Anionic Liposomes
Doxorubicin Liposomal
Immunoliposomes
Materials for liposomes
- Bacterial Lipids
- Bile Acids
- Bioactive Lipids
- Cationic Lipid Material
- Detergents
- Fatty Acid Modified Lipids
- Fluorescent Lipids
- GalNac Delivery System Lipids
- Headgroup Modified Lipids
- Neutral Lipids
- PEGylated Lipids
- Phosphatidic Acid (PA)
- Phosphatidylcholine (PC)
- Phosphatidylethanolamine (PE)
- Phosphatidylglycerol (PG)
- Phosphatidylserine (PS)
- Phospholipids
- Photoswitchable Lipids
- Sphingolipids
- Sterols
Nano-Liposomes
Clodronate Liposomes
ATP-Liposome
Cationic Liposomes
Liposomes for DNA/RNA Delivery
Get Quote
Online InquiryNano-Liposomes
Online InquiryBOC Sciences offers various types of liposome-based nano-gene vectors for our customers. All liposomes are prepared under sterile conditions.
IntroductionLiposomes Composition and Characterization
Liposomes were discovered in 1965 by Alec D Bangham when he observed phospholipids dissolved in water using electron microscopy. In 1968, the term "liposome" was formally proposed by Sessa. As a representative carrier, liposomes are widely used in the field of pharmacy, physics, chemistry, etc.
Liposomes are artificial membranes with a thickness of 5-7 nm and a diameter of 25-500 nm. When phospholipids are dissolved in water at high temperatures, hydrophobic tails converge and reach the air while hydrophilic heads merge with the aqueous phase. After stirring, closed vesicles with a bilayer structure are formed. Inside the vesicle, drugs with different polarities can be encapsulated, thus facilitating the penetration of polar macromolecules into the membrane. Furthermore, bilayer materials for liposome preparation can be either bilayer phospholipids spontaneously assembled in water or bilayer phospholipids formed after mixing and stirring. These phospholipids are usually categorized as Phosphatidylcholine(PC) and Phosphatidylethanolamines(PE). Currently, the most frequently used phospholipids for liposome preparation are lecithin and cholesterol.
Liposomes contain excellent properties, including:
- Well histocompatibility
- High cellular affinity
- Fast and convenient drug delivery route
- Capable of existing for an extended period around target cells
- High transdermal absorption efficiency
- Reduced drug toxicity
- Improved drug stabilization
Fig. 1 Schematic structure of liposome (Mohanta B C, 2019)
Nano-liposome Carriers
The nano-liposomal vector is a novel and effective gene delivery system where liposomes can carry plasmid DNA when combined with nanomaterials. The principle of action is that amino groups affected by pH in the molecular structure can neutralize negative charges of DNA and form a relatively small plasmid DNA. Thus, nano-liposome materials encapsulate DNA to avoid nuclease degradation.
Examples of nano-liposome carriers:
- Magnetic Liposomes
- Liposomal-gold Nanoparticles
- Quantum Dot Nano-liposomes
- Chitosan Nano-liposomes
- Upconversion Nano-liposomes
- Graphene Nano-liposomes
Advantages of Nano-liposome Carriers
- Good biocompatibility
- Improved therapeutic gene's efficiency in reaching target sites
- Reduced non-specific diffusion in normal organs
- Easy to rationalize modifications
Strategies to Enhance Transfection Efficiency of Nano-liposome Composites
- Trimming multicomponent nanomaterials to reduce particle sizes
- Modifying nano-liposome composite surfaces with targeted ligands to enhance target recognition
References
- Mohanta B C; et al. Lipid Based Nanoparticles: Current Strategies for Brain Tumor Targeting. 2019.
- Eskandari, V.; et al. Physical and chemical properties of nano-liposome, application in nano medicine. Journal of Computational Applied Mechanics, 52(4), pp. 751-767.