Abstract

Although the origin of disease and drug targets are primarily at intracellular space, such targeting is not achievable in currently available drugs. We and others recently show that molecular drugs can be transformed into nanodrug for better subcellular targeting with the enhanced therapeutic performance. This can be achieved via appropriate size and surface chemistry of colloidal nanodrug to control or bypass the endocytic uptake and intracellular trafficking processes. This approach can be adapted for enhanced drug performance with lower side effects.

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