ZA200302489B - Method for producing an extract from cannabis plant matter, containing a tetrahydrocannabinol and a cannabidiol and cannabis extracts. - Google Patents
Method for producing an extract from cannabis plant matter, containing a tetrahydrocannabinol and a cannabidiol and cannabis extracts. Download PDFInfo
- Publication number
- ZA200302489B ZA200302489B ZA200302489A ZA200302489A ZA200302489B ZA 200302489 B ZA200302489 B ZA 200302489B ZA 200302489 A ZA200302489 A ZA 200302489A ZA 200302489 A ZA200302489 A ZA 200302489A ZA 200302489 B ZA200302489 B ZA 200302489B
- Authority
- ZA
- South Africa
- Prior art keywords
- thc
- tetrahydrocannabinol
- extract
- cannabidiol
- pressure
- Prior art date
Links
- 229960004242 dronabinol Drugs 0.000 title claims description 167
- 239000000284 extract Substances 0.000 title claims description 111
- CYQFCXCEBYINGO-UHFFFAOYSA-N THC Natural products C1=C(C)CCC2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3C21 CYQFCXCEBYINGO-UHFFFAOYSA-N 0.000 title claims description 71
- CYQFCXCEBYINGO-IAGOWNOFSA-N delta1-THC Chemical compound C1=C(C)CC[C@H]2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3[C@@H]21 CYQFCXCEBYINGO-IAGOWNOFSA-N 0.000 title claims description 70
- ZTGXAWYVTLUPDT-UHFFFAOYSA-N cannabidiol Natural products OC1=CC(CCCCC)=CC(O)=C1C1C(C(C)=C)CC=C(C)C1 ZTGXAWYVTLUPDT-UHFFFAOYSA-N 0.000 title claims description 68
- 229950011318 cannabidiol Drugs 0.000 title claims description 67
- QHMBSVQNZZTUGM-UHFFFAOYSA-N Trans-Cannabidiol Natural products OC1=CC(CCCCC)=CC(O)=C1C1C(C(C)=C)CCC(C)=C1 QHMBSVQNZZTUGM-UHFFFAOYSA-N 0.000 title claims description 65
- PCXRACLQFPRCBB-ZWKOTPCHSA-N dihydrocannabidiol Natural products OC1=CC(CCCCC)=CC(O)=C1[C@H]1[C@H](C(C)C)CCC(C)=C1 PCXRACLQFPRCBB-ZWKOTPCHSA-N 0.000 title claims description 65
- QHMBSVQNZZTUGM-ZWKOTPCHSA-N cannabidiol Chemical compound OC1=CC(CCCCC)=CC(O)=C1[C@H]1[C@H](C(C)=C)CCC(C)=C1 QHMBSVQNZZTUGM-ZWKOTPCHSA-N 0.000 title claims description 63
- 241000218236 Cannabis Species 0.000 title claims 5
- 238000004519 manufacturing process Methods 0.000 title description 7
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 claims description 36
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 claims description 36
- 235000009120 camo Nutrition 0.000 claims description 34
- 235000005607 chanvre indien Nutrition 0.000 claims description 34
- 239000011487 hemp Substances 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 33
- 230000008569 process Effects 0.000 claims description 32
- 238000000605 extraction Methods 0.000 claims description 29
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 21
- 241000196324 Embryophyta Species 0.000 claims description 20
- 239000003814 drug Substances 0.000 claims description 20
- 229940079593 drug Drugs 0.000 claims description 18
- 229930002875 chlorophyll Natural products 0.000 claims description 15
- 235000019804 chlorophyll Nutrition 0.000 claims description 15
- 229930013930 alkaloid Natural products 0.000 claims description 14
- 150000001735 carboxylic acids Chemical class 0.000 claims description 14
- 239000000835 fiber Substances 0.000 claims description 13
- 244000025254 Cannabis sativa Species 0.000 claims description 12
- 150000002773 monoterpene derivatives Chemical class 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- 229930003658 monoterpene Natural products 0.000 claims description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 10
- 239000000470 constituent Substances 0.000 claims description 9
- 235000002577 monoterpenes Nutrition 0.000 claims description 9
- 229930004725 sesquiterpene Natural products 0.000 claims description 9
- 239000003463 adsorbent Substances 0.000 claims description 8
- 239000001752 chlorophylls and chlorophyllins Substances 0.000 claims description 8
- 229930003935 flavonoid Natural products 0.000 claims description 8
- 150000002215 flavonoids Chemical class 0.000 claims description 8
- 235000017173 flavonoids Nutrition 0.000 claims description 8
- -1 sesquiterpene hydrocarbons Chemical class 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 235000008697 Cannabis sativa Nutrition 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- 239000007858 starting material Substances 0.000 claims description 7
- 239000005909 Kieselgur Substances 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 239000000741 silica gel Substances 0.000 claims description 5
- 229910002027 silica gel Inorganic materials 0.000 claims description 5
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 239000011230 binding agent Substances 0.000 claims description 4
- WVOLTBSCXRRQFR-DLBZAZTESA-N cannabidiolic acid Chemical compound OC1=C(C(O)=O)C(CCCCC)=CC(O)=C1[C@H]1[C@H](C(C)=C)CCC(C)=C1 WVOLTBSCXRRQFR-DLBZAZTESA-N 0.000 claims description 4
- 239000000047 product Substances 0.000 claims description 4
- 239000001993 wax Substances 0.000 claims description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
- 235000012216 bentonite Nutrition 0.000 claims description 2
- 238000004061 bleaching Methods 0.000 claims description 2
- 239000001273 butane Substances 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 239000000395 magnesium oxide Substances 0.000 claims description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 2
- 239000001294 propane Substances 0.000 claims description 2
- WVOLTBSCXRRQFR-SJORKVTESA-N Cannabidiolic acid Natural products OC1=C(C(O)=O)C(CCCCC)=CC(O)=C1[C@@H]1[C@@H](C(C)=C)CCC(C)=C1 WVOLTBSCXRRQFR-SJORKVTESA-N 0.000 claims 2
- 238000004440 column chromatography Methods 0.000 claims 1
- 238000004128 high performance liquid chromatography Methods 0.000 claims 1
- 240000004308 marijuana Species 0.000 description 54
- 229930003827 cannabinoid Natural products 0.000 description 25
- 239000003557 cannabinoid Substances 0.000 description 25
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 18
- 229940065144 cannabinoids Drugs 0.000 description 16
- 238000007363 ring formation reaction Methods 0.000 description 8
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 7
- 239000002035 hexane extract Substances 0.000 description 7
- 238000000746 purification Methods 0.000 description 7
- 150000004354 sesquiterpene derivatives Chemical class 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 239000000469 ethanolic extract Substances 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- 238000000926 separation method Methods 0.000 description 6
