Evidence map›Paper›PMID 37382704›Full record

ArticleDiscover nano2023

Engineering of inhalable nano-in-microparticles for co-delivery of small molecules and miRNAs.

Marjan Motiei, Ondrej Mišík, Thanh Huong Truong, Frantisek Lizal, Petr Humpolíček, Vladimír Sedlařík, Petr Sáha

Open access · diamondAbstract read
In one paragraph

Article in Discover nano, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.9field-weighted citation impact, top 6% of its field
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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Dry Powder Inhalers for Delivery of Synthetic Biomolecules.Pharmaceuticals (Basel, Switzerland) · 2025
    Review
  7. Review
  8. Review
  9. Review
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

7 authors at 2 institutions in 1 country.

Marjan MotieiCentre of Polymer Systems, University Institute, TBU, Tr. Tomase Bati, 5678, Zlin, Czech Republic. motiei@utb.cz.
Ondrej MišíkFaculty of Mechanical Engineering, Brno University of Technology, Technicka 2896/2, 61669, Brno, Czech Republic.
Thanh Huong TruongCentre of Polymer Systems, University Institute, TBU, Tr. Tomase Bati, 5678, Zlin, Czech Republic.
Frantisek LizalFaculty of Mechanical Engineering, Brno University of Technology, Technicka 2896/2, 61669, Brno, Czech Republic.
Petr HumpolíčekCentre of Polymer Systems, University Institute, TBU, Tr. Tomase Bati, 5678, Zlin, Czech Republic.
Vladimír SedlaříkCentre of Polymer Systems, University Institute, TBU, Tr. Tomase Bati, 5678, Zlin, Czech Republic.
Petr SáhaCentre of Polymer Systems, University Institute, TBU, Tr. Tomase Bati, 5678, Zlin, Czech Republic.
Tomas Bata University in Zlín · CZBrno University of Technology · CZ

Funding

Czech Science Foundation GA 20-27653STomas Bata University in Zlin - DKRVO RP/CPS/2020/005
6 · The paper itself

Abstract

In this study, novel Trojan particles were engineered for direct delivery of doxorubicin (DOX) and miR-34a as model drugs to the lungs to raise local drug concentration, decrease pulmonary clearance, increase lung drug deposition, reduce systemic side effects, and overcome multi-drug resistance. For this purpose, targeted polyelectrolyte nanoparticles (tPENs) developed with layer-by-layer polymers (i.e., chitosan, dextran sulfate, and mannose-g-polyethyleneimine) were spray dried into a multiple-excipient (i.e., chitosan, leucine, and mannitol). The resulting nanoparticles were first characterized in terms of size, morphology, in vitro DOX release, cellular internalization, and in vitro cytotoxicity. tPENs showed comparable cellular uptake levels to PENs in A549 cells and no significant cytotoxicity on their metabolic activity. Co-loaded DOX/miR-34a showed a greater cytotoxicity effect than DOX-loaded tPENs and free drugs, which was confirmed by Actin staining. Thereafter, nano-in-microparticles were studied through size, morphology, aerosolization efficiency, residual moisture content, and in vitro DOX release. It was demonstrated that tPENs were successfully incorporated into microspheres with adequate emitted dose and fine particle fraction but low mass median aerodynamic diameter for deposition into the deep lung. The dry powder formulations also demonstrated a sustained DOX release at both pH values of 6.8 and 7.4.

Indexed as

ChitosanmiRNAsNano-in-microparticlesPulmonary deliverySmall molecules

Identifiers

PMID37382704
PMCPMC10214903
OpenAlexW4327861346

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.