AU587658B2 - Oral delivery of biologically active substances bound to vitamin b12, or analogues thereof - Google Patents
Oral delivery of biologically active substances bound to vitamin b12, or analogues thereofInfo
- Publication number
- AU587658B2 AU587658B2 AU65289/86A AU6528986A AU587658B2 AU 587658 B2 AU587658 B2 AU 587658B2 AU 65289/86 A AU65289/86 A AU 65289/86A AU 6528986 A AU6528986 A AU 6528986A AU 587658 B2 AU587658 B2 AU 587658B2
- Authority
- AU
- Australia
- Prior art keywords
- active substance
- carrier
- complex
- reacting
- vitamin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 239000013543 active substance Substances 0.000 title claims description 66
- RMRCNWBMXRMIRW-WYVZQNDMSA-L vitamin b12 Chemical group N([C@@H]([C@@]1(C)[C@@](C)(CC(N)=O)[C@H](CCC(N)=O)\C(N1[Co+]C#N)=C(/C)\C1=N\C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C\C1=N\C([C@H](C1(C)C)CCC(N)=O)=C/1C)[C@@H]2CC(N)=O)=C\1[C@]2(C)CCC(=O)NCC(C)OP([O-])(=O)O[C@H]1[C@@H](O)[C@@H](N2C3=CC(C)=C(C)C=C3N=C2)O[C@@H]1CO RMRCNWBMXRMIRW-WYVZQNDMSA-L 0.000 title 1
- FDJOLVPMNUYSCM-WZHZPDAFSA-L cobalt(3+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+3].N#[C-].N([C@@H]([C@]1(C)[N-]\C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C(\C)/C1=N/C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C\C1=N\C([C@H](C1(C)C)CCC(N)=O)=C/1C)[C@@H]2CC(N)=O)=C\1[C@]2(C)CCC(=O)NC[C@@H](C)OP([O-])(=O)O[C@H]1[C@@H](O)[C@@H](N2C3=CC(C)=C(C)C=C3N=C2)O[C@@H]1CO FDJOLVPMNUYSCM-WZHZPDAFSA-L 0.000 claims description 75
- 239000011715 vitamin B12 Substances 0.000 claims description 70
- 229930003779 Vitamin B12 Natural products 0.000 claims description 69
- 235000019163 vitamin B12 Nutrition 0.000 claims description 69
- 238000000034 method Methods 0.000 claims description 34
- 229960004927 neomycin Drugs 0.000 claims description 22
- 229930193140 Neomycin Natural products 0.000 claims description 21
- 239000003814 drug Substances 0.000 claims description 21
- 239000000427 antigen Substances 0.000 claims description 19
- 102000036639 antigens Human genes 0.000 claims description 19
- 108091007433 antigens Proteins 0.000 claims description 19
- 239000003431 cross linking reagent Substances 0.000 claims description 17
- RMRCNWBMXRMIRW-BYFNXCQMSA-M cyanocobalamin Chemical compound N#C[Co+]N([C@]1([H])[C@H](CC(N)=O)[C@]\2(CCC(=O)NC[C@H](C)OP(O)(=O)OC3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)C)C/2=C(C)\C([C@H](C/2(C)C)CCC(N)=O)=N\C\2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O RMRCNWBMXRMIRW-BYFNXCQMSA-M 0.000 claims description 14
- 230000008569 process Effects 0.000 claims description 14
- 102000004169 proteins and genes Human genes 0.000 claims description 13
- 108090000623 proteins and genes Proteins 0.000 claims description 13
- 239000005556 hormone Substances 0.000 claims description 12
- 229940088597 hormone Drugs 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 11
- 241000251539 Vertebrata <Metazoa> Species 0.000 claims description 10
- 229940029329 intrinsic factor Drugs 0.000 claims description 10
- 230000007246 mechanism Effects 0.000 claims description 10
- -1 PMSG Chemical compound 0.000 claims description 9
- 230000000694 effects Effects 0.000 claims description 9
- 230000032258 transport Effects 0.000 claims description 9
- 125000000524 functional group Chemical group 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 235000000639 cyanocobalamin Nutrition 0.000 claims description 7
- 239000011666 cyanocobalamin Substances 0.000 claims description 7
- 229960002104 cyanocobalamin Drugs 0.000 claims description 7
- 239000003085 diluting agent Substances 0.000 claims description 7
- 125000003346 cobalamin group Chemical group 0.000 claims description 6
- 230000008878 coupling Effects 0.000 claims description 6
- 238000010168 coupling process Methods 0.000 claims description 6
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- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 claims description 4
- 206010035148 Plague Diseases 0.000 claims description 4
- MUMGGOZAMZWBJJ-DYKIIFRCSA-N Testostosterone Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 MUMGGOZAMZWBJJ-DYKIIFRCSA-N 0.000 claims description 4
- 206010043376 Tetanus Diseases 0.000 claims description 4
- 241000607479 Yersinia pestis Species 0.000 claims description 4
- 238000005903 acid hydrolysis reaction Methods 0.000 claims description 4
- 230000000844 anti-bacterial effect Effects 0.000 claims description 4
- ZIHHMGTYZOSFRC-UWWAPWIJSA-M cobamamide Chemical compound C1(/[C@](C)(CCC(=O)NC[C@H](C)OP(O)(=O)OC2[C@H]([C@H](O[C@@H]2CO)N2C3=CC(C)=C(C)C=C3N=C2)O)[C@@H](CC(N)=O)[C@]2(N1[Co+]C[C@@H]1[C@H]([C@@H](O)[C@@H](O1)N1C3=NC=NC(N)=C3N=C1)O)[H])=C(C)\C([C@H](C/1(C)C)CCC(N)=O)=N\C\1=C/C([C@H]([C@@]\1(CC(N)=O)C)CCC(N)=O)=N/C/1=C(C)\C1=N[C@]2(C)[C@@](C)(CC(N)=O)[C@@H]1CCC(N)=O ZIHHMGTYZOSFRC-UWWAPWIJSA-M 0.000 claims description 4
- 235000006279 cobamamide Nutrition 0.000 claims description 4
- 239000011789 cobamamide Substances 0.000 claims description 4
- 206010013023 diphtheria Diseases 0.000 claims description 4
