Evidence map›Paper›PMID 27707522›Full record

ReviewTransfusion medicine reviews2017

Erythrocytes as Carriers for Drug Delivery in Blood Transfusion and Beyond.

Carlos H Villa, Douglas B Cines, Don L Siegel, Vladimir Muzykantov

Abstract readReview
In one paragraph

Review in Transfusion medicine reviews, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
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

39 citing papers in PubMed.

  1. Article
  2. Review
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  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
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  14. Review
  15. Review
  16. Article
  17. Review
  18. Drug transport by red blood cells.Frontiers in physiology · 2023
    Review
  19. Cell-based carrier for targeted hitchhiking delivery.Drug delivery and translational research · 2022
    Review
  20. 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

4 authors.

Carlos H VillaDepartment of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA. Electronic address: carlos.villa@uphs.upenn.edu.
Douglas B CinesPerelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Don L SiegelPerelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Vladimir MuzykantovPerelman School of Medicine, University of Pennsylvania, Philadelphia, PA.

Funding

TRANSFUSION MEDICINE RESEARCH TRAINING PROGRAMT32HL007775 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI SIEGEL, DONALD LAWRENCE · 1993 to 2023
$2.8M
Drug delivery by carrier erythrocytesR01HL121134 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI MUZYKANTOV, VLADIMIR R · 2014 to 2017
$2.6M
Targeted nanomedicine for ALI and I/RR01HL125462 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI MUZYKANTOV, VLADIMIR R · 2015 to 2018
$2.3M
NHLBI NIH HHS R01 HL121134NHLBI NIH HHS R01 HL125462NHLBI NIH HHS T32 HL007775
6 · The paper itself

Abstract

Red blood cells (RBCs) are innate carriers that can also be engineered to improve the pharmacokinetics and pharmacodynamics of many drugs, particularly biotherapeutics. Successful loading of drugs, both internally and on the external surface of RBCs, has been demonstrated for many drugs including anti-inflammatory, antimicrobial, and antithrombotic agents. Methods for internal loading of drugs within RBCs are now entering clinical use. Although internal loading can result in membrane disruption that may compromise biocompatibility, surface loading using either affinity or chemical ligands offers a diverse set of approaches for the production of RBC drug carriers. A wide range of surface determinants is potentially available for this approach, although there remains a need to characterize the effects of coupling agents to these surface proteins. Somewhat surprisingly, recent data also suggest that red cell-mediated delivery may confer tolerogenic immune effects. Questions remaining before widespread application of these technologies include determining the optimal loading protocol, source of RBCs, and production logistics, as well as addressing regulatory hurdles. Red blood cell drug carriers, after many decades of progress, are now poised to enter the clinic and broaden the potential application of RBCs in blood transfusion.

Indexed as

Blood TransfusionDrug CarriersDrug Delivery SystemsErythrocytesHumansDrug CarriersBiocompatibilityDrug deliveryImmunogenicityPharmacokineticsRed blood cells

Identifiers

PMID27707522
PMCPMC5161683

What OpenQuestion holds

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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.