6 February 2017 Enzyme-functionalized thin-cladding long-period fiber grating in transition mode at dispersion turning point for sugar-level and glucose detection
Author Affiliations +
Abstract
Enzyme-functionalized dual-peak long-period fiber grating (LPFG) inscribed in 80 - μ m -cladding B/Ge codoped single-mode fiber is presented for sugar-level and specific glucose detection. Before enzyme functionalization, the dual-peak LPFG was employed for refractive index sensing and sugar-level detection and high sensitivities of 4298.20    nm / RIU and 4.6696    nm / % were obtained, respectively. Glucose detection probe was attained by surface functionalization of the dual-peak LPFG via covalent binding with aminopropyl triethoxysilane used as a binding site. Optical micrographs confirmed the presence of enzyme. The surface-functionalized dual-peak LPFG was tested with D-(+)-glucose solution of different concentrations. While the peak 2 at the longer wavelength was suitable only to measure lower glucose concentration (0.1 to 1.6    mg / ml ) recording a high sensitivity of 12.21 ± 0.19    nm / ( mg / ml ) , the peak 1 at the shorter wavelength was able to measure a wider range of glucose concentrations (0.1 to 3.2    mg / ml ) exhibiting a maximum resonance wavelength shift of 7.12 ± 0.12    nm / mg / ml . The enzyme-functionalized dual-peak LPFG has the advantage of direct inscription of highly sensitive grating structures in thin-cladding fibre without etching, and most significantly, its sensitivity improvement of approximately one order of magnitude higher than previously reported LPFG and excessively tilted fibre grating (Ex-TFG) for glucose detection.
Badmos, Sun, Sun, Zhang, Yan, Lutsyk, Rozhin, and Zhang: Enzyme-functionalized thin-cladding long-period fiber grating in transition mode at dispersion turning point for sugar-level and glucose detection

1.

Introduction

Glucose, being the pivotal nutriment for human brain, muscles, and other body parts, essentially requires monitoring for any level imbalance to prevent malfunction and ensure healthy brain performance. Recent research findings have reported optical fiber-based biosensors with targeted applications in food safety,1 medical diagnosis,2,3 and environmental monitoring.45.6 Long-period fiber grating (LPFG) having the fundamental core mode coupled to the forward propagating cladding modes enables interaction between the propagating light and the ambient medium. This attribute allows LPFG to be utilized as a biosensor for direct probing of surrounding medium.

LPFG sensors have been reported to produce high-sensitivity resonant wavelength shift with the variation in refractive index (RI) of ambient medium, thereby offering label-free detection. Prominent citations on applications of LPFG-based biosensors include: antibody–antigen detection,7 chemical sensing,8 pH sensing,9 glucose detection,10 DNA,11,12 bacterial detection, and other medical diagnostic applications.13,14 Functionalizing the LPFG surface with molecular recognition elements such as enzymes, nucleic acids (DNA), antibodies, and antigens involves several bioreceptor immobilization methods which include covalent bonding,15,16 ionic bonding,17,18 absorption,19 avidin–biotin interaction, and cross-linking through a multifunctional reagent.20,21 While covalent bonding has been considered most effective of all the methods because it allows the active sites to remain chemically reactive and unobstructed, enzymes have also been considered usefully utilized as molecular recognition elements.

Dispersion turning point associated with dual-peak LPFG determines the condition of maximum sensitivity of cladding modes and occurs at longer wavelengths for lower order cladding modes with a shift to the shorter wavelength as the mode order increases.22 The high sensitivity exhibited by the dual-peak LPFG structure especially made in thin-cladding (80-μm diameter) fiber has prompted us to functionalize the dual-peak LPFG with enzyme for immunosensing of glucose. This serves as an alternative detection device to the prevalent electrochemical methods of glucose analysis. Here, we present an enzyme-functionalized, aqueous-dispersed, and actively targeted dual-peak LPFG with dispersion turning point in the near-infrared (NIR) region as a highly specific probe for sugar-level and glucose detection.

In previous reports, unmodified LPFGs have been used for nonselective analysis of very high-concentrated glucose solutions (300  mg/ml),23,24 but it offered insignificant changes in the RI and consequently no resonant wavelength shift. However, covalent immobilization methodology (conversion of glucose to gluconic acid) has been investigated for selective analysis of low-concentrated glucose solutions (0.1 to 3.0  mg/ml)10 and significant changes in the RI were obtained. This selective method was used in our research to show the correlation of the resonant wavelength shift of a dual-peak LPFG in a thin-cladding fiber to a range of D-(+)-glucose concentrations.

