ArticleNature chemistry2023
Uniform segmented platelet micelles with compositionally distinct and selectively degradable cores.
Article in Nature chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.
What it found
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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.
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Who cites it
21 citing papers in PubMed, 119 citations in OpenAlex.
- Polymer Platelets via Crystallization-Driven Self-Assembly of Block Copolymers: Precision Growth, Structural Complexity and Emerging Functions.Macromolecular rapid communications · 2026Review
- Preparation of polycaprolactone-based 2D platelets via living crystallization-driven self-assembly.Nature protocols · 2026Review
- Constructing and decoding tree-ring-like surface patterns on self-assembled polymer platelets.Nature communications · 2026Article
- Synthesis and applications of 1D and 2D nanoparticles prepared through crystallisation-driven self-assembly.Chemical science · 2026Review
- Near infrared light regulated crystallization-driven self-assembly: a versatile platform for controlled preparation of uniform π-conjugated functional nanostructures.Chemical science · 2026Article
- Supramolecular Assemblies of Self-Immolative Janus Dendrimers With Rapid Photodegradation Response.Small (Weinheim an der Bergstrasse, Germany) · 2026Article
- Supramolecular coupling of cylindrical micelles following seeded-growth.Nature communications · 2026Article
- Droplet-mediated kinetic-to-thermodynamic transition for the fabrication of uniform 1D and 2D nanostructures from conjugated homopolymers.Chemical science · 2026Article
- Time-Resolved SAXS Studies During the Synthesis of Hydrolytically Degradable Poly(ε-caprolactone)-Poly(N,N'-dimethylacrylamide) Diblock Copolymer Nanoparticles in Aqueous Media.Angewandte Chemie (International ed. in English) · 2026Article
- Uniform conjugated polymer rectangular platelets exhibiting long-range exciton diffusion.Nature materials · 2025Article
- Crystallization-driven two-dimensional assemblies from a phenothiazine-conjugated poly(l-lactide): redox-responsive tunable emission, white-light harvesting and surface-enabled nanoparticle decoration.Chemical science · 2025Article
- Deciphering Evolution, Function, and Observation of Crystallization-Driven Self-Assembly.Chemical reviews · 2025Review
- Regioselective on-surface crystallization of one-dimensional organic barcode-like heterostructures of MOFs with fluorescent stripe patterns.Nature communications · 2025Article
- Programmable Nanostructure Assembly of a Paclitaxel Derivative Enables Tunable Anticancer Therapy via Hydrogen Bond Engineering.ACS nano · 2025Article
- Crafting defects in two-dimensional organic platelets via seeded coassembly enables emergent molecular recognition.Nature communications · 2025Article
- Self-Assembly of the Block Copolymer Containing Discotic Mesogens Driven by Liquid Crystalline Ordering Effect.Polymers · 2024Article
- Semiaromatic Polyester-Ethers with Tunable Degradation Profiles.ACS macro letters · 2024Article
- Antibacterial Nanoplatelets via Crystallization-Driven Self-Assembly of Poly(l-lactide)-Based Block Copolymers.Biomacromolecules · 2024Article
- Concentric hollow multi-hexagonal platelets from a small molecule.Nature communications · 2024Article
- Enhancing the Scalability of Crystallization-Driven Self-Assembly Using Flow Reactors.ACS macro letters · 2023Article
Corrections and comments
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Authors and funding
7 authors at 3 institutions in 3 countries.
Funding
Abstract
The creation of nanoparticles with controlled and uniform dimensions and spatially defined functionality is a key challenge. The recently developed living crystallization-driven self-assembly (CDSA) method has emerged as a promising route to one-dimensional (1D) and 2D core-shell micellar assemblies by seeded growth of polymeric and molecular amphiphiles. However, the general limitation of the epitaxial growth process to a single core-forming chemistry is an important obstacle to the creation of complex nanoparticles with segmented cores of spatially varied composition that can be subsequently exploited in selective transformations or responses to external stimuli. Here we report the successful use of a seeded growth approach that operates for a variety of different crystallizable polylactone homopolymer/block copolymer blend combinations to access 2D platelet micelles with compositionally distinct segmented cores. To illustrate the utility of controlling internal core chemistry, we demonstrate spatially selective hydrolytic degradation of the 2D platelets-a result that may be of interest for the design of complex stimuli-responsive particles for programmed-release and cargo-delivery applications.
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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.