PL135416B1 - Method of obtaining a novel pharmacological preparation - Google Patents

Method of obtaining a novel pharmacological preparation Download PDF

Info

Publication number
PL135416B1
PL135416B1 PL1981232259A PL23225981A PL135416B1 PL 135416 B1 PL135416 B1 PL 135416B1 PL 1981232259 A PL1981232259 A PL 1981232259A PL 23225981 A PL23225981 A PL 23225981A PL 135416 B1 PL135416 B1 PL 135416B1
Authority
PL
Poland
Prior art keywords
water
weight
oil
ester
alcohol
Prior art date
Application number
PL1981232259A
Other languages
English (en)
Other versions
PL232259A1 (en
Original Assignee
Wellcome Found
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26276273&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PL135416(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Wellcome Found filed Critical Wellcome Found
Publication of PL232259A1 publication Critical patent/PL232259A1/xx
Publication of PL135416B1 publication Critical patent/PL135416B1/pl

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Classifications

    • 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
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52—Purines, e.g. adenine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0014—Skin, i.e. galenical aspects of topical compositions

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Dermatology (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Claims (2)

1.Zastrzezenie patentowe 1. Sposób wytwarzania nowego preparatu farmakologicznego typu olej w wodzie, do uzytku zewnetrznego, zawierajecego 9-/2-hydroksyetoksymetylo/guenine lub jej farmakologicznie dopusz¬ czalne sól lub ester, znamienny tym, ze 9-/2-hydroksyetoksymetylo/guenine lub Jej farmakologicznie dopuszczalne sól lub ester wprowadza sie do mieszaniny wody i misszajecego sie z wode alkoholu wielowodorotlenowego i przynajmniej czesc otrzymanej fazy wodnej emulguje sie z faze olejowe, po czym powstale emulsje typu olej w wodzie ewentualnie leczy sie z pozostale czescie fazy wodnej, przy czym alkohol wielowodorotlenowy stosuje sie w ilosci co najmniej 30% wagowych fezy wodnej calego preparatu.
2. Sposób wedlug zastrz. 1, znamienny tym, ze zarówno faze wodne jak i ole¬ jowe ogrzewa sie do temperatury okolo 40-80°C przed zemulgowanienw135 416 73. Sposób wedlug zaatrz. 1 albo 2, znamienny tym, ze stosuje sie 1-10% wagowych 9-/2-hydrokeyetokeymetylo/ guanlny lub jej soli lub estru, 30-50% wagowych alkoholu wlelowodorotlenowego i 20-40% wagowych wody, w stosunku do calej Ilosci preparatu.4. Sposób wedlug zaatrz. 3, znamienny tym, ze stosuje sie 2-5% wagowych 9-/2-hydroksyetoksymetylo/guenlny lub jej soli lub estru, 35-45% wagowych alkoholu wlelowodo¬ rotlenowego i 25-40% wagowych wody, w stosunku do calej ilosci preparatu.5. * Sposób wedlug zestrz. 1, znamienny tym, ze jako alkohol wielowodorotle- nowy stosuje sie glikol polietylenowy, butanodiol-1,3 lub gliceryne.6. Sposób wedlug zaatrz. 1, znamienny tym, ze stosuje sie faze olejowe za¬ wierajece co najmniej jeden emulgator.7. Sposób wedlug zastrz* 6, znamienny tym, ze jako emulgator stosuje sie alkohol cetostearylowy, alkohol mirystylowy, monostearynian gliceryny, laurylosiarczan sodowy, monostearynian poliokeyetylenosorbitanu, monostearynian sorbitanu lub monooleinian sorbitanu.8. 6. Sposób wedlug zestrz. 6, znamienny tym, ze stosuje sie faze olejowe za¬ wierajece takze tluszcz i/lub olej.9. Sposób wedlug zastrz. 8, znamienny tym, ze jako tluszcz i/lub olej sto¬ suje sie stearynian izocetylu, dwuestry glikolu propylenowego 1 kokosowych kwasów tluszczowych, mirystynian izopropylu, oleinian decylu, palmitynian izopropylu, stearynian butylu, palmitynian 2-etylohekaylu, biale miekka, parafine, ciekle parafine, oleje mineralne lub mieszany ester kwasu 2-etylokapronowego z mieszanine alkoholi cetylowego i ste»rylawego.10. Sposób wedlug zestrz. 1, znamienny tym, ze jako alkohol wielowodorotle- nowy stosuje sie glikol propylenowy. PL PL PL
PL1981232259A 1980-07-18 1981-07-17 Method of obtaining a novel pharmacological preparation PL135416B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8023645 1980-07-18
GB8033218A GB2080106B (en) 1980-07-18 1980-10-15 Acyclovin preparations

