Evidence map›Paper›PMID 40626548›Full record

ArticleACS applied materials & interfaces2025

Controlled Release of Microorganisms from Engineered Living Materials.

Manivannan Sivaperuman Kalairaj, Iris George, Sasha M George, Sofía E Farfán, Yoo Jin Lee, Laura K Rivera-Tarazona, Suitu Wang, Mustafa K Abdelrahman, Seelay Tasmim, Asaf Dana and 3 more

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Manivannan Sivaperuman KalairajDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States.ORCID 0000-0002-3218-7135
Iris GeorgeDepartment of Veterinary Pathobiology, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas 77843, United States.
Sasha M GeorgeDepartment of Materials Science and Engineering, Texas A&M University, College Station, Texas 77843, United States.ORCID 0009-0007-8640-3343
Sofía E FarfánDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States.
Yoo Jin LeeDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States.
Laura K Rivera-TarazonaDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States.
Suitu WangDepartment of Materials Science and Engineering, Texas A&M University, College Station, Texas 77843, United States.
Mustafa K AbdelrahmanDepartment of Materials Science and Engineering, Texas A&M University, College Station, Texas 77843, United States.
Seelay TasmimDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States.
Asaf DanaDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States.
Philippe E ZimmernDepartment of Urology, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.ORCID 0000-0002-7612-2042
Sargurunathan SubashchandraboseDepartment of Veterinary Pathobiology, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas 77843, United States.
Taylor H WareDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States.ORCID 0000-0001-7996-7393

Funding

Copper is a Host Effector in Protection Against Urinary Tract InfectionR01DK114224 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SUBASHCHANDRABOSE, SARGURUNATHAN · 2018 to 2022
$1.7M
Engineered Living Materials for the Delivery of Engineered Probiotics and TherapeuticsR56EB032395 · NIBIB · TEXAS ENGINEERING EXPERIMENT STATION · PI WARE, TAYLOR H · 2022 to 2022
$788k
NIBIB NIH HHS R56 EB032395NIDDK NIH HHS R01 DK114224
6 · The paper itself

Abstract

Probiotics offer therapeutic benefits by modulating the local microbiome, the host immune response, and the proliferation of pathogens. Probiotics have the potential to treat complex diseases, but their persistence or colonization is required at the target site for effective treatment. Although probiotic persistence can be achieved by repeated delivery, no biomaterial that releases clinically relevant doses of metabolically active probiotics in a sustained manner has been previously described. Here, we encapsulate stiff probiotic microorganisms within relatively less stiff hydrogels and show a generic mechanism where these microorganisms proliferate and induce hydrogel fracture, resulting in microbial release. Importantly, this fracture-based mechanism leads to microorganism release with zero-order release kinetics. Using this mechanism, small (∼1 μL) engineered living materials (ELMs) release >10

Indexed as

Biocompatible MaterialsEscherichia coliHydrogelsProbioticsDelayed-Action PreparationsBiocompatible MaterialsDelayed-Action PreparationsHydrogelscontrolled releaseengineered living materialsprobioticssustained releasezero-order release

Identifiers

PMID40626548
PMCPMC12278213

What OpenQuestion holds

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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.