- 239000002808 molecular sieve Substances 0.000 description 5
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 5
- CYQFCXCEBYINGO-DLBZAZTESA-N Dronabinol Natural products C1=C(C)CC[C@H]2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3[C@H]21 CYQFCXCEBYINGO-DLBZAZTESA-N 0.000 description 4
- 229910002091 carbon monoxide Inorganic materials 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 230000003400 hallucinatory effect Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 4
- 230000001105 regulatory effect Effects 0.000 description 4
- KZZKPJBKEJKNAK-UHFFFAOYSA-N Cannabisativin Natural products C1C(=O)NCCCCNCCCN2C(C(O)C(O)CCCCC)C=CCC21 KZZKPJBKEJKNAK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000006114 decarboxylation reaction Methods 0.000 description 3
- 230000000144 pharmacologic effect Effects 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- UVOLYTDXHDXWJU-UHFFFAOYSA-N Cannabichromene Chemical compound C1=CC(C)(CCC=C(C)C)OC2=CC(CCCCC)=CC(O)=C21 UVOLYTDXHDXWJU-UHFFFAOYSA-N 0.000 description 2
- UVOLYTDXHDXWJU-NRFANRHFSA-N Cannabichromene Natural products C1=C[C@](C)(CCC=C(C)C)OC2=CC(CCCCC)=CC(O)=C21 UVOLYTDXHDXWJU-NRFANRHFSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 239000004866 Hashish Substances 0.000 description 2
- 235000008694 Humulus lupulus Nutrition 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 208000019695 Migraine disease Diseases 0.000 description 2
- 208000007101 Muscle Cramp Diseases 0.000 description 2
- 208000002193 Pain Diseases 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000003797 alkaloid derivatives Chemical class 0.000 description 2
- 230000003474 anti-emetic effect Effects 0.000 description 2
- 230000003556 anti-epileptic effect Effects 0.000 description 2
- 239000001961 anticonvulsive agent Substances 0.000 description 2
- UAHWPYUMFXYFJY-UHFFFAOYSA-N beta-myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 description 2
- QXACEHWTBCFNSA-SFQUDFHCSA-N cannabigerol Chemical compound CCCCCC1=CC(O)=C(C\C=C(/C)CCC=C(C)C)C(O)=C1 QXACEHWTBCFNSA-SFQUDFHCSA-N 0.000 description 2
- QXACEHWTBCFNSA-UHFFFAOYSA-N cannabigerol Natural products CCCCCC1=CC(O)=C(CC=C(C)CCC=C(C)C)C(O)=C1 QXACEHWTBCFNSA-UHFFFAOYSA-N 0.000 description 2
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 2
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 2
- 231100000433 cytotoxic Toxicity 0.000 description 2
- 230000001472 cytotoxic effect Effects 0.000 description 2
- 230000004069 differentiation Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 229930182486 flavonoid glycoside Natural products 0.000 description 2
- 150000007955 flavonoid glycosides Chemical class 0.000 description 2
- 244000265144 hemp Species 0.000 description 2
- 206010027599 migraine Diseases 0.000 description 2
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 description 2
- 239000004081 narcotic agent Substances 0.000 description 2
- IRMPFYJSHJGOPE-UHFFFAOYSA-N olivetol Chemical compound CCCCCC1=CC(O)=CC(O)=C1 IRMPFYJSHJGOPE-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000002953 preparative HPLC Methods 0.000 description 2
- 238000004237 preparative chromatography Methods 0.000 description 2
- 230000000506 psychotropic effect Effects 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- NPNUFJAVOOONJE-ZIAGYGMSSA-N β-(E)-Caryophyllene Chemical compound C1CC(C)=CCCC(=C)[C@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-ZIAGYGMSSA-N 0.000 description 2
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 1
- XWFVRMWMBYDDFY-WCBMZHEXSA-N (1s,4r)-4-(2-hydroxypropan-2-yl)-1-methylcyclohex-2-en-1-ol Chemical compound CC(C)(O)[C@@H]1CC[C@](C)(O)C=C1 XWFVRMWMBYDDFY-WCBMZHEXSA-N 0.000 description 1
- TWKHUZXSTKISQC-UHFFFAOYSA-N 2-(5-methyl-2-prop-1-en-2-ylphenyl)-5-pentylbenzene-1,3-diol Chemical compound OC1=CC(CCCCC)=CC(O)=C1C1=CC(C)=CC=C1C(C)=C TWKHUZXSTKISQC-UHFFFAOYSA-N 0.000 description 1
- XJBOZKOSICCONT-UHFFFAOYSA-N 4,6,6-trimethylbicyclo[3.1.1]hept-2-ene Chemical compound CC1C=CC2C(C)(C)C1C2 XJBOZKOSICCONT-UHFFFAOYSA-N 0.000 description 1
- XWFVRMWMBYDDFY-UHFFFAOYSA-N 6-Angeloyl-3,6,9-Trihydroxy-7(11)-eremophilen-12,8-olide Natural products CC(C)(O)C1CCC(C)(O)C=C1 XWFVRMWMBYDDFY-UHFFFAOYSA-N 0.000 description 1
- NVEQFIOZRFFVFW-UHFFFAOYSA-N 9-epi-beta-caryophyllene oxide Natural products C=C1CCC2OC2(C)CCC2C(C)(C)CC21 NVEQFIOZRFFVFW-UHFFFAOYSA-N 0.000 description 1
- 208000030507 AIDS Diseases 0.000 description 1
- 206010006895 Cachexia Diseases 0.000 description 1
- 241000218235 Cannabaceae Species 0.000 description 1
- VBGLYOIFKLUMQG-UHFFFAOYSA-N Cannabinol Chemical compound C1=C(C)C=C2C3=C(O)C=C(CCCCC)C=C3OC(C)(C)C2=C1 VBGLYOIFKLUMQG-UHFFFAOYSA-N 0.000 description 1
- 208000000094 Chronic Pain Diseases 0.000 description 1
- 235000000604 Chrysanthemum parthenium Nutrition 0.000 description 1
- ORKZJYDOERTGKY-UHFFFAOYSA-N Dihydrocannabichromen Natural products C1CC(C)(CCC=C(C)C)OC2=CC(CCCCC)=CC(O)=C21 ORKZJYDOERTGKY-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 208000010412 Glaucoma Diseases 0.000 description 1
- GVGLGOZIDCSQPN-PVHGPHFFSA-N Heroin Chemical compound O([C@H]1[C@H](C=C[C@H]23)OC(C)=O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4OC(C)=O GVGLGOZIDCSQPN-PVHGPHFFSA-N 0.000 description 1
- 241000218228 Humulus Species 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 1
- 239000008896 Opium Substances 0.000 description 1
- 206010033892 Paraplegia Diseases 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241000489455 Sitta europaea Species 0.000 description 1
- 208000005392 Spasm Diseases 0.000 description 1
- 241000602316 Tanacetum parthenium Species 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 206010047700 Vomiting Diseases 0.000 description 1
- 208000010399 Wasting Syndrome Diseases 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- FAMPSKZZVDUYOS-UHFFFAOYSA-N alpha-Caryophyllene Natural products CC1=CCC(C)(C)C=CCC(C)=CCC1 FAMPSKZZVDUYOS-UHFFFAOYSA-N 0.000 description 1
- VYBREYKSZAROCT-UHFFFAOYSA-N alpha-myrcene Natural products CC(=C)CCCC(=C)C=C VYBREYKSZAROCT-UHFFFAOYSA-N 0.000 description 1
- 230000003444 anaesthetic effect Effects 0.000 description 1
- 239000002111 antiemetic agent Substances 0.000 description 1
- 230000036528 appetite Effects 0.000 description 1
