Evidence map›Paper›PMID 24628245›Full record

ArticleACS nano2014

Polydopamine-based simple and versatile surface modification of polymeric nano drug carriers.

Joonyoung Park, Tarsis F Brust, Hong Jae Lee, Sang Cheon Lee, Val J Watts, Yoon Yeo

Open access · greenAbstract read
In one paragraph

Article in ACS nano, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed
15.6field-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

123 citing papers in PubMed, 404 citations in OpenAlex.

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  14. Biomimetic fabricated tubular graftBioactive materials · 2025
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  16. Review
  17. Fast Screening of Tyrosinase Inhibitors inMolecules (Basel, Switzerland) · 2024
    Article
  18. Article
  19. Review
  20. Article

63 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

6 authors at 3 institutions in 2 countries.

Joonyoung ParkDepartment of Industrial and Physical Pharmacy, Purdue University , 575 Stadium Mall Drive, West Lafayette, Indiana 47907, United States.
Tarsis F Brust
Hong Jae Lee
Sang Cheon Lee
Val J Watts
Yoon Yeo
Purdue University West Lafayette · USKyung Hee University · KRKorea Institute of Science and Technology · KR

Funding

Transgenic Mouse Core Facility Shared Resource (TMCF-SR)P30CA023168 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI John Tesmer · 1985 to 2026
$43.4M
Quality Assurance and Quality Control Project Management: Improving Submissions and Study Conduct in the Human Subjects Research Prior Approval ProcessUL1TR002529 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI MOE, SHARON M, WIEHE, SARAH ELIZABETH · 2018 to 2022
$27.2M
Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
Environmentally-adaptive nanoparticles with focal irradiation for cancer therapyR01EB017791 · NIBIB · PURDUE UNIVERSITY · PI YEO, YOON · 2014 to 2018
$1.6M
NCATS NIH HHS UL1 TR001108NCI NIH HHS P30 CA023168NIBIB NIH HHS R01 EB017791
6 · The paper itself

Abstract

The surface of a polymeric nanoparticle (NP) is often functionalized with cell-interactive ligands and/or additional polymeric layers to control NP interaction with cells and proteins. However, such modification is not always straightforward when the surface is not chemically reactive. For this reason, most NP functionalization processes employ reactive linkers or coupling agents or involve prefunctionalization of the polymer, which are complicated and inefficient. Moreover, prefunctionalized polymers can lose the ability to encapsulate and retain a drug if the added ligands change the chemical properties of the polymer. To overcome this challenge, we use dopamine polymerization as a way of functionalizing NP surfaces. This method includes brief incubation of the preformed NPs in a weak alkaline solution of dopamine, followed by secondary incubation with desired ligands. Using this method, we have functionalized poly(lactic-co-glycolic acid) (PLGA) NPs with three representative surface modifiers: a small molecule (folate), a peptide (Arg-Gly-Asp), and a polymer [poly(carboxybetaine methacrylate)]. We confirmed that the modified NPs showed the expected cellular interactions with no cytotoxicity or residual bioactivity of dopamine. The dopamine polymerization method is a simple and versatile surface modification method, applicable to a variety of NP drug carriers irrespective of their chemical reactivity and the types of ligands.

Indexed as

NanoparticlesBetaineBiological TransportDrug CarriersFolic AcidHumansIndolesKB CellsLactic AcidOligopeptidesParticle SizePolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPolymersPolymethacrylic AcidsSafetyarginyl-glycyl-aspartic acidBetaineDrug CarriersFolic AcidIndolesLactic AcidOligopeptidespolycarboxybetaine methacrylatepolydopaminePolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPolymersPolymethacrylic Acids

Identifiers

PMID24628245
PMCPMC4107448
OpenAlexW2335405043

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.