Evidence map›Paper›PMID 21911015›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2012

A poly(ethylene glycol)-based surfactant for formulation of drug-loaded mucus penetrating particles.

Olcay Mert, Samuel K Lai, Laura Ensign, Ming Yang, Ying-Ying Wang, Joseph Wood, Justin Hanes

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 113 citations in OpenAlex.

  1. Review
  2. Hypotonic, gel-forming delivery system for vaginal drug administration.Journal of controlled release : official journal of the Controlled Release Society · 2024
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  20. Polymer conjugated retinoids for controlled transdermal delivery.Journal of controlled release : official journal of the Controlled Release Society · 2017
    Article
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 at 2 institutions in 1 country.

Olcay MertDepartment of Chemical and Biomolecular Engineering, Johns Hopkins University, 3400 N Charles Street, Baltimore, MD 21218, USA.
Samuel K Lai
Laura Ensign
Ming Yang
Ying-Ying Wang
Joseph Wood
Justin Hanes
Johns Hopkins University · USJohns Hopkins Medicine · US

Funding

Mucus penetrating nanoparticles for early stage cervical cancerR01CA140746 · NCI · JOHNS HOPKINS UNIVERSITY · PI HANES, JUSTIN S. · 2009 to 2010
$665k
Mucus-penetrating nanoparticles for sustained microbicide deliveryR21AI079740 · NIAID · JOHNS HOPKINS UNIVERSITY · PI CONE, RICHARD, HANES, JUSTIN S. · 2008 to 2009
$450k
Polymer nanoparticles that cross mucusR21HL089816 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI HANES, JUSTIN S. · 2008 to 2009
$449k
NCI NIH HHS R01 CA140746NCI NIH HHS R01CA140746NHLBI NIH HHS R21 HL089816NHLBI NIH HHS R21HL089816NIAID NIH HHS R21 AI079740NIAID NIH HHS R21AI079740
6 · The paper itself

Abstract

Mucosal surfaces are protected by a highly viscoelastic and adhesive mucus layer that traps most foreign particles, including conventional drug and gene carriers. Trapped particles are eliminated on the order of seconds to hours by mucus clearance mechanisms, precluding sustained and targeted drug and nucleic acid delivery to mucosal tissues. We have previously shown that polymeric coatings that minimize adhesive interactions with mucus constituents lead to particles that rapidly penetrate human mucus secretions. Nevertheless, a particular challenge in formulating drug-loaded mucus penetrating particles (MPP) is that many commonly used surfactants are either mucoadhesive, or do not facilitate efficient drug encapsulation. We tested a novel surfactant molecule for particle formulation composed of Vitamin E conjugated to 5 kDa poly(ethylene glycol) (VP5k). We show that VP5k-coated poly(lactide-co-glycolide) (PLGA) nanoparticles rapidly penetrate human cervicovaginal mucus, whereas PLGA nanoparticles coated with polyvinyl alcohol or Vitamin E conjugated to 1 kDa PEG were trapped. Importantly, VP5k facilitated high loading of paclitaxel, a frontline chemo drug, into PLGA MPP, with controlled release for at least 4 days and negligible burst release. Our results offer a promising new method for engineering biodegradable, drug-loaded MPP for sustained and targeted delivery of therapeutics at mucosal surfaces.

Indexed as

Antineoplastic Agents, PhytogenicCervix MucusChemistry, PharmaceuticalDrug CarriersHumansLactic AcidNanoparticlesPaclitaxelPolyethylene GlycolsPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerSurface-Active AgentsVitamin EAntineoplastic Agents, PhytogenicDrug CarriersLactic AcidPaclitaxelPolyethylene GlycolsPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerSurface-Active AgentsVitamin E

Identifiers

PMID21911015
PMCPMC3246104
OpenAlexW2059119804

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.