- 208000028104 epidemic louse-borne typhus Diseases 0.000 claims description 4
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 claims description 4
- 244000045947 parasite Species 0.000 claims description 4
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 4
- 229940124597 therapeutic agent Drugs 0.000 claims description 4
- 201000008827 tuberculosis Diseases 0.000 claims description 4
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- 230000004888 barrier function Effects 0.000 claims description 3
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- 210000004556 brain Anatomy 0.000 claims description 3
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- 230000002708 enhancing effect Effects 0.000 claims description 3
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- 229940047650 haemophilus influenzae Drugs 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 claims description 3
- 230000003248 secreting effect Effects 0.000 claims description 3
- XUDGDVPXDYGCTG-UHFFFAOYSA-N (2,5-dioxopyrrolidin-1-yl) 2-[2-(2,5-dioxopyrrolidin-1-yl)oxycarbonyloxyethylsulfonyl]ethyl carbonate Chemical group O=C1CCC(=O)N1OC(=O)OCCS(=O)(=O)CCOC(=O)ON1C(=O)CCC1=O XUDGDVPXDYGCTG-UHFFFAOYSA-N 0.000 claims description 2
- FXYPGCIGRDZWNR-UHFFFAOYSA-N (2,5-dioxopyrrolidin-1-yl) 3-[[3-(2,5-dioxopyrrolidin-1-yl)oxy-3-oxopropyl]disulfanyl]propanoate Chemical compound O=C1CCC(=O)N1OC(=O)CCSSCCC(=O)ON1C(=O)CCC1=O FXYPGCIGRDZWNR-UHFFFAOYSA-N 0.000 claims description 2
- JWDYCNIAQWPBHD-UHFFFAOYSA-N 1-(2-methylphenyl)glycerol Chemical compound CC1=CC=CC=C1OCC(O)CO JWDYCNIAQWPBHD-UHFFFAOYSA-N 0.000 claims description 2
- DWBCXGZVCAKDGO-UHFFFAOYSA-N 1-azido-4-[(4-azidophenyl)disulfanyl]benzene Chemical compound C1=CC(N=[N+]=[N-])=CC=C1SSC1=CC=C(N=[N+]=[N-])C=C1 DWBCXGZVCAKDGO-UHFFFAOYSA-N 0.000 claims description 2
- LAHCMYYCRFQUHP-UHFFFAOYSA-N 2-(4-azidophenyl)sulfanylisoindole-1,3-dione Chemical group C1=CC(N=[N+]=[N-])=CC=C1SN1C(=O)C2=CC=CC=C2C1=O LAHCMYYCRFQUHP-UHFFFAOYSA-N 0.000 claims description 2
- UPXRTVAIJMUAQR-UHFFFAOYSA-N 4-(9h-fluoren-9-ylmethoxycarbonylamino)-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid Chemical compound C1C(C(O)=O)N(C(=O)OC(C)(C)C)CC1NC(=O)OCC1C2=CC=CC=C2C2=CC=CC=C21 UPXRTVAIJMUAQR-UHFFFAOYSA-N 0.000 claims description 2
- JLLYLQLDYORLBB-UHFFFAOYSA-N 5-bromo-n-methylthiophene-2-sulfonamide Chemical compound CNS(=O)(=O)C1=CC=C(Br)S1 JLLYLQLDYORLBB-UHFFFAOYSA-N 0.000 claims description 2
- 244000146553 Ceiba pentandra Species 0.000 claims description 2
- 235000003301 Ceiba pentandra Nutrition 0.000 claims description 2
- 208000003495 Coccidiosis Diseases 0.000 claims description 2
- 241000282326 Felis catus Species 0.000 claims description 2
- 241000287828 Gallus gallus Species 0.000 claims description 2
- 102000004877 Insulin Human genes 0.000 claims description 2
- 108090001061 Insulin Proteins 0.000 claims description 2
- 102000014150 Interferons Human genes 0.000 claims description 2
- 108010050904 Interferons Proteins 0.000 claims description 2
- 206010023076 Isosporiasis Diseases 0.000 claims description 2
- 241000588747 Klebsiella pneumoniae Species 0.000 claims description 2
- 201000005505 Measles Diseases 0.000 claims description 2
- XADCESSVHJOZHK-UHFFFAOYSA-N Meperidine Chemical compound C=1C=CC=CC=1C1(C(=O)OCC)CCN(C)CC1 XADCESSVHJOZHK-UHFFFAOYSA-N 0.000 claims description 2
- RJQXTJLFIWVMTO-TYNCELHUSA-N Methicillin Chemical compound COC1=CC=CC(OC)=C1C(=O)N[C@@H]1C(=O)N2[C@@H](C(O)=O)C(C)(C)S[C@@H]21 RJQXTJLFIWVMTO-TYNCELHUSA-N 0.000 claims description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical class NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims description 2
- 241000194019 Streptococcus mutans Species 0.000 claims description 2
- 241000209140 Triticum Species 0.000 claims description 2
- 235000021307 Triticum Nutrition 0.000 claims description 2
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- 208000003152 Yellow Fever Diseases 0.000 claims description 2
- NDAUXUAQIAJITI-UHFFFAOYSA-N albuterol Chemical compound CC(C)(C)NCC(O)C1=CC=C(O)C(CO)=C1 NDAUXUAQIAJITI-UHFFFAOYSA-N 0.000 claims description 2
- 239000013566 allergen Substances 0.000 claims description 2
- 125000003368 amide group Chemical group 0.000 claims description 2
- 150000003931 anilides Chemical class 0.000 claims description 2
- 229940058303 antinematodal benzimidazole derivative Drugs 0.000 claims description 2
- 150000001556 benzimidazoles Chemical class 0.000 claims description 2
- 230000027455 binding Effects 0.000 claims description 2
- NXVYSVARUKNFNF-UHFFFAOYSA-N bis(2,5-dioxopyrrolidin-1-yl) 2,3-dihydroxybutanedioate Chemical group O=C1CCC(=O)N1OC(=O)C(O)C(O)C(=O)ON1C(=O)CCC1=O NXVYSVARUKNFNF-UHFFFAOYSA-N 0.000 claims description 2
- 210000004369 blood Anatomy 0.000 claims description 2
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- 235000013330 chicken meat Nutrition 0.000 claims description 2
