Literature DB >> 7425624

Microbial transformations of natural antitumor agents: use of solubilizing agents to improve yields of hydroxylated ellipticines.

M M Chien, J P Rosazza.   

Abstract

Aromatic hydroxylation of the antitumor alkaloid ellipticine by Aspergillus alliaceus results in the formation of both 8- and 9-hydroxyellipticines. Experiments designed to increase yields of microbial hydroxylation focused on enhancing the water solubility of ellipticine in aqueous fermentation media by use of wetting agents or solubilizing polymers, or both. Yields of hydroxylated metabolites were determined by high-performance liquid chromatography with the use of a mu-Bondapak-phenyl column and a mobile phase of acetonitrile--0.1% (NH4)2CO3 (1:1). Polyvinylpyrrolidone (molecular weight, 40,000) and polyoxyethylated vegetable oil (Emulphor 620) increased the water solubility of ellipticine and the yield of hydroxylated metabolites.

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Year:  1980        PMID: 7425624      PMCID: PMC291654          DOI: 10.1128/aem.40.4.741-745.1980

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  11 in total

1.  Possible complex formation between macromolecules and certain pharmaceuticals. X. The interaction of some phenolic compounds with polyethylene glycols, polypropylene glycols, and polyvinylpyrrolidone.

Authors:  D GUTTMAN; T HIGUCHI
Journal:  J Am Pharm Assoc Am Pharm Assoc       Date:  1956-10

2.  Study of possible complex formation between macromolecules and certain pharmaceuticals. I. Polyvinylpyrrolidone with sulfathiazole, procaine hydrochloride, sodium salicylate, benzyl penicillin, chloramphenicol, mandelic acid, caffeine, theophylline, and cortisone.

Authors:  T HIGUCHI; R KURAMOTO
Journal:  J Am Pharm Assoc Am Pharm Assoc       Date:  1954-07

3.  Study of possible complex formation between macromolecules and certain pharmaceuticals. II. Polyvinylpyrrolidone with p-aminobenzoic acid, aminopyrine, benzoic acid, salicylic acid, p-hydroxybenzoic acid, m-hydroxybenzoic acid, citric acid, and phenobarbital.

Authors:  T HIGUCHI; R KURAMOTO
Journal:  J Am Pharm Assoc Am Pharm Assoc       Date:  1954-07

4.  Physical state of phenanthrene for utilization by bacteria.

Authors:  R S Wodzinski; J E Coyle
Journal:  Appl Microbiol       Date:  1974-06

5.  Dissolution rates of high energy sulfathiazole--povidone coprecipitates II: characterization of form of drug controlling its dissolution rate via solubility studies.

Authors:  A P Simonelli; S C Mehta; W I Higuchi
Journal:  J Pharm Sci       Date:  1976-03       Impact factor: 3.534

6.  Antitumor activity of an acronycine-polyvinylpyrrolidone coprecipitate.

Authors:  G H Svoboda; M J Sweeney; W D Walkling
Journal:  J Pharm Sci       Date:  1971-02       Impact factor: 3.534

7.  Microbial transformations of natural antitumor agents. VIII. Formation of 8- and 9-hydroxyellipticines.

Authors:  M M Chien; J P Rosazza
Journal:  Drug Metab Dispos       Date:  1979 Jul-Aug       Impact factor: 3.922

8.  New method of solid-state dispersion for increasing dissolution rates.

Authors:  M Mayersohn; M Gibaldi
Journal:  J Pharm Sci       Date:  1966-11       Impact factor: 3.534

9.  Dissolution and absorption of the antineoplastic agent ellipticine.

Authors:  A Rahman; J C Cradock; J P Davignon
Journal:  J Pharm Sci       Date:  1978-05       Impact factor: 3.534

10.  Dissolution rates of high energy polyvinylpyrrolidone (PVP)-sulfathiazole coprecipitates.

Authors:  A P Simonelli; S C Mehta; W I Higuchi
Journal:  J Pharm Sci       Date:  1969-05       Impact factor: 3.534

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