provide emission outside the absorption bands of water, the rare-earth ions being preferably selected from the group consisting of Yb.sup.3+, Nd.sup.3+, Er.sup.3+, Tm.sup.3+, and Ho.sup.3+.

13. The sensor according to any of the previous claims, wherein the sensor comprises a plurality of resonators and a plurality of chambers, wherein the resonators are arranged such that each chamber comprises one resonator, wherein the sensor comprises a plurality of openings, each opening providing fluid communication between two adjacent chambers, and wherein the openings have different size.

14. A sensing system comprising: a sensor according to any of the previous claims, and a readout unit configured to receive the sensor and preferably comprising aligning means for aligning the sensor.

15. The sensing system according to claim 14, further comprising a laser configured to optically pump the at least one resonator when the sensor is received in the readout unit, a photodetector and processing electronics.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0080] To complete the description and provide for better understanding of the invention, a set of drawings is provided. Said drawings illustrate a preferred embodiment of the invention, which should not be interpreted as restricting the scope of the invention, but just as an example of how the invention can be carried out.

[0081] FIG. 1 shows the spectra of a ring resonator with a grating.

[0082] FIG. 2 shows |Ψ.sub.lc+1±Ψ.sub.lc−1|.sup.2 as a function of θ. The step function represents the distribution of molecules along the perimeter.

[0083] FIG. 3 schematically shows the degeneracy lifting of the spectra when analyte molecules are attached to part of the grating.

[0084] FIG. 4 shows the different responses upon biomarker detection of the passive and active embodiments of the biosensor according to the invention.

[0085] FIG. 5 shows experimental results on mode splitting of a self-referenced sensor according to the invention.

[0086] FIG. 6 shows experimental results on mode splitting of a self-referenced sensor according to the invention.

[0087] FIG. 7 shows the mode-splitting profile for the grating, along with the sensitivity of the sensor for different biomarker concentrations.

[0088] FIG. 8 schematically shows a sensor according to an embodiment of the present invention.

[0089] FIG. 9 schematically shows an embodiment wherein the grating is generated by adding to the resonator a layer of a different material on a top surface of the resonator.

[0090] FIG. 10 schematically shows an embodiment wherein the grating is fabricated by directly imprinting the antibodies onto the top surface of the resonator.

[0091] FIG. 11 schematically shows a sensor according to an embodiment of the present invention. In this embodiment the micro ring resonator has a grating on the sidewall over a part of its perimeter.

[0092] FIG. 12 shows a sensor according to an embodiment of the invention.

[0093] FIG. 13 shows a readout scheme for an active resonator according to the invention.

[0094] FIG. 14 shows an embodiment of a sensing system according to an embodiment of the invention.

[0095] FIG. 15 shows a flowchart of an embodiment of a method of operation of the invention.

[0096] FIG. 16 shows a flowchart of an embodiment of a method of operation of the invention.

[0097] FIG. 17 shows an embodiment of the sensor wherein the resonator is shaped as a non-circular loop.

DETAILED DESCRIPTION OF THE INVENTION

[0098] FIG. 1 (a) schematically shows a microring resonator of width ω and radius R with a grating. The refractive index varies periodically between n.sub.r and n.sub.r+Δn with a period

[00001]$d=\frac{\pi }{l_c}.$

[0099] A random surface roughness eventually results in changing the refractive index of the ring from n to n+Δn(θ). Being periodic, one may decompose the fluctuating index as

[00002]$\Delta n\left(\theta \right)=\underset{l=0}{\overset{\infty }{.Math.}}{c}_l\cos l\theta +s_l\sin l\theta$

[0100] In the most random case, where Δn(θ) is a white noise, all Fourier coefficients appearing above have the same modulus. However, in practice, it may be that some Fourier coefficients are significantly bigger than other. This would be expected if the process that induces surface roughness has some systematic component with well-defined length scale.

[0101] Here, we assume that there is a grating in the ring, which results in an effective modulation Δn(θ) of the refractive index given by

Δn(θ)=δcos(2l.sub.cθ)+ . . .

[0102] Above, the omitted terms are higher harmonics in the Fourier decomposition of Δn(θ) and δ is small compared to 1 so that in can be treated as a perturbation. The modulated refractive index plays with the electromagnetic field an analogous role as a periodic potential does for electrons in a crystal. Hence this results in a band gap in the frequency spectrum near the edge of the Brillouin zone, l=l.sub.c.

[0103] On the lower band of frequencies, the spectrum is given near l=l.sub.c by

[00003]$\omega \left(l\right)\sim {\omega }_o\left(l_c\right)-\left[\Delta \omega +k\frac{{\left(l-l_c\right)}^2}{2}\right]$

where Δω=0(δ) is the frequency gap.