- BYLXFSREGROOBJ-UVKKECPRSA-K cobalt(3+) [(2R,3S,4R,5S)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2R)-1-[3-[(2R,3R,4Z,7S,9Z,12S,13S,14Z,17S,18S,19R)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2,7,12,17-tetrahydro-1H-corrin-21-id-3-yl]propanoylamino]propan-2-yl] phosphate chloride Chemical compound [Cl-].[Co+3].C[C@H](CNC(=O)CC[C@]1(C)[C@@H](CC(N)=O)C2[N-]\C1=C(C)/C1=N/C(=C\C3=N\C(=C(C)/C4=N[C@]2(C)[C@@](C)(CC(N)=O)[C@@H]4CCC(N)=O)\[C@@](C)(CC(N)=O)[C@@H]3CCC(N)=O)/C(C)(C)[C@@H]1CCC(N)=O)OP([O-])(=O)O[C@@H]1[C@@H](CO)O[C@@H]([C@@H]1O)n1cnc2cc(C)c(C)cc12 BYLXFSREGROOBJ-UVKKECPRSA-K 0.000 claims description 2
- UUWYBLVKLIHDAU-UHFFFAOYSA-K cobalt(3+);[5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] 1-[3-[2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2,7,12,17-tetrahydro-1h-corrin-21-id-3-yl]propanoylamino]propan-2 Chemical compound [Co+3].[O-]N=O.OCC1OC(N2C3=CC(C)=C(C)C=C3N=C2)C(O)C1OP([O-])(=O)OC(C)CNC(=O)CCC1(C)C(CC(N)=O)C2[N-]\C1=C(C)/C(C(C\1(C)C)CCC(N)=O)=N/C/1=C\C(C(C/1(CC(N)=O)C)CCC(N)=O)=N\C\1=C(C)/C1=NC2(C)C(C)(CC(N)=O)C1CCC(N)=O UUWYBLVKLIHDAU-UHFFFAOYSA-K 0.000 claims description 2
- WBSXYJYELWQLCJ-UHFFFAOYSA-K cobalt(3+);[5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] 1-[3-[2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2,7,12,17-tetrahydro-1h-corrin-21-id-3-yl]propanoylamino]propan-2 Chemical compound O.[OH-].[Co+3].OCC1OC(N2C3=CC(C)=C(C)C=C3N=C2)C(O)C1OP([O-])(=O)OC(C)CNC(=O)CCC1(C)C(CC(N)=O)C2[N-]\C1=C(C)/C(C(C\1(C)C)CCC(N)=O)=N/C/1=C\C(C(C/1(CC(N)=O)C)CCC(N)=O)=N\C\1=C(C)/C1=NC2(C)C(C)(CC(N)=O)C1CCC(N)=O WBSXYJYELWQLCJ-UHFFFAOYSA-K 0.000 claims description 2
- 229960005452 cobamamide Drugs 0.000 claims description 2
- WUPRCGRRQUZFAB-DEGKJRJSSA-N corrin Chemical group N1C2CC\C1=C\C(CC/1)=N\C\1=C/C(CC\1)=N/C/1=C\C1=NC2CC1 WUPRCGRRQUZFAB-DEGKJRJSSA-N 0.000 claims description 2
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 claims description 2
- 239000000428 dust Substances 0.000 claims description 2
- AJJLGMCBXZSSSA-UHFFFAOYSA-N ethyl 4-(4-azidophenyl)sulfanylbutanimidothioate;hydrochloride Chemical compound Cl.CCSC(=N)CCCSC1=CC=C(N=[N+]=[N-])C=C1 AJJLGMCBXZSSSA-UHFFFAOYSA-N 0.000 claims description 2
- CKTNHGVJKUQEBM-UHFFFAOYSA-N ethylazanide Chemical compound CC[NH-] CKTNHGVJKUQEBM-UHFFFAOYSA-N 0.000 claims description 2
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- DQOCFCZRZOAIBN-WZHZPDAFSA-L hydroxycobalamin Chemical compound O.[Co+2].[N-]([C@@H]1[C@H](CC(N)=O)[C@@]2(C)CCC(=O)NC[C@@H](C)OP([O-])(=O)O[C@H]3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)\C2=C(C)/C([C@H](C\2(C)C)CCC(N)=O)=N/C/2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O DQOCFCZRZOAIBN-WZHZPDAFSA-L 0.000 claims description 2
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- 229940125396 insulin Drugs 0.000 claims description 2
- 229940079322 interferon Drugs 0.000 claims description 2
- MVZXTUSAYBWAAM-UHFFFAOYSA-N iron;sulfuric acid Chemical compound [Fe].OS(O)(=O)=O MVZXTUSAYBWAAM-UHFFFAOYSA-N 0.000 claims description 2
- 229960004184 ketamine hydrochloride Drugs 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
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- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/60—Medicinal preparations containing antigens or antibodies characteristics by the carrier linked to the antigen
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Description
ORAL DELIVERY OF BIOLOGICALLY ACTIVE SUBSTANCES BOUND TO VITAMIN B12, OR ANALOGUES THEREOF
TECHNICAL FIELD
The present invention relates to oral delivery systems. More particularly the invention relates to enhancing the absorption of active substances by administering these substances bound to vitamin B12 (VB12) or an analogue thereof.
BACKGROUND ART
The oral route of administration is perhaps the most preferable means of delivering an antigen or pharmaceutically active agent to man. This route does however suffer from the major disadvantage that there is generally poor uptake of antigens or pharmaceutically active agents by the gastrointestinal tract and some agents may be destroyed by prolonged exposure to proteolytic enzymes. In this regard, attemps to orally immunize man or animals in the past have met with limited success. Effective vaccination has generally only been achieved by the administration of large quantities of antigen or by combining parenteral priming with oral boosting. Recent work by us utilizing a number of molecules with the ability to bind to the intestinal mucosa has demonstrated effective oral immunization using low doses of these binding proteins or by coupling various antigens or haptens to these carriers. Uptake and delivery to the circulation of these molecules from the intestine seemed to be due to receptor mediated endocytosis.
It has been known for some time that a number of specific uptake mechanisms exist in the gut for uptake of dietary molecules. Thus there are specific uptake mechanisms for monosaccharides, disaccharides, amino acids and vitamins. Most of these uptake mechanisms depend upon the presence of a specific protein or enzyme such as monosaccharidase or disaccharidase situated in the mucosal lamina propria which binds to the molecule and transports it into the cells lining and lamina propria.
