Evidence map›Paper›PMID 29062065›Full record

ArticleScientific reports2017

A chloroquine-induced macrophage-preconditioning strategy for improved nanodelivery.

Joy Wolfram, Sara Nizzero, Haoran Liu, Feng Li, Guodong Zhang, Zheng Li, Haifa Shen, Elvin Blanco, Mauro Ferrari

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 1 pooled it
7.0field-weighted citation impact, top 2% 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

75 citing papers in PubMed, 1 synthesis or guideline pooled it, 135 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Engineered cargo-free nanoparticle decoys for phagocytic modulation of macrophages.Journal of controlled release : official journal of the Controlled Release Society · 2026
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  17. Combined Vorinostat and Chloroquine Inhibit Sodium-Iodide Symporter Endocytosis and Enhance Radionuclide Uptake In Vivo.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  18. Article
  19. Review
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15 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

9 authors at 3 institutions in 1 country.

Joy WolframDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, 77030, USA. wolfram.joy@mayo.edu.
Sara NizzeroDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Haoran LiuDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Feng LiDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Guodong ZhangDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Zheng LiDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Haifa ShenDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Elvin BlancoDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Mauro FerrariDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, 77030, USA. mferrari@houstonmethodist.org.
Houston Methodist · USCornell University · USRice University · US

Funding

Texas Center for Cancer NanomedicineU54CA151668 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2010 to 2014
$12.4M
TRANS-NETWORK PROJECTSU54CA143837 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CURLEY, STEVEN ALAN · 2009 to 2014
$10.8M
Transport Oncophysics CoreU54CA210181 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHANG, JENNY C-N, SHEN, HAIFA · 2016 to 2020
$9.3M
NCI NIH HHS U54 CA143837NCI NIH HHS U54 CA151668NCI NIH HHS U54 CA210181
6 · The paper itself

Abstract

Site-specific localization is critical for improving the therapeutic efficacy and safety of drugs. Nanoparticles have emerged as promising tools for localized drug delivery. However, over 90% of systemically injected nanocarriers typically accumulate in the liver and spleen due to resident macrophages that form the mononuclear phagocyte system. In this study, the clinically approved antimalarial agent chloroquine was shown to reduce nanoparticle uptake in macrophages by suppressing endocytosis. Pretreatment of mice with a clinically relevant dose of chloroquine substantially decreased the accumulation of liposomes and silicon particles in the mononuclear phagocyte system and improved tumoritropic and organotropic delivery. The novel use of chloroquine as a macrophage-preconditioning agent presents a straightforward approach for addressing a major barrier in nanomedicine. Moreover, this priming strategy has broad applicability for improving the biodistribution and performance of particulate delivery systems. Ultimately, this study defines a paradigm for the combined use of macrophage-modulating agents with nanotherapeutics for improved site-specific delivery.

Indexed as

AnimalsBiological TransportCell LineCell SurvivalChloroquineDrug CarriersEndocytosisHumansImmunity, InnateKupffer CellsMacrophagesMiceNanoparticlesChloroquineDrug Carriers

Identifiers

PMID29062065
PMCPMC5653759
OpenAlexW2766181274

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.