Evidence map›Paper›PMID 23751567›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2013

Scalable method to produce biodegradable nanoparticles that rapidly penetrate human mucus.

Qingguo Xu, Nicholas J Boylan, Shutian Cai, Bolong Miao, Himatkumar Patel, Justin Hanes

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.8field-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

44 citing papers in PubMed, 122 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

Qingguo XuThe Center for Nanomedicine, The Johns Hopkins University School of Medicine, 400 N. Broadway, Baltimore 21231, USA.
Nicholas J Boylan
Shutian Cai
Bolong Miao
Himatkumar Patel
Justin Hanes
Johns Hopkins Medicine · USJohns Hopkins University · US

Funding

ValidationU54CA151838 · NCI · JOHNS HOPKINS UNIVERSITY · PI POMPER, MARTIN G · 2010 to 2014
$11.9M
Mucus-penetrating nanoparticles for sustained microbicide deliveryR33AI079740 · NIAID · JOHNS HOPKINS UNIVERSITY · PI HANES, JUSTIN S. · 2010 to 2012
$1.4M
TGFb Modulation: Therapeutic Targeting for COPD-EmphysemaP50HL107190 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI NEPTUNE, ENID R · 2011 to 2012
$977k
NCI NIH HHS U54 CA151838NCI NIH HHS U54CA151838NHLBI NIH HHS P50 HL107190NHLBI NIH HHS P50HL107190NIAID NIH HHS R33 AI079740NIAID NIH HHS R33AI079740
6 · The paper itself

Abstract

Mucus typically traps and rapidly removes foreign particles from the airways, gastrointestinal tract, nasopharynx, female reproductive tract and the surface of the eye. Nanoparticles capable of rapid penetration through mucus can potentially avoid rapid clearance, and open significant opportunities for controlled drug delivery at mucosal surfaces. Here, we report an industrially scalable emulsification method to produce biodegradable mucus-penetrating particles (MPP). The emulsification of diblock copolymers of poly(lactic-co-glycolic acid) and polyethylene glycol (PLGA-PEG) using low molecular weight (MW) emulsifiers forms dense brush PEG coatings on nanoparticles that allow rapid nanoparticle penetration through fresh undiluted human mucus. In comparison, conventional high MW emulsifiers, such as polyvinyl alcohol (PVA), interrupts the PEG coating on nanoparticles, resulting in their immobilization in mucus owing to adhesive interactions with mucus mesh elements. PLGA-PEG nanoparticles with a wide range of PEG MW (1, 2, 5, and 10 kDa), prepared by the emulsification method using low MW emulsifiers, all rapidly penetrated mucus. A range of drugs, from hydrophobic small molecules to hydrophilic large biologics, can be efficiently loaded into biodegradable MPP using the method described. This readily scalable method should facilitate the production of MPP products for mucosal drug delivery, as well as potentially longer-circulating particles following intravenous administration.

Indexed as

Drug Delivery SystemsCurcuminDrug CompoundingFemaleHumansMucusNanoparticlesPermeabilityPolyethylene GlycolsPolyglactin 910Polyvinyl AlcoholCurcuminPolyethylene GlycolsPolyglactin 910poly(lactic-glycolic acid)-poly(ethyleneglycol) copolymerPolyvinyl AlcoholDrug deliveryEmulsificationMucus-penetrating particlesNanomedicineSurface PEG density

Identifiers

PMID23751567
PMCPMC3730524
OpenAlexW2046370080

What OpenQuestion holds

Textmetadata
LicenceTDM
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.