Two notable exceptions to these uptake mechanisms are found with iron transport and VB12 uptake. In both these cases a specific binding protein is released into the intestine, which binds to its ligand in the lumen of the gut.
Thus, during iron uptake in the intestine transferrin is released fro the stomach, binds to iron and is in turn bound by a receptor on the duodenal mucosa. The receptor-transferrin-iron complex is then taken up by receptor mediated endocytosis.
Similarly, the absorption of physiological amounts of VB12 by the
gut requires that it be complexed with a naturally occurring transport protein known as intrinsic factor (IF) (1-5). This protein is released into the lumen of the stomach by parietal cells in the fundus. Once bound to intrinsic factor, the VB12.IF complex interacts with a membrane bound receptor for IF located on the terminal ileum of the small intestine. The receptor-IF-VB12 complex is then internalized by a process of receptor mediated endocytosis (RME). Allen and Majerus (7) demonstrated that it is possible to chemically modify VB12, couple it to a resin and use the VBl-L-resin to affinity purify IF. This finding suggested to us that it may be possible to couple large macromolcules (such as the resin used by Allen and Majerus) to VB12 and to still preserve it's ability to interact specifically with intrinsic factor. By coupling molecules to VB12 in such a way as to preserve the ability of VB12 to interact with intrinsic factor it was hoped that we could use the natural uptake mechanism for VB12 deliver VB12 and various molecules coupled to it, to deliver various proteins, drugs or other pharmaceutically active molecules to the circulation.
It is thus the object of this invention to utilize the VB12 uptake mechanism to transport active substances such a drugs, hormones, antigenic material and the like, covalently coupled to VB12 or an analogue thereof, from the intestinal lumen into the circulation.
DISCLOSURE OF THE INVENTION
In a first embodiment the invention provides a complex which comprises at least one active substance linked to at least one carrier molecule which is VB12 or an analogue thereof wherein the ability of the carrier to undergo the binding reactions necessary for uptake and transport of VB12 in a vertebrate host and the activity of the active substance are substantially maintained.
In the context of the present invention, the term active substance includes all, part, an analogue, homologue, derivative or combination thereof, of a hormone, bio-active peptide, therapeutic agent, antigen or hapten.
Preferred active substances for delivery according to the invention include: hormones and bioactive peptides such as LHRH, insulin, testosterone, interferon, PMSG, HCG and inhibin; therapeutic agents such neomycin, salbutamol, pyrimethamine, penicillin G, methicillin, carbenicillin, pethidine, xylazine, ketamine hydrochloride, mephenesin and iron dextran; antigens or haptens including allergens, proteins, polysaccharides and secretary products such as grass pollens (for instance
barley and couch), weed pollens (e.g. clover, dock) tree pollens (e.g. ash, Cyprus), plant pollens (e.g. broom), epithelia (e.g. cat hair, dog hair, pig hair) and house dust mite, wheat chaff and kapok; a protein derived from or immunogens against influenza, measles, Rubella, smallpox, yellow fever, diphtheria, tetanus, cholera, plague, typhus, BCG, tuberculosis causing agents, Haemophilus influenzae, Neisseria catarrhalis, Klebsiella pneumoniae, pneumococci, streptococci; a secretory product derived from diphtheria, tetanus, cholera, plague, typhus, tuberculosis causing agents, Haemophilus influenzae, Neisseria catarrhalis, Klebsiel la pneumoniae, pneumococci, streptococci, Streptococcus mutans, or is derived from a malarial parasite or the causitive agent of coccidiosis in chickens.
Preferred analogues of VB12 include cyanocobalamin (CN-Cbl), aquocobalamin, adenosyl cobalamin, methyl cobalamin, hydroxycobalamin, cyanocobalamin carbanalide, and 5-o-methyl benzyl cobalmin [(5-OMeBza)CN-Cbl ] as well as the desdimethyl, monoethyl amide and the methyl amide analogues of all of the above. Also included are the various analogues and homologues of cobamamide such as coenzyme 812 and 5'-deoxyadenosyl cobalamin. Other analogues include chlorocobalamin, sulfitocobalamin, nitrocobalamin, thiocyanatocobalamin, benzimidazole derivatives such as; 5,6-dichloro- benzimidazole, 5-hydroxybenzimidazole, trimethylbenzimidazole, as well as adenosylcyanocobalmin [(Ade)CN-Cbl], cobalamin lactone, cobalamin lactam and the anilide, ethylamide, monocaboxylic and dicarboxylic acid derivatives of VB12 or its analogues.
Preferred derivatives of VB12 include the mono-, di- and tricaboxylic acid derivatives or the proprionamide derivatives of VB12. Carriers may also include analogues of VB12 in which the cobalt is replaced by zinc or nickel. The corrin ring of VB12 or its analogues may also be substituted with any substituent which does not effect its binding to IF.
In a preferred embodiment of the invention there is provided a comple comprising the lys-6 form of LHRH and VB12.
The complexes of this invention, of coupled active substances can be used to deliver these substances to any uni or multicellular organism with requirement for, and a specific transport mechanism for VB12. For example, bacteria resistant to a particular antibiotic where the resistance is mediated by the loss of ability to transport the antibiotic inside the cell could be overcome by this procedure. A VB12-antibiotic complex could thus be effectively delivered inside the bacterial cell via the VB12 transport mechanism. This could lead to an ability to reutilize a number of
antibiotics whose current use has become limited by development of bacterial resistance. Delivery of active substances, of the type described above, could be achieved to a wide variety or organisms, particularly parasites of humans or animals.
In another embodiment the invention provides a process for the production of a complex comprising, at least one active substarce linked to at lease one carrier molecule, said carrier molecule being VB12 or an analogue thereof, wherein the ability of the carrier to undergo the binding reactions necessary for uptake and transport of VB12 in a vertebrate host and the activity of the active substance are substantially maintained which process comprises one or more of the following steps: a) reacting the active substance with the carrier to form said complex: b) chemically modifying the active substance to provide at least one functional group capable of forming a chemical linkage, and reacting the active substance and carrier to form said complex; c) chemically modifying the carrier to provide at least one functional group capable of forming a chemical linkage and reacting the active substance and carrier to form said complex; d) chemically modifying the active substance and the carrier to provide functional groups capable of forming a chemical linkage, and reacting the active substance and carrier to form said complex; e) reacting the active substance with at least one cross-linking agent and reacting the active substance and the carrier molecule to form said complex; f) reacting the carrier with at least one cross-linking agent and reacting the active substance and carrier to form said complex; g) reacting the active substance and carrier with at least one cross-linking agent and reacting the active substance and carrier to form said complex.
