Evidence map›Paper›PMID 24235825›Full record

ArticleInternational journal of nanomedicine2013

The impact of PEGylation patterns on the in vivo biodistribution of mixed shell micelles.

Hongjun Gao, Jinjian Liu, Cuihong Yang, Tangjian Cheng, Liping Chu, Hongyan Xu, Aimin Meng, Saijun Fan, Linqi Shi, Jianfeng Liu

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

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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

14 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.

Hongjun GaoKey Laboratory of Functional Polymer Materials, Ministry of Education, and Institute of Polymer Chemistry, Nankai University, Tianjin, People's Republic of China.
Jinjian Liu
Cuihong Yang
Tangjian Cheng
Liping Chu
Hongyan Xu
Aimin Meng
Saijun Fan
Linqi Shi
Jianfeng Liu

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polyethylene glycol (PEG)-ylation is a widely used strategy to fabricate nanocarriers with a long blood circulation time. Further elaboration of the contribution of the surface PEGylation pattern to biodistribution is highly desirable. We fabricated a series of polyion complex (PIC) micelles PEGylated with different ratios (PEG2k and PEG550). The plasma protein adsorption, murine macrophage uptake, and in vivo biodistribution with iodine-125 as the tracer were systematically studied to elucidate the impact of PEGylation patterns on the biodistribution of micelles. We demonstrated that the PEGylated micelles with short hydrophilic PEG chains mixed on the surface were cleared quickly by the reticuloendothelial system (RES), and the single PEG2k PEGylated micelles could efficiently prolong the blood circulation time and increase their deposition in tumor sites. The present study extends the understanding of the PEGylation strategy to further advance the development of ideal nanocarriers for drug delivery and imaging applications.

Indexed as

MicellesAdsorptionAnalysis of VarianceAnimalsBlood ProteinsCell SurvivalDrug CarriersHep G2 CellsHumansIodine RadioisotopesMacrophagesMiceMice, Inbred BALB CMolecular WeightNanoparticlesNIH 3T3 CellsBlood ProteinsDrug CarriersIodine RadioisotopesMicellesPolyethylene Glycolsdrug deliveryin vivo biodistributionmacrophage uptakemixed shell micellesPEGylation

Identifiers

PMID24235825
PMCPMC3825670

What OpenQuestion holds

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Registered trials

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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.