WO1984002076A1 - Method of preparing controlled-release preparations for biologically active materials and resulting compositions - Google Patents
Method of preparing controlled-release preparations for biologically active materials and resulting compositions Download PDFInfo
- Publication number
- WO1984002076A1 WO1984002076A1 PCT/SE1983/000411 SE8300411W WO8402076A1 WO 1984002076 A1 WO1984002076 A1 WO 1984002076A1 SE 8300411 W SE8300411 W SE 8300411W WO 8402076 A1 WO8402076 A1 WO 8402076A1
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- WIPO (PCT)
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- phase
- cubic
- liquid crystalline
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- water
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 57
- 239000000203 mixture Substances 0.000 title claims abstract description 32
- 239000011149 active material Substances 0.000 title claims abstract description 15
- 239000003405 delayed action preparation Substances 0.000 title description 4
- 239000007788 liquid Substances 0.000 claims abstract description 43
- 239000000126 substance Substances 0.000 claims abstract description 17
- 230000000975 bioactive effect Effects 0.000 claims abstract description 15
- 239000000463 material Substances 0.000 claims abstract description 13
- 238000013270 controlled release Methods 0.000 claims abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 49
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 36
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 15
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 claims description 12
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 12
- RZRNAYUHWVFMIP-HXUWFJFHSA-N glycerol monolinoleate Natural products CCCCCCCCC=CCCCCCCCC(=O)OC[C@H](O)CO RZRNAYUHWVFMIP-HXUWFJFHSA-N 0.000 claims description 12
- 229940074096 monoolein Drugs 0.000 claims description 12
- 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 8
- KKEBXNMGHUCPEZ-UHFFFAOYSA-N 4-phenyl-1-(2-sulfanylethyl)imidazolidin-2-one Chemical compound N1C(=O)N(CCS)CC1C1=CC=CC=C1 KKEBXNMGHUCPEZ-UHFFFAOYSA-N 0.000 claims description 6
- 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 6
- 210000002969 egg yolk Anatomy 0.000 claims description 6
- -1 polyoxyethylene groups Polymers 0.000 claims description 6
- 239000002243 precursor Substances 0.000 claims description 5
- 239000007921 spray Substances 0.000 claims description 5
- 102000004877 Insulin Human genes 0.000 claims description 4
- 108090001061 Insulin Proteins 0.000 claims description 4
- 239000003093 cationic surfactant Substances 0.000 claims description 4
- PROQIPRRNZUXQM-ZXXIGWHRSA-N estriol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H]([C@H](O)C4)O)[C@@H]4[C@@H]3CCC2=C1 PROQIPRRNZUXQM-ZXXIGWHRSA-N 0.000 claims description 4
- 229940125396 insulin Drugs 0.000 claims description 4
- 239000004973 liquid crystal related substance Substances 0.000 claims description 4
- 239000003945 anionic surfactant Substances 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- 102000002322 Egg Proteins Human genes 0.000 claims description 2
- 108010000912 Egg Proteins Proteins 0.000 claims description 2
- 229930182555 Penicillin Natural products 0.000 claims description 2
- 210000000941 bile Anatomy 0.000 claims description 2
- 235000013345 egg yolk Nutrition 0.000 claims description 2
- 239000012705 liquid precursor Substances 0.000 claims description 2
- 229940049954 penicillin Drugs 0.000 claims description 2
- 239000000575 pesticide Substances 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims 6
- 229940067631 phospholipid Drugs 0.000 claims 3
- 150000003904 phospholipids Chemical class 0.000 claims 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 claims 2
- 239000003833 bile salt Substances 0.000 claims 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 2
- 239000002736 nonionic surfactant Substances 0.000 claims 2
