Evidence map›Paper›PMID 29416331›Full record

ArticleInternational journal of nanomedicine2018

Pharmacokinetics and in vitro/in vivo antitumor efficacy of aptamer-targeted Ecoflex

Erfaneh Ghassami, Jaleh Varshosaz, Ali Jahanian-Najafabadi, Mohsen Minaiyan, Parvin Rajabi, Effat Hayati

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Aptamers: precision tools for diagnosing and treating infectious diseases.Frontiers in cellular and infection microbiology · 2024
    Review
  3. Review
  4. Review
  5. Review
  6. Aptamer Nanomaterials for Ovarian Cancer Target Theranostics.Frontiers in bioengineering and biotechnology · 2022
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. HER-2 aptamer-targeted EcoflexIET nanobiotechnology · 2019
    Article
  17. Review
  18. Article
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 at 5 institutions in 3 countries.

Erfaneh GhassamiDepartment of Pharmaceutics, School of Pharmacy and Novel Drug Delivery Systems Research Centre.
Jaleh VarshosazDepartment of Pharmaceutics, School of Pharmacy and Novel Drug Delivery Systems Research Centre.
Ali Jahanian-NajafabadiDepartment of Pharmaceutical Biotechnology.
Mohsen MinaiyanDepartment of Pharmacology, School of Pharmacy.
Parvin RajabiDepartment of Pathology, Isfahan University of Medical Sciences, Isfahan.
Effat HayatiNorth Research Center, Pasteur Institute of Iran, Amol, Iran.
American Pharmacists Association · USIsfahan University of Medical Sciences · IRKindeva Drug Delivery (United States) · USPasteur Institute of Iran · IRPharmaceutical Biotechnology (Czechia) · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEpithelixal ovarian cancer is the fourth cause of cancer death in developed countries with 77% of ovarian cancer cases diagnosed with regional or distant metastasis, with poor survival rates. Docetaxel (DTX) is a well-known anticancer agent, with clinically proven efficacy in several malignancies, including ovarian cancer. However, the adverse effects caused by the active ingredient or currently marketed formulations could even deprive the patient of the advantages of treatment. Therefore, in the current study, polymeric nanoparticles (NPs) equipped with aptamer molecules as targeting agents were proposed to minimize the adverse effects and enhance the antitumor efficacy through directing the drug cargo toward its site of action. MATERIALS AND

methodsElectrospraying technique was implemented to fabricate poly (butylene adipate-co-butylene terephthalate) (Ecoflex

resultsThe obtained results demonstrated significantly enhanced in vitro cytotoxicity and cellular uptake of Apt-DTX-NPs in a HER-2-overexpressing cell line, comparing to DTX-NPs and the free drug. The results of in vivo studies indicated significant increment in pharmacokinetic parameters including the area under the plasma concentration-time curve, mean residence time, and elimination half-life. Significant increment in antitumor efficacy was also observed, probably due to the targeted delivery of DTX to the tumor site and enhanced cellular uptake as evaluated in the aforementioned tests.

conclusionHence, the proposed drug delivery system could be considered as an appropriate potential substitute for currently marketed DTX formulations.

Indexed as

AnimalsAntineoplastic AgentsAptamers, NucleotideCell Line, TumorDocetaxelDrug CarriersDrug Delivery SystemsErb-b2 Receptor Tyrosine KinasesFemaleHalf-LifeHumansMice, Inbred BALB CMice, NudeNanoparticlesOvarian NeoplasmsParticle SizeAntineoplastic AgentsAptamers, NucleotideDocetaxelDrug CarriersecoflexERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesPolyestersTaxoidsaptamerdocetaxelEcoflexelectrosprayingnanoparticlesovarian cancerpharmacokinetic

Identifiers

PMID29416331
PMCPMC5789074
OpenAlexW2785103187

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.