Next Article in Journal
Uncertainly Analysis of Two Types of Humidity Sensors by a Humidity Generator with a Divided-Flow System
Next Article in Special Issue
Miniaturized Bio-and Chemical-Sensors for Point-of-Care Monitoring of Chronic Kidney Diseases
Previous Article in Journal
mIoT Slice for 5G Systems: Design and Performance Evaluation
Previous Article in Special Issue
Three-Dimensional Blood Vessel Model with Temperature-Indicating Function for Evaluation of Thermal Damage during Surgery
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Split-Ring Resonator Sensor Penetration Depth Assessment Using In Vivo Microwave Reflectivity and Ultrasound Measurements for Lower Extremity Trauma Rehabilitation

1
Microwaves in Medical Engineering Group, Solid State Electronics, Department of Engineering Sciences, Angstrom Laboratory, Uppsala University, Box 534, SE 75121 Uppsala, Sweden
2
Department of Electronics and Communication, Amrita School of Engineering, Amrita Vishwa Vidyapeetham, Bengaluru , 560035, India
3
Department of surgery, Maastricht University Medical Center, PO Box 5800 6202 AZ Maastricht, The Netherlands
*
Authors to whom correspondence should be addressed.
Sensors 2018, 18(2), 636; https://doi.org/10.3390/s18020636
Submission received: 12 January 2018 / Revised: 14 February 2018 / Accepted: 19 February 2018 / Published: 21 February 2018
(This article belongs to the Special Issue Non-Invasive Biomedical Sensors)

Abstract

:
In recent research, microwave sensors have been used to follow up the recovery of lower extremity trauma patients. This is done mainly by monitoring the changes of dielectric properties of lower limb tissues such as skin, fat, muscle, and bone. As part of the characterization of the microwave sensor, it is crucial to assess the signal penetration in in vivo tissues. This work presents a new approach for investigating the penetration depth of planar microwave sensors based on the Split-Ring Resonator in the in vivo context of the femoral area. This approach is based on the optimization of a 3D simulation model using the platform of CST Microwave Studio and consisting of a sensor of the considered type and a multilayered material representing the femoral area. The geometry of the layered material is built based on information from ultrasound images and includes mainly the thicknesses of skin, fat, and muscle tissues. The optimization target is the measured S11 parameters at the sensor connector and the fitting parameters are the permittivity of each layer of the material. Four positions in the femoral area (two at distal and two at thigh) in four volunteers are considered for the in vivo study. The penetration depths are finally calculated with the help of the electric field distribution in simulations of the optimized model for each one of the 16 considered positions. The numerical results show that positions at the thigh contribute the highest penetration values of up to 17.5 mm. This finding has a high significance in planning in vitro penetration depth measurements and other tests that are going to be performed in the future.

1. Introduction

Penetration depth performance of sensors has been studied for many decades for multipurpose uses [1,2,3,4]. It could decisively affect how electromagnetic (EM) waves are absorbed, transmitted, and reflected in materials, especially in biological tissues. These penetration depth performances are used in dosimetry studies, including microwave technology, and they have brought about many new exciting therapeutic and diagnostic solutions [5,6]. Recent studies show that the association of the microwave technique with biological applications is growing rapidly [7,8,9,10,11,12,13].
For several reasons, hip fractures could be a valuable clinical application of this new technique. Hip fractures are one of the most common health issues among the elderly population nowadays as they cause significant morbidity and are often associated with increased mortality. Moreover, hip fractures lead to decreased mobility, mostly due to loss of muscle mass. Rehabilitation after a hip fracture is guided by clinical and radiological monitoring. For radiological monitoring, the gold standard is the use of X-ray, dual-energy X-ray absorptiometry (DEXA), and computed tomography (CT) images [14,15,16]. However, these techniques all have technical limitations and only provide some insight into the condition of calcified tissues. Clinical monitoring is limited as well, as it is guided by calculating mobility scores and observing gait patterns. Either monitoring method is not suitable to estimate the rehabilitation process, nor to determine the phase of rehabilitation for an individual at a certain time point. This leads to uncertainty for patients and care providers, but also to inefficiency in directing care to the appropriate patient who needs it most. Given the shortcomings of current monitoring techniques, the same rehabilitation regimen is imposed on all patients, instead of providing individualized care for those who need it and only observation and limited guidance for those who do well [17,18].
Therefore, there is an important clinical need to develop an effective, safe, portable, and rapid method for assessing the different healing stages of lower extremity injuries, such as hip fractures. A better understanding of the effective variations of the tissues affected during the rehabilitation of lower extremity fractures could lead to promising devices. Specifically, monitoring muscle tissue reliably may change clinical practice in the future. Our method is based on this observation as the key to answering that social need. Therefore, to understand those tissue variations from the clinical perspective, a comprehensive investigation is necessary and important. These effective variations could be correlated to the different healing stages, as can be seen in [19,20].
In a recent publication by Perez et al. [21], the authors demonstrated clinical measurement using Split-Ring Resonator (SRR) sensors operating at microwave frequency. The sensor has a large influence on the complementary dimension of the ring resonator compared to the T-coupling and ring resonator with the multilayer substrate. However, it gives minimal insight into the resolution with respect to the resonance frequency shift.
This paper presents the measurement and numerical analysis of an SRR sensor operating at the industrial, scientific, and medical radio (ISM) band (2.4–2.5 GHz) for studying the penetration depth in particular layers of multilayered biological tissue in terms of resonance frequency and permittivity variations. We utilize the same measurement configuration but with a range of different points on the femoral area to illustrate that the penetration depth is closely related to the variation of the biological tissue.
This paper is organized as follows. Section 2 describes the outline of material and methods of the sensor selectivity, clinical measurement approach, and numerical modelling procedures. Meanwhile, Section 3 explains in detail the results and discussion on the feature dependence of resonance frequency on position, permittivity analysis, and penetration depth and penetration analysis; this is followed by conclusions in Section 4.