A preferred process of the invention comprises;
(i) preparing the mono-acid derivative of VB12 by mild acid hydrolysis, and purifying the derivative;
(ii) chemically modifying an active substance to provide at least one functional group capable of forming a chemical linkage; and
(iii) reacting the modified active substance and mono-acid derivative of VB12 to form said complex.
The cross-linking agent may contain a disulfide bond or be cleavable
by acid, base or periodate. Examples of cross-linking agents include N-(4-azidophenylthio)phthalimide, 4,4'-dithiobisphenylazide, dithiobis- (succinimidylpropionate), dimethyl-3,3'-dithiobispropionimidate.2HCl, 3,3'-dithiobis-(su1fosuccinimidylpropionate), ethyl-4-azidophenyl-1,4-dithiobutyrimidate,HCl, N-succinimidyl-(4-azidophenyl)-1,3'-dithio- propionate, sulfosuccinimidyl-2-(m-azιdo-o-nitrobenzamido)-ethyl-l,3'- dithiopropionate, sulfosuccinimidyl-2-(p-azidosalicylamido)-ethyl- 1,3'dithiopropionate, N-succinimidyl-3-(2-pyridyldithio)propionate, sulfosuccinimidyl-(4-azidophenyldithio)-propionate, and 2-iminothiolane. Preferred cross-linking agents are disuccinimidyl tartrate and bis-[2-(succinimidyloxycarbonyloxy)-ethyl]sulfone.
Suitably, cross-linking of the carrier and active substance may be achieved by acid hydrolysis of the amide groups of the propionamide side chains adjacent to rings A, B and C of VB12 and coupling to suitable groups of the active substance.
In a further embodiment of the invention there is provided a medicament which comprises a complex according to the invention together with a pharmaceutically acceptable carrier or diluent.
Examples of pharmaceutically acceptable carriers and diluents include typical carriers and diluents such as sodium bicarbonate solutions and similar diluents which neutralize stomach acid or have similar buffering capacity, glycols, oils, oil-in-water or water-in-oil emulsions, and include medicaments in the form of emulsions, gels, pastes and viscous colloidal dispersions. The medicament may be presented in capsule, tablet, slow release or elixir form or as a gel or paste. Furthermore, the medicament may be provided as a live stock feed or as food suitable for human consumption.
The invention also provides an antibacterial formulation comprising a complex according to the invention, in which the active substance is an antibacterial active substance together with a carrier or diluent therefor.
In another embodiment the invention provides a method of enhancing a host vertebrate's respone to an orally administered active substance which method comprises the oral administration of an effective amount of said active substance as a complex according to the invention, or of a medicament according to the invention.
The invention also provides a method of selectively modulating the magnitude and/or type of immune response to an antigen or hapten, which method comprises orally administering an effective amount of said antigen or
hapten as a complex according to the invention, or of a medicament according to the invention.
The invention also provides a method of delivering an active substance to any unicellular or multicel lular organism, including bacteria, protozoa, or parasites, which has a requirement for VB12 as well as a specific uptake mechanism for the same, which method comprises administering a complex of the invention to the organism. In this manner bacteria which are resistant to an antibiotic due to the loss of their ability to transport the antibiotic into the cell could be once again made sensitive to the antibiotic by coupling the antibiotic to VB12 and using the natural VB12 uptake system of the bacteria to deliver the antibiotic into the cell. In this fashion a number of antibiotics whose use has been discontinued due to the occurrence of bacterial resistance could regain pharmacological significance.
In a further embodiment of the invention there is provided a method of delivering an active substance across the blood/brain barrier or across the placenta into a developing foetus by administering a complex of the invention. Delivery of such substances would occur through the natural VB12 uptake mechanisms at these barriers.
BEST MODE FOR CARRYING OUT THE INVENTION Materials
Bovine serun albumen (BSA), VB12, p-nitrophenol , LHRH acetate salt, and neomycin sulfate were all purchased from Sigma Chemical Co. St Louis, Mo. USA.
1-ethyl-3-(dimethylaminopropyl)carbodiimide HCl (EDAC) was obtained from BIORAD Labs, California, while N,N'dicyclohexylcarbodiimide (DCC) was purchased from Fluka.
PREPARATION 1 Monocarboxyl -Derivative of VB12
The acid derivative of VB12 can readily be prepared by hydrolysing native VB12 for 72h in 0.4M HCl at room temperature. The reaction is stopped by passing the hydrolystate down an ion-exchange column of DOWEX AG1-X8. The flow through containing the monoacid VB12 is lyophilized and resuspended in 0.2M pyridine and adjusted to pH9.05 with 1M ammonium hydroxide. The solution is then passed down a Sephadex QAE A25 previously equilibrated with 0.2M pyridine and the monoacid eludated with a gradient from 0.4M pyridine to 0.4M, 0.16M acetic acid. The fractions containing the purified mono-acid are pooled and lyophilized.
The-foilowing examples illustrate preferred embodiments of the invention and should not be construed as limiting theron.
The monocarboxyl VB12 can be covalently crossl inked to any ami no containing compound by the use of a suitable carbodiimide.
EXAMPLE 1 VB12-BSA
VB12-BSA complex was formed by mixing an equal weight of C00H-B12 with BSA in distilled water, the pH was adjusted to 6.5 with IM NaOH and an equal weight of solid EDAC was added to the solution and allowed to react overnight. Free, unreacted COOH-B12 was removed by chromatography of Sephadex G-25, followed by repeated ethanol precipitation of the VB12-BSA complex.
EXAMPLE 2 VB12-LVS-6-LHRH
Monocarboxyl VB12 plus 1.5 equivalents of n-hydroxysuccinamide were dissolved in cold (4ºC) dimethyl formamide (DMF). To this solution was added 1.1 equivalents of dicyclohexyl carbodiimide (DCC) in DMF. The solutions were warmed to room temperature and allowed to react for 1 hour. Lys-6-LHRH dissolved in DMF containing triethylamine was added and allowed to react overnight. The resultant complex was separated from the free reactants by chromatography on Sephades G-25 followed by reverse phase HPLC.
