Nampeng, Jindapa
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Item type:Publication, A Novel Approach for Optimizing Molecularly Imprinted Polymer Composition in Electrochemical Detection of Collagen Peptides(2025-11-01) ;Vongmanee, Naphatsawan; ;Rattanapithan, Katesirin ;Sriwichai, PhuritasineeCollagen peptides are key structural proteins that play an important role in maintaining the integrity and proper function of multiple tissues in the human body. Their breakdown is recognized as an important biomarker for various degenerative conditions, including the loss of muscle mass, joint and bone disorders, and compromised skin health. Current analytical approaches for collagen detection, such as ultraviolet spectrometry, enzyme-linked immunosorbent assay (ELISA), high-performance liquid chromatography (HPLC), and histochemical staining, are widely used but often expensive, time-consuming, and reliant on specific laboratory instrumentation, limiting their practicality for routine or rapid diagnostics. This study reports a novel biosensor for collagen peptide detection based on molecularly imprinted polymers (MIPs) integrated with screen-printed electrodes (SPEs). Electrochemical measurements revealed a clear correlation between collagen concentration and current response, confirming effective molecular binding within the imprinted matrix. The optimized MIP-modified electrode exhibited a detection range of 0.1–1000 µg/mL with a limit of detection (LOD) of 1.0106 µg/mL, limit of quantification (LOQ) of 4.46 µg/mL, sensitivity of 8.3816, and correlation coefficient (R<sup>2</sup> = 0.9436). These results highlight strong selectivity and sensitivity toward collagen peptides. The proposed MIP-based biosensor provides a rapid, low-cost platform for detecting collagen degradation products and holds potential for early diagnosis and future clinical applications in degenerative disease monitoring. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, C. albicans Detection with Electrochemical Sensors by Using Molecular Imprinted Polymer Technique(2026-03-01) ;Vongmanee, Naphatsawan; ; Candida albicans (C. albicans) is an opportunistic fungal pathogen and a major cause of nosocomial infections, especially in immunocompromised patients. Conventional diagnostic approaches such as blood culture and biochemical assays are accurate but require multi-step sample processing and prolonged turnaround times, limiting their applicability for rapid clinical screening. In the present study, we developed an electrochemical biosensor based on molecularly imprinted polymer (MIP) technology for the rapid and selective detection of intact C. albicans cells. The MIP layer was electropolymerized onto a screen-printed carbon electrode (SPCE), forming selective recognition cavities complementary to the fungal morphology. Electrochemical characterization and detection were performed using cyclic voltammetry in phosphate-buffered saline (PBS). The system demonstrated a wide linear detection range, enabling reliable quantification of C. albicans across concentrations spanning from 1 to 10<sup>4</sup> CFU/mL and achieved an ultralow limit of detection (LOD) of 1.30 CFU/mL, demonstrating high sensitivity. High selectivity was confirmed against E. coli, S. aureus, and P. aeruginosa, demonstrating that the imprinted cavities effectively distinguish fungal cells from bacterial contaminants. These findings highlight the promise of MIP-based electrochemical biosensors as a simple, low-cost, and portable alternative for early fungal diagnostics.
