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Understanding the disassembly process is significant for constructing well-defined and multifunctional supramolecular structures. Nowadays, fluorescent microscopy is used as a common technique to observe a real-time disassembly process. However, the addition of the fluorescent probes into nonfluorescent systems might influence the disassembly due to the weak supramolecular interactions. Therefore, it is urgent to explore a novel strategy to monitor supramolecular disassembly in the absence of fluorophores. In this work, we developed a simple and rapid strategy to understand the supramolecular disassembly process based on confined microenvironment-regulated electrochemiluminescence (ECL). It is disclosed that the addition of competitive guests could disassemble the supramolecular architectures and destroy the confined spaces, decreasing the ECL intensity as a result of the reduction of the chemical transformation efficiency of the coreactant. This developed nanoconfinement-tuned ECL strategy offers a simple method to monitor supramolecular disassembly in real time without the addition of any fluorescent dye. It is anticipated that the proposed strategy could be beneficial for a deep understanding of supramolecular disassembly, promoting the design and preparation of new-generation supramolecular assemblies with advanced functions.
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http://dx.doi.org/10.1021/acs.analchem.5c01961 | DOI Listing |
Mater Today Bio
October 2025
School of Public Health, Key Laboratory of Emergency and Trauma of Ministry of Education, Hainan Medical University, Haikou, 571199, China.
The development of controllable nanoplatforms with disease-specific responsiveness and programmable therapeutic functions is vital for treating complex cardiovascular diseases such as atherosclerosis. Herein, we present an intelligent, next-generation nanoplatform (HALA@AgS) that integrates enzyme-responsive dual-drug delivery with NIR-II imaging-guided photothermal therapy (PTT), enabling triple-stimuli synergy of enzyme, light, and multi-drug co-activation. This modular design enables stable nanoassemblies with high drug-loading capacity and selective disassembly in enzyme-rich plaque microenvironments, achieving controlled dual-drug release exceeding 80 % within 72 h.
View Article and Find Full Text PDFBiomaterials
August 2025
Department of Anesthesiology and Perioperative Medicine, The Second Affiliated Hospital of Anhui Medical University, 678 Furong Road, Hefei, 230601, China; Key Laboratory of Anesthesiology and Perioperative Medicine of Anhui Higher Education Institutes, Anhui Medical University, 678 Furong Road, Hef
Activation of p38 mitogen-activated protein kinase plays an important role in the progression of ventricular muscle inflammation after myocardial ischemia-reperfusion (MI/R). The inhibition of p38 activation in ischemic myocardium can reduce ventricular muscle remodeling post-MI. However, owing to the dynamic change of p38 in ischemic myocardium after MI, the clinical therapeutic effect of p38 inhibitors is insufficient.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou 325001, China; Terahertz Technology Innovation Research Institute, Terahertz Spectrum and Imaging Technology Cooperative Innovation Center, Shanghai Key Lab of Modern Optical System, School of Optical-Electrical and Computer Engin
Precise engineering of hydrophobic microenvironments in synthetic peptide-catecholamine co-assemblies remains challenging for tunable fluorescence. Hierarchical nanostructures were constructed through sequence-specific peptide encoding (GYK tripeptide and Ac-IIIGYK-NH₂ hexapeptide) and co-assembly with catecholamines of graded hydrophobicity. Structural dynamics were analyzed via molecular simulations, HPLC, AFM, and spectroscopy.
View Article and Find Full Text PDFJ Control Release
August 2025
Hunan Provincial Key Laboratory of Animal Models and Molecular Medicine, State Key Laboratory of Chemo/Bio-Sensing and Chemometrics, School of Biomedical Sciences, Hunan University, Changsha 410082, China; Shenzhen Research Institute, Hunan University, Shenzhen 518000, Guangdong Province, China. Ele
Enzyme-instructed self-assembly has emerged as a powerful tool to engineer selective functional materials. However, its reverse process, enzyme-instructed disassembly, has been largely overlooked despite its critical implications in pharmaceutical research. This study introduces a new approach employing enzyme-instructed peptide disassembly to selectively inhibit cancer cells.
View Article and Find Full Text PDFChemistryOpen
August 2025
CPCV, Department of Chemistry, Ecole Normale Supérieure, PSL University, Sorbonne Université, CNRS, 75005, Paris, France.
Pseudo-rotaxanes are reversibly interlocked molecules with at least one linear molecule threaded into a macrocycle and, contrary to rotaxanes, an advantageous ability to be dissociated. Cyclodextrins constitute attracting macrocyclic host entities to build such dynamic structures for their oligosaccharide nature, conic shape, amphiphilic character and biocompatibility. Here we show that using an azobenzene DNA intercalator as a guest allows to build a pseudo-rotaxane combining several remarkable properties, including light-controlled assembly/disassembly, photoreversible chirality and fluorescence, as well as the capability to affect the melting temperature of double-stranded DNA through intercalator host-guest complexation.
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