- 235000019789 appetite Nutrition 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- NPNUFJAVOOONJE-UHFFFAOYSA-N beta-cariophyllene Natural products C1CC(C)=CCCC(=C)C2CC(C)(C)C21 NPNUFJAVOOONJE-UHFFFAOYSA-N 0.000 description 1
- 230000001851 biosynthetic effect Effects 0.000 description 1
- 244000213578 camo Species 0.000 description 1
- 229960003453 cannabinol Drugs 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- NPNUFJAVOOONJE-UONOGXRCSA-N caryophyllene Natural products C1CC(C)=CCCC(=C)[C@@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-UONOGXRCSA-N 0.000 description 1
- 229940117948 caryophyllene Drugs 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 229960003920 cocaine Drugs 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000000824 cytostatic agent Substances 0.000 description 1
- HCAWPGARWVBULJ-IAGOWNOFSA-N delta8-THC Chemical compound C1C(C)=CC[C@H]2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3[C@@H]21 HCAWPGARWVBULJ-IAGOWNOFSA-N 0.000 description 1
- 229960002069 diamorphine Drugs 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000008157 edible vegetable oil Substances 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- GCFHZZWXZLABBL-UHFFFAOYSA-N ethanol;hexane Chemical compound CCO.CCCCCC GCFHZZWXZLABBL-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000008384 feverfew Nutrition 0.000 description 1
- 238000007380 fibre production Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 230000000762 glandular Effects 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- YCOZIPAWZNQLMR-UHFFFAOYSA-N heptane - octane Natural products CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 230000004410 intraocular pressure Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229910000833 kovar Inorganic materials 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000036651 mood Effects 0.000 description 1
- 229960005181 morphine Drugs 0.000 description 1
- 201000006417 multiple sclerosis Diseases 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 229960001027 opium Drugs 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000007965 phenolic acids Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 229940043263 traditional drug Drugs 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/78—Ring systems having three or more relevant rings
- C07D311/80—Dibenzopyrans; Hydrogenated dibenzopyrans
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/54—Improvements relating to the production of bulk chemicals using solvents, e.g. supercritical solvents or ionic liquids
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Medical Informatics (AREA)
- Biotechnology (AREA)
- Botany (AREA)
- Alternative & Traditional Medicine (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Neurology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines Containing Plant Substances (AREA)
- Pyrane Compounds (AREA)
- Extraction Or Liquid Replacement (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10051427A DE10051427C1 (de) | 2000-10-17 | 2000-10-17 | Verfahren zur Herstellung eines Tetrahydrocannabinol- und Cannabidiol-haltigen Extraktes aus Cannabis-Pflanzenmaterial sowie Cannabis-Extrakte |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200302489B true ZA200302489B (en) | 2004-07-05 |
Family
ID=7660081
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200302489A ZA200302489B (en) | 2000-10-17 | 2003-03-31 | Method for producing an extract from cannabis plant matter, containing a tetrahydrocannabinol and a cannabidiol and cannabis extracts. |
Country Status (25)
| Country | Link |
|---|---|
| US (5) | USRE49434E1 (ru) |
| EP (1) | EP1326598B1 (ru) |
| JP (1) | JP4146225B2 (ru) |
| KR (1) | KR20030040522A (ru) |
| CN (1) | CN1202818C (ru) |
| AT (1) | ATE303142T1 (ru) |
| AU (2) | AU2002218242B2 (ru) |
| BR (1) | BR0114717A (ru) |
| CA (1) | CA2424356A1 (ru) |
| CY (1) | CY1105011T1 (ru) |
| CZ (1) | CZ2003843A3 (ru) |
| DE (2) | DE10051427C1 (ru) |
| DK (1) | DK1326598T3 (ru) |
| EA (1) | EA004520B1 (ru) |
| ES (1) | ES2243580T3 (ru) |
| HU (1) | HU227796B1 (ru) |
| IL (1) | IL155185A0 (ru) |
| MX (1) | MXPA03003295A (ru) |
| NZ (1) | NZ525118A (ru) |
| PL (1) | PL206679B1 (ru) |
| PT (1) | PT1326598E (ru) |
| SK (1) | SK287668B6 (ru) |
| UA (1) | UA74203C2 (ru) |
| WO (1) | WO2002032420A1 (ru) |
| ZA (1) | ZA200302489B (ru) |
Families Citing this family (205)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6730519B2 (en) * | 1998-10-26 | 2004-05-04 | The University Of Mississippi | Method of preparing delta-9-tetrahydrocannabinol |
| DE10051427C1 (de) * | 2000-10-17 | 2002-06-13 | Adam Mueller | Verfahren zur Herstellung eines Tetrahydrocannabinol- und Cannabidiol-haltigen Extraktes aus Cannabis-Pflanzenmaterial sowie Cannabis-Extrakte |
| US10004684B2 (en) | 2001-02-14 | 2018-06-26 | Gw Pharma Limited | Pharmaceutical formulations |
| EP1361864B9 (en) * | 2001-02-14 | 2014-07-09 | GW Pharma Limited | Liquid spray formulations for buccal delivery of cannabinoids |
| US8034843B2 (en) | 2002-02-01 | 2011-10-11 | Gw Pharma Limited | Compositions comprising cannabinoids for treatment of nausea, vomiting, emesis, motion sickness or like conditions |
| GB0202385D0 (en) * | 2002-02-01 | 2002-03-20 | Gw Pharma Ltd | Compositions for the treatment of nausea,vomiting,emesis,motion sicknes or like conditions |
| IL148244A0 (en) * | 2002-02-19 | 2002-09-12 | Yissum Res Dev Co | Anti-nausea and anti-vomiting activity of cannabidiol compounds |
| DE10226494A1 (de) * | 2002-06-14 | 2004-01-08 | Lts Lohmann Therapie-Systeme Ag | Filmförmige mucoadhäsive Darreichungsformen zur Verabreichung von Cannabis-Wirkstoffen |
| AU2003261187B2 (en) | 2002-07-18 | 2009-10-22 | Phasex Corporation | Reduction of constituents in tobacco |
| US10730906B2 (en) * | 2002-08-01 | 2020-08-04 | Nuevolutions A/S | Multi-step synthesis of templated molecules |
| GB2391865B (en) * | 2002-08-14 | 2005-06-01 | Gw Pharma Ltd | Improvements in the extraction of pharmaceutically active components from plant materials |
| WO2004016277A2 (en) * | 2002-08-14 | 2004-02-26 | Gw Pharma Limited | Extraction of pharmaceutically active cannabinoids from plant materials |
| US7344736B2 (en) * | 2002-08-14 | 2008-03-18 | Gw Pharma Limited | Extraction of pharmaceutically active components from plant materials |
| US6946150B2 (en) * | 2002-08-14 | 2005-09-20 | Gw Pharma Limited | Pharmaceutical formulation |
| US10538373B2 (en) | 2002-08-14 | 2020-01-21 | Gw Pharma Limited | Pharmaceutical formulation |
| GB0222077D0 (en) | 2002-09-23 | 2002-10-30 | Gw Pharma Ltd | Methods of preparing cannabinoids from plant material |
| GB2393182B (en) * | 2002-09-23 | 2007-03-14 | Gw Pharma Ltd | Method of preparing cannabidiol from plant material |
| US20040248970A1 (en) * | 2003-04-10 | 2004-12-09 | Webster G.R. Barrie | CBD-delta8-THC composition |
| EP1559423A1 (en) * | 2004-02-02 | 2005-08-03 | Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno | Medicinal acidic cannabinoids |
| GB2418612A (en) * | 2004-10-01 | 2006-04-05 | Gw Pharma Ltd | Inhibition of tumour cell migration with cannabinoids |
| DE102005028937B4 (de) * | 2005-06-22 | 2009-07-23 | Bionorica Ag | Verfahren zur Herstellung von Dronabinol |
| US7597910B2 (en) * | 2005-08-20 | 2009-10-06 | Slgm Medical Research Institute | Compositions and methods for treating prostate disorders |
| AU2006297300B2 (en) | 2005-09-29 | 2012-05-10 | Albany Molecular Research, Inc. | Process for production of delta-9-tetrahydrocannabinol |
| GB2434312B (en) | 2006-01-18 | 2011-06-29 | Gw Pharma Ltd | Cannabinoid-containing plant extracts as neuroprotective agents |
| DE102007046086A1 (de) * | 2007-09-26 | 2009-04-09 | Heinz Prof. Dr. Letzel | Pflanzenextrakt aus THC-armen Cannabis zur Behandlung von Erkrankungen |
| GB2460672B (en) * | 2008-06-04 | 2012-01-04 | Gw Pharma Ltd | Cannabinoids in combination with non-cannabinoid chemotherapeutic agents that are alkylating agents |
| BRPI1010302A2 (pt) * | 2009-04-03 | 2017-06-27 | Synthetic Genomics Inc | composições e métodos para tratamento, inibição ou prevenção do desenvolvimento de uma doença patogênica de planta e método de extermínio, inibição ou prevenção do desenvolvimento de um organismo |
| WO2010150245A1 (en) * | 2009-06-24 | 2010-12-29 | Tikun Olam Ltd. | Pharmaceutical and cosmeceutical compositions containing cannabis flower and seed extracts |
| GB2471523A (en) * | 2009-07-03 | 2011-01-05 | Gw Pharma Ltd | Use of tetrahydrocannibivarin (THCV) and optionally cannabidiol (CBD) in the treatment of epilepsy |
| GB2478595B (en) | 2010-03-12 | 2018-04-04 | Gw Pharma Ltd | Phytocannabinoids in the treatment of glioma |
| US8445034B1 (en) | 2010-11-02 | 2013-05-21 | Albert L Coles, Jr. | Systems and methods for producing organic cannabis tincture |
| GB2487712B (en) * | 2011-01-04 | 2015-10-28 | Otsuka Pharma Co Ltd | Use of the phytocannabinoid cannabidiol (CBD) in combination with a standard anti-epileptic drug (SAED) in the treatment of epilepsy |
| GB201111261D0 (en) | 2011-07-01 | 2011-08-17 | Gw Pharma Ltd | Cannabinoids for use in the treatment of neuro-degenerative diseases or disorders |
| GB2514054A (en) | 2011-09-29 | 2014-11-12 | Gw Pharma Ltd | A pharmaceutical composition comprising the phytocannabinoids cannabidivarin (CBDV) and cannabidiol (CBD) |
| EP4137142A1 (en) | 2013-03-14 | 2023-02-22 | Purple Mundo, Inc. | Bioactive concentrates and uses thereof |
| MX2015013202A (es) | 2013-03-15 | 2016-04-07 | Biotech Inst Llc | Cultivo, produccion, procesamiento y uso de cannabis de especialidad. |
| US10441617B2 (en) | 2013-03-15 | 2019-10-15 | Biotech Institute, Llc | Breeding, production, processing and use of medical cannabis |
| GB2516814B (en) | 2013-06-19 | 2016-08-31 | Otsuka Pharma Co Ltd | Use of phytocannabinoids for increasing radiosensitivity in the treatment of cancer |
| EP3052602A4 (en) | 2013-10-04 | 2017-06-14 | Natural Extraction Services, LLC | Method and apparatus for extracting botanical oils |
| GB2536150A (en) * | 2013-11-11 | 2016-09-07 | The Werc Shop Llc | Solvent-free processing, system and methods |
| WO2015122484A1 (ja) * | 2014-02-13 | 2015-08-20 | ウシオ電機株式会社 | 大麻成分の抽出方法、大麻成分の検査用デバイス及び大麻成分の検査方法 |
| WO2015142574A1 (en) | 2014-03-21 | 2015-09-24 | St & T International, Inc. | Cannabis extraction method and compositions |
| US9186386B2 (en) | 2014-04-17 | 2015-11-17 | Gary J. Speier | Pharmaceutical composition and method of manufacturing |
| US9044390B1 (en) | 2014-04-17 | 2015-06-02 | Gary J. Speier | Pharmaceutical composition and method of manufacturing |
| US10319475B1 (en) | 2014-06-13 | 2019-06-11 | Enigami Systems, Inc. | Method and apparatus for determining relationships between medications and symptoms |
| GB2530001B (en) | 2014-06-17 | 2019-01-16 | Gw Pharma Ltd | Use of cannabidiol in the reduction of convulsive seizure frequency in treatment-resistant epilepsy |
| US10610512B2 (en) | 2014-06-26 | 2020-04-07 | Island Breeze Systems Ca, Llc | MDI related products and methods of use |
| WO2016004121A1 (en) * | 2014-07-01 | 2016-01-07 | MJAR Holdings, LLC | High cannabidiol cannabis strains |
| WO2016004410A1 (en) | 2014-07-02 | 2016-01-07 | Cannavest Corp. | Novel process for generating hemp oil with a high cannabidiol (cbd) content |
| US10897915B2 (en) | 2014-08-15 | 2021-01-26 | Blacklist Holdings, Inc. | Method for making coffee products containing cannabis ingredients |
| US9565865B2 (en) | 2014-08-15 | 2017-02-14 | Imbue LLC | Method for making coffee products containing cannabis ingredients |
| US9649575B2 (en) | 2014-09-03 | 2017-05-16 | Hopkins Holdings Llc | Organic oil extraction device |
| US10117891B2 (en) | 2014-09-16 | 2018-11-06 | India Globalization Capital, Inc. | Cannabinoid composition for treating pain |
| GB2531278A (en) | 2014-10-14 | 2016-04-20 | Gw Pharma Ltd | Use of cannabidiol in the treatment of intractable epilepsy |
| GB2531282A (en) | 2014-10-14 | 2016-04-20 | Gw Pharma Ltd | Use of cannabinoids in the treatment of epilepsy |
| CA3135893C (en) * | 2014-10-21 | 2023-11-14 | United Cannabis Corp. | Cannabis extracts and methods of preparing and using same |
| WO2016097425A1 (de) | 2014-12-19 | 2016-06-23 | Thc Pharm Gmbh | Cbd-haltiges getränk |
| WO2016105514A1 (en) | 2014-12-23 | 2016-06-30 | Biotech Institute, Llc | A reliable and robust method for the analysis of cannabinoids and terpenes in cannabis |
| CA2977421C (en) * | 2015-01-22 | 2022-10-18 | Phytoplant Research S.L. | Methods of purifying cannabinoids, compositions and kits thereof |
| EP3247359A4 (en) | 2015-01-25 | 2018-08-08 | India Globalization Capital, Inc. | Composition and method for treating seizure disorders |
