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Study · Animal study (in vivo) · rat · 2019

5 results

Long-term oral administration of Exendin-4 to control type 2 diabetes in a rat model.

Suzuki K, Kim KS, Bae YH

Journal of controlled release : official journal of the Controlled Release Society18 Dec 2018Cited by 56 (Europe PMC)

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 study5

3 results from studies that gave the peptide. No result from this study comes from people.

  1. 01AnimalAnimal study (in vivo)Pharmacokinetics

    In rats, oral EL-CSG had relative bioavailability of 19.5% versus subcutaneous Ex-4.

    In plain wordsIn rats, oral EL-CSG had 19.5% relative bioavailability versus subcutaneous Ex-4.

    Outcome
    Not applicableRelative oral bioavailability
    Study

    ratn: not reported in source

    type 2 diabetes rat model
    Comparator
    subcutaneous Ex-4 20 μg/kg
    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    200 μg/kg · oralAs given in this study (rat).

    Source sentences

    Summary
    In rat models, a single oral dose (200 μg/kg) of EL-CSG showed a relative oral bioavailability of 19.5%, compared with subcutaneous administration (20 μg/kg), and sustained pharmacokinetics for up to 72 h.
  2. 02AnimalAnimal study (in vivo)Pharmacokinetics

    In rats, a single oral EL-CSG dose sustained pharmacokinetics for up to 72 h.

    In plain wordsIn rats, oral EL-CSG sustained pharmacokinetics for up to 72 h.

    Outcome
    Not applicableSustained pharmacokinetics
    Study

    ratn: not reported in source

    type 2 diabetes rat model
    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    200 μg/kg · oralAs given in this study (rat).

    Source sentences

    Summary
    In rat models, a single oral dose (200 μg/kg) of EL-CSG showed a relative oral bioavailability of 19.5%, compared with subcutaneous administration (20 μg/kg), and sustained pharmacokinetics for up to 72 h.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In rats, oral EL-CSG had overall effects assessed by HbA1c, weight and lipids equivalent to or better than injected free Ex-4.

    In plain wordsIn rats, overall effects of oral EL-CSG were equivalent to or better than injected free Ex-4.

    Outcome
    MixedOverall long-term pharmacodynamic effects
    Study

    ratn: not reported in source

    type 2 diabetes rat model
    Comparator
    daily subcutaneous free Ex-4 20 μg/kg
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    300 μg/kg daily · oral · four weeksAs given in this study (rat).

    Source sentences

    Summary
    The overall long-term pharmacodynamic effects, assessed by hemoglobin A1c (HbA1c), body weight, and blood lipid concentrations, of daily oral EL-CSG (300 μg/kg) for four weeks were equivalent to or better than daily subcutaneous injections of free Ex-4 solution (20 μg/kg).

Studies that did not test the peptide alone2

In this study, Exenatide (exendin-4) 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 Exenatide (exendin-4).

  1. 04LabNot a test of Exenatide (exendin-4) aloneIn vitro (cell-free)Activity measurement

    In lab tests, EL-CSG liposomes had an Ex-4 loading efficiency of 77%.

    In plain wordsIn lab tests, EL-CSG liposomes loaded Ex-4 with 77% efficiency.

    Outcome
    Not applicableLoading efficiency
    Study

    n: not reported in source

    EL-CSG liposomes
    Outcome group
    Pharmacokinetics · Pharmacology

    Measurements

    Loading efficiency
    77%
    EL-CSG

    Source sentences

    Summary
    The Ex-4 loading efficiency was 77% and the loading content in the nanoparticles was 1 wt-%.

    In this study, Exenatide (exendin-4) 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 Exenatide (exendin-4).

  2. 05LabNot a test of Exenatide (exendin-4) aloneIn vitro (cell-free)Activity measurement

    In lab tests, Ex-4 loading content was 1 wt-%.

    In plain wordsIn lab tests, Ex-4 loading content was 1 wt-%.

    Outcome
    Not applicableLoading content
    Study

    n: not reported in source

    EL-CSG liposomes
    Outcome group
    Pharmacokinetics · Pharmacology

    Source sentences

    Summary
    The Ex-4 loading efficiency was 77% and the loading content in the nanoparticles was 1 wt-%.

    In this study, Exenatide (exendin-4) 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 Exenatide (exendin-4).

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

    22 Oct 2026, 02:26 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 18:59 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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