Dual-Mode Detection of Urinary Chemokine and Ion Imbalance of BPS/IC Patients Toward Therapeutic Efficacy Assessment

IF 2.2 Q3 ENGINEERING, ELECTRICAL & ELECTRONIC
Tanzila Noushin;Jinwon Jeong;Muhammad Luqman Haider;Yun Ting Hsia;Jeong Bong Lee
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引用次数: 0

Abstract

Bladder pain syndrome/interstitial cystitis (BPS/IC) is a chronic urological condition characterized by pelvic pain and urinary urgency, often misdiagnosed due to symptom overlap with other analogous disorders. The absence of specific, noninvasive biomarkers complicates its diagnosis and hinders effective monitoring of disease progression and therapeutic response. C-C motif chemokine ligand 5 (CCL5) is recognized as a potential inflammatory biomarker for BPS/IC, while urinary potassium (K+) levels reflect epithelial barrier dysfunction. In this letter, we present a novel screen-printed, low-cost, and rapid electrochemical sensor for simultaneous point-of-care detection of CCL5 and K+ in urine samples. The sensor employs immunosensing and ion-selective membrane strategies to achieve excellent sensitivity, selectivity, and operational stability, having a low detection limit of 60 fg/mL and 80 pM for CCL5 and K+ ion sensing electrodes. The dual-detection approach offers valuable insights into both inflammatory status and urothelial integrity, holds promise for early diagnosis and therapeutic strategy with improved patient stratification, and real-time personalized monitoring in BPS/IC.
BPS/IC患者尿趋化因子及离子失衡双模检测对疗效评价的意义
膀胱疼痛综合征/间质性膀胱炎(BPS/IC)是一种以盆腔疼痛和尿急为特征的慢性泌尿系统疾病,常因症状与其他类似疾病重叠而误诊。特异性、非侵入性生物标志物的缺乏使其诊断复杂化,并阻碍了对疾病进展和治疗反应的有效监测。C-C基元趋化因子配体5 (CCL5)被认为是BPS/IC的潜在炎症生物标志物,而尿钾(K+)水平反映上皮屏障功能障碍。在这封信中,我们提出了一种新型的丝网印刷,低成本,快速电化学传感器,用于同时在护理点检测尿液样本中的CCL5和K+。该传感器采用免疫传感和离子选择性膜策略,具有出色的灵敏度、选择性和操作稳定性,对CCL5和K+离子传感电极具有60 fg/mL和80 pM的低检测限。双重检测方法提供了对炎症状态和尿路上皮完整性的宝贵见解,有望通过改进患者分层和BPS/IC的实时个性化监测来进行早期诊断和治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
IEEE Sensors Letters
IEEE Sensors Letters Engineering-Electrical and Electronic Engineering
CiteScore
3.50
自引率
7.10%
发文量
194
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