Evidence map›Paper›PMID 26346426›Full record

ArticleInternational journal of nanomedicine2015

Tumor-targeting, pH-sensitive nanoparticles for docetaxel delivery to drug-resistant cancer cells.

Tuan Hiep Tran, Thiruganesh Ramasamy, Ju Yeon Choi, Hanh Thuy Nguyen, Thanh Tung Pham, Jee-Heon Jeong, Sae Kwang Ku, Han-Gon Choi, Chul Soon Yong, Jong Oh Kim

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2015. 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
5.3field-weighted citation impact, top 4% 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, 76 citations in OpenAlex.

  1. Review
  2. MnOPharmaceutics · 2026
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  14. HER-2 aptamer-targeted EcoflexIET nanobiotechnology · 2019
    Article
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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

10 authors at 3 institutions in 1 country.

Tuan Hiep TranCollege of Pharmacy, Yeungnam University, Dae-Dong, South Korea.
Thiruganesh RamasamyCollege of Pharmacy, Yeungnam University, Dae-Dong, South Korea.
Ju Yeon ChoiCollege of Pharmacy, Yeungnam University, Dae-Dong, South Korea.
Hanh Thuy NguyenCollege of Pharmacy, Yeungnam University, Dae-Dong, South Korea.
Thanh Tung PhamCollege of Pharmacy, Yeungnam University, Dae-Dong, South Korea.
Jee-Heon JeongCollege of Pharmacy, Yeungnam University, Dae-Dong, South Korea.
Sae Kwang KuCollege of Korean Medicine, Daegu Haany University, Gyeongsan, South Korea.
Han-Gon ChoiCollege of Pharmacy, Hanyang University, Hanyangdaehak-ro, Sangnok-gu, Ansan, South Korea.
Chul Soon YongCollege of Pharmacy, Yeungnam University, Dae-Dong, South Korea.
Jong Oh KimCollege of Pharmacy, Yeungnam University, Dae-Dong, South Korea.
Yeungnam University · KRDaegu Haany University · KRHanyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The attachment of polyethylene glycol (PEG) increases the circulation time of drug-containing nanoparticles; however, this also negatively affects cellular uptake. To overcome this problem, unique lipid polymer hybrid (LPH) nanoparticles were developed with a pH-responsive PEG layer that detached prior to cell uptake. Docetaxel (DTX) was incorporated into the lipid core of the nanoparticles, which was then shielded with the pH-responsive block co-polymer polyethylene glycol-b-polyaspartic acid (PEG-b-PAsp) using a modified emulsion method. The optimized LPH nanoparticles were ~200 nm and had a narrow size distribution. Drug release from DTX-loaded LPH (DTX-LPH) nanoparticles was pH-sensitive, which is beneficial for tumor targeting. More importantly, DTX-LPH nanoparticles were able to effectively induce apoptosis in cancer cells. The negative surface charge and PEG shell of vehicle remarkably enhanced the blood circulation and physiological activity of DTX-LPH nanoparticles compared with that of free DTX. The nanoparticles were also found to reduce the size of tumors in tumor-bearing xenograft mice. The in vivo anticancer effect of DTX-LPH nanoparticles was further confirmed by the elevated levels of caspase-3 and poly ADP ribose polymerase found in the tumors after treatment. Thus, the results suggest that this novel LPH system could be an effective new treatment for cancer.

Indexed as

Drug Resistance, NeoplasmParticle SizeAnimalsAntineoplastic AgentsApoptosisCaspase 3Cell Line, TumorCell SurvivalDocetaxelDrug Delivery SystemsEmulsionsHumansHydrogen-Ion ConcentrationLipidsMaleMCF-7 CellsAntineoplastic AgentsCaspase 3DocetaxelEmulsionsLipidsMicellesPoly(ADP-ribose) PolymerasesPolyethylene GlycolsTaxoidsantitumordocetaxeldrug delivery systemspH-sensitivepolyaspartic acid

Identifiers

PMID26346426
PMCPMC4552257
OpenAlexW2230774605

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.