[go: up one dir, main page]

FR2598080A1 - Fluid for peritonial dialysis, containing, in particular, a compound of the verapamil type - Google Patents

Fluid for peritonial dialysis, containing, in particular, a compound of the verapamil type Download PDF

Info

Publication number
FR2598080A1
FR2598080A1 FR8701351A FR8701351A FR2598080A1 FR 2598080 A1 FR2598080 A1 FR 2598080A1 FR 8701351 A FR8701351 A FR 8701351A FR 8701351 A FR8701351 A FR 8701351A FR 2598080 A1 FR2598080 A1 FR 2598080A1
Authority
FR
France
Prior art keywords
dialysis
compound
fluid
mval
formula
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.)
Granted
Application number
FR8701351A
Other languages
French (fr)
Other versions
FR2598080B1 (en
Inventor
Sunder M Lal
Zbylut J Twardowski
Karl D Nolph
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
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 BASF SE filed Critical BASF SE
Publication of FR2598080A1 publication Critical patent/FR2598080A1/en
Application granted granted Critical
Publication of FR2598080B1 publication Critical patent/FR2598080B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/275Nitriles; Isonitriles

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Fluids for peritonial dialysis, which contain a compound of formula I in which the substituents R<1> to R<5> are identical or different and represent hydrogen atoms or C1 to C4 alkoxy groups, or their enantiomers.

Description

Les personnes affectées d'une insuffisance rénale doivent se soumettre à un traitement par dialyse. Une méthode de ce genre est la dialyse péritonéale continue ambulatoire (DPCA), qui peut être effectuée par les personnes concernées. Elle consiste à introduire dans la cavité péritonéale, par l'intermédiaire d'un cathéter péritonéal, un liquide de dialyse approprié, contenu dans une poche, t i le retirer au bout dun certain temps. Le liquide est ensuite échangé contre un liquide de dialyse frais et la dialyse est poursuivie.People with kidney failure should undergo dialysis treatment. One such method is continuous ambulatory peritoneal dialysis (CAPD), which can be performed by those affected. It consists of introducing into the peritoneal cavity, via a peritoneal catheter, an appropriate dialysis fluid, contained in a bag, t i withdrawing it after a certain time. The fluid is then exchanged for fresh dialysis fluid and dialysis is continued.

Or on a trouvé qu'on peut améliorer sensiblement les conditions de dialyse et l'efficacité de la dialyse en additionnant le liquide de dialyse de certaines substances.However, it has been found that the dialysis conditions and the efficiency of the dialysis can be significantly improved by adding certain substances to the dialysis liquid.

L'invention a pour objet des liquides pour dialyse pdrito- néale, caractérisés par le fait qu'ils contiennent, outre les composants usuels, 0,001 à 0,1 % en poids dtun composé de formule I

Figure img00010001

dans laquelle les substitutants R1 à R3 sont identiques ou différents et représentent des atomes d'hydrogène ou des groupes alcoxy en C1 à C4, ou leurs énantiomères.The subject of the invention is liquids for peritoneal dialysis, characterized in that they contain, in addition to the usual components, 0.001 to 0.1% by weight of a compound of formula I
Figure img00010001

wherein the substitutes R1 to R3 are the same or different and represent hydrogen atoms or C1 to C4 alkoxy groups, or their enantiomers.

Pour préparer les liquides selon l'invention on additionne des solutions de dialyse péritonéale usuelles de 0,001 à 0,09 *, de préférence 0,001 à 0,01 *, en poids, d'un compo sé de formule I, de préférence sous forme d'un sel d'un acide physiologiquement acceptable. To prepare the liquids according to the invention are added customary peritoneal dialysis solutions of 0.001 to 0.09 *, preferably 0.001 to 0.01 *, by weight, of a compound of formula I, preferably in the form of a salt of a physiologically acceptable acid.

Les composés de formule I, ainsi que leurs sels diacides physiologiquement acceptables, sont décrits dans DE-PS 1 154 810, DE-PS 2 o39 923, DE-PS 2 059 983 et EP-OS 147 707.The compounds of formula I, as well as their physiologically acceptable diacid salts, are described in DE-PS 1 154 810, DE-PS 2 039 923, DE-PS 2 059 983 and EP-OS 147 707.

L'addition des composés de formule I permet d'augmenter sensiblement l'élimination de substances contenues dans l'urine, en particulier de l'urée, de sorte que les poches contenant le liquide de dialyse ne doivent plus être échangées aussi souvent. Au surplus, les effets secondaires qui se manifestent par suite de la perte de protéine, due à la dialyse péritonéale, sont fortement diminués.The addition of the compounds of formula I makes it possible to significantly increase the elimination of substances contained in the urine, in particular urea, so that the bags containing the dialysis liquid no longer have to be exchanged as often. In addition, the side effects which manifest themselves as a result of the loss of protein, due to peritoneal dialysis, are greatly reduced.

