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SELECTBIO Conferences Nanomedicine & LNPs Asia 2026

Nanomedicine & LNPs Asia 2026 Agenda



Co-Located Conference Agendas

Nanomedicine & LNPs Asia 2026 | Organoids & Organs-on-Chips Asia 2026 | 

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Saturday, 21 November 2026

08:00

Conference Registration, Materials Pick-Up, Coffee, Tea and Networking

09:00

Nan ZhangConference Chair

Welcome and Introduction by Conference Co-Chairperson
Nan Zhang, Associate Professor, University College Dublin, Ireland

09:10

Liang  ZhaoConference Chair

Welcome and Introduction by Conference Co-Chairperson
Liang Zhao, Associate Professor, Beijing University of Technology, China


Session Title: Conference Opening Plenary Session

09:20

Chwee Teck LimPlenary Presentation

Presentation Details to be Confirmed.
Chwee Teck Lim, NUS Society Chair Professor, Department of Biomedical Engineering, Institute for Health Innovation & Technology (iHealthtech), Mechanobiology Institute, National University of Singapore, Singapore

09:50

Yoon-Kyoung ChoPlenary Presentation

Engineering Liquid Biopsy: From Automated Exosome Analysis to Hand-Powered Point-of-Care Diagnostics
Yoon-Kyoung Cho, Professor, Biomedical Engineering and Dean, UNIST (Ulsan National Institute of Science & Technology), Korea South

Liquid biopsy is transforming precision medicine by enabling minimally invasive access to circulating biomarkers for disease detection and monitoring. Among these biomarkers, extracellular vesicles (EVs) offer exceptional promise due to their molecular richness and stability. However, widespread clinical and global deployment of liquid biopsy technologies remains limited by challenges in sensitivity, automation, cost, and accessibility.

In this talk, I will present our engineering approach based on centrifugal microfluidics to address these challenges across diverse clinical settings, spanning fully automated laboratory systems to hand-powered point-of-care diagnostics. First, I will describe our lab-on-a-disc platforms for high-performance EV analysis, which enable rapid and automated isolation of nanoscale EVs from biological fluids. Building on this foundation, I will introduce a digital EV profiling strategy that allows direct, amplification-free detection of tumor-derived EV RNAs from unprocessed plasma, substantially improving sensitivity for clinically relevant mutations and treatment monitoring. I will then expand beyond centralized laboratories to introduce hand-powered centrifugal diagnostic tools designed for extreme point-of-care environments. These platforms harness manual rotation to perform bacterial enrichment and nanoplasmonic sensing, enabling rapid, electricity-free identification of infectious pathogens with high precision. Together, these technologies illustrate how microfluidic engineering can unify advanced molecular diagnostics with scalable, low-cost solutions, accelerating the translation of liquid biopsy and precision diagnostics from the laboratory to real-world clinical and global health applications.

10:20

Noo Li JeonPlenary Presentation

High-Throughput Reproducible Organ-on-a-Chip Platform: A New Strategy for Drug Validation
Noo Li Jeon, Professor, Seoul National University, Korea South

Accurate prediction of human drug responses during the preclinical stage is essential for successful drug development, yet conventional 2D cultures and animal models often fail to mimic complex human physiology. This seminar introduces an advanced Organ-on-a-Chip (OoC) platform designed to provide a robust validation stage for the drug discovery pipeline.

Our system moves beyond laboratory-scale research by establishing mass-production processes and high experimental reproducibility suitable for the biotech industry. By co-culturing patient-derived 3D tumor spheroids with cancer-associated fibroblasts (CAFs), we have precisely recapitulated the dense stroma and vascular microenvironments of solid tumors.

This platform allows for the evaluation of how small-molecule therapies and large biologics, as well as such as Antibody-Drug Conjugates (ADCs), penetrate the tumor microenvironment. We will present data on patient-specific efficacy and vascular toxicity resulting from endothelial barrier disruption. By combining highly reproducible chip design with sophisticated tumor modeling, this translational research platform significantly enhances clinical predictability and overcomes the limitations of traditional preclinical models.

10:50

Mid-Morning Coffee and Tea Break -- Visit Exhibitors and View Posters

11:30

Lorena DiéguezPlenary Presentation

Presentation Details to be Confirmed.
Lorena Diéguez, Leader of the Medical Devices Research Group, INL- International Iberian Nanotechnology Laboratory, Portugal

12:00

Lining (Arnold) JuConference Chair

Personalized 3D Vessel-on-a-Chip and Digital Twins for Thrombotic Risk Assessment and Drug Screening
Lining (Arnold) Ju, Professor and Snow Fellow, School of Biomedical Engineering, The University of Sydney, Australia

This presentation will introduce state-of-the-art 3D microvessel-on-a-chip platforms designed to recapitulate patient-specific vascular anatomies. By integrating microfluidics, hydrogels, and 3D bioprinting, our laboratory has developed "Physical Twins" that model complex hemodynamic flow disturbances and biomechanical thrombosis. Combined with AI-driven "Digital Twins" mapped from clinical CT angiography, this advanced organ-on-a-chip technology enables the personalized assessment of stroke risk, high-throughput antithrombotic drug screening, and the translation of mechanobiology insights into rapid point-of-care diagnostics.

12:30

Chenzhong LiPlenary Presentation

Presentation Details to be Confirmed.
Chenzhong Li, X.Q. Deng Presidential Chair Professor, The Chinese University of Hong Kong, Shenzhen, China

13:00

Networking Buffet Lunch in the Hotel Restaurant -- Network and Engage over Lunch

14:00

Bacterial Membrane Vesicles-Inspired Antimicrobial Drug Delivery Systems and Vaccines
Xin Ding, Professor, Sun Yat-sen University, China

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