| US10830780B2 (en) | 2015-01-26 | 2020-11-10 | Biotech Institute, Llc | Apparatus and methods for sample analysis and classification based on terpenes and cannabinoids in the sample |
| AU2016215094B2 (en) * | 2015-02-05 | 2019-09-26 | Colorado Can Llc | Purified CBD and CBDA, and methods, compositions and products employing CBD or CBDA |
| EP3061510A1 (de) | 2015-02-27 | 2016-08-31 | Bionorica Ethics GmbH | CPC Verteilungschromatographie von Cannabinoiden |
| EP3274321B8 (en) | 2015-03-23 | 2019-10-23 | Echo Pharmaceuticals B.V. | Cannabidiol isolate from industrial-hemp and use thereof in pharmaceutical and/or cosmetic preparations |
| BG112018A (bg) | 2015-05-22 | 2016-11-30 | "Побелч-Гле" Оод | Метод за получаване на канабиноиден извлек от коноп |
| EP3307291A1 (en) * | 2015-06-09 | 2018-04-18 | Total Health Care I | Process for extraction, separation and purification of cannabinoids, flavonoids and terpenes from cannabis |
| GB2539472A (en) | 2015-06-17 | 2016-12-21 | Gw Res Ltd | Use of cannabinoids in the treatment of epilepsy |
| US10092855B2 (en) | 2015-07-16 | 2018-10-09 | Fritz Chess | CO2 extraction and filtration system |
| US10596159B2 (en) | 2015-08-12 | 2020-03-24 | India Globalization Capital, Inc. | Method and composition for treating cachexia and eating disorders |
| US20170071992A1 (en) * | 2015-09-15 | 2017-03-16 | Mrx Xtractors Llc | Method and system for extracting compounds from plants and plant based materials |
| EP3150264A1 (de) | 2015-09-30 | 2017-04-05 | Bionorica Ethics GmbH | Vakuumdestillation zur anreicherung von cbd |
| US9950976B1 (en) * | 2015-10-27 | 2018-04-24 | CLS Labs, Inc. | Cannabidiol extraction and conversion process |
| EP3367831A4 (en) * | 2015-10-30 | 2019-08-14 | Nisarga Biotech Private Limited | THERAPEUTIC COMPOSITIONS COMPRISING VEGETABLE EXTRACTS AND ESSENTIAL OILS FOR SMOKING AND SPRAYING |
| EP3175897B1 (de) | 2015-12-04 | 2018-04-04 | Evonik Degussa GmbH | Verbessertes verfahren zur extraktion von aromastoffen aus fetthaltigen und/oder wässrigen flüssigphasen |
| US10028987B1 (en) | 2015-12-22 | 2018-07-24 | Chocowaska Cooperative, Inc. | Cannabis-infused milk |
| CN105505565A (zh) * | 2015-12-28 | 2016-04-20 | 贵州航天乌江机电设备有限责任公司 | 一种萃取富含大麻二酚的工业大麻油的方法 |
| US20170202895A1 (en) * | 2016-01-18 | 2017-07-20 | Kevin Anthony Hugh | Cannabis Pellets |
| US10328361B2 (en) | 2016-02-25 | 2019-06-25 | Jeffrey M. Skell | Extracting substances from botanical matter |
| WO2017151980A1 (en) | 2016-03-03 | 2017-09-08 | Segreti Louis M | Cannabis-based bioactive formulations and methods for use thereof |
| US10842772B1 (en) | 2016-03-03 | 2020-11-24 | Segreti Louis Michael | Cannabis-based bioactive formulations and methods for use thereof |
| US10307447B2 (en) | 2016-03-07 | 2019-06-04 | Stephen Goldner | Freeze dry process |
| US10045515B2 (en) * | 2016-03-07 | 2018-08-14 | Jeffrey T Cooper | Edible, retrievable animal items |
| GB2548873B (en) | 2016-03-31 | 2020-12-02 | Gw Res Ltd | Use of Cannabidiol in the Treatment of SturgeWeber Syndrome |
| US11305212B2 (en) | 2016-04-06 | 2022-04-19 | Kiinja Corporation | Multifunctional vessels for extraction and fractionation of extracts from biomass |
| US10625175B2 (en) | 2016-04-06 | 2020-04-21 | Kiinja Corporation | Extractor for high pressure extraction of a matrix |
| US10933013B1 (en) | 2016-04-25 | 2021-03-02 | Ethan D Dean | Oral hygiene compositions containing extract of cannabis plant |
| US9901607B2 (en) | 2016-04-28 | 2018-02-27 | Mark J. Silen | Smokeless cannabis composition and method of manufacture |
| US10617974B2 (en) | 2016-05-02 | 2020-04-14 | Natural Extraction Systems, LLC | Method and apparatus for extracting botanical oils |
| US10456709B2 (en) | 2016-05-10 | 2019-10-29 | Green Mill Supercritical, Inc. | Dispersion flow device for extraction vessel and methods of use |
| US10499584B2 (en) | 2016-05-27 | 2019-12-10 | New West Genetics | Industrial hemp Cannabis cultivars and seeds with stable cannabinoid profiles |
| EP3471746A4 (en) | 2016-06-15 | 2020-02-26 | India Globalization Capital, Inc. | METHOD AND COMPOSITION FOR TREATING EPILEPTIC DISORDERS |
| EP3475402B1 (en) | 2016-06-24 | 2023-08-02 | Cool Clean Technologies, LLC | Method of extraction of cannabinoids using liquid carbon dioxide |
| GB2551986A (en) | 2016-07-01 | 2018-01-10 | Gw Res Ltd | Parenteral formulations |
| GB2551987A (en) | 2016-07-01 | 2018-01-10 | Gw Res Ltd | Oral cannabinoid formulations |
| EP3493799A4 (en) * | 2016-08-03 | 2020-04-01 | Zelda Therapeutics Operations Pty Ltd | CANNABIS |
| KR20190034576A (ko) * | 2016-08-03 | 2019-04-02 | 젤다 테라퓨틱스 오퍼레이션즈 피티와이 엘티디 | 카나비스 조성물 |
| GB2553139A (en) | 2016-08-25 | 2018-02-28 | Gw Res Ltd | Use of cannabinoids in the treatment of multiple myeloma |
| WO2018071452A1 (en) | 2016-10-11 | 2018-04-19 | Growblox Life Sciences L.L.C. | Cannabinoid-containing complex mixtures for the treatment of neurodegenerative diseases |
| CA3033166C (en) | 2016-11-14 | 2021-12-14 | Ag Equipment Ip Holding Company, Inc. | Mobile supercritical extractor system with evaporator chamber having cones and related methods |
| JP2020515379A (ja) * | 2016-12-01 | 2020-05-28 | ナチュラル イクストゥラクション システムズ，エルエルシー | マイクロ波剤を利用した急速植物性油蒸留装置 |
| US10239808B1 (en) | 2016-12-07 | 2019-03-26 | Canopy Holdings, LLC | Cannabis extracts |
| GB2557921A (en) | 2016-12-16 | 2018-07-04 | Gw Res Ltd | Use of cannabinoids in the treatment of angelman syndrome |
| CA3048841A1 (en) | 2016-12-30 | 2018-07-05 | X Traxion, Llc | Extraction of compounds from cannabis |
| AU2018207955B2 (en) * | 2017-01-14 | 2022-10-06 | Herbolea Biotech S.R.L. | Enzyme-assisted lipid-based extraction and stabilization of phyto-cannabinoids and terpens and products obtained thereof |
| AU2018215200B2 (en) | 2017-02-01 | 2022-12-15 | Gbs Global Biopharma, Inc. | Cannabinoid-containing complex mixtures for the treatment of mast cell-associated or basophil-mediated inflammatory disorders |
| GB2559774B (en) | 2017-02-17 | 2021-09-29 | Gw Res Ltd | Oral cannabinoid formulations |
| US10702495B2 (en) | 2017-02-20 | 2020-07-07 | Nexien Biopharma, Inc. | Method and compositions for treating dystrophies and myotonia |
| EP3600361A4 (en) | 2017-03-24 | 2021-01-06 | Trait Biosciences, Inc. | HIGH LEVEL IN VIVO BIOSYNTHESIS AND ISOLATION OF WATER-SOLUBLE CANNABINOIDS IN PLANT SYSTEMS |
| US10596485B2 (en) | 2017-04-03 | 2020-03-24 | Fritz Chess | Multi-functional distiller |
