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Hussain et al. Soft Sci. 2025, 5, 21  https://dx.doi.org/10.20517/ss.2025.02     Page 3 of 19

               due to the photonic bandgap (λ ) exhibited by CLCNs, which can be shifted to different wavelengths in
                                          PBG
                                                                                  [44]
                                                                                                     [45]
               response to external stimuli such as pH [41,42] , temperature , mechanical stress , or organic solvents . To
                                                                [43]
               enhance the hydrophilicity and responsiveness of CLCNs in aqueous environments, researchers have
               developed interpenetrating polymer networks (IPNs) integrated with CLCNs, making them ideal for
               biosensing applications . Several CLCN-IPN films have been fabricated on glass substrates for the analysis
                                   [46]
               of human body fluids [47-50] . The IPN typically consists of a weak polyelectrolyte hydrogel, which can undergo
               volumetric changes when exposed to external stimuli. These changes in volume directly alter the helical
               pitch of the CLCN, resulting in a visible color shift. Specifically, an increase in volume induces a red shift,
               while a decrease (or shrinkage) causes a blue shift. Unlike traditional dye-based sensors that rely on
               chemical colors which can degrade over time, CLCN-IPNs provide stable photonic colors that do not
               fade . Their solid structure and durability allow them to remain functional across a wide range of
                   [51]
               temperatures, making them long-lasting and reliable for various biosensing applications.

               Despite significant progress in wearable photonic biosensors, many existing technologies still face
               challenges in terms of usability, real-time monitoring, and integration into practical applications. In
               response to these limitations, we have developed a novel optical photonic sensor based on a CLCN-IPN
               system, seamlessly integrated into a soft wearable microfluidic device. Unlike conventional colorimetric
               sweat sensors that rely on intensity-based dye changes, our system utilizes structural photonic color shifts
               that provide stable, real-time detection without requiring an external power source or electronic
               components. A key innovation of our device lies in its enzyme-functionalized CLCN-IPN hydrogel
               network, which ensures high selectivity, mechanical flexibility, and durability for prolonged wear. The
               microfluidic polydimethylsiloxane (PDMS) patch is carefully designed to enable efficient sweat collection,
               controlled fluid flow, and reduced contamination risk, ensuring accurate and interference-free biomarker
               detection. Furthermore, the dynamic λ  shifts in response to biomarker concentration changes allow for
                                                PBG
               intuitive, naked-eye detection, eliminating the need for sophisticated optical instrumentation. By combining
               optical photonic sensing with microfluidic engineering, our platform bridges the gap between laboratory-
               based detection methods and practical, on-body health monitoring, offering a scalable, user-friendly, and
               cost-effective solution for real-time sweat analysis. This advancement represents a significant step forward
               in wearable biosensing, providing a battery-free, power-independent, and non-invasive diagnostic tool for
               monitoring glucose, lactate, and urea in human sweat.


               EXPERIMENTAL
               Materials
               Materials 1,4-Bis-[4-(6-acryloyloxyhexyloxy)benzoyloxy]-2-methylbenzene (RM82), 4-Methoxyphenyl 4-
               ((6-(acryloyloxy)hexyl)oxy)benzoate (RM105), (3R,3aS,6aS)-hexahydrofuro[3,2-b]furan-3,6-diyl bis(4-(4-
               ((4-(acryloyloxy)butoxy)carbonyloxy)benzoyloxy)benzoate) (DK756), and 4-Cyano-4’-pentylbiphenyl
               (5CB) were sourced from Daken Chemical Limited, China. Trichloro(1H,1H,2H,2H-perfluorooctyl)silane
               (PFOTS), 3-(trimethoxysilyl)propyl methacrylate (TMSPMA), acrylic acid (AA), 2-(dimethylamino)ethyl
               methacrylate  (DMAEMA),  tri(propylene  glycol)  diacrylate  (TPGDA),  phenylbis(2,4,6-
               trimethylbenzoyl)phosphine oxide (PI), N-(3-dimethylaminopropyl)-N’-ethylcarbodiimide hydrochloride
               (EDC), N-hydroxysuccinimide (NHS), magnesium chloride (MgCl ), acetone, and ethanol were procured
                                                                         2
               from Sigma Aldrich (USA). Urea, urease, sodium L-lactate, lactate oxidase (LOx), glucose, and glucose
               oxidase were also obtained from Sigma Aldrich. Calcium chloride dihydrate (CaCl ·2H O) and sodium
                                                                                        2
                                                                                            2
               chloride (NaCl) were received from Merk, USA. Potassium chloride (KCl) was obtained from PanReac,
               Spain. All chemicals were used as received without further purification unless otherwise noted. Glass slides
               (Euruslide, United Kingdom) were pre-cleaned with water and ethanol before use. Milli-Q water was
               employed for all reagent preparations.
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