“…In fact, its bioavailability reaches only 1% after oral administration (Liu et al, 2016). Several delivery strategies have been employed to overcome these obstacles, such as designing emulsions (Ma, et al, 2017), micelles (Wang & Gao, 2018), hydrogels (Zheng, Zhang, Chen, Luo, & McClements, 2017) , nanoparticles (C. Tan, Xie, Zhang, Cai, & Xia, 2016), applying electrospun fibres (Alehosseini, Gomez-Mascaraque, Martinez-Sanz, & Lopez-Rubio, 2019), creating phospholipid complexes (Maiti, Mukherjee, Gantait, Saha, & Mukherjee, 2007) and using liposomal systems (Alavi, Haeri, & Dadashzadeh, 2017;Karewicz et al, 2013;Liu, Liu, Zhu, Gan, & Le, 2015;Pu, Tang, Li, Li, & Sun, 2019).…”