2. Materials and Methods

2.1. Sensor Selection

In this study we used two designs of sensor—Split-Ring Resonator (SRR) and Capacitive Split-Ring Resonator (CSRR)—based on a previous study by Perez et al. [21]. These sensors were used to observe the penetration depth from different parameters such as resonance frequency fr, effective permittivity εeff, and tissue thickness ts. Furthermore, the signal that penetrated through different tissue layers was investigated in terms of its electric field (E-field) to analyze the signal penetration depth.
The arrangement of the first sensor consists of three multilayer substrates, as shown in Figure 1. In particular, the sensor consists of a subminiature version A (SMA) connector, coaxially fed T-shaped microstrip line fabricated on the bottom substrate layer, having a dielectric permittivity of 4.5 and a height of 0.64 mm. A split ring is fabricated on the intermediate layer, and the electric field from the ring extends to the tissue through the top superstrate layer, which also acts as a coupling medium. The SRR dimensions include the top layer of superstrate with W and L = 25.0 mm; the intermediate layer, with R1= 8.6 mm and R2 = 5.8 mm; and the bottom layer with T1= 9.2 mm, T2 = 4.2 mm, W = 30.0 mm, L = 30.0 mm, and the gap width of split-ring resonator, Gap = 0.8 mm. Rogers TMM4 and TMM6 were used for the substrate and superstrate, respectively.
With this done, to go further into sensor optimization, we propose other variants of the ring resonator structure: a Capacitively fed Split Single Circular Ring (CSSCR) resonator. The sensor has two layers—a resonator layer and a matching layer. The resonator layer corresponds to the microstrip resonator structure. The matching layer consists basically of a superstrate which acts as a coupling medium to the target to allow more energy to be radiated into the human tissues and to obtain enhanced and stable resonance characteristics while illuminating the targets. These two sensors were then optimized and employed in clinical measurements.