[0104] The corresponding eigenmode are now given by

Ψ.sub.l≈Φ.sub.l+Φ.sub.l−2lc

where Φ.sub.m is an eigenmode of azimuthal number m of the resonator in the absence of refractive index modulation, that is when Δn(θ)=0.

[0105] Similarly, on the upper side of the band gap, the spectrum is given by

[00004]$\omega \left(l\right)\sim {\omega }_o\left(l_c\right)-\left[\Delta \omega +k\frac{{\left(l-l_c\right)}^2}{2}\right]$

with the corresponding eigenmodes approximately given by

X.sub.l≈Φ.sub.l−Φ.sub.l−2lc

[0106] Focusing now on the lower band, the modes with labels Ψ.sub.lc+p and Ψ.sub.lc−p are degenerate, as shown in FIG. 1 (b). Therefore, any combination aΨ.sub.lc+p+bΨ.sub.lc−p forms an eigenmode with approximate frequency ω(I.sub.c+p) given by

[00005]$\omega \left(l_c+p\right)\sim {\omega }_o\left(l_c\right)-\left[\Delta \omega +k\frac{p^2}{2}\right]$

[0107] FIG. 1 (b) shows the spectra of a ring resonator of width w and radius R with a grating, where the refractive index varies periodically between n.sub.r and n.sub.r+Δn, as shown in FIG. 1(a). Here, R=50 μm, ω=700 nm, n.sub.r=1.65, Δn=−0.02 and l.sub.c=490. The upper branch of resonances corresponds to eigenmodes of the form X.sub.l, while the lower branch corresponds to Ψ.sub.l.

[0108] For modelling a microring as the ones used in the embodiments of the present invention, a cavity mode is considered, with electric field ε, magnetic field H and frequency ω. If the cavity is perturbed by a material with distributed polarizability a, a polarization

P=αε

will result. Then, a frequency shift δω and wavelength shift δλ will be produced according to the formula

[00006]$-\frac{\delta \omega }{\omega }=\frac{\mathrm{\delta \lambda }}{\lambda }=\frac{\int \int \int {ℰ}^{*}.Math.\alpha ℰ\mathrm{dV}}{\int \int \int \left(ϵ{.Math.ℰ.Math.}^2+\mu {.Math.H.Math.}^2\right)\mathrm{dV}}$

[0109] For assessing the frequency shift, the following integral has been used

U=∫∫∫ε*.Math.αεdV

[0110] In a particular embodiment, urine has been flown only over one quarter of the ring perimeter, in particular in the range 3π/4<θ<5π/4. Then, the eigenmodes

Ψ.sub.lc+1+Ψ.sub.lc−1 and Ψ.sub.lc+1−Ψ.sub.lc−1

experience the maximal and minimal frequency shift, respectively. These two particular combinations are the new eigenmodes in the presence of the urine polarisation P and their frequency difference (U.sub.+-U.sub.−) is the mode splitting.

[0111] In order to derive the this result, we consider a pristine microring without grating, with a perfectly smooth surface, whose azimuthal dependence is characterized by their angular number l:

[00007]$\Phi \equiv \left\{\begin{array}{c}{E}_l\left(r,z\right)\\ H_l\left(r,z\right)\end{array}\right\}{e}^{\mathrm{il}\theta -i{\omega }_0\left(l\right)t}$

[0112] This equation can be simplified in the limit of large l.sub.c, with l=l.sub.c±p and p=O(1). Indeed, in that limit,

[00008]$\left\{\begin{array}{c}{E}_{\pm l}\left(r,z\right)\\ H_{\pm l}\left(r,z\right)\end{array}\right\}\sim \left\{\begin{array}{c}{E}_{lc}\left(r,z\right)\\ H_{lc}\left(r,z\right)\end{array}\right\}$

and, consequently,

[00009]${\Psi }_l\sim \left\{\begin{array}{c}{E}_{lc}\left(r,z\right)\\ H_{lc}\left(r,z\right)\end{array}\right\}\left(e^{il\theta }+e^{i\left(l-2l_c\right)\theta }\right)e^{-i\omega \left(l\right)t}.fwdarw.{\Psi }_{l+p}\sim \left\{\begin{array}{c}{E}_{lc}\left(r,z\right)\\ H_{lc}\left(r,z\right)\end{array}\right\}{e}^{ip\theta }2\cos \left(l_c\theta \right)e^{-i\omega \left(l\right)t}$

[0113] Hence, with a field given by

[00010]${\Psi }_{lc+1}+{\Psi }_{lc-1}\sim \left\{\begin{array}{c}{E}_{lc}\left(r,z\right)\\ H_{lc}\left(r,z\right)\end{array}\right\}4\cos \left(l_c\theta \right)\cos \left(\theta \right)e^{-i\omega \left(l\right)t}$

