Claims for Patent: 8,609,142

Summary for Patent: 8,609,142

Title:	Drug loaded polymeric nanoparticles and methods of making and using same
Abstract:	The present disclosure generally relates to methods of making nanoparticles having about 0.2 to about 35 weight percent of a therapeutic agent; and about 10 to about 99 weight percent of biocompatible polymer such as a diblock poly(lactic) acid-poly(ethylene)glycol.
Inventor(s):	Troiano; Greg (Pembroke, MA), Figa; Michael (Allston, MA), Sabnis; Abhimanyu (Arlington, MA)
Assignee:	BIND Therapeutics, Inc. (Cambridge, MA)
Application Number:	13/713,553
Patent Claims:	1. A method of preparing a plurality of therapeutic nanoparticles, comprising: combining a therapeutic agent, a first polymer, and optionally a second polymer, with an organic solvent to form a first organic phase having about 5 to about 50% solids, and wherein the first or second polymer, if present, is selected from the group consisting of PLA, PLGA, PEG, and copolymers thereof; combining the first organic phase with a first aqueous solution to form a second phase; emulsifying the second phase to form an emulsion phase; quenching the emulsion phase to form a quenched phase; adding a drug solubilizer to the quenched phase to form a solubilized phase of unencapsulated therapeutic agent; and filtering the solubilized phase to recover the target-specific nanoparticles, thereby forming a slurry of therapeutic nanoparticles having a diameter of about 80 nm to about 150 nm. 2. The method of claim 1, wherein emulsifying the second phase comprises: emulsifying the second phase to form a coarse emulsion, and emulsifying the coarse emulsion to form a fine emulsion phase. 3. The method of claim 1, wherein the organic solvent comprises a solvent chosen from: ethyl acetate, benzyl alcohol, methylene chloride, chloroform, toluene, methyl ethyl ketone, dimethyl formamide, dimethyl sulfoxide, acetone, acetonitrile, acetic acid, Tween 80 and Span 80, and combinations of two or more thereof. 4. The method of claim 1, wherein the aqueous solution comprises a reagent chosen from: sodium cholate, ethyl acetate, benzyl alcohol or combinations thereof. 5. The method of claim 2, wherein emulsifying the second phase comprises using a rotor stator homogenizer, probe sonicator, stir bar, or high pressure homogenizer. 6. The method of claim 2 wherein emulsifying the coarse emulsion comprises using a high pressure homogenizer. 7. The method of claim 6, wherein emulsifying the primary emulsion comprises about 2 to about 3 passes through the homogenizer. 8. The method of claim 6, wherein the homogenizer feed pressure is about 2000 to about 8000 psi per interaction chamber. 9. The method of claim 6, wherein the homogenizer comprises multiple interaction chambers. 10. The method of claim 1, wherein quenching is at least partially performed at a temperature of about 5.degree. C. or less. 11. The method of claim 1, wherein quenching is performed at about 0.degree. C. to about 5.degree. C. 12. The method of claim 1, wherein the quenching comprises the addition of water to the emulsion phase with a quench: emulsion ratio of about 8:1 to about 5:1. 13. The method of claim 1, wherein the the quenching comprises the addition of water to the emulsion phase with a quench: emulsion ratio of about 2:1 to about 40:1. 14. The method of claim 1, wherein the drug solubilizer is selected from the group consisting of Tween 80, Tween 20, polyvinyl pyrrolidone, cyclodextran, sodium dodecyl sulfate, and sodium cholate. 15. The method of claim 1, wherein the drug solubilizer is selected from the group consisting of diethylnitrosamine, sodium acetate, urea, glycerin, propylene glycol, glycofurol, poly(ethylene)glycol, bris(polyoxyethyleneglycolddodecyl ether, sodium benzoate, and sodium salicylate. 16. The method of claim 1, wherein the ratio of drug solubilizer to therapeutic agent is about 100:1 to about 10:1. 17. The method of claim 1, wherein filtering comprises using a tangential flow filtration system. 