Exemple1
On prépare une solution aqueuse contenant 134mval/1de
Na+, 3,5 mval/l de Ca+, 1,0 mval/lde Mg+, 103,5mval/l deCl-, 35,0mval/l de lactate, 15 g/l de glucose et 10 mg/l de Vérapamil - HCl (formule I, R=R=R4=R5=OCH3,
R =H), et on l'introduit, dans des conditions aseptiques, dans des poches en plastique de 2 1, que l'on enferme ensuite dans des enveloppes stérilisées.
Example1
An aqueous solution is prepared containing 134mval / 1de
Na +, 3.5 mval / l of Ca +, 1.0 mval / l of Mg +, 103.5 mval / l of Cl-, 35.0 mval / l of lactate, 15 g / l of glucose and 10 mg / l of Verapamil - HCl (formula I, R = R = R4 = R5 = OCH3,
R = H), and introduced, under aseptic conditions, into 2 L plastic bags, which are then enclosed in sterilized envelopes.

Exemple 2
On prépare une solution aqueuse contenant 134 mval/l de Na+, 2,0 mwal/l de R+, 3,5 mval/l de Ca2+, 1,0 mval/l de
Mg+, 105,5 mval/l de Cl-,35,0 mval/l de lactate, 35 g/l de glucose et 2 mg/l deGallopamil, HCl (formule I,
R-R5 = OCH3), et on l'introduit, dans des conditions aseptiques, dans des poches en plastique de 2 q, que l'on enferme ensuite dans des enveloppes stérilisées.
Example 2
An aqueous solution is prepared containing 134 mval / l of Na +, 2.0 mwal / l of R +, 3.5 mval / l of Ca2 +, 1.0 mval / l of
Mg +, 105.5 mval / l of Cl-, 35.0 mval / l of lactate, 35 g / l of glucose and 2 mg / l of Gallopamil, HCl (formula I,
R-R5 = OCH3), and is introduced, under aseptic conditions, into 2 q plastic bags, which are then enclosed in sterilized envelopes.

Claims (1)

RevendicationClaim Liquides pour dialyse péritonéale, caractérisés par le fait qu'ils contiennent, outre les composants usuels, 0,001 & à 0,1 % en poids d'un composé de formule ILiquids for peritoneal dialysis, characterized in that they contain, in addition to the usual components, 0.001 & 0.1% by weight of a compound of formula I
Figure img00030001
Figure img00030001
dans laquelle les substituants R1 & R5 sont identiques ou différents et représentent des atomes d'hydrogène ou des groupes alcoxy en C1 à 64, ou leurs énantiomères. wherein the substituents R1 & R5 are the same or different and represent hydrogen atoms or C1 to 64 alkoxy groups, or their enantiomers.
FR8701351A 1986-02-06 1987-02-04 LIQUID FOR PERITONEAL DIALYSIS, CONTAINING IN PARTICULAR A COMPOUND OF THE NATURE OF VERAPAMIL Expired - Lifetime FR2598080B1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19863603660 DE3603660C2 (en) 1986-02-06 1986-02-06 Improved peritoneal dialysis

Publications (2)

Publication Number Publication Date
FR2598080A1 true FR2598080A1 (en) 1987-11-06
FR2598080B1 FR2598080B1 (en) 1992-12-31

Family

ID=6293518

Family Applications (1)

Application Number Title Priority Date Filing Date
FR8701351A Expired - Lifetime FR2598080B1 (en) 1986-02-06 1987-02-04 LIQUID FOR PERITONEAL DIALYSIS, CONTAINING IN PARTICULAR A COMPOUND OF THE NATURE OF VERAPAMIL

Country Status (2)

Country Link
DE (1) DE3603660C2 (en)
FR (1) FR2598080B1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997044025A1 (en) * 1996-05-23 1997-11-27 G.D. Searle & Co. Pharmaceutical compositions containing non-racemic verapamil and process for optimizing the pharmaceutical activity of r- and s-verapamil

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0159678A1 (en) * 1984-04-20 1985-10-30 The Cancer Institute Of Japanese Foundation For Cancer Research Use of 5-[(3,4-dimethoxyphenethyl)methylamino]-2-(3,4-dimethoxy-phenyl)-2-isopropylvaleronitrile

