Design of fine particles for pulmonary drug delivery

作者：Weers Jeffry G^*; Tarara Thomas E; Clark Andrew R

来源：Expert Opinion on Drug Delivery, 2007, 4(3): 297-313.

DOI：10.1517/17425247.4.3.297

• absorption enhancer
• aerosol
• amorphous glass
• anti-infective
• dry powder inhaler
• immunoglobulin
• inhalation
• particle engineering
• peptide
• porous particle
• powder formulation
• protein
• pulmonary drug delivery
• spray drying
• spray freeze drying
• supercritical fluid
• systemic drug administration
• vaccine

Particle design for inhalation is characterized by advances in particle processing methods and the utilization of new excipients. Processing methods such as spray drying allow control over critical particle design features, such as particle size and distribution, surface energy, surface rugosity, particle density, surface area, porosity and microviscosity. Control of these features has enabled new classes of therapeutics to be delivered by inhalation. These include therapeutics that have a narrow therapeutic index, require a high delivered dose, and/or elicit their action systemically. Engineered particles are also being utilized for immune modulation, with exciting advances being made in the delivery of antibodies and inhaled vaccines. Continued advances are expected to result in 'smart' therapeutics capable of active targeting and intracellular trafficking.

• 出版日期2007-5