EP1521598A1 - Adjuvant containing xenon - Google Patents
Adjuvant containing xenonInfo
- Publication number
- EP1521598A1 EP1521598A1 EP03762626A EP03762626A EP1521598A1 EP 1521598 A1 EP1521598 A1 EP 1521598A1 EP 03762626 A EP03762626 A EP 03762626A EP 03762626 A EP03762626 A EP 03762626A EP 1521598 A1 EP1521598 A1 EP 1521598A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- adjuvant
- drugs
- xenon
- brain
- medicament
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000002671 adjuvant Substances 0.000 title claims abstract description 60
- 229910052724 xenon Inorganic materials 0.000 title claims abstract description 53
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 title claims abstract description 53
- 239000003814 drug Substances 0.000 claims abstract description 92
- 239000000126 substance Substances 0.000 claims abstract description 12
- -1 analgesic Substances 0.000 claims abstract description 10
- 230000000202 analgesic effect Effects 0.000 claims abstract description 8
- 239000000812 cholinergic antagonist Substances 0.000 claims abstract description 4
- 239000000219 Sympatholytic Substances 0.000 claims abstract description 3
- 239000000150 Sympathomimetic Substances 0.000 claims abstract description 3
- 150000001413 amino acids Chemical class 0.000 claims abstract description 3
- 230000000844 anti-bacterial effect Effects 0.000 claims abstract description 3
- 229940035678 anti-parkinson drug Drugs 0.000 claims abstract description 3
- 230000001754 anti-pyretic effect Effects 0.000 claims abstract description 3
- 230000000840 anti-viral effect Effects 0.000 claims abstract description 3
- 239000000935 antidepressant agent Substances 0.000 claims abstract description 3
- 229940005513 antidepressants Drugs 0.000 claims abstract description 3
- 239000002221 antipyretic Substances 0.000 claims abstract description 3
- 239000002876 beta blocker Substances 0.000 claims abstract description 3
- 239000005556 hormone Substances 0.000 claims abstract description 3
- 229940088597 hormone Drugs 0.000 claims abstract description 3
- 230000000324 neuroprotective effect Effects 0.000 claims abstract description 3
- 230000002445 parasympatholytic effect Effects 0.000 claims abstract description 3
- 230000001499 parasympathomimetic effect Effects 0.000 claims abstract description 3
- 230000002048 spasmolytic effect Effects 0.000 claims abstract description 3
- 230000000948 sympatholitic effect Effects 0.000 claims abstract description 3
- 230000001975 sympathomimetic effect Effects 0.000 claims abstract description 3
- 239000011782 vitamin Substances 0.000 claims abstract description 3
- 229940088594 vitamin Drugs 0.000 claims abstract description 3
- 229930003231 vitamin Natural products 0.000 claims abstract description 3
- 235000013343 vitamin Nutrition 0.000 claims abstract description 3
- 239000002269 analeptic agent Substances 0.000 claims abstract 2
- 230000003555 analeptic effect Effects 0.000 claims abstract 2
- 230000003474 anti-emetic effect Effects 0.000 claims abstract 2
- 230000003556 anti-epileptic effect Effects 0.000 claims abstract 2
- 239000001961 anticonvulsive agent Substances 0.000 claims abstract 2
- 239000002111 antiemetic agent Substances 0.000 claims abstract 2
- 239000003795 chemical substances by application Substances 0.000 claims abstract 2
- 239000002895 emetic Substances 0.000 claims abstract 2
- 229940079593 drug Drugs 0.000 claims description 71
- 239000000932 sedative agent Substances 0.000 claims description 25
- 230000001624 sedative effect Effects 0.000 claims description 20
- 239000000730 antalgic agent Substances 0.000 claims description 10
- 210000004556 brain Anatomy 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 10
- 229940035676 analgesics Drugs 0.000 claims description 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 9
- 229940000425 combination drug Drugs 0.000 claims description 8
- 208000035475 disorder Diseases 0.000 claims description 8
- 238000011321 prophylaxis Methods 0.000 claims description 8
- 206010012289 Dementia Diseases 0.000 claims description 6
- 206010061285 Mental disorder due to a general medical condition Diseases 0.000 claims description 6
- 239000013543 active substance Substances 0.000 claims description 6
- 229940125723 sedative agent Drugs 0.000 claims description 6
- 238000011282 treatment Methods 0.000 claims description 6
- 230000001154 acute effect Effects 0.000 claims description 5
- 208000028867 ischemia Diseases 0.000 claims description 5
- FTOAOBMCPZCFFF-UHFFFAOYSA-N 5,5-diethylbarbituric acid Chemical compound CCC1(CC)C(=O)NC(=O)NC1=O FTOAOBMCPZCFFF-UHFFFAOYSA-N 0.000 claims description 4
- 208000030507 AIDS Diseases 0.000 claims description 4
- 208000024827 Alzheimer disease Diseases 0.000 claims description 4
- 208000019695 Migraine disease Diseases 0.000 claims description 4
- 208000018737 Parkinson disease Diseases 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 4
- VIROVYVQCGLCII-UHFFFAOYSA-N amobarbital Chemical compound CC(C)CCC1(CC)C(=O)NC(=O)NC1=O VIROVYVQCGLCII-UHFFFAOYSA-N 0.000 claims description 4
- 229940035674 anesthetics Drugs 0.000 claims description 4
- 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 claims description 4
- 239000003193 general anesthetic agent Substances 0.000 claims description 4
- 239000003589 local anesthetic agent Substances 0.000 claims description 4
- 230000004770 neurodegeneration Effects 0.000 claims description 4
- 208000015122 neurodegenerative disease Diseases 0.000 claims description 4
- WEXRUCMBJFQVBZ-UHFFFAOYSA-N pentobarbital Chemical compound CCCC(C)C1(CC)C(=O)NC(=O)NC1=O WEXRUCMBJFQVBZ-UHFFFAOYSA-N 0.000 claims description 4
- 208000011580 syndromic disease Diseases 0.000 claims description 4
- 206010061218 Inflammation Diseases 0.000 claims description 3
- PIWKPBJCKXDKJR-UHFFFAOYSA-N Isoflurane Chemical compound FC(F)OC(Cl)C(F)(F)F PIWKPBJCKXDKJR-UHFFFAOYSA-N 0.000 claims description 3
- 206010063837 Reperfusion injury Diseases 0.000 claims description 3
- 208000006011 Stroke Diseases 0.000 claims description 3
- 208000030886 Traumatic Brain injury Diseases 0.000 claims description 3
- 230000003444 anaesthetic effect Effects 0.000 claims description 3
- 229940125717 barbiturate Drugs 0.000 claims description 3
- 230000002490 cerebral effect Effects 0.000 claims description 3
- 230000001684 chronic effect Effects 0.000 claims description 3
- 230000004054 inflammatory process Effects 0.000 claims description 3
- 229960002725 isoflurane Drugs 0.000 claims description 3
- 229960005015 local anesthetics Drugs 0.000 claims description 3
- 230000004112 neuroprotection Effects 0.000 claims description 3
- 238000002560 therapeutic procedure Methods 0.000 claims description 3
- ZKMNUMMKYBVTFN-HNNXBMFYSA-N (S)-ropivacaine Chemical compound CCCN1CCCC[C@H]1C(=O)NC1=C(C)C=CC=C1C ZKMNUMMKYBVTFN-HNNXBMFYSA-N 0.000 claims description 2
- LEBVLXFERQHONN-UHFFFAOYSA-N 1-butyl-N-(2,6-dimethylphenyl)piperidine-2-carboxamide Chemical compound CCCCN1CCCCC1C(=O)NC1=C(C)C=CC=C1C LEBVLXFERQHONN-UHFFFAOYSA-N 0.000 claims description 2
- FDQGNLOWMMVRQL-UHFFFAOYSA-N Allobarbital Chemical compound C=CCC1(CC=C)C(=O)NC(=O)NC1=O FDQGNLOWMMVRQL-UHFFFAOYSA-N 0.000 claims description 2
- VMIYHDSEFNYJSL-UHFFFAOYSA-N Bromazepam Chemical compound C12=CC(Br)=CC=C2NC(=O)CN=C1C1=CC=CC=N1 VMIYHDSEFNYJSL-UHFFFAOYSA-N 0.000 claims description 2
- GJSURZIOUXUGAL-UHFFFAOYSA-N Clonidine Chemical compound ClC1=CC=CC(Cl)=C1NC1=NCCN1 GJSURZIOUXUGAL-UHFFFAOYSA-N 0.000 claims description 2
- 206010012218 Delirium Diseases 0.000 claims description 2
- VTUSIVBDOCDNHS-UHFFFAOYSA-N Etidocaine Chemical compound CCCN(CC)C(CC)C(=O)NC1=C(C)C=CC=C1C VTUSIVBDOCDNHS-UHFFFAOYSA-N 0.000 claims description 2
- 208000026097 Factitious disease Diseases 0.000 claims description 2
- 208000023105 Huntington disease Diseases 0.000 claims description 2
- NNJVILVZKWQKPM-UHFFFAOYSA-N Lidocaine Chemical compound CCN(CC)CC(=O)NC1=C(C)C=CC=C1C NNJVILVZKWQKPM-UHFFFAOYSA-N 0.000 claims description 2
- FTLDJPRFCGDUFH-UHFFFAOYSA-N Oxethazaine Chemical compound C=1C=CC=CC=1CC(C)(C)N(C)C(=O)CN(CCO)CC(=O)N(C)C(C)(C)CC1=CC=CC=C1 FTLDJPRFCGDUFH-UHFFFAOYSA-N 0.000 claims description 2
- 208000002193 Pain Diseases 0.000 claims description 2
- KCLANYCVBBTKTO-UHFFFAOYSA-N Proparacaine Chemical compound CCCOC1=CC=C(C(=O)OCCN(CC)CC)C=C1N KCLANYCVBBTKTO-UHFFFAOYSA-N 0.000 claims description 2
- 206010052276 Pseudodementia Diseases 0.000 claims description 2
- ZTVQQQVZCWLTDF-UHFFFAOYSA-N Remifentanil Chemical compound C1CN(CCC(=O)OC)CCC1(C(=O)OC)N(C(=O)CC)C1=CC=CC=C1 ZTVQQQVZCWLTDF-UHFFFAOYSA-N 0.000 claims description 2
- PPTYJKAXVCCBDU-UHFFFAOYSA-N Rohypnol Chemical compound N=1CC(=O)N(C)C2=CC=C([N+]([O-])=O)C=C2C=1C1=CC=CC=C1F PPTYJKAXVCCBDU-UHFFFAOYSA-N 0.000 claims description 2
- 206010040070 Septic Shock Diseases 0.000 claims description 2
- 208000007271 Substance Withdrawal Syndrome Diseases 0.000 claims description 2
- 206010048010 Withdrawal syndrome Diseases 0.000 claims description 2
- 239000000556 agonist Substances 0.000 claims description 2
- 229960000880 allobarbital Drugs 0.000 claims description 2
- 102000030484 alpha-2 Adrenergic Receptor Human genes 0.000 claims description 2
- 108020004101 alpha-2 Adrenergic Receptor Proteins 0.000 claims description 2
- VREFGVBLTWBCJP-UHFFFAOYSA-N alprazolam Chemical compound C12=CC(Cl)=CC=C2N2C(C)=NN=C2CN=C1C1=CC=CC=C1 VREFGVBLTWBCJP-UHFFFAOYSA-N 0.000 claims description 2
- 229960004538 alprazolam Drugs 0.000 claims description 2
- 229940024606 amino acid Drugs 0.000 claims description 2
- 229960001301 amobarbital Drugs 0.000 claims description 2
- 230000001093 anti-cancer Effects 0.000 claims description 2
- 230000000843 anti-fungal effect Effects 0.000 claims description 2
- 229940121375 antifungal agent Drugs 0.000 claims description 2
- 229940125716 antipyretic agent Drugs 0.000 claims description 2
- 229960003153 aprobarbital Drugs 0.000 claims description 2
- UORJNBVJVRLXMQ-UHFFFAOYSA-N aprobarbital Chemical compound C=CCC1(C(C)C)C(=O)NC(=O)NC1=O UORJNBVJVRLXMQ-UHFFFAOYSA-N 0.000 claims description 2
- 229960002319 barbital Drugs 0.000 claims description 2
- 229940049706 benzodiazepine Drugs 0.000 claims description 2
- 150000001557 benzodiazepines Chemical class 0.000 claims description 2
- 229950002261 brallobarbital Drugs 0.000 claims description 2
- DYODAJAEQDVYFX-UHFFFAOYSA-N brallobarbital Chemical compound BrC(=C)CC1(CC=C)C(=O)NC(=O)NC1=O DYODAJAEQDVYFX-UHFFFAOYSA-N 0.000 claims description 2
- 229960002729 bromazepam Drugs 0.000 claims description 2
- 229960003150 bupivacaine Drugs 0.000 claims description 2
- 230000003788 cerebral perfusion Effects 0.000 claims description 2
- RNFNDJAIBTYOQL-UHFFFAOYSA-N chloral hydrate Chemical compound OC(O)C(Cl)(Cl)Cl RNFNDJAIBTYOQL-UHFFFAOYSA-N 0.000 claims description 2
- 229960002327 chloral hydrate Drugs 0.000 claims description 2
- 229960001747 cinchocaine Drugs 0.000 claims description 2
- PUFQVTATUTYEAL-UHFFFAOYSA-N cinchocaine Chemical compound C1=CC=CC2=NC(OCCCC)=CC(C(=O)NCCN(CC)CC)=C21 PUFQVTATUTYEAL-UHFFFAOYSA-N 0.000 claims description 2
- 229960002896 clonidine Drugs 0.000 claims description 2
- 229960003920 cocaine Drugs 0.000 claims description 2
- 208000010877 cognitive disease Diseases 0.000 claims description 2
- 230000003931 cognitive performance Effects 0.000 claims description 2
- 239000002872 contrast media Substances 0.000 claims description 2
- 229940039231 contrast media Drugs 0.000 claims description 2
- 229960004138 cyclobarbital Drugs 0.000 claims description 2
- WTYGAUXICFETTC-UHFFFAOYSA-N cyclobarbital Chemical compound C=1CCCCC=1C1(CC)C(=O)NC(=O)NC1=O WTYGAUXICFETTC-UHFFFAOYSA-N 0.000 claims description 2
- 230000000120 cytopathologic effect Effects 0.000 claims description 2
- 230000003001 depressive effect Effects 0.000 claims description 2
- 229960003537 desflurane Drugs 0.000 claims description 2
- DPYMFVXJLLWWEU-UHFFFAOYSA-N desflurane Chemical compound FC(F)OC(F)C(F)(F)F DPYMFVXJLLWWEU-UHFFFAOYSA-N 0.000 claims description 2
- 229960004253 dexmedetomidine Drugs 0.000 claims description 2
- HRLIOXLXPOHXTA-NSHDSACASA-N dexmedetomidine Chemical compound C1([C@@H](C)C=2C(=C(C)C=CC=2)C)=CN=C[N]1 HRLIOXLXPOHXTA-NSHDSACASA-N 0.000 claims description 2