| WO2018217803A2 (en) | 2017-05-22 | 2018-11-29 | Growblox Life Sciences L.L.C. | Myrcene-containing complex mixtures targeting trpv1 |
| EP3641754A4 (en) * | 2017-06-19 | 2021-03-10 | Zelda Therapeutics Operations Pty Ltd | COMPOSITION AGAINST SLEEP APNEA AND RELATED TREATMENTS |
| CN107365622A (zh) * | 2017-06-20 | 2017-11-21 | 云南汉木森生物科技有限责任公司 | 一种大麻蜡的提取方法 |
| EA031411B1 (ru) * | 2017-06-26 | 2018-12-28 | Товарищество С Ограниченной Ответственностью "Казахстанская Фармацевтическая Компания "Далафарм" | Способ получения экстракта из растительной массы конопли |
| US10189762B1 (en) * | 2017-07-07 | 2019-01-29 | Orochem Technologies, Inc. | Process for purification and separation of cannabinoids, from dried hemp and cannabis leaves |
| AU2018301674B2 (en) | 2017-07-11 | 2024-03-28 | Trait Biosciences, Inc. | Generation of water-soluble cannabinoid compounds in yeast and plant cell suspension cultures and compositions of matter |
| EP3650018B1 (en) * | 2017-07-18 | 2022-09-07 | Deyi Pharmarmaceutical Ltd. | Application of cannabidiol in treatment of pulmonary hypertension |
| CN107325881A (zh) * | 2017-07-28 | 2017-11-07 | 云南汉木森生物科技有限责任公司 | 大麻花叶油的萃取方法及其大麻花叶油产品 |
| CN107344908A (zh) * | 2017-07-28 | 2017-11-14 | 云南汉木森生物科技有限责任公司 | 大麻二酚的萃取方法及其大麻二酚产品 |
| CN107227198A (zh) * | 2017-07-28 | 2017-10-03 | 云南汉木森生物科技有限责任公司 | 高提取率的大麻花叶油提取方法及其大麻花叶油 |
| US10272360B2 (en) | 2017-08-05 | 2019-04-30 | Priya Naturals, Inc. | Phytochemical extraction system and methods to extract phytochemicals from plants including plants of the family Cannabaceae sensu stricto |
| CA3072322A1 (en) | 2017-08-07 | 2019-02-04 | Massachusetts Institute Of Technology | Systems and methods for separating cannabis-derived compounds using chromatography with liquid or supercritical carbon dioxide |
| US10500525B2 (en) | 2017-08-17 | 2019-12-10 | Curtis Hare | Method for producing an extract from cannabis plant matter |
| US10286336B2 (en) * | 2017-08-24 | 2019-05-14 | Medxtractor Corp. | Extraction process using supercritical carbon dioxide |
| CA3072768C (en) * | 2017-08-27 | 2024-06-11 | Rhodes Technologies | Pharmaceutical compositions for the treatment of ophthalmic conditions |
| EP3449992A1 (en) | 2017-09-04 | 2019-03-06 | Bionorica Ethics GmbH | Recovery of acidic cannabinoids from plant material |
| EP3453397A1 (en) | 2017-09-12 | 2019-03-13 | Albert Jan Dijkstra | Processes for the isolation of a cannabinoid extract and product from cannabis plant material |
| WO2019051560A1 (en) * | 2017-09-15 | 2019-03-21 | Zelda Therapeutics Operations Pty Ltd | COMPOSITION AND METHOD OF TREATMENT OF AUTISM |
| EP3461545A1 (de) | 2017-09-30 | 2019-04-03 | Bionorica Ethics GmbH | Kurzwegdestillation im vakuum zur anreicherung von naturstoffen |
| NZ764977A (en) * | 2017-10-30 | 2023-01-27 | Whistler Tech Corp | Terpene enrichment methods and systems |
| US11083765B2 (en) * | 2017-12-15 | 2021-08-10 | Andrew Scott Davis | Hemp leaf chew composition and method for producing |
| GB2569961B (en) | 2018-01-03 | 2021-12-22 | Gw Res Ltd | Pharmaceutical |
| CA3089994A1 (en) | 2018-01-31 | 2019-08-08 | Canopy Holdings, LLC | Hemp powder |
| CN112105606A (zh) * | 2018-03-07 | 2020-12-18 | 索卡蒂科技俄勒冈有限公司 | 大麻素的连续分离以及大麻素向δ8-四氢大麻酚和δ9-四氢大麻酚的转化 |
| DE102018001959A1 (de) | 2018-03-10 | 2019-09-12 | Florian Frey | Thermisches Trennverfahren zur Anreicherung von Cannabinoiden |
| EP3539637A1 (en) * | 2018-03-13 | 2019-09-18 | CLS Labs, Inc. | Cannabidiol extraction and conversion process |
| EP3773528B1 (en) | 2018-04-09 | 2024-01-10 | Portland Technology Holdings LLC | Hemp extract for treatment of pain in animals |
| US20190308116A1 (en) * | 2018-04-10 | 2019-10-10 | Craig Alan Brodersen | Solvent based cannabinoid extraction process with improved efficiency, safety, quality, which yields a homogenous and pasteurized product |
| CN108654134A (zh) * | 2018-05-08 | 2018-10-16 | 北京中农腾达科技有限公司 | 医用大麻中四氢大麻酚萃取方法 |
| US11946016B2 (en) | 2018-06-14 | 2024-04-02 | Biosoma B.V. | Process for the extraction of oil-soluble components from plant material |
| US10897925B2 (en) | 2018-07-27 | 2021-01-26 | Joseph Pandolfino | Articles and formulations for smoking products and vaporizers |
| US20200035118A1 (en) | 2018-07-27 | 2020-01-30 | Joseph Pandolfino | Methods and products to facilitate smokers switching to a tobacco heating product or e-cigarettes |
| WO2020153931A2 (en) * | 2018-08-10 | 2020-07-30 | Huron Botanicals, Llc | Methods for extracting constituents from plant material and apparatus and products thereof |
| US10669248B2 (en) | 2018-08-10 | 2020-06-02 | Natural Extraction Systems, LLC | Methods to chemically modify cannabinoids |
| US10822320B2 (en) | 2018-08-10 | 2020-11-03 | Natural Extraction Systems, LLC | Methods to purify cannabinoids |
| US11324718B2 (en) | 2018-10-09 | 2022-05-10 | Sartorius Chromatography Equipment | Method for purifying cannabinoids |
| EP3864000A4 (en) | 2018-10-10 | 2022-08-10 | Treehouse Biosciences, Inc. | CANNABIGEROL SYNTHESIS |
| WO2020101731A1 (en) * | 2018-11-13 | 2020-05-22 | Cbd Inc. | Methods, devices, and systems for processing of plant-based matter |
| US20220001297A1 (en) * | 2018-11-20 | 2022-01-06 | Hexo Operations Inc. | Process for selectively extracting cannabinoids from cannabis plant materials |
| US11660283B2 (en) | 2018-12-19 | 2023-05-30 | Joyn Botanicals Ltd. | Cannabinoid-containing composition |
| US10888596B1 (en) | 2018-12-28 | 2021-01-12 | Cold Baked LLC | Method of preparing Cannabis extracts |
| CN113631162A (zh) * | 2019-01-11 | 2021-11-09 | 艾瑞利慕健康有限责任公司 | 用于将cbd转化为thc的新颖方法和相关工具 |
| US10493377B1 (en) | 2019-02-06 | 2019-12-03 | Heinkel Filtering Systems, Inc. | Biomass extraction and centrifugation systems and methods |
| US10765966B2 (en) | 2019-02-06 | 2020-09-08 | Heinkel Filtering Systems. Inc. | Biomass extraction and centrifugation systems and methods |
| US11147805B2 (en) | 2019-02-07 | 2021-10-19 | Medipure Pharmaceuticals Inc. | Cannabinoid receptor agonists and serine hydrolase enzyme inhibitor based anxiolytic therapeutic product |
| WO2020168421A1 (en) * | 2019-02-19 | 2020-08-27 | Agrima Scientific Corp. | Cyclodextrin inclusion complexes of cannabis extracts |
| WO2020169221A1 (en) | 2019-02-20 | 2020-08-27 | Synbionik Gmbh | Production of plant-based active substances (e.g. cannabinoids) by recombinant microorganisms |
