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Research Article

Quality by design in formulation and process development for a freeze-dried, small molecule parenteral product: a case study

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Pages 549-576 | Received 29 Nov 2010, Accepted 03 Aug 2011, Published online: 20 Sep 2011

References

  • Snee RD, Cini P, Kamm JJ, Meyers CA. Quality by design: Shortening the path to acceptance. Pharmpro.com 2008; Feb.
  • Snee RD. Quality by design: Four years and three myths later. Pharmaceut Process 2009; Feb:14–16.
  • Stamatis DH. (1995). Failure mode and effect analysis: FMEA from theory to execution,, Milwaukee, WI: ASQC Quality Press.
  • Yarwood RJ, Moore WD, Collett JH. Liquid chromatographic analysis of ethacrynic acid and degradation products in pharmaceutical systems. J Pharm Sci 1985;74:220–223.
  • Merck Index, Thirteenth Edition, Published by Merck Research Laboratories, Whitehouse Station, NJ, 2001, page 663.
  • Gupta VD. Quantitation of ethacrynic acid by high pressure liquid chromatography. Drug Dev Ind Pharm 1982; 8:869–82.
  • Yarwood RJ, Collett JH. Influence of storage on the crystalline structure of freeze-dried sodium ethacrynate. Drug Dev Ind Pharm 1985; 11:461–72.
  • Yarwood RJ, Phillips AJ, Collett JH. Processing factors influencing the stability of freeze dried sodium ethacrynate. Drug Dev Ind Pharm 1986; 12:2157–70.
  • Shamblin SL, Hancock BC, Pikal MJ. Coupling between chemical reactivity and structural relaxation in pharmaceutical glasses. Pharm Res 2006;23:2254–2268.
  • Wang B, Pikal MJ. The impact of thermal treatment on the stability of freeze dried amorphous pharmaceuticals: I. Dimer formation in sodium ethacrynate. J Pharm Sci 2010;99:663–682.
  • Searles JA, Carpenter JF, Randolph TW. Annealing to optimize the primary drying rate, reduce freezing-induced drying rate heterogeneity, and determine T(g)’ in pharmaceutical lyophilization. J Pharm Sci 2001;90:872–887.
  • Johnson JW, Nail SL. Methodology for in-process determination of residual water in freeze-dried products. Dev Biol Std 1992;74:137–51.
  • Patel SM, Doen T, Pikal MJ. Determination of end point of primary drying in freeze-drying process control. AAPS Pharm Sci Tech 2010;11(1):73–84.
  • Gieseler H, Kessler WJ, Finson M, Davis SJ, Mulhall PA, Bons V et al. Evaluation of tunable diode laser absorption spectroscopy for in-process water vapor mass flux measurements during freeze drying. J Pharm Sci 2007;96:1776–1793.
  • Searles JA. Observation and implications of sonic water vapor flow during freeze drying. Am Pharmaceut Rev 2004; 7:58–68.

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