Publications (2)

Publication Number Publication Date
PL232259A1 PL232259A1 (en) 1983-07-04
PL135416B1 true PL135416B1 (en) 1985-10-31

Family

ID=26276273

Family Applications (1)

Application Number Title Priority Date Filing Date
PL1981232259A PL135416B1 (en) 1980-07-18 1981-07-17 Method of obtaining a novel pharmacological preparation

Country Status (30)

Country Link
EP (1) EP0044543B1 (pl)
AR (1) AR225680A1 (pl)
AT (1) AT381025B (pl)
AU (1) AU547391B2 (pl)
BG (1) BG60450B2 (pl)
CA (1) CA1172169A (pl)
CS (1) CS229674B2 (pl)
CY (1) CY1309A (pl)
DD (1) DD203464A5 (pl)
DE (1) DE3163982D1 (pl)
DK (1) DK149191C (pl)
ES (1) ES504046A0 (pl)
FI (1) FI76255C (pl)
GB (1) GB2080106B (pl)
GR (1) GR75104B (pl)
HK (1) HK95485A (pl)
HU (1) HU185936B (pl)
IE (1) IE51120B1 (pl)
IL (1) IL63351A (pl)
IT (1) IT1171399B (pl)
MC (1) MC1408A1 (pl)
MY (1) MY8600389A (pl)
NO (1) NO155038C (pl)
NZ (1) NZ197744A (pl)
PH (1) PH16308A (pl)
PL (1) PL135416B1 (pl)
PT (1) PT73391B (pl)
RO (1) RO82678A (pl)
SG (1) SG72085G (pl)
ZW (1) ZW17181A1 (pl)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0095813A3 (en) * 1982-06-01 1985-05-08 THE PROCTER & GAMBLE COMPANY Penetrating topical pharmaceutical compositions containing 9-(2-hydroxyethoxymethyl) guanine
US4557934A (en) 1983-06-21 1985-12-10 The Procter & Gamble Company Penetrating topical pharmaceutical compositions containing 1-dodecyl-azacycloheptan-2-one
GB8602346D0 (en) * 1986-01-30 1986-03-05 Wellcome Found Antiviral combinations
GB8917959D0 (en) * 1989-08-05 1989-09-20 Beecham Group Plc Pharmaceutical formulation
GB9001886D0 (en) * 1990-01-26 1990-03-28 Beecham Group Plc Pharmaceutical formulation
US6469015B1 (en) 1990-01-26 2002-10-22 Novartis International Pharmaceutical Ltd Pharmaceutical formulation
EP0773091A3 (en) * 1992-03-20 1998-04-01 Unichema Chemie B.V. Release composition
DK169121B1 (da) * 1992-09-09 1994-08-22 Gea Farmaceutisk Fabrik As Antiviralt virksom farmaceutisk olie-i-vand-emulsion indeholdende 9-[(2-hydroxyethoxy)methyl]guanin (acyclovir) eller et salt eller en ester deraf
DE4416674C2 (de) * 1994-05-11 1997-01-30 Rentschler Arzneimittel Topische Zubereitung enthaltend Aciclovir
DE19517147C2 (de) * 1995-05-10 1999-07-01 Hexal Pharmaforschung Gmbh Aciclovir-Zubereitung
AU2036297A (en) * 1996-03-20 1997-10-10 Glaxo Group Limited Topical formulations of aciclovir
GB9611167D0 (en) * 1996-05-29 1996-07-31 Glaxo Group Ltd Medicaments
GB9718568D0 (en) 1997-09-03 1997-11-05 Chauvin Pharmaceuticals Limite Compositions
GB9718791D0 (en) * 1997-09-05 1997-11-12 Glaxo Group Ltd Medicaments
ITMI981528A1 (it) * 1998-07-03 2000-01-03 Recordati Ind Chimica E Farma Formulazioni topiche di aciclovir
US7223387B2 (en) 1998-11-18 2007-05-29 Medivir Ab Antiviral formulations comprising propylene glycol and an isopropyl alkanoic acid ester
GB9828620D0 (en) * 1998-12-23 1999-02-17 Glaxo Group Ltd Medicaments
RU2179851C1 (ru) * 2000-12-21 2002-02-27 Открытое акционерное общество "Химико-фармацевтический комбинат "Акрихин" Противовирусный фармацевтический состав
RU2175230C1 (ru) * 2001-01-23 2001-10-27 Открытое акционерное общество "Химико-фармацевтический комбинат "Акрихин" Фармацевтическая композиция с противовирусной активностью и способ ее получения
FR2837102B1 (fr) * 2002-03-18 2004-10-08 Palbian Snc Composition a l'etat de gel aqueux, procede de fabrication et utilisation pour la fabrication d'un medicament, notamment antiherpetique
ATE396732T1 (de) * 2004-04-05 2008-06-15 Liomont S A De C V Lab Neue antivirale pharmazeutische zusammensetzung
EP2005824A1 (de) † 2007-06-21 2008-12-24 Bayer CropScience AG Wirkstoffsuspensionen in Glycerin
WO2017029298A1 (en) 2015-08-17 2017-02-23 Sanovel Ilac Sanayi Ve Ticaret A.S. A topical antiviral composition

