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Dry powder aerosol containing muco-inert particles for excipient enhanced growth pulmonary drug delivery.
Chai, Guihong; Hassan, Amr; Meng, Tuo; Lou, Lihua; Ma, Jonathan; Simmers, Russell; Zhou, Lei; Rubin, Bruce K; Zhou, Qi Tony; Longest, P Worth; Hindle, Michael; Xu, Qingguo.
Afiliação
  • Chai G; Department of Pharmaceutics, Virginia Commonwealth University, Richmond, VA, USA.
  • Hassan A; Department of Pharmaceutics, Virginia Commonwealth University, Richmond, VA, USA.
  • Meng T; Department of Pharmaceutics, Virginia Commonwealth University, Richmond, VA, USA.
  • Lou L; Department of Pharmaceutics, Virginia Commonwealth University, Richmond, VA, USA.
  • Ma J; Department of Pediatrics, Children's Hospital of Richmond, Virginia Commonwealth University, Richmond, VA, USA.
  • Simmers R; Department of Pharmaceutics, Virginia Commonwealth University, Richmond, VA, USA; Department of Physics, College of Humanities & Sciences, Virginia Commonwealth University, Richmond, VA, USA.
  • Zhou L; Department of Physiology and Biophysics, Virginia Commonwealth University, Richmond, VA, USA.
  • Rubin BK; Department of Pediatrics, Children's Hospital of Richmond, Virginia Commonwealth University, Richmond, VA, USA.
  • Zhou QT; Department of Industrial and Physical Pharmacy, College of Pharmacy, Purdue University, West Lafayette, IN, USA.
  • Longest PW; Department of Pharmaceutics, Virginia Commonwealth University, Richmond, VA, USA; Department of Mechanical and Nuclear Engineering, Virginia Commonwealth University, Richmond, VA, USA.
  • Hindle M; Department of Pharmaceutics, Virginia Commonwealth University, Richmond, VA, USA.
  • Xu Q; Department of Pharmaceutics, Virginia Commonwealth University, Richmond, VA, USA; Department of Ophthalmology, Massey Cancer Center, Center for Pharmaceutical Engineering, and Institute for Structural Biology, Drug Discovery & Development (ISB3D), Virginia Commonwealth University, Richmond, VA,
Nanomedicine ; 29: 102262, 2020 10.
Article em En | MEDLINE | ID: mdl-32623017
ABSTRACT
Tenacious sputum poses a critical diffusion barrier for aerosol antibiotics used to treat cystic fibrosis (CF) lung infection. We conducted a proof-of-concept study using dense poly(ethylene glycol) coated polystyrene nanoparticles (PS-PEG NPs) as model muco-inert particles (MIPs) formulated as a powder using an excipient enhanced growth (EEG) strategy, aiming to minimize extrathoracic airway loss, maximize deposition in the airway and further overcome the sputum barrier in the CF lungs. The EEG aerosol formulation containing PS-PEG MIPs was prepared by spray drying and produced discrete spherical particles with geometric diameter of approximately 2 µm; and >80% of the powder dose was delivered from a new small-animal dry powder inhaler (DPI). The MIPs released from the EEG aerosol had human airway mucus and CF sputum diffusion properties comparable to the suspension formulation. These properties make this formulation a promising pulmonary drug delivery system for CF lung infections.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistemas de Liberação de Medicamentos / Fibrose Cística / Nanopartículas / Pulmão / Pneumopatias Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistemas de Liberação de Medicamentos / Fibrose Cística / Nanopartículas / Pulmão / Pneumopatias Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article