In vitro characterization and in vivo comparison of the pulmonary outcomes of Poractant alfa and Calsurf in ventilated preterm rabbits.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 06 06 2019
accepted: 12 02 2020
entrez: 14 3 2020
pubmed: 14 3 2020
medline: 23 6 2020
Statut: epublish

Résumé

Poractant alfa and Calsurf are two natural surfactants widely used in China for the treatment of neonatal respiratory distress syndrome, which are extracted from porcine and calf lungs, respectively. The purpose of this experimental study was to compare their in vitro characteristics and in vivo effects in the improvement of pulmonary function and protection of lung injury. The biophysical properties, ultrastructure, and lipid composition of both surfactant preparations were respectively analysed in vitro by means of Langmuir-Blodgett trough (LBT), atomic force microscopy (AFM), and liquid-chromatography mass-spectrometry (LC-MS). Then, as core pharmacological activity, both head-to-head (100 and 200 mg/kg for both surfactants) and licensed dose comparisons (70 mg/kg Calsurf vs. 200 mg/kg Poractant alfa) between the two surfactants were conducted as prophylaxis in preterm rabbits with primary surfactant deficiency, assessing survival time and rate and dynamic compliance of the respiratory system (Cdyn). Intrapulmonary surfactant pools, morphometric volume density as alveolar expansion (Vv), and lung injury scores were determined post mortem. AFM and LC-MS analysis revealed qualitative differences in the ultrastructure as well as in the lipid composition of both preparations. Calsurf showed a longer plateau region of the LBT isotherm and lower film compressibility. In vivo, both surfactant preparations improved Cdyn at any dose, although maximum benefits in terms of Vv and intrapulmonary surfactant pools were seen with the 200 mg/kg dose in both surfactants. The group of animals treated with 200 mg/kg of Poractant alfa showed a prolonged survival time and rate compared to untreated but ventilated controls, and significantly ameliorated lung injury compared to Calsurf at any dose, including 200 mg/kg. The overall outcomes suggest the pulmonary effects to be dose dependent for both preparations. The group of animals treated with 200 mg/kg of Poractant alfa showed a significant reduction of mortality. Compared to Calsurf, Poractant alfa exerted better effects if licensed doses were compared, which requires further investigation.

Identifiants

pubmed: 32168331
doi: 10.1371/journal.pone.0230229
pii: PONE-D-19-15621
pmc: PMC7069639
doi:

Substances chimiques

Biological Products 0
Phospholipids 0
Pulmonary Surfactants 0
poractant alfa KE3U2023NP

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0230229

Déclaration de conflit d'intérêts

The study was supported by Chiesi Farmaceutici S.p.A, which owns the marketing rights for Poractant alfa. The company contributed to the study design but had neither influence on the performance, analysis, and interpretation of experimental data nor in writing the manuscript. BP, SC, and FS are employees of Chiesi Farmaceutici S.p.A. XM served as consultant for Chiesi in this study. YD is a recipient of research grants from the National Natural Science Foundation (No. 81501288) and Shanghai Municipal Commission of Health (Project Young Physician Investigator). This does not alter our adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

Xiaojing Guo (X)

Departments of Pediatrics and Neonatology, Children's Hospital of Fudan University, Shanghai, China.

Siwei Luo (S)

Departments of Pediatrics and Neonatology, Children's Hospital of Fudan University, Shanghai, China.

Davide Amidani (D)

Department of Research and Development, Chiesi Farmaceutici, Parma, Italy.

Claudio Rivetti (C)

Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.

Giuseppe Pieraccini (G)

CISM Mass Spectrometry Centre, Department of Health Sciences, University of Florence, Firenze, Italy.

Barbara Pioselli (B)

Department of Research and Development, Chiesi Farmaceutici, Parma, Italy.

Silvia Catinella (S)

Department of Research and Development, Chiesi Farmaceutici, Parma, Italy.

Xabi Murgia (X)

Department of Drug Delivery, Helmholtz Institute for Pharmaceutical Research, Saarbrücken, Saarland, Germany.

Fabrizio Salomone (F)

Department of Research and Development, Chiesi Farmaceutici, Parma, Italy.

Yaling Xu (Y)

Departments of Pediatrics and Neonatology, Children's Hospital of Fudan University, Shanghai, China.

Ying Dong (Y)

Departments of Pediatrics and Neonatology, Children's Hospital of Fudan University, Shanghai, China.

Bo Sun (B)

Departments of Pediatrics and Neonatology, Children's Hospital of Fudan University, Shanghai, China.

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