EXAMPLE 3 VB12-Neomycin
The total acid hydro! i sate of VB12 was adjusted to pH6.5 with NaOH, an equal weight of neomycin sulfate was added to the solution followed by an equal weight of EDAC. The conjugation was allowed to proceed overnight after which the conjugate was separated from unreacted reagents by chromatography on G-25 and reverse phase HPLC.
All reactions and purification procedures were monitored by thin layer chromatography. The degree of VB12 substitution of BSA was determined by spectrophotometric scanning of the conjugate using O.D.278 extinction values of 0.6 and 11.5, for lmg/ml solutions of BSA and VB12, respectively, and an O.D.361 of 20.4 for VB12.
Female C57B1/6J mice (18-22g) were obtained from the Animal Resources Centre (Perth, Western Australia). All mice received conjugate preparations in 0.5ml of 0.1M carbonate/bicarbonate buffer pH9.5 using a specially
prepared feeding needle. Mice were fed on days 0 and 14. On day 21 the mice were bled from the orbital plexus. Antibody titres of serum were determined by ELISA using alkaline phosphatase conjugated anti-mouse serum.
EXAMPLE 4 Stimulation of serum antibodies following oral administration of
VB12-BSA complex
The possible potential for VB12 deliver protein molecules, covalently linked to it, from the intestine to the circulation was investigated. The immune response generated to this complex was compared to that generated by the protein fed alone or together with VB12, or to the protein injected intramuscularly.
As seen in Table 1, feeding mice with microgram quantities of BSA or FGG coupled to VB12 resulted in the stimulation of significant serum antibody responses to the BSA or FGG respectively. Feeding of either protein in similar amounts or in a 50 fold excess either mixed with VB12 or without VB12 resulted in the stimulation of no anti-BSA or anti-FGG antibodies. Feeding of these VB12-protein complexed was also capable of stimulating good cellular immunity (as measured by the footpad assay for DTH
* The reciprocal of the antiserum dilution that gave an ELISA reading of 0.5 afer 45min. at 37 C on day 21 after initial feeding. Each value represents the mean of 15 mice ±1 standard deviation. Mice received two feedings of antigen (50μg) on days 1 and 14. On day 21 mice were bled from the retro orbital plaxus and the antibody titres measured by ELISA as described previously (Russell-Jones et al., 1984). Each protein molecule was substituted with an average of 5 VB12 groups.
+ Footpad swelling was measured in mm using a microcaliper. All groups received a 50μg priming dose of antigen followed by challenge with lOμg of the immunizing antigen in the right foot and 10μg of ovalbumen in the left footpad. Swelling was measured after 24h.
EXAMPLE 5 Oral delivery of VB12-LHRH as a means of stimulating ovulation Although a number of hormones as oestrogen and progesterone are actively absorbed upon oral administration, there are may other which have little effect when given per os. Noteable amongst these hormones is the peptide hormone lutenizing hormone releasing hormone (LHRH), or gonadotrophin releasing hormone (GnRH). This hormone is normally secreted by the anterior pituitary and is responsible for the control of release of lutenizng hormone (LH) and follicle stimulating hormone ( FSH) . Parenteral i njecti ons of LHRH have previ ously been shown to be effective in stimulating FSH and LH release, however orally presented
LHRH has Little effect. Many studies have been performed on varying the sequence of LHRH, with the result that a number of agonists and antagonists have now been identified. Perhaps one of the most powerful agonists identified to date is the D-Lys-6 analogue of LHRH (D-Lys-6.LHRH). As the epsilon amino group on the lysine of this analogue is readily accessible for peptide cross-linking it was decided to usfi the DCC method to link monocarboxyl VB12 to D-Lys6.LHRH and to tsst if s efficacy upon oral administration.
The. D-lys-6 analogue of LHRH was synthesized by us and purified by reverse, ptrase HPLC. The purified analogue was coupled to monocarboxyl VB12 using DCC as described in Example 2. The conjugated product was purified by Sephadex G-25 chromatography in 10% acetic acid, followed by HPLC Chromatography.
Mature C57B1/6J female mice were treated in the following fashion:- On day 0 all mice received a subcutaneous (s/c) superovulating dose of pregnant mare serum gonadotraphin (PMSG) to stimulate the growth of ovarian follicles. After 48 hours mice received various doses of LHRH, Lys-6-LHRH or saline. On day 3 mice were sacrificed and examined for ovulation. Ovulation was assessed by examining for the presence of corpora haemorrhagica on the ovaries using a stereoscopic microscope at 80X power.
The results below show that by coupling Lys-6-LRH to VB12 it is possible to deliver the analogue orally and to still observe a biological effect as exemplified by it's ability to stimulate ovulation in developing follicles. The inability of this preparatin to exert it's effect when injected intravenously presumably reflects the rapid clearance of free VB12 when it is not complexed to transcobalamin II.
EXAMPLE 6
A number of drugs including the antibiotic, neomycin, are highly effective antibiotics when injected parenterally, however they are completely ineffective when given orally as they cannot be transported across the intestinal epithelium. It was therefore decided to see if VB12 could act as a carrier for an antibiotic (neomycin) which normally has no effect upon a systemic infection when the antibiotic was given orally.
Neomycin was covalently linked to VB12 as described in Example 3 and fed to mice infected with S. typhimurium.
Oral administration of neomycin, or neomycin plus VB12 was not able to eliminate systemic infection with S. typhimurium. When neomycin was coupled to VB12, however, a significant quantity of the conjugate was transported across the intestinal epithelium and was capable of eliminating a systemic Salmonella infection. Table 3 shows that mice infected with S. typhimurium could be saved by either feeding VB12.neomycin conjugate (lmg total dose) or by the i.m. injection of neomycin or VB12. neomycin (both lmg total dose). AH other treatments failed to prevent death due to infection. In addition, the extent to which orally presented VB12. neomycin was capable of clearing infective particles from the liver and spleen of experimental animals suggests that, at least for this dosage, VB12. neomycin is comparable to and i.m. injection of neomycin alone or the neomycin.VB12 conjugate (Table 5).
Male-C57B1/6J mice (/group) were fed 1x106 S. typhimurium on day 0. On day 3 mice received either saline, VB12, VB12 + neomycin (Neomycin+VB12) , VB12 coupled to neomycin (Neomycin-VB12) , or neomycin alone. A total dose of lmg was administered as five smaller doses each separated by 12 hours. Neomycin was coupled to VB12 and the conjugate purified as outlined in Example 3.
