Evidence map›Paper›PMID 30063243›Full record

ArticleBiotechnology and bioengineering2019

Bioprocess decision support tool for scalable manufacture of extracellular vesicles.

Kelvin S Ng, James A Smith, Matthew P McAteer, Benjamin E Mead, Jamie Ware, Felix O Jackson, Alison Carter, Lino Ferreira, Kim Bure, Jon A Rowley and 3 more

Abstract read
In one paragraph

Article in Biotechnology and bioengineering, 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
–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

18 citing papers in PubMed.

  1. Review
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  12. Co-delivery systems: hope for clinical application?Drug delivery and translational research · 2022
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  16. The emerging role of exosomes as novel therapeutics: Biology, technologies, clinical applications, and the next.American journal of reproductive immunology (New York, N.Y. : 1989) · 2021
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  18. 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

13 authors.

Kelvin S NgHarvard-MIT Division of Health Sciences and Technology, Cambridge, Massachusetts.
James A SmithNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.ORCID 0000-0003-2634-0268
Matthew P McAteerDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, Charlestown, Massachusetts.
Benjamin E MeadHarvard-MIT Division of Health Sciences and Technology, Cambridge, Massachusetts.
Jamie WareThe Oxford-UCL Centre for the Advancement of Sustainable Medical Innovation, University of Oxford, Oxford, UK.
Felix O JacksonThe Oxford-UCL Centre for the Advancement of Sustainable Medical Innovation, University of Oxford, Oxford, UK.
Alison CarterDepartment of Paediatrics, University of Oxford, Oxford, UK.
Lino FerreiraUniversity of Coimbra, Center for Neuroscience and Cell Biology, Portugal.
Kim BureThe Oxford-UCL Centre for the Advancement of Sustainable Medical Innovation, University of Oxford, Oxford, UK.
Jon A RowleyRoosterBio, Frederick, Maryland.
Brock ReeveHarvard Stem Cell Institute, Cambridge, Massachusetts.
David A BrindleyHarvard Stem Cell Institute, Cambridge, Massachusetts.
Jeffrey M KarpHarvard-MIT Division of Health Sciences and Technology, Cambridge, Massachusetts.

Funding

Engineered Induction of a Stem Cell Homing ResponseR01HL095722 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI KARP, JEFFREY MICHAEL · 2010 to 2018
$3.9M
Medical Research Council UK MR/K501256/NHLBI NIH HHS R01 HL095722
6 · The paper itself

Abstract

Newly recognized as natural nanocarriers that deliver biological information between cells, extracellular vesicles (EVs), including exosomes and microvesicles, provide unprecedented therapeutic opportunities. Large-scale and cost-effective manufacturing is imperative for EV products to meet commercial and clinical demands; successful translation requires careful decisions that minimize financial and technological risks. Here, we develop a decision support tool (DST) that computes the most cost-effective technologies for manufacturing EVs at different scales, by examining the costs of goods associated with using published protocols. The DST identifies costs of labor and consumables during EV harvest as key cost drivers, substantiating a need for larger-scale, higher-throughput, and automated technologies for harvesting EVs. Importantly, we highlight a lack of appropriate technologies for meeting clinical demands, and propose a potentially cost-effective solution. This DST can facilitate decision-making very early on in development and be used to predict, and better manage, the risk of process changes when commercializing EV products.

Indexed as

Decision Support TechniquesBiotechnologyExtracellular Vesiclescostseconomicsexosomesextracellular vesiclesmanufacturingscale-up

Identifiers

PMID30063243
PMCPMC6322973

What OpenQuestion holds

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LicenceCC BY
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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.