Crosslinked polymer nano-assemblies and uses thereof

Patent metadata

Field	Value
Publication number	US-9795689-B2
Application number	US-201314421882-A
Country	US
Kind code	B2
Filing date	Sep 10, 2013
Priority date	Sep 11, 2012
Publication date	Oct 24, 2017
Grant date	Oct 24, 2017

Abstract

The invention provides powerful methods and compositions for designing, selecting, fine-tuning and optimizing polymer nanogel and other supramolecular assemblies for various properties including, for example, particle size, density and morphology, guest loading capacity and encapsulation stability, and dynamic release control.

First claim

The invention claimed is:

1. A method for modifying the release rate of an encapsulated guest in a polymer nanogel host, comprising preparing the polymer nanogel host in an aqueous environment having a kosmotropic or chaotropic agent, wherein the kosmotropic or chaotropic agent is present at a concentration suitable for achieving the desired guest release rate,
wherein the polymer nanogel host comprises a block co-polymer having the structural formula:

wherein
each of R 1 , R′ 1 and R″ 1 is independently a hydrogen, C 1 -C 12 alkyl group, or halogen;
each of R 2 , R′ 2 , R″ 2 , R 3 , R′ 3 and R″ 3 is independently a hydrogen, (C 1 -C 16 ) alkyl, (C 1 -C 16 ) alkyloxy, or halogen;
each of L 1 , L 2 and L 3 is independently a linking group;
each of S 1 , S 2 and S 3 is independently a single bond or a spacer group;
W is a hydrophilic group;
X is a group comprising a crosslinking moiety;
Y is a hydrophobic group; and
each of i, j and k is independently a positive number.

2. The method of claim 1 , comprising preparing the polymer nanogel in an aqueous environment having a kosmotropic agent.

3. The method of claim 1 , comprising preparing the polymer nanogel in an aqueous environment having a chaotropic agent.

4. The method of claim 2 , wherein the kosmotropic agent is selected from the group consisting of sulfate (SO 4 2− ), phosphate (PO 4 3− ), hydrogenphosphates (HPO 4 2− ), hydroxide (OH − ), magnesium (Mg 2+ ), calcium (Ca 2+ ), sodium (Na + ), lithium (Li + ), proton (H + ), trialkylamine oxide (R 3 N + O − ), proline, ectoine, glycine betaine, and trehalose.

5. The method of claim 4 , wherein the kosmotropic agent is a sulfate (SO 4 2− ).

6. The method of claim 3 , wherein the chaotropic agent is selected from the group consisting of thiocyanates (SCN − ), dihydrogenphosphates (H 2 PO 4 − ), bisulfates (HSO 4 − ), bicarbonates (HCO 3 − ), iodides (I − ), bromides (Br − ), chlorides (Cl − ), nitrates (NO 3 − ), ammonium (NH 4 + ), cesium (Cs + ), potassium (K + ), guanidinium ((NH 2 ) 3 C + ), tetraalkylammonium (R 4 N + ), and urea.

7. The method of claim 6 , wherein the chaotropic agent is a thiocyanate (SCN − ).

8. The method of claim 2 , wherein the kosmotropic agent is present at a concentration from about 1 mM to about 5 M.

9. The method of claim 3 , wherein the chaotropic agent is present at a concentration from about 1 mM to about 5 M.

10. The method of claim 1 , wherein the polymer nanogel comprises a crosslinked network of polymer molecules and non-covalently encapsulated therein a guest releasable upon partial or complete de-crosslinking of the crosslinked network of polymer molecules.

11. The method of claim 1 , wherein each of R 2 , R′ 2 , R″ 2 , R 3 , R′ 3 and R″ 3 is a hydrogen, and each of R 1 , R′ 1 and R″ 1 is a methyl group.

12. The method of claim 11 , wherein each of L 1 , L 2 and L 3 is

13. The method of claim 11 , wherein W comprises a charged group and/or a zwitterionic group.

14. The method of claim 12 , wherein W comprises

wherein p is an integer from about 1 to about 40.

15. The method of claim 12 , wherein Y comprises a hydrocarbon chain.

16. The method of claim 15 , wherein X comprises a disulfide moiety, an acetal moiety and/or an enzyme-sensitive linker.

17. The method of claim 16 , wherein X comprises a disulfide moiety.

18. The method of claim 16 , wherein X comprises an acetal moiety.

19. The method of claim 16 , wherein X comprises an enzyme-sensitive linker.

Assignees

• Univ Massachusetts

Inventors

• Thayumanavan Sankaran

Classifications

• A61P25/04

  Centrally acting analgesics, e.g. opioids · CPC title

• C08L33/14

  of esters containing halogen, nitrogen, sulfur, or oxygen atoms in addition to the carboxy oxygen · CPC title

• C08F8/12

  Hydrolysis · CPC title

• A61K47/42

  Proteins; Polypeptides; Degradation products thereof; Derivatives thereof, e.g. albumin, gelatin or zein (oligopeptides having up to five amino acids {A61K47/183}; polyamino acids A61K47/34) · CPC title

• C08F8/44

  Preparation of metal salts or ammonium salts · CPC title