Dr. Xin Ding, Professor at Sun Yat-sen University School of Medicine (Assistant Dean), is a Global Top 2% Scientist (Stanford, 2025) and Guangdong (China) Youth Top Talent. His research focused on nanomedicine against drug-resistant infections, developing breakthrough technologies: Bacterial membrane vesicles-inspired targeted nanovesicles (Sci. Adv. 2024) & hybrid nanovaccines (J. Extracell. Vesicles 2024) overcoming Gram-negative barriers; Resistance-reversing nanocomplexes restoring colistin efficacy (ACS Nano 2023); Smart ROS nanogenerators eradicating H. pylori while preserving microbiome (Adv. Sci. 2023). He has published >30 publications (corresponding/first author) and 10+ patents. He is an award-winning educator, he guided students to win National Gold Medal (11th Medical Innovation Competition, Best Academic Award, Top 10 nationally).
Bacterial Membrane Vesicles-Inspired Antimicrobial Drug Delivery Systems and Vaccines
Saturday, 21 November 2026 at 14:00
Add to Calendar ▼2026-11-21 14:00:002026-11-21 15:00:00Europe/LondonBacterial Membrane Vesicles-Inspired Antimicrobial Drug Delivery Systems and VaccinesNanomedicine and LNPs Asia 2026 in Shenzhen, ChinaShenzhen, ChinaSELECTBIOenquiries@selectbiosciences.com
Multidrug-resistant bacterial infections pose a critical threat to global health, demanding innovative antimicrobial strategies. Biological barriers – including biofilms and the dual-membrane architecture of Gram-negative bacteria – fundamentally limit intracellular drug delivery. Capitalizing on the innate cell-penetrating capacity of outer membrane vesicles (OMVs), we engineered three targeted therapeutic platforms: 1. OMV-based antimicrobial delivery systems that efficiently transport repurposed rifampicin to homologous Gram-negative pathogens, establishing a novel drug rediscovery paradigm; 2. Hybrid membrane vesicles (HMVs) integrating neutrophil membranes with OMVs to simultaneously neutralize LPS toxicity and confer infection microenvironment-targeting capability, achieving dual-pathogen eradication in systemic and pulmonary infections; 3. Multiantigenic nanovaccines fabricated by fusing OMVs with bacterial antigen-adsorbed macrophage membranes, which eliminate pathogens through direct bacteriolysis and toxin neutralization, yielding 100% survival in sepsis models and >99.9% bacterial clearance in pneumonia. Collectively, our engineered vesicle platforms overcome fundamental delivery barriers, transforming OMVs from biological components into robust therapeutic pipelines against intractable Gram-negative infections.
Add to Calendar ▼2026-11-21 00:00:002026-11-22 00:00:00Europe/LondonNanomedicine and LNPs Asia 2026Nanomedicine and LNPs Asia 2026 in Shenzhen, ChinaShenzhen, ChinaSELECTBIOenquiries@selectbiosciences.com