References
- Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68(6):394–424. doi:https://doi.org/10.3322/caac.21492
- van Baal JO, van Noorden CJ, Nieuwland R, Van de Vijver KK, Sturk A, van Driel WJ, Kenter GG, Lok CA. Development of peritoneal carcinomatosis in epithelial ovarian cancer: a review. J Histochem Cytochem. 2018;66(2):67–83. doi:https://doi.org/10.1369/0022155417742897
- Kastelein AW, Vos LM, de Jong KH, van Baal JO, Nieuwland R, van Noorden CJ, Roovers J-PW, Lok CA. Embryology, anatomy, physiology and pathophysiology of the peritoneum and the peritoneal vasculature. Semin Cell Dev Biol. 2019;92:27–36. doi:https://doi.org/10.1016/j.semcdb.2018.09.007
- Halkia E, Chrelias G, Chrelias C, Esquivel J. 2017 update on ovarian cancer peritoneal carcinomatosis multimodal-treatment considerations. Gastroenterol Res Pract. 2018;2018:5284814. doi:https://doi.org/10.1155/2018/5284814
- Pujade-Lauraine E, Hilpert F, Weber B, Reuss A, Poveda A, Kristensen G, Sorio R, Vergote I, Witteveen P, Bamias A, et al. Bevacizumab combined with chemotherapy for platinum-resistant recurrent ovarian cancer: the AURELIA open-label randomized phase III trial. Obstetrical Gynecol Surv. 2014;69(7):402–4. doi:https://doi.org/10.1097/01.ogx.0000452705.82050.e4
- Kamba T, McDonald D. Mechanisms of adverse effects of anti-VEGF therapy for cancer. Br J Cancer. 2007;96(12):1788–95. doi:https://doi.org/10.1038/sj.bjc.6603813
- Yousefzadi M, Riahi-Madvar A, Hadian J, Rezaee F, Rafiee R, Biniaz M. Toxicity of essential oil of Satureja khuzistanica: in vitro cytotoxicity and anti-microbial activity. J Immunotoxicol. 2014;11(1):50–5. doi:https://doi.org/10.3109/1547691X.2013.789939
- Bou DD, Lago JHG, Figueiredo CR, Matsuo AL, Guadagnin RC, Soares MG, Sartorelli P. Chemical composition and cytotoxicity evaluation of essential oil from leaves of Casearia sylvestris, its main compound α-zingiberene and derivatives. Molecules. 2013;18(8):9477–87. doi:https://doi.org/10.3390/molecules18089477
- Afoulous S, Ferhout H, Raoelison EG, Valentin A, Moukarzel B, Couderc F, Bouajila J. Chemical composition and anticancer, antiinflammatory, antioxidant and antimalarial activities of leaves essential oil of Cedrelopsis grevei. Food Chem Toxicol. 2013;56:352–62. doi:https://doi.org/10.1016/j.fct.2013.02.008
- Fogang HPD, Maggi F, Tapondjou LA, Womeni HM, Papa F, Quassinti L, Bramucci M, Vitali LA, Petrelli D, Lupidi G, et al . In vitro biological activities of seed essential oils from the Cameroonian spices Afrostyrax lepidophyllus Mildbr. and Scorodophloeus zenkeri Harms rich in sulfur-containing compounds. Chem Biodivers. 2014;11(1):161–9. doi:https://doi.org/10.1002/cbdv.201300237
- Keawsa-Ard S, Liawruangrath B, Liawruangrath S, Teerawutgulrag A, Pyne SG. Chemical constituents and antioxidant and biological activities of the essential oil from leaves of Solanum spirale. Nat Prod Commun. 2012;7(7):1–4.
- Amin T, Thakur M. Linum usitatissimum L.(Flaxseed)–A multifarious functional food. Online Int Interdiscip Res J. 2014;4(1):220–38.
- Hussain S, Anjum FM, Butt MS, Khan MI, Asghar A. Physical and sensoric attributes of flaxseed flour supplemented cookies. Turk J Biol. 2006;30(2):87–92.
- Banerjee K, Thiagarajan P. Linum usitatissimum L.(Flax) plant and its seed oil a review. JCHPS. 2015;8(4):623–8.
- Basli A, Belkacem N, Amrani I. Health benefits of phenolic compounds against cancers. In Phenolic compounds-biological activity. London: InTechOpen; 2017. p. 193–210.
- Azrad M, Vollmer RT, Madden J, Dewhirst M, Polascik TJ, Snyder DC, Ruffin MT, Moul JW, Brenner DE, Demark-Wahnefried W. Flaxseed-derived enterolactone is inversely associated with tumor cell proliferation in men with localized prostate cancer. J Med Food. 2013;16(4):357–60. doi:https://doi.org/10.1089/jmf.2012.0159
- Portt L, Norman G, Clapp C, Greenwood M, Greenwood MT. Anti-apoptosis and cell survival: A review. Biochim Biophys Acta. 2011;1813(1):238–59. doi:https://doi.org/10.1016/j.bbamcr.2010.10.010
- Xu D, Wang C, Shen X, Yu Y, Rui Y, Zhang D, Zhou Z. Apoptotic block in colon cancer cells may be rectified by lentivirus mediated overexpression of caspase-9. Acta Gastroenterol Belg. 2013;76(4):372–80.
- Nishitani Yukuyama M, Tomiko Myiake Kato E, Lobenberg R, Araci Bou-Chacra N. Challenges and future prospects of nanoemulsion as a drug delivery system. Curr Pharm Des. 2017;23(3):495–508. doi:https://doi.org/10.2174/1381612822666161027111957
- Solans C, Izquierdo P, Nolla J, Azemar N, Garcia-Celma MJ. Nano-emulsions. Curr Opin Colloid Interface Sci. 2005;10(3–4):102–10. doi:https://doi.org/10.1016/j.cocis.2005.06.004
- Date AA, Desai N, Dixit R, Nagarsenker M. Self-nanoemulsifying drug delivery systems: formulation insights, applications and advances. Nanomedicine (Lond). 2010;5(10):1595–616. doi:https://doi.org/10.2217/nnm.10.126
- Mahdi Jafari S, He Y, Bhandari B. Nano-emulsion production by sonication and microfluidization—a comparison. Int J Food Prop. 2006;9(3):475–85. doi:https://doi.org/10.1080/10942910600596464
- Sarker DK. Engineering of nanoemulsions for drug delivery. Curr Drug Deliv. 2005;2(4):297–310. doi:https://doi.org/10.2174/156720105774370267
- Wasan KM. Role of lipid excipients in modifying oral and parenteral drug delivery: Basic principles and biological examples. Hoboken (NJ): Wiley; 2007.
- Unger EC, Porter T, Culp W, Labell R, Matsunaga T, Zutshi R. Therapeutic applications of lipid-coated microbubbles. Adv Drug Deliv Rev. 2004;56(9):1291–314. doi:https://doi.org/10.1016/j.addr.2003.12.006
- Constantinides PP, Han J, Davis SS. Advances in the use of tocols as drug delivery vehicles. Pharm Res. 2006;23(2):243–55. doi:https://doi.org/10.1007/s11095-005-9262-9
- Constantinides PP, Chaubal MV, Shorr R. Advances in lipid nanodispersions for parenteral drug delivery and targeting. Adv Drug Deliv Rev. 2008;60(6):757–67. doi:https://doi.org/10.1016/j.addr.2007.10.013
- Ghosh V, Saranya S, Mukherjee A, Chandrasekaran N. Cinnamon oil nanoemulsion formulation by ultrasonic emulsification: investigation of its bactericidal activity. J Nanosci Nanotechnol. 2013;13(1):114–22. doi:https://doi.org/10.1166/jnn.2013.6701
- Qian C, McClements DJ. Formation of nanoemulsions stabilized by model food-grade emulsifiers using high-pressure homogenization: factors affecting particle size. Food Hydrocolloids. 2011;25(5):1000–8. doi:https://doi.org/10.1016/j.foodhyd.2010.09.017
- Sun H, Liu K, Liu W, Wang W, Guo C, Tang B, Gu J, Zhang J, Li H, Mao X, et al. Development and characterization of a novel nanoemulsion drug-delivery system for potential application in oral delivery of protein drugs. Int J Nanomed. 2012;7:5529–43. doi:https://doi.org/10.2147/IJN.S36071
- Sanaeimehr Z, Javadi I, Namvar F. Antiangiogenic and antiapoptotic effects of green-synthesized zinc oxide nanoparticles using Sargassum muticum algae extraction. Cancer Nanotechnol. 2018;9(1):3. doi:https://doi.org/10.1186/s12645-018-0037-5
- Stetefeld J, McKenna SA, Patel TR. Dynamic light scattering: a practical guide and applications in biomedical sciences. Biophys Rev. 2016;8(4):409–27. doi:https://doi.org/10.1007/s12551-016-0218-6
- Salopek B, Krasic D, Filipovic S. Measurement and application of zeta-potential. Rudarsko-Geolosko-Naftni Zbornik. 1992;4(1):147.
