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Background: Methotrexate (MTX) is an antineoplastic drug used in high doses to treat different types of cancer. Its mechanism of action relies on the structural similarities to folic acid (FA), interfering in the metabolic pathway of FA. Due to the narrow therapeutic window and high cytotoxicity, MTX therapeutic drug monitoring is mandatory in high-dose administration schemes.
Results: A new nanosensor (NS) based on luminescent silver nanoclusters (AgNC) and metallic ions was developed to selectively determine MTX in samples containing its molecular analog FA. Notably, changes in the AgNC fluorescence signal are induced in the presence of MTX and FA, and this phenomenon was exploited to develop a sensing platform for quantitating non-fluorescent MTX in the presence of FA. The selectivity and sensitivity of the NS were improved by including Al and Mg, and their concentrations were optimized by design-of-experiment and response surface methodology tools. Analysis of excitation-emission fluorescence matrices by Multivariate curve resolution-alternating least squares allowed exploiting the advantages of the analyte-induced fluorescence changes since it can cope with deviations from multilinearity occurring upon NS interaction with MTX. The sensing strategy reached limits of detection and quantitation of 0.3 μmol L and 0.9 μmol L, respectively.
Significance: These findings support the method's applicability for quantitating MTX at clinically relevant concentrations in the presence of its molecular analog, without requiring exhaustive sample pretreatment. The developed sensing platform represents a simple, selective, sensitive, and cost-effective approach for quantitating non-fluorescent MTX in the presence of FA.
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http://dx.doi.org/10.1016/j.aca.2025.344259 | DOI Listing |
Curr Opin Microbiol
September 2025
Department of Molecular Biosciences, The Wenner-Gren Institute, Science for Life Laboratory, Stockholm University, Stockholm, Sweden. Electronic address:
Many bacteria have complex pleomorphic lifecycles - a feature particularly widespread across the class Alphaproteobacteria of the phylum Pseudomonadota. While research on bacteria with pleomorphic lifecycles has for many years focused on the dimorphic bacterium Caulobacter crescentus, more recent studies on less established alphaproteobacterial model bacteria have uncovered diverse variations of bacterial pleomorphism. Here, we provide an overview of the diversity and evolution of the complex lifecycles among dimorphic Alphaproteobacteria and highlight the presence of analogous lifecycles in unrelated bacteria across the bacterial domain.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Department of Chemistry, State Key Laboratory of Porous Materials for Separation and Conversion, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, and iChEM, Fudan University, Shanghai 200438, China. Electronic address:
We present a coordination-inspired strategy for assembling binary nanocrystal superlattices (BNSLs) using CdSe nanotetrapods as symmetry-encoding building blocks. Exploiting their intrinsic tetrahedral geometry, which mimics the sp hybridization of carbon atoms in a diamond lattice, we encode spatially defined binding sites that guide regioselective coassembly with spherical nanocrystals. By tuning the size ratio between components, we achieve both three-dimensional and two-dimensional BNSLs with long-range structural order.
View Article and Find Full Text PDFOrg Biomol Chem
September 2025
Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of Bioorganic Chemistry, Sienkiewicza 112, 90-363 Łódź, Poland.
We present the application of the oxathiaphospholane method for the synthesis of novel P-stereodefined phosphorothioate N-modified morpholino analogs, showcasing its potential for creating therapeutically relevant compounds. Additionally, we provide valuable structural insights into their stereochemistry, including a detailed analysis of stereochemical configurations. We also report on the enzymatic stability of these compounds in 10% (v/v) fetal bovine serum (FBS), thereby mimicking conditions.
View Article and Find Full Text PDFMol Divers
September 2025
State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi, 830011, Xinjiang, China.
Aurora kinases are a group of serine/threonine kinases essential for cell mitosis, comprising Aurora A, B, and C. However, the Aurora B is overexpressed in multiple tumors and the aurone has been proved to exhibit potent inhibitory activity against Aurora B kinase by our group. The indolinone was considered as an aurone scaffold hopping analog, and the indolinone-based Aurora B inhibitor library (3577 molecules) was constructed by FBDD strategy.
View Article and Find Full Text PDFInflammopharmacology
September 2025
Centre for Research Impact & Outcome, Chitkara College of Pharmacy, Chitkara University, Rajpura, Punjab, 140401, India.
The NOD‑like receptor family pyrin domain containing 3 (NLRP3) inflammasome is a key molecular complex that amplifies inflammatory cascades by maturing interleukin‑1 beta (IL-1β) and interleukin‑18 (IL-18) and inducing pyroptosis. It serves as a major driver and co-driver of numerous diseases associated with chronic inflammation. Dysregulated NLRP3 activation contributes to the progression of disorders such as rheumatoid arthritis, inflammatory bowel disease, neurodegenerative diseases and atherosclerosis.
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