Claims for Patent: 9,724,279

Summary for Patent: 9,724,279

Title:	Core-shell particles, preparation process thereof, and composition containing the same
Abstract:	Disclosed herein are core-shell particles and process for preparing the same. The core-shell particles include a functional core, a multilayer or porous shell surrounding the functional core and polymeric tails extending from the shell. The functional core includes an antimicrobial agent or an antitumor agent. Also disclosed herein are pharmaceutical or health care compositions containing the core-shell particles.
Inventor(s):	Shieh; Dar-Bin (Tainan, TW)
Assignee:	SYNEURX INTERNATIONAL CORP. (Taipei, TW)
Application Number:	14/438,556
Patent Claims:	1. A multilayer core-shell particle, comprising, (a) a functional core; (b) one or more composite shell layers encapsulating the functional core, wherein each composite shell layer comprises, (b1) a first polymeric layer made of a first polymer that is oppositely charged to the functional core, wherein the first polymeric layer encapsulates the functional core, (b2) a plurality of first di- or trivalent ion-containing nanoparticles adhering onto the outer surface of the first polymeric layer, (b3) a second polymeric layer made of the first polymer, wherein the second polymeric layer covers the first polymeric layer and the plurality of di- or trivalent ion-containing nanoparticles, and (b4) a third polymeric layer made of a second polymer that is oppositely charged to the first polymer, wherein the third polymeric layer encapsulates the second polymeric layer; (c) an outermost shell layer, comprising a fourth polymeric layer and a plurality of second di- or trivalent ion-containing nanoparticles, wherein the fourth polymeric layer is made of a third polymer that has the same charge as the first polymer and encapsulates the one or more composite shell layers, while the plurality of second di- or trivalent ion-containing nanoparticles adhere onto the outer surface of the fourth polymeric layer; and (d) a plurality of polymeric tails respectively extending from the outer surface of the outermost shell layer, wherein the plurality of polymeric tails comprise a fourth polymer. 2. The multilayer core-shell particle of claim 1, wherein the multilayer core-shell particle comprises 2 to 40 composite shell layers. 3. The multilayer core-shell particle of claim 1, wherein the functional core comprises an antimicrobial agent selected from the group consisting of, sodium fluoride, calcium fluoride, acidulated phosphate fluoride, stannous fluoride, triclosan, chlorhexidine, amikacin, gentamicin, kanamycin, neomycin, netilmicin, tobramycin, paromomycin, spectinomycin, geldanamycin, herbimycin, rifaximin, streptomycin, loracarbef, ertapenem, doripenem, imipenem, cilastatin, meropenem, cefadroxil, cefazolin, cefalotin, cefalexin, cefaclor, cefamandole, cefoxitin, cefprozil, cefuroxime, cefixime, cefdinir, cefditoren, cefoperazone, cefotaxime, cefpodoxime, ceftazidime, ceftibuten, ceftizoxime, ceftriaxone, cefepime, ceftaroline fosamil, ceftobiprole, teicoplanin, vancomycin, telavancin, clindamycin, lincomycin, daptomycin, azithromycin, clarithromycin, dirithromycin, erythromycin, roxithromycin, troleandomycin, telithromycin, spiramycin, aztreonam, furazolidone, nitrofurantoin, linezolid, posizolid, radezolid, torezolid, amoxicillin, ampicillin, azlocillin, carbenicillin, cloxacillin, dicloxacillin, flucloxacillin, mezlocillin, methicillin, nafcillin, oxacillin, penicillin G, penicillin V, piperacillin, penicillin G, temocillin, ticarcillin, clavulanate, sulbactam, tazobactam, bacitracin, colistin polymyxin B, ciprofloxacin, enoxacin, gatifloxacin, levofloxacin, lomefloxacin, moxifloxacin, nalidixic acid, norfloxacin, ofloxacin, trovafloxacin, grepafloxacin, sparfloxacin, temafloxacin, mafenide, sulfacetamide, sulfadiazine, silver sulfadiazine, sulfadimethoxine, sulfamethizole, sulfamethoxazole, sulfanilimide, sulfasalazine, sulfisoxazole, trimethoprim-sulfamethoxazole, sulfonamidochrysoidine, demeclocycline, doxycycline, minocycline, oxytetracycline, tetracycline, clofazimine, dapsone, capreomycin, cycloserine, ethambutol, ethionamide, isoniazid, pyrazinamide, rifampicin, rifabutin, rifapentine, streptomycin, arsphenamine, chloramphenicol, fosfomycin, fusidic acid, metronidazole, mupirocin, platensimycin, quinupristin, dalfopristin, thiamphenicol, tigecycline, tinidazole and trimethoprim. 4. The multilayer core-shell particle of claim 1, wherein the functional core comprises a whitening agent selected from the group consisting of, hydrogen peroxide, carbamide peroxide, and zinc oxide. 5. The multilayer core-shell particle of claim 1, wherein the functional core comprises an antitumor agent selected from the group consisting of, actinomycin, all-trans retinoic acid, alitretinoin, azacitidine, azathioprine, bevacizumab, bexarotene, bleomycin, bortezomib, carboplatin, capecitabine, cetuximab, cisplatin, chlorambucil, cyclophosphamide, cytarabine, daunorubicin, docetaxel, doxifluridine, doxorubicin, epirubicin, epothilone A-F, erlotinib, etoposide, fluorouracil, gemcitabine, gefitinib, hydroxyurea, idarubicin, imatinib, ipilimumab, irinotecan, mechlorethamine, melphalan, mercaptopurine, methotrexate, mitoxantrone, ocrelizumab, ofatumumab, oxaliplatin, paclitaxel, panitumab, pemetrexed, rituximab, romidepsin, tafluposide, teniposide, tioguanine, topotecan, tretinoin, valrubicin, vemurafenib, vinblastine, vincristine, vindesine, vinorelbine, vismodegib, and vorinostat. 6. The multilayer core-shell particle of claim 1, wherein the first and second di-or trivalent ion-containing nanoparticles respectively comprise a material selected from the group consisting of hydroxyapatite, fluoroapatite, calcium phosphate, calcium fluoride, zinc oxide, silicate, titanium oxide and a combination thereof. 7. The multilayer core-shell particle of claim 1, wherein at least one of the first, second and third polymers is a cationic polymer selected from the group consisting of, polyarginine, polylysine, polyhistidine, poly-ornithine, polyethyleneimine, polypropyleneimine, poly(allylamine), polystyrene-maleic acid, gelatin, and chitosan. 8. The multilayer core-shell particle of claim 1, wherein at least one of the first, second and third polymers is an anionic polymer selected from the group consisting of, polyacrylic acid, polymethacrylic acid, polycrotonic acid, polyaspartic acid, polyglutamic acid, polylactic acid, poly(lactic-co-glycolic) acid, hyaluronic acid, alginic acid, polystyrene sulfonate, carrageenan, poly(methylene-co-guanidine), polyphosphoric acid, and pamidronic acid. 9. The multilayer core-shell particle of claim 1, wherein the fourth polymer is selected from the group consisting of, polyarginine, polylysine, polyhistidine, poly-ornithine, polyethyleneimine, polypropyleneimine, poly(allylamine), polystyrene-maleic acid, gelatin, chitosan, polyacrylic acid, polymethacrylic acid, polycrotonic acid, polyaspartic acid, polyglutamic acid, polylactic acid, poly(lactic-co-glycolic) acid, hyaluronic acid, and alginic acid, polystyrene sulfonate, carrageenan, poly(methylene-co-guanidine), polyphosphoric acid, or pamidronic acid, xanthan gum, polycarbophil, poly(methylvinyl ether-co-maleic anhydride), shellac, agar, pectin, polyvinyl acetate phthalate, guar gum, polyethylene glycol, dextrin, polydextrose, and polyethylene oxide. 10. The multilayer core-shell particle of claim 1, wherein the total thickness of the one or more composite shell layers and the outermost shell is about 0.5 to 1,000 nm. 11. The multilayer core-shell particle of claim 1, wherein the average diameter of the multilayer core-shell particle is about 50 to 50,000 nm. 12. The multilayer core-shell particle of claim 1, wherein the multilayer core-shell particle is cubic-shaped, needle-shaped, spherical-shaped, pyramidal-shaped or polygonal cylindrical-shaped. 13. The multilayer core-shell particle of claim 1, wherein the multilayer core-shell particle is a pH-sensitive particle. 14. The multilayer core-shell particle of claim 1, wherein the functional core comprises sodium fluoride; the first, third and fourth polymers are polyacrylic acid; the second polymer is polyethyleneimine; the first and second di- or trivalent ion-containing nanoparticles are respectively composite nanoparticles made of hydroxyapatite, fluoroapatite and calcium fluoride; and the multilayer core-shell particle has 4 to 10 composite shell layers. 