In vitro investigation of anti-inflammatory activity of propolis/saffron extract/curcumin-loaded ZIF8 nanoparticles and their potential application for treating osteoarthritis
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
van den Bosch MH. Osteoarthritis year in review 2020: biology. Osteoarthr Cartil. 2021;29(2): 143–50. doi: 10.1016/j.joca.2020.10.006van den BoschMH.Osteoarthritis year in review 2020: biology. . 2021;29(2): 143–50. doi: 10.1016/j.joca.2020.10.006Open DOISearch in Google Scholar
Cai X, Yuan S, Zeng Y, Wang C, Yu N, Ding C. New trends in pharmacological treatments for osteoarthritis. Front Pharmacol. 2021;12: 645842. doi: 10.3389/fphar.2021.645842CaiXYuanSZengYWangCYuNDingC.New trends in pharmacological treatments for osteoarthritis. . 2021;12: 645842. doi: 10.3389/fphar.2021.645842Open DOISearch in Google Scholar
Li X-Z, Zhang SN. Recent advance in treatment of osteoarthritis by bioactive components from herbal medicine. Chin Med. 2020;15(1): 80. doi: 10.1186/s13020-020-00363-5LiX-ZZhangSN.Recent advance in treatment of osteoarthritis by bioactive components from herbal medicine. . 2020;15(1): 80. doi: 10.1186/s13020-020-00363-5Open DOISearch in Google Scholar
Arias C, Vásquez B, Salazar LA. Propolis as a potential therapeutic agent to counteract age-related changes in cartilage: an in vivo study. Int J Mol Sci. 2023;24(18): 14272. doi: 10.3390/ijms241814272AriasCVásquezBSalazarLA.Propolis as a potential therapeutic agent to counteract age-related changes in cartilage: an in vivo study. . 2023;24(18): 14272. doi: 10.3390/ijms241814272Open DOISearch in Google Scholar
Boneva B, Marchev A, Amirova K, Ganova P, Georgiev M, Tchorbanov A, Mihaylova N. Crocus sativus extract as a biological agent for disease-modifying gherapy of collagenase-induced mouse model of osteoarthritis. Life (Basel). 2023;13(4): 894. doi: 10.3390/life13040894BonevaBMarchevAAmirovaKGanovaPGeorgievMTchorbanovAMihaylovaN.Crocus sativus extract as a biological agent for disease-modifying gherapy of collagenase-induced mouse model of osteoarthritis. . 2023;13(4): 894. doi: 10.3390/life13040894Open DOISearch in Google Scholar
Zeng L, Yu G, Hao W, Yang K, Chen H. The efficacy and safety of Curcuma longa extract and curcumin supplements on osteoarthritis: a systematic review and meta-analysis. Biosci Rep. 2021;41(6): BSR20210817. doi: 10.1042/BSR20210817ZengLYuGHaoWYangKChenH.The efficacy and safety of Curcuma longa extract and curcumin supplements on osteoarthritis: a systematic review and meta-analysis. . 2021;41(6): BSR20210817. doi: 10.1042/BSR20210817Open DOISearch in Google Scholar
Almuhayawi MS. Propolis as a novel antibacterial agent. Saudi J Biol Sci. 2020;27(11): 3079–3086. doi: 10.1016/j.sjbs.2020.09.016AlmuhayawiMS.Propolis as a novel antibacterial agent. . 2020;27(11): 3079–3086. doi: 10.1016/j.sjbs.2020.09.016Open DOISearch in Google Scholar
Silva H, Francisco R, Saraiva A, Francisco S, Carrascosa C, Raposo A. The cardiovascular therapeutic potential of propolis—a comprehensive review. Biology (Basel). 2021;10(1): 27. doi: 10.3390/biology10010027SilvaHFranciscoRSaraivaAFranciscoSCarrascosaCRaposoA.The cardiovascular therapeutic potential of propolis—a comprehensive review. . 2021;10(1): 27. doi: 10.3390/biology10010027Open DOISearch in Google Scholar
Xing B, Li S, Yang J, Lin D, Feng Y, Lu J, Shao Q. Phytochemistry, pharmacology, and potential clinical applications of saffron: a review. J Ethnopharmacol. 2021;281: 114555. doi: 10.1016/j.jep.2021.114555XingBLiSYangJLinDFengYLuJShaoQ.Phytochemistry, pharmacology, and potential clinical applications of saffron: a review. . 2021;281: 114555. doi: 10.1016/j.jep.2021.114555Open DOISearch in Google Scholar