It is possible to covalently couple VB12 to proteins (FGG and BSA), hormones (LHRH) and antibiotics (neomycin) and to utilize the natural active uptake mechanism for VB12 to transport these molecules form the lumen of the gut into the systemic circulation while retaining full immunogenicity and/or biological activity of the molecules coupled to VB12. The importance of these finding lie in the potential use of VB12 as a specific carrier of highly potent hormones, antibiotics and vasoactive peptides which currently must be repeatedly administered by injection at considerable costs and inconvenience.
INDUSTRIAL APPLICABILITY The present invention provides a simple and novel technique for the specific oral presentation of various molecules previously incapable of being transported across the gut in significant amounts or in producing a significant systemic immune response upon oral feeding of various antigens. These antigens would not normally elicit an immune response when fed unless very large quantities of antigen were administered. Similarly various active molecules which are normally only poorly absorbed from the intestine can be covalently linked to VB12 and so render them susceptable to intestinal uptake.
REFERENCES
1. Castle, W.B. N. Engl . 3 . Med, 24, 603-611 (1953)
2. Fox, H.J., Castle, W.B. Am. J. Med. Sci ., 203, 18-26
3. Hoedemaeker, P.J., Abies J., Wachters, 3 .3 . , Averds, A., Nieweg, H.O. Lab. Invest., 15, 1163-1169 (1966)
4. Allen, R.H. Majerus, P.W. 3 . Biol. Chem.,; 247, 7702-7708 (1972)
5. Allen, R.H. Majerus, P.W. 3. Biol. Chem.,; 247, 7709-7717 (1972)
6. Grasbech, R. Progr. Haematol . 6, 233-260 (1969)
7. Allen, R.H. Majerus, P.W. 3. Biol. Chem.,; 247, 7695-7701 (1972)
8. Russel-Jones, G.J., Gotschlich, E.C. Blake, M.S. 3. Exp. Med., 160, 1476- (1984)
9. Sedgwick, J.D. Holt, P.G. 3 . Immunol. Meth., 87 37-44 (1986)
Claims (29)
1. A complex comprising at least one active substance linked to at lease one carrier molecule, said carrier molecule being vitamin B12 or an analogue thereof, wherein the ability of the carrier to undergo the binding reactions necessary for uptake and transport of vitamin B12 in a vertebrate host and the activity of the active substance are substantially maintained.
2. A complex according to claim 1, wherein the active substance is selected from: all, part, analogues, homologues, derivatives or combinations thereof of a hormone, a bioactive peptide or therapeutic agent.
3. A complex according to claim 2, wherein the active substance is a hormone selected from LHRH, insulin, testosterone, interferon, PMSG, HCG, or inhibin.
4. A complex according to claim 2, wherein the active substance is the lys-6 form of LHRH.
5. A complex according to claim 2, wherein said active substance is a therapeutic agent selected from neomycin, salbutamol, cloridine, penicillin G, methicillin, carbenicill in, pethidine, xylazine, ketamine hydrochloride, mephenesin or iron dextran.
6. A complex according to claim 1, wherein the substance is selected from all, part, analogues, homologues, derivatives or combinations thereof of an antigen or hapten.
7. A complex according to claim 6, wherein said antigen or hapten is an allergen, protein, polysaccharide or secretory product.
8. A complex according to claim 6, wherein said antigen or hapten is selected from: grass pollen, weed pollen, tree pollen, plant pollen, cat hair, dog hair, pig hair or, other epithelia, house dust mite, wheat chaff, kapok; a protein derived from or immunogens against influenza, measles, Rubella, smallpox, yellow fever, diphtheria, tetanus, cholera, plague, typhus, BCG, tuberculosis causing agents, Haemophilus influenzae, Neisseria catarrhalis, Klebsiel la pneumoniae, pneumococci, streptococci; a secretory product derived from diphtheria, tetanus, cholera, plague, typhus, tuberculosis causing agents, Haemophi 1 us influenzae, Neisseria catarrhal is, Klebsiella pneumoniae, pneumococci, streptococci, Streptococcus mutans, or is derived from a malarial parasite or the causitive agent of coccidiosis in chickens.
9. A complex according to claim l, wherein the carrier is: cyanocobalamin, aquocobalamin, adenosyl cobalamin, methyl cobalamin, hydroxycobalamin, cyanocobalamin carbanalide, 5-o-methyl benzyl cobalmin, the desdi methyl, monoethyl amide and the methylamide analogues all of the above, analogues and homologues of cobamamide, coenzyme B12, 5'-deoxy- adenosylcobalamine, chlorocobalamin, sulfitocobalamin, nitrocobalamin, thiocyanatocobalamin, benzimidazole derivatives, adenosylcyanocobalmin, cobalamin lactone, cobalamin lactam and the anilide, ethyl amide, propionamide, monocaboxylic and dicarboxylic acid derivatives of vitamin B12 or its analogues.
10. A complex according to claim 1, wherein the carrier is a vitamin B12 analogue in which the Co is replaced by Ni or Zn.
11. A complex according to claim 1, wherein the carrier is a vitamin B12 analogue in which the corrin ring is substituted with a substituent which does not effect binding to intrinsic factor.
12. A process for the production of a complex according to claim 1, which process comprises one or more of the following steps: a) reacting the active substance with the carrier to form said complex: b) chemically modifying the active substance to provide at least one functional group capable of forming a chemical linkage, and reacting the active substance and carrier to form said complex; c) chemically modifying the carrier to provide at least one functional group capable of forming a chemical linkage and reacting the active substance and carrier to form said complex; d) chemically modifying the active substance and the carrier to provide functional groups capable of forming a chemical linkage, and reacting the active substance and carrier to form said complex; e) reacting the active substance with at least one cross-linking agent and reacting the active substance and the carrier molecule to form said complex; f) reacting the carrier with at least one cross-linking agent and reacting the active substance and carrier to form said complex; g) reacting the active substance and carrier with at least one cross-linking agent and reacting the active substance and carrier to form said complex.
