Literature DB >> 17722087

Antimicrobial preservative use in parenteral products: past and present.

Brian K Meyer1, Alex Ni, Binghua Hu, Li Shi.   

Abstract

The following review provides a comprehensive summary of antimicrobial preservatives that are commonly used in licensed parenteral products to date. The information reviewed includes the general properties of the preservatives, the doses and frequency of their use, the classes of the preserved products (peptide, protein, vaccine, and small molecule products), the interactions with other formulation components, and the criteria commonly used for their selection in parental product formulations. It was revealed that phenol and benzyl alcohol are the two most common antimicrobial preservatives used in peptide and protein products, while phenoxyethanol is the most frequently used preservative in vaccines. Benzyl alcohol or a combination of methylparaben and propylparaben are generally found in small molecule parenteral formulations. The key criteria for antimicrobial preservative selection are the preservative's dose, antimicrobial functionality, and effect on the active ingredient. Additionally, the use of spectroscopic techniques (circular dicroism (CD) and fluorescence) and differential scanning calorimetry (DSC) were identified as common techniques used in evaluating an antimicrobial preservative for its impact on the conformational stability of peptide, protein, and vaccine antigens. The future use of preservatives is also discussed, including antimicrobial agents such as peptides, and regulatory requirements for antimicrobial effectiveness testing. (c) 2007 Wiley-Liss, Inc.

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Year:  2007        PMID: 17722087     DOI: 10.1002/jps.20976

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  26 in total

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2.  Crystal structures of β-primeverosidase in complex with disaccharide amidine inhibitors.

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3.  Interactions Between Peptide and Preservatives: Effects on Peptide Self-Interactions and Antimicrobial Efficiency In Aqueous Multi-Dose Formulations.

Authors:  P Heljo; A Ross; I E Zarraga; A Pappenberger; H-C Mahler
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4.  Role of partial protein unfolding in alcohol-induced protein aggregation.

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5.  New FDA draft guidance on immunogenicity.

Authors:  Ashwin Parenky; Heather Myler; Lakshmi Amaravadi; Karoline Bechtold-Peters; Amy Rosenberg; Susan Kirshner; Valerie Quarmby
Journal:  AAPS J       Date:  2014-03-29       Impact factor: 4.009

6.  Ligand binding assay critical reagents and their stability: recommendations and best practices from the Global Bioanalysis Consortium Harmonization Team.

Authors:  Lindsay E King; Esme Farley; Mami Imazato; Jeannine Keefe; Masood Khan; Mark Ma; K Susanne Pihl; Priya Sriraman
Journal:  AAPS J       Date:  2014-04-01       Impact factor: 4.009

Review 7.  Factors affecting the physical stability (aggregation) of peptide therapeutics.

Authors:  Karolina L Zapadka; Frederik J Becher; A L Gomes Dos Santos; Sophie E Jackson
Journal:  Interface Focus       Date:  2017-10-20       Impact factor: 3.906

8.  Effect of antimicrobial preservatives on partial protein unfolding and aggregation.

Authors:  Regina L Hutchings; Surinder M Singh; Javier Cabello-Villegas; Krishna M G Mallela
Journal:  J Pharm Sci       Date:  2012-11-20       Impact factor: 3.534

9.  Mechanisms of m-cresol-induced protein aggregation studied using a model protein cytochrome c.

Authors:  Surinder M Singh; Regina L Hutchings; Krishna M G Mallela
Journal:  J Pharm Sci       Date:  2011-01-12       Impact factor: 3.534

10.  Parabens abatement from surface waters by electrochemical advanced oxidation with boron doped diamond anodes.

Authors:  Joaquín R Domínguez; Maria J Muñoz-Peña; Teresa González; Patricia Palo; Eduardo M Cuerda-Correa
Journal:  Environ Sci Pollut Res Int       Date:  2016-07-23       Impact factor: 4.223

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