Nano-Biomechanical Analysis of a Corticosteroid Drug for Targeted Delivery into the Alveolar Air—Water Interface Using Molecular Dynamics Simulation

The enhancement of drug delivery into the lung surfactant is facilitated by research on the interaction between drugs and the lung surfactant. Drug designers must have a thorough theoretical understanding of a drug before performing clinical tests to reduce the experimental cost. The current study uses a coarse-grained molecular dynamics (MD) approach with the MARTINI force field to parameterize the corticosteroid drug mometasone furoate, which is used to treat lung inflammation. Here, we investigate the accurate parametrization of drug molecules and validate the parameters with the help of umbrella sampling simulations. A collection of thermodynamic parameters was studied during the parametrization procedure. The Gibbs free energy gradient was used to calculate the partition coefficient value of mometasone furoate, which was approximately 10.49 based on our umbrella sampling simulation. The value was then matched with the experimental and predicted the partition coefficient of the drug, showing good agreement. The drug molecule was then delivered into the lung surfactant monolayer membrane at the alveolar air–water interface, resulting a concentration-dependent drop in surface tension while controlling the underlying continual compression–expansion of alveoli that maintains the exhalation–inhalation respiratory cycle. The dynamical properties of the monolayer demonstrate that the drug’s capacity to diffuse into the monolayer is considerably diminished in larger clusters, and this effect is intensified when there are more drug molecules present in the monolayer. The monolayer microstructure analysis shows that the drug concentration controls monolayer morphology. The results of this investigation may be helpful for corticosteroid drug delivery into the lung alveoli, which can be applied to comprehend how the drug interacts with lung surfactant monolayers or bilayers.

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Publication Details

Journal
Micro
Published
2025-09-25
DOI
https://doi.org/10.3390/micro5040044
Primary Topic
Inhalation and Respiratory Drug Delivery
Type
article
Field-Weighted Citation Impact
0.00

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article

Nano-Biomechanical Analysis of a Corticosteroid Drug for Targeted Delivery into the Alveolar Air—Water Interface Using Molecular Dynamics Simulation

Suvash C. Saha, Toufik Tayeb Naas, Shakhawat Hossain, Akram Hossain et al.
Micro
Inhalation and Respiratory Drug Delivery
article

Nano-Biomechanical Analysis of a Corticosteroid Drug for Targeted Delivery into the Alveolar Air—Water Interface Using Molecular Dynamics Simulation

Suvash C. Saha, Toufik Tayeb Naas, Shakhawat Hossain, Akram Hossain, Md. Zohurul Islam, Kwang‐Yong Kim, Khalid Bin Kaysar
article en

Abstract

The enhancement of drug delivery into the lung surfactant is facilitated by research on the interaction between drugs and the lung surfactant. Drug designers must have a thorough theoretical understanding of a drug before performing clinical tests to reduce the experimental cost. The current study uses a coarse-grained molecular dynamics (MD) approach with the MARTINI force field to parameterize the corticosteroid drug mometasone furoate, which is used to treat lung inflammation. Here, we investigate the accurate parametrization of drug molecules and validate the parameters with the help of umbrella sampling simulations. A collection of thermodynamic parameters was studied during the parametrization procedure. The Gibbs free energy gradient was used to calculate the partition coefficient value of mometasone furoate, which was approximately 10.49 based on our umbrella sampling simulation. The value was then matched with the experimental and predicted the partition coefficient of the drug, showing good agreement. The drug molecule was then delivered into the lung surfactant monolayer membrane at the alveolar air–water interface, resulting a concentration-dependent drop in surface tension while controlling the underlying continual compression–expansion of alveoli that maintains the exhalation–inhalation respiratory cycle. The dynamical properties of the monolayer demonstrate that the drug’s capacity to diffuse into the monolayer is considerably diminished in larger clusters, and this effect is intensified when there are more drug molecules present in the monolayer. The monolayer microstructure analysis shows that the drug concentration controls monolayer morphology. The results of this investigation may be helpful for corticosteroid drug delivery into the lung alveoli, which can be applied to comprehend how the drug interacts with lung surfactant monolayers or bilayers.

MicroVol. 5(4)
University of Technology Sydney (AU), Inha University (KR), Ziane Achour University of Djelfa (DZ), Jerash University (JO)
University Grants Commission of Bangladesh, University Grants Commission, University of Technology Sydney, Jashore University of Science and Technology
Openalex Percentile: Top 62%
Inhalation and Respiratory Drug Delivery
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