6, 7-Coumarin-heterocyclic hybrids: a comprehensive review of their natural sources, synthetic approaches, and bioactivity

NM Zeki, YF Mustafa - Journal of Molecular Structure, 2024 - Elsevier
The hybridization of heterocycles presents a key opportunity to craft innovative multicyclic
compounds with enhanced biological activity. Coumarins, being broadly prevalent natural …

Diagnosis and management of fibrotic interstitial lung diseases

BF Collins, F Luppi - Clinics in Chest Medicine, 2021 - chestmed.theclinics.com
Although idiopathic pulmonary fibrosis (IPF) is the most well studied among the fibrotic
interstitial lung diseases (ILDs), non-IPF fibrotic lung diseases may also have a progressive …

Evaluation of nitric oxide fluctuation via a fast, responsive fluorescent probe in idiopathic pulmonary fibrosis cells and mice models

F Xu, Q Wang, L Jiang, F Zhu, L Yang, S Zhang… - Analytical …, 2022 - ACS Publications
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, and fatal interstitial pneumonia
with unknown pathogenesis. Early diagnosis and therapeutic intervention are essential for …

A mitochondrial-targeted near-infrared fluorescent probe for visualizing the fluctuation of hypochlorite acid in idiopathic pulmonary fibrosis mice

S Li, P Wang, Y Liu, K Yang, R Zhong, D Cheng… - Analytica Chimica …, 2023 - Elsevier
Idiopathic pulmonary fibrosis (IPF) is a chronic inflammatory disease destroying lungs
irreversibly with high mortality rates. There are challenges in diagnosing IPF and treating it …

A near-infrared fluorescent probe for evaluating glutamyl transpeptidase fluctuation in idiopathic pulmonary fibrosis cell and mice models

N He, Y Wang, Y Huang, X Wang, L Chen… - Sensors and Actuators B …, 2020 - Elsevier
Idiopathic pulmonary fibrosis (IPF), whose early diagnosis and effective treatment still
remain the focus of clinical studies, is a chronic, irreversible and finally fatal pulmonary …

[PDF][PDF] Idiopathic pulmonary fibrosis: where do we stand and how far to go

V Singh, I Ulasov, S Gupta, A Singh, VK Roy… - Discov …, 2024 - researchgate.net
Idiopathic pulmonary fibrosis is a progressive and incurable lung disease characterized by
collagen deposition, alveolar inflammation, fibroblast proliferation, and the destruction of …

Clinical characteristics of individuals with interstitial lung diseases and indication of end-of-life care

G Krinski, LD Bertin, HA Pimpão, H Silva… - Journal of Clinical …, 2023 - mdpi.com
End-of-life care (EOLC) is palliative support provided in the last 6 months to 1 year of a
patient's life. Although there are established criteria for its indication, few studies describe …

Palliative care for interstitial lung disease: A nationwide survey of pulmonary specialists

T Fujisawa, N Akiyama, T Morita, T Koyauchi… - …, 2023 - Wiley Online Library
Abstract Background and Objective Interstitial lung disease (ILD) is progressive with high
symptom burdens and poor prognosis. Patients with ILD need optimal palliative care to …

Management of patients with fibrosing interstitial lung diseases

LE Morrow, D Hilleman… - American Journal of …, 2022 - academic.oup.com
Purpose This article summarizes the appropriate use and pharmacology of treatments for
fibrosing interstitial lung diseases, with a specific focus on the antifibrotic agents nintedanib …

End-of-life care for idiopathic pulmonary fibrosis patients with acute exacerbation

N Akiyama, T Fujisawa, T Morita, T Koyauchi… - Respiratory …, 2022 - Springer
Background Acute exacerbation (AE) is a major cause of death in patients with idiopathic
pulmonary fibrosis (IPF). AE-IPF patients require optimal palliative care; however, the real …