Lipid-based multi-compartment drug delivery systems have gained
significant attention due to their ability to enhance drug solubility, improve
bioavailability, and enable controlled release. These systems are particularly
useful for delivering hydrophobic drugs, biologics, and gene therapies,
providing a versatile platform for targeted and sustained drug delivery. Analytical
modeling of such systems is crucial for optimizing their design, predicting
drug release kinetics, and ensuring efficacy and safety.
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