[0114] We find

[00011]$U=U_{+}=16\int \int E_{l_c}^{*}\left(r,z\right).Math.\alpha E_{l_c}\left(r,z\right)\mathrm{rdrdz}\times {\int }_{\frac{3\pi }{4}}^{\frac{5\pi }{4}}{\cos }^2\left(l_c\theta \right){\cos }^2\left(\theta \right)d\theta .fwdarw.2\left(2+\pi \right)\int \int E_{l_c}^{*}\left(r,z\right).Math.\alpha E_{l_c}\left(r,z\right)\mathrm{rdrdz}$

[0115] On the other hand, with

[00012]${\Psi }_{lc+1}-{\Psi }_{lc-1}\sim \left\{\begin{array}{c}{E}_{lc}\left(r,z\right)\\ H_{lc}\left(r,z\right)\end{array}\right\}4i\sin \left(l_c\theta \right)\cos \left(\theta \right)e^{-i\omega \left(l\right)t}$

[0116] We obtain

[00013]$U=U_{-}=-16\int \int E_{l_c}^{*}\left(r,z\right).Math.\alpha E_{l_c}\left(r,z\right)\mathrm{rdrdz}\times {\int }_{\frac{3\pi }{4}}^{\frac{5\pi }{4}}{\cos }^2\left(l_c\theta \right){\sin }^2\left(\theta \right)d\theta .fwdarw.2\left(2-\pi \right)\int \int E_{l_c}^{*}\left(r,z\right).Math.\alpha E_{l_c}\left(r,z\right)\mathrm{rdrdz}$

[0117] The difference is

U.sub.+−U.sub.−=4π∫∫E.sub.l.sub.c*(r,z).Math.αE.sub.l.sub.c(r,z)rdrdz

[0118] Eventually the splitting is given by

[00014]$\frac{\delta {\lambda }_{+}-{\mathrm{\delta \lambda }}_{-}}{\lambda }=\frac{2\int \int E_{l_c}^{*}\left(r,z\right).Math.\alpha E_{l_c}\left(r,z\right)rdrdz}{\int \int \int \left(ϵ{.Math.E_{l_c}\left(r,z\right).Math.}^2+\mu {.Math.H_{l_c}\left(r,z\right).Math.}^2\right)rdrdz}$

[0119] To illustrate the difference between U.sub.+ and U.sub.−, one may simply plot the square modulus of Ψ.sub.lc+1±Ψ.sub.lc−1 along the perimeter and compare it with the distribution of a along that perimeter.

[0120] Said difference is schematically shown in FIG. 2.

[0121] FIG. 3 (a) shows a functionalized ring according to an embodiment of the invention, which is being supplied with water through two different channels, each one communicating a fluid sample to a different half of the ring. In this embodiment, water flows through both upper and bottom channels. Therefore, no analyte molecules binding events have occurred. As a consequence, FIG. 3 (c) shows the degeneracy of the spectra when in absence of analyte molecules.

[0122] FIG. 3 (b) shows the functionalized ring of FIG. 3 (a) being supplied with a solution of water and molecules through one of the channels, thus showing analyte molecules attached to its perimeter. Accordingly, FIG. 3 (d) shows the degeneracy lifting of the spectra when analyte molecules are attached to one half of the ring.

[0123] FIG. 4 shows the contrast in the emission linewidth between the passive and active embodiments of a self-referenced sensor according to the present invention. Apart from the splitting in the frequency domain (beatnote) due to the presence of the grating, the active case (i.e., resonators with doped material providing a gain medium making them capable of operating as a laser) shows narrower peaks, which leads to higher precision in the detection of the beatnote.

[0124] FIG. 5 shows the results of an experiment testing the self-referencing capabilities of a sensor according to the invention. On one side, it is shown how the peaks in which the signal is split by the mode splitting (Peak 1 and Peak 2) shift. In this particular case, only Peak 1 is shown as an example. As a function of time, the RIU (Refractive Index Unit) is modified, by increasing every 500 s the concentration of the liquid flowing over the sensor. It can be observed that Peak 1 shifts its resonance frequency accordingly.

[0125] On the other side, the mode splitting of the sensor, this is, the beatnote variation resulting of subtracting the frequency of Peak 2 to Peak 1, is displayed as a function of time. In contrast with the variation of Peak 1 with the bulk refractive index as a consequence of the increase in the concentration of the liquid flowing over the sensor, said beatnote does not vary.

[0126] FIG. 6 shows an experiment in which temperature is varied in a similar manner in which RIU was varied in the experiment carried out in FIG. 5. It can be observed that, whereas Peak 1 shifts subsequently with temperature variation, again, the beatnote remains substantially constant.