- 102000004169 proteins and genes Human genes 0.000 claims 2
- 108090000623 proteins and genes Proteins 0.000 claims 2
- 150000003431 steroids Chemical class 0.000 claims 2
- 239000002888 zwitterionic surfactant Substances 0.000 claims 2
- PROQIPRRNZUXQM-UHFFFAOYSA-N (16alpha,17betaOH)-Estra-1,3,5(10)-triene-3,16,17-triol Natural products OC1=CC=C2C3CCC(C)(C(C(O)C4)O)C4C3CCC2=C1 PROQIPRRNZUXQM-UHFFFAOYSA-N 0.000 claims 1
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 claims 1
- FDCJDKXCCYFOCV-UHFFFAOYSA-N 1-hexadecoxyhexadecane Chemical compound CCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCC FDCJDKXCCYFOCV-UHFFFAOYSA-N 0.000 claims 1
- LVPFIQLQEJUWCB-UHFFFAOYSA-N 2,2-diethyl-3-hexyl-3-sulfobutanedioic acid Chemical compound CCCCCCC(C(O)=O)(S(O)(=O)=O)C(CC)(CC)C(O)=O LVPFIQLQEJUWCB-UHFFFAOYSA-N 0.000 claims 1
- 125000000174 L-prolyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])[C@@]1([H])C(*)=O 0.000 claims 1
- 125000002877 alkyl aryl group Chemical group 0.000 claims 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 150000008051 alkyl sulfates Chemical class 0.000 claims 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 claims 1
- 150000008052 alkyl sulfonates Chemical class 0.000 claims 1
- 239000003242 anti bacterial agent Substances 0.000 claims 1
- 229940088710 antibiotic agent Drugs 0.000 claims 1
- 229940093761 bile salts Drugs 0.000 claims 1
- 230000003115 biocidal effect Effects 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 210000001217 buttock Anatomy 0.000 claims 1
- NOLXQSVNNIIHMV-UHFFFAOYSA-L disodium;2,2-diethyl-3-hexyl-3-sulfobutanedioate Chemical group [Na+].[Na+].CCCCCCC(C([O-])=O)(S(O)(=O)=O)C(CC)(CC)C([O-])=O NOLXQSVNNIIHMV-UHFFFAOYSA-L 0.000 claims 1
- WRZXKWFJEFFURH-UHFFFAOYSA-N dodecaethylene glycol Chemical compound OCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO WRZXKWFJEFFURH-UHFFFAOYSA-N 0.000 claims 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical group [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 claims 1
- 239000012530 fluid Substances 0.000 claims 1
- JOJLFGHXRDJIBQ-UHFFFAOYSA-L magnesium;2,2-diethyl-3-hexyl-3-sulfobutanedioate Chemical compound [Mg+2].CCCCCCC(C([O-])=O)(S(O)(=O)=O)C(CC)(CC)C([O-])=O JOJLFGHXRDJIBQ-UHFFFAOYSA-L 0.000 claims 1
- 102000039446 nucleic acids Human genes 0.000 claims 1
- 108020004707 nucleic acids Proteins 0.000 claims 1
- 150000007523 nucleic acids Chemical class 0.000 claims 1
- 150000003180 prostaglandins Chemical class 0.000 claims 1
- NRHMKIHPTBHXPF-TUJRSCDTSA-M sodium cholate Chemical group [Na+].C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 NRHMKIHPTBHXPF-TUJRSCDTSA-M 0.000 claims 1
- 239000011573 trace mineral Substances 0.000 claims 1
- 235000013619 trace mineral Nutrition 0.000 claims 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims 1
- 239000011782 vitamin Substances 0.000 claims 1
- 229940088594 vitamin Drugs 0.000 claims 1
- 229930003231 vitamin Natural products 0.000 claims 1
- 235000013343 vitamin Nutrition 0.000 claims 1
- 239000012736 aqueous medium Substances 0.000 abstract description 2
- 239000012071 phase Substances 0.000 description 114
- 239000000243 solution Substances 0.000 description 12
- 238000009792 diffusion process Methods 0.000 description 11
- JQWAHKMIYCERGA-UHFFFAOYSA-N (2-nonanoyloxy-3-octadeca-9,12-dienoyloxypropoxy)-[2-(trimethylazaniumyl)ethyl]phosphinate Chemical compound CCCCCCCCC(=O)OC(COP([O-])(=O)CC[N+](C)(C)C)COC(=O)CCCCCCCC=CCC=CCCCCC JQWAHKMIYCERGA-UHFFFAOYSA-N 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- OGQYPPBGSLZBEG-UHFFFAOYSA-N dimethyl(dioctadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC OGQYPPBGSLZBEG-UHFFFAOYSA-N 0.000 description 6
- 229940079593 drug Drugs 0.000 description 6
- 239000003814 drug Substances 0.000 description 6
- 230000003628 erosive effect Effects 0.000 description 6
- 230000002209 hydrophobic effect Effects 0.000 description 6