15. A process for preparing a multilayer core-shell particle of claim 1, and the process comprises the steps of: (a) forming the one or more composite shell layers encapsulating the functional core, wherein each composite shell layer is formed by the steps of, (a1) mixing the functional core with a first polymer to form a first particle, wherein the first particle has a first polymeric layer of the first polymer and encapsulates the functional core, and the first polymer and the functional core are oppositely-charged, (a2) mixing the first particle with a plurality of first di- or trivalent ion-containing nanoparticles to form a second particle, wherein the second particle has the first di- or trivalent ion-containing nanoparticles adhering onto the outer surface of the first particle, (a3) mixing the second particle with the first polymer to form a third particle, wherein the third particle has a second polymeric layer of the first polymer and encapsulates the second particle, and (a4) mixing the third particle with a second polymer to form a fourth particle, wherein the fourth particle has a third polymeric layer of the second polymer and encapsulates the third particle, and the first polymer and the second polymer are oppositely-charged; (b) forming the outermost shell layer encapsulating the one or more composite shell layers by the steps of, (b1) mixing the fourth particle with a third polymer to form a fifth particle, wherein the fifth particle has a fourth polymeric layer of the third polymer and encapsulates the fourth particle, and the third polymer has the same charge as the first polymer, and (b2) mixing the fifth particle with a plurality of second di- or trivalent ion-containing nanoparticles to form a sixth particle, wherein the sixth particle has the plurality of second di- or trivalent ion-containing nanoparticles adhering onto the outer surface of the fourth polymeric layer; and (c) forming the plurality of polymeric tails respectively extending from the outer surface of the outermost shell layer by mixing the sixth particle with a fourth polymer, wherein the fourth polymer is a cationic, anionic or neutral polymer. 16. The process of claim 15, wherein the step (a) is repeated 2 to 40 times before the step (b) is performed, and thereby forms 2 to 40 composite shell layers. 17. The process of claim 15, wherein the functional core comprises an antimicrobial agent selected from the group consisting of, sodium fluoride, calcium fluoride, acidulated phosphate fluoride, stannous fluoride, triclosan, chlorhexidine, amikacin, gentamicin, kanamycin, neomycin, netilmicin, tobramycin, paromomycin, spectinomycin, geldanamycin, herbimycin, rifaximin, streptomycin, loracarbef, ertapenem, doripenem, imipenem, cilastatin, meropenem, cefadroxil, cefazolin, cefalotin, cefalexin, cefaclor, cefamandole, cefoxitin, cefprozil, cefuroxime, cefixime, cefdinir, cefditoren, cefoperazone, cefotaxime, cefpodoxime, ceftazidime, ceftibuten, ceftizoxime, ceftriaxone, cefepime, ceftaroline fosamil, ceftobiprole, teicoplanin, vancomycin, telavancin, clindamycin, lincomycin, daptomycin, azithromycin, clarithromycin, dirithromycin, erythromycin, roxithromycin, troleandomycin, telithromycin, spiramycin, aztreonam, furazolidone, nitrofurantoin, linezolid, posizolid, radezolid, torezolid, amoxicillin, ampicillin, azlocillin, carbenicillin, cloxacillin, dicloxacillin, flucloxacillin, mezlocillin, methicillin, nafcillin, oxacillin, penicillin G, penicillin V, piperacillin, penicillin G, temocillin, ticarcillin, clavulanate, sulbactam, tazobactam, bacitracin, colistin polymyxin B, ciprofloxacin, enoxacin, gatifloxacin, levofloxacin, lomefloxacin, moxifloxacin, nalidixic acid, norfloxacin, ofloxacin, trovafloxacin, grepafloxacin, sparfloxacin, temafloxacin, mafenide, sulfacetamide, sulfadiazine, silver sulfadiazine, sulfadimethoxine, sulfamethizole, sulfamethoxazole, sulfanilimide, sulfasalazine, sulfisoxazole, trimethoprim-sulfamethoxazole, sulfonamidochrysoidine, demeclocycline, doxycycline, minocycline, oxytetracycline, tetracycline, clofazimine, dapsone, capreomycin, cycloserine, ethambutol, ethionamide, isoniazid, pyrazinamide, rifampicin, rifabutin, rifapentine, streptomycin, arsphenamine, chloramphenicol, fosfomycin, fusidic acid, metronidazole, mupirocin, platensimycin, quinupristin, dalfopristin, thiamphenicol, tigecycline, tinidazole and trimethoprim. 