[0127] FIG. 7 shows the results of different mode-splitting simulations for a resonator according to an embodiment of the present invention. To test the response of the resonator with a grating upon biomarker concentration, several biolayers with different thicknesses have been considered. As it can be seen in the two correlated graphs (a) and (b), the splitting increases monotonously with the number of binding events. This is, as the layer thickness increases as shown with the linear fit in graph (b) (for the selected values of layer thickness (nm) (0, 2, 4, 6, 8, 10)), the mode splitting also increases (having the corresponding peak values shown in graph (a) for the selected values of layer thickness).

[0128] FIG. 8 schematically shows a sensor (1) according to an embodiment of the present invention. Specifically, the sensor (1) comprises a micro ring resonator (2) embodied as a looped optical waveguide, namely a circular optical waveguide, and an optical waveguide (3) for coupling with the looped optical waveguide (2). In this embodiment the micro ring resonator (2) has part of the ring perimeter covered by a grating (5). This grating (5) induces a mode splitting that varies upon binding of molecules to pre-determined sections of the grating (5). In the figure the grating (5) is schematically represented with grey squares.

[0129] In this embodiment the ring resonator (2) is made of Al.sub.2O.sub.3 doped with Ytterbium, which allows using the micro ring resonator (2) in an active mode. In the active mode the micro ring resonator (2) operates as a laser, emitting one or several frequencies that are associated to resonator modes within the gain spectrum of the doping material (in this embodiment Ytterbium). Narrowing of the emission linewidth occurs after lasing threshold. A ˜200 kHz linewidth was measured for a device with output power in the tens of microwatts

[0130] There are different ways in which the grating (5) can be provided.

[0131] FIG. 9 schematically shows an embodiment wherein the grating (5) is generated by adding to a top surface of the micro ring resonator (2) a layer of a different material. In this embodiment the micro ring resonator (2) is made of Al.sub.2O.sub.3 and the material of the grating (5) is SiO.sub.2. The grating (5) can cover the full circumference of the micro ring resonator (2) of just a portion of it.

[0132] Selective functionalization (6) of the grating (5), either by different materials or lift-off process of the functionalization (6), permits the immobilization of analyte receptors and the subsequent attachment of analyte molecules to only part of the grating (5), thus inducing a variation of the induced splitting as a function of the number of analyte molecules attached to the surface of the grating (5). In this embodiment the grating (5) is selectively functionalized with silane (6) to achieve selective immobilization of antibodies on the grating (5). The analyte receptors, which in this embodiment are antibodies, can be immobilized over the full perimeter of the micro ring resonator (2) or over only a part of it. A biolayer (7) is also shown in FIG. 9, the biolayer (7) comprising the antibodies immobilized on the grating (5) and captured proteins.

[0133] FIG. 10 schematically shows an embodiment wherein the grating (5) is provided on the micro ring resonator (2) by directly imprinting analyte receptors onto a top surface of the functionalized (6) micro ring resonator (2). Thus, in this embodiment the functionalization (6) is arranged on the micro ring resonator (2) to form a grating (5). The grating (5) of analyte receptors can cover the full perimeter of the micro ring resonator (2) or only a part of it. In this embodiment the micro ring resonator (2) is made of Al.sub.2O.sub.3 and the analyte receptors are antibodies. A biolayer (7) is also shown in FIG. 10, the biolayer (7) comprising the antibodies immobilized on the grating (5) and captured biomarkers.

[0134] In the embodiments of FIGS. 8 to 10 the grating (5) is arranged on the top surface of the micro ring resonator (2). FIG. 11 schematically shows a sensor (1) according to an embodiment wherein the grating (5) is arranged on a sidewall over a part of the perimeter of a micro ring resonator (2). Corrugation of the sidewall, corresponding to the grating (5), is represented by rectangles in the figure.

[0135] FIG. 12 shows a sensor (1) according to an embodiment of the invention. In this embodiment a micro ring resonator (2) has a grating (5) covering its full perimeter. However, only a quarter of the grating (5) is functionalized (6) and covered with analyte receptors.

[0136] In FIG. 12 the grating (5) is represented with grey squares and the functionalization (6) is represented with white triangles.

