ArticleAAPS PharmSciTech2026
Development of a New Aerosol Delivery System for Administering Aerosol Surfactant Therapy to Preterm Infants Through a Laryngeal Mask Airway.
Article in AAPS PharmSciTech, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Transnasal Administration of Surfactant Aerosol to the Lungs of Infants Using Direct Interfaces - Lessons Learned from Computational Fluid Dynamics.Pharmaceutical research · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In this study, aerosol surfactant therapy administered through a laryngeal mask airway (LMA) was investigated as an alternative to the more invasive approach of surfactant liquid bolus instillation, which carries significant risks to infants with respiratory distress syndrome. Combining a recently developed synthetic lung surfactant excipient enhanced growth (SLS-EEG) dry powder formulation with a novel LMA aerosol delivery system (LMA-ADS) was intended to avoid the side effects associated with current liquid bolus therapies. A new patient connection system (PCS) was developed for introducing the aerosol from an infant air-jet DPI into the LMA. Using in vitro benchtop studies with a 1.5 kg preterm infant extrathoracic model, the effectiveness of a co-flow (CF) strategy was investigated for improving lung delivery efficiencies of the aerosol. Next, different tubing sizes and aerosolization parameters were explored using laser diffraction to quantify their effects on aerosol size distribution metrics, and insights gained were implemented to develop four PCS designs. The best-performing PCS was tested with a realistic pulmonary mechanics (PM) model. Large-diameter tubing (> 1 mm diameter) was shown to produce large aerosol size increases that could be minimized with smaller-diameter tubing. Following integration of 0.8 mm inner diameter tubing, all PCS designs were capable of at least ~ 24% lung delivery efficiency (based on loaded dose) with the best-performing PCS reaching ~ 29%, which represented a > 1.7-fold improvement from baseline. PM simulations confirmed safe delivery pressures with only minor reductions in aerosol transmission. Therefore, the LMA-ADS could be a promising alternative for effective aerosol surfactant therapies.
Indexed as
Identifiers
42026389What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.