- 239000000306 component Substances 0.000 description 5
- 238000012377 drug delivery Methods 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 4
- 239000000006 Nitroglycerin Substances 0.000 description 4
- 241000209140 Triticum Species 0.000 description 4
- 235000021307 Triticum Nutrition 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229960003711 glyceryl trinitrate Drugs 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 3
- 229960000907 methylthioninium chloride Drugs 0.000 description 3
- 238000010587 phase diagram Methods 0.000 description 3
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 2
- 206010013911 Dysgeusia Diseases 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 238000002441 X-ray diffraction Methods 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- 239000003708 ampul Substances 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 239000000787 lecithin Substances 0.000 description 2
- 229940067606 lecithin Drugs 0.000 description 2
- 235000010445 lecithin Nutrition 0.000 description 2
- 150000002632 lipids Chemical class 0.000 description 2
- 239000000693 micelle Substances 0.000 description 2
- 235000019371 penicillin G benzathine Nutrition 0.000 description 2
- 229940056360 penicillin g Drugs 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 210000002784 stomach Anatomy 0.000 description 2
- 230000002459 sustained effect Effects 0.000 description 2
- XWTYSIMOBUGWOL-UHFFFAOYSA-N (+-)-Terbutaline Chemical group CC(C)(C)NCC(O)C1=CC(O)=CC(O)=C1 XWTYSIMOBUGWOL-UHFFFAOYSA-N 0.000 description 1
- 108010068370 Glutens Proteins 0.000 description 1
- 241000271915 Hydrophis Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 101100400378 Mus musculus Marveld2 gene Proteins 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 239000003613 bile acid Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 238000002144 chemical decomposition reaction Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 206010012601 diabetes mellitus Diseases 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- 238000002481 ethanol extraction Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 235000021312 gluten Nutrition 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229940126701 oral medication Drugs 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- CMDGQTVYVAKDNA-UHFFFAOYSA-N propane-1,2,3-triol;hydrate Chemical compound O.OCC(O)CO CMDGQTVYVAKDNA-UHFFFAOYSA-N 0.000 description 1
- 238000001472 pulsed field gradient Methods 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- KFVSLSTULZVNPG-UHFFFAOYSA-N terbutaline sulfate Chemical compound [O-]S([O-])(=O)=O.CC(C)(C)[NH2+]CC(O)C1=CC(O)=CC(O)=C1.CC(C)(C)[NH2+]CC(O)C1=CC(O)=CC(O)=C1 KFVSLSTULZVNPG-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/127—Liposomes
- A61K9/1274—Non-vesicle bilayer structures, e.g. liquid crystals, tubules, cubic phases, cochleates; Sponge phases
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/829—Liposomes, e.g. encapsulation
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2984—Microcapsule with fluid core [includes liposome]
Definitions
- Amphiphilic substances i.e. substances with both hydrophilic and hydrophobic (lipophilic) groups, spontaneously tend to self- associate in aqueous systems forming various types of aggregates.
- a typical example is shown in Figure 1 in "Cubic Mesomorphic Pha ⁇ ses" (R.R. Balmbra, J.S. Clunie and J.F. Goodman, Nature, 222, 1159 (1969)), in which an increasing amount of amphiphile in water gives rise to icellar, cubic, hexagonal and lamellar phases.
- the struc ⁇ tures of these phases are well-known, except for the cubic phases, since there are a number of cubic phases, some of which remain to be determined in detail.
- Al l phases are thermodynamical ly stabl e and have therefore no tendency to phase separate with time (unl ess chemical decompo ⁇ si tion occurs) , and they wi l l al so form spontaneously.