18. The process of claim 15, wherein the functional core comprises a whitening agent selected from the group consisting of, hydrogen peroxide, carbamide peroxide, and zinc oxide. 19. The process of claim 15, wherein the functional core comprises an antitumor agent selected from the group consisting of, actinomycin, all-trans retinoic acid, alitretinoin, azacitidine, azathioprine, bevacizumab, bexarotene, bleomycin, bortezomib, carboplatin, capecitabine, cetuximab, cisplatin, chlorambucil, cyclophosphamide, cytarabine, daunorubicin, docetaxel, doxifluridine, doxorubicin, epirubicin, epothilone A-F, erlotinib, etoposide, fluorouracil, gemcitabine, gefitinib, hydroxyurea, idarubicin, imatinib, ipilimumab, irinotecan, mechlorethamine, melphalan, mercaptopurine, methotrexate, mitoxantrone, ocrelizumab, ofatumumab, oxaliplatin, paclitaxel, panitumab, pemetrexed, rituximab, romidepsin, tafluposide, teniposide, tioguanine, topotecan, tretinoin, valrubicin, vemurafenib, vinblastine, vincristine, vindesine, vinorelbine, vismodegib, and vorinostat. 20. The process of claim 15, wherein the first and second di- or trivalent ion-containing nanoparticles respectively comprise a material selected from the group consisting of hydroxyapatite, fluoroapatite, calcium phosphate, calcium fluoride, zinc oxide, silicate, titanium oxide and a combination thereof. 21. The process of claim 15, wherein at least one of the first, second and third polymers is a cationic polymer selected from the group consisting of, polyarginine, polylysine, polyhistidine, poly-ornithine, polyethyleneimine, polypropyleneimine, poly(allylamine), polystyrene-maleic acid, gelatin, and chitosan. 22. The process of claim 15, wherein at least one of the first, second and third polymers is an anionic polymer selected from the group consisting of, polyacrylic acid, polymethacrylic acid, polycrotonic acid, polyaspartic acid, polyglutamic acid, polylactic acid, poly(lactic-co-glycolic) acid, hyaluronic acid, alginic acid, polystyrene sulfonate, carrageenan, poly(methylene-co-guanidine), polyphosphoric acid, and pamidronic acid. 23. The process of claim 15, wherein the fourth polymer is selected from the group consisting of, polyarginine, polylysine, polyhistidine, poly-ornithine, polyethyleneimine, polypropyleneimine, poly(allylamine), polystyrene-maleic acid, gelatin, chitosan, polyacrylic acid, polymethacrylic acid, polycrotonic acid, polyaspartic acid, polyglutamic acid, polylactic acid, poly(lactic-co-glycolic) acid, hyaluronic acid, and alginic acid, polystyrene sulfonate, carrageenan, poly(methylene-co-guanidine), polyphosphoric acid, or pamidronic acid, xanthan gum, polycarbophil, poly(methylvinyl ether-co-maleic anhydride), shellac, agar, pectin, polyvinyl acetate phthalate, guar gum, polyethylene glycol, dextrin, polydextrose, and polyethylene oxide. 24. The process of claim 15, wherein the functional core comprises sodium fluoride; the first, third and fourth polymers are polyacrylic acid; the second polymer is polyethyleneimine; the first and second di- or trivalent ion-containing nanoparticles are respectively composite nanoparticles made of hydroxyapatite, fluoroapatite and calcium fluoride; and the multilayer core-shell particle has 4 to 10 composite shell layers. 25. A pharmaceutical or health care composition, comprising, an effective amount of the multilayer core-shell particles of claim 1, and a pharmaceutically acceptable excipient. 26. The pharmaceutical or health care composition of claim 25, wherein the pharmaceutical or health care composition is an oral care composition. 27. The pharmaceutical or health care composition of claim 26, wherein the respective functional core of the multilayer core-shell particles comprises an antimicrobial agent selected from the group consisting of, sodium fluoride, calcium fluoride, acidulated phosphate fluoride, stannous fluoride, triclosan, and chlorhexidine. 