2.

Materials and Methods

2.1.

LPFG Inscription and Spectral Characteristics

The prevalent point-by-point inscription method was used to fabricate dual-peak LPFGs of 300-μm period on single-mode thin-cladding boron–germanium-doped fiber (80-μm B/Ge CA3596/877F/C—Nortel). An ultraviolet (UV) light source from a frequency-doubled argon (Ar+) laser at 244 nm (Sabre Fred, Coherent) was used for the LPFG inscription. The grating fabrication parameters include a period of 300  μm, grating length of 12 mm, scanning speed of 0.2  mm/s, and laser power of 145 mW. UV radiation propagating through the fiber core causes index modulation according to the phase matching condition:25

(1)

β01βcladdingm=2πΛ,m=2,3,4,5,,
where β01 and βcladdingm are the propagation constants of the fundamental core mode and the m’th-order copropagating cladding mode, respectively, and Λ is the grating period. As a result of the parabolic characteristic of group index of higher-order cladding modes, a dispersion turning point was observed on the LPFG phase curve as |dλres/dΛ|. For a given radius, the phase matching condition is met concurrently with one cladding mode in the positive dispersion region and the other in the negative dispersion region, thereby generating dual-peak resonances.22 We have theoretically simulated the cladding mode curves of the 80-μm-diameter cladding fiber with 4.8-μm core size for LPFGs with different periods and the results are plotted in Fig. 1(a). Due to the reduction in the fiber cladding diameter (80  μm), the dispersion turning point has shifted to a lower order cladding mode curve region as compared with the normal 125-μm-cladding fiber. As per our calculation result shown in Fig. 1(a), the turning point for an LPFG with 300-μm period in 80-μm thin-cladding fiber is associated with the cladding mode HE1,4.

Fig. 1

(a) The simulated cladding mode curves of LPFGs of different periods in 80-μm-diameter cladding fiber with 4.8-μm core size and (b) measured transmission spectrum of 80-μm-cladding LPFG showing dual peak in NIR region.

JBO_22_2_027003_f001.png

According to the mode curves shown in Fig. 1(a), we see the paired attenuation bands of the dual-peak LPFG with a 300-μm period in an 80-μm-cladding fiber would appear at the HE1,6 with wavelengths of 1520 and 1740 nm. The real-time transmission spectrum evolution of the dual-peak LPFG with a 300-μm grating period monitored on an optical spectrum analyzer (OSA AQ6375B-YOKOGAWA) as shown in Fig. 1(b) exhibits a dual-peak feature with the first of the dual attenuation peaks appearing at 1567.53  nm termed “peak 1” while the other peak at the longer wavelength, 1787.16  nm, is termed “peak 2.” Both resonance wavelengths are broadly in agreement with the simulated wavelengths of the dual peaks. These dual attenuation peaks are generated from the light coupling from the core mode to high-sensitivity HE1,6 (dual peak) cladding mode, thereby interacting with the surrounding medium more responsively via evanescent fields. External perturbation effect on the evanescent fields induces changes in the effective index of the cladding mode, thus causing optically measurable wavelength shifts of the LPFG dual peaks according to the following equation:26

(2)

λm,res=[neff,core01(λm,n1,n2)neff,clad0  m(λm,n1,n3)]Λ,
where λm,res is the resonant wavelength due to coupling between fundamental core mode and the m’th cladding mode, neff,core01 and neff,clad0  m are the effective indices of the fundamental core mode and the cladding mode, respectively, while the RIs of the core, cladding, and ambient medium are denoted by n1, n2, and n3, respectively. It is clear from this mechanism that LPFGs are capable of detecting changes when a target bioanalyte interacts with a recognition element on their surfaces.12,27 In the evaluation, the response of the dual-peak LPFG to external perturbations was carried out: first, by characterizing the temperature sensitivity (20°C to 80°C); then, by exposure to wide range of surrounding RI gels (1.305 to 1.444 RIU); sugar solutions of different concentrations (0% to 60%), and finally, different glucose concentrations (0.0 to 3.2  mg/ml) after the surface has been enzyme functionalized.

2.2.

