Evidence map›Paper›PMID 30880491›Full record

ArticleDrug delivery2019

Combined using of paclitaxel and salinomycin active targeting nanostructured lipid carriers against non-small cell lung cancer and cancer stem cells.

Jianwen Zhou, Mingshuang Sun, Shanshan Jin, Li Fan, Wenquan Zhu, Xiaoyu Sui, Lixin Cao, Chunrong Yang, Cuiyan Han

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Advanced drug delivery platforms target cancer stem cells.Asian journal of pharmaceutical sciences · 2025
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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

9 authors at 3 institutions in 1 country.

Jianwen Zhoua School of Pharmacy , Jiamusi Medical University , Jiamusi , China.
Mingshuang Sunc School of Pharmacy , Taishan Medical University , Taian , China.
Shanshan Jind Department of Pharmaceutical Preparations , Beijing Dezhong Wanquan Medicine Technology Co., Ltd , Beijing , China.
Li Fane Research Institute of Medicine & Pharmacy, Qiqihar Medical University , Qiqihar , China.
Wenquan Zhub School of Pharmacy , Qiqihar Medical University , Qiqihar , China.
Xiaoyu Suib School of Pharmacy , Qiqihar Medical University , Qiqihar , China.
Lixin Caof Department of Orthopedics , the First Affiliated Hospital of Qiqihar Medical University , Qiqihar , China.
Chunrong Yanga School of Pharmacy , Jiamusi Medical University , Jiamusi , China.
Cuiyan Hanb School of Pharmacy , Qiqihar Medical University , Qiqihar , China.
Qiqihar Medical University · CNJiamusi University · CNTaishan Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The existing of avidity cancer stem cells (CSCs) made it an optical strategy to kill cancer cells and CSCs at the same time. Here, we constructed a CSCs specific nanocarrier naming T-S-NLC using the CD133+ targeting peptide TISWPPR (TR) as the targeting moiety attached to the distal end of PEG on salinomycin (Sal) loaded nanostructured lipid carriers (NLC), its pharmaceutical characteristics proved it 128.73 ± 2.09 nm, anionic spheroid with sustained release profile. It's in vitro targeting effect in CD133+ CSCs indicated that it exhibited superior CSCs internalization over non-modified NLC or free drug. Afterwards, it was used in combination with previously designed EGFR specific A-P-NLC (AEYLR peptide-PEG-modified paclitaxel loaded NLC) to achieve the goal to kill the cancer cells and CSCs, simultaneously. The in vitro tumor targeting effect of T-S-NLC + A-P-NLC was affirmed by cellular uptake and proliferation inhibition effect in NCI-H1299 and S180 cell lines showing advanced results over single preparation groups. In vivo tumor targeting effect in S180 tumor-bearing mice also validated the better tumor accumulative effect of the combined group. Last but not least, the in vivo antitumor effect strongly identified the greater tumor suppression effect of T-S-NLC + A-P-NLC than single preparation groups or combined use of free drugs while maintaining a good living state of the mice. To sum up, the combined usage of PTX and Sal active targeting NLC naming A-P-NLC + T-S-NLC which killed cancer cells and CSCs at the same time was a promising drug delivery system.

Indexed as

AnimalsAntineoplastic AgentsCarcinoma, Non-Small-Cell LungCell Line, TumorDrug CarriersDrug Delivery SystemsHumansLipidsLung NeoplasmsMiceNanostructuresNeoplastic Stem CellsPaclitaxelParticle SizePeptidesPolyether PolyketidesAntineoplastic AgentsDrug CarriersLipidsPaclitaxelPeptidesPolyether PolyketidesPolyethylene GlycolsPyranssalinomycinactive targetingcombined therapyNanostructured lipid carrierspaclitaxelsalinomycin

Identifiers

PMID30880491
PMCPMC6427498
OpenAlexW2921303823

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.