Solid lipid microparticles as a sustained release system for pulmonary drug delivery

Séverine Jaspart, Pascal Bertholet, Géraldine Piel, Jean-Michel Dogné, Luc Delattre, Brigitte Evrard

Research output: Contribution to journalArticlepeer-review


The controlled release of drugs for pulmonary delivery is a research field which has been so far rather unexploited but is currently becoming increasingly attractive. The introduction part of this research article first details the potential advantages of solid lipid microparticles (SLMs) as drug carrier compared to liposomes and polymeric microspheres. The aim of this work is to use SLMs to impart a sustained release profile to a model drug, salbutamol acetonide (SA). SA was synthesized from salbutamol in order to increase the lipophilicity of this molecule and thereby to increase its incorporation efficiency into SLMs. SA-loaded SLMs were then produced by a hot emulsion technique followed by high-shear homogenisation and the manufacturing parameters were optimized using the experimental design methodology in order to reach a suitable particle size for pulmonary administration. Scanning electron micrographs showed that SLMs are spherical, have a smooth surface and that SA crystallizes outside of the particles when the drug loading is higher than 20%. This was confirmed by X-ray diffraction. SA in vitro release study from SLMs showed that the release rate increased with SA loading but remained in every case lower than the dissolution rate of pure SA.
Original languageEnglish
Pages (from-to)47-56
Number of pages10
JournalEuropean journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft für Pharmazeutische Verfahrenstechnik e.V
Issue number1
Publication statusPublished - Jan 2007


  • Administration, Inhalation
  • Albuterol
  • Bronchodilator Agents
  • Calorimetry, Differential Scanning
  • Chemistry, Pharmaceutical
  • Crystallography, X-Ray
  • Delayed-Action Preparations
  • Drug Carriers
  • Drug Compounding
  • Humans
  • Kinetics
  • Lipids
  • Microscopy, Electron, Scanning
  • Particle Size
  • Respiratory System
  • Solubility
  • Technology, Pharmaceutical


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