Characterization of a cyclosporine solid dispersion for inhalation

被引:0
作者
Gerrit S. Zijlstra
Michiel Rijkeboer
Dirk Jan van Drooge
Marc Sutter
Wim Jiskoot
Marco van de Weert
Wouter L. J. Hinrichs
Henderik W. Frijlink
机构
[1] University of Groningen,Department of Pharmaceutical Technology and Biopharmacy
[2] The Netherlands,Department of Pharmaceutics
[3] Utrecht Institute for Pharmaceutical Sciences (UIPS),Division of Drug Delivery Technology
[4] Leiden/Amsterdam Center for Drug Research (LACDR),Department of Pharmaceutics and Analytical Chemistry, Faculty of Pharmaceutical Sciences
[5] University of Copenhagen,undefined
来源
The AAPS Journal | / 9卷
关键词
DPI; Cyclosporine A; solid dispersion; FTIR; aerosol; large porous particles;
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摘要
For lung transplant patients, a respirable, inulin-based solid dispersion containing cyclosporine A (CsA) has been developed. The solid dispersions were prepared by spray freezedrying. The solid dispersion was characterized by water vapor uptake, specific surface area analysis, and particle size analysis. Furthermore, the mode of inclusion of CsA in the dispersion was investigated with Fourier transform infrared spectroscopy. Finally, the dissolution behavior was determined and the aerosol that was formed by the powder was characterized. The powder had large specific surface areas (∼160 m2). The water vapor uptake was dependent linearly on the drug load. The type of solid dispersion was a combination of a solid solution and solid suspension. At a 10% drug load, 55% of the CsA in the powder was in the form of a solid solution and 45% as solid suspension. At 50% drug load, the powder contained 90% of CsA as solid suspension. The powder showed excellent dispersion characteristics as shown by the high emitted fraction (95%), respirable fraction (75%), and fine-particle fraction (50%). The solid dispersions consisted of relatively large (x50≈7 μm), but low-density particles (ρ≈0.2 g/cm3). The solid dispersions dissolved faster than the physical mixture, and inulin dissolved faster than CsA. The spray freeze-drying with inulin increased the specific surface area and wettability of CsA. In conclusion, the developed powder seems suitable for inhalation in the local treatment of lung transplant patients.
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  • [1] Corcoran TE(2004)Preservation of posttransplant lung function with aerosol cyclosporin Eur Respir J 23 378-383
  • [2] Smaldone GC(1997)Dose-related reserval of acute lung rejection by aerosolized cyclosporine Am J Respir Crit Care Med 155 1690-1698
  • [3] Dauber JH(2006)A randomized trial of inhaled cyclosporine in lung-transplant recipients N Engl J Med 354 141-150
  • [4] Iacono AT(2003)Lung deposition and pharmacokinetics of cyclosporine after aerosolization in lung transplant patients Pharm Res. 20 252-256
  • [5] Smaldone GC(1999)Can tobramycin inhalation be improved with a jet nebulizer? Ther Drug Monit 21 618-624
  • [6] Keenan RJ(1997)The science of nebulised drug delivery Thorax 52 S31-S44
  • [7] Iacono AT(1997)Pharmacokinetics of aerosolized tobramycin in adult patients with cystic fibrosis Antimicrob Agents Chemother 41 184-187
  • [8] Johnson BA(1996)Exothermic-endothermic heat of solution shift of cyclosporin A related to poloxamer 188 behavior in aqueous solutions Int J Pharm 130 75-81
  • [9] Grgurich WF(2004)Incorporation of lipophilic drugs in sugar glasses by lyophilization using a mixture of water and tertiary butyl alcohol as solvent J Pharm Sci 93 713-725
  • [10] Burckart GJ(2002)Dry pow der inhalation of antibiotics in cystic fibrosis therapy: part 2. Inhalation of a novel colistin dry powder formulation: a feasibility study in healthy volunteers and patients Eur J Pharm Biopharm. 54 25-32