Evidence map›Paper›PMID 31114197›Full record

ArticleInternational journal of nanomedicine2019

Targeted lipid nanoparticle delivery of calcitriol to human monocyte-derived macrophages in vitro and in vivo: investigation of the anti-inflammatory effects of calcitriol.

Aisha Rafique, Anders Etzerodt, Jonas H Graversen, Søren K Moestrup, Frederik Dagnæs-Hansen, Holger Jon Møller

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The Immune Microenvironment in Liver Cancer: From Analysis to Targeting.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  5. Review
  6. Nano-Enhanced Diets: Advancing Metabolic Dysfunction-Related Steatotic Liver Disease (MASLD) - A Review.Diabetes, metabolic syndrome and obesity : targets and therapy · 2025
    Review
  7. Review
  8. Impact of calcitriol and PGDDrug delivery and translational research · 2024
    Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Targeting of CD163International journal of molecular sciences · 2020
    Review
  16. Review
  17. Article
  18. Review
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 1 country.

Aisha RafiqueDepartment of Clinical Biochemistry, Aarhus University Hospital, Aarhus, Denmark, araf@clin.au.dk.
Anders EtzerodtInstitute of Biomedicine, Aarhus University, Aarhus, Denmark.
Jonas H GraversenDepartment of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Søren K MoestrupDepartment of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Frederik Dagnæs-HansenInstitute of Biomedicine, Aarhus University, Aarhus, Denmark.
Holger Jon MøllerDepartment of Clinical Biochemistry, Aarhus University Hospital, Aarhus, Denmark, araf@clin.au.dk.
Aarhus University · DKAarhus University Hospital · DKUniversity of Southern Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVitamin D PURPOSE: The main purpose of this study was to encapsulate and specifically target calcitriol to macrophages and investigate the anti-inflammatory properties of calcitriol in vitro and in vivo.

methodsIn this study we have designed and developed near-infrared calcitriol PEGylated nanoparticles (PEG-LNP(Cal)) using a microfluidic mixing technique and modified lipid nanoparticles (LNPs) to target the M specific endocytic receptor CD163. We have investigated LNP cellular uptake and anti-inflammatory effect in LPS-induced M in vitro by flow cytometry, confocal microscopy and gene expression analyses. LNP pharmacodynamics, bio-distribution and organ specific LNP accumulation was also investigated in mice in vivo.

resultsIn vitro, we observed the specific uptake of PEG-LNP(Cal)-hCD163 in human M, which was significantly higher than the non-specific uptake of control PEG-LNP(Cal)-IgG(h) in M. Pretreatment with encapsulated calcitriol was able to attenuate intracellular TNF-expression, and M surface marker HLA-DR expression more efficiently than free calcitriol in LPS-induced M in vitro. Encapsulated calcitriol diminished mRNA gene levels of TNF-, NF-B, MCP-1 and IL-6, while upregulating IL-10. TNF- and IL-6 protein secretion also decreased. In mice, an in vivo pharmacodynamic study of PEG-LNP(Cal) showed a rapid clearance of IgG and CD163 modified LNPs compared to PEG-LNP(Cal). Antibody modified PEG-LNP(Cal) accumulated in the liver, spleen and kidney, whereas unmodified PEG-LNP(Cal) accumulation was only observed in the liver.

conclusionOur results show that calcitriol can be effectively targeted to M. Our data confirms the anti-inflammatory properties of calcitriol and this may be a potential way to deliver high dose bioactive calcitriol to M during inflammation in vivo.

Indexed as

AnimalsAntibodiesAntigens, CDAntigens, Differentiation, MyelomonocyticAnti-Inflammatory AgentsCalcitriolCD163 AntigenChemokinesDrug CompoundingGene Expression RegulationHumansInflammationInflammation MediatorsLipidsMacrophagesMice, Inbred C57BLAntibodiesAntigens, CDAntigens, Differentiation, MyelomonocyticAnti-Inflammatory AgentsCalcitriolCD163 AntigenChemokinesInflammation MediatorsLipidsReceptors, Cell SurfaceRNA, Messenger1.25(OH)2D3calcitriolCD163 targeted drug deliverygene expression analysesin vivo pharmacodynamicslipid nanoparticlesmacrophagespro-inflammatory cytokines

Identifiers

PMID31114197
PMCPMC6488164
OpenAlexW2936279625

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.