| CN113874481A (zh) | 2019-03-13 | 2021-12-31 | 埃尔蒂沃科技有限公司 | 自动提取、储存和封装脂肪族化合物的装置、系统和方法 |
| CN109796311A (zh) * | 2019-03-25 | 2019-05-24 | 黑龙江阳光工业大麻研究院 | 一种从废弃试剂中提纯大麻二酚的方法 |
| JP2022529931A (ja) * | 2019-04-17 | 2022-06-27 | シルバー スタリオン ゲーエムベーハー | 大麻からのカンナビノイド、フラボノイド、およびテルペンの抽出 |
| US11370767B2 (en) | 2019-04-23 | 2022-06-28 | Soma Oil Llc | Cannabis processing systems and methods |
| EP3750528A1 (en) | 2019-06-11 | 2020-12-16 | Nexien Biopharma, Inc. | Compositions for treating dystrophies and myotonia |
| AU2020303897A1 (en) | 2019-06-28 | 2022-03-03 | Gbs Global Biopharma, Inc. | Treatment of pain using allosteric modulator of TRPV1 |
| CN110229135A (zh) * | 2019-07-10 | 2019-09-13 | 朱法科 | 色谱生产高纯度四氢大麻酚的方法 |
| US12036485B1 (en) * | 2019-07-16 | 2024-07-16 | Green Vault Systems, LLC | Continuous flow cold water extraction |
| CN110511119A (zh) * | 2019-08-13 | 2019-11-29 | 云南飞久逍科技有限公司 | 一种大麻二酚的提取方法 |
| CN110423187A (zh) * | 2019-08-22 | 2019-11-08 | 哈尔滨工业大学 | 一种隧道超声与热循环蒸馏联用萃取大麻二酚（cbd）方法 |
| CA3152012A1 (en) * | 2019-08-23 | 2021-03-04 | Canopy Growth Corporation | Methods for converting thc-rich cannabinoid mixtures into cbn-rich cannabinoid mixtures |
| US12023601B2 (en) * | 2019-09-09 | 2024-07-02 | Alden Botanica LLC | Carbon dioxide extraction processes, devices, methods, and systems |
| US11021675B2 (en) * | 2019-09-13 | 2021-06-01 | Thar Process, Inc. | Process for producing refined oils from botanical plant matter using a supercritical fluid |
| US11542243B1 (en) | 2019-09-26 | 2023-01-03 | FusionFarms, LLC | Method of converting delta9-THC to delta10-THC and the purification of the delta10-THC by crystallization |
| EP3997113A4 (en) * | 2019-10-02 | 2023-06-28 | Chiaranussati, Suchad | Humus treatment process with active neurological substances |
| GB2588456B (en) * | 2019-10-25 | 2023-02-01 | Gw Res Ltd | Cannabinoid compound |
| GB2588457B (en) * | 2019-10-25 | 2022-12-21 | Gw Res Ltd | Cannabinoid compound |
| US10751640B1 (en) | 2019-10-30 | 2020-08-25 | Heinkel Filtering Systems, Inc. | Cannabidiol isolate production systems and methods |
| US10858303B1 (en) | 2019-10-30 | 2020-12-08 | Heinkel Filtering Systems, Inc. | Cannabidiol isolate production systems and methods |
| CN110732159A (zh) * | 2019-11-05 | 2020-01-31 | 大连大学 | 一种连续型分级式高效萃取装置 |
| US11351476B2 (en) | 2020-01-07 | 2022-06-07 | Agrify Corporation | Method for chemical separation of cannabinoids |
| CN111135810B (zh) * | 2020-01-22 | 2022-08-23 | 苏州汇通色谱分离纯化有限公司 | 一种大麻二酚分离专用色谱分离介质的制备方法 |
| US10919828B1 (en) * | 2020-02-14 | 2021-02-16 | Aicardo Roa-Espinosa | Process for manufacturing cannabidiol |
| GB202002754D0 (en) | 2020-02-27 | 2020-04-15 | Gw Res Ltd | Methods of treating tuberous sclerosis complex with cannabidiol and everolimus |
| CA3172215A1 (en) * | 2020-03-20 | 2021-09-23 | Reinhold Penner | Cannabinoid compositions |
| EP4153306A4 (en) * | 2020-05-22 | 2024-06-26 | Ilera Derm LLC | COMPOSITIONS FOR TREATING ACNE AND DERMATOLOGICAL DISEASES |
| KR102463377B1 (ko) * | 2020-06-16 | 2022-11-07 | 한국과학기술연구원 | 연속식 마이크로웨이브 조사에 의해 테트라히드로칸나비놀의 함량비율이 증가된 칸나비스속 식물 추출물의 제조방법, 및 그 칸나비스속 식물 추출물을 포함하는 조성물 |
| CN113801727A (zh) * | 2020-06-16 | 2021-12-17 | 晨光生物科技集团股份有限公司 | 一种制备高品质工业大麻油的工业化方法 |
| US11667619B2 (en) | 2020-07-06 | 2023-06-06 | Gaia Botanicals Llc | Synthesis and purification of cannabinol from cannabidiol |
| US11160757B1 (en) | 2020-10-12 | 2021-11-02 | GW Research Limited | pH dependent release coated microparticle cannabinoid formulations |
| US12029718B2 (en) | 2021-11-09 | 2024-07-09 | Cct Sciences, Llc | Process for production of essentially pure delta-9-tetrahydrocannabinol |
| CN112279752B (zh) * | 2020-10-30 | 2022-11-11 | 云南芙雅生物科技有限公司 | 用于工业大麻的大麻素二氧化碳超临界提取方法 |
| EP4006006A1 (en) * | 2020-11-27 | 2022-06-01 | Bridge Farm Nurseries Limited | Production of cannabidiol from hemp using subcritical liquid carbon dioxide |
| US20240308943A1 (en) * | 2020-11-29 | 2024-09-19 | Aphios Corporation | Extraction, separation and purification of cannabinoids from cannabis staiva and other marijuana biomass |
| CN112645802A (zh) * | 2020-12-10 | 2021-04-13 | 云南昆船环保技术有限公司 | 一种有效去除四氢大麻酚的大麻二酚广谱油制备方法 |
| KR20220084761A (ko) * | 2020-12-14 | 2022-06-21 | 강원대학교산학협력단 | 헴프 껍질 추출물을 포함하는 인지기능 개선용 조성물 |
| JP2024500611A (ja) | 2020-12-23 | 2024-01-10 | エム－フォー、エルエルシー | カンナビノイドの抽出および精製 |
| CN114685268B (zh) * | 2020-12-31 | 2024-02-02 | 上海医药工业研究院 | 一种大麻二酚酸的提取方法及纯化方法 |
| US11242328B1 (en) * | 2021-02-25 | 2022-02-08 | Acid Neutral Alkaline Laboratory | Heterogeneous catalyst and method for preparation of aromatic tricyclic pyrans |
| CN113073009A (zh) * | 2021-04-21 | 2021-07-06 | 云南康贝特生物科技有限公司 | 一种同时提取工业大麻芳香水和提高工业大麻原料cbd含量的前处理干燥方法 |
| US11352337B1 (en) * | 2021-06-02 | 2022-06-07 | Acid Neutral Alkaline Laboratory | Zeolite catalyst and method for preparation of aromatic tricyclic pyrans |
| KR102461951B1 (ko) * | 2021-09-23 | 2022-11-03 | 재단법인춘천바이오산업진흥원 | 반응표면분석법을 활용한 대마 초임계 추출 최적화 |
| CN114088680B (zh) * | 2021-10-14 | 2023-06-27 | 安徽中科赛飞尔科技有限公司 | 一种染发样品中痕量毒品的快速检测方法 |
| EP4242201A1 (en) | 2022-03-11 | 2023-09-13 | Bridge Farm Nurseries Limited | Cannabinoids extraction and conversion |
| WO2023240221A2 (en) * | 2022-06-11 | 2023-12-14 | Trait Biosciences, Inc. | System and methods for sequential desorption of cannabidiol (cbd) glycoside species |
| WO2023244646A1 (en) * | 2022-06-15 | 2023-12-21 | Zaiput Flow Technologies LLC | Systems and methods for separation of chemical species, such as cannabinoids, using multiple liquid phases |
| US11810645B1 (en) | 2022-07-14 | 2023-11-07 | Cannamatrix Inc. | System and method of making predictions of mature cannabis plants from seedling information |
| DE102022004596A1 (de) | 2022-12-08 | 2024-06-13 | Biosynth Gmbh | Neuartige Cannabinoid-Oligosaccharide |
| EP4431169A1 (en) | 2023-03-17 | 2024-09-18 | Siegfried AG | Method of purifying cannabinoid components from plant extracts |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3477856A (en) | 1965-11-10 | 1969-11-11 | Us Agriculture | Process for extraction of flavors |
| US4123559A (en) | 1971-06-03 | 1978-10-31 | Studiengesellschaft Kohle Mbh | Process for the production of spice extracts |
| GB1576729A (en) | 1976-10-13 | 1980-10-15 | Brewing Patents Ltd | Method of making an iso-acid preparation from hops |
| DE2827002B2 (de) | 1978-06-20 | 1980-09-04 | Adam Dr. 8421 St Johann Mueller | Verfahren zum Behandeln von Hopfen mit CO2 als Extraktionsmittel |