2.2. Clinical Measurement Approach

Data were gathered from four consenting volunteers during the Complex Fracture Orthopedic Rehabilitation (COMFORT) measurement campaign at the Telge Rehabilitation Center, Södertälje, Sweden. The data collection was carried out under ethical approval (2016/698-31/1) from Sweden. Since the region around the femur bone is of particular interest in the case of lower extremity injuries, four different positions on the femoral area were used for data collection, as shown in Figure 2a:
  • Anterior of the distal femur 3 cm above the patella.
  • Lateral (outside) of the distal femur.
  • Anterior of the thigh (10 cm above patella) midlength.
  • Lateral of the thigh midlength, same level as the front thigh.
The SRR sensor was attached to each participant’s hip by using a stretchable strap. The sensor was then aligned to the anterior and lateral hip direction as shown in Figure 2b,c and connected to the network analyzer (MiniVNA Tiny-mRS radio solution). The measurement was performed over an operating frequency from 1 to 3 GHz, which is in the range of the operating frequency of the sensor (2.78 GHz) (without tissue surface contact). During clinical measurement, Positions 1 to 4 (distal femur and thigh) were selected for data collection, and further analysis was required to study the penetration depth.
Data collection was done by following the standard protocol at the rehabilitation center. The participants were requested to undergo control measurement using ultrasound (US) with help from a radiologist. The US images we obtained for this clinical measurement were taken from Positions 1 to 4 and are shown in Supplementary Figures S1–S4. The thickness of individual tissues (skin, fat, and muscle) and their composition were obtained from US images of the distal femur and thigh (anterior/lateral) and are summarized in Table 1.
The anterior and lateral lower extremity was kept immobile during US measurements to reduce artefacts. The data collection was repeated if any change in protocol was detected by the physician. To ensure consistent results, S11 was measured three times for any given position. A numerical model was made and validated using the information extracted from US and S-parameter measurements. This model is described in detail in the following subsection. The thickness of each tissue layer was obtained from the US measurement, and can typically be distinguished by observing the grey scale (contrast) between adjacent areas displayed on the US images.

2.3 Numerical Model

The proposed sensor was numerically simulated using Computer Simulation Technology (CST Studio, 2017, SIMULIA, Darmstadt, Germany) based on US tissue thickness measurements. Figure 3 shows the process of extracting the dielectric properties of different tissues and subsequent derivation of signal penetration depth using S11 data and US images. The thickness of tissue layers was fixed, the target S11 was obtained from measurement, and an initial estimate of dielectric properties was obtained from the literature. Then the dielectric properties were optimized to result in the simulated S11 that matches the target measured S11 obtained from volunteer measurement with a maximum convergence limit of 10%. The S11 data collected from the volunteers were imported into CST in the 1–3 GHz frequency range and were defined as the response of the model. The dielectric parameter of the CST model was optimized for the response thus defined.
The numerical results have given valuable information on the effective permittivity εeff and conductivity σ, expressed in S/m. Specifically, this numerical study demonstrates a characterization of tissue properties over a microwave frequency range 2.4–2.6 GHz. These frequencies overlap with the industrial, scientific, and medical radio (ISM) frequency band, which is free to be used in medical applications. This band was chosen as it covers the frequency range of interest for the sensor and the system. Additionally, this model was developed to estimate the signal penetration depth based on analyzing the E-field distribution in the layered tissue model. In order to characterize the penetration depth in the system, observations were made from the simulated E-field and the results were correlated. The penetration depth offers good information on the stipulated E-field distribution for analyzing sensor performance and at the same time can be used in extensive clinical measurements.

3. Results and Analysis

3.1. Permittivity Analysis

The tissue dielectric data reported in literature [22,23,24,25] (for 1–3 GHz) for skin, fat, and muscle were used as initial tissue properties for training (iteration) of the numerical model (as described in Table 2). The real part of relative permittivity, εr, and conductivity, σ, expressed in S/m were taken into consideration for the dielectric properties of the tissues.
We further investigated the effective permittivity values of tissues by examining each position on a simulated numerical model. In particular, the properties consist of the relative permittivity and conductivity, for which the numerical model was trained. The S11 data measured at the different femoral positions of the volunteer were used as the target data to train the proposed model to obtain an effective permittivity for different volunteer tissues. Among all the tissue layers, the muscle layer has the highest dielectric properties and can detune the sensor resonance more. It can be seen that the variation in dielectric properties ∆εr and ∆σ of Volunteer 1 is 0.2 and 0.06, respectively, compared to the literature data. In particular, for εr, the accuracy is within 0.38%, while for σ, the accuracy is within 3.45%.

3.2. Dependence of Resonance Frequency on Position

In this section, we present the results of S11 data measurements and their analysis. A general trend observed in the experiment is that the tissue thickness and position point influence the resonance frequency of the sensors. In Figure 4a–d, individual measurements from Positions 1 to 4 are presented. For calculations based on the shifted resonance frequency ∆fr, the highest frequency shift was obtained at Position 1, as shown in Figure 4a, for Volunteer 3 with 30.1 MHz. The lowest calculated ∆fr is at Position 4 for Volunteer 4 with 17.1 MHz. From these results, it is evident that the variation of tissue thickness at each position has an impact on the resonance frequency shift.
The influence of material properties can also be observed with respect to resonance frequency, fr, for various measurement setups. The data shows that the resonance frequency may shift downwards from the free-space resonance frequency of the sensor when thicker muscle tissue is present at the concerned position. The resonance frequency may move towards free-space resonance of the sensor when the muscle layer is thinner.
Similarly, for Position 3 of Volunteer 3, the ∆fr was higher, and the corresponding muscle thickness was measured to be 49.7 mm. From all ∆fr observations, it can be seen that the thicker muscle tissue caused a larger shifting of resonance frequency compared to the thinner muscle tissue.

