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Review ArticleReview

Excipients and Their Role in Approved Injectable Products: Current Usage and Future Directions

Sandeep Nema and Ronald J. Brendel
PDA Journal of Pharmaceutical Science and Technology May 2011, 65 (3) 287-332; DOI: https://doi.org/10.5731/pdajpst.2011.00634
Sandeep Nema
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  • For correspondence: Sandeep.nema@pfizer.com
Ronald J. Brendel
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Abstract

This review article is a current survey of excipients used in approved injectable products. Information provided includes concentration ranges, function, frequency of use, and role in dosage form. This article is an update of a paper published more than a decade ago (reference 11). Since then many new products have been approved. Safety concerning excipients has evolved as the scientific community continues to learn about their usage. New excipients are being used in early phases of clinical trials to support novel therapeutic entities like RNAi, aptamers, anti-sense, fusion proteins, monoclonal antibodies, and variant scaffolds. Because these excipients are not inert, various pharmacopoeias are responding with monographs or informational chapters addressing excipient functionality. The final sections of this article discuss new excipients, serving specific needs that traditional excipients are unable to provide and for which safety studies are necessary to support a novel excipient for marketing applications.

LAY ABSTRACT: Excipients are added to parenteral dosage forms to serve a variety of functions including stabilization and as vehicles. This review article is a survey of excipients used in approved injectable products. Information provided includes excipient concentrations, functional roles, and frequency of use. This article is an update of an article originally published over a decade ago. Since then new products have been approved and safety concerns have evolved as the scientific community has learned about the usage of excipients. In addition, new excipients are being used in early phases of clinical trials to support novel therapeutic entities such as RNAi, aptamers, anti-sense, fusion proteins, monoclonal antibodies, and variant scaffolds. Because these excipients are not inert, various pharmacopoeias are responding with monographs or informational chapters addressing excipient functionality. The final sections of this article discuss new excipients, serving specific needs that traditional excipients are unable to provide and for which safety studies are necessary to support a novel excipient for marketing applications.

  • Antioxidant
  • Buffer
  • Chelating agent
  • Excipients
  • Inactive ingredients
  • Injectable
  • Parenteral
  • Surfactant
  • © PDA, Inc. 2011
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PDA Journal of Pharmaceutical Science and Technology: 65 (3)
PDA Journal of Pharmaceutical Science and Technology
Vol. 65, Issue 3
May/June 2011
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Excipients and Their Role in Approved Injectable Products: Current Usage and Future Directions
Sandeep Nema, Ronald J. Brendel
PDA Journal of Pharmaceutical Science and Technology May 2011, 65 (3) 287-332; DOI: 10.5731/pdajpst.2011.00634

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Excipients and Their Role in Approved Injectable Products: Current Usage and Future Directions
Sandeep Nema, Ronald J. Brendel
PDA Journal of Pharmaceutical Science and Technology May 2011, 65 (3) 287-332; DOI: 10.5731/pdajpst.2011.00634
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  • Article
    • Abstract
    • I. Introduction
    • II. Types of Excipients
    • III. Regulatory Perspective
    • IV. Criteria for the Selection of Excipient and Supplier
    • V. Safety Issues
    • VI. Future Directions
    • Acknowledgements
    • References
  • Figures & Data
  • References
  • Info & Metrics
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  • A Risk Assessment and Risk-Based Approach Review of Pre-Use/Post-Sterilization Integrity Testing (PUPSIT)
  • A Review of Artificial Intelligence and Machine Learning in Product Life Cycle Management
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