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Alkaline phosphatase (ALP) is an important hydrolase found in mammalian tissues and plays a crucial role in numerous fundamental physiological processes within organisms by means of dephosphorylation. From a clinical perspective, the level of ALP is regarded as a vital indicator for numerous diseases, including neurological disorders, diabetes, and hepatocellular carcinoma. In this study, a novel dual-mode assay system was developed with the objective of facilitating quantitative ALP detection. This method used a G-quadruplex dimer (Di-G4) to enhance the signal, resulting in the quantification of the ALP concentration in either fluorescence or colorimetric mode. Under optimal conditions, wide linear ranges (fluorescence mode, 1-200 U L; colorimetric mode, 1-300 U L) were achieved with excellent limits of detection (fluorescence mode, 0.79 U L; colorimetric mode, 1 U L). The proposed method was employed for the detection of ALP in human serum samples and yielded satisfactory results. The advantageous characteristics of this method, including high sensitivity, simple operation and low cost, suggest that it has considerable application potential in the diagnosis and treatment of clinical diseases.
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http://dx.doi.org/10.1039/d5ay00934k | DOI Listing |
Anal Chim Acta
November 2025
Guangxi Key Laboratory of Natural Polymer Chemistry and Physics, Key Laboratory of Nanobiosensor Analysis, College of Chemistry and Materials, Nanning Normal University, Nanning, 530001, PR China. Electronic address:
Background: Hexavalent chromium ions (Cr(VI)), a notorious toxic heavy metal pollutant with proven carcinogenicity, endangers human health and the environment. Meanwhile, l-ascorbic acid (L-AA), a vital biological antioxidant, has abnormal levels closely tied to various diseases. Developing efficient synchronous detection methods for these two key analytes is of great value in clinical and environmental monitoring.
View Article and Find Full Text PDFTalanta
September 2025
Glyn O. Phillips Hydrocolloid Research Centre, National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Key Laboratory of Fermentation Engineering of Ministry of Education, Key Laboratory of Industrial Microbiology in Hubei Province, School of Life and Health Sciences, Hubei Univer
Given rising consumer demands for meat safety and quality assurance, developing an intuitive, cost-effective, and user-friendly sensor platform for real-time monitoring of perishable meat freshness is important. Herein, this study developed an innovative chitosan/agarose/blueberry anthocyanin (CS/AG/BA) hydrogel label system for visual real-time freshness tracking of perishable proteins through smartphone-assisted colorimetric analysis. Through systematic optimization of CS/AG compositional ratios (3:7-7:3) and pH conditions (2.
View Article and Find Full Text PDFMikrochim Acta
September 2025
Henan Agricultural University, Zhengzhou, 450002, China.
A dual-mode aptasensor was engineered for aflatoxin B (AFB) detection by functional integration of peroxidase-mimetic Au@CeO core-shell nanostructures with emissive carbon dots (CDs). The Au@CeO nanocomposite, synthesized via spontaneous redox reaction, exhibited enhanced peroxidase-like activity due to abundant Ce/oxygen vacancies facilitating hydroxyl radical generation. The aptasensor utilizes a competitive binding mechanism, where AFB competed with immobilized Au@CeO-CDs-Apt1 probes for binding sites, resulting in inversely proportional colorimetric and fluorescent signals.
View Article and Find Full Text PDFAnal Chem
September 2025
State Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Second Provincial General Hospital, The Fifth Affiliated Hospital, Guangzhou Red Cross Hospital, College of Pharmacy, Jinan University, Guangzhou 510632, China.
Rapid and precise detection of () is crucial for early diagnosis, treatment of infectious ailments, and controlling outbreaks. Herein, we present a rapid, streamlined, and sensitive method for screening based on a hollow copper/platinum interspersed graphene oxide nanosheets (Cu/Pt-GO)-mediated cascade responsiveness strategy. The Cu/Pt-GO nanozymes were proposed to catalyze the colorless 3,3',5,5'-tetramethylbenzidine (TMB) to colored oxidized TMB (oxTMB) with enhanced SERS signals, achieving colorimetric/SERS dual-model detection.
View Article and Find Full Text PDFACS Omega
August 2025
VinUni-Illinois Smart Health Center, VinUniversity, Hanoi 100000, Vietnam.
Accurate and accessible glucose detection is essential for clinical diagnostics, point-of-care testing, food safety, and biosensing applications. In this study, we present a simple, scalable, and dual-mode glucose sensor that integrates commercial potassium permanganate (KMnO) with glucose oxidase to enable sensitive and selective detection in the clinically critical range of 1-5 mM. Leveraging the strong oxidative power and distinct optical characteristics of KMnO, the sensor operates via both absorbance measurement at 400 nm and visual colorimetric analysis, displaying a clear color change from purple to pink and yellow upon reaction with glucose.
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