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Study · Animal study (in vivo) · rat · 2021

7 results

Simultaneous incorporation of PTH(1-34) and nano-hydroxyapatite into Chitosan/Alginate Hydrogels for efficient bone regeneration.

Zou Z, Wang L, Zhou Z, Sun Q, Liu D, Chen Y, Hu H, Cai Y, Lin S, Yu Z, Tan B, Guo W, Ling Z, Zou X

Bioactive materials7 Dec 2020Cited by 83 (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: CC BY-NC-ND. Results still quote short attributed sentences.

Results from this study7

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

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In rats with cranial defects, hydrogel containing nHAP and PTH(1-34) promoted bone regeneration compared with hydrogel containing nHAP.

    In plain wordsIn rats with skull defects, hydrogel containing nHAP and PTH(1-34) improved bone regeneration compared with hydrogel containing nHAP.

    Outcome
    IncreaseCranial bone regeneration versus nHAP hydrogel
    Study

    ratn: not reported in source

    rat cranial defect
    Comparator
    hydrogel with nHAP
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    Dose not stated · implantationAs given in this study (rat).

    Source sentences

    Summary
    Implantation of the complex hydrogel into a rat cranial defect model led to efficient bone regeneration compared to the rats treated with the hydrogel alone or with nHAP, indicating the simultaneous therapeutic effect of nHAP and PTH during the treatment process.
  2. 02LabIn vitro (cells)Efficacy outcome

    In BMSCs, increasing PTH(1-34) content in hydrogels enhanced osteogenic differentiation.

    In plain wordsIn lab tests, increasing PTH(1-34) content in hydrogels increased bone-forming differentiation compared with lower content.

    Outcome
    IncreasePTH-content-dependent osteogenic differentiation
    Study

    ratn: not reported in source

    rat bone marrow mesenchymal stem cells
    Comparator
    lower PTH(1-34) hydrogel content
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    Dose not stated

    Source sentences

    Summary
    We found that increasing the content of PTH(1-34) in the hydrogels resulted in enhanced osteogenic differentiation of BMSCs.

Studies that did not test the peptide alone5

In this study, Teriparatide (PTH 1-34) 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 Teriparatide (PTH 1-34).

  1. 03AnimalNot a test of Teriparatide (PTH 1-34) aloneAnimal study (in vivo)Efficacy outcome

    In rats with cranial defects, hydrogel containing nHAP and PTH(1-34) promoted bone regeneration compared with hydrogel alone.

    In plain wordsIn rats with skull defects, hydrogel containing nHAP and PTH(1-34) improved bone regeneration compared with hydrogel alone.

    Outcome
    IncreaseCranial bone regeneration versus hydrogel
    Study

    ratn: not reported in source

    rat cranial defect
    Comparator
    hydrogel alone
    Outcome group
    Bone and joint · Musculoskeletal

    Source sentences

    Summary
    Implantation of the complex hydrogel into a rat cranial defect model led to efficient bone regeneration compared to the rats treated with the hydrogel alone or with nHAP, indicating the simultaneous therapeutic effect of nHAP and PTH during the treatment process.

    In this study, Teriparatide (PTH 1-34) 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 Teriparatide (PTH 1-34).

  2. 04LabNot a test of Teriparatide (PTH 1-34) aloneIn vitro (cells)Safety outcome

    In rat bone marrow mesenchymal stem-cell experiments, hydrogel containing nHAP and PTH(1-34) showed strong biocompatibility.

    In plain wordsIn lab tests with rat bone marrow cells, hydrogel containing nHAP and PTH(1-34) showed strong biocompatibility.

    Outcome
    Not applicableBiocompatibility
    Study

    ratn: not reported in source

    rat bone marrow mesenchymal stem cells
    Outcome group
    Adverse events · Musculoskeletal

    Source sentences

    Summary
    In vitro experiments showed that the hydrogel containing nHAP and PTH(1-34) exhibited strong biocompatibility and facilitated osteogenic differentiation of rat bone marrow mesenchymal stem cells (rBMSCs) via the Notch signaling pathway, as shown by the upregulated expression of osteogenic-related proteins.

    In this study, Teriparatide (PTH 1-34) 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 Teriparatide (PTH 1-34).

  3. 05LabNot a test of Teriparatide (PTH 1-34) aloneIn vitro (cells)Efficacy outcome

    In rat bone marrow mesenchymal stem cells, hydrogel containing nHAP and PTH(1-34) facilitated osteogenic differentiation via Notch signaling.

    In plain wordsIn rat cells, hydrogel containing nHAP and PTH(1-34) promoted development into bone-forming cells through Notch signaling.

    Outcome
    IncreaseOsteogenic differentiation
    Study

    ratn: not reported in source

    rat bone marrow mesenchymal stem cells
    Outcome group
    Bone and joint · Musculoskeletal

    Source sentences

    Summary
    In vitro experiments showed that the hydrogel containing nHAP and PTH(1-34) exhibited strong biocompatibility and facilitated osteogenic differentiation of rat bone marrow mesenchymal stem cells (rBMSCs) via the Notch signaling pathway, as shown by the upregulated expression of osteogenic-related proteins.

    In this study, Teriparatide (PTH 1-34) 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 Teriparatide (PTH 1-34).

  4. 06LabNot a test of Teriparatide (PTH 1-34) aloneIn vitro (cells)Mechanism

    In rat bone marrow mesenchymal stem cells, hydrogel containing nHAP and PTH(1-34) increased osteogenic-related protein expression.

    In plain wordsIn rat cells, hydrogel containing nHAP and PTH(1-34) increased proteins associated with bone formation.

    Outcome
    IncreaseOsteogenic-related protein expression
    Study

    ratn: not reported in source

    rat bone marrow mesenchymal stem cells
    Outcome group
    Bone and joint · Musculoskeletal

    Source sentences

    Summary
    In vitro experiments showed that the hydrogel containing nHAP and PTH(1-34) exhibited strong biocompatibility and facilitated osteogenic differentiation of rat bone marrow mesenchymal stem cells (rBMSCs) via the Notch signaling pathway, as shown by the upregulated expression of osteogenic-related proteins.

    In this study, Teriparatide (PTH 1-34) 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 Teriparatide (PTH 1-34).

  5. 07LabNot a test of Teriparatide (PTH 1-34) aloneIn vitro (cell-free)Activity measurement

    In hydrogel tests, mechanical properties were almost maintained after adding nHAP and PTH(1-34).

    In plain wordsIn lab tests, hydrogel mechanical properties were almost unchanged after adding nHAP and PTH(1-34).

    Outcome
    Direction not reportedHydrogel mechanical properties
    Study

    n: not reported in source

    chitosan/alginate hydrogels
    Comparator
    hydrogel before nHAP and PTH(1-34) addition
    Outcome group
    Bone and joint · Musculoskeletal

    Source sentences

    Summary
    Rheological characterizations revealed that the mechanical properties of the hydrogels were almost maintained upon the addition of nHAP and PTH(1-34).

    In this study, Teriparatide (PTH 1-34) 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 Teriparatide (PTH 1-34).

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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