3.3. Penetration Depth Analysis

To intuitively analyze and compare the performances of two sensors, the electric field distribution was studied in this section. We further investigated the penetration depth by examining each position of items of interest. Figure 5a,b show the results of the E-field distribution with respect to tissue thickness. The variation in the E-field distribution across different tissues for Positions 1 and 2 shows the penetration depth of the SRR sensor for the respective positions. In this section, the actual position of E-field was obtained from the Ez axis. The E-field along the Ez axis perpendicular to the sensor plane was considered. The starting point of the Ez axis was taken at the maximum E-field strength which happens to be at the interface of the sensor and skin surface. The distribution of the E-field was observed along the Ez axis through the different tissue layers of the volunteer until the E-field died off. In this case, the penetration depth was obtained from 11.5 to 18 mm. According to the data from tissue thickness based on US measurements, the total E-field covered at least 46.3% of the distance from the skin to the muscle boundary.
The differences in penetration depth at Positions 3 and 4 are plotted in Figure 5c,d. As shown in Figure 5d, the changing trend of penetration depth was similar between all the volunteer measurements. Considering the data of tissue thickness, the penetration depth was found to be higher when a thicker fat layer is present. Thus, it is observed that the thickness of the fat layer had a great impact on the E-field distribution. Since fat tissue has inherently low water content it shows very low frequency dispersion in its dielectric properties. It can be seen in Figure 5a–d that the E-field extends throughout the fat layer (2.5–10 mm on average on the tissue thickness axis) and the E-field intensity increases at the boundary between skin and fat. Therefore, the thickness of the fat tissue has a higher significance on the measured S11 values compared to its dielectric properties. In this scenario, at the operating frequency of 2.45 GHz, Volunteer 4 gives a higher indication of a larger penetration depth, calculated to be 18.5 mm. As mentioned, the penetration depth demonstrates a clear dependence with tissue thickness, especially for the fat layer. The depth was gradually decreased once the E-field arrives at an average fat thickness of 9.2 mm. This is due to the fact that E-field penetrates more in the fat tissues because of its lower conductivity.
On the other hand, considering the fact that the tissue properties are those of a lossy medium [22,23,24], the E-fields are induced in the human body when the human body is exposed to the RF electromagnetic field [26,27,28]. Therefore, as a result, the signal penetration depth for this measurement scenario depends on the thickness of tissue with lower conductivity such as the fat layer. The magnitude of the E-field that enters the fat tissue will not attenuate quickly. The thickness of fat tissue does not impact the proportion of the field that is transmitted into it; only the contrast between the skin and the fat and the thickness of the first layer the field has travelled through (skin) determine the field magnitude that propagates into the fat layer.
Furthermore, the correlation between E-field and distance can be explained by using the relationship of power propagation and its absorption in the fat layer. As the thickness is increased, the power will be more easily transmitted into fat because of its lower loss compared to other tissue layers. Therefore, the E-field extent represents the percentage increase in the E-field magnitude in the fat layer. It is calculated using the following equation:
E Field   Extent = ( ( Max Min ) 1 ) ×   100 %
where Max is the maximum E-field in the fat layer and Min is the minimum E-field at the skin–fat interface.
Moreover, there was lower E-field propagation at Positions 1 and 2 as shown in Figure 6a,b, respectively. Thus, the E-field propagation at Position 2 for Volunteer 1 decreased rapidly due to a small transition in between the fat and muscle boundary.
On the other hand, as shown in Figure 6c,d, the E-field propagation at Positions 3 and 4 was almost the same in the range of a 20.8–21.5% increase in attenuation level. All these scenarios might be explained by [29,30], which is related to the influence of the fat layer as a channel medium for intrabody communication. According to these findings, the signal transmission can be improved with the thickness of the fat and muscle tissues. The signal transmission is analyzed with respect to the length and thickness of the tissue channel.
From one side it is clear that the CSRR sensor shows better penetration characteristics since there is more electric field energy penetrating the different tissue layers, showing an improvement with respect to its predecessor, the SRR structure. From the other side it is possible to see that SRR has a better field distribution in muscle and bone, making it preferable for distal femur positions, while CSRR is preferable for thigh positions because of its higher energy in the fat layer.

