References
- Spencer, J. P. E. Proceedings of the Third International Scientific Symposium on Tea and Human Health: Role of Flavonoids in the Diet Metabolism of Tea Flavonoids in the Gastrointestinal Tract 1, 2. J. Nutr. 2003, 133, 3255–3261.
- Yang, C.; Wang, H. Cancer Preventive Activities of Tea Catechins. Molecules. 2016, 21, 1679. DOI: https://doi.org/10.3390/molecules21121679.
- Higdon, J. V.; Frei, B. Tea Catechins and Polyphenols: Health Effects, Metabolism, and Antioxidant Functions. Crit Rev Food Sci Nutr 2003, 43, 89–143. DOI: https://doi.org/10.1080/10408690390826464.
- Zaveri, N. T. Green Tea and Its Polyphenolic Catechins: Medicinal Uses in Cancer and Noncancer Applications. Life Sci. 2006, 78, 2073–2080. DOI: https://doi.org/10.1016/j.lfs.2005.12.006.
- Roychoudhury, S.; Agarwal, A.; Virk, G.; Cho, C. L. Potential Role of Green Tea Catechins in the Management of Oxidative Stress-Associated Infertility. Reprod. Biomed. Online. 2017, 34, 487–498. DOI: https://doi.org/10.1016/j.rbmo.2017.02.006.
- Chen, W.; Zhu, X.; Lu, Q.; Zhang, L.; Wang, X.; Liu, R. C-Ring Cleavage Metabolites of Catechin and Epicatechin Enhanced Antioxidant Activities through Intestinal Microbiota. Food Res Int 2020, 135, 109271. DOI: https://doi.org/10.1016/j.foodres.2020.109271.
- Sies, H. Oxidative Stress: Oxidants and Antioxidants. Exp. Physiol. 1997, 82, 291–295. DOI: https://doi.org/10.1113/expphysiol.1997.sp004024.
- Ramassamy, C. Emerging Role of Polyphenolic Compounds in the Treatment of Neurodegenerative Diseases: A Review of Their Intracellular Targets. Eur. J. Pharmacol. 2006, 545, 51–64. DOI: https://doi.org/10.1016/j.ejphar.2006.06.025.
- Lim, J.; Kim, D. K.; Shin, H.; Hamaker, B. R.; Lee, B. H. Different Inhibition Properties of Catechins on the Individual Subunits of Mucosal α-Glucosidases as Measured by Partially-Purified Rat Intestinal Extract. Food Funct. 2019, 10, 4407–4413. DOI: https://doi.org/10.1039/c9fo00990f.
- Steele, V. E.; Kelloff, G. J.; Balentine, D.; Boone, C. W.; Mehta, R.; Bagheri, D.; Sigman, C. C.; Zhu, S.; Sharma, S. Comparative Chemopreventive Mechanisms of Green Tea, Black Tea and Selected Polyphenol Extracts Measured by in Vitro Bioassays. Carcinogenesis. 2000, 21, 63–67. DOI: https://doi.org/10.1093/carcin/21.1.63.
- Min, K.; Kwon, T. K. Anticancer Effects and Molecular Mechanisms of Epigallocatechin-3-Gallate. Integr. Med. Res. 2014, 3, 16–24. DOI: https://doi.org/10.1016/j.imr.2013.12.001.
- Yang, C. S.; Wang, X.; Lu, G.; Picinich, S. C. Cancer Prevention by Tea: Animal Studies, Molecular Mechanisms and Human Relevance. Nat. Rev. Cancer. 2009, 9, 429–439. DOI: https://doi.org/10.1038/nrc2641.
- Yuan, J. M.; Sun, C.; Butler, L. M. Tea and Cancer Prevention: Epidemiological Studies. Pharmacol. Res. 2011, 64, 123–135. DOI: https://doi.org/10.1016/j.phrs.2011.03.002.
