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Study · Not a test of the peptide alone · 2026

13 results

Oral Colon- and Mitochondria-Targeted Nanoparticles Alleviate Ulcerative Colitis by Reeducating Macrophage Polarization via SIRT3/FOXO3a-Mediated Mitochondrial Restoration.

Mei R, Zhang R, Li Z, Luo J, Zhang X, Zhang T, Lv G, Zhang J, Liang B, Yan Y

Journal of gastroenterology and hepatology24 Aug 2026

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study13

No result from this study comes from a test of the peptide.

Studies that did not test the peptide alone13

In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Elamipretide (SS-31).

  1. 01AnimalNot a test of Elamipretide (SS-31) aloneAnimal study (in vivo)Pharmacokinetics

    In mice with DSS-induced colitis, oral KSF@SS31@S100Ns accumulated in inflamed colons.

    In plain wordsIn mice with colitis, the swallowed nanoparticles collected in the inflamed colon.

    Outcome
    IncreaseAccumulation in inflamed colon
    Study

    mousen: not reported in source

    DSS-induced colitis
    Outcome group
    Pharmacokinetics · Gastrointestinal

    Source sentences

    Summary
    In vivo, oral KSF@SS31@S100Ns accumulated in inflamed colons, reduced disease severity, suppressed pro-inflammatory cytokines, elevated IL-10, restored tight-junction proteins, and increased M2 macrophages.
    1 context sentence
    Summary · context
    Efficacy and mechanisms were evaluated in a DSS-induced colitis mouse model.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  2. 02AnimalNot a test of Elamipretide (SS-31) aloneAnimal study (in vivo)Efficacy outcome

    In mice with DSS-induced colitis, oral KSF@SS31@S100Ns reduced disease severity.

    In plain wordsIn mice with colitis, the swallowed nanoparticles reduced how severe the disease was.

    Outcome
    DecreaseDisease severity
    Study

    mousen: not reported in source

    DSS-induced colitis
    Outcome group
    Gastrointestinal protection · Gastrointestinal

    Source sentences

    Summary
    In vivo, oral KSF@SS31@S100Ns accumulated in inflamed colons, reduced disease severity, suppressed pro-inflammatory cytokines, elevated IL-10, restored tight-junction proteins, and increased M2 macrophages.
    1 context sentence
    Summary · context
    Efficacy and mechanisms were evaluated in a DSS-induced colitis mouse model.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  3. 03AnimalNot a test of Elamipretide (SS-31) aloneAnimal study (in vivo)Efficacy outcome

    In mice with DSS-induced colitis, oral KSF@SS31@S100Ns suppressed pro-inflammatory cytokines.

    In plain wordsIn mice with colitis, the swallowed nanoparticles lowered inflammatory signal proteins.

    Outcome
    DecreasePro-inflammatory cytokines
    Study

    mousen: not reported in source

    DSS-induced colitis
    Outcome group
    Inflammation markers · Gastrointestinal

    Source sentences

    Summary
    In vivo, oral KSF@SS31@S100Ns accumulated in inflamed colons, reduced disease severity, suppressed pro-inflammatory cytokines, elevated IL-10, restored tight-junction proteins, and increased M2 macrophages.
    1 context sentence
    Summary · context
    Efficacy and mechanisms were evaluated in a DSS-induced colitis mouse model.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  4. 04AnimalNot a test of Elamipretide (SS-31) aloneAnimal study (in vivo)Efficacy outcome

    In mice with DSS-induced colitis, oral KSF@SS31@S100Ns elevated IL-10.

    In plain wordsIn mice with colitis, the swallowed nanoparticles raised IL-10, an anti-inflammatory protein.

    Outcome
    IncreaseIL-10
    Study

    mousen: not reported in source

    DSS-induced colitis
    Outcome group
    Inflammation markers · Gastrointestinal

    Source sentences

    Summary
    In vivo, oral KSF@SS31@S100Ns accumulated in inflamed colons, reduced disease severity, suppressed pro-inflammatory cytokines, elevated IL-10, restored tight-junction proteins, and increased M2 macrophages.
    1 context sentence
    Summary · context
    Efficacy and mechanisms were evaluated in a DSS-induced colitis mouse model.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  5. 05AnimalNot a test of Elamipretide (SS-31) aloneAnimal study (in vivo)Efficacy outcome

    In mice with DSS-induced colitis, oral KSF@SS31@S100Ns restored tight-junction proteins.

