Creative Biolabs-Lipid Based Drug Delivery

Virosomes

Introduction Virosomes-based Drug Delivery

As a leader in the field of targeted delivery system research and development, Creative Biolabs is committed to providing the most comprehensive liposome development services for our global clients. Creative Biolabs has accumulated abundant experience in the successful completion of many targeted delivery system-related projects.

Introduction

Virosomes are a type of reconstituted viral envelopes composed of membrane lipids and viral spike glycoproteins, which avoid viral genetic material. Virosomal technology has been used in vaccines delivery successfully for many years. Influenza virus is most widely used for virosome production. They are spherical, unilamellar vesicle structure with a mean diameter of 150 nm. Virosomes are not able to replicate but are pure fusion-active vesicles. Virosomes contain functional viral envelope glycoproteins compared with liposomes, i.e. influenza virus hemagglutinin (HA) and neuraminidase (NA) intercalated in the phospholipid bilayer membrane. Different bilayer components of virosomes possess distinct characteristics.

Fig.1 Composition of a virosome derived from virus. (Creative Biolabs Original)Fig.1 Composition of a virosome derived from virus.

Virosomes-based Drug Delivery

The virosome presents one of the optimal drug delivery systems and it can be optimized for maximum incorporation of the drug or the best physiological effect by modifying the content or type of lipids in the membrane. On the surface of the virosomes, a variety of ligands like cytokines, peptides and monoclonal antibodies can be adopted. Besides, tumor-specific monoclonal antibody fragments (Fab) also can be linked to virosomes for targeting the carrier to selected tumor cells. For the targeted delivery of the encapsulated drugs, virosomes selectively recognize through binding molecules to the target cell. Virosomal HA induces receptor-mediated uptake of the virosome into an endosome in the target cell. The endolysosomal pathway can protect the drug from degradation because the drugs are transported directly into the cytosol of the cell. This feature of virosomes is especially critical for cancer therapies, which often have severe side effects because of the toxicity of the agents. The mechanism of protection of incorporated pharmaceutically active substances is a major advantage of the virosomal carrier system and is clearly distinct from other liposomal and proteoliposomal carrier systems.

Fig.2 Mechanism of drug delivery to the target cell using virosome technology. (Creative Biolabs Original)Fig.2 Mechanism of drug delivery to the target cell using virosome technology.

Virosomes represent an innovative, broadly applicable drug carrier systems that have been applied commonly in various treatments and preventions of cancer, neurodegenerative disorders and infectious diseases. To date, a large number of pharmaceutically active substances like antibiotics, cytostatics, nucleic acids, fungicides and antigens can be encapsulated into the virosomal carrier.

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For Research Use Only. Not For Clinical Use

Supports

Formulation Science Background of Liposome Research Highlights
Resources Technical Supports Featured Services Knowledge Center
Optimizing LNP Molar Ratios for Transfection Efficiency
Scalability Challenges in mRNA-LNP Manufacturing
Beyond mRNA: LNP Delivery for CRISPR/Cas9
Cationic Lipids Evolution: DOTAP to Ionizable Lipids
LNP Storage Stability: Lyophilization vs. Liquid
Modulating LNP Biodistribution: Overcoming Liver Accumulation
Active vs. Passive Targeting (EPR): A Guide to Tumor Drug Delivery
Immunoliposomes: Comparing Pre-insertion vs. Post-insertion Techniques
Crossing the BBB: Advances in Transferrin and Peptide-Modified Liposomes
pH-Responsive Liposomes for Tumor Microenvironment
Thermosensitive Liposomes combined with HIFU
Aptamer-Modified Liposomes: A Cost-Effective Antibody Alternative
Ethosomes vs Transfersomes for Dermal Delivery
Strategies for Encapsulating Poorly Water-Soluble Small Molecules in Liposomes
Multivesicular Liposomes: The Architecture of Sustained Release
Mechanisms of Liposomal Adjuvants in Enhancing Vaccine Immune Response
Protecting Enzymatic Activity: Liposomal Encapsulation Strategies for Enzymes
Cryo-TEM vs. DLS: Interpreting Discrepancies in Liposome Particle Size Data
Validating In Vitro Release Methods: Dialysis vs. Sample Separation Techniques
Predicting Long-Term Stability of Liposomal Suspensions using Zeta Potential
Troubleshooting Low Liposome Encapsulation Efficiency
Application of Multi-omics Analysis in Liposome Toxicology Assessment
The Ultimate Guide to Liposome Preparation
Fluorescent Liposomes for Cellular Uptake: Labeling, Controls, and Troubleshooting
How to Design Stealth Liposomes for Long Circulation
Homemade vs. Commercial Kits: Why Standardization Matters in Liposome Research

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