Evidence map›Paper›PMID 33367332›Full record

ArticleBiomaterials science2021

Milk exosomes with enhanced mucus penetrability for oral delivery of siRNA.

Matthew R Warren, Chenzhen Zhang, Armin Vedadghavami, Krister Bokvist, Pradeep K Dhal, Ambika G Bajpayee

Open access · bronzeAbstract read
In one paragraph

Article in Biomaterials science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

68 citing papers in PubMed, 135 citations in OpenAlex.

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  14. Exosome isolation based on polyethylene glycol (PEG): a review.Molecular and cellular biochemistry · 2025
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8 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 2 institutions in 4 countries.

Matthew R WarrenDepartments of Bioengineering, Northeastern University, Boston, MA 02115, USA. warren.ma@husky.neu.edu zhang.chenz@husky.neu.edu vedadghavami.a@husky.neu.edu.
Chenzhen ZhangDepartments of Bioengineering, Northeastern University, Boston, MA 02115, USA. warren.ma@husky.neu.edu zhang.chenz@husky.neu.edu vedadghavami.a@husky.neu.edu.
Armin VedadghavamiDepartments of Bioengineering, Northeastern University, Boston, MA 02115, USA. warren.ma@husky.neu.edu zhang.chenz@husky.neu.edu vedadghavami.a@husky.neu.edu.
Krister BokvistSanofi SA Global R&D, Frankfurt am Main, Germany. krbo13@hotmail.com.
Pradeep K DhalSanofi SA Global R&D, Waltham, MA 02451, USA. Pradeep.dhal@sanofi.com.ORCID http://orcid.org/0000-0002-7059-855X
Ambika G BajpayeeDepartments of Bioengineering, Northeastern University, Boston, MA 02115, USA. warren.ma@husky.neu.edu zhang.chenz@husky.neu.edu vedadghavami.a@husky.neu.edu and Mechanical Engineering, Northeastern University, Boston, MA 02115, USA. a.bajpayee@northeastern.edu.ORCID http://orcid.org/0000-0002-8458-7464
Northeastern University · USSanofi (France) · FR

Funding

Anti-catabolic drug anchored cationic exosomes for cartilage targeting and repairR21EB028385 · NIBIB · NORTHEASTERN UNIVERSITY · PI BAJPAYEE, AMBIKA GOEL · 2019 to 2021
$628k
NIBIB NIH HHS R21 EB028385
6 · The paper itself

Abstract

Bovine milk-derived exosomes have recently emerged as a promising nano-vehicle for the encapsulation and delivery of macromolecular biotherapeutics. Here we engineer high purity bovine milk exosomes (mExo) with modular surface tunability for oral delivery of small interfering RNA (siRNA). We utilize a low-cost enrichment method combining casein chelation with differential ultracentrifugation followed by size exclusion chromatography, yielding mExo of high concentration and purity. Using in vitro models, we demonstrate that negatively charged hydrophobic mExos can penetrate multiple biological barriers to oral drug delivery. A hydrophilic polyethylene glycol (PEG) coating was introduced on the mExo surface via passive, stable hydrophobic insertion of a conjugated lipid tail, which significantly reduced mExo degradation in acidic gastric environment and enhanced their permeability through mucin by over 3× compared to unmodified mExo. Both mExo and PEG-mExo exhibited high uptake by intestinal epithelial cells and mediated functional intracellular delivery of siRNA, thereby suppressing the expression of the target green fluorescence protein (GFP) gene by up to 70%. We also show that cationic chemical transfection is significantly more efficient in loading siRNA into mExo than electroporation. The simplicity of isolating high purity mExo in high concentrations and equipping them with tunable surface properties, demonstrated here, paves way for the development of mExo as an effective, scalable platform technology for oral drug delivery of siRNA.

Indexed as

ExosomesAnimalsCattleDrug Delivery SystemsMilkMucusPolyethylene GlycolsRNA, Small InterferingPolyethylene GlycolsRNA, Small Interfering

Identifiers

PMID33367332
PMCPMC8205963
OpenAlexW3111375902

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.