Vafaei S, Wu X, Tu J, Nematollahi-Mahani SN. The effects of crocin on bone and cartilage diseases. Front Pharmacol. 2022;12: 830331. doi: 10.3389/fphar.2021.830331VafaeiSWuXTuJNematollahi-MahaniSN.The effects of crocin on bone and cartilage diseases. . 2022;12: 830331. doi: 10.3389/fphar.2021.830331Open DOISearch in Google Scholar
Beevers CS, Huang S. Pharmacological and clinical properties of curcumin. Botanics: Targets Therapy. 2011(1): 5–18.BeeversCSHuangS.Pharmacological and clinical properties of curcumin. . 2011(1): 5–18.Search in Google Scholar
Henrotin Y, Priem F, Mobasheri A. Curcumin: a new paradigm and therapeutic opportunity for the treatment of osteoarthritis: curcumin for osteoarthritis management. Springerplus. 2013;2: 1–9. doi: 10.1186/2193-1801-2-56HenrotinYPriemFMobasheriA.Curcumin: a new paradigm and therapeutic opportunity for the treatment of osteoarthritis: curcumin for osteoarthritis management. . 2013;2: 1–9. doi: 10.1186/2193-1801-2-56Open DOISearch in Google Scholar
Bonifacio BV, da Silva PB, Dos Santos Ramos MA, Silveira Negri KM, Bauab TM, Chorilli M. Nanotechnology-based drug delivery systems and herbal medicines: a review. Int J Nanomedicine. 2014;9: 1–15.BonifacioBVda SilvaPBDos Santos RamosMASilveira NegriKMBauabTMChorilliM.Nanotechnology-based drug delivery systems and herbal medicines: a review. . 2014;9: 1–15.Search in Google Scholar
Wang Q, Sun Y, Li S, Zhang P, Yao Q. Synthesis and modification of ZIF-8 and its application in drug delivery and tumor therapy. RSC Advances. 2020;10(62): 37600–37620. DOI: 10.1039/D0RA07950BWangQSunYLiSZhangPYaoQ.Synthesis and modification of ZIF-8 and its application in drug delivery and tumor therapy. . 2020;10(62): 37600–37620. DOI: 10.1039/D0RA07950BOpen DOISearch in Google Scholar
Cai W, Zhang W, Chen Z. Magnetic Fe3O4@ ZIF-8 nanoparticles as a drug release vehicle: pH-sensitive release of norfloxacin and its antibacterial activity. Colloids Surf B. 2023;223: 113170. doi: 10.1016/j.colsurfb.2023.113170CaiWZhangWChenZ.Magnetic Fe3O4@ ZIF-8 nanoparticles as a drug release vehicle: pH-sensitive release of norfloxacin and its antibacterial activity. . 2023;223: 113170. doi: 10.1016/j.colsurfb.2023.113170Open DOISearch in Google Scholar
Zhang H, Zhao M, Lin Y. Stability of ZIF-8 in water under ambient conditions. Microporous Mesoporous Mater. 2019;279: 201–210. doi: 10.1016/j.micromeso.2018.12.035ZhangHZhaoMLinY.Stability of ZIF-8 in water under ambient conditions. . 2019;279: 201–210. doi: 10.1016/j.micromeso.2018.12.035Open DOISearch in Google Scholar
Xie H, Liu X, Huang Z, Xu L, Bai R, He F, et al. Nanoscale zeolitic imidazolate framework (ZIF)–8 in cancer theranostics: current challenges and prospects. Cancers (Basel). 2022;14(16): 3935. doi: 10.3390/cancers14163935’XieHLiuXHuangZXuLBaiRHeFNanoscale zeolitic imidazolate framework (ZIF)–8 in cancer theranostics: current challenges and prospects. . 2022;14(16): 3935. doi: 10.3390/cancers14163935’Open DOISearch in Google Scholar
Jin L, Wang S, Chen C, Qiu X, Wang C-C. ZIF-8 nanoparticles induce behavior abnormality and brain oxidative stress in adult zebrafish (Danio rerio). Antioxidants (Basel). 2023;12(7): 1345. doi: 10.3390/antiox12071345JinLWangSChenCQiuXWangC-C.ZIF-8 nanoparticles induce behavior abnormality and brain oxidative stress in adult zebrafish (Danio rerio). . 2023;12(7): 1345. doi: 10.3390/antiox12071345Open DOISearch in Google Scholar
Li Z, Shao Y, Yang Y, Zan J. Zeolitic imidazolate framework-8: a versatile nanoplatform for tissue regeneration. Front Bioeng Biotechnol. 2024;12: 1386534. doi: 10.3389/fbioe.2024.1386534LiZShaoYYangYZanJ.Zeolitic imidazolate framework-8: a versatile nanoplatform for tissue regeneration. . 2024;12: 1386534. doi: 10.3389/fbioe.2024.1386534Open DOISearch in Google Scholar