Enzyme Functionalization of LPFG Surface

The entire sample solutions were prepared by analytical-grade reagents and deionized water. All reagents used were purchased from Sigma Aldrich: sodium acetate (SA) buffer (form: liquid; S7899); D-(+)-glucose (form: powder; G7021); (3-aminopropyl) triethoxysilane (APTES) (form: liquid; A3648); and glucose oxidase (from Aspergillus niger) (form: buffered aqueous solution; G0543). The LPFG enzyme functionalization started with the cleaning process [Fig. 2(a)]. Here, the fiber was absolutely immersed in HNO3 solution (5%  v/v; 2  h; 40°C) with a view to removing all contaminations, then washed thoroughly with deionized water and ethanol intermittently. Thereafter, the contamination-free fiber was immersed in H2SO4 solution (95%v/v in H2O2; 1  h; room temperature) to activate the hydroxyl groups (OH) on the fiber surface. The fiber was left to dry under an incandescent lamp (40 W; 240 V; 24  h; 40°C).

Fig. 2

Enzyme functionalization of LPFG surface: (a) cleaning process, (b) silanization process, and (c) glucose oxidase immobilization.

JBO_22_2_027003_f002.png

Afterward, it was submerged in (3-aminopropyl) triethoxysilane (APTES/ethanoic solution, 10%  v/v) which incubates the OH-activated fiber in the silanization process for 30 min at room temperature in order to covalently link the NH3+ groups of the APTES molecules to the OH group on the fiber surface [Fig. 2(b)]. Note, the NH3+ group of the APTES molecules has been reportedly used to absorb biomolecules with negative charges like glucose oxidase and Escherichia coli bacteria.10,13 Then it was rinsed with deionized water and ethanol to remove noncovalently absorbed silane compounds.

Finally, glucose oxidase was immobilized on the NH2 functionalized dual-peak LPFG surface [Fig. 2(c)] by immersion in 5  mg/ml buffered solution (SA) of glucose oxidase for 2  h. During the incubation, glucose oxidase COOH groups bonded with the NH3+ groups of the APTES molecules through covalent interaction. The enzyme-functionalized surface was later rinsed with SA buffer and left to dry in air. Each stage of the enzyme functionalization processes was examined under optical microscope (Zeiss Axioskop 2 mot plus upright Microscope) and the micrograph images taken are shown in Fig. 3.

Fig. 3

Optical microscopic images of (a) cleaned optical fiber, (b) silanized optical fiber, (c) enzyme-functionalized optical fiber observed under transmitted light, and (d) enzyme’s (fluorescent) presence on optical fiber surface.

JBO_22_2_027003_f003.png

The optical microscope transmission path (100 W halogen—HAL 100) was used to observe the cleaned fiber, APTES-treated fiber, and glucose oxidase immobilized fiber [Figs. 3(a)3(c)]. Optical recognition of the presence of glucose oxidase was as a result of its fluorescence property when observed under optical fluorescent microscopy (100×; ex. 479 nm; light source: 200-W metal halide arc lamp; 110 to 250 VAC; 2 A; 50 to 60 Hz; 5°C to 30°C—Lumen 200PRO) [Fig. 3(d)]. For better controlled measurement, the APTES-treated fiber was first observed under the fluorescent microscopy but no fluorescence property was detected; therefore, the fluorescence property is attributed only to the presence of glucose oxidase molecules. From the optical microscopic images obtained in Fig. 3, with each micrograph depicting each functionalization stage, it is evident that the surface of the fiber has been uniformly functionalized with the protocol used for the silanization and enzyme immobilization.

2.3.

Experimental Setup for Glucose Detection

Figure 4 shows the experimental setup for the surrounding medium RI (SRI) sensing. The dual-peak LPFG fiber was mounted at each end on two three-dimensional translation stages (Thorlabs) with the grating region centralized above a test solution platform that was fixed to a micrometer stage (1 in., 25 mm, Thorlabs) that is capable of vertical movement in either direction. Clean glass slides were placed intermittently on the platform as each solution of different RIs was applied. One end of the fiber was connected to a supercontinuum light source (950 nm—mid-IR; Fianium) and the other end to the input port of the OSA. When light was transmitted through the fiber while the grating region was exposed in air, spectral measurement was taken on the OSA and recorded as reference. Subsequent submergence of the fiber in different solutions caused wavelength shift with respect to the reference as observed on the OSA and all transmission spectra were recorded.

Fig. 4

Experimental setup of enzyme-functionalized LPFG biosensor for glucose detection.

JBO_22_2_027003_f004.png

The experimental setup for sensing all the test solutions (index gel, sugar solution, and glucose solution) is the same as Fig. 4 while that of the temperature measurement is a mere replacement of the micrometer stage by a Peltier connected to a temperature controller (ILX Lightwave). For the thermal measurement, supercontinuum light was transmitted through the fiber while the dual-peak LPFG is mounted on the Peltier. The temperature range of 20°C to 80°C in steps of 10°C was applied to the dual-peak LPFG and the transmission spectral response was measured using the OSA.

