Publications by authors named "Xingjin Li"

Directly assembling drugs into mesoporous nanoformulations will be greatly favored due to the combination of enhanced drug delivery efficiency and mesostructure-enabled nanobio interactions. However, such an approach is hindered due to the lack of understanding of polymer nanoparticles' formation mechanism, especially the relationship between polymerization, self-assembly, and the nucleation process. Here, by investigating the levodopa and dopamine polymerization process, we identify π-cation interaction as pivotal in the self-assembly and nucleation control of dopa molecules.

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Article Synopsis
  • Microemulsion systems can create nano/microstructures, but there's a lack of understanding in controlling how these structures form at the interface.
  • The researchers propose a new method called nucleation-inhibited microemulsion interfacial assembly to create polydopamine microvesicles (PDA MVs), which resemble cell shapes and are about 1 µm in size.
  • When modified with antibodies, these PDA MVs significantly boost T-cell activation compared to solid nanoparticles, demonstrating their potential as effective artificial antigen-presenting cells.
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One-dimensional (1D) nanomaterials have sparked widespread research interest owing to their fascinating physicochemical properties, however, the direct self-assembly of 1D porous nanomaterials and control over their porosity still presents a grand challenge. Herein, we report a monomicelle oriented self-assembly approach to fabricate 1D mesoporous nanostructures with uniform diameter, high aspect ratio and ordered mesostructure. This strategy features the introduction of hexamethylenetetramine as a curing agent, which can subtly control the monomicelle self-assembly kinetics, thus enabling formation of high-quality 1D ordered mesostructures.

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Although recent studies have reported that long non-coding RNA (lncRNA) is involved in the development of ischemic acute kidney injury (AKI), the exact function and regulatory mechanism of lncRNAs in ischemic AKI remain largely unknown. Herein, we found that ischemic injury promoted the expression of lncRNA 148400 in mouse proximal tubule-derived cell line (BUMPT) and C57BL/6J mice. Furthermore, the lncRNA148400 mediates ischemic injury-induced apoptosis of BUMPT cells.

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The optical properties of cost-effective Ag-Cu bimetallic nanocrystals, with synergistically enhanced catalytic and biological activities, are limited within ultraviolet-visible region due to lack of morphology control. In order to overcome this constraint, two-dimensional (2D) Ag-Cu bimetallic heterostructures were designed and synthesized by a seed-mediated colloidal growth method. The conformal Cu domain was epitaxially deposited on Ag nanoplates with different spatial configuration under retention of their 2D shape.

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Synopsis of recent research by authors named "Xingjin Li"

  • - Xingjin Li's recent research primarily focuses on the development of novel nanostructures for drug delivery and biomedical applications, emphasizing the importance of controlled self-assembly techniques to enhance efficiency and efficacy.
  • - Key findings include the identification of cation-π interactions in mesoporous levodopa formulations to improve drug assembly for Parkinson's treatment, and the innovative use of nucleation-inhibited emulsion methods to create polydopamine microvesicles that mimic cellular characteristics.
  • - Additionally, Li's studies explore the synthesis of one-dimensional porous nanostructures with tailored mesophases and the role of long non-coding RNAs in ischemic acute kidney injury, highlighting the interplay between material science and biological mechanisms.