[0137] FIG. 13 schematically shows a readout unit for the sensors (1) of FIGS. 8, 11 and 12 when working in an active mode. The readout unit comprises a laser diode pump (21) to optically pump the micro ring/micro disk resonator (2) laser and a fast photodetector (23) followed by an RF spectrum analyser (REF) (33). The system further comprises a Wavelength Division Multiplexing unit (WDM) (34), which enables bidirectional transmission through the straight optical waveguide (3), multiplexing the pump laser (21) and the backward lasing power (31). In an embodiment the photodetector (23) is a photodiode. If the splitting is within or below the GHz range, then conventional electronics can be used to detect the beating between the splitted modes. In this way, the readout unit can be made portable and inexpensive. In FIGS. 8, 11 and 12 the pump laser (21), the backward lasing power (31) and the forward lasing power (32) are schematically represented with arrows. In these figures a straight optical waveguide (3) is also shown, separated from the micro ring resonator (2) by a gap (4), but sufficiently near to allow optical coupling.

[0138] Although the embodiment of FIG. 13 operates in an active mode, in other embodiments the sensors (1) work in a passive mode. In a particular embodiment, if operated as a passive device, during the operation of the sensor (1), the resonator (2) can be excited by a laser with a spectral bandwidth that is large enough to include the two split resonances. In this embodiment the readout unit comprises the laser and a photodetector.

[0139] In another particular embodiment of the passive mode, the readout unit comprises a tunable laser along with a photodetector (23) for scanning the resonances of the resonator (2), so that the peak position of the two split resonances can be detected. Even if the embodiments of FIGS. 8, 11 and 12 have been described referring to a micro ring resonator (2), in other embodiments the resonator (2) is embodied as a disk and the above description is also applicable to said disk resonators (2).

[0140] FIG. 14 shows an embodiment of a sensing system (100) according to the invention. The sensing system (100) comprises a sensor (1) and a readout unit (20) configured to receive the sensor (1).

[0141] In this embodiment the sensor (1) is a disposable cartridge configured for the detection of a plurality of N biomarkers related to the indication of cancer, preferably N being 4 or more. The sensor (1) has one resonator (2.1, 2.2, . . . 2.N) per biomarker, that is, a total number of N resonators (2.1, 2.2, . . . 2.N). Each resonator (2.1, 2.2, . . . 2.N) is embodied as a looped optical waveguide shaped as a circular ring (2.1, 2.2, . . . 2.N). The sensor (1) further comprises N substantially straight optical waveguides (3.1, 3.2, . . . 3.N) for optical coupling with the circular rings (2.1, 2.2, . . . 2.N). The resonator rings (2.1, 2.2, . . . 2.N) comprise a grating (not shown in FIG. 14) and are functionalized (6) for the immobilization of analyte receptors for the binding of biomarkers associated to the respective cancer type (one type of biomarker per resonator).

[0142] The number N of resonators in the sensor (1) provides the number of biomarkers that can be analyzed simultaneously, with one sensor (1) and one fluid sample. A higher number of resonators (2.1, 2.2, . . . 2.N) allows more biomarkers to be analyzed simultaneously with one sample, which results in more information and better quality to the user in the form of indication of different cancer classes and/or cancer development stages by different biomarkers with one measurement. Also, it results in an increase in detection probability of a specific cancer class and specific cancer status, by using a higher number of different biomarkers for detecting the same class or specific stage of cancer. On the other side, a higher number of resonators (2.1, 2.2, . . . 2.N) would imply that different antibodies for different biomarkers gather biomarker molecules at different speeds, so in case of a higher number of biomarkers it would be more difficult to arrange the optimum time of contact with the sample, therefore making the system (100) calibration more complex. Therefore, a preferred number of resonators (2.1, 2.2, . . . 2.N) is between 8 and 16.

[0143] The readout unit (20) is the non-disposable part of the sensing system (100). In this embodiment the readout unit (20) contains N optical sources (21.1, 21.2, . . . 21.N) and N optical detectors (23.1, 23.2, . . . 23.N). The optical sources (21.1, 21.2, . . . 21.N) are preferably integrated laser components. In this embodiment the readout unit (20) comprises one optical source (21.1, 21.2, . . . 21.N) per resonator (2.1, 2.2, . . . 2.N). In another embodiment, the readout unit (20) comprises a single laser source (21.1, 21.2, . . . 21.N) and the light is splitted into N number of channels either by a fiber based 1×N splitter or a 1×N splitter integrated on the sensor (1) or on the readout unit (20).