- Al l phases are characterized by having distinct hydrophi l ic and hydrophobic domains , which give them the possibil i ty to dissolve (solubil ize) or disperse both water-sol ubl e and water-insol ubl e compounds .
- the cubic liquid crystalline phase may crudely be characteri ⁇ zed as being either of the water-discontinuous or oil-discontinuous droplet type, or of the bi -continuous type.
- the droplet structures may thus be either of a "water-soluble” or of a "water-insoluble” type.
- B -continuous structures of cubic phase have been determined by V. Luzatti et al . (Nature, 2__, 701 (1967)) and K. Larsson et al . (Chem. Phys. Li ids, 27, 321 (1980)). All the different forms of cu ⁇ bic phases can be used in control led-rel ease preparations which the following discussion will explain.
- the cubic liquid crystalline phase can also be described as erodible or non-erodible depending on its behaviour in excess water. Furthermore, the rate of erosion depends on, besides temperature and agitation, the appearance of the phase diagram for the actual amphiphile. This dependence is extremely strong and the rate of erosion may vary by several orders of magnitude. The following three examples will illustrate the erodible and non-erodible types of cu ⁇ bic phases at a temperature of 37 °C.
- Figure 7 (monoolein-water) in "Food Emu! si - fiers and Their Associations with Water” (N. Krog and J.B. Laurid- sen, in “Food Emulsions” (ed. S. Friberg), Marcel Dekker Inc. (1976)), shows a cubic phase which will, when in water, be in equilibrium with a monomer solution of amphiphile in water ⁇ .Q ⁇ ⁇ M) . This cubic phase will stay unchanged in excess water (at " least for extremely long times).
- an erodible or a non-erodible cubic phase in a control! ed-rel ease preparation depends on the required rate pro ⁇ file, the solubility of the compound, which rate one wants to con ⁇ trol etc.
- an eroding cubic phase may act as a source for mo ⁇ lecular! y dissolved drug.
- the use of erodible cubic pha- ses is ⁇ ot limited to water- insoluble compounds, but may also be used if a relatively fast release profile is desired, or if an ini ⁇ tial protection of a pharmaceutical compound (which may be subject to chemical degradation in contact with the high acidity of the gas ⁇ tric juice) is required.
- Non-eroding cubic phases stable in water, may be used for app ⁇ lications where longer release times are desirable. Both water- soluble and water-insoluble compounds can be used in this kind of cubic phase.
- the release rate of a bioactive substance from a non- erodible cut-vic phase may either be determined by the outer surface of the cubic phase towards the surrounding aqueous medium or the interfaces between hydrophilic and hydrophobic domain within the cubic phase, depending on whether the cubic phase is mono- or bi- continuous and the nature (hydrophilic, hydrophobic or amphiphilic) r of the bioactive compound.
- OMP Fine adjustments of the release rate in any kind of cub i c phase can be made by the addition of salt, glycerol , ethylene glycol , propylene glycol or any similar amphiphile of low molecular weight.
- Our invention relates to a method for preparing a control led- release composition for biologically active materials, the composi ⁇ tion consisting of chemical substances capable of forming a cubic liquid crystalline phase, or any other type of liquid crystalline phase, and the bioactive material, the method which comprises:
- the invention also comprises the intermediate phases formed, the product cubic phases, their use and carrier compositions including
- biologically active material and “bioactive material” as used throughout the specification and claims mean a compound or composition which, when present in an effective amount, reacts with and/or affects living cells and organisms.
- liquid crystalline phase denotes an intermediate state between solid crystals and isotropic liquids, cha- racterized by long-range order and short-range properties close to those of a simple liquid or solution (H. Keller and R. Hatz, in “Handbook of Liquid Crystals", Verlag Chemie, Weinheim(1980)).
- cubic liquid crystalline phase and “cubic phase” as used herein mean a thermodynamical ly stable, viscous and optically isotropic phase made of at least amphiphilic substance(s) and water.