4. Conclusions

In this paper, with the participation of four consenting volunteers, S11 measurements were made and tissue thickness information from US images was obtained for the femoral area. Numerical models were created and the effective permittivity of individual tissues was derived. The numerical model was used to simulate the E-field distribution following a penetration depth calculation. It was observed that the resonance frequency has substantial dependence on the specific measurement position on the femoral area. The penetration depth at any given position also depends on the thickness of tissue with lower conductivity, such as the fat layer. As a key result of this study, this proposed method can be used to estimate penetration depth by using sensor S11 measurements and tissue thickness provided from US images. Preliminary results are, therefore, encouraging and suggest the effectiveness of using noninvasive methods to monitor tissue variations, especially during lower extremity fracture rehabilitation.

Supplementary Materials

The following are available online at https://www.mdpi.com/1424-8220/18/2/636/s1, Figure S1: Measured tissue thickness of (a) position 1 (b) position 2 (c) position 3 and (d) position 4 for Volunteer 1 performed using Ultrasound tool. Figure S2: Measured tissue thickness of (a) position 1 (b) position 2 (c) position 3 and (d) position 4 for Volunteer 2 performed using Ultrasound tool. Figure S3: Measured tissue thickness of (a) position 1 (b) position 2 (c) position 3 and (d) position 4 for Volunteer 3 performed using Ultrasound tool. Figure S4: Measured tissue thickness of (a) position 1 (b) position 2 (c) position 3 and (d) position 4 for Volunteer 4 performed using Ultrasound tool.

Acknowledgments

This work was financially supported by Majlis Amanah Rakyat (MARA), VR project grant —Osteodiagnonsis (2017-04644) and EUREKA Eurostars project COMFORT E!9655. The authors also thank Ann Granqvist, Boxplay Alleato, and Martin Österblad, physiotherapists at Telge Rehabilitation center, Södertälje, Sweden, for their valuable help in data collection.