    In plain wordsIn mice with colitis, the swallowed nanoparticles restored proteins that seal the gut wall.

    Outcome
    IncreaseTight-junction proteins
    Study

    mousen: not reported in source

    DSS-induced colitis
    Outcome group
    Gastrointestinal protection · Gastrointestinal

    Source sentences

    Summary
    In vivo, oral KSF@SS31@S100Ns accumulated in inflamed colons, reduced disease severity, suppressed pro-inflammatory cytokines, elevated IL-10, restored tight-junction proteins, and increased M2 macrophages.
    1 context sentence
    Summary · context
    Efficacy and mechanisms were evaluated in a DSS-induced colitis mouse model.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  6. 06AnimalNot a test of Elamipretide (SS-31) aloneAnimal study (in vivo)Efficacy outcome

    In mice with DSS-induced colitis, oral KSF@SS31@S100Ns increased M2 macrophages.

    In plain wordsIn mice with colitis, the swallowed nanoparticles increased anti-inflammatory macrophages.

    Outcome
    IncreaseM2 macrophages
    Study

    mousen: not reported in source

    DSS-induced colitis
    Outcome group
    Immune response · Gastrointestinal

    Source sentences

    Summary
    In vivo, oral KSF@SS31@S100Ns accumulated in inflamed colons, reduced disease severity, suppressed pro-inflammatory cytokines, elevated IL-10, restored tight-junction proteins, and increased M2 macrophages.
    1 context sentence
    Summary · context
    Efficacy and mechanisms were evaluated in a DSS-induced colitis mouse model.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  7. 07LabNot a test of Elamipretide (SS-31) aloneIn vitro (cells)Activity measurement

    In macrophages, SS‑31 on the kaempferol nanoparticles enhanced macrophage uptake and mitochondrial localization.

    In plain wordsIn cells, the SS‑31 on the nanoparticles helped macrophages take them up and bring them to mitochondria.

    Outcome
    IncreaseMacrophage uptake and mitochondrial localization
    Study

    n: not reported in source

    LPS-stimulated RAW264.7 cells
    Outcome group
    Mitochondrial function · Immune and inflammation

    Source sentences

    Summary
    SS-31 enhanced macrophage uptake and mitochondrial localization.
    1 context sentence
    Summary · context
    Mitochondrial function, macrophage polarization, and SIRT3/FOXO3a signaling were assessed in LPS-stimulated RAW264.7 cells.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  8. 08LabNot a test of Elamipretide (SS-31) aloneIn vitro (cells)Mechanism

    In LPS-stimulated RAW264.7 cells, KSF@SS31Ns restored mitochondrial membrane potential.

    In plain wordsIn cells, the nanoparticles restored mitochondrial membrane potential.

    Outcome
    IncreaseMitochondrial membrane potential
    Study

    n: not reported in source

    LPS-stimulated RAW264.7 cells
    Outcome group
    Mitochondrial function · Immune and inflammation

    Source sentences

    Summary
    In vitro, KSF@SS31Ns restored mitochondrial membrane potential and ATP, reduced ROS, promoted mitophagy, and shifted macrophages toward the M2 phenotype via SIRT3/FOXO3a activation.
    1 context sentence
    Summary · context
    Mitochondrial function, macrophage polarization, and SIRT3/FOXO3a signaling were assessed in LPS-stimulated RAW264.7 cells.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  9. 09LabNot a test of Elamipretide (SS-31) aloneIn vitro (cells)Mechanism

    In LPS-stimulated RAW264.7 cells, KSF@SS31Ns restored ATP.

    In plain wordsIn cells, the nanoparticles restored energy (ATP) levels.

    Outcome
    IncreaseATP level
    Study

    n: not reported in source

    LPS-stimulated RAW264.7 cells
    Outcome group
    Mitochondrial function · Immune and inflammation

    Source sentences

    Summary
    In vitro, KSF@SS31Ns restored mitochondrial membrane potential and ATP, reduced ROS, promoted mitophagy, and shifted macrophages toward the M2 phenotype via SIRT3/FOXO3a activation.
    1 context sentence
    Summary · context
    Mitochondrial function, macrophage polarization, and SIRT3/FOXO3a signaling were assessed in LPS-stimulated RAW264.7 cells.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  10. 10LabNot a test of Elamipretide (SS-31) aloneIn vitro (cells)Mechanism

    In LPS-stimulated RAW264.7 cells, KSF@SS31Ns reduced ROS.

    In plain wordsIn cells, the nanoparticles reduced harmful oxygen molecules.

    Outcome
    DecreaseROS
    Study

    n: not reported in source

    LPS-stimulated RAW264.7 cells
    Outcome group
    Inflammation markers · Immune and inflammation

    Source sentences

    Summary
    In vitro, KSF@SS31Ns restored mitochondrial membrane potential and ATP, reduced ROS, promoted mitophagy, and shifted macrophages toward the M2 phenotype via SIRT3/FOXO3a activation.
    1 context sentence
    Summary · context
    Mitochondrial function, macrophage polarization, and SIRT3/FOXO3a signaling were assessed in LPS-stimulated RAW264.7 cells.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  11. 11LabNot a test of Elamipretide (SS-31) aloneIn vitro (cells)Mechanism

    In LPS-stimulated RAW264.7 cells, KSF@SS31Ns promoted mitophagy.

    In plain wordsIn cells, the nanoparticles promoted the clearing of damaged mitochondria.

    Outcome
    IncreaseMitophagy
    Study

    n: not reported in source

    LPS-stimulated RAW264.7 cells
    Outcome group
    Mitochondrial function · Immune and inflammation

    Source sentences

    Summary
    In vitro, KSF@SS31Ns restored mitochondrial membrane potential and ATP, reduced ROS, promoted mitophagy, and shifted macrophages toward the M2 phenotype via SIRT3/FOXO3a activation.
    1 context sentence
    Summary · context
    Mitochondrial function, macrophage polarization, and SIRT3/FOXO3a signaling were assessed in LPS-stimulated RAW264.7 cells.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  12. 12LabNot a test of Elamipretide (SS-31) aloneIn vitro (cells)Mechanism

    In LPS-stimulated RAW264.7 cells, KSF@SS31Ns shifted macrophages toward the M2 phenotype via SIRT3/FOXO3a activation.

    In plain wordsIn cells, the nanoparticles shifted macrophages to an anti-inflammatory type through SIRT3 and FOXO3a signals.

    Outcome
    IncreaseM2 macrophage polarization via SIRT3/FOXO3a
    Study

    n: not reported in source

    LPS-stimulated RAW264.7 cells
    Outcome group
    Immune response · Immune and inflammation

    Source sentences

    Summary
    In vitro, KSF@SS31Ns restored mitochondrial membrane potential and ATP, reduced ROS, promoted mitophagy, and shifted macrophages toward the M2 phenotype via SIRT3/FOXO3a activation.
    1 context sentence
    Summary · context
    Mitochondrial function, macrophage polarization, and SIRT3/FOXO3a signaling were assessed in LPS-stimulated RAW264.7 cells.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

  13. 13LabNot a test of Elamipretide (SS-31) aloneIn vitro (cell-free)Other

    The KSF@SS31@S100Ns nanoparticles showed uniform size, high stability and pH-dependent release.

    In plain wordsIn lab tests, the nanoparticles had an even size, stayed stable and released their load depending on pH.

    Outcome
    Not applicableNanoparticle size, stability and release
    Study

    n: not reported in source

    nanoparticles
    Outcome group
    Formulation, delivery and stability · Pharmacology

    Measurements

    Particle size
    ≈ 307 nm

    Source sentences

    Summary
    Nanoparticles showed uniform size (~307 nm), high stability, and pH-dependent release.
    1 context sentence
    Summary · context
    Kaempferol-loaded silk fibroin (SF) nanoparticles were conjugated with SS-31 peptide and coated with pH-sensitive Eudragit S100.

    In this study, Elamipretide (SS-31) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Elamipretide (SS-31).

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    10 Oct 2026, 08:19 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 02:47 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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