- 229960003529 diazepam Drugs 0.000 claims description 2
- AAOVKJBEBIDNHE-UHFFFAOYSA-N diazepam Chemical compound N=1CC(=O)N(C)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 AAOVKJBEBIDNHE-UHFFFAOYSA-N 0.000 claims description 2
- 229960003976 etidocaine Drugs 0.000 claims description 2
- 229960002200 flunitrazepam Drugs 0.000 claims description 2
- 229960003528 flurazepam Drugs 0.000 claims description 2
- SAADBVWGJQAEFS-UHFFFAOYSA-N flurazepam Chemical compound N=1CC(=O)N(CCN(CC)CC)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1F SAADBVWGJQAEFS-UHFFFAOYSA-N 0.000 claims description 2
- 229950003051 fomocaine Drugs 0.000 claims description 2
- CVHGCWVMTZWGAY-UHFFFAOYSA-N fomocaine Chemical compound C=1C=C(COC=2C=CC=CC=2)C=CC=1CCCN1CCOCC1 CVHGCWVMTZWGAY-UHFFFAOYSA-N 0.000 claims description 2
- 229960003132 halothane Drugs 0.000 claims description 2
- BCQZXOMGPXTTIC-UHFFFAOYSA-N halothane Chemical compound FC(F)(F)C(Cl)Br BCQZXOMGPXTTIC-UHFFFAOYSA-N 0.000 claims description 2
- 230000035987 intoxication Effects 0.000 claims description 2
- 231100000566 intoxication Toxicity 0.000 claims description 2
- 201000010901 lateral sclerosis Diseases 0.000 claims description 2
- 229960004194 lidocaine Drugs 0.000 claims description 2
- 229960003019 loprazolam Drugs 0.000 claims description 2
- UTEFBSAVJNEPTR-RGEXLXHISA-N loprazolam Chemical compound C1CN(C)CCN1\C=C/1C(=O)N2C3=CC=C([N+]([O-])=O)C=C3C(C=3C(=CC=CC=3)Cl)=NCC2=N\1 UTEFBSAVJNEPTR-RGEXLXHISA-N 0.000 claims description 2
- 229960002409 mepivacaine Drugs 0.000 claims description 2
- INWLQCZOYSRPNW-UHFFFAOYSA-N mepivacaine Chemical compound CN1CCCCC1C(=O)NC1=C(C)C=CC=C1C INWLQCZOYSRPNW-UHFFFAOYSA-N 0.000 claims description 2
- 229960002455 methoxyflurane Drugs 0.000 claims description 2
- RFKMCNOHBTXSMU-UHFFFAOYSA-N methoxyflurane Chemical compound COC(F)(F)C(Cl)Cl RFKMCNOHBTXSMU-UHFFFAOYSA-N 0.000 claims description 2
- 229960002238 methylpentynol Drugs 0.000 claims description 2
- QXLPXWSKPNOQLE-UHFFFAOYSA-N methylpentynol Chemical compound CCC(C)(O)C#C QXLPXWSKPNOQLE-UHFFFAOYSA-N 0.000 claims description 2
- 206010027599 migraine Diseases 0.000 claims description 2
- 208000005264 motor neuron disease Diseases 0.000 claims description 2
- 201000006417 multiple sclerosis Diseases 0.000 claims description 2
- 229940005483 opioid analgesics Drugs 0.000 claims description 2
- 229960000986 oxetacaine Drugs 0.000 claims description 2
- 230000036407 pain Effects 0.000 claims description 2
- 229960003868 paraldehyde Drugs 0.000 claims description 2
- SQYNKIJPMDEDEG-UHFFFAOYSA-N paraldehyde Chemical compound CC1OC(C)OC(C)O1 SQYNKIJPMDEDEG-UHFFFAOYSA-N 0.000 claims description 2
- 239000000734 parasympathomimetic agent Substances 0.000 claims description 2
- 229940005542 parasympathomimetics Drugs 0.000 claims description 2
- 229960001412 pentobarbital Drugs 0.000 claims description 2
- 229960002695 phenobarbital Drugs 0.000 claims description 2
- DDBREPKUVSBGFI-UHFFFAOYSA-N phenobarbital Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NC(=O)NC1=O DDBREPKUVSBGFI-UHFFFAOYSA-N 0.000 claims description 2
- 229960001896 pramocaine Drugs 0.000 claims description 2
- DQKXQSGTHWVTAD-UHFFFAOYSA-N pramocaine Chemical compound C1=CC(OCCCC)=CC=C1OCCCN1CCOCC1 DQKXQSGTHWVTAD-UHFFFAOYSA-N 0.000 claims description 2
- 229960001807 prilocaine Drugs 0.000 claims description 2
- MVFGUOIZUNYYSO-UHFFFAOYSA-N prilocaine Chemical compound CCCNC(C)C(=O)NC1=CC=CC=C1C MVFGUOIZUNYYSO-UHFFFAOYSA-N 0.000 claims description 2
- 229960004919 procaine Drugs 0.000 claims description 2
- MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 claims description 2
- 229960003981 proparacaine Drugs 0.000 claims description 2
- 230000002285 radioactive effect Effects 0.000 claims description 2
- 229960003394 remifentanil Drugs 0.000 claims description 2
- 229960001549 ropivacaine Drugs 0.000 claims description 2
- 229960002060 secobarbital Drugs 0.000 claims description 2
- KQPKPCNLIDLUMF-UHFFFAOYSA-N secobarbital Chemical compound CCCC(C)C1(CC=C)C(=O)NC(=O)NC1=O KQPKPCNLIDLUMF-UHFFFAOYSA-N 0.000 claims description 2
- 230000036303 septic shock Effects 0.000 claims description 2
- 229960004739 sufentanil Drugs 0.000 claims description 2
- GGCSSNBKKAUURC-UHFFFAOYSA-N sufentanil Chemical compound C1CN(CCC=2SC=CC=2)CCC1(COC)N(C(=O)CC)C1=CC=CC=C1 GGCSSNBKKAUURC-UHFFFAOYSA-N 0.000 claims description 2
- 229940064707 sympathomimetics Drugs 0.000 claims description 2
- 229950006609 tolycaine Drugs 0.000 claims description 2
- UDKICLZCJWQTLS-UHFFFAOYSA-N tolycaine Chemical compound CCN(CC)CC(=O)NC1=C(C)C=CC=C1C(=O)OC UDKICLZCJWQTLS-UHFFFAOYSA-N 0.000 claims description 2
- 229960005392 vinylbital Drugs 0.000 claims description 2
- KGKJZEKQJQQOTD-UHFFFAOYSA-N vinylbital Chemical compound CCCC(C)C1(C=C)C(=O)NC(=O)NC1=O KGKJZEKQJQQOTD-UHFFFAOYSA-N 0.000 claims description 2
- 201000006474 Brain Ischemia Diseases 0.000 claims 2
- 208000018152 Cerebral disease Diseases 0.000 claims 2
- FJIKWRGCXUCUIG-HNNXBMFYSA-N (3s)-7-chloro-5-(2-chlorophenyl)-3-hydroxy-1-methyl-3h-1,4-benzodiazepin-2-one Chemical compound O=C([C@H](O)N=1)N(C)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1Cl FJIKWRGCXUCUIG-HNNXBMFYSA-N 0.000 claims 1
- 208000014644 Brain disease Diseases 0.000 claims 1
- 206010008120 Cerebral ischaemia Diseases 0.000 claims 1
- SEQDDYPDSLOBDC-UHFFFAOYSA-N Temazepam Chemical compound N=1C(O)C(=O)N(C)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 SEQDDYPDSLOBDC-UHFFFAOYSA-N 0.000 claims 1
- 229940125683 antiemetic agent Drugs 0.000 claims 1
- 229960003965 antiepileptics Drugs 0.000 claims 1
- 239000000939 antiparkinson agent Substances 0.000 claims 1
- 230000023555 blood coagulation Effects 0.000 claims 1
- 150000003943 catecholamines Chemical class 0.000 claims 1
- 206010008118 cerebral infarction Diseases 0.000 claims 1
- 229960000305 enflurane Drugs 0.000 claims 1
- JPGQOUSTVILISH-UHFFFAOYSA-N enflurane Chemical compound FC(F)OC(F)(F)C(F)Cl JPGQOUSTVILISH-UHFFFAOYSA-N 0.000 claims 1
- 230000005764 inhibitory process Effects 0.000 claims 1
- 230000000302 ischemic effect Effects 0.000 claims 1
- 229960004033 lormetazepam Drugs 0.000 claims 1