3.

Results and Discussion

3.1.

Response to External Perturbations

In order to optimize the performance of a biosensor, it is important to know all the constraints imposed by the sensing components. The dual-peak LPFG sensitivity to temperature was carried out to ascertain the level of cross-sensitivity of this sensor, which has been a major drawback for all LPFG sensors. Figure 5(a) plots the wavelength shift of the dual-peak LPFG in thin-cladding fiber against variation in temperature (20°C to 80°C). As shown clearly in the figure, the dual peaks exhibit opposite movement with increasing temperature, which testifies the dual-peak feature as the coupled two cladding modes of the same order are situated very close to but on the opposite sites of the dispersion turning point. From the plots, we calculate the temperature sensitivities of the dual peaks: 867.39±17.07  pm/°C and 676.03±26.95  pm/°C for peaks 1 and 2, respectively. In comparison with normal LPFGs, the typical temperature sensitivity of this dual-peak LPFG is relatively higher, which will impose a cross-sensitivity issue and must be taken into the consideration if the sensor is operated in an environment with fluctuation of thermal condition. Therefore, as the results of the temperature sensing measurement have shown that the dual-peak LPFG is prone to cross-sensitivity, the experiments for both sugar-level and glucose detection were strictly carried out under constant room temperature (21±1°C).

Fig. 5

(a) Plots of resonant wavelength variation against temperature; and (b) plots of resonant wavelength shift against surrounding medium RI variation of the 300-μm-period dual-peak LPFG in thin-cladding fiber.

JBO_22_2_027003_f005.png

However, there are situations in which several external perturbations coexist and the optical responses of LPFGs are generally a convolution of all these influences. Hence, to compensate for cross-sensitivity, an alternative is to either combine the LPFG structure with another grating structure (such as FBG) so as to facilitate simultaneous measurement of multiple parameters26 or modify the LPFG structure in order to be temperature insensitive such as LPFG in photonic crystal fiber28 or LPFG with rotary grooves carved by high-frequency CO2-laser pulses.29

According to Eq. (2), the LPFG resonant wavelength depends on the effective index of the cladding mode, which in turn is dependent on the RI of the surrounding medium. Therefore, as the surrounding medium RI increases there is a corresponding shift in the resonant wavelength. The dual-peak LPFG was then first investigated as an RI sensor at a constant room temperature of 21°C. To evaluate the RI sensitivity of the dual-peak LPFG, a series of index gels, 1.305 to 1.444 (Cargile), were employed to probe the response of the dual-peak LPFG to SRI variation. High SRI sensitivities were obtained, as shown in Fig. 5(b): peak 1 and peak 2 recorded sensitivities of 425.29 and 882.38  nm/RIU in the RI range of 1.305 to 1.404 and 1991.10 and 4298.20  nm/RIU in the RI range of 1.412 to 1.444. It is interesting to note that both peaks show higher RI sensitivity in the second RI range, but the RI sensitivity of peak 2 is almost twice of that of peak 1. This is a maximum recorded total-peak separation of 460  nm which is 23% improvement compared to 374  nm earlier reported for light cladding-etched dual-peak LPFG.30 Although, an RI sensitivity of 8734  nm/RIU,31 which is much higher than ours, has been achieved on a thin-cladding dual-peak LPFG, the grating fiber was etched off from original 80  μm to only 35  μm, undoubtedly reducing the mechanical strength of the grating and increasing its fragility, thus limiting its applicability.

Raw sugar (turbinado sugar) has been known to contain several useful nutrients (100 g of turbinado sugar contains—100 mg potassium, 85 mg calcium, 23 mg magnesium, 3.9 mg phosphorous, and 1.3 mg iron) and less calories, and therefore is healthier than white sugar.32 Solutions of different concentrations (0% to 60%) were made with the turbinado sugar and deionized water for sugar-level sensing using the same dual-peak LPFG at room temperature. Figure 6(a) shows the real-time shifting of the dual peaks in opposite directions with peak 1 shifting toward the shorter wavelength (blueshifting) while peak 2 drifts toward the longer wavelength (redshifting) as the concentration of the sugar solution increases. Both peaks recorded relatively high sensitivities to sugar-level detection with peak 1 showing a negative correlation coefficient of 0.8550 and 2.4642  nm/% for the sugar concentration levels of 0% to 30% and 30% to 60%, respectively, while peak 2 shows stronger positive correlation coefficients of 1.4592 and 4.6696  nm/% for the same two ranges [Fig. 6(b)]. From Fig. 6, it can be observed that peak 1 blueshifts by 100  nm while peak 2 redshifts by 200  nm for the entire sugar concentration (0% to 60%) which are significantly higher than 19.8  nm peak redshift reported for concentration of hemoglobin in sugar solution30 as the sensitivity of our thin-cladding dual-peak LPFG has achieved over one order of magnitude improvement.

