Evidence map›Paper›PMID 34401226›Full record

ReviewActa pharmaceutica Sinica. B2022

Pulmonary delivery of siRNA against acute lung injury/acute respiratory distress syndrome.

Makhloufi Zoulikha, Qingqing Xiao, George Frimpong Boafo, Marwa A Sallam, Zhongjian Chen, Wei He

Abstract readReview
In one paragraph

Review in Acta pharmaceutica Sinica. B, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 137 papers.

0numbers the graph read from it
0cells of the map it votes in
137citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

137 citing papers in PubMed.

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77 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Makhloufi ZoulikhaDepartment of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing 211198, China.
Qingqing XiaoDepartment of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing 211198, China.
George Frimpong BoafoDepartment of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing 211198, China.
Marwa A SallamDepartment of Industrial Pharmacy, Faculty of Pharmacy, Alexandria University, Alexandria 21521, Egypt.
Zhongjian ChenShanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai 200443, China.
Wei HeDepartment of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing 211198, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of small interfering RNAs (siRNAs) has been under investigation for the treatment of several unmet medical needs, including acute lung injury/acute respiratory distress syndrome (ALI/ARDS) wherein siRNA may be implemented to modify the expression of pro-inflammatory cytokines and chemokines at the mRNA level. The properties such as clear anatomy, accessibility, and relatively low enzyme activity make the lung a good target for local siRNA therapy. However, the translation of siRNA is restricted by the inefficient delivery of siRNA therapeutics to the target cells due to the properties of naked siRNA. Thus, this review will focus on the various delivery systems that can be used and the different barriers that need to be surmounted for the development of stable inhalable siRNA formulations for human use before siRNA therapeutics for ALI/ARDS become available in the clinic.

Indexed as

AAV, adeno-associated virusAgo-2, argonaute 2ALI/ARDSALI/ARDS, acute lung injury/acute respiratory distress syndromeAM, alveolar macrophageATI, alveolar cell type IATII, alveolar cell type IIAV, adenovirusCellular uptakeCFDA, China Food and Drug AdministrationCOPD, chronic obstructive pulmonary diseaseCPP, cell-penetrating peptideCS, cigarette smokeCXCR4, C–X–C motif chemokine receptor type 4DAMPs, danger-associated molecular patternsDC-Chol, 3β-(N-(N′,N′-dimethylethylenediamine)-carbamoyl) cholesterolDDAB, dimethyldioctadecylammonium bromideDODAP, 1,2-dioleyl-3-dimethylammonium-propaneDODMA, 1,2-dioleyloxy-N,N-dimethyl-3-aminopropaneDOGS, dioctadecyl amido glycin spermineDOPC, 1,2-dioleoyl-sn-glycero-3-phosphocholineDOPE, 1,2-dioleoyl-l-α-glycero-3-phosphatidylethanolamineDOSPA, 2,3-dioleyloxy-N-[2-(sperminecarboxamido)ethyl]-N,N-dimethyl-1-propanaminiumDOTAP, 1,2-dioleoyl-3-trimethylammonium-propaneDOTMA, N-[1-(2,3-dioleoyloxy)propyl]-N,N,N-trimethylammoniumDPI, dry powder inhalerDPPC, 1,2-dipalmitoyl-sn-glycero-3-phosphocholineDrug deliverydsDNA, double-stranded DNAdsRNA, double-stranded RNAEC, endothelial celleggPG, l-α-phosphatidylglycerolEndosomal escapeEPC, egg phosphatidylcholineEpiC, epithelial cellEXOs, exosomesFDA, US Food and Drug AdministrationHALI, hyperoxic acute lung injuryHem-CLP, hemorrhagic shock followed by cecal ligation and puncture septic challengeHMGB1, high-mobility group box 1HMVEC, human primary microvascular endothelial cellHNPs, hybrid nanoparticlesICAM-1, intercellular adhesion molecule-1IFN, interferonsInflammatory diseasesLPS, lipopolysaccharidesMEND, multifunctional envelope-type nano deviceMIF, macrophage migration inhibitory factormiRNA, microRNAmRNA, messenger RNAMyd88, myeloid differentiation primary response 88NanoparticlesNETs, neutrophil extracellular trapsNF-κB, nuclear factor kappa BN/P ratio, nitrogen /phosphate ratioNPs, nanoparticlesPAI-1, plasminogen activator inhibitor-1PAMAM, polyamidoaminePAMPs, pathogen-associated molecular patternsPDGFRα, platelet-derived growth factor receptor-αPD-L1, programmed death ligand-1pDNA, plasmid DNAPEEP, positive end-expiratory pressurePEG, polyethylene glycolPEI, polyethyleneiminePFC, perfluorocarbonPF, pulmonary fibrosisPLGA, poly(d,l-lactic-co-glycolic acid)PMs, polymeric micellesPRR, pattern recognition receptorPS, pulmonary surfactantPulmonary administrationRIP2, receptor-interacting protein 2RISC, RNA-induced silencing complexRNAi, RNA interferenceROS, reactive oxygen speciesshRNA, short RNAsiRNAsiRNA, small interfering RNASLN, solid lipid nanoparticleSNALP, stable nucleic acid lipid particleTGF-β, transforming growth factor-βTLR, Toll-like receptorTNF-α, tumor necrosis factor-αVALI, ventilator-associated lung injuryVILI, ventilator-induced lung injury

Identifiers

PMID34401226
PMCPMC8359643

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.