- 229960003793 midazolam Drugs 0.000 claims 1
- DDLIGBOFAVUZHB-UHFFFAOYSA-N midazolam Chemical compound C12=CC(Cl)=CC=C2N2C(C)=NC=C2CN=C1C1=CC=CC=C1F DDLIGBOFAVUZHB-UHFFFAOYSA-N 0.000 claims 1
- 229960001454 nitrazepam Drugs 0.000 claims 1
- KJONHKAYOJNZEC-UHFFFAOYSA-N nitrazepam Chemical compound C12=CC([N+](=O)[O-])=CC=C2NC(=O)CN=C1C1=CC=CC=C1 KJONHKAYOJNZEC-UHFFFAOYSA-N 0.000 claims 1
- 229960004535 oxazepam Drugs 0.000 claims 1
- ADIMAYPTOBDMTL-UHFFFAOYSA-N oxazepam Chemical compound C12=CC(Cl)=CC=C2NC(=O)C(O)N=C1C1=CC=CC=C1 ADIMAYPTOBDMTL-UHFFFAOYSA-N 0.000 claims 1
- 229960002078 sevoflurane Drugs 0.000 claims 1
- DFEYYRMXOJXZRJ-UHFFFAOYSA-N sevoflurane Chemical compound FCOC(C(F)(F)F)C(F)(F)F DFEYYRMXOJXZRJ-UHFFFAOYSA-N 0.000 claims 1
- 229960003188 temazepam Drugs 0.000 claims 1
- 229960003386 triazolam Drugs 0.000 claims 1
- JOFWLTCLBGQGBO-UHFFFAOYSA-N triazolam Chemical compound C12=CC(Cl)=CC=C2N2C(C)=NN=C2CN=C1C1=CC=CC=C1Cl JOFWLTCLBGQGBO-UHFFFAOYSA-N 0.000 claims 1
- 239000007789 gas Substances 0.000 abstract description 40
- 230000003217 anti-cancerogenic effect Effects 0.000 abstract 1
- 230000001430 anti-depressive effect Effects 0.000 abstract 1
- 230000001857 anti-mycotic effect Effects 0.000 abstract 1
- 239000002543 antimycotic Substances 0.000 abstract 1
- 230000015271 coagulation Effects 0.000 abstract 1
- 238000005345 coagulation Methods 0.000 abstract 1
- 239000003176 neuroleptic agent Substances 0.000 abstract 1
- 230000000701 neuroleptic effect Effects 0.000 abstract 1
- 229940125725 tranquilizer Drugs 0.000 abstract 1
- 239000003204 tranquilizing agent Substances 0.000 abstract 1
- 230000002936 tranquilizing effect Effects 0.000 abstract 1
- 150000003722 vitamin derivatives Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 11
- 230000029058 respiratory gaseous exchange Effects 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000011261 inert gas Substances 0.000 description 4
- 206010002091 Anaesthesia Diseases 0.000 description 3
- 230000037005 anaesthesia Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
- JILCEWWZTBBOFS-UHFFFAOYSA-N 4-(methylamino)antipyrine Chemical compound O=C1C(NC)=C(C)N(C)N1C1=CC=CC=C1 JILCEWWZTBBOFS-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- XADCESSVHJOZHK-UHFFFAOYSA-N Meperidine Chemical compound C=1C=CC=CC=1C1(C(=O)OCC)CCN(C)CC1 XADCESSVHJOZHK-UHFFFAOYSA-N 0.000 description 2
- LOUPRKONTZGTKE-WZBLMQSHSA-N Quinine Chemical compound C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-WZBLMQSHSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000017531 blood circulation Effects 0.000 description 2
- OROGSEYTTFOCAN-DNJOTXNNSA-N codeine Chemical compound C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC OROGSEYTTFOCAN-DNJOTXNNSA-N 0.000 description 2
- 229940083761 high-ceiling diuretics pyrazolone derivative Drugs 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
- 229960000482 pethidine Drugs 0.000 description 2
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 229940058287 salicylic acid derivative anticestodals Drugs 0.000 description 2
- 150000003872 salicylic acid derivatives Chemical class 0.000 description 2
- WVYADZUPLLSGPU-UHFFFAOYSA-N salsalate Chemical compound OC(=O)C1=CC=CC=C1OC(=O)C1=CC=CC=C1O WVYADZUPLLSGPU-UHFFFAOYSA-N 0.000 description 2
- 238000009423 ventilation Methods 0.000 description 2
- TVYLLZQTGLZFBW-ZBFHGGJFSA-N (R,R)-tramadol Chemical compound COC1=CC=CC([C@]2(O)[C@H](CCCC2)CN(C)C)=C1 TVYLLZQTGLZFBW-ZBFHGGJFSA-N 0.000 description 1
- DPSHMGYUJQNALR-UHFFFAOYSA-N 2,3-diphenylpropane-1,2-diol Chemical compound C=1C=CC=CC=1C(O)(CO)CC1=CC=CC=C1 DPSHMGYUJQNALR-UHFFFAOYSA-N 0.000 description 1
- BSYNRYMUTXBXSQ-FOQJRBATSA-N 59096-14-9 Chemical compound CC(=O)OC1=CC=CC=C1[14C](O)=O BSYNRYMUTXBXSQ-FOQJRBATSA-N 0.000 description 1
- USSIQXCVUWKGNF-UHFFFAOYSA-N 6-(dimethylamino)-4,4-diphenylheptan-3-one Chemical compound C=1C=CC=CC=1C(CC(C)N(C)C)(C(=O)CC)C1=CC=CC=C1 USSIQXCVUWKGNF-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- QTGIAADRBBLJGA-UHFFFAOYSA-N Articaine Chemical compound CCCNC(C)C(=O)NC=1C(C)=CSC=1C(=O)OC QTGIAADRBBLJGA-UHFFFAOYSA-N 0.000 description 1
- 235000001258 Cinchona calisaya Nutrition 0.000 description 1
- 208000005189 Embolism Diseases 0.000 description 1
- MOIJZWWOFOQFMH-UHFFFAOYSA-M Gentisic acid sodium Chemical compound [Na+].OC1=CC=C(O)C(C([O-])=O)=C1 MOIJZWWOFOQFMH-UHFFFAOYSA-M 0.000 description 1
- 206010065390 Inflammatory pain Diseases 0.000 description 1
- ALFGKMXHOUSVAD-UHFFFAOYSA-N Ketobemidone Chemical compound C=1C=CC(O)=CC=1C1(C(=O)CC)CCN(C)CC1 ALFGKMXHOUSVAD-UHFFFAOYSA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- JUUFBMODXQKSTD-UHFFFAOYSA-N N-[2-amino-6-[(4-fluorophenyl)methylamino]-3-pyridinyl]carbamic acid ethyl ester Chemical compound N1=C(N)C(NC(=O)OCC)=CC=C1NCC1=CC=C(F)C=C1 JUUFBMODXQKSTD-UHFFFAOYSA-N 0.000 description 1
- RGPDEAGGEXEMMM-UHFFFAOYSA-N Nefopam Chemical compound C12=CC=CC=C2CN(C)CCOC1C1=CC=CC=C1 RGPDEAGGEXEMMM-UHFFFAOYSA-N 0.000 description 1
- 239000008896 Opium Substances 0.000 description 1
- BRUQQQPBMZOVGD-XFKAJCMBSA-N Oxycodone Chemical compound O=C([C@@H]1O2)CC[C@@]3(O)[C@H]4CC5=CC=C(OC)C2=C5[C@@]13CCN4C BRUQQQPBMZOVGD-XFKAJCMBSA-N 0.000 description 1
- SKZKKFZAGNVIMN-UHFFFAOYSA-N Salicilamide Chemical compound NC(=O)C1=CC=CC=C1O SKZKKFZAGNVIMN-UHFFFAOYSA-N 0.000 description 1
- 206010039897 Sedation Diseases 0.000 description 1
- 208000007536 Thrombosis Diseases 0.000 description 1
- UJLFQHSVIUGIOA-UHFFFAOYSA-N [O].[Xe] Chemical compound [O].[Xe] UJLFQHSVIUGIOA-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 208000007502 anemia Diseases 0.000 description 1
- VEQOALNAAJBPNY-UHFFFAOYSA-N antipyrine Chemical compound CN1C(C)=CC(=O)N1C1=CC=CC=C1 VEQOALNAAJBPNY-UHFFFAOYSA-N 0.000 description 1
- 229960003831 articaine Drugs 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- JFKWZVQEMSKSBU-UHFFFAOYSA-N benzyl 2-hydroxy-2-phenylacetate Chemical compound C=1C=CC=CC=1C(O)C(=O)OCC1=CC=CC=C1 JFKWZVQEMSKSBU-UHFFFAOYSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 230000008499 blood brain barrier function Effects 0.000 description 1