Author Contributions

Syaiful Redzwan performed the clinical measurement approach and numerical model analysis. Jacob Velander did the same for dielectric property measurement. Mauricio David Perez and Robin Augustine wrote the introduction and discussion. Robin Augustine was also involved in the supervision of the project. Syaiful Redzwan did the analysis of the combination on dielectric properties, clinical work, and wrote most of the paper. Noor Badariah was involved in the dielectric property campaign. Parul Mathur and Dhanesh Kurup worked on data collection. Taco Blokhuis provided consultation on the clinical perspective. All authors participated in meetings, discussed the methods and the scope of the paper, and commented on the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Zhang, T.; Zhang, L.; Zhao, S.; Jiang, L.; Chai, L. A Statistic model developed to estimate the penetration depth using passive microwave remote sensing. In Proceedings of the 2012 IEEE International on Geoscience and Remote Sensing Symposium, Munich, Germany, 22–27 July 2012; pp. 666–669. [Google Scholar]
  2. Scorza, A.; Lupi, G.; Sciuto, S.A.; Bini, F.; Marinozzi, F. A novel approach to a phantom-based method for maximum depth of penetration measurement in diagnostic ultrasound: A preliminary study. In Proceedings of the 2015 IEEE International Symposium on Medical Measurements and Application, Turin, Italy, 7–9 May 2015; pp. 369–374. [Google Scholar]
  3. Meaney, P.M.; Gregory, A.P.; Seppala, J.; Lahtinen, T. Open-ended coaxial dielectric probe effective penetrative depth determination. IEEE Trans. Microw. Theory Techn. 2016, 64, 915–923. [Google Scholar] [CrossRef]
  4. Porter, E.; O’Halloran, M. Investigation of Histology Region in Dielectric Measurements of Heterogenous Tissues. IEEE Trans. Antennas Propag. 2017, 65, 5541–5552. [Google Scholar] [CrossRef]
  5. Yilmaz, T.; Foster, R.; Hao, Y. Broadband tissue mimicking phantoms and a patch resonator for evaluating noninvasive monitoring of blood glucose levels. IEEE Trans. Antennas Propag. 2014, 62, 3064–3075. [Google Scholar] [CrossRef]
  6. Choi, H.; Naylon, J.; Luzio, S.; Beutler, J.; Birchall, J.; Martin, C.; Porch, A. Design and in vitro interference test of microwave noninvasive blood glucose monitoring sensor. IEEE Trans. Microw. Theory Techn. 2015, 63, 3016–3025. [Google Scholar] [CrossRef] [PubMed]
  7. Paffi, A.; Merla, C.; Pinto, R.; Lovisolo, G.A.; Liberti, M.; Marino, C.; Repacholi, M.; Apollonio, F. Microwave Exposure Systems for In Vivo Biological Experiments: A Systematic Review. IEEE Trans. Microw. Theory Tech. 2013, 61, 1980–1993. [Google Scholar] [CrossRef]
  8. Raman, S.; Augustine, R.; Rydberg, A. Noninvasive Osseointegration analysis of skull implants. IEEE Trans. Antennas Propag. 2014, 62, 5431–5436. [Google Scholar] [CrossRef]
  9. Odelstad, E.; Raman, S.; Rydberg, A.; Augustine, R. Experimental Procedure for Determination of the Dielectric Properties of Biological Samples in the 2–50 GHz Range. IEEE J. Transl. Eng. Health Med. 2014, 2, 1–8. [Google Scholar] [CrossRef] [PubMed]
  10. Lee, D.; Velander, J.; Blokhuis, T.J.; Kim, K.; Augustine, R. Preliminary study on monitoring the progression of osteoporosis using UWB radar technique in distal femur model. Electron. Lett. 2016, 52, 589–590. [Google Scholar] [CrossRef]
  11. Redzwan, S.; Asan, N.B.; Velander, J.; Lee, D.; Perez, M.D.; Raaben, M.; Blokhuis, T.J.; Augustine, R. Frequency domain analysis of hip fracture using microwave split ring resonators sensor on phantom model. In Proceedings of the 2016 IEEE Asian-Pacific Conference on Applied Electromagnetics, Langkawi, Malaysia, 11–13 December 2016; pp. 244–247. [Google Scholar]
  12. Augustine, R.; Kurup, D.G.; Raman, S.; Lee, D.; Kim, K.; Rydberg, A. Bone mineral density analysis using ultra wide band microwave measurement. In Proceedings of the 2015 IEEE MTT-S International Microwave and RF Conference, Hyderabad, India, 10–12 December 2015; pp. 102–104. [Google Scholar]
  13. Augustine, R.; Kurup, D.G.; Redzwan, S.; Mathur, P.; Raman, S.; Lee, D.; Kim, K. Microwave reflectivity analysis of bone mineral density using ultra wide band antenna. Microw. Opt. Technol. Lett. 2017, 59, 21–26. [Google Scholar] [CrossRef]
  14. Shankar, N.; Vijay, A.; Ligesh, A.S.; Kumar, A.; Anburajan, M. Comparison of Singh’s index with Dual energy X-ray Absorptiometry (DEXA) in evaluating post-menopausal lower extremity. In Proceedings of the IEEE Conference on Electronics Computer Technology, Kanyakumari, India, 8–10 April 2011; pp. 361–364. [Google Scholar]
  15. Mobashsher, A.T.; Abbosh, A.M. Developments of tomography and radar-based head imaging systems. In Proceedings of the 2015 International Symposium on Antennas and Propagation, Hobart, Tasmania, Australia, 9–12 November 2015; pp. 1–3. [Google Scholar]
  16. LeBlanc, K.; Muncie, H.L.; LeBlanc, L.L. Hip fracture: Diagnosis, treatment, and secondary prevention. Am. Fam. Physician. 2014, 89, 945–951. [Google Scholar] [PubMed]
  17. Reuling, E.M.B.P.; Sierevelt, I.N.; van den Bekerom, M.P.J.; Hilverdink, E.F.; Schnater, J.M.; van Dijk, C.N.; Goslings, J.C.; Raaymakers, E.L.F.B. Predictors of functional outcome following femoral neck fractures treated with an arthroplasty: Limitations of the Harris hip score. Arch Orthop Trauma Surg. 2011, 132, 249–256. [Google Scholar] [CrossRef] [PubMed]
  18. Pettersson, J.; Palmerius, K.L.; Knutsson, H.; Wahlstrom, O.; Tillander, B.; Borga, M. Simulation of Patient Specific Cervical Hip Fracture Surgery with a Volume Haptic Interface. IEEE Trans Biomed Eng. 2008, 55, 1255–1265. [Google Scholar] [CrossRef] [PubMed]
  19. Baumgartner, R.N.; Stauber, P.M.; Koehler, K.M.; Romero, L.; Garry, P.J. Associations of fat and muscle masses with bone mineral in elderly men and women. Am. J. Clin. Nutr. 1996, 63, 365–372. [Google Scholar] [CrossRef] [PubMed]