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2059985C3 (en) * 1970-12-05 1979-10-04 Knoll Ag, 6700 Ludwigshafen Right-handed, basic substituted phenylacetonitriles, processes for their preparation and pharmaceuticals containing these compounds
DE2059923C3 (en) * 1970-12-05 1979-01-25 Knoll Ag, 6700 Ludwigshafen 1-a-Isopropyl-o - [(N-methyl-N-homoveratryl) v-aminopropyl] -3,4-dimethoxyphenylacetonitrile, process for its preparation and pharmaceuticals containing it
DE3344755A1 (en) * 1983-12-10 1985-06-20 Basf Ag, 6700 Ludwigshafen 1,7-DIPHENYL-3-METHYLAZA-7-CYAN-8-METHYL-NONANES FOR USE IN THE FIGHT AGAINST DISEASES

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0159678A1 (en) * 1984-04-20 1985-10-30 The Cancer Institute Of Japanese Foundation For Cancer Research Use of 5-[(3,4-dimethoxyphenethyl)methylamino]-2-(3,4-dimethoxy-phenyl)-2-isopropylvaleronitrile

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997044025A1 (en) * 1996-05-23 1997-11-27 G.D. Searle & Co. Pharmaceutical compositions containing non-racemic verapamil and process for optimizing the pharmaceutical activity of r- and s-verapamil
US5955500A (en) * 1996-05-23 1999-09-21 G. D. Searle & Co. Pharmaceutical compositions containing non-racemic verapamil and process for optimizing the pharmaceutical activity of R- and S-verapamil

Also Published As

Publication number Publication date
FR2598080B1 (en) 1992-12-31
DE3603660C2 (en) 1994-09-15
DE3603660A1 (en) 1987-09-03

Similar Documents

Publication Publication Date Title
KR910000143B1 (en) Process for preparing 3-hydroxybutanoic acid or salts derived from these acids
US4889634A (en) Dialysate solution containing hydroxypropyl-beta-cyclodextrin and method of using same
DE69527660T2 (en) Osmotic agent for peritoneal dialysis
EP0316993B1 (en) Pharmaceutical compositions containing a derivative of 3-hydroxy-butanoic acid chosen among oligomers of this acid and among esters of this acid or of these oligomers with 1,3-butane-diol
JP2005514174A (en) Bicarbonate-based solutions for dialysis therapy
HUE028700T2 (en) Method for solubilizing, separating, removing and reacting carboxylic acids in oils, fats, aqueous or organic solutions by means of micro- or nanoemulsification
EP0270545A1 (en) Medicinal composition.
EP1753437A1 (en) Bicarbonate-based peritoneal dialysis solutions
US4952575A (en) Solutions of oxaphosphorins having improved stability and process for the preparation thereof
JPS5869810A (en) Improved peritoneal dialysis solution
Etteldorf et al. Intermittent peritoneal dialysis in the treatment of experimental salicylate intoxication
FR2598080A1 (en) Fluid for peritonial dialysis, containing, in particular, a compound of the verapamil type
HUT66136A (en) Process for preparing a pharmaceutical comp. to peritoneal dyalisis
EP0614366B1 (en) Use of creatine phosphate or phosphoenolpyruvic acid for the treatment of tumours
Fisher et al. Death in neonatal calf diarrhoea. Pt. II: The role of oxygen and potassium
FR2584405A1 (en) FUROSEMIDE SALTS, PHARMACEUTICAL COMPOSITION CONTAINING THEM AND PROCESS FOR THEIR PREPARATION
FR2487195A1 (en) METHOD AND COMPOSITION FOR LOWERING CHOLESTEROL CONTENT IN BLOOD
US3856964A (en) Concentrate for infusion purposes containing 5,5-diphenylhydantoin sodium
FR2491950A1 (en) INSTANTLY PREPARED CULTURE MEDIUM FOR MICROBIOLOGY AND BACTERIOLOGY AND STERILIZATION METHOD THEREOF
DE2216242A1 (en) Dishwashing and cleaning agents for mucous membranes
EP0243336B1 (en) Pharmaceutical compositions for the treatment of intermittent claudication
FR2696933A3 (en) Solns. for perfusion contg. thioctic acid salt - are useful in treatment of liver disorders, hepatic lesions, diabetic or alcoholic poly-neuropathies etc
Friend Iron ascorbate in the treatment of anemia
CN108451974A (en) A kind of aspartic acid Multiple electrolytes injection and preparation method thereof
JP3049280B2 (en) Nutrition infusion bag

Legal Events

Date Code Title Description
TP Transmission of property
ST Notification of lapse