GB658467A - Improvements relating to the production of preparations of penicillin salts - Google Patents

Improvements relating to the production of preparations of penicillin salts

Info

Publication number
GB658467A
GB658467A GB24781/49A GB2478149A GB658467A GB 658467 A GB658467 A GB 658467A GB 24781/49 A GB24781/49 A GB 24781/49A GB 2478149 A GB2478149 A GB 2478149A GB 658467 A GB658467 A GB 658467A
Authority
GB
United Kingdom
Prior art keywords
penicillin
salt
water
preparations
salts
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.)
Expired
Application number
GB24781/49A
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.)
KAERNBOLAGET AB
Original Assignee
KAERNBOLAGET AB
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 KAERNBOLAGET AB filed Critical KAERNBOLAGET AB
Publication of GB658467A publication Critical patent/GB658467A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D499/00Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D499/21Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring with a nitrogen atom directly attached in position 6 and a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2
    • C07D499/22Salts with organic bases; Complexes with organic compounds
    • C07D499/24Salts with organic bases; Complexes with organic compounds with acyclic or carbocyclic compounds containing amino radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)

Abstract

Preparations of penicillin salts difficulty soluble in water, which preparations contain water, or in which the penicillin salt in the course of production comes into contact with water, are stabilized by dissolving in the aqueous phase the cation of the penicillin salt so that there is present an excess of the cation of the penicillin salt over and above that combined in the penicillin salt. Such salts are procaine penicillin and aluminium penicillin. The aqueous solution may contain other substances such as hydrophyllic colloids, e.g. carboxymethyl cellulose, carboxymethyl starch, alkali metal salts of alginic acid and pectins and amylopectin, alkali metal salts, e.g. sodium chloride, and preservatives, e.g. methyl p-hydroxybenzoate. An example is given of a procaine penicillin injection in which the said salt is suspended in an aqueous solution of procaine hydrochloride, sodium carboxymethyl cellulose, sodium chloride and methyl p-hydroxybenzoate.ALSO:Preparations of penicillin salts difficultly soluble in water, which preparations contain water, or in which the penicillin salt in the course of production comes into contact with water, are characterized in that to the aqueous phase is added the cation of the penicillin salt so that there is present an excess of the cation of the penicillin salt over and above that combined in the penicillin salt. Such salts are procaine penicillin and aluminium penicillin. The aqueous solution may contain other substances such as hydrophillic colloids, e.g. carboxymethyl cellulose carboxymethyl starch alkali metal salts of alginic acid and pectins and amylopectin, alkali metal salts, e.g. sodium chloride and preserving agents, e.g. methyl p-hydroxybenzoate. An example is given of a procaine penicillin injection in which the said salt is suspended in an aqueous solution of procaine hydrochloride, sodium carboxymethyl cellulose, sodium chloride and methyl p-hydroxybenzoate. The preparations may be water-containing ointments, injections and lozenges.
GB24781/49A 1949-09-09 1949-09-27 Improvements relating to the production of preparations of penicillin salts Expired GB658467A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE658467X 1949-09-09

Publications (1)

Publication Number Publication Date
GB658467A true GB658467A (en) 1951-10-10

Family

ID=20314248

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24781/49A Expired GB658467A (en) 1949-09-09 1949-09-27 Improvements relating to the production of preparations of penicillin salts

Country Status (1)

Country Link
GB (1) GB658467A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2715092A (en) * 1951-04-06 1955-08-09 Chimiotherapie Lab Franc Organic penicillin salt solutions and method of making same
US2731387A (en) * 1951-05-15 1956-01-17 Schenley Ind Inc Aqueous suspension of procaine penicillin
US2734845A (en) * 1956-02-14 Aqueous suspension of procaine penicil-
US2734846A (en) * 1956-02-14 Aqueous suspension of procaine penicil-
US2738300A (en) * 1954-12-24 1956-03-13 Smith Kline French Lab Stable aqueous penicillin preparation
US2749274A (en) * 1952-05-06 1956-06-05 Bristol Lab Inc Stable aqueous procaine penicillin suspension
US2870063A (en) * 1955-07-05 1959-01-20 Mallinckrodt Chemical Works X-ray contrast composition comprising substantially amylose-free amylopectin in aqueous solution of contrast agent
US2903395A (en) * 1956-03-30 1959-09-08 Pfizer & Co C Aqueous calcium dioxytetracycline antibiotic composition
EP1190719A1 (en) * 2000-08-17 2002-03-27 B. Braun Melsungen Ag Colloidal pharmacomodulation of injected pharmaceutical compositions

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2734845A (en) * 1956-02-14 Aqueous suspension of procaine penicil-
US2734846A (en) * 1956-02-14 Aqueous suspension of procaine penicil-
US2715092A (en) * 1951-04-06 1955-08-09 Chimiotherapie Lab Franc Organic penicillin salt solutions and method of making same
US2731387A (en) * 1951-05-15 1956-01-17 Schenley Ind Inc Aqueous suspension of procaine penicillin
US2749274A (en) * 1952-05-06 1956-06-05 Bristol Lab Inc Stable aqueous procaine penicillin suspension
US2738300A (en) * 1954-12-24 1956-03-13 Smith Kline French Lab Stable aqueous penicillin preparation
US2870063A (en) * 1955-07-05 1959-01-20 Mallinckrodt Chemical Works X-ray contrast composition comprising substantially amylose-free amylopectin in aqueous solution of contrast agent
US2903395A (en) * 1956-03-30 1959-09-08 Pfizer & Co C Aqueous calcium dioxytetracycline antibiotic composition
EP1190719A1 (en) * 2000-08-17 2002-03-27 B. Braun Melsungen Ag Colloidal pharmacomodulation of injected pharmaceutical compositions

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