  20. Jagan, G.; Palanikumar, N.; Varun-Miranda, A.; Florence, S. Development of a Planar Sensor for Monitoring Orthopaedic Health. In Proceedings of the 2016 IRF International Conference, Chennai, India, 20 March 2016; pp. 71–75. [Google Scholar]
  21. Perez, M.D.; Redzwan, S.; Velander, J.; Raaben, M.; Asan, N.B.; Blokhuis, T.J.; Augustine, R. Microwave sensors for new approach in monitoring hip fracture healing. In Proceedings of the 2017 IEEE European Conference on Antenna and Propagation, Paris, France, 19–24 April 2017; pp. 1838–1842. [Google Scholar]
  22. Gabriel, C.; Gabriel, S.; Corthout, E. The dielectric properties of biological tissues: I. Literature survey. Phys. Med. Biol. 1996, 41, 2231–2249. [Google Scholar] [CrossRef] [PubMed]
  23. Gabriel, S.; Lau, R.; Gabriel, C. The dielectric properties of biological tissues: II. Measurements in the frequency range 10 Hz to 20 GHz. Phys. Med. Biol. 1996, 41, 2251–2269. [Google Scholar] [CrossRef] [PubMed]
  24. Gabriel, S.; Lau, R.; Gabriel, C. The dielectric properties of biological tissues: III. Parametric models for the dielectric spectrum of tissues. Phys. Med. Biol. 1996, 41, 2271–2293. [Google Scholar] [CrossRef] [PubMed]
  25. NirEmf Ifac. Home Page. Available online: http://niremf.ifac.cnr.it (accessed on 19 February 2018).
  26. Vallauri, R.; Bertin, G.; Piovano, B.; Gianola, P. Electromagnetic field zones around an antenna for human exposure assessment: Evaluation of the human exposure to EMFs. IEEE Antennas Propag. Mag. 2015, 57, 53–63. [Google Scholar] [CrossRef]
  27. King, R.W.P. Electric fields induced in cells in the bodies of amateur radio operators by their transmitting antennas. IEEE Trans. Microw. Theory Tech. 2000, 48, 2155–2158. [Google Scholar] [CrossRef]
  28. King, R.W.P. Electric current and electric field induced in the human body when exposed to an incident electric field near the resonant frequency. IEEE Trans. Microw. Theory Tech. 2000, 48, 1537–1543. [Google Scholar] [CrossRef]
  29. Asan, N.B.; Noreland, D.; Hassan, E.; Redzwan, S.; Rydberg, A.; Blokhuis, T.J.; Carlsson, P.-O.; Voigt, T.; Augustine, R. Intra-body microwave communication through adipose tissue. Healthc Technol Lett. 2017, 4, 115–121. [Google Scholar] [CrossRef] [PubMed]
  30. Asan, N.B.; Penichet, C.P.; Redzwan, S.; Noreland, D.; Hassan, E.; Rydberg, A.; Blokhuis, T.J.; Voigt, T.; Augustine, R. Data Packet Transmission through Fat Tissue for Wireless Intra-Body Networks. IEEE J. Electromag. RF Microw. Med. Biol. 2017, 1, 1–9. [Google Scholar] [CrossRef]
Figure 1. (a) Side view of the proposed multilayer sensor. The bottom layer consists of TMM4 substrate and the ground plane, the middle layer consists of TMM4 substrate and the T-patch, and the top layer consists of TMM6 superstrate and the split-ring resonator (SRR) patch; (b) Top views of the prototype of the SRR and (c) capacitive split-ring resonator (CSRR).
Figure 1. (a) Side view of the proposed multilayer sensor. The bottom layer consists of TMM4 substrate and the ground plane, the middle layer consists of TMM4 substrate and the T-patch, and the top layer consists of TMM6 superstrate and the split-ring resonator (SRR) patch; (b) Top views of the prototype of the SRR and (c) capacitive split-ring resonator (CSRR).
Sensors 18 00636 g001
Figure 2. (a) The proposed sensor positions. (b,c) Implemented positions of SRR sensors on the two positions consisting of the distal femur and thigh.
Figure 2. (a) The proposed sensor positions. (b,c) Implemented positions of SRR sensors on the two positions consisting of the distal femur and thigh.
Sensors 18 00636 g002
Figure 3. Method of extracting the dielectric profile of different tissues and hence the signal penetration depth using S11 data and US images.
Figure 3. Method of extracting the dielectric profile of different tissues and hence the signal penetration depth using S11 data and US images.
Sensors 18 00636 g003
Figure 4. Measured S11 data versus frequency response for four volunteers from difference position measurements.
Figure 4. Measured S11 data versus frequency response for four volunteers from difference position measurements.
Sensors 18 00636 g004aSensors 18 00636 g004b
Figure 5. Plot of the E-field penetration as a function of tissue thickness from different positions.
Figure 5. Plot of the E-field penetration as a function of tissue thickness from different positions.
Sensors 18 00636 g005aSensors 18 00636 g005b
Figure 6. E-field penetration from fat transition boundary in between skin and muscle.
Figure 6. E-field penetration from fat transition boundary in between skin and muscle.
Sensors 18 00636 g006
Table 1. Ultrasound (US) measurement of different tissue thicknesses from volunteers.
Table 1. Ultrasound (US) measurement of different tissue thicknesses from volunteers.
VolunteerLayerPosition 1 (mm)Position 2 (mm)Position 3 (mm)Position 4 (mm)
1Skin3.01.92.62.3
Fat6.15.87.211.5
Muscle15.414.435.528.6
2Skin2.32.32.42.7
Fat5.68.05.38.7
Muscle16.318.044.637.2
3Skin2.92.42.32.3
Fat10.18.87.211.0
Muscle19.723.549.744.2
4Skin2.52.52.52.5
Fat8.914.320.120.4
Muscle11.716.735.624.2
Table 2. Numerical data for different effective permittivity and conductivity.
Table 2. Numerical data for different effective permittivity and conductivity.
VolunteerLayerLiterature [25]Positions 1 and 2 (derived dielectric properties)Positions 3 and 4 (derived dielectric properties)
εrσ (S/m)εrσ (S/m)εrσ (S/m)
/Skin38.01.5/
Fat5.30.1
Muscle52.71.74
1Skin/34.21.338.01.5
Fat5.30.15.30.1
Muscle58.01.952.91.8
2Skin/37.91.431.91.2
Fat5.20.16.20.1
Muscle52.91.761.22.1
3Skin/34.21.330.41.2
Fat4.80.114.70.12
Muscle58.01.952.91.8
4Skin/34.11.230.21.3
Fat4.70.125.270.15
Muscle57.91.952.61.75

