Abstract

Direct lung administration of budesonide in combination with surfactant reduces the incidence of bronchopulmonary dysplasia. Although the therapy is currently undergoing clinical development, the lung distribution of budesonide throughout the premature neonatal lung has not yet been investigated. Here, we applied mass spectrometry imaging (MSI) to investigate the surfactant-assisted distal lung distribution of budesonide. Unlabeled budesonide was either delivered using saline as a vehicle (n = 5) or in combination with a standard dose of the porcine surfactant Poractant alfa (n = 5). These lambs were ventilated for one minute, and then the lungs were extracted for MSI analysis. Another group of lambs (n = 5) received the combination of budesonide and Poractant alfa, followed by two hours of mechanical ventilation. MSI enabled the label-free detection and visualization of both budesonide and the essential constituent of Poractant alfa, the porcine surfactant protein C (SP-C). 2D ion intensity images revealed a non-uniform distribution of budesonide with saline, which appeared clustered in clumps. In contrast, the combination therapy showed a more homogeneous distribution of budesonide throughout the sample, with more budesonide distributed towards the lung periphery. We found similar distribution patterns for the SP-C and budesonide in consecutive lung tissue sections, indicating that budesonide was transported across the lungs associated with the exogenous surfactant. After two hours of mechanical ventilation, the budesonide intensity signal in the 2D ion intensity maps dropped dramatically, suggesting a rapid lung clearance and highlighting the relevance of achieving a uniform surfactant-assisted lung distribution of budesonide early after delivery to maximize the anti-inflammatory and maturational effects throughout the lung.

Highlights

  • Bronchopulmonary dysplasia (BPD) is a chronic lung disease affecting premature neonates born at low gestational ages (GA)

  • The NEUROSIS trial demonstrated that early inhaled budesonide delivered with a pressurized metered-dose inhaler reduced the incidence of BPD in babies with a GA ranging between 23 and 27 weeks [5]

  • There were no differences in the male-to-female ratio or in the GA of the animals, a marginally significant difference was found in the birthweight comparisons (p = 0.027, one-way ANOVA) with animals in the SF+BUD 10 having a lower mean birth weight

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Summary

Introduction

Bronchopulmonary dysplasia (BPD) is a chronic lung disease affecting premature neonates born at low gestational ages (GA). Direct lung administration of budesonide has been proven to be an effective therapy for treating premature neonates at high risk of developing BPD [5,6,7]. The method consists of a combination therapy of budesonide (0.25 mg/kg) mixed with 100 mg/kg of surfactant (Beractant, Survanta® , Abbott Laboratories, Abbott Park, IL, USA) delivered as an intratracheal bolus [6,12]. This delivery strategy guarantees a high initial lung bioavailability of budesonide and takes advantage of the good spreading properties of surfactant to boost budesonide’s lung distribution

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