Evidence map›Paper›PMID 26955270›Full record

ArticleInternational journal of nanomedicine2016

Development of a robust pH-sensitive polyelectrolyte ionomer complex for anticancer nanocarriers.

Chaemin Lim, Yu Seok Youn, Kyung Soo Lee, Ngoc Ha Hoang, Taehoon Sim, Eun Seong Lee, Kyung Taek Oh

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. A charge-reversible nanocarrier using PEG-PLL (-International journal of nanomedicine · 2017
    Article
  7. 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.

Chaemin LimDepartment of Pharmaceutical Sciences, College of Pharmacy, Chung-Ang University, Seoul, South Korea; Department of Pharmaceutical Sciences, College of Pharmacy, Chung-Ang University, Seoul, South Korea.
Yu Seok YounDepartment of Pharmaceutical Sciences, School of Pharmacy, Sungkyunkwan University, Suwon, South Korea; Department of Pharmaceutical Sciences, College of Pharmacy, Chung-Ang University, Seoul, South Korea.
Kyung Soo LeeDepartment of Pharmaceutical Sciences, College of Pharmacy, Chung-Ang University, Seoul, South Korea.
Ngoc Ha HoangDepartment of Pharmaceutical Sciences, College of Pharmacy, Chung-Ang University, Seoul, South Korea.
Taehoon SimDepartment of Pharmaceutical Sciences, College of Pharmacy, Chung-Ang University, Seoul, South Korea.
Eun Seong LeeDivision of Biotechnology, The Catholic University of Korea, Gyeonggi-do, South Korea.
Kyung Taek OhDepartment of Pharmaceutical Sciences, College of Pharmacy, Chung-Ang University, Seoul, South Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A polyelectrolyte ionomer complex (PIC) composed of cationic and anionic polymers was developed for nanomedical applications. Here, a poly(ethylene glycol)-poly(lactic acid)-poly(ethylene imine) triblock copolymer (PEG-PLA-PEI) and a poly(aspartic acid) (P[Asp]) homopolymer were synthesized. These polyelectrolytes formed stable aggregates through electrostatic interactions between the cationic PEI and the anionic P(Asp) blocks. In particular, the addition of a hydrophobic PLA and a hydrophilic PEG to triblock copolyelectrolytes provided colloidal aggregation stability by forming a tight hydrophobic core and steric hindrance on the surface of PIC, respectively. The PIC showed different particle sizes and zeta potentials depending on the ratio of cationic PEI and anionic P(Asp) blocks (C/A ratio). The doxorubicin (dox)-loaded PIC, prepared with a C/A ratio of 8, demonstrated pH-dependent behavior by the deprotonation/protonation of polyelectrolyte blocks. The drug release and the cytotoxicity of the dox-loaded PIC (C/A ratio: 8) increased under acidic conditions compared with physiological pH, due to the destabilization of the formation of the electrostatic core. In vivo animal imaging revealed that the prepared PIC accumulated at the targeted tumor site for 24 hours. Therefore, the prepared pH-sensitive PIC could have considerable potential as a nanomedicinal platform for anticancer therapy.

Indexed as

Drug Delivery SystemsAnimalsBreast NeoplasmsCell SurvivalDoxorubicinDrug CarriersFemaleHydrogen-Ion ConcentrationHydrophobic and Hydrophilic InteractionsIminesMiceMice, Inbred BALB CMicellesMice, NudeNanoparticlesPolyethylene GlycolsDoxorubicinDrug CarriersIminesMicellesmonomethoxypolyethyleneglycol-polylactide block copolymerPolyethylene Glycolspoly(ethylene imine)PolyethylenesPolymersanimal imagingnanomedicinePEG-PLA-PEIpH-sensitivepolyelectrolyte ionomer complex

Identifiers

PMID26955270
PMCPMC4768899

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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.