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Pickering emulsions (PEs), where water-in-oil (w/o) droplets are stabilized by nanoparticles (NPs), offer a promising platform for biocatalysis by providing a large interfacial area crucial for efficient substrate conversion. While several lipase catalyzed reactions in PEs have been demonstrated, the exact interfacial structure is unknown. This study focuses on the interfacial network formed by NPs and lipase (CRL) at the octanol/water-interface by varying pH and NP charge. By applying different methods, the location of lipases within a PE was identified and the enzyme concentration profile quantified for the first time. Positively charged nanoparticles (NP+) adsorbed at the o/w-interface together with CRL to form a network-structure. The relation between individual and simultaneous adsorption showed a constant value of 0.75 for the investigated pH range. Negatively charged particles (NP-) did not adsorb spontaneously at the negatively charged octanol/water-interface and therefore showed no influence on the enzyme adsorption behavior. Interfacial shear rheology measurements further revealed distinct elastic behavior of the enzyme-particle network due to attractive interactions between positively charged nanoparticles and CRL. This was shown by a 4.4-fold increase in the interfacial storage modulus. In contrast, repulsive interactions─either between CRL and positively charged particles at low pH or with negatively charged particles─did not enhance the elastic response of CRL at the interface. Confocal laser scanning microscopy of prepared PE droplets showed an interfacial CRL layer thickness of 0.75 μm for NP+ and 0.51 μm for NP-. Using NP+ results in a 30% higher interfacial enzyme concentration, indicating a more compact layer structure. These insights contribute to optimizing biocatalytic systems using PEs for industrial applications and provide a basis for the quantitative analysis of the interfacial layer in a Pickering emulsion.
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http://dx.doi.org/10.1021/acs.langmuir.5c02459 | DOI Listing |
ACS Appl Mater Interfaces
September 2025
Affiliated Hospital of Shandong Second Medical University, Shandong Second Medical University, Weifang, Shandong 261053, P.R. China.
Decades of antibiotic misuse have spurred an antimicrobial resistance crisis, creating an urgent demand for alternative treatment options. Although phototherapy has therapeutic potential, the efficacy of the most advanced photosensitizers (PS) is essentially limited by aggregation-induced quenching, which significantly reduces their therapeutic effect. To address these challenges, we developed a cationic metallocovalent organic framework (CRuP-COF) via a solvent-mediated dual-reaction synthesis strategy.
View Article and Find Full Text PDFWorld J Urol
September 2025
Division of Urology, University of Montreal Hospital Centre, Montreal, QC, Canada.
Purpose: To report the level of knowledge, impressions, and satisfaction of Urology readers, authors, and editorial boards regarding Open Access (OA) publishing in the field of Urology and to determine their satisfaction with the current OA models.
Methods: We developed an online, five-section cross-sectional survey including 23 questions. To recruit participants, we used mixed methods to obtain responses based on a simple random sampling and convenience sampling.
J Mater Chem B
September 2025
School of Materials Science and Engineering, Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates, South China University of Technology, Guangzhou, 510640, China.
Antibacterial photodynamic therapy offers a promising approach for combating both susceptible and multidrug-resistant pathogens. However, conventional photosensitizers have limitations in terms of poor binding specificity and weak penetration for pathogens. In this study, we developed synergistic photobactericidal polymers that integrate hydrophilic toluidine blue O (TBO) with the lipophilic penetration enhancer citronellol (CT).
View Article and Find Full Text PDFSmall
September 2025
Institute of Chemistry, Academia Sinica, Taipei, 115201, Taiwan.
Achieving high capacitance while maintaining rapid charge transport and structural stability remains a major challenge in the design of battery-type supercapacitor electrodes. Herein, a molecularly engineered strategy is presented for constructing hierarchical hybrid electrodes by integrating petal-like NiCu-LDH nanosheets onto 3D HBC-x (x = H, F, OMe)-functionalized CNT paper via a one-step hydrothermal process. The incorporation of HBC effectively mitigates CNT agglomeration and constructs an interconnected conductive framework that enhances charge transport, shortens ion diffusion paths, and reduces internal resistance.
View Article and Find Full Text PDFLangmuir
September 2025
Process Engineering in Life Science Engineering, HTW Berlin, Wilhelminenhofstraße 75 A, 12459 Berlin, Germany.
Pickering emulsions (PEs), where water-in-oil (w/o) droplets are stabilized by nanoparticles (NPs), offer a promising platform for biocatalysis by providing a large interfacial area crucial for efficient substrate conversion. While several lipase catalyzed reactions in PEs have been demonstrated, the exact interfacial structure is unknown. This study focuses on the interfacial network formed by NPs and lipase (CRL) at the octanol/water-interface by varying pH and NP charge.
View Article and Find Full Text PDF