- Walimbe, T.; Panitch, A.; Sivasankar, P. M. A Review of Hyaluronic Acid and Hyaluronic Acid-Based Hydrogels for Vocal Fold Tissue Engineering. J. Voice. 2017, 31, 416–423. DOI: https://doi.org/10.1016/j.jvoice.2016.11.014.
- Jung, Y. D.; Kim, M. S.; Shin, B. A.; Chay, K. O.; Ahn, B. W.; Liu, W.; Bucana, C. D.; Gallick, G. E.; Ellis, L. M. EGCG, a Major Component of Green Tea, Inhibits Tumour Growth by Inhibiting VEGF Induction in Human Colon Carcinoma Cells. Br. J. Cancer. 2001, 84, 844–850. DOI: https://doi.org/10.1054/bjoc.2000.1691.
- Vittorio, O.; Cirillo, G.; Iemma, F.; Di Turi, G.; Jacchetti, E.; Curcio, M.; Barbuti, S.; Funel, N.; Parisi, O. I.; Puoci, F.; Picci, N. Dextran-Catechin Conjugate: A Potential Treatment against the Pancreatic Ductal Adenocarcinoma. Pharm. Res. 2012, 29, 2601–2614. DOI: https://doi.org/10.1007/s11095-012-0790-9.
- Al-Hazzani, A. A.; Alshatwi, A. A. Catechin Hydrate Inhibits Proliferation and Mediates Apoptosis of SiHa Human Cervical Cancer Cells. Food Chem. Toxicol. 2011, 49, 3281–3286. DOI: https://doi.org/10.1016/j.fct.2011.09.023.
- Alshatwi, A. A. Catechin Hydrate Suppresses MCF-7 Proliferation through TP53/Caspase-Mediated Apoptosis. J. Exp. Clin. Cancer Res. 2010, 29, 1–9. DOI: https://doi.org/10.1186/1756-9966-29-167.
- Leone, M.; Zhai, D.; Sareth, S.; Kitada, S.; Reed, J. C.; Pellecchia, M. Cancer Prevention by Tea Polyphenols is Linked to Their Direct Inhibition of Antiapoptotic Bcl-2-Family Proteins. Cancer Res. 2003, 63, 8118–8121.
- Pfeffer, C. M.; Singh, A. T. K. Apoptosis: A Target for Anticancer Therapy. Int. J. Mol. Sci. 2018, 19, 448. DOI: https://doi.org/10.3390/ijms19020448..
- Ezzat, H. M.; Elnaggar, Y. S. R.; Abdallah, O. Y. Improved Oral Bioavailability of the Anticancer Drug Catechin Using Chitosomes: Design, In-Vitro Appraisal and In-Vivo Studies. Int. J. Pharm. 2019, 565, 488–498. DOI: https://doi.org/10.1016/j.ijpharm.2019.05.034.
- Senapati, S.; Mahanta, A. K.; Kumar, S.; Maiti, P. Controlled Drug Delivery Vehicles for Cancer Treatment and Their Performance. Signal Transduct. Target. Ther. 2018, 3, 1–19. DOI: https://doi.org/10.1038/s41392-017-0004-3.
- Davda, J.; Labhasetwar, V. Characterization of Nanoparticle Uptake by Endothelial Cells. Int. J. Pharm. 2002, 233, 51–59. DOI: https://doi.org/10.1016/s0378-5173(01)00923-1.
- Behzadi, S.; Serpooshan, V.; Tao, W.; Hamaly, M. A.; Alkawareek, M. Y.; Dreaden, E. C.; Brown, D.; Alkilany, A. M.; Farokhzad, O. C.; Mahmoudi, M. Cellular Uptake of Nanoparticles: Journey Inside the Cell. Chem. Soc. Rev. 2017, 46, 4218–4244. DOI: https://doi.org/10.1039/c6cs00636a.
- Parveen, S.; Sahoo, S. K. Polymeric Nanoparticles for Cancer Therapy. J. Drug Target. 2008, 16, 108–123. DOI: https://doi.org/10.1080/10611860701794353.
