Optimizing protein delivery rate from silk fibroin hydrogel using silk fibroin-mimetic peptides conjugation.
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
23 Feb 2024
23 Feb 2024
Historique:
received:
27
06
2023
accepted:
03
02
2024
medline:
24
2
2024
pubmed:
24
2
2024
entrez:
23
2
2024
Statut:
epublish
Résumé
Controlled release of proteins, such as growth factors, from biocompatible silk fibroin (SF) hydrogel is valuable for its use in tissue engineering, drug delivery, and other biological systems. To achieve this, we introduced silk fibroin-mimetic peptides (SFMPs) with the repeating unit (GAGAGS)
Identifiants
pubmed: 38395958
doi: 10.1038/s41598-024-53689-7
pii: 10.1038/s41598-024-53689-7
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
4428Subventions
Organisme : Research Assistantship Funding from Faculty of Science, Chulalongkorn University
ID : RAF_2562_012
Organisme : Program Management Unit for Human Resources & Institutional Development, Research, and Innovation
ID : B05F640156
Organisme : Basic Science Research Program through the National Research Foundation of Korea (NRF) by the Ministry of Education
ID : 2020R1I1A1A01073559
Organisme : Brain Pool program of the National Research Foundation (NRF) by the Korean government (MOE and MSIT)
ID : 2021H1D3A2A02045561
Organisme : Brain Pool program of the National Research Foundation (NRF) by the Korean government (MOE and MSIT)
ID : RS-2023-00208587
Organisme : Thailand Science research and Innovation Fund Chulalongkorn University
ID : CU_FRB65_hea (74)_168_21_34
Organisme : The Asahi Glass Foundation through CU-AGF grant 2022
ID : RES_66_111_2100_011
Organisme : Institute for the Promotion of Teaching Science and Technology (IPST) under the Research Fund for DPST Graduate with First Placement
ID : 08/2559
Organisme : Center of Excellence in Molecular Crop, Chulalongkorn University
ID : CE66-042_2300_009
Informations de copyright
© 2024. The Author(s).
Références
Park, K. Controlled drug delivery systems: Past forward and future back. J. Control Release 190, 3–8 (2014).
doi: 10.1016/j.jconrel.2014.03.054
pubmed: 24794901
pmcid: 4142099
Nguyen, T. P. et al. Silk fibroin-based biomaterials for biomedical applications: A review. Polymers 11, 1933 (2019).
doi: 10.3390/polym11121933
pubmed: 31771251
pmcid: 6960760
Watchararot, T., Prasongchean, W. & Thongnuek, P. Angiogenic property of silk fibroin scaffolds with adipose-derived stem cells on chick chorioallantoic membrane. R. Soc. Open Sci. 8, 201618 (2021).
doi: 10.1098/rsos.201618
pubmed: 33959331
pmcid: 8074929
Manissorn, J. et al. Osteogenic enhancement of silk fibroin-based bone scaffolds by forming hybrid composites with bioactive glass through GPTMS during sol-gel process. Mater. Today Commun. 26, 101730 (2021).
doi: 10.1016/j.mtcomm.2020.101730
Li, G. & Sun, S. Silk fibroin-based biomaterials for tissue engineering applications. In Molecules (2022).
Duangpakdee, A. et al. Crosslinked silk fibroin/gelatin/hyaluronan blends as scaffolds for cell-based tissue engineering. Molecules 26, 3191 (2021).
doi: 10.3390/molecules26113191
pubmed: 34073542
pmcid: 8198693
Mita, K., Ichimura, S. & James, T. C. Highly repetitive structure and its organization of the silk fibroin gene. J. Mol. Evol. 38, 583–592 (1994).
doi: 10.1007/BF00175878
pubmed: 7916056
Hu, X., Kaplan, D. & Cebe, P. Determining beta-sheet crystallinity in fibrous proteins by thermal analysis and infrared spectroscopy. Macromolecules 39, 6161–6170 (2006).
doi: 10.1021/ma0610109
de Moraes, M. A., AlbrechtMahl, C. R., FerreiraSilva, M. & Beppu, M. M. Formation of silk fibroin hydrogel and evaluation of its drug release profile. J. Appl. Polym. Sci. https://doi.org/10.1002/app.41802 (2015).
doi: 10.1002/app.41802
Zhong, T. et al. Silk fibroin/copolymer composite hydrogels for the controlled and sustained release of hydrophobic/hydrophilic drugs. Int. J. Pharm. 494, 264–270 (2015).
