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The Gradual Release of Alendronate for the Treatment of Critical Bone Defects in Osteoporotic and Control Rats

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378041%3A_____%2F23%3A00580757" target="_blank" >RIV/68378041:_____/23:00580757 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11110/23:10466456 RIV/00216208:11140/23:10466456 RIV/00064165:_____/23:10466456

  • Result on the web

    <a href="https://www.dovepress.com/the-gradual-release-of-alendronate-for-the-treatment-of-critical-bone--peer-reviewed-fulltext-article-IJN" target="_blank" >https://www.dovepress.com/the-gradual-release-of-alendronate-for-the-treatment-of-critical-bone--peer-reviewed-fulltext-article-IJN</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2147/IJN.S386784" target="_blank" >10.2147/IJN.S386784</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    The Gradual Release of Alendronate for the Treatment of Critical Bone Defects in Osteoporotic and Control Rats

  • Original language description

    Purpose: Osteoporosis is a severe health problem with social and economic impacts on society. The standard treatment consists of the systemic administration of drugs such as bisphosphonates, with alendronate (ALN) being one of the most common. Nevertheless, complications of systemic administration occur with this drug. Therefore, it is necessary to develop new strategies, such as local administration.Methods: In this study, emulsion/dispersion scaffolds based on W/O emulsion of PCL and PF68 with ALN, containing hydroxyapatite (HA) nanoparticles as the dispersion phase were prepared using electrospinning. Scaffolds with different release kinetics were tested in vitro on the co-cultures of osteoblasts and osteoclast-like cells, isolated from adult osteoporotic and control rats. Cell viability, proliferation, ALP, TRAP and CA II activity were examined. A scaffold with a gradual release of ALN was tested in vivo in the bone defects of osteoporotic and control rats.Results: The release kinetics were dependent on the scaffold composition and the used system of the poloxamers. The ALN was released from the scaffolds for more than 22 days. The behavior of cells cultured in vitro on scaffolds with different release kinetics was comparable. The difference was evident between cell co-cultures isolated from osteoporotic and control animals. The PCL/HA scaffold show slow degradation in vivo and residual scaffold limited new bone formation inside the defects. Nevertheless, the released ALN supported bone formation in the areas surrounding the residual scaffold. Interestingly, a positive effect of systemic administration of ALN was not proved.Conclusion: The prepared scaffolds enabled tunable control release of ALN. The effect of ALN was proved in vitro and in in vivo study supported peri-implant bone formation.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30404 - Biomaterials (as related to medical implants, devices, sensors)

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2023

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    International Journal of Nanomedicine

  • ISSN

    1178-2013

  • e-ISSN

    1178-2013

  • Volume of the periodical

    18

  • Issue of the periodical within the volume

    mar.

  • Country of publishing house

    NZ - NEW ZEALAND

  • Number of pages

    20

  • Pages from-to

    541-560

  • UT code for WoS article

    000927119000001

  • EID of the result in the Scopus database

    2-s2.0-85147427143