- Indoria, S.; Singh, V.; Hsieh, M. F. Recent Advances in Theranostic Polymeric Nanoparticles for Cancer Treatment: A Review. Int. J. Pharm. 2020, 582, 119314. DOI: https://doi.org/10.1016/j.ijpharm.2020.119314.
- Sahiner, N. One Step Poly(Quercetin) Particle Preparation as Biocolloid and its Characterization. Colloids Surfaces A Physicochem. Eng. Asp. 2014, 452, 173–180. DOI: https://doi.org/10.1016/j.colsurfa.2014.03.097.
- Sahiner, N.; Sagbas, S.; Aktas, N.; Silan, C. Inherently Antioxidant and Antimicrobial Tannic Acid Release from Poly(Tannic Acid) Nanoparticles with Controllable Degradability. Colloids Surfaces B Biointerfaces. 2016, 142, 334–343. DOI: https://doi.org/10.1016/j.colsurfb.2016.03.006.
- Andrews, N. C. Forging a Field: The Golden Age of Iron Biology. Blood. 2008, 112, 219–230. DOI: https://doi.org/10.1182/blood-2007-12-077388.
- Zhou, T.; Ma, Y.; Kong, X.; Hider, R. C. Design of Iron Chelators with Therapeutic Application. Dalton Trans. 2012, 41, 6371–6389. DOI: https://doi.org/10.1039/c2dt12159j.
- Hatcher, H. C.; Singh, R. N.; Torti, F. M.; Torti, S. V. Synthetic and Natural Iron Chelators: Therapeutic Potential and Clinical Use. Future Med. Chem. 2009, 1, 1643–1670. DOI: https://doi.org/10.4155/fmc.09.121.
- Buss, J.; Torti, F.; Torti, S. The Role of Iron Chelation in Cancer Therapy. Curr. Med. Chem. 2003, 10, 1021–1034. DOI: https://doi.org/10.2174/0929867033457638.
- Tang, H.; Huang, L.; Zhao, D.; Sun, C.; Song, P. Interaction Mechanism of Flavonoids on Bovine Serum Albumin: Insights from Molecular Property-Binding Affinity Relationship. Spectrochim. Acta A Mol. Biomol. Spectrosc. 2020, 239, 118519. DOI: https://doi.org/10.1016/j.saa.2020.118519.
- Estrada Valencia, M.; Herrera-Arozamena, C.; de Andrés, L.; Pérez, C.; Morales-García, J. A.; Pérez-Castillo, A.; Ramos, E.; Romero, A.; Viña, D.; Yáñez, M.; et al. Neurogenic and Neuroprotective Donepezil-Flavonoid Hybrids with Sigma-1 Affinity and Inhibition of Key Enzymes in Alzheimer’s disease. Eur. J. Med. Chem. 2018, 156, 534–553. DOI: https://doi.org/10.1016/j.ejmech.2018.07.026.
- Forester, S. C.; Gu, Y.; Lambert, J. D. Inhibition of Starch Digestion by the Green Tea Polyphenol, (-)-epigallocatechin-3-gallate. Mol. Nutr. Food Res. 2012, 56, 1647–1654. DOI: https://doi.org/10.1002/mnfr.201200206.
- Li, Y.; Ma, D.; Sun, D.; Wang, C.; Zhang, J.; Xie, Y.; Guo, T. Total Phenolic, Flavonoid Content, and Antioxidant Activity of Flour, Noodles, and Steamed Bread Made from Different Colored Wheat Grains by Three Milling Methods. Crop J. 2015, 3, 328–334. DOI: https://doi.org/10.1016/j.cj.2015.04.004.
- Tadapaneni, R. K.; Banaszewski, K.; Patazca, E.; Edirisinghe, I.; Cappozzo, J.; Jackson, L.; Burton-Freeman, B. Effect of High-Pressure Processing and Milk on the Anthocyanin Composition and Antioxidant Capacity of Strawberry-Based Beverages. J. Agric. Food Chem. 2012, 60, 5795–5802. DOI: https://doi.org/10.1021/jf2035059.