28. The pharmaceutical or health care composition of claim 26, wherein the respective functional core of the multilayer core-shell particles comprises a whitening agent selected from the group consisting of, hydrogen peroxide, carbamide peroxide, and zinc oxide. 29. The pharmaceutical or health care composition of claim 25, wherein the pharmaceutical or health care composition is an antimicrobial composition. 30. The pharmaceutical or health care composition of claim 29, wherein the respective functional core of the multilayer core-shell particles comprises an antimicrobial agent selected from the group consisting of amikacin, gentamicin, kanamycin, neomycin, netilmicin, tobramycin, paromomycin, spectinomycin, geldanamycin, herbimycin, rifaximin, streptomycin, loracarbef, ertapenem, doripenem, imipenem, cilastatin, meropenem, cefadroxil, cefazolin, cefalotin, cefalexin, cefaclor, cefamandole, cefoxitin, cefprozil, cefuroxime, cefixime, cefdinir, cefditoren, cefoperazone, cefotaxime, cefpodoxime, ceftazidime, ceftibuten, ceftizoxime, ceftriaxone, cefepime, ceftaroline fosamil, ceftobiprole, teicoplanin, vancomycin, telavancin, clindamycin, lincomycin, daptomycin, azithromycin, clarithromycin, dirithromycin, erythromycin, roxithromycin, troleandomycin, telithromycin, spiramycin, aztreonam, furazolidone, nitrofurantoin, linezolid, posizolid, radezolid, torezolid, amoxicillin, ampicillin, azlocillin, carbenicillin, cloxacillin, dicloxacillin, flucloxacillin, mezlocillin, methicillin, nafcillin, oxacillin, penicillin G, penicillin V, piperacillin, penicillin G, temocillin, ticarcillin, clavulanate, sulbactam, tazobactam, bacitracin, colistin polymyxin B, ciprofloxacin, enoxacin, gatifloxacin, levofloxacin, lomefloxacin, moxifloxacin, nalidixic acid, norfloxacin, ofloxacin, trovafloxacin, grepafloxacin, sparfloxacin, temafloxacin, mafenide, sulfacetamide, sulfadiazine, silver sulfadiazine, sulfadimethoxine, sulfamethizole, sulfamethoxazole, sulfanilimide, sulfasalazine, sulfisoxazole, trimethoprim-sulfamethoxazole, sulfonamidochrysoidine, demeclocycline, doxycycline, minocycline, oxytetracycline, tetracycline, clofazimine, dapsone, capreomycin, cycloserine, ethambutol, ethionamide, isoniazid, pyrazinamide, rifampicin, rifabutin, rifapentine, streptomycin, arsphenamine, chloramphenicol, fosfomycin, fusidic acid, metronidazole, mupirocin, platensimycin, quinupristin, dalfopristin, thiamphenicol, tigecycline, tinidazole and trimethoprim. 31. The pharmaceutical or health care composition of claim 25, wherein the pharmaceutical or health care composition is an antitumor composition. 32. The pharmaceutical or health care composition of claim 31, wherein the respective functional core of the multilayer core-shell particles comprises an antitumor agent selected from the group consisting of, actinomycin, all-trans retinoic acid, alitretinoin, azacitidine, azathioprine, bevacizumab, bexarotene, bleomycin, bortezomib, carboplatin, capecitabine, cetuximab, cisplatin, chlorambucil, cyclophosphamide, cytarabine, daunorubicin, docetaxel, doxifluridine, doxorubicin, epirubicin, epothilone A-F, erlotinib, etoposide, fluorouracil, gemcitabine, gefitinib, hydroxyurea, idarubicin, imatinib, ipilimumab, irinotecan, mechlorethamine, melphalan, mercaptopurine, methotrexate, mitoxantrone, ocrelizumab, ofatumumab, oxaliplatin, paclitaxel, panitumab, pemetrexed, rituximab, romidepsin, tafluposide, teniposide, tioguanine, topotecan, tretinoin, valrubicin, vemurafenib, vinblastine, vincristine, vindesine, vinorelbine, vismodegib, and vorinostat. 33. A method for selectively inhibiting the growth or metabolism of cariogenic and/or periodontopathic microorganisms in a subject, comprising, administering the oral care composition of claim 26 to the oral cavity of the subject; and allowing the adhesion of the multilayer core-shell particles or the porous core-shell particles to the oral surface of the subject.

Details for Patent 9,724,279

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Genentech, Inc.	RITUXAN	rituximab	Injection	103705	11/26/1997		2032-10-26
Idec Pharmaceuticals Corp.	RITUXAN	rituximab	Injection	103737	02/19/2002		2032-10-26
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Novartis Pharmaceuticals Corporation	ARZERRA	ofatumumab	Injection	125326	04/01/2011		2032-10-26