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[Erythromycin ethylsuccinate obtaining possibilities]. / Posibilitati de obtinere a etil-succinatului de eritromicina.
Stan, Catalina Daniela; Stefanache, Alina; Tântaru, Gladiola; Poiata, Antonia; Dumitrache, M; Diaconu, D E; Profire, Lenuta.
Affiliation
  • Stan CD; Disciplina de Industria Medicamentului si Biotehnologii Farmaceutice, Facultatea de Farmacie, Universitatea de Medicina si Farmacie Gr.T. Popa Iasi.
Rev Med Chir Soc Med Nat Iasi ; 112(4): 1104-9, 2008.
Article in Ro | MEDLINE | ID: mdl-20209795
ABSTRACT
UNLABELLED In this study we tried to improve the erythromycin ethylsuccinate obtaining, having in view to separate the erythromycin ester by crystallization in water. MATERIAL AND

METHODS:

The erythromycin acylation and the erythromycin ethylsuccinate crystallization were realized, following the next

steps:

1. the acylation of the erythromycin with a methylene chloride solution of monoethylsuccinyl chloride, at 25-28 degrees C for 3 hours in the presence of NaHCO3; 2. the transfer of the erythromycin ethylsuccinate from methylene chloride solution in acetone solution by distillation of mixture methylene chloride acetone 11 at 25-28 degrees C; 3. erythromycin ethylsuccinate separation by crystallization in water at pH = 8-8.5 and 5 degrees C for 90 minutes. The quality control for the erythromycin ester was performed according to the Xth edition of Romanian Pharmacopoeia standards using national standard for erythromycin ethylsuccinate and national standard for erythromycin with an activity of 1 937 U and 2.02% humidity. The Micrococcus luteus ATCC 9341 was used as a test microorganism and a thin layer cromatography was performed for qualitative control.

RESULTS:

13.1 g of erythromycin ethylsuccinate were obtained with an output of the process of 82.02%. Using water for the separation of erythromycin ethylsuccinate the output of the process is greater (82.02%) than in case of using petroleum ether (74.14%) or hexane (80.25%). The thin layer cromatography revealed an Rf = 0.56 and the microbiological activity of the erythromycin ethylsuccinate was 98.7% compared with the standard.

CONCLUSIONS:

Using water instead of hexane or petroleum ether is gainful for the separation of erythromycin ethylsuccinate from the reaction medium. The obtained erythromycin ethylsuccinate corresponds to the Xth edition of Romanian Pharmacopoeia standards. So, the raw materials consumption is decreased, the costs are cut down, the obtained product purity is high and the output of the process is greater.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Erythromycin Ethylsuccinate / Micrococcus luteus / Anti-Bacterial Agents Type of study: Qualitative_research Limits: Humans Language: Ro Journal: Rev Med Chir Soc Med Nat Iasi Year: 2008 Type: Article
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Collection: 01-internacional Database: MEDLINE Main subject: Erythromycin Ethylsuccinate / Micrococcus luteus / Anti-Bacterial Agents Type of study: Qualitative_research Limits: Humans Language: Ro Journal: Rev Med Chir Soc Med Nat Iasi Year: 2008 Type: Article