- Sudan, R.; Bhagat, M.; Gupta, S.; Singh, J.; Koul, A. Iron (FeII) Chelation, Ferric Reducing Antioxidant Power, and Immune Modulating Potential of Arisaema Jacquemontii (Himalayan Cobra Lily). Biomed. Res. Int. 2014, 2014, 179865–179867. DOI: https://doi.org/10.1155/2014/179865.
- Aghebati-Maleki, A.; Dolati, S.; Ahmadi, M.; Baghbanzhadeh, A.; Asadi, M.; Fotouhi, A.; Yousefi, M.; Aghebati-Maleki, L. Nanoparticles and Cancer Therapy: Perspectives for Application of Nanoparticles in the Treatment of Cancers. J. Cell. Physiol. 2020, 235, 1962–1972. DOI: https://doi.org/10.1002/jcp.29126.
- Tang, D. W.; Yu, S. H.; Ho, Y. C.; Huang, B. Q.; Tsai, G. J.; Hsieh, H. Y.; Sung, H. W.; Mi, F. L. Characterization of Tea Catechins-Loaded Nanoparticles Prepared from Chitosan and an Edible Polypeptide. Food Hydrocoll. 2013, 30, 33–41. DOI: https://doi.org/10.1016/j.foodhyd.2012.04.014.
- Pervin, M.; Unno, K.; Ohishi, T.; Tanabe, H.; Miyoshi, N.; Nakamura, Y. Beneficial Effects of Green Tea Catechins on Neurodegenerative Diseases. Molecules. 2018, 23, 1–17. DOI: https://doi.org/10.3390/molecules23061297.
- Matsui, T.; Tanaka, T.; Tamura, S.; Toshima, A.; Tamaya, K.; Miyata, Y.; Tanaka, K.; Matsumoto, K. Αlpha-Glucosidase Inhibitory Profile of Catechins and Theaflavins. J. Agric. Food Chem. 2007, 55, 99–105. DOI: https://doi.org/10.1021/jf0627672.
- Cheng, Z.; Zhang, Z.; Han, Y.; Wang, J.; Wang, Y.; Chen, X.; Shao, Y.; Cheng, Y.; Zhou, W.; Lu, X.; Wu, Z. A Review on anti-Cancer Effect of Green Tea Catechins. J. Funct. Foods. 2020, 74, 104172. DOI: https://doi.org/10.1016/j.jff.2020.104172.
- Stenius, U.; Hogberg, J.; Duerksen-Hughes, P. R.; Yang, J.; Duerksen-Hughes, P. Re: Yang, J. and Duerksen-Hughes, P. (1998) A New Approach To Identifying Genotoxic Carcinogens: P53 Induction as an Indicator of Genotoxic Damage. Carcinogenesis 1999, 20, 181–182. DOI: https://doi.org/10.1093/carcin/20.1.181.
- Kanwar, J.; Taskeen, M.; Mohammad, I.; Huo, C.; Chan, T. H.; Dou, Q. P. Recent Advances on Tea Polyphenols. Front. Biosci. 2012, 4, 111–131. DOI: https://doi.org/10.2741/363.
- Granado-Serrano, A. B.; Martín, M. A.; Haegeman, G.; Goya, L.; Bravo, L.; Ramos, S. Epicatechin Induces NF-kappaB, Activator Protein-1 (AP-1) and Nuclear Transcription Factor Erythroid 2p45-Related Factor-2 (Nrf2) Via Phosphatidylinositol-3-Kinase/Protein Kinase B (PI3K/AKT) and Extracellular Regulated Kinase (ERK) Signalling in HepG2 Cells. Br. J. Nutr. 2010, 103, 168–179. DOI: https://doi.org/10.1017/S0007114509991747.
