ArticleSmall science2025
Immobilization of Enzyme-Polymer Hybrids and Nanozymes Through Electrostatic Interactions: Toward Multicatalytic Microreactors with Controlled Nanoarchitecture.
Article in Small science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Microglia encapsulation in nanozyme-loaded hydrogels: response to oxidative stress and inflammation.Nanomedicine (London, England) · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The optimal allocation of catalysts and their precise compartmentalization are vital to ensure efficient cascade reactions. The layer-by-layer approach offers the possibility of assembling various building blocks onto templates of different sizes and shapes, thus representing a powerful tool for fabricating multicatalytic reactors with controlled nanoarchitecture. However, this process usually relies on electrostatic interactions between building blocks, which means a limitation when working with natural enzymes. Accordingly, both the loading capacity and control over membrane architecture are compromised by the inherent surface charge of the enzymes. Here, this study introduces a modular strategy to assemble engineered enzyme-polymer hybrids and inorganic nanozymes onto colloidal templates, giving rise to multicatalytic reactors. The surface charge of the engineered enzyme-polymer hybrids can be finely tuned, allowing their à-la-carte assembly into multilayer membranes. Following this approach, the distance between catalytic units and their arrangement on colloidal templates at the nano- and micrometer scale can be precisely controlled, resulting in optimized configurations with enhanced cascade efficiency. The synthesized multicatalytic reactors can reduce the metabolic activity of human pancreatic stellate cells, confirming their functional activity in biological microenvironments and highlighting their potential for biomedical applications.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.