| ZA802802B (en) | 1979-05-24 | 1981-05-27 | Brewing Patents Ltd | Preparation of hop extracts rich in particular constituents |
| US4279824A (en) | 1979-11-01 | 1981-07-21 | Mckinney Laurence O | Method and apparatus for processing herbaceous plant materials including the plant cannabis |
| DE3368377D1 (en) | 1982-04-16 | 1987-01-29 | Nestle Sa | Lipid composition for oral, enteral or parenteral feeding |
| BE896610A (fr) * | 1982-05-06 | 1983-08-16 | Hop Developments Ltd | Extraction d'une matiere vegetale en utilisant de l'anhydride carbonique |
| DE3704850A1 (de) * | 1987-02-16 | 1988-08-25 | Mueller Adam | Verfahren zur herstellung von chinin aus chinarinde durch extraktion mit ueberkritischer co(pfeil abwaerts)2(pfeil abwaerts) |
| DE4100441A1 (de) * | 1991-01-09 | 1992-07-16 | Mack Chem Pharm | Verfahren zur herstellung von 6,12-dihydro-6-hydroxy-cannabidiol und dessen verwendung zur herstellung von trans-delta-9-tetrahydrocannabinol |
| US5474668A (en) * | 1991-02-11 | 1995-12-12 | University Of Arkansas | Petroleum-wax separation |
| US5120558A (en) | 1991-05-01 | 1992-06-09 | Norac Technologies Inc. | Process for the supercritical extraction and fractionation of spices |
| CA2111084C (fr) | 1992-04-29 | 2004-07-06 | Roger-Marc Nicoud | Procede et dispositif de fractionnement d'un melange en lit mobile simule en presence d'un gaz comprime, d'un fluide supercritique ou d'un liquide subcritique |
| CA2126698A1 (en) * | 1992-12-07 | 1994-06-23 | Muraleedharan G. Nair | Process for the isolation and purification of taxol and taxanes from taxus spp. |
| DE4316620A1 (de) * | 1993-05-18 | 1994-11-24 | Mueller Extract Co Gmbh | Verfahren und Vorrichtung zur Herstellung von Squalen aus Olivenölrückständen |
| DE19654945C2 (de) * | 1996-07-29 | 1998-05-20 | Mueller Extract Co Gmbh | Im wesentlichen nikotinfreies Tabakaromaöl sowie Verfahren zu dessen Herstellung |
| EP0908185A1 (de) | 1997-10-13 | 1999-04-14 | Max Zeller Söhne AG | Verfahren zur Herstellung von Heilpflanzenextrakten |
| DE19800330C2 (de) * | 1998-01-07 | 2002-09-26 | Delta 9 Pharma Gmbh | Pharmazeutisch wirksamer CO¶2¶-Extrakt aus Tanacetum parthenium |
| JPH11292777A (ja) | 1998-04-08 | 1999-10-26 | Lion Corp | フォルスコリン含有抽出物及びその抽出物を含有する組成物 |
| US6365416B1 (en) * | 1998-10-26 | 2002-04-02 | The University Of Mississippi | Method of preparing delta-9-tetrahydrocannabinol |
| US6403126B1 (en) * | 1999-05-26 | 2002-06-11 | Websar Innovations Inc. | Cannabinoid extraction method |
| US6319524B1 (en) | 1999-11-19 | 2001-11-20 | U.S. Nutraceuticals | Saw palmetto composition and associated methods |
| DE10051427C1 (de) | 2000-10-17 | 2002-06-13 | Adam Mueller | Verfahren zur Herstellung eines Tetrahydrocannabinol- und Cannabidiol-haltigen Extraktes aus Cannabis-Pflanzenmaterial sowie Cannabis-Extrakte |
| FR2930256B1 (fr) | 2008-04-22 | 2011-10-07 | Lafarge Platres | Enduit de finition convenant pour support acoustique |
-
2000
- 2000-10-17 DE DE10051427A patent/DE10051427C1/de not_active Expired - Lifetime
-
2001
- 2001-10-16 UA UA2003032364A patent/UA74203C2/ru unknown
- 2001-10-16 DE DE50107311T patent/DE50107311D1/de not_active Expired - Lifetime
- 2001-10-16 US US17/219,170 patent/USRE49434E1/en active Active
- 2001-10-16 CN CNB018174442A patent/CN1202818C/zh not_active Expired - Fee Related
- 2001-10-16 PT PT01987666T patent/PT1326598E/pt unknown
- 2001-10-16 SK SK329-2003A patent/SK287668B6/sk not_active IP Right Cessation
- 2001-10-16 AU AU2002218242A patent/AU2002218242B2/en not_active Ceased
- 2001-10-16 AU AU1824202A patent/AU1824202A/xx active Pending
- 2001-10-16 EA EA200300485A patent/EA004520B1/ru not_active IP Right Cessation
- 2001-10-16 CA CA002424356A patent/CA2424356A1/en not_active Abandoned
- 2001-10-16 JP JP2002535658A patent/JP4146225B2/ja not_active Expired - Fee Related
- 2001-10-16 WO PCT/EP2001/011967 patent/WO2002032420A1/de active IP Right Grant
- 2001-10-16 HU HU0303002A patent/HU227796B1/hu not_active IP Right Cessation
- 2001-10-16 DK DK01987666T patent/DK1326598T3/da active
- 2001-10-16 EP EP01987666A patent/EP1326598B1/de not_active Revoked
- 2001-10-16 KR KR10-2003-7004918A patent/KR20030040522A/ko active Search and Examination
- 2001-10-16 US US10/399,362 patent/US8895078B2/en not_active Ceased
- 2001-10-16 IL IL15518501A patent/IL155185A0/xx not_active IP Right Cessation
- 2001-10-16 ES ES01987666T patent/ES2243580T3/es not_active Expired - Lifetime
- 2001-10-16 PL PL362446A patent/PL206679B1/pl not_active IP Right Cessation
- 2001-10-16 AT AT01987666T patent/ATE303142T1/de active
- 2001-10-16 MX MXPA03003295A patent/MXPA03003295A/es active IP Right Grant
- 2001-10-16 BR BR0114717-0A patent/BR0114717A/pt not_active Application Discontinuation
- 2001-10-16 NZ NZ525118A patent/NZ525118A/en not_active IP Right Cessation
- 2001-10-16 CZ CZ2003843A patent/CZ2003843A3/cs unknown
-
2003
- 2003-03-31 ZA ZA200302489A patent/ZA200302489B/en unknown
-
2005
- 2005-09-12 CY CY20051101101T patent/CY1105011T1/el unknown
-
2014
- 2014-05-13 US US14/276,165 patent/US10870632B2/en not_active Expired - Lifetime
-
2020
- 2020-06-25 US US16/911,716 patent/US20210017145A1/en not_active Abandoned
- 2020-12-16 US US17/123,929 patent/US20210188798A1/en not_active Abandoned
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US20210017145A1 (en) | Process for producing an extract containing tetrahydrocannabinol and cannabidiol from cannabis plant material, and cannabis extracts | |
| US10604464B2 (en) | Process for purification and separation of cannabinoids, from dried hemp and cannabis leaves | |
| US10751380B2 (en) | Compound and method for treating spasms, inflammation and pain | |
| JP2021042233A (ja) | 大麻抽出物ならびにその調製方法および使用方法 | |
| CA2872528C (en) | Cannabis plant isolate comprising .delta.9-tetrahydrocannabinol and a method for preparing such an isolate | |
| CA2986895A1 (en) | Process for extraction, separation and purification of cannabinoids, flavonoids and terpenes from cannabis | |
| US6174531B1 (en) | Methods of preparation of bioginkgo | |
| EP2015645A2 (en) | Extracts and methods comprising cinnamon species | |
| JP2010500974A (ja) | 新規のユーカリ抽出物、その調製方法およびその治療利用法 | |
| CA2391454A1 (en) | Cannabinoid extraction method | |
| EA031411B1 (ru) | Способ получения экстракта из растительной массы конопли |