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Study · Not a test of the peptide alone · 2025

7 results

A thorough LC-MS/MS strategy to quantify abaloparatide in rat plasma: method development, validation and application.

Kong Y, Li X, Li Y, Tan Y, Li T, Xiao Y, Zhang L, Yu Q, Rong R

Analytical methods : advancing methods and applications2 Oct 2025

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 study7

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

Studies that did not test the peptide alone7

In this study, Abaloparatide (Tymlos) 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 Abaloparatide (Tymlos).

  1. 01LabNot a test of Abaloparatide (Tymlos) aloneIn vitro (cell-free)Other

    In rat plasma analysis, abaloparatide separation on a positively charged surface hybrid column gave reliable chromatography without strong ion-pairing reagents.

    In plain wordsIn lab tests, a positively charged column reliably separated abaloparatide without strong ion-pairing reagents.

    Outcome
    Not applicableChromatographic separation
    Study

    ratn: not reported in source

    rat plasma LC-MS/MS assay
    Outcome group
    Analytical methods and detection · Pharmacology

    Source sentences

    Summary
    Plasma samples were purified by protein precipitation, and abaloparatide was then chromatographically separated on a positively charged surface hybrid column, which offered reliable chromatographic results without the addition of any strong ion-pairing reagents.

    In this study, Abaloparatide (Tymlos) 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 Abaloparatide (Tymlos).

  2. 02LabNot a test of Abaloparatide (Tymlos) aloneIn vitro (cell-free)Other

    In an LC-MS/MS assay, the selected abaloparatide ion transition was 566.512 to 632.488.

    In plain wordsIn lab tests, the assay selected a specific abaloparatide ion transition for detection.

    Outcome
    Not applicableMass spectrometry ion transition
    Study

    ratn: not reported in source

    rat plasma LC-MS/MS assay
    Outcome group
    Analytical methods and detection · Pharmacology

    Source sentences

    Summary
    Ion transitions of m/z 566.512 (7+) → 632.488 for abaloparatide and 687.05 (6+) → 787.26 for the internal standard (teriparatide) were selected for multiple-reaction mass spectrometry detections.

    In this study, Abaloparatide (Tymlos) 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 Abaloparatide (Tymlos).

  3. 03LabNot a test of Abaloparatide (Tymlos) aloneIn vitro (cell-free)Other

    In rat plasma, the abaloparatide assay was accurate and precise over 0.02 to 8 ng mL-1.

    In plain wordsIn lab tests, the abaloparatide assay was accurate and precise over the reported concentration range.

    Outcome
    Not applicableValidated quantification range
    Study

    ratn: not reported in source

    rat plasma LC-MS/MS assay
    Outcome group
    Analytical methods and detection · Pharmacology

    Measurements

    Validated concentration range
    0.02 to 8 ng/mL
    rat plasma assay

    Source sentences

    Summary
    The method was validated over a range of 0.02 to 8 ng mL-1 and was further demonstrated to be accurate and precise.

    In this study, Abaloparatide (Tymlos) 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 Abaloparatide (Tymlos).

  4. 04LabNot a test of Abaloparatide (Tymlos) aloneIn vitro (cell-free)Other

    In rat plasma analysis, abaloparatide recovery was 88.7-103%.

    In plain wordsIn lab tests, abaloparatide recovery from plasma was 88.7-103%.

    Outcome
    Not applicableAbaloparatide recovery
    Study

    ratn: not reported in source

    rat plasma LC-MS/MS assay
    Outcome group
    Analytical methods and detection · Pharmacology

    Measurements

    Recovery
    88.7 to 103%
    abaloparatide

    Source sentences

    Summary
    Meanwhile, the method presented acceptable recoveries for abaloparatide (88.7-103%) and the internal standard (102%), and there was no significant matrix effect.

    In this study, Abaloparatide (Tymlos) 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 Abaloparatide (Tymlos).

  5. 05LabNot a test of Abaloparatide (Tymlos) aloneIn vitro (cell-free)Other

    In rat plasma analysis, the abaloparatide assay showed no significant matrix effect.

    In plain wordsIn lab tests, the abaloparatide assay showed no significant plasma matrix effect.

    Outcome
    No significant changeMatrix effect
    Study

    ratn: not reported in source

    rat plasma LC-MS/MS assay
    Outcome group
    Analytical methods and detection · Pharmacology

    Source sentences

    Summary
    Meanwhile, the method presented acceptable recoveries for abaloparatide (88.7-103%) and the internal standard (102%), and there was no significant matrix effect.

    In this study, Abaloparatide (Tymlos) 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 Abaloparatide (Tymlos).

  6. 06LabNot a test of Abaloparatide (Tymlos) aloneIn vitro (cell-free)Other

    In rat plasma, abaloparatide remained stable under the reported refrigerated, frozen-storage and freeze-thaw conditions.

    In plain wordsIn lab tests, abaloparatide remained stable under the reported refrigerated, frozen-storage and freeze-thaw conditions.

    Outcome
    No significant changeStability under handling and storage conditions
    Study

    ratn: not reported in source

    rat plasma LC-MS/MS assay
    Outcome group
    Analytical methods and detection · Pharmacology

    Source sentences

    Summary
    Abaloparatide was proved to be stable under the conditions of 4 °C for 2 h at -80 °C for 50 days and three freeze-thaw cycles (-80 °C to 4 °C).

    In this study, Abaloparatide (Tymlos) 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 Abaloparatide (Tymlos).

  7. 07LabNot a test of Abaloparatide (Tymlos) aloneIn vitro (cell-free)Other

    In rats, the abaloparatide assay was successfully applied to a pharmacokinetic study after subcutaneous administration.

    In plain wordsIn lab tests, the assay successfully measured abaloparatide for a rat pharmacokinetic study after subcutaneous administration.

    Outcome
    Not applicableApplication to rat pharmacokinetics
    Study

    ratn: not reported in source

    rat plasma LC-MS/MS assay
    Outcome group
    Analytical methods and detection · Pharmacology

    Source sentences

    Summary
    The method was successfully applied to the pharmacokinetic study of abaloparatide in rats after subcutaneous administration.

    In this study, Abaloparatide (Tymlos) 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 Abaloparatide (Tymlos).

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, 02:25 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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