- the cubic phase can be unambiguously identified from the
- any other liquid crystalline phase as used in the claims mean thermodynamically stable optically anisotropic phases like lamellar, hexagonal and reversed hexagonal liquid crystalline phases made of at least amphiphilic substance(s) and water.
- the method of the invention is useful to make liquid crystalline phases, especially cubic phases, which in turn are usefully employed in a rich variety of processes.
- the liquid crystalline phases may be used to enhance the bioavai lability of medications, oral drug delivery, rectal drug delivery, transderma! drug delivery and drug delivery through inhalation.
- the cubic liquid crystalline phases produced by the method of the invention may also be employed to encapsulate pesticides, feromones, compounds for sustained slow- release to effect the growth of plants and the Tike.
- the precursor of the cubic phase in the form of a liquid or a
- OMPI solid as described in claim 2 may also be utilized.
- a dispersion of the phase can be prepared, which can be utilized as a spray suitable for inhalation.
- the present invention involves the dissolution or dispersion of a bioactive material in a cubic liquid crystal composed of water and amphiphilic compound(s) or the preparation of a cubic phase in which the bioactive material occurs as an integral part.
- the cubic phase may form only in the presence of the bio ⁇ active material.
- the bioactive material is to be used only in small amounts, its dissolution in a known cubic phase is a more ty ⁇ pical procedure.
- one can in the preparation of con- trolled-release compositions according to the present invention make use of existing knowledge on phase behaviour of amphiphilic systems.
- phase dia ⁇ gram is not available or, in the case mentioned above, where the existence of a cubic phase may be dependent on the bioactive material used, then s-ome phase studies are a prerequisite to the application of the invention.
- the approximate region of existen ⁇ ce of the cubic phase (concentrations and temperature) and the pha ⁇ ses existing at higher (and depending on mode of employment occasio ⁇ nally also lower) water contents must be determined.
- Such studies involve visual observations but in particular observations in a po-
- the rates of release of bioactive materials according to the present invention can as described above be determined either by an erosion process or a molecular diffusion process or a combination of both.
- a molecular diffusion process is rate-limiting, useful information on the factors determining the release rate can be obtained in self-diffusion studies.
- Such self-diffusion measure ⁇ ments are very useful in predicitng how and which factors should be modified to obtain a required release rate.
- Self-diffusion studies in connection with the present invention have been made both using the classical pulsed field-gradient nuclear magnetic resonance spin- echo method (E.O. Stejskal and J.E. Tanner, J. Chem.
- the self-diffusion of hydrophilic com ⁇ ponent is ca. eight times as fast as that of hydrophobic component.
- self-diffusion coefficients of the order of 10 "12 m 2 s ⁇ can be achieved and control led.
- Figure 1 shows the phase diagram of the ternary system monoolein- egg yolk lecithin-water at about 40 C
- Figure 2 shows the amount of dye released versus square root of time for the system monoolein-water (including dye) at
- Figure 3 shows the amount of dye released versus square root of time for the system monoolein-egg yolk lecithin-water (including dye) at 37 °C and
- Figure 4 shows the amount of dye released versus square root of time for the system monoolein-glycerol -water (including dye) at 37 °C.
- an amphiphilic sys ⁇ tem which shows the advantages of the present invention is the three- component system monoolein-egg yolk lecithin-water. Its phase dia ⁇ gram is not completely known, but the cubic phase is wel! established, as seen in Figure 1.
- One advantage with this system is the fact that all components occur as natural parts in both animals and plants, which among other things make them attractive for pharmaceutical use.
- the system offers many possibilities for controlled- release preparations with various properties. For example, by vary ⁇ ing the relative amounts of onoolein and egg yolk lecithin, cubic phases of the non-erodible (low lecithin content) or erodible (high lecithin content) type may be formed.
- the system also allows glyce ⁇ rol, ethylene glycol or propylene glycol to be incorporated to app ⁇ reciable amounts without destroying the cubic structure.
- Glycerol is preferred for toxicological reasons and it acts as a highly effec- tive release rate modulator. When water is replaced by glycerol the cubic phase is stil! formed, with only a minor increase in swel ⁇ ling.