doi: 10.1016/j.ijpharm.2015.08.035
pubmed: 26283278
Lu, Q. et al. Stabilization and release of enzymes from silk films. Macromol. Biosci. 10, 359–368 (2010).
doi: 10.1002/mabi.200900388
pubmed: 20217856
Hofmann, S. et al. Silk fibroin as an organic polymer for controlled drug delivery. J. Control. Release 111, 219–227 (2006).
doi: 10.1016/j.jconrel.2005.12.009
pubmed: 16458987
Chattopadhyay, S., Murphy, C. J., McAnulty, J. F. & Raines, R. T. Peptides that anneal to natural collagen in vitro and ex vivo. Org. Biomol. Chem. 10, 5892–5897 (2012).
doi: 10.1039/c2ob25190f
pubmed: 22522497
pmcid: 3395758
Matsumoto, A. et al. Mechanisms of silk fibroin sol-gel transitions. J. Phys. Chem. B 110, 21630–21638 (2006).
doi: 10.1021/jp056350v
pubmed: 17064118
Wojcik-Pastuszka, D. et al. Evaluation of the release kinetics of a pharmacologically active substance from model intra-articular implants replacing the cruciate ligaments of the knee. Materials 12, 1202 (2019).
doi: 10.3390/ma12081202
pubmed: 31013801
pmcid: 6515312
Manan, F. A. A. et al. Drug release profiles of mitomycin c encapsulated quantum dots-chitosan nanocarrier system for the possible treatment of non-muscle invasive bladder cancer. Pharmaceutics 13, 1379 (2021).
doi: 10.3390/pharmaceutics13091379
pubmed: 34575455
pmcid: 8469644
Laomeephol, C. et al. Phospholipid-induced silk fibroin hydrogels and their potential as cell carriers for tissue regeneration. J. Tissue Eng. Regen. Med. 14, 160–172 (2020).
doi: 10.1002/term.2982
pubmed: 31671250
Tungtasana, H. et al. Tissue response and biodegradation of composite scaffolds prepared from Thai silk fibroin, gelatin and hydroxyapatite. J. Mater. Sci. Mater. Med. 21, 3151–3162 (2010).
doi: 10.1007/s10856-010-4159-5
pubmed: 20976530
Ritger, P. L. & Peppas, N. A. A simple equation for description of solute release II. Fickian and anomalous release from swellable devices. J. Control. Release 5, 37–42 (1987).
doi: 10.1016/0168-3659(87)90035-6
Puerta, M., Peresin, M. S. & Restrepo-Osorio, A. Effects of chemical post-treatments on structural and physicochemical properties of silk fibroin films obtained from silk fibrous waste. Front. Bioeng. Biotechnol. 8, 523949 (2020).
doi: 10.3389/fbioe.2020.523949
pubmed: 33344426
pmcid: 7738614
Sapudom, J. et al. Degradation products of crosslinked silk fibroin scaffolds modulate the immune response but not cell toxicity. J. Mater. Chem. B 11, 3607–3616 (2023).
doi: 10.1039/D3TB00097D
pubmed: 37013997
Pritchard, E. M. & Kaplan, D. L. Silk fibroin biomaterials for controlled release drug delivery. Expert Opin. Drug Deliv. 8, 797–811 (2011).
doi: 10.1517/17425247.2011.568936
pubmed: 21453189
Li, J. & Mooney, D. J. Designing hydrogels for controlled drug delivery. Nat. Rev. Mater. https://doi.org/10.1038/natrevmats.2016.71 (2016).
doi: 10.1038/natrevmats.2016.71
pubmed: 29657852
pmcid: 5898614
Yan, L. P. et al. Tumor growth suppression induced by biomimetic silk fibroin hydrogels. Sci. Rep. 6, 31037 (2016).
doi: 10.1038/srep31037
pubmed: 27485515
pmcid: 4971568
Partlow, B. P. et al. Highly tunable elastomeric silk biomaterials. Adv. Funct. Mater. 24, 4615–4624 (2014).
doi: 10.1002/adfm.201400526
pubmed: 25395921
pmcid: 4225629
Huemmerich, D. et al. Primary structure elements of spider dragline silks and their contribution to protein solubility. Biochemistry 43, 13604–13612 (2004).
