SE512655C2 - Medication for infusion treatment - Google Patents

Medication for infusion treatment

Info

Publication number
SE512655C2
SE512655C2 SE9303787A SE9303787A SE512655C2 SE 512655 C2 SE512655 C2 SE 512655C2 SE 9303787 A SE9303787 A SE 9303787A SE 9303787 A SE9303787 A SE 9303787A SE 512655 C2 SE512655 C2 SE 512655C2
Authority
SE
Sweden
Prior art keywords
medication
soln
infusion
solution
durability
Prior art date
Application number
SE9303787A
Other languages
Swedish (sv)
Other versions
SE9303787L (en
SE9303787D0 (en
Inventor
Nil Dizdar
Original Assignee
Medmera Sweden Hb C O Nil Dizd
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
Application filed by Medmera Sweden Hb C O Nil Dizd filed Critical Medmera Sweden Hb C O Nil Dizd
Priority to SE9303787A priority Critical patent/SE512655C2/en
Publication of SE9303787D0 publication Critical patent/SE9303787D0/en
Publication of SE9303787L publication Critical patent/SE9303787L/en
Publication of SE512655C2 publication Critical patent/SE512655C2/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0019Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
    • A61K31/198Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/08Solutions

Landscapes

  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)

Abstract

Medication comprises an infusion soln. with L-dopa dissolved in hydrochloric acid and buffered with Addex-THAM to a degree of acidity so that the soln. maintains its properties, is tissue-tolerable and maintainable for periods permitting its use in clinical practice. The pH of the medication is 4.0-6.0 and sodium pyrosulphite is used to stabilise the soln. and improve its durability. The durability is pH-dependent and at pH 4.5 is 3 days.

Description

512 655 BESKRIVNING Stamlösning L-dopa 50 mg/ml Levodopum 5 g HCL 1 mol/131 g Natfii pyrosulfis 0.5 g Aqua ad injectabila ad 100 ml Lös upp levodopa i saltsyrai en 100 ml kolv. 512 655 DESCRIPTION Stock solution L-dopa 50 mg / ml Levodopum 5 g HCL 1 mol / 131 g Nat fi i pyrosul g s 0.5 g Aqua ad injectable ad 100 ml Dissolve levodopa in hydrochloric acid in a 100 ml flask.

Väg upp natriumpyrosulflt i en 10 ml injektionsflaska och tillsätt 2 ml sterilt vatten för upplösning.Weigh sodium pyrosul in a 10 ml syringe and add 2 ml of sterile water for dissolution.

Tillsätt 50 ml vatten till kolven med levodopa.Add 50 ml of water to the flask with levodopa.

Tillsätt natriumpyrosulfitlösningen. Lösningen blir klar och ljusgul.Add the sodium pyrosul solution. The solution becomes clear and light yellow.

Häll över i 100 ml mätkolv och fyll på vatten till märket.Pour into a 100 ml graduated flask and add water to the mark.

Sterilfiltrera ned i en 100 ml injektionsflaska. Använd Sterivex GV-filter 0.22 pm.Sterile filter into a 100 ml syringe box. Use Sterivex GV filter 0.22 pm.

L-dopa 5 mg/ml - infusionsvätska Levodopum 50 mg/ml (stamlösning) 20 ml Addex-Tham 2ml Glucos 50 mg/ml ad 200 ml Använd Glucos 50 mg/ml infusionsvätska 200 ml flaska.L-dopa 5 mg / ml - infusion solution Levodopum 50 mg / ml (stock solution) 20 ml Addex-Tham 2ml Glucos 50 mg / ml ad 200 ml Use Glucos 50 mg / ml solution for infusion 200 ml fl ash.

Sug ur uträknad mängd (enligt ovanstående exempel 22 ml) Glucos ur flaskan.Suck the calculated amount (according to the above example 22 ml) of glucose from the bottle.

Tillsätt Levodopa stamlösning i uträknad mängd (20 ml).Add Levodopa stock solution in calculated amount (20 ml).

Tillsätt Addex-Tham (2ml), pH ligger då mellan 4 och 6.Add Addex-Tham (2ml), the pH is then between 4 and 6.

Ljusskydda under förvaring och infusion.Light protection during storage and infusion.

Hållbarhet 3 dygn.Shelf life 3 days.

Claims (2)

1. 512 655 Patentansökning nr. 9303787-7 Patentkrav l. En infusionslösning för medicinskt bruk som kännetecknas av att L-dopa är löst i saltsyra (HCI) och därefter buífrad med Addex-THAM till en stabil lösning med surhetsgrad pH 4,0-6,0. Infusionslösningen stabiliseras med natriumpyrosulfit, varvid dess egenskaper vad gäller vävnadstolerabilitet och hållbarhet bibehålls.1. 512 655 Patent application no. 9303787-7 Claim 1. An infusion solution for medical use which is characterized in that L-dopa is dissolved in hydrochloric acid (HCl) and then buffered with Addex-THAM to a stable solution with an acidity of pH 4.0-6.0. The infusion solution is stabilized with sodium pyrosul, retaining its tissue tolerance and durability properties. 2. Infiisionslösningen enligt krav l kännetecknas av att hållbarheten är pH- beroende. Vid pH 4,5 är hållbarheten minst 3 dygn.The injection solution according to Claim 1 is characterized in that the shelf life is pH-dependent. At pH 4.5, the shelf life is at least 3 days.
SE9303787A 1993-11-17 1993-11-17 Medication for infusion treatment SE512655C2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SE9303787A SE512655C2 (en) 1993-11-17 1993-11-17 Medication for infusion treatment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE9303787A SE512655C2 (en) 1993-11-17 1993-11-17 Medication for infusion treatment

Publications (3)

Publication Number Publication Date
SE9303787D0 SE9303787D0 (en) 1993-11-17
SE9303787L SE9303787L (en) 1995-05-18
SE512655C2 true SE512655C2 (en) 2000-04-17

Family

ID=20391770

Family Applications (1)

Application Number Title Priority Date Filing Date
SE9303787A SE512655C2 (en) 1993-11-17 1993-11-17 Medication for infusion treatment

Country Status (1)

Country Link
SE (1) SE512655C2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006006929A1 (en) 2004-07-12 2006-01-19 Dizlin Medical Design Ab Infusion and injection solution of levodopa
US8815950B2 (en) 2003-08-29 2014-08-26 Janssen Biotech, Inc. Pharmaceutical compositions and method of using levodopa and carbidopa
WO2018224501A1 (en) 2017-06-05 2018-12-13 Dizlin Pharmaceuticals Ab Levodopa infusion solution

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8815950B2 (en) 2003-08-29 2014-08-26 Janssen Biotech, Inc. Pharmaceutical compositions and method of using levodopa and carbidopa
EP2298281A1 (en) 2004-07-12 2011-03-23 Dizlin Medical Design AB Infusion and injection solution of Levodopa
JP2015227341A (en) * 2004-07-12 2015-12-17 ディズリン・メディカル・デザイン・アクチボラゲットDizlin Medical Design Ab Infusion and injection solution of levodopa
AU2005262918B2 (en) * 2004-07-12 2010-12-23 Dizlin Medical Design Ab Infusion and injection solution of Levodopa
WO2006006929A1 (en) 2004-07-12 2006-01-19 Dizlin Medical Design Ab Infusion and injection solution of levodopa
JP2013028609A (en) * 2004-07-12 2013-02-07 Dizlin Medical Design Ab Levodopa infusion solution and injection solution
US8735382B2 (en) 2004-07-12 2014-05-27 Dizlin Medical Design Ab Infusion and injection solution of levodopa
EA012415B1 (en) * 2004-07-12 2009-10-30 Дизлин Медикал Дизайн Аб Infusion and injection solution of levodopa
JP2008505966A (en) * 2004-07-12 2008-02-28 ディズリン・メディカル・デザイン・アクチボラゲット Infusion and injection of levodopa
US20140221489A1 (en) * 2004-07-12 2014-08-07 Dizlin Medical Design Ab Infusion and Injection Solution of Levodopa
US9248113B2 (en) 2004-07-12 2016-02-02 Dizlin Medical Design Ab Infusion and injection solution of Levodopa
WO2018224501A1 (en) 2017-06-05 2018-12-13 Dizlin Pharmaceuticals Ab Levodopa infusion solution
CN110753538A (en) * 2017-06-05 2020-02-04 迪兹林制药公司 Levodopa infusion solutions
EP3838263A1 (en) 2017-06-05 2021-06-23 Dizlin Pharmaceuticals AB Levodopa infusion solution
AU2018280745B2 (en) * 2017-06-05 2023-03-09 Dizlin Pharmaceuticals Ab Levodopa infusion solution
US11633353B2 (en) 2017-06-05 2023-04-25 Dizlin Pharmaceuticals Ab Levodopa infusion solution

Also Published As

Publication number Publication date
SE9303787L (en) 1995-05-18
SE9303787D0 (en) 1993-11-17

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