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The aim of this study was to obtain degradable poly(Llactide-co-glycolide) (PLGA) microparticles (MPs) with a controlled size for bottom-up bone tissue engineering. The particles were produced using the classical single water/oil emulsification method by mixing with a magnetic stirrer and by using a novel approach based on the application of a microfluidic device. This study involved a thorough investigation of different concentrations of PLGA and poly(vinyl alcohol) (PVA) during microparticle fabrication. The oil phase was PLGA dissolved in dichloromethane or ethyl acetate at 1%, 2% and 4% w/v concentrations. The water phase was an aqueous solution of PVA at concentrations of 0.5%, 1%, 2%, 2.5%, 4% and 5% w/v. The size and size distribution of the MPs were evaluated with an optical microscope. Obtained MPs were incubated in contact with osteoblast-like MG-63 cells and after days 1 and 3, the cell viability was evaluated using the reduction of resazurin and the fluorescence live/dead staining. The results showed that for each concentration of PVA, the size of the MPs increased with an increase in the concentration of PLGA in the oil phase. The MPs obtained with the use of the microfluidic device were characterized by a smaller size and lower polydispersity compared to those obtained with emulsification by mixing. Both methods resulted in the generation of MPs cytocompatible with MG-63 cells, what paves the way to consider them as scaffolds for bottom-up tissue engineering.
Czasopismo
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Tom
Strony
18--22
Opis fizyczny
Bibliogr. 16 poz., rys., tab., wykr., zdj.
Twórcy
autor
- AGH University of Krakow, Faculty of Materials Science and Ceramics, Department of Biomaterials and Composites, al. A. Mickiewicza 30, 30-059 Krakow, Poland
- AGH University of Krakow, Faculty of Materials Science and Ceramics, Department of Biomaterials and Composites, al. A. Mickiewicza 30, 30-059 Krakow, Poland
autor
- AGH University of Krakow, Faculty of Materials Science and Ceramics, Department of Biomaterials and Composites, al. A. Mickiewicza 30, 30-059 Krakow, Poland
Bibliografia
- [1] Liu Z., Yuan X., Liu M., Fernandes G., Zhang Y., Yang S., Ionita C.N., Yang S.: Antimicrobial Peptide Combined with BMP2-Modified Mesenchymal Stem Cells Promotes Calvarial Repair in an Osteolytic Model. Molecular Therapy 26(1) (2018) 199-207. https://doi.org/10.1016/j.ymthe.2017.09.011
- [2] Kang Y., Jabbari, E., Yang Y.: Integrating Top‐Down and Bottom‐Up Scaffolding Tissue Engineering Approach for Bone Regeneration. In: Micro and Nanotechnologies in Engineering Stem Cells and Tissues, 1st ed., Ramalingam M., Jabbari E., Ramakrishna S., Khademhosseini A. Eds. Wiley (2013) 142-158. https://doi.org/10.1002/9781118574775.ch6.
- [3] Schmidt T., Xiang Y., Bao X., Sun T.: A Paradigm Shift in Tissue Engineering: From a Top–Down to a Bottom–Up Strategy. Processes 9(6) (2021) 935. https://doi.org/10.3390/pr9060935.
- [4] Nichol J.W., Khademhosseini A.: Modular tissue engineering: engineering biological tissues from the bottom up. Soft Matter 5(7) (2009) 1312-1319. https://doi.org/10.1039/b814285h.
- [5] Jin S., Xia X., Huang J., Yuan C., Zuo Y., Li Y., Li J.: Recent advances in PLGA-based biomaterials for bone tissue regeneration. Acta Biomater. 127(2021) 56-79. https://doi.org/10.1016/j.actbio.2021.03.067.
- [6] Martins C., Sousa F., Araújo F., Sarmento B.: Functionalizing PLGA and PLGA Derivatives for Drug Delivery and Tissue Regeneration Applications. Adv Healthc Mater. 7(1) (2018). https://doi.org/10.1002/adhm.201701035.
- [7] Kim G., Gavande V., Shaikh V., Lee W-K.: Degradation Behavior of Poly(Lactide-Co-Glycolide) Monolayers Investigated by Langmuir Technique: Accelerating Effect. Molecules. 28(12) (2023) 4810. https://doi.org/10.3390/molecules28124810
- [8] Mielan B., Sousa D.M., Krok-Borkowicz M., Eloy P., Dupont C., Lamghari M., Pamuła E.: Polymeric Microspheres/Cells/Extracellular Matrix Constructs Produced by Auto-Assembly for Bone Modular Tissue Engineering. Int J Mol Sci. 22(15) (2021) 7897. https://doi.org/10.3390/ijms22157897
- [9] Mielan B., Pamuła E.: Optimizing manufacturing conditions of polymer microspheres as cell carriers for modular tissue engineering. Eng.Biomat. 156 (2020) 2-9. https://doi.org/10.34821/eng.biomat.156.2020.2-9
- [10] Lin Z., Wu J., Qiao W., Zhao Y., Wong K.H.M., Chu P.K., Bian L., Wu S., Zheng Y., Cheung K.M.C., Leung F., Yeung K.W.K.: Precisely controlled delivery of magnesium ions thru sponge-like monodisperse PLGA/nano-MgO-alginate core-shell microsphere device to enable in-situ bone regeneration. Biomaterials. 174 (2018) 1-16. https://doi.org/10.1016/j.biomaterials.2018.05.011.
- [11] Li W., Zhang L., Ge X., Xu B., Zhang W., Qu L., Choi C.H., Xu J., Zhang A., Lee H., Weitz D.A.: Microfluidic fabrication of microparticles for biomedical applications. Chem Soc Rev. 47(15) (2018) 5646-5683. https://doi.org/10.1039/c7cs00263g.
- [12] Fluigent. Microfluidic Droplet Production Method [online]. https://www.fluigent.com/resources-support/expertise/expertise-reviews/droplet-and-particle-generation-in-microfluidics/microfluidic-droplet-production-method. Accessed: Jun. 21, 2023.
- [13] Pudełko I., Moskwik A., Kwiecień K., Kriegseis S., KrokBorkowicz M., Schickle K., et al. Porous Zirconia Scaffolds Functionalized with Calcium Phosphate Layers and PLGA Nanoparticles Loaded with Hydrophobic Gentamicin. International Journal of Molecular Sciences 24(9) (2023) 8400. https://doi.org/10.3390/ijms24098400
- [14] Rumian Ł., Wolf-Brandstetter C., Rößler S., Reczyńska K., Tiainen H., Haugen H.J., Scharnweber D., Pamuła E.: Sodium alendronate loaded poly(l-lactide- co-glycolide) microparticles immobilized on ceramic scaffolds for local treatment of bone defects. Regenerative Biomaterials 8(3) (2021) rbaa012. https://doi.org/10.1093/rb/rbaa012
- [15] Cichoń E., Czechowska J.P., Krok-Borkowicz M., Allinson S.L., Stępień K., Smith A., Pamuła E., Douglas T.E.L., Zima A.: Biosurfactants as foaming agents in calcium phosphate bone cements. Biomaterials Advance 145 (2023) 213273. https://doi.org/10.1016/j.bioadv.2022.213273
- [16] ISO 10993-5:2009. Biological evaluation of medical devices. Part 5: Tests for in vitro cytotoxicity
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Bibliografia
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