Novel formulation of dehydrated lipid vesicles for controlled release of active pharmaceutical ingredient via inhalation
A pharmaceutically active, lipid-based technology for the treatment of asthma and other conditions
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[0272] It has been found according to the present invention that when a high percentage of vesicle protector stabilizers and / or plasticizers are contained in liposomes, said vesicle protector stabilizers and / or plasticizers such as glycerol and fatty acid sucrose esters, which The molar percentage is generally between 0.1% and 40%. During or after freeze-drying or spray-drying and rehydration process, albuterol or other pharmaceutical active ingredients can successfully maintain the shape of lipid vesicles and remain in liposome vesicles. Medium delayed release.
[0273] According to the present invention, it is also found that the pharmaceutically active ingredient / lipid / stabilizer and / or plasticizer composition of the present invention has many improved properties, such as less leakage of the pharmaceutically active ingredient from liposomal vesicles, lower drug The toxicity and side effects of the drug can be controlled, the solubility and encapsulation rate of the drug can...
Embodiment 1
[0305] Aqueous multilamellar vesicles (MLVs) were prepared by conventional lipid membrane hydration methods, and small unilamellar vesicles (SUVs) were subsequently produced by extrusion. Lipids and albuterol were dissolved in chloroform and methanol, respectively, and the solutions were mixed with lipids and albuterol at the indicated molar ratios. The mixture was dried under a nitrogen stream to form a uniform lipid film, and then placed under vacuum overnight to remove residual organic solvents. The lipid film was hydrated in 10 mM Tris-isotonic saline buffer (10 mM Tris, 137 mM NaCl, and pH 7.4 at 25°C). The final concentration of lipid was controlled at 5-20mg / ml. The mixture was then kept at 80°C (above the transition temperature of all lipids) for 60 minutes to allow the liposomal structure to solidify. During curing, it was vortexed 3 times at the beginning, middle and end time points respectively and the stirring was continued for 5 minutes each time. The obtained ...
Embodiment 2
[0312] A mixture of part of DOPC or DOTAP and the active ingredient (albuterol, 0.04mmol) in a molar ratio of 1:2 was dissolved in 4ml of ethanol. Salbutamol liposome dispersions were formed by injecting the lipid / pharmaceutical active ingredient / ethanol solution into 50 ml of pH 7.4 phosphate buffer. Liposomes were extruded through 0.4 or 0.2 μm polycarbonate membranes to form liposome vesicles with uniform size distribution.
[0313] Determination of Encapsulation Efficiency
[0314] 150 μL of freshly prepared liposome samples were centrifuged with an AvantiJ-E centrifuge (JA-20, 17400×g, 6° C., and 20 min) through a MicroconY-10 centrifugal filter device (Millipore) with a molecular weight cut-off of 10 KD. The albuterol concentration in the centrifuged solution was determined spectrophotometrically at 276 nm. This concentration represents the albuterol concentration in the continuous phase of the liposomes (non-encapsulated albuterol). Spectrophotometry was also used to...
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