About: Pulmonary delivery of nanostructured lipid carriers for effective repurposing of salinomycin as an antiviral agent

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About: Pulmonary delivery of nanostructured lipid carriers for effective repurposing of salinomycin as an antiviral agent Goto Sponge NotDistinct Permalink

An Entity of Type : schema:ScholarlyArticle, within Data Space : wasabi.inria.fr associated with source document(s)

Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	Pulmonary delivery of nanostructured lipid carriers for effective repurposing of salinomycin as an antiviral agent
Creator	B#, Kumar Golla, Kumar Kiran, Sai Phani Kumar, Chirravuri Phani, Chirravuri Pindiproli, Likitha Pindiprolu, S Ramachandra, R Sampath, Venu
Source	Elsevier; Medline; PMC
abstract	Coronavirus disease outbreak caused a severe public health burden all over the world. Salinomycin (SAL) is a broad-spectrum antibiotic that had drawn attention in selective targeting of cancer and viral infections. Recent drug screen identified SAL as a potent antiviral agent against SARS-CoV-2. In this review we discuss the potential of pulmonary delivery of SAL using nanostructured lipid carriers (NLCs) against SARS-CoV-2.
has issue date	2020-05-30(xsd:dateTime)
bibo:doi	10.1016/j.mehy.2020.109858
bibo:pmid	32516655
has license	no-cc
sha1sum (hex)	df11423d4426b254dc353c855eb8a83a8a76d6f6
schema:url	https://doi.org/10.1016/j.mehy.2020.109858
resource representing a document's title	Pulmonary delivery of nanostructured lipid carriers for effective repurposing of salinomycin as an antiviral agent
has PubMed Central identifier	PMC7260485
has PubMed identifier	32516655
schema:publication	Med Hypotheses
resource representing a document's body	covid:df11423d4426b254dc353c855eb8a83a8a76d6f6#body_text
is schema:about of	named entity 'caused' named entity 'identified' named entity 'Journal' named entity 'public health' named entity 'lipid' named entity 'cytosol' named entity 'enveloped viruses' named entity 'viral RNA' named entity 'first-pass metabolism' named entity 'SARS-CoV-2' named entity 'SARS-CoV-2' named entity 'adhesion' named entity 'virus entry' named entity 'viral infections' named entity 'nanometers' named entity 'ionophore' named entity 'COVID' named entity 'lipid' named entity 'FDA' named entity 'transmembrane' named entity 'infection' named entity 'lung' named entity 'SARS-CoV-2' named entity 'protein' named entity 'burden' named entity 'drug screen' named entity 'repurposing' named entity 'SARS-CoV-2' named entity 'Salinomycin' named entity 'antiviral agent' named entity 'lipid' named entity 'endosomal' named entity 'lysosomal' named entity 'Drug repurposing' named entity 'interact' named entity 'spike protein' named entity 'ectodomain' named entity 'ACE2' named entity 'cytoplasmic' named entity 'antibacterial' named entity 'coronavirus' named entity 'SARS-CoV-2' named entity 'Angiotensin-Converting Enzyme' named entity '5.5' named entity 'cell membranes' named entity 'NLCs' named entity 'vaccines' named entity 'Ionophores' named entity 'SARS-CoV-2' named entity 'biocompatible' named entity 'SARS-CoV-2' named entity 'endosomes' named entity 'lung' named entity 'host cells' named entity 'viral RNA' named entity 'approved drugs' named entity 'NLCs' named entity 'infection' named entity 'Coronaviruses' named entity 'membrane fusion' named entity 'NLCs' named entity 'SARS-CoV-2' named entity 'SARS-CoV-2' named entity 'NLCs' named entity 'MERS-CoV' named entity 'antiviral' named entity 'Streptomyces albus' named entity 'membrane fusion' named entity 'proteolytic cleavage' named entity 'antiviral agent' named entity 'antiviral agent' named entity 'cytosol' named entity 'Coronaviruses'

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