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Research ArticleResearch

Delamination Propensity of Pharmaceutical Glass Containers by Accelerated Testing with Different Extraction Media

Emanuel Guadagnino and Daniele Zuccato
PDA Journal of Pharmaceutical Science and Technology March 2012, 66 (2) 116-125; DOI: https://doi.org/10.5731/pdajpst.2012.00853
Emanuel Guadagnino
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  • For correspondence: eguadag@libero.it
Daniele Zuccato
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  • Article
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References

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PDA Journal of Pharmaceutical Science and Technology: 66 (2)
PDA Journal of Pharmaceutical Science and Technology
Vol. 66, Issue 2
March/April 2012
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Delamination Propensity of Pharmaceutical Glass Containers by Accelerated Testing with Different Extraction Media
Emanuel Guadagnino, Daniele Zuccato
PDA Journal of Pharmaceutical Science and Technology Mar 2012, 66 (2) 116-125; DOI: 10.5731/pdajpst.2012.00853

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Delamination Propensity of Pharmaceutical Glass Containers by Accelerated Testing with Different Extraction Media
Emanuel Guadagnino, Daniele Zuccato
PDA Journal of Pharmaceutical Science and Technology Mar 2012, 66 (2) 116-125; DOI: 10.5731/pdajpst.2012.00853
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  • Characterization of a Novel Particle in a Pharmaceutical Drug Product
  • Investigating the Effects of the Chemical Composition on Glass Corrosion: A Case Study for Type I Vials
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  • Introducing the Alba(R) Primary Packaging Platform. Part 2: Inorganic Extractables Evaluation
  • Complexing Agents and pH Influence on Chemical Durability of Type I Molded Glass Containers
  • Historical Review of Glasses Used for Parenteral Packaging
  • Development of Conductivity Method as an Alternative to Titration for Hydrolytic Resistance Testing Used for Evaluation of Glass Vials Used in Pharmaceutical Industry
  • Comparative Delamination Study to Demonstrate the Impact of Container Quality and Nature of Buffer System
  • A Biopharmaceutical Industry Perspective on the Control of Visible Particles in Biotechnology-Derived Injectable Drug Products
  • Comparison of Acid Titration, Conductivity, Flame Photometry, ICP-MS, and Accelerated Lamellae Formation Techniques in Determining Glass Vial Quality
  • Particulate Study on NeoProfen, a Neonatal Injectable Product
  • Filtration of Glass Delamination Particles with West Pharmaceutical Vial Adapters
  • Materials in Manufacturing and Packaging Systems as Sources of Elemental Impurities in Packaged Drug Products: A Literature Review
  • Implementation of a High-Throughput Ion Chromatographic Assay To Assess Glass Degradation in Drug Product Formulations
  • A Quick Test To Monitor the Delamination Propensity of Glass Containers
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