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Excipient Enhanced Growth Aerosol Surfactant Replacement Therapy in an In Vivo Rat Lung Injury Model.
Kamga Gninzeko, Franck J; Valentine, Michael S; Tho, Cindy K; Chindal, Sahil R; Boc, Susan; Dhapare, Sneha; Momin, Mohammad Abdul Motalib; Hassan, Amr; Hindle, Michael; Farkas, Dale R; Longest, P Worth; Heise, Rebecca L.
Affiliation
  • Kamga Gninzeko FJ; Department of Biomedical Engineering, Virginia Commonwealth University, Richmond, Virginia, USA.
  • Valentine MS; Department of Biomedical Engineering, Virginia Commonwealth University, Richmond, Virginia, USA.
  • Tho CK; Department of Biomedical Engineering, Virginia Commonwealth University, Richmond, Virginia, USA.
  • Chindal SR; Department of Biomedical Engineering, Virginia Commonwealth University, Richmond, Virginia, USA.
  • Boc S; Department of Pharmaceutics, and Virginia Commonwealth University, Richmond, Virginia, USA.
  • Dhapare S; Department of Pharmaceutics, and Virginia Commonwealth University, Richmond, Virginia, USA.
  • Momin MAM; Department of Pharmaceutics, and Virginia Commonwealth University, Richmond, Virginia, USA.
  • Hassan A; Department of Pharmaceutics, and Virginia Commonwealth University, Richmond, Virginia, USA.
  • Hindle M; Department of Pharmaceutics, and Virginia Commonwealth University, Richmond, Virginia, USA.
  • Farkas DR; Department of Mechanical and Nuclear Engineering, Virginia Commonwealth University, Richmond, Virginia, USA.
  • Longest PW; Department of Mechanical and Nuclear Engineering, Virginia Commonwealth University, Richmond, Virginia, USA.
  • Heise RL; Department of Biomedical Engineering, Virginia Commonwealth University, Richmond, Virginia, USA.
J Aerosol Med Pulm Drug Deliv ; 33(6): 314-322, 2020 12.
Article in En | MEDLINE | ID: mdl-32453638
ABSTRACT

Background:

In neonatal respiratory distress syndrome, breathing support and surfactant therapy are commonly used to enable the alveoli to expand. Surfactants are typically delivered through liquid instillation. However, liquid instillation does not specifically target the small airways. We have developed an excipient enhanced growth (EEG) powder aerosol formulation using Survanta®.

Methods:

EEG Survanta powder aerosol was delivered using a novel dry powder inhaler via tracheal insufflation to surfactant depleted rats at nominal doses of 3, 5, 10, and 20 mg of powder containing 0.61, 0.97, 1.73, and 3.46 mg of phospholipids (PL), whereas liquid Survanta was delivered via syringe instillation at doses of 2 and 4 mL/kg containing 18.6 and 34 mg of PL. Ventilation mechanics were measured before and after depletion, and after treatment. We hypothesized that EEG Survanta powder aerosol would improve lung mechanics compared with instilled liquid Survanta in surfactant depleted rats. Results and

Conclusion:

EEG Survanta powder aerosol at a dose of 0.61 mg PL significantly improved lung compliance and elastance compared with the liquid Survanta at a dose of 18.6 mg, which represents improved primary efficacy of the aerosol at a 30-fold lower dose of PL. There was no significant difference in white blood cell count of the lavage from the EEG Survanta group compared with liquid Survanta. These results provide an in vivo proof-of-concept for EEG Survanta powder aerosol as a promising method of surfactant replacement therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pulmonary Surfactants / Lung Injury Limits: Animals Language: En Journal: J Aerosol Med Pulm Drug Deliv Journal subject: TERAPIA POR MEDICAMENTOS Year: 2020 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pulmonary Surfactants / Lung Injury Limits: Animals Language: En Journal: J Aerosol Med Pulm Drug Deliv Journal subject: TERAPIA POR MEDICAMENTOS Year: 2020 Document type: Article Affiliation country: United States