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3892857A (en) * 1972-11-24 1975-07-01 Squibb & Sons Inc Steroid formulation
ZA738657B (en) * 1973-01-05 1974-10-30 Hoffmann La Roche Emulsions
GB1478009A (en) * 1973-04-02 1977-06-29 Glaxo Lab Ltd Pharmaceutical compositions
US4199574A (en) * 1974-09-02 1980-04-22 Burroughs Wellcome Co. Methods and compositions for treating viral infections and guanine acyclic nucleosides
GB1543907A (en) * 1975-02-19 1979-04-11 Dermal Labor Ltd Steroid compositions
US3934013A (en) * 1975-02-21 1976-01-20 Syntex (U.S.A.) Inc. Pharmaceutical composition
US4049802A (en) * 1975-03-19 1977-09-20 Research Corporation Zinc sulfadiazine and its use in the treatment of burns
GB1554720A (en) * 1975-07-10 1979-10-24 Nyegaard & Co As Pyridthione derivatives
US4144332A (en) * 1976-01-05 1979-03-13 The Regents Of The University Of Michigan Process for alleviating proliferative skin diseases
DE2847975A1 (de) * 1978-11-04 1980-05-14 Merck Patent Gmbh Verfahren zur bindung von freiem formaldehyd in pharmazeutischen und kosmetischen zubereitungen

Also Published As

Publication number Publication date
PT73391A (en) 1981-08-01
AU7307381A (en) 1982-01-21
NO155038B (no) 1986-10-27
DD203464A5 (de) 1983-10-26
NO812464L (no) 1982-01-19
IT8148925A0 (it) 1981-07-17
CY1309A (en) 1985-12-06
DK321681A (da) 1982-01-19
FI812257L (fi) 1982-01-19
NO155038C (no) 1987-02-04
ATA318081A (de) 1986-01-15
IL63351A0 (en) 1981-10-30
ES8305363A1 (es) 1983-04-01
PH16308A (en) 1983-09-05
SG72085G (en) 1986-05-02
HK95485A (en) 1985-12-06
FI76255B (fi) 1988-06-30
AR225680A1 (es) 1982-04-15
MC1408A1 (fr) 1982-07-16
AU547391B2 (en) 1985-10-17
CA1172169A (en) 1984-08-07
GR75104B (pl) 1984-07-13
BG60450B2 (bg) 1995-04-28
NZ197744A (en) 1983-05-10
IE811617L (en) 1982-01-18
GB2080106B (en) 1984-03-07
GB2080106A (en) 1982-02-03
DK149191C (da) 1986-09-08
MY8600389A (en) 1986-12-31
RO82678A (ro) 1984-05-23
IT8148925A1 (it) 1983-01-17
EP0044543B1 (en) 1984-06-06
EP0044543A1 (en) 1982-01-27
ES504046A0 (es) 1983-04-01
PL232259A1 (en) 1983-07-04
IE51120B1 (en) 1986-10-01
HU185936B (en) 1985-04-28
PT73391B (en) 1983-06-15
FI76255C (fi) 1990-03-14
AT381025B (de) 1986-08-11
DE3163982D1 (en) 1984-07-12
IL63351A (en) 1983-10-31
DK149191B (da) 1986-03-10
ZW17181A1 (en) 1983-02-23
IT1171399B (it) 1987-06-10
CS229674B2 (en) 1984-06-18

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