Evidence map›Paper›PMID 29973592›Full record

ArticleNature communications2018

Rapid transport of deformation-tuned nanoparticles across biological hydrogels and cellular barriers.

Miaorong Yu, Lu Xu, Falin Tian, Qian Su, Nan Zheng, Yiwei Yang, Jiuling Wang, Aohua Wang, Chunliu Zhu, Shiyan Guo and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
12.2field-weighted citation impact, top 1% 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

74 citing papers in PubMed, 289 citations in OpenAlex.

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14 more citing papers are in PubMed but not listed here.

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

14 authors at 4 institutions in 2 countries.

Miaorong YuShanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Lu XuSchool of Pharmacy, Shenyang Pharmaceutical University, 110016, Shenyang, China.
Falin TianCAS Key Laboratory for Nanosystem and Hierarchy Fabrication, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Chinese Academy of Sciences, 100190, Beijing, China.
Qian SuUniversity of Chinese Academy of Sciences, NO.19A Yuquan Road, 100049, Beijing, China.
Nan ZhengSchool of Pharmacy, Shenyang Pharmaceutical University, 110016, Shenyang, China.
Yiwei YangShanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Jiuling WangUniversity of Chinese Academy of Sciences, NO.19A Yuquan Road, 100049, Beijing, China.
Aohua WangShanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Chunliu ZhuShanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Shiyan GuoShanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
XinXin ZhangShanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Yong GanShanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China. ygan@simm.ac.cn.
Xinghua ShiUniversity of Chinese Academy of Sciences, NO.19A Yuquan Road, 100049, Beijing, China. shixh@nanoctr.cn.ORCID http://orcid.org/0000-0001-5012-3453
Huajian GaoSchool of Engineering, Brown University, Providence, RI, 02912, USA. huajian_Gao@brown.edu.
Chinese Academy of Sciences · CNShenyang Pharmaceutical University · CNBrown University · USShanghai Institute of Materia Medica · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 11272327National Natural Science Foundation of China (National Science Foundation of China) 11422215National Natural Science Foundation of China (National Science Foundation of China) 81373356National Natural Science Foundation of China (National Science Foundation of China) 81573378National Natural Science Foundation of China (National Science Foundation of China) 81773651
6 · The paper itself

Abstract

To optimally penetrate biological hydrogels such as mucus and the tumor interstitial matrix, nanoparticles (NPs) require physicochemical properties that would typically preclude cellular uptake, resulting in inefficient drug delivery. Here, we demonstrate that (poly(lactic-co-glycolic acid) (PLGA) core)-(lipid shell) NPs with moderate rigidity display enhanced diffusivity through mucus compared with some synthetic mucus penetration particles (MPPs), achieving a mucosal and tumor penetrating capability superior to that of both their soft and hard counterparts. Orally administered semi-elastic NPs efficiently overcome multiple intestinal barriers, and result in increased bioavailability of doxorubicin (Dox) (up to 8 fold) compared to Dox solution. Molecular dynamics simulations and super-resolution microscopy reveal that the semi-elastic NPs deform into ellipsoids, which enables rotation-facilitated penetration. In contrast, rigid NPs cannot deform, and overly soft NPs are impeded by interactions with the hydrogel network. Modifying particle rigidity may improve the efficacy of NP-based drugs, and can be applicable to other barriers.

Indexed as

Drug CarriersAdministration, OralAnimalsAntibiotics, AntineoplasticBiological TransportCell Line, TumorDiffusionDoxorubicinDrug CompoundingElasticityHardnessHumansHydrogelsMaleMiceMice, NudeAntibiotics, AntineoplasticDoxorubicinDrug CarriersHydrogelsPolylactic Acid-Polyglycolic Acid Copolymer

Identifiers

PMID29973592
PMCPMC6031689
OpenAlexW2811460842

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.