Shi L, Wu J, Qiao X, Ha Y, Peng C, Wu R. In situ biomimetic mineralization on ZIF-8 for smart drug delivery. ACS Biomater Sci Eng. 2020;6(8): 4595–4603. doi: 10.1021/acsbiomaterials.0c00935ShiLWuJQiaoXHaYPengCWuR.In situ biomimetic mineralization on ZIF-8 for smart drug delivery. . 2020;6(8): 4595–4603. doi: 10.1021/acsbiomaterials.0c00935Open DOISearch in Google Scholar
Chen P, He M, Chen B. Size- and dose-dependent cytotoxicity of ZIF-8 based on single cell analysis. Ecotoxicol Environ Saf. 2020;205: 111110. doi: 10.1016/j.ecoenv.2020.111110ChenPHeMChenB.Size- and dose-dependent cytotoxicity of ZIF-8 based on single cell analysis. . 2020;205: 111110. doi: 10.1016/j.ecoenv.2020.111110Open DOISearch in Google Scholar
Yang C, Wen J, Xue Z, Yin X, Li Y, Yuan L. The accumulation and toxicity of ZIF-8 nanoparticles in Corbicula fluminea. J Environ Sci (China). 2023;127: 91–101. doi: 10.1016/j.jes.2022.03.020YangCWenJXueZYinXLiYYuanL.The accumulation and toxicity of ZIF-8 nanoparticles in Corbicula fluminea. . 2023;127: 91–101. doi: 10.1016/j.jes.2022.03.020Open DOISearch in Google Scholar
Ramos A, Miranda JD. Propolis: a review of its antiinflammatory and healing actions. J VA TiTD. 2007;13: 697–710. doi: 10.1590/S1678-91992007000400002RamosAMirandaJD.Propolis: a review of its antiinflammatory and healing actions. . 2007;13: 697–710. doi: 10.1590/S1678-91992007000400002Open DOISearch in Google Scholar
Zulhendri F, Lesmana R, Tandean S, Christoper A, Chandrasekaran K, Irsyam I, et al. Recent update on the anti-inflammatory activities of propolis. Molecules. 2022;27(23): 8473. doi: 10.3390/molecules27238473ZulhendriFLesmanaRTandeanSChristoperAChandrasekaranKIrsyamIRecent update on the anti-inflammatory activities of propolis. . 2022;27(23): 8473. doi: 10.3390/molecules27238473Open DOISearch in Google Scholar
Borrelli F, Maffia P, Pinto L, Ianaro A, Russo A, Capasso F, Ialenti A. Phytochemical compounds involved in the anti-inflammatory effect of propolis extract. Fitoterapia. 2002;73: S53–S63. doi: 10.1016/S0367-326X(02)00191-0BorrelliFMaffiaPPintoLIanaroARussoACapassoFIalentiA.Phytochemical compounds involved in the anti-inflammatory effect of propolis extract. . 2002;73: S53–S63. doi: 10.1016/S0367-326X(02)00191-0Open DOISearch in Google Scholar
Valenzuela-Barra G, Castro C, Figueroa C, Barriga A, Silva X, Las Heras B, et al. Anti-inflammatory activity and phenolic profile of propolis from two locations in Región Metropolitana de Santiago, Chile. J Ethnopharmacol. 2015;168: 37–44. doi: 10.1016/j.jep.2015.03.050Valenzuela-BarraGCastroCFigueroaCBarrigaASilvaXLas HerasBAnti-inflammatory activity and phenolic profile of propolis from two locations in Región Metropolitana de Santiago, Chile. . 2015;168: 37–44. doi: 10.1016/j.jep.2015.03.050Open DOISearch in Google Scholar
Hsieh CY, Li LH, Rao YK, Ju TC, Nai YS, Chen YW, Hua KF. Mechanistic insight into the attenuation of gouty inflammation by Taiwanese green propolis via inhibition of the NLRP3 inflammasome. J Cell Physiol. 2019;234(4): 4081–4094. doi: 10.1002/jcp.27204HsiehCYLiLHRaoYKJuTCNaiYSChenYWHuaKF.Mechanistic insight into the attenuation of gouty inflammation by Taiwanese green propolis via inhibition of the NLRP3 inflammasome. . 2019;234(4): 4081–4094. doi: 10.1002/jcp.27204Open DOISearch in Google Scholar
Puspasari A, Harijanti K, Soebadi B, Hendarti HT, Radithia D, Ernawati DS. Effects of topical application of propolis extract on fibroblast growth factor-2 and fibroblast expression in the traumatic ulcers of diabetic Rattus norvegicus. J Oral Maxillofac Pathol. 2018;22(1): 54–58. DOI: 10.4103/jomfp.JOMFP_82_17PuspasariAHarijantiKSoebadiBHendartiHTRadithiaDErnawatiDS.Effects of topical application of propolis extract on fibroblast growth factor-2 and fibroblast expression in the traumatic ulcers of diabetic Rattus norvegicus. . 2018;22(1): 54–58. DOI: 10.4103/jomfp.JOMFP_82_17Open DOISearch in Google Scholar