18. The method of claim 1, wherein filtering comprises filtering at a first temperature of about 0.degree. C. to about 5.degree. C. 19. The method of claim 18, further comprising filtering at a second temperature of about 20.degree. C. to about 30.degree. C. 20. The method of claim 19, wherein filtering comprises processing about 1 to about 6 diavolumes at about 0.degree. C. to about 5.degree. C. and processing at least one diavolume at about 20.degree. C. to about 30.degree. C. 21. The method of claim 19, wherein filtering comprises processing about 1 to about 6 diavolumes at about 0.degree. C. to about 5.degree. C. and processing about one diavolume to about 15 diavolumes at about 20.degree. C. to about 30.degree. C. 22. The method of claim 17, wherein filtering comprises processing different diavolumes at different distinct temperatures. 23. The method of claim 1, further comprising purifying the solubilized phase before said filtering to substantially remove said organic solvent, unencapsulated therapeutic agent, and/or drug solubilizer. 24. The method of claim 1, further comprising sterilely filtering the slurry of therapeutic nanoparticles using a filtration train at a controlled rate. 25. The method of claim 24, wherein the filtration train comprises a depth filter and a sterile filter. 26. The method of claim 1, wherein the first polymer is bound to a ligand having a molecular weight of less than about 1000 g/mol. 27. The method of claim 26, wherein the ligand is a low-molecular weight PSMA ligand. 28. The method of claim 27, wherein the low-molecular weight PSMA ligand is selected from the group consisting of ##STR00034## and enantiomers, stereoisomers, rotamers, tautomers, diastereomers, or racemates thereof; wherein R is independently selected from the group consisting of NH.sub.2, SH, OH, CO.sub.2H, C.sub.1-6-alkyl that is substituted with NH.sub.2, SH, OH or CO.sub.2H, and phenyl that is substituted with NH.sub.2, SH, OH or CO.sub.2H, and wherein R serves as the point of covalent attachment to the first polymer. 29. The method of claim 27, wherein the low-molecular weight PSMAligand is ##STR00035## and enantiomers, stereoisomers, rotamers, tautomers, diastereomers, or racemates thereof; wherein the NH.sub.2 groups serve as the point of covalent attachment to the first polymer. 30. The method of claim 1, wherein the first polymer is poly(lactic) acid-block-poly(ethylene)glycol or poly(lactic) acid-co-glycolic acid-block-poly(ethylene)glycol. 31. The method of claim 30, wherein the first polymer is not bound to a ligand. 32. The method of claim 1, wherein the therapeutic agent is docetaxel. 33. The method of claim 1, wherein the therapeutic agent is selected from the group consisting of chemotherapeutic agents such as doxorubicin (adriamycin), mitoxantrone, gemcitabine (gemzar), daunorubicin, procarbazine, mitomycin, cytarabine, etoposide, methotrexate, 5-fluorouracil (5-FU), vinblastine, vincristine, bleomycin, paclitaxel (taxol), docetaxel (taxotere), aldesleukin, asparaginase, busulfan, carboplatin, cladribine, camptothecin, CPT-11, 10-hydroxy-7-ethylcamptothecin (SN38), dacarbazine, S-I capecitabine, ftorafur, 5'deoxyflurouridine, UFT, eniluracil, deoxycytidine, 5-azacytosine, 5-azadeoxycytosine, allopurinol, 2-chloroadenosine, trimetrexate, aminopterin, methylene-10-deazaaminopterin (MDAM), oxaplatin, picoplatin, tetraplatin, satraplatin, platinum-DACH, ormaplatin, CI-973, JM-216, and analogs thereof, epirubicin, etoposide phosphate, 9-aminocamptothecin, 10,11-methylenedioxycamptothecin, karenitecin, 9-nitrocamptothecin, TAS 103, vindesine, L-phenylalanine mustard, ifosphamidemefosphamide, perfosfamide, trophosphamide carmustine, semustine, epothilones A-E, tomudex, 6-mercaptopurine, 6-thioguanine, amsacrine, etoposide phosphate, karenitecin, acyclovir, valacyclovir, ganciclovir, amantadine, rimantadine, lamivudine, zidovudine, bevacizumab, trastuzumab, rituximab, and 5-Fluorouracil, methotrexate, budesonide, sirolimus vincristine, and combinations thereof.

Details for Patent 8,609,142

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Recordati Rare Diseases, Inc.	ELSPAR	asparaginase	For Injection	101063	01/10/1978		2028-06-16
Clinigen, Inc.	PROLEUKIN	aldesleukin	For Injection	103293	05/05/1992		2028-06-16
Genentech, Inc.	RITUXAN	rituximab	Injection	103705	11/26/1997		2028-06-16