[0144] In this embodiment the sensor (1) is provided with an input port (11) for the entry of a fluid sample into the sensor (1) and a container (12) for collecting the fluid sample after the fluid sample passes through the ring resonators (2.1, 2.2, . . . 2.N). In this embodiment the sensor (1) comprises a plurality of analysis chambers (22.1, 22.2, . . . 22.N) and the resonators (2.1, 2.2, . . . 2.N) are arranged such that each analysis chamber (22.1, 22.2, . . . 22.N) comprises one resonator (2.1, 2.2, . . . 2.N). The sensor (1) has a plurality of openings (19), each opening (19) providing fluid communication between two adjacent analysis chambers (22.1, 22.2, . . . 22.N). The inlet port (11), the analysis chambers (22.1, 22.2, . . . 22.N) and the container (12) are arranged such that after introduction of the fluid sample through the inlet port (11), the fluid sample passes through the analysis chambers (22.1, 22.2, . . . 22.N) until reaching the container (12). The pass of the fluid sample from the inlet port (11) to the container (12) within the sensor (1) can be achieved and/or facilitated by the effect of gravity, by putting the sensor (1) in a position such that the inlet port (11) and the container (12) are substantially placed in a vertical plane, with the inlet port (11) placed at a higher position than the container (12). In an embodiment the openings (19) providing fluid communication between two adjacent analysis chambers (22.1, 22.2, . . . 22.N) have different sizes in order to regulate the exposure time of the fluid sample to the analyte receptors in each analysis chamber (22.1, 22.2, . . . 22.N). However, other means to regulate the exposure time of the fluid sample to the analyte receptors in each analysis chamber (22.1, 22.2, . . . 22.N) may be provided.

[0145] The fluid sample may be of human or animal origin. This includes blood, secretion or emulsions made of solid biologic material and is preferably but not necessarily urine. The optical sources (21.1, 21.2, . . . 21.N) introduce light into each N optical waveguides (3.1, 3.2, . . . 3.N), passing through the resonators (2.1, 2.2, . . . 2.N) and initiating resonance in each resonator (2.1, 2.2, . . . 2.N). The resonators (2.1, 2.2, . . . 2.N) have analyte receptors, specifically antibodies related to the dedicated biomarker, and the presence of the related biomarker causes a shift in optical resonance frequency. N optical waveguides (3.1, 3.2, . . . 3.N) approach N optical detectors (23.1, 23.2, . . . 23.N), in this particular example laser detector diodes. In this embodiment N optical sources (21.1, 21.2, . . . 21.N) and N optical detectors (23.1, 23.2, . . . 23.N), are within the readout unit (20). In other embodiments, the optical sources (21.1, 21.2, . . . 21.N) and/or the optical detectors (23.1, 23.2, . . . 23.N) may be arranged in the sensor (1).

[0146] The optical detectors (23.1, 23.2, . . . 23.N) are able to detect the level and frequency of optical signals. In the case of passive sensors (1), the laser sources (21.1, 21.2, . . . 21.N) are tunable to be able to scan over the resonance. The optical detectors (23.1, 23.2, . . . 23.N) are used to detect the backward lasing light (31). In a preferred embodiment the disposable sensor (1) has mechanical means to be connected to the non-disposable readout unit (20) of the sensing system (100) so that active optical alignment is not necessary. The optical detectors (23.1, 23.2, . . . 23.N) have a specific dynamic range to detect the minimum and maximum of the expected signal spectrum.

[0147] In this embodiment the readout unit (20) contains a signal processing module (24), a communications interface (25) and a supporting electronic unit (26). In this embodiment the readout unit (20) additionally comprises an operation start button (28) and a data processing done indicator (29).

[0148] In this embodiment the signal processing module (24) includes a signal conditioning unit (241), an analog to digital conversion (ADC) unit (242) and a digital processing unit (243). The signal processing module (24) is configured to measure the beatnote variation coming from optical detectors (23.1, 23.2, . . . 23.N).

[0149] The signal conditioning unit (241) contains amplification of the analog signal coming from the optical detectors (23.1, 23.2, . . . 23.N), as well as analog filtering. The purpose of the signal conditioning unit (241) is to provide a noise-free analog signal to be adequately captured by the analog to digital conversion unit (242), such that the complete dynamic range of the signal may be correctly covered with the best possible resolution. Signal conditioning unit (241) may have also analog down conversion functionalities, if the realized beatnote variation is too large to be detected by analog digital conversion electronics.

[0150] For each dedicated resonator (2.1, 2.2, . . . 2.N), the processing results provide information on the beatnote variation, being associated with probability of detection that is further analyzed. For each biomarker, being related to each resonator (2.1, 2.2, . . . 2.N), the sensing system (100) has a predefined mapping structure to perform classification of data obtained from the sensor (1). This means that for each biomarker type the sensing system (100) knows the mapping between beatnote variation, detection probability and information on the biomarker concentration. Therefore, the beatnote variation is monitored over time and correlated with the analyte concentration. In an embodiment the mapping results from a previous calibration of the sensing system and/or of the sensor. In an embodiment the mapping is stored in a memory of the readout unit and/or is remotely stored is a separate device accessible from the readout unit.