Share and Cite

MDPI and ACS Style

Mohd Shah, S.R.; Velander, J.; Mathur, P.; Perez, M.D.; Asan, N.B.; Kurup, D.G.; Blokhuis, T.J.; Augustine, R. Split-Ring Resonator Sensor Penetration Depth Assessment Using In Vivo Microwave Reflectivity and Ultrasound Measurements for Lower Extremity Trauma Rehabilitation. Sensors 2018, 18, 636. https://doi.org/10.3390/s18020636

AMA Style

Mohd Shah SR, Velander J, Mathur P, Perez MD, Asan NB, Kurup DG, Blokhuis TJ, Augustine R. Split-Ring Resonator Sensor Penetration Depth Assessment Using In Vivo Microwave Reflectivity and Ultrasound Measurements for Lower Extremity Trauma Rehabilitation. Sensors. 2018; 18(2):636. https://doi.org/10.3390/s18020636

Chicago/Turabian Style

Mohd Shah, Syaiful Redzwan, Jacob Velander, Parul Mathur, Mauricio D. Perez, Noor Badariah Asan, Dhanesh G. Kurup, Taco J. Blokhuis, and Robin Augustine. 2018. "Split-Ring Resonator Sensor Penetration Depth Assessment Using In Vivo Microwave Reflectivity and Ultrasound Measurements for Lower Extremity Trauma Rehabilitation" Sensors 18, no. 2: 636. https://doi.org/10.3390/s18020636

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop