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Deep learning–enabled investigation on non-invasive glucose detection using miniaturized pentagonal slotted microstrip patch antenna (MPSMA)

Published online by Cambridge University Press:  28 July 2026

Rahul Krishnan
Affiliation:
Faculty of Engineering and Built Science, Lincoln University College, Petaling Jaya, Malaysia Department of ECE, Sree Buddha College of Engineering, Alappuzha, India
Priyanka Das
Affiliation:
School of Electronics Engineering, Vellore Institute of Technology, Chennai, India
V. Shiva Prasad Nayak*
Affiliation:
Department of EECE, GITAM Deemed to be University, Hydrabad, India Department of Electronics and Communication Engineering, Amity University Hyderabad, Telangana, India
Inam Ullah Khan
Affiliation:
Faculty of Computing and Informatics, Multimedia University, Cyberjaya, Malaysia
Sai Kiran Oruganti
Affiliation:
Faculty of Engineering and Built Science, Lincoln University College, Petaling Jaya, Malaysia
*
Corresponding author: V. Shiva Prasad Nayak; Email: shiva6221@gmail.com
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Abstract

A miniaturized pentagonal slotted microstrip patch antenna (MPSMA) is designed using FR4 substrate at 4.2 GHz for non-invasive glucose sensing applications. The MPSMA design was optimized for maximal impedance matching, S11, Voltage Standing Wave Ratio (VSWR), efficiency, gain, and directivity. Simulated results were experimentally validated using a vector network analyzer inside an anechoic chamber. The proposed MPSMA achieved a notable return loss of −36.36 dB, a VSWR of 1.0308, efficiency of 75.4 %, gain of 1.5 dBi, and directivity of 2.879 dBi, confirming its performance. A detailed analysis was carried out by placing the antenna near various concentrations of glucose solution (10%–50%), which indicates a significant shift in the resonant frequency and reflection characteristics of the antenna. Principal component analysis was applied for identifying distinct characteristics between various glucose concentrations. The glucose sensing capability of the proposed MPSMA was validated by using a multilayer finger model designed in CST Studio software that mimics real tissue characteristics (Cole–Cole model). The detailed analysis on the multilayer finger model as well as the beaker solution setup highlights the potential of MPSMA in non-invasive glucose monitoring. Further deep learning is implemented using the experimental data for the prediction of glucose from the S11 data. Convolutional neural network classifier results are balanced across most classes. Around most glucose concentrations, true and predicted values are close, with minor overestimation around 4000 mg/dL. The proposed solution is inexpensive and has the potential for diabetes treatment, which ensures the feasibility integration of microstrip antenna technology into next-generation biomedical sensing platforms.

Information

Type
Research Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2026. Published by Cambridge University Press in association with The European Microwave Association.
Figure 0

Figure 1. (a) Proposed MPSMA design. (b) Iteration of the proposed MPSMA design. (c) S11 comparison of various patch iterations of the proposed MPSMA. (d) Proposed MPSMA ground plane iteration. (e) S11 comparison of various ground length (GL) iterations.Figure 1 long description.

Figure 1

Table 1. Dimensions of proposed MPSMATable 1 long description.

Figure 2

Figure 2. (a) Comparison between reflection characteristics of the proposed antenna by equivalent circuit modeling and full-wave simulations. (b) Fabricated MPSMA. (c) Comparison of the tested vs simulated S11. (d) Comparison of the tested vs simulated VSWR.Figure 2 long description.

Figure 3

Table 2. Comparison of the tested vs simulated VSWRTable 2 long description.

Figure 4

Figure 3. Block diagram for multilayer finger model simulation setup.

Figure 5

Figure 4. Multilayer finger model.

Figure 6

Figure 5. S11 comparison with and without the finger model.

Figure 7

Table 3. Comparison of physical properties for the human finger modelTable 3 long description.

Figure 8

Figure 6. (a) Frequency vs S11 response for various blood glucose concentrations. (b) PCA of S11 vs glucose concentration. (c) 2D scatter plot (PC1 vs PC2). (d) Various positions of the finger model placement.Figure 6 long description.

Figure 9

Table 4. Comparison of frequency vs S11 for various blood glucose concentrationsTable 4 long description.

Figure 10

Figure 7. S11 vs frequency for shifting of finger position (a) 0 mg, (b) 500 mg, (c) 2000 mg, and (d) 8000 mg.Figure 7 long description.

Figure 11

Table 5. Comparison of S11 and frequency across finger shifts and glucose concentrationsTable 5 long description.

Figure 12

Figure 8. (a) Block diagram for beaker setup. (b) Beaker setup modeled in CST. (c) Antenna, beaker, and solution. (d) Various glucose solution concentrations. (e) Beaker setup testing in VNA.Figure 8 long description.

Figure 13

Table 6. Comparison of S11 vs frequency for various glucose concentrationsTable 6 long description.

Figure 14

Figure 9. (a) Measured S11 for various glucose concentrations. (b) Comparison of S11 (simulation vs measurement). (c) CNN architecture for glucose level classification. (d) Confusion matrix. (e) ROC curves. (f) Class distribution plot.Figure 9 long description.

Figure 15

Table 7. Comparison table for simulated vs measured S11Table 7 long description.