[0151] In an embodiment the analyte receptors attached to the resonators (2.1, 2.2, . . . 2.N) are N antibodies configured for the binding of a cancer biomarker, wherein the cancer biomarkers are selected from the following list of biomarkers: [0152] PSA, for prostate cancer [0153] Engrailed 2, for prostate cancer [0154] MSMbeta for prostate cancer [0155] HAS-1, for bladder cancer: [0156] HAS-2, for bladder cancer: [0157] HYAL-3, for bladder cancer: [0158] Cytokeratin 20 (CK20), for bladder cancer: [0159] CAIX, for renal cancer: [0160] Aquaporin1, for renal cancer: [0161] Adipophilin, for renal cancer: [0162] IL8, for bladder cancer [0163] MMP9, for bladder cancer [0164] MMP10, for bladder cancer [0165] SERPINA1, for bladder cancer [0166] VEGFA, for bladder cancer [0167] ANG, for bladder cancer [0168] CA9, for bladder cancer [0169] APOE, for bladder cancer [0170] SDC1, for bladder cancer [0171] SERPINE1, for bladder cancer [0172] HYAL1, for bladder cancer [0173] CXCL 1, for bladder cancer [0174] CXCR7, for bladder cancer [0175] SDF1beta, for bladder cancer

[0176] The information acquired from the sensor (1) is classified and provided, preferably together with biofluid sample and sensor (1) identification, to the supporting electronic unit (26). In this embodiment the supporting electronic unit (26) includes Human Machine Interface (HMI) unit (261), a power supply (262) and a controlling unit (263). In the supporting electronic unit (26) the information may be: [0177] stored on the associated memory, where one of the options can be a removable memory realization like a Secure Digital (SD) card or flash memory; [0178] provided to the communications interface (25); and/or [0179] provided to the HMI unit (261).

[0180] The HMI unit (261) provides interaction with the user by multimedia or mechanical means, including interaction with a display of the non-disposable readout unit (20), displaying one or more of the following results: biomarker detection, probability of dedicated biomarker detection, cancer class probability detection or indication, time information, environment information such as temperature, disposable part identification, apparatus status, such as battery status, apparatus readiness to perform and/or apparatus activity, using any applicable graphical and/or textual means. The HMI unit (261) can also provide information by electrically generated sound, such as information on sensing system (100) status information and/or on activity results, by using a loudspeaker being part of the readout unit (20). Thus, warnings or status indications like “data analysis process started”, “data analysis process completed”, “battery low” or “ready to perform”, are addressed. Also, mechanical vibrations could be performed as status warnings or status indications like “data analysis process started”, “data analysis process completed”, “battery low” or “ready to perform”.

[0181] The controlling unit (263) may be implemented as micro-controller software code or may be integrated as extra software code of the processor unit (24) performing digital signal processing (243), which preferably is a CPU, like an ARM class microprocessor. Alternatively, the controlling unit (263) may be implemented as a unit separate from the digital signal processing unit (243). The controlling unit (263) takes part in the status of sensing system (100), including environment and power status control as well as control of the sensing system's (100) functional blocks. It also interacts with the HMI unit (261). The controlling unit (263) provides information on the presence of disposable sensor (1) inserted in non-disposable readout unit (20), information on the type of disposable sensor (1), as well as on the operation of start button (28) and data processing done indicator (29).

[0182] Operation start button (28) is advantageously realized by soft pressure system button technology which allows for good water-proof realization. Operation start button (28) is advantageously realized with an optical indicator system showing in one color the “status done” signal, in another color the “ready for sensor acquisition” signal, and in a third color the “no cartridge attached” signal.

[0183] In this embodiment the communications interface (25) comprises a wireless connection interface (251) and a wired connection interface (252). This allows communication from the readout unit (20) to the world outside of the sensing system (100). In a preferred embodiment, the wired connection interface (252) has one or more of the following wired communication means: USB connector, Ethernet connection, CAN based cable connection, LIN Based connector cable connection, SPI wired connection, UART wired connection. The wired connection interface (252) can enable communication to the cloud or to a remote memory on user PC or user network. The wireless connection interface (251) may be realized by a plurality of short range and log range wireless means, including: 2G, 3G, LTE mobile communication interface and/or other long range, cellular, communication methods; wireless LAN, Bluetooth, short range communication methods in ISM bands.

[0184] The readout unit (20) may include a memory for the storage of information, such as a cartridge reference number and/or findings of the executed data acquisition and data processing procedures when the sample is analyzed. This may allow for better tracking and system (100) optimization. Also, the readout unit (20) may include a detector, preferably based on RFID technology, for the detection of an identifier (16), preferably a passive RF ID tag, located on the sensor (1).