Fig. 6

(a) Transmission spectral evolution of 80-μm-cladding dual-peak LPFG to varying concentrations of turbinado sugar solution; and (b) plot of resonant wavelength shift of peak 1 and peak 2 against sugar solution.

JBO_22_2_027003_f006.png

Since sucrose is sugar found naturally in fruits, vegetables, and sugar cane, monitoring of sugar level in industrial aqueous solutions can utilize this sensor for broader applications. The inclusion of the RI sensing and raw sugar solution detection experiments are specifically used to show the versatility of this sensor as not only being restricted to biosensing but also could find applications in food processing and environmental monitoring.

3.2.

Glucose Detection with Enzyme Functionalized Dual-Peak LPFG

The enzyme functionalization of the dual-peak LPFG made it a biosensor for biomolecule detection. The specific enzyme (glucose oxidase) immobilized on the surface of the LPFG enables interaction with the surrounding glucose solution. Different concentrations of D-(+)-glucose was prepared in SA buffer (pH 5.2), which is a suitable reagent for this catalytic reaction. Equation (3) expresses the interaction of the glucose solution with glucose oxidase showing the conversion of D-(+)-glucose to gluconic acid with concurrent release of hydrogen peroxide [1 unit of glucose oxidase (200 units/mg) oxidizes 1.0  μm of D-(+)-glucose to D-gluconic acid and H2O2 per minute at pH5.1, 35°C].

(3)

D-(+)-Glucose+O2+H2OGlucose oxidaseD-Gluconicacid+H2O2.

This interaction causes change in the RI of the ambient medium and thus induces resonant wavelength shift in the transmission spectrum as observed on the OSA. After applying each glucose solution, deionized water was used to rinse the solution off the fiber surface to restore resonant peak back to the reference point and make ready for the next measurement of subsequent solutions. An average interaction time of 60  s was observed for each test solution (glucose solution). It was also observed that after enzyme functionalization of the LPFG surface, the dual-peak shifted around 15  nm from the initial position in air. Peak 1 was observed at around 1565  nm and peak 2 around 1802  nm as against initial positions. Figure 7(a) shows the transmission spectral evolution of peak 1 of the dual-peak LPFG in glucose solutions of different concentrations, showing the resonant peak drifting away from the initial reference position toward the shorter wavelength.

Fig. 7

(a) Transmission spectral evolution of peak 1 (of the dual-peak LPFG) to varying concentrations of SA buffer/D-(+)-glucose solution at different concentrations [inset: glucose solution (0.1 to 3.2  mg/ml)] and (b) plots of resonant wavelength shift of the dual-peak LPFG against glucose concentration (inset: regular residual of peak 2).

JBO_22_2_027003_f007.png

The test solutions (SA buffer/glucose) cover the glucose concentration range 0.1 to 3.2  mg/ml [Fig. 7(a), inset]. The obtained transmission spectra (peak 1) shows ~30  nm blueshift with respect to the varying glucose solutions. However, as peak 2 redshifted, the concentration range was limited to lower values of between 0.1 and 1.6  mg/ml to be measured as the longest wavelength the light source can emit at around 2  μm. As shown in Fig. 7(b), for the glucose concentration range 0.1 to 3.2  mg/ml, peak 1 has exhibited a linear response with a sensitivity of 7.115±0.119  nm/(mg/ml), while for the lower glucose concentration range 0.1 to 1.6  mg/ml, peak 2 recorded a higher sensitivity of 12.211±0.189  nm/(mg/ml). From the results, we observe that the enzyme-functionalized dual-peak LPFG gives a linear response in the glucose concentration range (0.1 to 3.2  mg/ml). In comparison with the previous reports, the sensitivity 7.115  nm/(mg/ml) for peak 1 is approximately one order of magnitude higher than 0.806  nm/(mg/ml) reported for normal LPFG10 and 0.298  nm/(mg/ml) reported for 81°-TFG33 in similar glucose concentration range (0.1 to 3.2  mg/ml).

