Evidence map›Paper›PMID 28860753›Full record

ArticleInternational journal of nanomedicine2017

pH-sensitive and folic acid-targeted MPEG-PHIS/FA-PEG-VE mixed micelles for the delivery of PTX-VE and their antitumor activity.

Yan Di, Ting Li, Zhihong Zhu, Fen Chen, Lianqun Jia, Wenbing Liu, Xiumei Gai, Yingying Wang, Weisan Pan, Xinggang Yang

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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.

Yan DiDepartment of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University.
Ting LiDepartment of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University.
Zhihong ZhuDepartment of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University.
Fen ChenKey Laboratory of Ministry of Education for TCM Viscera-State Theory and Applications, Liaoning University of Traditional Chinese Medicine.
Lianqun JiaKey Laboratory of Ministry of Education for TCM Viscera-State Theory and Applications, Liaoning University of Traditional Chinese Medicine.
Wenbing LiuKey Laboratory of Structure-Based Drug Design & Discovery, Shenyang Pharmaceutical University, Ministry of Education, Shenyang, China.
Xiumei GaiDepartment of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University.
Yingying WangDepartment of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University.
Weisan PanDepartment of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University.
Xinggang YangDepartment of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to simultaneously introduce pH sensitivity and folic acid (FA) targeting into a micelle system to achieve quick drug release and to enhance its accumulation in tumor cells. Paclitaxel-(+)-α-tocopherol (PTX-VE)-loaded mixed micelles (PHIS/FA/PM) fabricated by poly(ethylene glycol) methyl ether-poly(histidine) (MPEG-PHIS) and folic acid-poly(ethylene glycol)-(+)-α-tocopherol (FA-PEG-VE) were characterized by dynamic light scattering and transmission electron microscopy (TEM). The mixed micelles had a spherical morphology with an average diameter of 137.0±6.70 nm and a zeta potential of -48.7±4.25 mV. The drug encapsulation and loading efficiencies were 91.06%±2.45% and 5.28%±0.30%, respectively. The pH sensitivity was confirmed by changes in particle size, critical micelle concentration, and transmittance as a function of pH. MTT assay showed that PHIS/FA/PM had higher cytotoxicity at pH 6.0 than at pH 7.4, and lower cytotoxicity in the presence of free FA. Confocal laser scanning microscope images demonstrated a time-dependent and FA-inhibited cellular uptake. In vivo imaging confirmed that the mixed micelles targeted accumulation at tumor sites and the tumor inhibition rate was 85.97%. The results proved that the mixed micelle system fabricated by MPEG-PHIS and FA-PEG-VE is a promising approach to improve antitumor efficacy.

Indexed as

alpha-TocopherolAnimalsAntineoplastic Agents, PhytogenicDrug CarriersDrug LiberationDynamic Light ScatteringFemaleFolic AcidHumansHydrogen-Ion ConcentrationMCF-7 CellsMiceMicellesMicroscopy, Electron, TransmissionNeoplasmsPaclitaxelalpha-TocopherolAntineoplastic Agents, PhytogenicDrug CarriersFolic AcidMicellesmonomethoxypolyethylene glycolPaclitaxelPolyethylene Glycolsdrug deliveryfolic acid targetingin vivo antitumor activitymixed micellespH sensitive

Identifiers

PMID28860753
PMCPMC5566413

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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.