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Tracheal stent implantation serves as a critical intervention for tracheal stenosis, where biodegradable magnesium (Mg) alloy stents have emerged as promising alternatives due to their ability to eliminate long-term complications associated with permanent stents. However, the uneven stress distribution on the stent often leads to premature failure through localized rapid degradation and structural collapse. This study systematically investigated the biomechanical interactions between biodegradable stents and tracheal tissues to guide optimized stent design. The mechanical properties of tracheal cartilage under physiological curvature conditions were quantitatively characterized using custom-designed tissue fixtures. Finite element analysis was employed to simulate Mg alloy stent interaction with the trachea during both normal breathing and coughing, which revealed that the stent's regions adjacent to the cartilage and membranous wall junction are high-risk regions for fractures. To address these challenges, the non-uniform stent design was proposed to enhance radial support and distribute stresses more evenly, thereby improving the resistance to localized degradation and premature fracture. The findings provide biomechanical insights and technical strategies for the development of biodegradable tracheal stents.
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http://dx.doi.org/10.1016/j.jbiomech.2025.112757 | DOI Listing |
J Pediatr Surg
September 2025
Hospital de Clínicas de Porto Alegre (HCPA), Rua Ramiro Barcelos, 2350, Santa Cecília, 90035-003, Porto Alegre, Rs, Brazil; Universidade Federal do Rio Grande do Sul (UFRGS), Rua Ramiro Barcelos, 2400, Santa Cecília, 90035-003, Porto Alegre, RS, Brazil.
Background: Obstructions of the tracheobronchial tree can result from various etiologies. Most cases of tracheal stenosis or tracheomalacia are associated with patient-specific anatomical and functional abnormalities, making treatment challenging. Despite progress in the development of tracheal support devices, the optimal or near-optimal stent design remains elusive.
View Article and Find Full Text PDFSci Rep
September 2025
Pharmacology Department, Medical Research and Clinical Studies Institute, National Research Centre (ID: 60014618), 33 ELBohouth St. (former EL Tahrir St.), P.O. 12622, Dokki, Cairo, Egypt.
Idiopathic pulmonary fibrosis (IPF) is one of the rapidly progressing interstitial lung illnesses. Bleomycin (Bleo) is used as a chemotherapeutic agent for the treatment of lymphoma patients. The major side effects of Bleo include lung fibrosis, characterized by the accumulation of inflammatory cells.
View Article and Find Full Text PDFExp Lung Res
September 2025
State Key Laboratory of Respiratory Disease, Guangzhou Chest Hospital, Guangzhou, China.
Recent studies have shown that fine particulate matter (PM2.5) exposure is a key harmful risk factor for chronic obstructive pulmonary disease (COPD) and PM2.5-associated ferroptosis plays an important role during the process of airway oxidative stress.
View Article and Find Full Text PDFRespir Res
August 2025
Center of Emergency and Critical Medicine, Jinshan Hospital of Fudan University, 1508 Longhang Rd, Shanghai, 201508, China.
Background: E-cigarette or vaping product use-associated Lung Injury (EVALI) has become a public health concern since 2019, with vitamin E acetate (VEA) identified as a potential causative agent. While previous studies have used whole-body VEA aerosol exposure or intratracheal instillation models, these approaches may introduce confounding exposure routes or do not fully reflect real-world vaping conditions. To better understand VEA-induced EVALI, there remains a need for an animal model that isolates airway exposure and closely mimics human vaping behaviour.
View Article and Find Full Text PDFSci Rep
August 2025
Computational Sciences Laboratory, Department of Mechanical and Manufacturing Engineering, University of Cyprus, Nicosia, Cyprus.
The effective delivery of pharmaceuticals to the respiratory tract is significantly influenced by the three-dimensional covalent network structure of mucus and the motility of cilia within the airway surface liquid (ASL). This study investigates the dissolution and absorption of three distinct drugs-Salbutamol sulfate (SAL), Tiotropium bromide (TIO), and Rifampicin (RIF)-in the ASL, focusing on individual particles of each drug with an initial diameter of 5 µm. A three-dimensional numerical model that characterizes mucus as a nonlinear viscoelastic fluid was employed for this analysis.
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