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Excess consumption of caffeine (>400 mg/day/adult) can lead to adverse health effects. Recent introduction of caffeinated products (gums, jelly beans, energy drinks) might lead to excessive consumption, especially among children and nursing mothers, hence attracting the Food and Drug Administration's attention and product withdrawals. An "in-home" test will aid vigilant consumers in detecting caffeine in beverages and milk easily and quickly, thereby restricting its consumption. Known diagnostic methods lack speed and sensitivity. We report a caffeine dehydrogenase (Cdh)-based test which is highly sensitive (1-5 ppm) and detects caffeine in beverages and mother's milk in 1 min. Other components in these complex test samples do not interfere with the detection. Caffeine-dependent reduction of the dye iodonitrotetrazolium chloride results in shades of pink proportional to the levels in test samples. This test also estimates caffeine levels in pharmaceuticals, comparable to high-performance liquid chromatography. The Cdh-based test is the first with the desired attributes of a rapid and robust caffeine diagnostic kit.
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http://dx.doi.org/10.1021/jf501598c | DOI Listing |
Haematologica
September 2025
Department of Biochemistry and Molecular Genetics, University of Colorado Denver - Anschutz Medical Campus, Aurora, CO, USA; Omix Technologies Inc, Aurora, CO.
Caffeine is the most widely consumed psychoactive substance globally, yet its peripheral physiological effects remain incompletely understood. Leveraging comprehensive data from 13,091 blood donors in the REDS RBC-Omics study, we identify caffeine as a significant modulator of red blood cell (RBC) storage quality and transfusion outcomes. Elevated caffeine levels were reproducible across multiple donations from 643 recalled donors, selected based on their extremes in hemolytic propensity.
View Article and Find Full Text PDFSci Rep
August 2025
Chemistry Department, Biochemistry Division, Faculty of Science, Cairo University, Giza, 12613, Egypt.
Energy drinks are rapidly gaining prominence in the global beverage industry, with projected sales reaching $60 billion within the next five years. These beverages often contain high levels of caffeine and the amino acid taurine, among other ingredients. The increasing consumption of energy drinks by children has sparked concerns regarding potential caffeine toxicity.
View Article and Find Full Text PDFInt J Mol Sci
July 2025
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud University, Riyadh 12372, Saudi Arabia.
Nonspecific toxicity to normal and malignant cells restricts the clinical utility of many anticancer drugs. In particular, anemia in cancer patients develops due to drug-induced toxicity to red blood cells (RBCs). The anticancer alkaloid, cepharanthine (CEP), elicits distinct forms of cell death including apoptosis and autophagy, but its cytotoxicity to RBCs has not been investigated.
View Article and Find Full Text PDFNutrients
July 2025
Department of Microscopic Morphology, Discipline of Genetics, Genomic Medicine Centre "Victor Babes", University of Medicine and Pharmacy, 300041 Timisoara, Romania.
: Inter-individual metabolic responses to caffeine are shaped by CYP1A2 clearance rate and by concurrent lipid- or glucose-lowering drugs. We investigated how habitual caffeine intake relates to serum cholesterol and fasting glucose under different CYP1A2 rs762551 genotypes and statin or oral antidiabetic (OAD) use. : A prospective cross-sectional analysis was performed on 358 adults (AA = 65, AC = 163, CC = 130) with recorded genotype, daily caffeine intake, total cholesterol, fasting glucose, and medication status.
View Article and Find Full Text PDFChem Biol Interact
October 2025
Department of Pharmacology, Wuhan University School of Basic Medical Science, Wuhan, 430071, China; Hubei Provincial Key Laboratory of Developmentally Originated Disorder, Wuhan, 430071, China. Electronic address:
Our previous study has confirmed that the occurrence of fetal-originated disease is related to the changes in the developmental programming of adrenal in offspring. The aim of this study was to investigate the effects of prenatal caffeine exposure (PCE) on adrenal developmental programming in offspring rats and the underlying mechanisms. Here, PCE inhibited adrenal morphology and steroidogenic function in female and male offspring, and the suppression persisted in female offspring up to postnatal week 28 (PW28), while no significant changes in male offspring.
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