- Mehmood, S.; Wang, L.; Yu, H.; Haq, F.; Amin, B. U.; Uddin, M. A.; Fahad, S.; Haroon, M.; Shen, D.; Ni, Z. Preparation of Poly(Cyclotriphosphazene-Co-Piperazine) Nanospheres and Their Drug Release Behavior. Int. J. Polym. Mater. Polym. Biomater. 2020, 1–9. DOI: https://doi.org/10.1080/00914037.2020.1809407.
- Feng, Z.; Xu, J.; Ni, C. Preparation of Redox Responsive Modified Xanthan Gum Nanoparticles and the Drug Controlled Release. Int. J. Polym. Mater. Polym. Biomater. 2020, 1–8. DOI: https://doi.org/10.1080/00914037.2020.1767618.
- Paudel, K. R.; Wadhwa, R.; Tew, X. N.; Lau, N. J. X.; Madheswaran, T.; Panneerselvam, J.; Zeeshan, F.; Kumar, P.; Gupta, G.; Anand, K.; et al. Rutin Loaded Liquid Crystalline Nanoparticles Inhibit Non-Small Cell Lung Cancer Proliferation and Migration In Vitro. Life Sci. 2021, 276, 119436. DOI: https://doi.org/10.1016/j.lfs.2021.119436.
- Sun, T.; Zhang, Y. S.; Pang, B.; Hyun, D. C.; Yang, M.; Xia, Y. Engineered Nanoparticles for Drug Delivery in Cancer Therapy. Angew. Chemie. 2014, 53, 12320–12364. DOI: https://doi.org/10.1002/anie.201403036.
- Brigger, I.; Dubernet, C.; Couvreur, P. Nanoparticles in Cancer Therapy and Diagnosis. Adv. Drug Deliv. Rev. 2002, 54, 631–651. (02)00044-3. DOI: https://doi.org/10.1016/s0169-409x(02)00044-3.
- Luo, Y. L.; Zhang, X. Y.; Fu, J. Y.; Xu, F.; Chen, Y. S. Novel Temperature and pH Dual-Sensitive PNIPAM/CMCS/MWCNT Semi-IPN Nanohybrid Hydrogels: Synthesis, Characterization, and DOX Drug Release. Int. J. Polym. Mater. Polym. Biomater. 2017, 66, 398–409. DOI: https://doi.org/10.1080/00914037.2016.1233418.
- Brewer, M. S. Natural Antioxidants: Sources, Compounds, Mechanisms of Action, and Potential Applications. Compr. Rev. Food Sci. Food Saf. 2011, 10, 221–247. DOI: https://doi.org/10.1111/j.1541-4337.2011.00156.x.
- Sánchez-Rangel, J. C.; Benavides, J.; Heredia, J. B.; Cisneros-Zevallos, L.; Jacobo-Velázquez, D. A. The Folin-Ciocalteu Assay Revisited: Improvement of its Specificity for Total Phenolic Content Determination. Anal. Methods. 2013, 5, 5990–5999. DOI: https://doi.org/10.1039/c3ay41125g.
- Hider, R. C.; Liu, Z. D.; Khodr, H. H. Metal Chelation of Polyphenols. In Methods in Enzymology, 2001, 335, 190–203. DOI: https://doi.org/10.1016/S0076-6879(01)35243-6.
- Liu, G.; Garrett, M. R.; Men, P.; Zhu, X.; Perry, G.; Smith, M. A. Nanoparticle and Other Metal Chelation Therapeutics in Alzheimer Disease. Biochim. Biophys. Acta. 2005, 1741, 246–252. DOI: https://doi.org/10.1016/j.bbadis.2005.06.006.
- Simsek, M.; Quezada-Calvillo, R.; Ferruzzi, M. G.; Nichols, B. L.; Hamaker, B. R. Dietary Phenolic Compounds Selectively Inhibit the Individual Subunits of Maltase-Glucoamylase and Sucrase-Isomaltase with the Potential of Modulating Glucose Release. J. Agric. Food Chem. 2015, 63, 3873–3879. DOI: https://doi.org/10.1021/jf505425d.