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The rational design of nanozymes with remarkable catalytic activity remains pivotal for advancing colorimetric biosensing platforms. Graphitic carbon nitride (g-CN) has emerged as a captivating photocatalytic material given its cost-effectiveness, ease of fabrication and outstanding stability. However, its practical implementation as a light-responsive nanozyme is fundamentally constrained by suboptimal catalytic activity. Herein, cobalt was incorporated into g-CN nanosheets, giving rise to the formation of cobalt-doped graphitic carbon nitride nanosheets (Co/g-CN), which significantly enhanced its light-responsive oxidase-mimicking activity primarily attributed to its notably enhanced visible light absorption capacity and optimized photo-generated charge carrier separation/transfer efficiency. When exposed to visible light illumination, Co/g-CN triggered the chromogenic reaction by facilitating the oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) owing to the generation of hydrogen oxide, singlet oxygen and photogenerated holes. Furthermore, capitalizing on the inhibitory effect of thiocholine on the TMB oxidation, a new colorimetric method was established to determine acetylcholinesterase (AChE) activity. This colorimetric method enabled determination of AChE activity ranging from 0.1-15 mU/mL, achieving a remarkably low detection limit of 0.04 mU/mL. Moreover, it was effectively utilized to ascertain AChE activity in serum samples with desirable results. Additionally, it was successfully applied to detect AChE inhibitor. This work not only advances the modulation of catalytic activities in light-responsive nanozymes, but also presents an innovative perspective for AChE activity determination.
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http://dx.doi.org/10.1016/j.jcis.2025.137968 | DOI Listing |
Cephalalgia
September 2025
Department of Molecular Physiology and Biophysics, University of Iowa, Iowa City, IA, USA.
Migraine is a complex neurological disorder involving multiple neuropeptides that modulate nociceptive and sensory pathways. The most studied peptide is calcitonin gene-related peptide (CGRP), which is a well-established migraine trigger and therapeutic target. Recently, another peptide, pituitary adenylate cyclase-activating polypeptide (PACAP), has emerged as an alternative target for migraine therapeutics.
View Article and Find Full Text PDFAnn Palliat Med
September 2025
Brown University Health Cancer Institute, Providence, RI, USA; Division of Geriatrics and Palliative Medicine, Department of Medicine, Alpert Medical School of Brown University, Providence, RI, US.
ancreatic cancer is an aggressive disease and often presents at an advanced stage with no curative options. The disease is often characterized by rapid progression, limited or short-lived responsiveness to standard therapies, and a profound impact on patients' quality of life. Despite advances in targeted therapies and immunotherapy, curative outcomes remain elusive for the majority of patients with advanced or high-grade disease with a 5-year survival rate of less than 10%.
View Article and Find Full Text PDFCNS Neurosci Ther
September 2025
College of Biomedical Engineering and Technology, Tianjin Medical University, Tianjin, China.
Background: Neurological diseases such as stroke or Parkinson's disease are often accompanied by weakening or loss of proprioception, which seriously affects the motor control ability of the patients. However, proprioception rehabilitation is challenging due to the pain caused by impaired joints and the hard efforts that patients have to make during training. This study investigated the cross-transfer effect of short-term visuomotor training to the untrained wrist from the trained wrist, from both views of behavioral results and brain activity analyses.
View Article and Find Full Text PDFFuture Med Chem
September 2025
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Anadolu University, Eskişehir, Turkey.
In this review, the primary aim is to examine non-azole ring systems that have analgesic activity and, where applicable, to establish structure - activity relationships (SARs) with the nine major pathways, prostaglandin synthesis inhibition, opioid receptor modulation, sodium channel blockade, enhancement of serotonin and norepinephrine levels, cannabinoid receptor (CBR) binding, N-methyl-D-aspartate (NMDA) receptor antagonism, transient receptor potential cation channel subfamily V member 1 (TRPV1) antagonism, and P2X purinergic receptor blockade, have been described for pain relief. Analgesic effects have been observed in compounds containing ring systems such as piperidine, piperazine, pyridine, pyridazine, pyrazine, morpholine, thiomorpholine, pyran, thiopyran, indane, benzofuran, benzothiophene, quinoline, quinazoline, and chromene. These ring systems were classified in the whole study, first according to their molecular weights and then by bioisosteric similarity as same as first part.
View Article and Find Full Text PDFJ Sci Med Sport
August 2025
Eastern Health Clinical School, Monash University, Australia; Eastern Health Emergency Medicine Program, Australia. Electronic address:
Objectives: To explore differences in beliefs towards running in adults with and without chronic low back pain.
Design: This convergent mixed methods cross-sectional study compared adults with chronic low back pain (n = 39) to pain-free adults with a history of chronic low back pain (n = 28) and a low back pain naive control group (n = 71).
Methods: Beliefs towards running (activity specific beliefs questionnaire; range: 1-4 points), pain intensity (101-point visual analogue scale), disability (Oswestry Disability Index), and habitual physical activity (International Physical Activity Questionnaire) were analysed.