- Badgwell D, Bast RC. Jr, Early detection of ovarian cancer. Dis Markers. 2007;23(5–6):397–410. doi:https://doi.org/10.1155/2007/309382
- Dawane JS, Pandit VA. Understanding redox homeostasis and its role in cancer. J Clin Diagn Res. 2012;6(10):1796–802. doi:https://doi.org/10.7860/JCDR/2012/4947.2654
- DeBerardinis RJ, Lum JJ, Hatzivassiliou G, Thompson CB. The biology of cancer: metabolic reprogramming fuels cell growth and proliferation. Cell Metab. 2008;7(1):11–20. doi:https://doi.org/10.1016/j.cmet.2007.10.002
- Pistritto G, Trisciuoglio D, Ceci C, Garufi A, D'Orazi G. Apoptosis as anticancer mechanism: function and dysfunction of its modulators and targeted therapeutic strategies. Aging (Albany NY), 2016;8(4):603–19. doi:https://doi.org/10.18632/aging.100934
- Sznarkowska A, Kostecka A, Meller K, Bielawski KP. Inhibition of cancer antioxidant defense by natural compounds. Oncotarget. 2017;8(9):15996–6016. doi:https://doi.org/10.18632/oncotarget.13723
- Labi V, Erlacher M. How cell death shapes cancer. Cell Death Dis. 2015;6(3):e1675. doi:https://doi.org/10.1038/cddis.2015.20
- Zhao Y, Adjei AA. Targeting angiogenesis in cancer therapy: moving beyond vascular endothelial growth factor. Oncologist. 2015;20(6):660–73. doi:https://doi.org/10.1634/theoncologist.2014-0465
- Ur Rashid H, Xu Y, Muhammad Y, Wang L, Jiang J. Research advances on anticancer activities of matrine and its derivatives: An updated overview. Eur J Med Chem. 2019;161:205–38. doi:https://doi.org/10.1016/j.ejmech.2018.10.037
- Reza KH. Nanoemulsion as a novel transdermal drug delivery system. Int J Pharm Sci Res. 2011;2(8):1938.
- Anantharaju PG, Gowda PC, Vimalambike MG, Madhunapantula SV. An overview on the role of dietary phenolics for the treatment of cancers. Nutr J. 2016;15(1):99. doi:https://doi.org/10.1186/s12937-016-0217-2
- Abotaleb M, Samuel S, Varghese E, Varghese S, Kubatka P, Liskova A, Büsselberg D. Flavonoids in cancer and apoptosis. Cancers. 2018;11(1):28. doi:https://doi.org/10.3390/cancers11010028
- Sharma N, Bansal M, Visht S, Sharma P, Kulkarni G. Nanoemulsion: A new concept of delivery system. Chronicles Young Sci. 2010;1(2):2.
- Nirmala MJ, Durai L, Gopakumar V, Nagarajan R. Anticancer and antibacterial effects of a clove bud essential oil-based nanoscale emulsion system. Int J Nanomed. 2019;14:6439–50. doi:https://doi.org/10.2147/IJN.S211047
- Kubatka P, Uramova S, Kello M, Kajo K, Samec M, Jasek K, Vybohova D, Liskova A, Mojzis J, Adamkov M. Anticancer activities of Thymus vulgaris L. in experimental breast carcinoma in vivo and in vitro. Int J Mol Sci. 2019;20(7):1749. doi:https://doi.org/10.3390/ijms20071749
- Maragheh AD, Tabrizi MH, Karimi E, Seyedi SMR, Khatamian N. Producing the sour cherry pit oil nanoemulsion and evaluation of its anti-cancer effects on both breast cancer murine model and MCF-7 cell line. J Microencapsul. 2019;36(4):399–409. doi:https://doi.org/10.1080/02652048.2019.1638460
- Ezzat SM, Shouman SA, Elkhoely A, Attia YM, Elsesy MS, El Senousy AS, Choucry MA, El Gayed SH, El Sayed AA, Sattar EA, et al. Anticancer potentiality of lignan rich fraction of six Flaxseed cultivars. Sci Rep. 2018;8(1):544. doi:https://doi.org/10.1038/s41598-017-18944-0
- Jungeström MB, Thompson LU, Dabrosin C. Flaxseed and its lignans inhibit estradiol-induced growth, angiogenesis, and secretion of vascular endothelial growth factor in human breast cancer xenografts in vivo. Clin Cancer Res. 2007;13(3):1061–7. doi:https://doi.org/10.1158/1078-0432.CCR-06-1651