[0185] FIG. 15 shows a flowchart showing the method of operation of the sensing system (100) according to an embodiment of the invention, the method comprising the following steps from the user perspective: [0186] Inserting (1010) the sensor (1) in the readout unit (20) of the sensing system (100). [0187] Putting (1020) a fluid sample in the input port (11) of the sensor (1). [0188] Initiating (1030) the electronics of the readout unit (20), together with the optical sources (21) and optical detectors (23) by pressing operation start button (28). [0189] Allowing the biomarker detection to be performed until a visual indication of completed processing is shown (1040) by the data processing done indicator (29) of the readout unit (20). [0190] Acquiring (1050) from the HMI unit (261) the analysis results, specifically indication of cancer biomarkers presence or absence in the fluid sample, the presence indication being preferably accompanied with a probability indication. [0191] Optionally, the analysis results and/or details of cancer biomarker signal processing data are made available on an external device like a computer, portable computer, tablet, mobile phone and/or data cloud, the data being transmitted (1060) from the readout unit (20) through the communications interface (25), via wireless (251) and/or wired (252) means. The concentration of biomarkers will be determined from the calibrated sensor (1). [0192] The user removes (1070) the sensor (1) from the readout unit (20), optionally disposing the remaining fluid sample through an output of the container (12). The sensor (1) may also be disposed and/or recycled.

[0193] Optionally, initial operation settings can be obtained (1001) from an external system, such as a data cloud, a computer or a mobile platform, or can be inserted (1002) using the HMI entity (261).

[0194] With reference to FIG. 16, the method of operation of the sensing system (100) according to an embodiment of the invention comprises the following steps from the functional perspective: [0195] The optical sources (21.1, 21.2, . . . 21.N) generate (2010) optical signal emissions with a dedicated wavelength. The optical sources (21.1, 21.2, . . . 21.N) are preferably lasers. [0196] Fluid sample, influenced by gravity, passes (2020) from the inlet port (11) to the first chamber (22.1), where the first resonator (2.1) is present, and subsequently passes through the other chambers (22.2, . . . 22.N) until ending in the container (12). [0197] The optical waveguides (3.1, 3.2, . . . 3.N) are coupled with the resonators (2.1, 2.2, . . . 2.N), inducing the resonance processes (2030). The resonators (2.1, 2.2, . . . 2.N) have antibodies related to the dedicated biomarker, the antibodies being immobilized on the resonators (2.1, 2.2, . . . 2.N) surface. [0198] The resonators (2.1, 2.2, . . . 2.N) interact with the fluid sample entered into the sensor (1). If the fluid sample contains biomarker molecules matching antibodies immobilized on the resonator (2.1, 2.2, . . . 2.N), the biomarker molecules will attach selectively to the part of the resonator (2.1, 2.2, . . . 2.N) where the antibodies are immobilized, inducing (2040) a variation of the beatnote that is proportional to the concentration of biomarkers in the fluid sample. [0199] The optical detectors (23.1, 23.2, . . . 23.N) detect (2050) the beatnote variation and provide analog signal information. [0200] The signal processing module (24) performs (2060) sequential analog signal conditioning, analog to digital signal conversion and digital signal processing to detect for each resonator (2.1, 2.2, . . . 2.N) the existence of beatnote variation and the value of the beatnote variation. [0201] HMI unit (261) shows (2070) the analysis results. [0202] Optionally, the communications interface (25) sends (2080) the analysis results and/or details of cancer biomarker signal processing data to an external device like a computer, portable computer, tablet, mobile phone and/or data cloud, the data being transmitted (2080) from the readout unit (20) through the communications interface (25), via wireless (251) and/or wired (252) means.

[0203] In summary, the following two cases can be obtained: [0204] The optical signal passing by the resonators (2.1, 2.2, . . . 2.N) will have no change of beatnote, if fluid sample does not contain dedicated biomarkers. [0205] In contrast, if the beatnote change is observed, a dedicated biomarker is detected in fluid sample. Evaluating the value of beatnote variation by applying dedicated calibration processing algorithms, combined with duration of fluid sample interchange with the resonators (2.1, 2.2, . . . 2.N) will lead to information of relevant biomarker molecule concentration in fluid sample. This biomarker molecule concentration information in fluid sample, indirectly yields information about the probability of relevant cancer detection.

[0206] FIG. 17 shows an embodiment of the sensor wherein the resonator (2) is shaped as a non-circular loop. Also, a non-straight optical waveguide (3) for coupling with the resonator (2) is shown. The resonator (2) and the waveguide (3) can be designed with different sections, what provides the design process with more flexibility. This is, the shape of the resonator (2) permits engineering of the sensitivity and tolerance for manufacturability errors as well as to tailor the coupling of both pump and signal independently, and to tune the length of the resonator (2), everything without affecting the coupling region. Different sections of the resonator (2) and the waveguide (3) are identified in FIG. 17 with dash lines.