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Solubilizing Systems for Parenteral Formulation Development—Small Molecules

  • JAMES E. KIPP
Part of the Biotechnology: Pharmaceutical Aspects book series (PHARMASP, volume VI)

Abstract

“Parenteral” is defined1 as “situated or occurring outside the intestine, and especially introduced otherwise than by way of the intestines”—pertaining to essentially any administration route other than enteral. This field is obviously too broad for an adequate focus in one book, let alone one chapter. Many have nonetheless used the term synonymously with injectable drug delivery. We restrict ourselves to this latter usage. This would thus include intravenous, intramuscular, subcutaneous, intrathecal, and subdural injection. In this chapter we discuss the theoretical and practical aspects of solubilizing small molecules for injectable formulation development and will examine the role of surfactants and other excipients in more recent parenteral delivery systems such as liposomes, solid-drug nanoparticles and particulate carriers.

Keywords

Cloud Point Dispersion Force Leuprolide Acetate Methylprednisolone Acetate Solubilizing System 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer 2007

Authors and Affiliations

  • JAMES E. KIPP
    • 1
  1. 1.BioPharma SolutionsBaxter Healthcare CorporationRound LakeUSA

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