- Example 1 A cubic liquid crystalline phase is formed by mixing 0.6 g of monoolein (Nu-chek-prep Inc., USA) and 0.4 g of a 2.8 mM aqueous solution of methylene blue. The re ⁇ lease of the dye in 100 ml water was studied at 37 C by monitoring the increasing absorbance at 664 nm. The resulting release curve is shown in Figure 2, which gi- ves the amount of dye released versus square root of time. As seen in the figure the curve is linear between about 20 in to 24 h, which is to be expected for a re ⁇ lease preparation of the matrix type ("Sustained and Con ⁇ trolled Release Drug Delivery Systems", Marcel Dekker Inc. (1978)). As an alternative to the monoolein mentioned above, an industrially distilled product was used.
- Example 2 Figure 3 shows the release profile for one cubic phase where egg yolk lecithin was incorporated.
- the composition of the cubic phase was (monoolein/egg yolk lecithin/dye- solution) (48.0/12.0/40.0) (w/w).
- the figure clearly re ⁇ veals that the release profile may be altered by the addi ⁇ tion of egg yolk lecithin.
- Example 3 ⁇ igure 4 shows corresponding release curves for cubic phase where some water were replaced by glycerol.
- Example 4 0.6 g of monoolein was mixed with 0.4 g of a 7.5 % (w/w) aqueous solution of terbutaline sulphate (other names are Bricanyl and F ⁇ air ; used for the treatment of asthma) in an ampoule, which was sealed. After 24 h at 40 °C a glass-clear cubic liquid crystalline phase was obtained. It is also possible to replace up to 15 % (w/w) of the water by glycerol, and still obtain the cubic phase.
- terbutaline sulphate other names are Bricanyl and F ⁇ air ; used for the treatment of asthma
- Example 5 0.6 g of monoolein was mixed with 0.4 g water and 0.5 g of oestrio! (other names are Ovesterin , Triodurin and Triovex ; used for the treatment of vaginal desease).
- the ampoule was sealed and after about 24 h at 40 C a glass-clear cubic liquid crystalline phase was obtained.
- Example 6 0.6 g of monoolein was mixed with 0.4 g of water and 0.2 g of 2-amino-l-phenylpropano! hydrochloride (other names Lunerin and Rinomar ; used for treatment of Nicol- ses in the nose). The mixture was placed at 40 C for about 24 h, and the saturated cubic phase obtained (with respect to 2-amino-1-phenylpropano! hydrochloride) was ⁇ heated to 100 °C for about ten minutes, and then shaked extensively during cooling, in order to disperse the rest of the drug in the cubic phase. Transderma! application of cubic phases
- the following example describes a method to make a mixture of monoolein and egg yolk lecithin on a molecular level, and how to use c this mixture together with nitroglycerin and water to make a cubic phase suitable for transderma! control! ed-rel ease.
- Example 7 A mixture of 90 g monoolein and 30 g egg yolk lecithin is dissolved in 800 g of ethanol , 95% (v/v). The solvent is
- the example below describes how the cubic liquid crystalline phase precursor may be used to protect a patient against bad taste and to protect the drug against degradation in the stomach.
- the drug is benzylpenicillin. 5
- Example 8 Benzylpenicillin is pressed into tablets of 0.3 g accor ⁇ ding to conventional techniques.
- the tablets are coated with monoolein in an ethanol solution using a fluidized bed, and then covered with a thin film of sugar.
- Such a 0 Goating will also give a total protection against taste disturbance due to the penicillin in the mouth, and a control!ed-release function so that the benzylpenicill in is protected against acidic degradation in the stomach, whereas it is exposed for absorbtion in the small intes- 5 tine due to the solubilization of the coat by bile acids
- Galactoyl-diglycerides can be isolated from plants or prepared synthetically, and monogalactoyl-diglycerides form reversed hexago ⁇ nal phases with any amount of water above 5% (w/w).
- the example be ⁇ low describes a method to prepare reversed hexagonal liquid crystal ⁇ line phase from galactoyl-diglycerides.
- Example 9 Saturate water with acetylsalicyl ic acid and add 20 g of this solution to 80 g of monogalactoyl-diglyceride isola ⁇ ted from wheat ⁇ pids by column chromatography.
