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Verified CAS / Academic Author3 Decoded Studies

Prof. BAO Yan

Sun Yat-sen University

Research Publications & English Decoded Briefs

Showing 3 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3873-7

Multifunctional Melamine Foam Composites Featuring Asymmetric Conductive Networks for Highly Absorptive EMI Shielding and Infrared Stealth

The escalating demand for lightweight, multifunctional stealth materials in modern protective applications necessitates integrated solutions against electromagnetic interference (EMI), infrared (IR) detection, and incendiary threats. This study presents an innovative melamine foam (MF)-based composite featuring an asymmetric dual-nano conductive network, achieving absorption-dominated EMI shielding, IR stealth, and flame retardancy. Inspired by the Salisbury screen, the composite employs MF as an interlayer and flame-retardant thermoplastic polyurethane (TPU) nanofiber membrane as a substrate. The architecture comprises a carbon nanotubes (CNTs)-modified impedance matching nanofiber layer as the top absorber and a silver nanoparticles (AgNPs)-modified nanofiber layer as the highly conductive reflective bottom. Precise control of CNTs content and interlayer thickness enables tunable electromagnetic wave (EMW) absorption, yielding a low reflection coefficient of 0.03 and a high EMI shielding effectiveness of 79.23 dB at a total thickness of 4.40 mm. Even at 1.40 mm, effective absorption-dominated shielding is maintained. The performance remains stable under ultrasonic, compression, and bending tests, demonstrating high durability. The mechanism underlying absorption-dominated EMI shielding at reduced thickness, relying on destructive interference of EMWs enabled by the asymmetric dual-nano conductive network, is thoroughly elucidated. Additionally, the composite exhibits superior IR stealth and self-extinguishing properties. This work offers a feasible strategy for designing high-performance stealth materials with strong potential for personnel and communication equipment protection.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3360-x

A conjugate strategy capable of targeting bacteria and selectively being activated at infection sites

The clinical utility of colistin, a last-resort antibiotic against multidrug-resistant Gram-negative pathogens, is severely constrained by dose-limiting nephrotoxicity (up to 60% incidence) and poor infection-site targeting. Existing prodrug approaches, such as colistin methanesulfonate, rely on slow, non-selective hydrolysis that reduces systemic toxicity but also diminishes antibacterial efficacy at the infection foci. Here we report a conjugate strategy that combines infection-activatable release with bacterial targeting. A series of colistin prodrugs were synthesized by attaching a reactive oxygen species (ROS)-responsive phenylboronic acid linker to all primary amines of colistin, followed by covalent conjugation to sugars via boronic acid–diol complexation. The lead candidate, lactosyl-functionalized colistin prodrug (LaP-Col), exhibited minimal toxicity toward normal tissues and actively targeted bacteria. LaP-Col displayed a maximum tolerated dose exceeding that of colistin by more than 20-fold and minimal nephrotoxicity. In a murine model of Pseudomonas aeruginosa pneumonia, intravenous LaP-Col accumulated in infected lungs, effectively killed bacteria, and significantly improved therapeutic efficacy and survival rates. This prodrug architecture offers a generalizable route to mitigate the inherent toxicity of potent antimicrobial peptides while enhancing site-specific targeting.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3475-2

Second-generation rotaxane ion transporters: boosting transport activity via enhanced transport flux across lipid bilayers

Rotaxane-based synthetic ion transporters have demonstrated potential in mimicking natural transmembrane machinery, yet first-generation systems suffer from low transport activity, with EC50 values in the micromolar range. This study reports a second-generation rotaxane transporter design that addresses this limitation by modifying the ring component to a tricyclic architecture (TCE) incorporating two K+ recognition sites. The TCE ring enables the transport of two K+ ions per shuttle cycle, resulting in a tenfold reduction in EC50 compared to first-generation transporters that possess only one K+ recognition site. Further implementation of a cooperative shuttle-relay mechanism, using [3]R-TCE2 where two rings traverse the thread within the lipid membrane, achieved an EC50 value as low as 60 nM (0.18 mol% relative to lipid). This represents one of the highest K+ transport activities reported for molecular machine-based transporters. The findings provide a robust technical foundation for mimicking natural channel functions and support potential biomedical applications, including therapeutic agents and biosensing platforms.