- 230000036770 blood supply Effects 0.000 description 1
- 210000001218 blood-brain barrier Anatomy 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- RMRJXGBAOAMLHD-IHFGGWKQSA-N buprenorphine Chemical compound C([C@]12[C@H]3OC=4C(O)=CC=C(C2=4)C[C@@H]2[C@]11CC[C@]3([C@H](C1)[C@](C)(O)C(C)(C)C)OC)CN2CC1CC1 RMRJXGBAOAMLHD-IHFGGWKQSA-N 0.000 description 1
- 229960001736 buprenorphine Drugs 0.000 description 1
- 239000002327 cardiovascular agent Substances 0.000 description 1
- 229940125692 cardiovascular agent Drugs 0.000 description 1
- LOUPRKONTZGTKE-UHFFFAOYSA-N cinchonine Natural products C1C(C(C2)C=C)CCN2C1C(O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-UHFFFAOYSA-N 0.000 description 1
- 229960004126 codeine Drugs 0.000 description 1
- WDEFBBTXULIOBB-WBVHZDCISA-N dextilidine Chemical compound C=1C=CC=CC=1[C@@]1(C(=O)OCC)CCC=C[C@H]1N(C)C WDEFBBTXULIOBB-WBVHZDCISA-N 0.000 description 1
- 229960003701 dextromoramide Drugs 0.000 description 1
- INUNXTSAACVKJS-OAQYLSRUSA-N dextromoramide Chemical compound C([C@@H](C)C(C(=O)N1CCCC1)(C=1C=CC=CC=1)C=1C=CC=CC=1)N1CCOCC1 INUNXTSAACVKJS-OAQYLSRUSA-N 0.000 description 1
- 229960004193 dextropropoxyphene Drugs 0.000 description 1
- XLMALTXPSGQGBX-GCJKJVERSA-N dextropropoxyphene Chemical compound C([C@](OC(=O)CC)([C@H](C)CN(C)C)C=1C=CC=CC=1)C1=CC=CC=C1 XLMALTXPSGQGBX-GCJKJVERSA-N 0.000 description 1
- 229960000616 diflunisal Drugs 0.000 description 1
- HUPFGZXOMWLGNK-UHFFFAOYSA-N diflunisal Chemical compound C1=C(O)C(C(=O)O)=CC(C=2C(=CC(F)=CC=2)F)=C1 HUPFGZXOMWLGNK-UHFFFAOYSA-N 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 229940120889 dipyrone Drugs 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 229960000514 ethenzamide Drugs 0.000 description 1
- SBNKFTQSBPKMBZ-UHFFFAOYSA-N ethenzamide Chemical compound CCOC1=CC=CC=C1C(N)=O SBNKFTQSBPKMBZ-UHFFFAOYSA-N 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 229960002428 fentanyl Drugs 0.000 description 1
- IVLVTNPOHDFFCJ-UHFFFAOYSA-N fentanyl citrate Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O.C=1C=CC=CC=1N(C(=O)CC)C(CC1)CCN1CCC1=CC=CC=C1 IVLVTNPOHDFFCJ-UHFFFAOYSA-N 0.000 description 1
- NOOCSNJCXJYGPE-UHFFFAOYSA-N flunixin Chemical compound C1=CC=C(C(F)(F)F)C(C)=C1NC1=NC=CC=C1C(O)=O NOOCSNJCXJYGPE-UHFFFAOYSA-N 0.000 description 1
- 229960000588 flunixin Drugs 0.000 description 1
- 229960003667 flupirtine Drugs 0.000 description 1
- 238000002695 general anesthesia Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- OROGSEYTTFOCAN-UHFFFAOYSA-N hydrocodone Natural products C1C(N(CCC234)C)C2C=CC(O)C3OC2=C4C1=CC=C2OC OROGSEYTTFOCAN-UHFFFAOYSA-N 0.000 description 1
- WVLOADHCBXTIJK-YNHQPCIGSA-N hydromorphone Chemical compound O([C@H]1C(CC[C@H]23)=O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O WVLOADHCBXTIJK-YNHQPCIGSA-N 0.000 description 1
- 229960001410 hydromorphone Drugs 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 229960003029 ketobemidone Drugs 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 230000006386 memory function Effects 0.000 description 1
- 229960000365 meptazinol Drugs 0.000 description 1
- JLICHNCFTLFZJN-HNNXBMFYSA-N meptazinol Chemical compound C=1C=CC(O)=CC=1[C@@]1(CC)CCCCN(C)C1 JLICHNCFTLFZJN-HNNXBMFYSA-N 0.000 description 1
- LVWZTYCIRDMTEY-UHFFFAOYSA-N metamizole Chemical compound O=C1C(N(CS(O)(=O)=O)C)=C(C)N(C)N1C1=CC=CC=C1 LVWZTYCIRDMTEY-UHFFFAOYSA-N 0.000 description 1
- 229960001797 methadone Drugs 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229960004610 morazone Drugs 0.000 description 1
- OOGNFQMTGRZRAB-UHFFFAOYSA-N morazone Chemical compound CC1C(C=2C=CC=CC=2)OCCN1CC(C1=O)=C(C)N(C)N1C1=CC=CC=C1 OOGNFQMTGRZRAB-UHFFFAOYSA-N 0.000 description 1
- 229960005181 morphine Drugs 0.000 description 1
- NETZHAKZCGBWSS-CEDHKZHLSA-N nalbuphine Chemical compound C([C@]12[C@H]3OC=4C(O)=CC=C(C2=4)C[C@@H]2[C@]1(O)CC[C@@H]3O)CN2CC1CCC1 NETZHAKZCGBWSS-CEDHKZHLSA-N 0.000 description 1
- 229960000805 nalbuphine Drugs 0.000 description 1
- UZHSEJADLWPNLE-GRGSLBFTSA-N naloxone Chemical compound O=C([C@@H]1O2)CC[C@@]3(O)[C@H]4CC5=CC=C(O)C2=C5[C@@]13CCN4CC=C UZHSEJADLWPNLE-GRGSLBFTSA-N 0.000 description 1
- 229960004127 naloxone Drugs 0.000 description 1
- 229960000751 nefopam Drugs 0.000 description 1
- 230000035771 neuroregeneration Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229960001027 opium Drugs 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 229960002085 oxycodone Drugs 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 229960005489 paracetamol Drugs 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- VOKSWYLNZZRQPF-GDIGMMSISA-N pentazocine Chemical compound C1C2=CC=C(O)C=C2[C@@]2(C)[C@@H](C)[C@@H]1N(CC=C(C)C)CC2 VOKSWYLNZZRQPF-GDIGMMSISA-N 0.000 description 1
- 229960005301 pentazocine Drugs 0.000 description 1
- 230000003864 performance function Effects 0.000 description 1
- 239000002831 pharmacologic agent Substances 0.000 description 1
- 229960005222 phenazone Drugs 0.000 description 1
- 229960001286 piritramide Drugs 0.000 description 1
- IHEHEFLXQFOQJO-UHFFFAOYSA-N piritramide Chemical compound C1CC(C(=O)N)(N2CCCCC2)CCN1CCC(C#N)(C=1C=CC=CC=1)C1=CC=CC=C1 IHEHEFLXQFOQJO-UHFFFAOYSA-N 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229960002189 propyphenazone Drugs 0.000 description 1
- PXWLVJLKJGVOKE-UHFFFAOYSA-N propyphenazone Chemical compound O=C1C(C(C)C)=C(C)N(C)N1C1=CC=CC=C1 PXWLVJLKJGVOKE-UHFFFAOYSA-N 0.000 description 1
- 229960000948 quinine Drugs 0.000 description 1
- JZWFDVDETGFGFC-UHFFFAOYSA-N salacetamide Chemical compound CC(=O)NC(=O)C1=CC=CC=C1O JZWFDVDETGFGFC-UHFFFAOYSA-N 0.000 description 1
- 229950009280 salacetamide Drugs 0.000 description 1
- 229960000581 salicylamide Drugs 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 229960000953 salsalate Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000036280 sedation Effects 0.000 description 1
- IMCGHZIGRANKHV-AJNGGQMLSA-N tert-butyl (3s,5s)-2-oxo-5-[(2s,4s)-5-oxo-4-propan-2-yloxolan-2-yl]-3-propan-2-ylpyrrolidine-1-carboxylate Chemical compound O1C(=O)[C@H](C(C)C)C[C@H]1[C@H]1N(C(=O)OC(C)(C)C)C(=O)[C@H](C(C)C)C1 IMCGHZIGRANKHV-AJNGGQMLSA-N 0.000 description 1
- 229960001402 tilidine Drugs 0.000 description 1
- 229960004380 tramadol Drugs 0.000 description 1
- TVYLLZQTGLZFBW-GOEBONIOSA-N tramadol Natural products COC1=CC=CC([C@@]2(O)[C@@H](CCCC2)CN(C)C)=C1 TVYLLZQTGLZFBW-GOEBONIOSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Definitions
- the invention relates to a medicament containing xenon.
- WO 02/22141 A2 describes the use of xenon or xenon-containing gases as medicaments, in particular cardiovascular agents.
- ischemic pulmonary disease Many pharmacological agents reach the target site (site of action) in a patient's body via the bloodstream. If blood flow to a part of the body is restricted, the active substances cannot reach the site of action in sufficient quantities. Anemia of the blood in individual parts of the organ due to insufficient blood supply is called ischemia. Ischemia arises, for example, from thrombosis or embolism. Serious circulatory disorders in the brain occur in the event of a stroke.
- adjuvants are substances that support the effectiveness of a medication.
- the invention is based, to improve the drug supply or drug supply of parts of the body, in particular the brain, the task.
- the invention relates to an adjuvant with the features described in claim 1.
- BESTATIGUNGSKOPIE Xenon or xenon-containing gases are used as an adjuvant or as part of an adjuvant.
- the adjuvant particularly supports drugs whose active ingredient or agents are transported through the bloodstream. Medicines with one or more active substances transported via the bloodstream are referred to here as hemogenic drugs. Preferred drugs supported by the adjuvant are drugs which are intended to have an effect in the brain (cerebral drugs), in particular hemogenic cerebral drugs.
- the adjuvant is preferably administered by inhalation.
- the adjuvant is therefore preferably used as an inhalation medication.
- Adjuvant and assisted medicament used together are considered to be a combination preparation or combination medication, wherein adjuvant and assisted medicament are administered together in one medicament (the adjuvant is included in the medicament) or as separate medications.
- the combination drug consisting of a xenone-containing drug, the adjuvant, and another drug (the drug supported by the adjuvant) is used for the simultaneous, separate or chronological use of the drugs (the components of the combination drug).
- the combination drug preferably consists of an inhalation drug containing xenon (e.g. xenon or a gas containing xenon) and a hemogenic drug, e.g. an oral or parenteral drug.
- the adjuvant or inhalation medication contains gaseous xenon in a pharmacologically or therapeutically effective amount, in particular in a sedative, sedative, subanalgesic, analgesic, subhypnotically, hypnotically effective, subanesthetically or anesthetically effective amount, concentration or dosage.
- the subanesthetic amounts of xenon are to be understood as those amounts, concentrations or dosages of xenon which are suitable for general anesthesia not suffice.
- Subscribing amounts of xenon are to be understood as those amounts, concentrations or dosages of xenon which are insufficient for sedation.
- the subhypnotic amounts of xenon are to be understood as amounts, concentrations or dosages of xenon which are insufficient for the initiation and maintenance of sleep.
- Amounts, concentrations or dosages of xenon which are not sufficient for an analgesic effect are to be understood as subanalgesic or analgesically effective amounts of xenon.
- the combination drug is usually used in humans or mammals.
- the drugs combined with the adjuvant include, in addition to drugs with pharmacologically active substances (active ingredients), diagnostics, X-ray contrast media, radioactive isotopes.
- the adjuvant is e.g. used in combination with an antiviral, antibacterial, antifungal, neuroprotective, anticancer, sedative, analgesic or anesthetic substance, especially with opioids (e.g. sufentanil, remifentanil), anesthetics, volatile anesthetics (e.g. methoxyflurane, halothane, desflurane, isoflurane, isoflurane) ), ⁇ 2 adrenoceptor agonists (e.g.
- Clonidine, dexmedetomidine) or catechoamines are organic substances.
- the adjuvant is advantageously combined with parasympathomimetics, parasympatholytics, spasmolytics, sympathomimetics, sympatholytics, ß-receptor blockers, tranquillizers, neuroleptics, antidepressants, sedatives (analgesics), antipyretics, migraine drugs, antiparkinsonian drugs, analgesics, analgesics, analgesics Substances, amino acids, vitamins or hormones.
- the adjuvant is also used with drugs to inhibit NOS, with drugs to treat migraines, with drugs to treat septic shock, multiple sclerosis, inflammation or inflammatory pain.
- the adjuvant is used, for example, with drugs for the treatment and / or prophylaxis of stroke, reperfusion damage, brain trauma, circulatory disorders in the brain, cerebral perfusion disorder, cognitive disorders or post-ischemia syndrome.
- the adjuvant is also used with a drug for neuroprotection, a drug for the prophylaxis and / or therapy of cognitive performance disorders, a drug for improving the oxygen supply in the brain or a drug for promoting blood circulation in the brain.
- the combination medicaments include, in particular, the adjuvant and a medicament for the therapy of diseases in which there is a loss of brain performance and memory functions, e.g. B. in the course of pathological aging processes such as Parkinson's disease, Alzheimer's disease, organic brain syndrome (organic brain syndrome), AIDS dementia, depressive pseudo-dementia, dementia syndromes, delirium as acute organic brain syndromes, intoxications, withdrawal syndromes or cytopathic disorders.
- diseases in which there is a loss of brain performance and memory functions e.g. B. in the course of pathological aging processes such as Parkinson's disease, Alzheimer's disease, organic brain syndrome (organic brain syndrome), AIDS dementia, depressive pseudo-dementia, dementia syndromes, delirium as acute organic brain syndromes, intoxications, withdrawal syndromes or cytopathic disorders.