- the wheat lipids are easily obtained by ethanol extraction of wheat flour or wheat gluten. After a few days equilibrium has been reached as seen by the homogeneous appearance in the polarizing microscope.
- the final example describes a method to make a precursor of the cubic phase in liquid form, which is suitable for spray inhalation of insul in.
- Example 10 A saturated solution of insulin in water is prepared.
- Insulin keeps its native conformation both in the liquid phase used to give the aerosol as well as in the cubic phase-formed at contact between droplets and water in the mu- cous layer where absorption takes place.
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP84500018A JPS60500256A (en) | 1982-11-26 | 1983-11-25 | Method of preparing controlled release formulations for biologically active materials and resulting compositions |
AT83903841T ATE33938T1 (en) | 1982-11-26 | 1983-11-25 | METHODS OF MANUFACTURE OF COMPOSITIONS WITH CONTROLLED ADMINISTRATION OF BIOLOGICALLY ACTIVE MATERIALS. |
DE8383903841T DE3376467D1 (en) | 1982-11-26 | 1983-11-25 | Method of preparing controlled-release preparations for biologically active materials |
AU23396/84A AU2339684A (en) | 1982-11-26 | 1983-11-25 | Method of preparing controlled-release preparations for bio- |
DK362284A DK166752B1 (en) | 1982-11-26 | 1984-07-24 | Process for producing preparations having a regulated release of biologically active materials |
NO843023A NO173315C (en) | 1982-11-26 | 1984-07-25 | Process for preparing liquid crystals with controlled release of a biologically active material |
FI842983A FI83036C (en) | 1982-11-26 | 1984-07-26 | A process for the preparation of a composition which releasably controls a biologically active substance |
US08/313,543 US5753259A (en) | 1982-11-26 | 1994-09-27 | Method of preparing controlled-release preparations for biologically active materials and resulting compositions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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SE8206744A SE8206744D0 (en) | 1982-11-26 | 1982-11-26 | PREPARATION FOR CONTROLLED RELEASE OF SUBSTANCES |
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WO1984002076A1 true WO1984002076A1 (en) | 1984-06-07 |
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PCT/SE1983/000411 WO1984002076A1 (en) | 1982-11-26 | 1983-11-25 | Method of preparing controlled-release preparations for biologically active materials and resulting compositions |
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US (2) | US5151272A (en) |
EP (1) | EP0126751B2 (en) |
JP (1) | JPS60500256A (en) |
AT (1) | ATE33938T1 (en) |
AU (2) | AU2339684A (en) |
DE (1) | DE3376467D1 (en) |
DK (1) | DK166752B1 (en) |
FI (1) | FI83036C (en) |
NO (1) | NO173315C (en) |
SE (1) | SE8206744D0 (en) |
WO (1) | WO1984002076A1 (en) |
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Also Published As
Publication number | Publication date |
---|---|
US5753259A (en) | 1998-05-19 |
DK362284A (en) | 1984-07-24 |
DE3376467D1 (en) | 1988-06-09 |
FI842983A (en) | 1984-07-26 |
DK362284D0 (en) | 1984-07-24 |
AU1819388A (en) | 1988-10-27 |
EP0126751A1 (en) | 1984-12-05 |
NO173315C (en) | 1993-12-01 |
NO173315B (en) | 1993-08-23 |
AU615453B2 (en) | 1991-10-03 |
DK166752B1 (en) | 1993-07-12 |
EP0126751B2 (en) | 1993-01-20 |
FI83036C (en) | 1991-05-27 |
FI83036B (en) | 1991-02-15 |
FI842983A0 (en) | 1984-07-26 |
SE8206744D0 (en) | 1982-11-26 |
ATE33938T1 (en) | 1988-05-15 |
EP0126751B1 (en) | 1988-05-04 |
US5151272A (en) | 1992-09-29 |
AU2339684A (en) | 1984-06-18 |
NO843023L (en) | 1984-07-25 |
JPS60500256A (en) | 1985-02-28 |
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