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Solid-state stability of spray-dried insulin powder for inhalation: Chemical kinetics and structural relaxation modeling of Exubera above and below the glass transition temperature. Journal of pharmaceutical sciences [J Pharm Sci] Journal article

 
TitleSolid-state stability of spray-dried insulin powder for inhalation: Chemical kinetics and structural relaxation modeling of Exubera above and below the glass transition temperature.
Author(s)Sadrzadeh N, Miller DP, Lechuga-Ballesteros D, Harper NJ, Stevenson CL, Bennett DB 
InstitutionNektar Therapeutics, 150 Industrial Road, San Carlos, California 94070.
SourceJ Pharm Sci 2009 Oct 20.
AbstractThe effect of temperature on the chemical stability of an amorphous spray-dried insulin powder formulation (Exubera)(R) was evaluated in the solid state at constant moisture content. The chemical stability of the powder was assessed using reversed-phase high-performance liquid chromatography (RP-HPLC) and high-performance-size exclusion chromatography (HP-SEC). The major degradants in spray-dried insulin produced during heat stressing were identified as A21-desamidoinsulin (A21) and high molecular weight protein (HMWP). As expected, the rates of formation of A21 and HMWP were observed to increase with temperature. A stretched-time kinetic model (degradation rate is proportional to the square root of time) was applied to the degradant profiles above and below the glass transition temperature (T(g)) and apparent reaction rate constants were determined. Below T(g), isothermal enthalpy of relaxation measurements were used to assess the effect of temperature on molecular mobility. The formation of A21 and HMWP was found to follow an Arrhenius temperature dependence above and below the T(g). Comparison of reaction rate constants to those estimated from structural relaxation experiments suggests that the reaction pathways to form A21 and HMWP below the T(g) may be coupled with the molecular motions involved in structural relaxation. (c) 2009 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci.
LanguageENG
Pub Type(s)JOURNAL ARTICLE
PubMed ID19844959
  
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