- the adjuvant is advantageously used in combination with medication for chronic neurodegenerative diseases such as Huntington's disease, amyotropic lateral sclerosis, Parkinson's disease, AIDS dementia, Alzheimer's disease or acute neurodegenerative diseases such as ischemia of the brain and neurotrauma.
- chronic neurodegenerative diseases such as Huntington's disease, amyotropic lateral sclerosis, Parkinson's disease, AIDS dementia, Alzheimer's disease or acute neurodegenerative diseases such as ischemia of the brain and neurotrauma.
- the adjuvant is advantageously used in combination with sedative substances, in particular with centrally sedative substances.
- the sedative substances are usually organic substances that have a sedative effect.
- the sedative substances are usually contained in a medicament (sedative medication, sedative or sedative) which is administered with the adjuvant, in particular as a combination preparation or combination medication.
- Such combination preparations or combination medicaments therefore generally consist of a xenone-containing medicament as an adjuvant and a sedative medication for simultaneous, separate or chronologically graded i.
- Such a combination drug preferably consists of an inhalation drug with xenon or a gas containing xenon and an orally or parenterally administered sedative drug.
- the adjuvant or inhalation drug is e.g. administered in a sedative or sedative amount, concentration or dosage.
- Sedative drugs or active substances are e.g. long-acting barbiturates such as barbital or phenobarbital, medium-long and short-acting barbiturates such as allobarbital, amobarbital, aprobarbital, brallobarbital,
- the adjuvant enhances known sedatives.
- conventional sedatives can be administered in lower doses, which can significantly reduce or avoid side effects.
- the adjuvant is also used in combination with an analgesic.
- the combination preparation or combination medicament generally consists of a xenone-containing medication and an analgesic for simultaneous, separate or staggered use, in particular for the treatment and prophylaxis of pain.
- the combination medicament preferably consists of an inhalation medication with xenon or a gas containing xenon and an orally or parenterally administered analgesic.
- Analgesics or analgesic agents are analgesics with morphine-like effects such as buprenorphine, cetobemidone, codeine, dextromoramide,
- Other analgesics are salicylic acid derivatives, pyrazolone derivatives and aminophenol derivatives.
- Salicylic acid derivatives are acetylsalicylic acid, benorilat, diflunisal, ethenzamide gentisate sodium, salacetamide, salicylamide, salicylic acid or salsalate.
- Pyrazolone derivatives are metamizole (noramidopyrine), morazone, phenazone or propyphenazone.
- An aminophenol derivative is paracetamol.
- Other analgesics are quinine, flunixin, flupirtine or benzyl phenylglycol (benzyl mandelate, benzyl almondate).
- the adjuvant is also used in combination with a local anesthetic.
- Local anesthetics are e.g. Articaine, Benzovain, Bupivacaine, Butanilicain, Butoxycain, Cinchocaine, Cocaine, Etidocaine, Fomocaine, Lidocaine, Mepivacaine, Oxetacaine, Oxybuprocain, Pramocaine, Prilocaine, Procaine, Proxymetacaine, Ropivacaine, Tolycaine or Tetra.
- the supported medication can also be a mixture of two or more local anesthetics.
- the adjuvant is preferably used as a breathing gas mixture containing xenon and oxygen.
- the adjuvant provided or the adjuvant produced directly during use, in particular in the immediate vicinity of the patient is, for example, a gas mixture which contains 1 to 80 vol B. balance oxygen).
- the drug that is administered to the patient advantageously contains xenon in subanesthetic amounts.
- the subanesthetic amounts of xenon are those amounts or concentrations of xenon that are insufficient for anesthesia. These are generally amounts of up to 70% by volume xenon, preferably up to 65% by volume, particularly preferably up to 60% by volume, in particular up to 50% by volume xenon. Accordingly, pure xenon is dosed into the patient's breathing gas in the concentrations mentioned.
- the breathing gas supplied to the patient contains, for example, 5 to 60% by volume, 5 to 50% by volume, 5 to 40% by volume, 5 to 30% by volume or 5 to 20% by volume xenon.
- a dosage of xenon in the breathing gas with a low concentration, for example 1 to 35 vol.%, 5 to 25 vol. % Xenon in the breathing gas may be beneficial.
- the gaseous adjuvant preferably contains one or more gases or gaseous substances at body temperature and normal pressure.
- Usable gas mixtures are, for example, xenon-oxygen gas mixtures or gas mixtures of xenon and one or more inert gases such as nitrogen or an inert gas (eg helium) or xenon-oxygen-inert gas gas mixtures.
- Suitable gas mixtures are described in WO 02/22141 A2, to which reference is hereby made.
- Gaseous xenon (pure xenon) is generally provided as a compressed gas in pressurized gas containers such as pressurized gas cylinders or pressurized cans. Gas mixtures containing xenon can also be provided in pressurized gas containers. The gaseous drug can also be provided in a container as a liquefied gas or gas mixture or in a work hardened form.
- the adjuvant is usually administered with a ventilator with a gas metering unit or with an anesthesia machine.
- the adjuvant is advantageously produced directly for use from the pure gases, for example by mixing xenon, oxygen and, if appropriate, an inert gas (for example with the aid of an anesthesia machine or a gas metering device) in close proximity to the patient.
- gaseous adjuvant in particular xenon and oxygen or a breathing gas
- concentrations of the gas components are advantageously varied during ventilation.
- the device and the different methods of gas metering, in particular the continuous and discontinuous gas metering with constant or variable gas component concentration, are in the
- the adjuvant or combination drug is also administered, for example, with a heart-lung machine.
- the combination drug is used in the following manner. First, a gas containing xenon is administered in an anesthetic and / or sedative effective amount as an adjuvant. In the next phase of the graded administration of the drug, the hemogenic drug is administered.
- the adjuvant is usually administered to the patient as a dry, moist gas or water vapor-saturated gas.
- the adjuvant is also, for example, a liquid preparation that contains xenon.
- a liquid preparation is described in DE 19933704 A1, to which reference is hereby made.