In order to ascertain the RI cross-sensitivity in the glucose detection, an experiment was carried out using the bare dual-peak LPFG (without surface functionalization with glucose oxidase) in the same glucose concentration range (0.1 to 3.2  mg/ml). The result shows that peak 1 recorded a sensitivity of 0.595  nm/(mg/ml) that is 8.36% of the initial sensitivity of 7.115  nm/(mg/ml) when the dual-peak LPFG was surface-functionalized with glucose oxidase. Therefore, the chemical interaction on the fiber surface between the glucose oxidase and the SA buffer/glucose solutions contributed the remaining 91.64% of the wavelength shift. In other words, the effect of RI cross-sensitivity to the glucose detection is 0.08. The significantly improved sensitivity in comparison with earlier reports in Refs. 10 and 33 coupled with inherent high mechanical strength make this dual-peak LPFG sensor a viable and applicable alternative for supporting the instantaneous detection of the glucose concentration. Note, to ensure reproducibility of the result, the experiment was repeated three times with the glucose oxidase replenished for each repeated experiment, and the whole procedure shown in Fig. 2 was reiterated. The repeatability standard deviation of the experimental data was calculated to be 0.02.

4.

Conclusion

In summary, enzyme-functionalized dual-peak LPFG inscribed in B/Ge codoped 80-μm-cladding single-mode fiber has been demonstrated and investigated for sugar-level and glucose concentration detection. Before the enzyme functionalization, the dual-peak LPFG has been investigated for RI sensing and a sensitivity of 4298.20  nm/RIU has been achieved, which is a significant 23% improvement in total-peak separation as against an earlier report on light cladding-etched dual-peak LPFG. Also, sugar solution has been investigated for level concentration range 0% to 60%, and a significant peak-wavelength shift of 200  nm has been achieved for the entire concentration range which is remarkably higher than 19.8  nm peak-wavelength shift earlier reported for concentration of hemoglobin in sugar solution. After the enzyme functionalization of the fiber surface, the dual-peak LPFG has been investigated for glucose concentration detection. The glucose detection has shown markedly high sensitivities of 12.211±0.189  nm/(mg/ml) (0.1 to 1.6  mg/ml) for peak 2 and 7.115±0.119  nm/(mg/ml) (0.1 to 3.2  mg/ml) for peak 1 which is one order of magnitude higher than earlier glucose detection results reported for normal LPFG and 81°-TFG. This dual-peak LPFG sensor, as a useful alternative, may find applications in food safety, medical diagnosis, and environmental monitoring.

Disclosures

We declare that there is no conflict of interest regarding this manuscript.

Acknowledgments

This work was supported by the Marie Curie International Incoming Fellowships (FP7-PEOPLE-2013-IIF, Grant Nos. 623473 and 913473). P.L. acknowledges support of EU FP ‘Horizon-2020’ Marie Skłodowska-Curie Individual Fellowship (FOC4SIP, #654733).

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Biography

Abdulyezir A. Badmos received his BSc and MSc degrees in electrical/electronic engineering from the University of Lagos, Nigeria, in 2005 and 2008, respectively. He joined Aston Institute of Photonics Technologies, Aston University, Birmingham, UK, in April 2014 as a research student. His PhD research area includes optical fiber grating fabrication and nanocharacterization of in-fiber grating for biosensing applications. His research topic centers on “Advance optical fiber gratings for nanostructural characterization and biosensing applications.” He is a member of SPIE.

Biographies for the other authors are not available.

© The Authors. Published by SPIE under a Creative Commons Attribution 3.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
Abdulyezir A. Badmos, Abdulyezir A. Badmos, Qizhen Sun, Qizhen Sun, Zhongyuan Sun, Zhongyuan Sun, Junxi Zhang, Junxi Zhang, Zhijun Yan, Zhijun Yan, Petro Lutsyk, Petro Lutsyk, Alex Rozhin, Alex Rozhin, Lin Zhang, Lin Zhang, } "Enzyme-functionalized thin-cladding long-period fiber grating in transition mode at dispersion turning point for sugar-level and glucose detection," Journal of Biomedical Optics 22(2), 027003 (6 February 2017). https://doi.org/10.1117/1.JBO.22.2.027003 . Submission: Received: 13 October 2016; Accepted: 10 January 2017
Received: 13 October 2016; Accepted: 10 January 2017; Published: 6 February 2017
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