doi: 10.1021/bi048983q
pubmed: 15491167
Humenik, M., Magdeburg, M. & Scheibel, T. Influence of repeat numbers on self-assembly rates of repetitive recombinant spider silk proteins. J. Struct. Biol. 186, 431–437 (2014).
doi: 10.1016/j.jsb.2014.03.010
pubmed: 24657229
Wang, X. et al. Silk microspheres for encapsulation and controlled release. J. Control. Release 117, 360–370 (2007).
doi: 10.1016/j.jconrel.2006.11.021
pubmed: 17218036
Reeves, A. R., Spiller, K. L., Freytes, D. O., Vunjak-Novakovic, G. & Kaplan, D. L. Controlled release of cytokines using silk-biomaterials for macrophage polarization. Biomaterials 73, 272–283 (2015).
doi: 10.1016/j.biomaterials.2015.09.027
pubmed: 26421484
pmcid: 4605898
Elango, J. et al. The relationship of rheological properties and the performance of silk fibroin hydrogels in tissue engineering application. Process Biochem. 125, 198–211 (2023).
doi: 10.1016/j.procbio.2022.12.012
Roy, S., Sharma, A. & Ghosh, S. Macrophage polarization profiling on native and regenerated silk biomaterials. ACS Biomater. Sci. Eng. 8, 659–671 (2022).
doi: 10.1021/acsbiomaterials.1c01432
pubmed: 35089695
Midha, S., Tripathi, R., Geng, H., Lee, P. D. & Ghosh, S. Elucidation of differential mineralisation on native and regenerated silk matrices. Mater. Sci. Eng. C Mater. Biol. Appl. 68, 663–674 (2016).
doi: 10.1016/j.msec.2016.06.041
pubmed: 27524066
Su, D. et al. Enhancing mechanical properties of silk fibroin hydrogel through restricting the growth of beta-sheet domains. ACS Appl. Mater. Interfaces 9, 17489–17498 (2017).
doi: 10.1021/acsami.7b04623
pubmed: 28470062
Johari, N., Moroni, L. & Samadikuchaksaraei, A. Tuning the conformation and mechanical properties of silk fibroin hydrogels. Eur. Polym. J. 134, 109842 (2020).
doi: 10.1016/j.eurpolymj.2020.109842
Wu, N. et al. Investigation on the structure and mechanical properties of highly tunable elastomeric silk fibroin hydrogels cross-linked by gamma-ray radiation. ACS Appl. Bio Mater. 3, 721–734 (2020).
doi: 10.1021/acsabm.9b01062
pubmed: 35019416
Zimmer, M. Green fluorescent protein (GFP): Applications, structure, and related photophysical behavior. Chem. Rev. 102, 759–781 (2002).
doi: 10.1021/cr010142r
pubmed: 11890756
Keten, S., Xu, Z., Ihle, B. & Buehler, M. J. Nanoconfinement controls stiffness, strength and mechanical toughness of beta-sheet crystals in silk. Nat. Mater. 9, 359–367 (2010).
doi: 10.1038/nmat2704
pubmed: 20228820
Huang, W., Ling, S., Li, C., Omenetto, F. G. & Kaplan, D. L. Silkworm silk-based materials and devices generated using bio-nanotechnology. Chem. Soc. Rev. 47, 6486–6504 (2018).
doi: 10.1039/C8CS00187A
pubmed: 29938722
pmcid: 6113080
Li, P., Zhong, Y., Wang, X. & Hao, J. Enzyme-regulated healable polymeric hydrogels. ACS Cent. Sci. 6, 1507–1522 (2020).
doi: 10.1021/acscentsci.0c00768
pubmed: 32999926
pmcid: 7517121
Jolayemi, O. L. et al. Protein-based biostimulants to enhance plant growth—state-of-the-art and future direction with sugar beet as an example. In Agronomy (2022)
Rojas, J. E. U. et al. Silk fibroin hydrogels for potential applications in photodynamic therapy. Biopolymers 110, e23245 (2019).
doi: 10.1002/bip.23245
pubmed: 30548859
Calixto, G., Yoshii, A. C., Rocha e Silva, H., Stringhetti Ferreira Cury, B. & Chorilli, M. Polyacrylic acid polymers hydrogels intended to topical drug delivery: Preparation and characterization. Pharm. Dev. Technol. 20, 490–496 (2015).
doi: 10.3109/10837450.2014.882941
pubmed: 25975700