Claims for Patent: 11,179,336

Summary for Patent: 11,179,336

Title:	Manufacturing of bupivacaine multivesicular liposomes
Abstract:	Embodiments of the present application relate to commercial manufacturing processes for making bupivacaine multivesicular liposomes (MVLs) using independently operating dual tangential flow filtration modules.
Inventor(s):	Hall; Jeffrey S. (San Diego, CA), Turnbull; David J. (San Diego, CA), Grigsby, Jr.; John J. (San Diego, CA), Ardekani; Soroush M. (San Diego, CA), Davis; Paige N. (San Diego, CA), Garcia; Louie D. (San Diego, CA), Kurz; Stephanie M. (San Diego, CA), Los; Kathleen D. A. (San Diego, CA)
Assignee:	Pacira Pharmaceuticals, Inc. (San Diego, CA)
Application Number:	17/319,956
Patent Claims:	1. A composition of bupivacaine encapsulated multivesicular liposomes (MVLs), comprising: bupivacaine residing inside a plurality of internal aqueous chambers of the MVLs separated by lipid membranes, wherein the lipid membranes comprise 1, 2-dierucoylphosphatidylcholine (DEPC), 1, 2-dipalmitoyl-sn-glycero-3 phospho-rac-(1-glycerol) (DPPG), and at least one neutral lipid, the plurality of internal aqueous chambers of the MVLs also comprise lysine; and an aqueous medium in which the bupivacaine encapsulated MVLs are suspended; wherein the plurality of internal aqueous chambers of the MVLs has a pH of about 5.5; wherein the bupivacaine concentration in the composition is from about 11.3 mg/mL to about 17.0 mg/mL, wherein erucic acid concentration in the composition is about 23 .mu.g/mL or less after the composition is stored at 25.degree. C. for one month, and wherein the composition has a shelf life of up to 2 years when stored at 2-8.degree. C. 2. The composition of claim 1, wherein the composition has a pH of about 7.1 after the composition is stored at 25.degree. C. for one month. 3. The composition of claim 1, wherein the erucic acid concentration in the composition is about 38 .mu.g/mL or less after the composition is stored at 25.degree. C. for two months. 4. The composition of claim 3, wherein the composition has a pH of about 7.1 after the composition is stored at 25.degree. C. for two months. 5. The composition of claim 1, wherein the erucic acid concentration in the composition is about 54 .mu.g/mL or less after the composition is stored at 25.degree. C. for three month. 6. The composition of claim 5, wherein the composition has a pH of about 6.9 after the composition is stored at 25.degree. C. for three months. 7. The composition of claim 1, wherein the erucic acid concentration in the composition is about 99 .mu.g/mL or less after the composition is stored at 25.degree. C. for six months. 8. The composition of claim 7, wherein the composition has a pH of about 6.5 after the composition is stored at 25.degree. C. for six months. 9. The composition of claim 1, wherein the lipid membranes further comprise cholesterol and tricaprylin. 10. The composition of claim 1, wherein the encapsulated lysine concentration in the bupivacaine encapsulated MVLs composition is about 0.030 .mu.g/mL to about 0.032 .mu.g/mL. 11. The composition of claim 1, wherein the bupivacaine concentration in the composition is about 13.3 mg/mL. 12. The composition of claim 1, wherein the composition comprises less than about 5% by weight unencapsulated bupivacaine. 13. The composition of claim 1, wherein the composition comprises less than about 8% by weight unencapsulated bupivacaine when stored at 2-8.degree. C. for up to 2 years. 14. The composition of claim 1, wherein the percent packed particle volume (% PPV) of the bupivacaine encapsulated multivesicular liposomes in the composition is about 35% to 40%. 15. The composition of claim 1, wherein the encapsulated bupivacaine is in a salt form. 16. The composition of claim 15, wherein the encapsulated bupivacaine is in the form of bupivacaine phosphate. 17. A method of treating or ameliorating pain in a subject in need thereof, comprising administering a composition of claim 1 to the subject. 18. The method of claim 14, wherein the administration is via local infiltration to a surgical site to provide local analgesia. 19. The method of claim 14, wherein the administration is via interscalene brachial plexus nerve block or femoral nerve block to provide regional analgesia. 20. The method of claim 14, wherein the pain is postsurgical pain.