Customizable
Our nanoparticles are engineered for modularity, allowing precise adaptation to various payloads, whether you are delivering nucleic acids, proteins, or gene-editing tools. This flexibility ensures compatibility with diverse therapeutic strategies.
Delivering Diverse Genetic Tools
From pDNA and mRNA to siRNA and CRISPR components, our carriers are optimized to transport a wide spectrum of genetic materials, supporting cutting-edge applications in gene and cell therapy.
Enhanced Targeting Capacity
Using advanced surface chemistry and functionalization techniques, our systems can home in on specific cell types or tissues, reducing systemic side effects and increasing therapeutic efficacy.
Low Immunogenicity
Built from biocompatible materials and designed to avoid triggering immune reactions, our nanoparticles prioritize patient safety, especially in repeat dosing scenarios.
Cost-effective Scale-up
Our platforms offer scalable manufacturing techniques, enabling a seamless transition from research to commercial production without compromising quality or performance.
Stable and Shelf-Ready Formulations
Our nanoparticles offer excellent physicochemical stability, enabling longer shelf life and simplified storage requirements, crucial for global distribution and real-world clinical deployment.