Crosslinked polymer nano-assemblies and uses thereof
The invention provides a novel system of nano-assemblies and related method for delivery of therapeutic, diagnostic or imaging agent to biological sites. The compositions and methods of the invention enable the syntheses of novel polymeric nano-assemblies (nanoparticles) under non-emulsion conditions with the incorporation of hydrophobic guest molecules. The versatilities and advantages of the polymer nanoparticles of the invention include: (i) the guest molecules (e.g., drug molecules) can be readily incorporated non-covalently within the nanoparticles; (ii) the surface of the nanoparticles are functionalizable; (iii) the non-covalently encapsulated guest molecule (payload) can be released in response to a biologically relevant stimulus at the target site; (iv) the payload is held by the polymeric nanoparticle before being internalized in cells and can be released within the cellular interiors; (v) encapsulating lipophilic small molecules within its crosslinked interiors and binding proteins on its surface through electrostatic interactions; (vi) facile synthetic methods for ligand functionalization that can be utilized to decorate nanogels with cell targeting ligands that facilitate receptor-dependent cellular uptake, and (vii) the payload release kinetics is tunable and controllable.
1. A nano-assembly for controlled delivery of a therapeutic or diagnostic agent to a biological site, comprising:
a water-soluble polymer host comprising a crosslinked network of a random co-polymer having the structural formula:
wherein
p is an integer from about 1 to about 20,
the co-polymer has a molecular weight from about 1,000 to about 100,000,
the ratio of i:j is in the range from about 2:8 to about 8:2, and from about 1% to about 95% of j is substituted by k,
a guest molecule comprising a therapeutic, diagnostic, or imaging agent non-covalently associated with the polymer host, wherein the therapeutic or diagnostic agent is releasable upon partial or complete de-crosslinking of the crosslinked network of polymer molecules at or near the biological site, and
a targeting moiety selected from an antibody, an aptamer, a peptide, and a small molecule ligand, covalently linked to or non-covalently associated with the polymer host.
2. The nano-assembly of claim 1 , wherein the crosslinked network of polymer molecules is crosslinked both inter-molecularly and intra-molecularly.
3. The nano-assembly of claim 1 , wherein the de-crosslinking of the crosslinked polymer molecules is due to a biological or chemical stimulus at the biological site.
4. The nano-assembly of claim 3 , wherein the stimulus is a pH value at the biological site.
5. The nano-assembly of claim 1 , wherein the stimulus is induced by an external light signal.
6. The nano-assembly of claim 1 , wherein the loading weight percentage of the guest molecule is from about 2% to about 70%.
7. The nano-assembly of claim 6 , wherein the crosslinked network of polymer molecules have a crosslinking density from about 5% to about 60%, relative to the total number of structural units in the polymer.