13. A process according to claim 12, comprising:
(i) preparing the mono-acid derivative of vitamin B12 by mild acid hydrolysis, and purifying said derivative;
(ii) chemically modifying an active substance to provide at least one functional group capable of forming a chemical linkage; and (iii) reacting the modified active substance and mono-acid derivative of vitamin B12 to form said complex.
14. A process according to claim 12, wherein the chemical cross-linking of active substance and carrier is by acid hydrolysis of the amide groups of the propionamide side chains adjacent to rings A, B and C of vitamin B12 and coupling to suitable groups of the active substance.
15. A process according to claim 12, wherein the cross-linking agent is a cleavable cross-linking agent containing a disulfide bond.
16. A process according to claim 12, wherein the cross-linking agent is cleavable by acid.
17. A process according to claim 12, wherein the cross-linking agent is cleavable by periodate.
18. A process according to claim 12, wherein the cross-linking agent is cleavable by base.
19. A process according to claim 12, wherein the cross-linking agent is N-(4-azidophenylthio)phthalimide, 4,4'-dithiobisphenylazide, dithiobis- (succinimidylpropionate), dimethyl-3,3'-dithiobispropionimidate.2HCl, 3,3'-dithiobis(sulfosuccinimidylpropionate), ethyl-4-azidophenyl-
1,4-dithiobutyrimidate.HCl, N-succinimιdyl-(4-azidophenyl)-1,3'-dithio- propionate, sulfosuccinimidyl-2-(m-azido-o-nitrobenzamido)-ethyl-1,3'- dithiopropionate, sulfosuccinimidyl-2-(p-azidosalicylamido)-ethyl- 1,3'-dithiopropionate, N-succinimidyl-3-(2-pyridyldithιo)propionate, sulfosuccinimidy1-(4-azidophenyldithio)-propionate, or 2-iminothiolane.
20. A process according to claim 12, wherein the cross-linking agent is disuccinimidyl tartrate.
21. A proces according to claim 12, wherein the cross-linking agent is bis-[2-(succinimidyloxycarbonyloxy)-ethyl]-sulfone.
22. A medicament which comprises a complex according to claim 1, together with a pharmaceutically acceptable carrier or diluent therefor.
23. A medicament according to claim 22, wherein said medicament is in capsule, tablet, slow release, elixir, gel or paste form or is enteric coated.
24. An antibacterial formulation comprising a complex according to claim 1, in which the active substance is an antibacterial active substance together with a carrier or diluent therefor.
25. A method of enhancing a vertebrate's respone to an orally administered active substance which method comprises the oral administration of an effective amount of said active substance to said vertebrate as a complex according to claim 1, or if a medicament according to claim 22.
26. A method of selectively modulating the magnitude and/or type of immune response to an antigen or hapten in a vertebrate, which method comprises orally administering an effective amount of said antigen or hapten to said vertebrate as a complex according to claim 1, or of a medicament according to claim 22.
27. A method of delivering an active substance across the blood/brain barrier in a vertebrate requiring said active substance to be transported into the brain, which method comprises administering to said vertebrate, an effective amount of said active substance in the form of a complex according to claim 1, or of a medicament according to claim 22.
28. A method of delivering an active substance to a foetus requiring said active substance, which method comprises administering to a pregnant mammal, an effective amount of said active substance in the form of a complex according to claim 1, or of a medicament according to claim 22.
29. A method of delivering an active substance to a unicellular or multicellular organism which has a requirement for vitamin B12 and a specific uptake mechanism for vitamin B12, which method comprises administering a complex according to claim 1 , or a medicament according to claim 22, to said organism, or applying a formulation according to claim 24, to a locus at which said organism occurs or is likely to occur.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU65289/86A AU587658B2 (en) | 1985-10-10 | 1986-10-10 | Oral delivery of biologically active substances bound to vitamin b12, or analogues thereof |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AUPH283885 | 1985-10-10 | ||
| AUPH2838 | 1985-10-10 | ||
| AU65289/86A AU587658B2 (en) | 1985-10-10 | 1986-10-10 | Oral delivery of biologically active substances bound to vitamin b12, or analogues thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU6528986A AU6528986A (en) | 1987-05-05 |
| AU587658B2 true AU587658B2 (en) | 1989-08-24 |
Family
ID=25634659
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU65289/86A Ceased AU587658B2 (en) | 1985-10-10 | 1986-10-10 | Oral delivery of biologically active substances bound to vitamin b12, or analogues thereof |
Country Status (1)
| Country | Link |
|---|---|
| AU (1) | AU587658B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU620512B2 (en) * | 1989-05-02 | 1992-02-20 | Arlington, Eileen Alexis | Therapeutic uses of cyanocobalamin |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU706979B2 (en) * | 1993-05-20 | 1999-07-01 | Biotech Australia Pty Limited | LHRH antagonists |
| JPH08510260A (en) * | 1993-05-20 | 1996-10-29 | バイオテック・オーストラリア・プロプライエタリー・リミテッド | LHRH antagonist |
| AU692485B2 (en) * | 1993-12-14 | 1998-06-11 | Bomac Laboratories Limited | A medicament, pack containing a medicament, and a method of administering a medicament |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU5402786A (en) * | 1985-02-25 | 1986-08-28 | Xoma Corporation | Antibody hybrid molecules and process for their preparation |
| EP0228568A1 (en) * | 1985-12-05 | 1987-07-15 | Anawa München Aktiengesellschaft Biologische Laboratorien | Carrier bioactivated by antibodies covalently bound to its surface |
-
1986
- 1986-10-10 AU AU65289/86A patent/AU587658B2/en not_active Ceased
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU5402786A (en) * | 1985-02-25 | 1986-08-28 | Xoma Corporation | Antibody hybrid molecules and process for their preparation |
| EP0228568A1 (en) * | 1985-12-05 | 1987-07-15 | Anawa München Aktiengesellschaft Biologische Laboratorien | Carrier bioactivated by antibodies covalently bound to its surface |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU620512B2 (en) * | 1989-05-02 | 1992-02-20 | Arlington, Eileen Alexis | Therapeutic uses of cyanocobalamin |
Also Published As
| Publication number | Publication date |
|---|---|
| AU6528986A (en) | 1987-05-05 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PC | Assignment registered |
Owner name: ACCESS PHARMACEUTICALS AUSTRALIA PTY. LTD. Free format text: FORMER OWNER WAS: BIOTECHNOLOGY AUSTRALIA PTY. LTD. |
|
| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |