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Liposomes for Loading Hydrophobic Drugs
Liposomes for Loading Hydrophobic Drugs
Catalog # | Pkg Size | Price(USD) | Quantity | Buy this product |
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R-R-5668 | 5ml | 340.00 | + Add to cart |
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R-R-5668 | 10ml | 600.00 | + Add to cart |
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Product description
Liposomes for Loading Hydrophobic Drugs (5.0mL). This pre-formed liposome product is created for post loading of hydrophobic small molecule compounds into liposomes. The process of drug incorporation is very straight-forward. Then simply add an aliquot of drug solution (prepared in a water-miscible solvent such as ethanol, DMSO and etc.) into the liposome suspension. The drug molecules can be incorporated into the lipid bilayers by the nature of hydrophobic interactions. The drug solubility therefore could be significantly enhanced. Liposomal drug concentration of 1-2 mg/mL could be achieved for most lipophilic drugs. PEGylation of the liposomes provides not only better formulation stability but also the potential of achieving prolonged in vivo blood circulation. The finished drug loaded formulations are suitable for either in vitro testing or in vivo studies.
Appearance | N/A |
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Total lipid content | 220 mgs in 5 mL |
Lipid concentration | 50mM |
Mean particle size | 100 nm (90-120 nm) |
Buffer solution | PBS pH 7.0 – 7.4 (phosphate buffered saline) |
Storage | 2-8 °C |
Transportation | 4-25℃ temperature for up to 2 weeks |
Stability | 6 months |
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