Landscapes
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
Claims
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10230544 | 2002-07-05 | ||
| DE10230544 | 2002-07-05 | ||
| DE10236760 | 2002-08-10 | ||
| DE10236760 | 2002-08-10 | ||
| DE10236761 | 2002-08-10 | ||
| DE10236762 | 2002-08-10 | ||
| DE10236762 | 2002-08-10 | ||
| DE10236761 | 2002-08-10 | ||
| PCT/EP2003/007186 WO2004004782A1 (en) | 2002-07-05 | 2003-07-04 | Adjuvant containing xenon |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP1521598A1 true EP1521598A1 (en) | 2005-04-13 |
Family
ID=30119186
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP03762626A Withdrawn EP1521598A1 (en) | 2002-07-05 | 2003-07-04 | Adjuvant containing xenon |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20050255169A1 (en) |
| EP (1) | EP1521598A1 (en) |
| JP (1) | JP2006508040A (en) |
| CN (1) | CN1665542A (en) |
| AU (1) | AU2003249959A1 (en) |
| WO (1) | WO2004004782A1 (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20100203156A1 (en) * | 2009-02-09 | 2010-08-12 | Meiler Steffen E | Xenon as a treatment for hemoglobinopathy |
| CA2824948C (en) * | 2011-02-07 | 2020-06-02 | Rich Products Corporation | Method for preserving cells and cell cultures |
| CN103565745A (en) | 2012-08-10 | 2014-02-12 | 德克萨斯州大学系统董事会 | Neuroprotective liposome compositions and methods for treating stroke |
| RU2506944C1 (en) * | 2012-09-24 | 2014-02-20 | Александр Юрьевич Верховский | Method for improving transdermal permeability of therapeutic or cosmetic topical preparations, method for dermal administration of liquid xenon |
| FR2996459B1 (en) | 2012-10-09 | 2015-02-06 | Air Liquide | USE OF AN ARGON / XENON MIXTURE TO PREVENT OR TREAT THE NEUROLOGICAL CONSEQUENCES OF A SEPTIC SHOCK |
| FR2996458B1 (en) * | 2012-10-09 | 2015-02-27 | Air Liquide | USE OF XENON TO PREVENT OR TREAT THE NEUROLOGICAL CONSEQUENCES OF A SEPTIC SHOCK |
| JP6625966B2 (en) | 2013-03-15 | 2019-12-25 | ボード・オブ・リージエンツ,ザ・ユニバーシテイ・オブ・テキサス・システム | Noble gas-rich liquids and methods for their preparation and use |
| FR3007983B1 (en) * | 2013-07-08 | 2015-06-26 | Air Liquide | ASSOCIATION OF XENON AND AN NMDA RECEPTOR ANTAGONIST TO FIGHT NEURODEGENERATIVE DISEASE |
| FR3027226B1 (en) * | 2014-10-17 | 2017-12-08 | L'air Liquide Sa Pour L'etude Et L'exploitation Des Procedes Georges Claude | MEDICAMENT FOR TREATING A DISEASE RELATED TO A DYSFUNCTION OF THE DOPAMINERGIC SYNAPTIC TRANSMISSION |
| EP3313384A4 (en) * | 2015-06-23 | 2019-04-03 | Nobilis Therapeutics, Inc. | Therapeutic immune modulation using noble gas compositions |
| CN116746574A (en) * | 2023-05-31 | 2023-09-15 | 广西田园生化股份有限公司 | Pesticide adjuvants and preparation methods and applications thereof, and pesticide compositions including the same and applications thereof |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1601366A (en) * | 1977-06-21 | 1981-10-28 | Nat Res Dev | Lasers |
| FR2538704B1 (en) * | 1983-01-03 | 1986-02-28 | France Prod Oxygenes Co | CONTRAST PRODUCT OF TOMODENSITOMETRY IMAGES |
| US5228434A (en) * | 1991-07-16 | 1993-07-20 | Praxair Technology, Inc. | Mixture for anesthesia |
| US5099834A (en) * | 1991-07-16 | 1992-03-31 | Union Carbide Industrial Gases Technology Corporation | Method for anesthesia |
| DE69617719D1 (en) * | 1995-10-20 | 2002-01-17 | Air Liquide | PHARMACEUTICAL COMPOSITION OF NITROGEN MONOXIDE |
| DE19709704C2 (en) * | 1997-03-10 | 1999-11-04 | Michael Georgieff | Use of a liquid preparation of xenon for intravenous administration when inducing and / or maintaining anesthesia |
| DE19910986C2 (en) * | 1999-03-11 | 2001-06-07 | Aga Ab | Use of xenon in the treatment of neurointoxication |
| GB9913677D0 (en) * | 1999-06-11 | 1999-08-11 | Imperial College | Formulation |
| FR2812545B1 (en) * | 2000-08-03 | 2003-03-28 | Air Liquide Sante Int | INHALABLE DRUG AEROSOL FOR TREATMENT OR PREVENTION OF SWEETNESS |
| DE10045829A1 (en) * | 2000-09-14 | 2002-04-04 | Messer Griesheim Gmbh | Volatile anesthetic with xenon |
-
2003
- 2003-07-04 US US10/518,067 patent/US20050255169A1/en not_active Abandoned
- 2003-07-04 AU AU2003249959A patent/AU2003249959A1/en not_active Abandoned
- 2003-07-04 WO PCT/EP2003/007186 patent/WO2004004782A1/en not_active Ceased
- 2003-07-04 JP JP2004518712A patent/JP2006508040A/en active Pending
- 2003-07-04 CN CN038159945A patent/CN1665542A/en active Pending
- 2003-07-04 EP EP03762626A patent/EP1521598A1/en not_active Withdrawn
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2004004782A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2006508040A (en) | 2006-03-09 |
| CN1665542A (en) | 2005-09-07 |
| US20050255169A1 (en) | 2005-11-17 |
| AU2003249959A1 (en) | 2004-01-23 |
| WO2004004782A1 (en) | 2004-01-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Bortolami et al. | Practical use of opioids in cats: a state-of-the-art, evidence-based review | |
| Özalevli et al. | The effect of adding intrathecal magnesium sulphate to bupivacaine–fentanyl spinal anaesthesia | |
| DE69523301T2 (en) | A NARCOTIC AEROSOL FORMULATION | |
| Aronson | Meyler's side effects of analgesics and anti-inflammatory drugs | |
| JP2003113074A (en) | Dosage form | |
| Reza et al. | Preemptive analgesic effect of ketamine in patients undergoing elective cesarean section | |
| EP1521598A1 (en) | Adjuvant containing xenon | |
| Schwagmeier et al. | Pharmacokinetics of intranasal alfentanil | |
| EP3551166B1 (en) | Topical phenytoin for use in the treatment of peripheral neuropathic pain | |
| WO2018106108A1 (en) | Topical pharmaceutical composition containing phenytoin and a (co -)an algesic for the treatment of chronic pain | |
| DE2222039A1 (en) | Narcotic drugs | |
| DE60122015T2 (en) | TREATMENT OF AFFECTIVE DISORDERS BY COMBINED EFFECT OF A NICOTINE RECEPTOR AGONIST AND A MONOAMINERGIC SUBSTANCE | |
| CA2961936C (en) | Intranasal compositions for treatment of neurological and neurodegenerative diseases and disorders | |
| Comelon et al. | Tapentadol versus oxycodone analgesia and side effects after laparoscopic hysterectomy: a randomised controlled trial | |
| WO2002022141A2 (en) | Xenon as medicament | |
| EP2367546B1 (en) | Combination of local anesthetic and analgesic for relieving breast pain | |
| EP1420789B1 (en) | USE OF ACTIVE INGREDIENTS HAVING A µ-OPIOID RECEPTOR AGONIST ACTION AND AN OPIOID RECEPTOR ANTAGONIST ACTION, AS COMBINATION DRUGS FOR THE TREATMENT OF CANCER | |
| WO2003105871A1 (en) | Cerebral protection with a gas comprising xenon | |
| Wajima et al. | Severe lightning pain after subarachnoid block in a patient with neuropathic pain of central origin: which drug is best to treat the pain? | |
| Chandrakar et al. | Use of Patient Controlled Analgesia Using IV Tramadol and IV Nalbuphine for Postoperative Pain Management after Major Abdominal Surgery-A Comparative Study | |
| Merhavy et al. | Anesthetic Drugs: A Comprehensive Overview for Primary Care | |
| DE60316927T2 (en) | USE OF DEVAZEPIDE AS PAIN | |
| DE19712398A1 (en) | Oral use of (+) - 0-demethyltramadol as a pain reliever | |
| Hassoon et al. | ANALGESIA WITH REMIFENTANIL IN GENERAL ANESTHESIA IN LARGE OPERATION | |
| Cooley et al. | Insight into anesthetic drugs |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| 17P | Request for examination filed |
Effective date: 20050207 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LI LU MC NL PT RO SE SI SK TR |
|
| AX | Request for extension of the european patent |
Extension state: AL LT LV MK |
|
| RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: AIR LIQUIDE DEUTSCHLAND GMBH |
|
| DAX | Request for extension of the european patent (deleted) | ||
| RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: REYLE-HAHN, MATTHIAS Inventor name: NEU, PETER Inventor name: PILGER, CARSTEN |
|
| 17Q | First examination report despatched |
Effective date: 20080606 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
| 18D | Application deemed to be withdrawn |
Effective date: 20081217 |