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Nanomedicine for acute respiratory distress syndrome: The latest application, targeting strategy, and rational design

Authors :
Ting Yang
Li Kong
Zhiping Zhang
Conglian Yang
Xiong Liu
Kexin Cui
Qi Qiao
Source :
Acta Pharmaceutica Sinica B, Vol 11, Iss 10, Pp 3060-3091 (2021), Acta Pharmaceutica Sinica. B
Publication Year :
2021
Publisher :
Elsevier BV, 2021.

Abstract

Acute respiratory distress syndrome (ARDS) is characterized by the severe inflammation and destruction of the lung air-blood barrier, leading to irreversible and substantial respiratory function damage. Patients with coronavirus disease 2019 (COVID-19) have been encountered with a high risk of ARDS, underscoring the urgency for exploiting effective therapy. However, proper medications for ARDS are still lacking due to poor pharmacokinetics, non-specific side effects, inability to surmount pulmonary barrier, and inadequate management of heterogeneity. The increased lung permeability in the pathological environment of ARDS may contribute to nanoparticle-mediated passive targeting delivery. Nanomedicine has demonstrated unique advantages in solving the dilemma of ARDS drug therapy, which can address the shortcomings and limitations of traditional anti-inflammatory or antioxidant drug treatment. Through passive, active, or physicochemical targeting, nanocarriers can interact with lung epithelium/endothelium and inflammatory cells to reverse abnormal changes and restore homeostasis of the pulmonary environment, thereby showing good therapeutic activity and reduced toxicity. This article reviews the latest applications of nanomedicine in pre-clinical ARDS therapy, highlights the strategies for targeted treatment of lung inflammation, presents the innovative drug delivery systems, and provides inspiration for strengthening the therapeutic effect of nanomedicine-based treatment.<br />Graphical abstract Nanomedicine has demonstrated great potential in achieving specific targeting and amplifying therapeutic efficiency. This review focuses on the recent breakthroughs and targeting strategies to provide insights into nanomedicine for acute respiratory distress syndrome treatment.Image 1

Subjects

Subjects :
RBD, receptor-binding domains
ARDS
MSC, mesenchymal stem cells
PLGA, poly(lactic-co-glycolic acid)
MPO, myeloperoxidase
NAC, N-acetylcysteine
Review
ICAM-1, intercellular adhesion molecule-1
TNF-α, tumor necrosis factor-α
SDC1, syndecan-1
scFv, single chain variable fragments
PC, phosphatidylcholine
0302 clinical medicine
EphA2, ephrin type-A receptor 2
BALF, bronchoalveolar lavage fluid
PECAM-1, platelet-endothelial cell adhesion molecule
Pathophysiologic feature
PEG, poly(ethylene glycol)
Acute lung injury
cRGD, cyclic arginine glycine-D-aspartic acid
Respiratory function
General Pharmacology, Toxicology and Pharmaceutics
IKK, IκB kinase
PCB, poly(carboxybetaine)
COVID-19, coronavirus disease 2019
HO-1, heme oxygenase-1
DPPC, dipalmitoylphosphatidylcholine
0303 health sciences
EPCs, endothelial progenitor cells
Acute respiratory distress syndrome
TPP, triphenylphosphonium cation
RBC, red blood cells
SP, surfactant protein
EVs, extracellular vesicles
MPMVECs, mouse pulmonary microvascular endothelial cells
DOPE, phosphatidylethanolamine
ECM, extracellular matrix
CD, cyclodextrin
Nanomedicine
medicine.anatomical_structure
H2O2, hydrogen peroxide
030220 oncology & carcinogenesis
Targeting strategy
Drug delivery
iNOS, inducible nitric oxide synthase
LPS, lipopolysaccharide
Esbp, E-selectin-binding peptide
NETs, neutrophil extracellular traps
medicine.medical_specialty
PS-PEG, poly(styrene-b-ethylene glycol)
PDE4, phosphodiesterase 4
NF-κB, nuclear factor-κB
S1PLyase, sphingosine-1-phosphate lyase
RM1-950
ACE2, angiotensin-converting enzyme 2
SARS-CoV-2, severe acute respiratory syndrome coronavirus 2
Siglec, sialic acid-binding immunoglobulin-like lectin
GNP, peptide-gold nanoparticle
Anti-inflammatory therapy
Se, selenium
03 medical and health sciences
PDA, polydopamine
ROS, reactive oxygen species
Pharmacotherapy
medicine
NE, neutrophil elastase
PEI, polyetherimide
SARS, severe acute respiratory syndrome
CLP, cecal ligation and perforation
TLR, toll-like receptor
Intensive care medicine
EPR, enhanced permeability and retention
FcgR, Fcγ receptor
AM, alveolar macrophages
ARDS, acute respiratory distress syndrome
YSA, YSAYPDSVPMMS
030304 developmental biology
Lung
PEVs, platelet-derived extracellular vesicles
business.industry
AEC II, alveolar type II epithelial cells
MERS, Middle East respiratory syndrome
Therapeutic effect
COVID-19
DOTAP, 1-diolefin-3-trimethylaminopropane
medicine.disease
DOX, doxorubicin
IL, interleukin
rSPANb, anti-rat SP-A nanobody
Middle East respiratory syndrome
BSA, bovine serum albumin
SORT, selective organ targeting
Therapeutics. Pharmacology
Nanocarriers
ELVIS, Extravasation through Leaky Vasculature and subsequent Inflammatory cell-mediated Sequestration
business

Details

ISSN :
22113835
Volume :
11
Database :
OpenAIRE
Journal :
Acta Pharmaceutica Sinica B
Accession number :
edsair.doi.dedup.....eb7076f0b91326b1dc05f8b3eaf861f6