Kumar Rachna M, Kumar Hitesh, Bhatt Tanvi, Jain Rupshee, Panchal Kanan, Chaurasiya Akash, Jain Vikas
Department of Pharmaceutics, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Mysuru 570015, India.
Department of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Mysuru 570015, India.
Pharmaceuticals (Basel). 2023 Jan 28;16(2):196. doi: 10.3390/ph16020196.
Cancer is one of the major causes of mortality, globally. Cancerous cells invade normal cells and metastasize to distant sites with the help of the lymphatic system. There are several mechanisms involved in the development and progression of cancer. Several treatment strategies including the use of phytoconstituents have evolved and been practiced for better therapeutic outcomes against cancer. Fisetin is one such naturally derived flavone that offers numerous pharmacological benefits, i.e., antioxidant, anti-inflammatory, antiangiogenic, and anticancer properties. It inhibits the rapid growth, invasiveness, and metastasis of tumors by hindering the multiplication of cancer cells, and prompts apoptosis by avoiding cell division related to actuation of caspase-9 and caspase-8. However, its poor bioavailability associated with its extreme hydrophobicity hampers its clinical utility. The issues related to fisetin delivery can be addressed by adapting to the developmental aspects of nanomedicines, such as formulating it into lipid or polymer-based systems, including nanocochleates and liposomes. This review aims to provide in-depth information regarding fisetin as a potential candidate for anticancer therapy, its properties and various formulation strategies.
癌症是全球主要的死亡原因之一。癌细胞会侵入正常细胞,并借助淋巴系统转移至远处。癌症的发生和发展涉及多种机制。为了获得更好的抗癌治疗效果,已经出现并实践了多种治疗策略,包括使用植物成分。非瑟酮就是这样一种天然衍生的黄酮类化合物,具有多种药理益处,即抗氧化、抗炎、抗血管生成和抗癌特性。它通过阻碍癌细胞的增殖来抑制肿瘤的快速生长、侵袭和转移,并通过避免与半胱天冬酶 -9 和半胱天冬酶 -8 激活相关的细胞分裂来促使细胞凋亡。然而,其极低的疏水性导致的低生物利用度阻碍了它的临床应用。与非瑟酮递送相关的问题可以通过适应纳米药物的发展方向来解决,例如将其制成基于脂质或聚合物的系统,包括纳米耳蜗状结构和脂质体。本综述旨在提供有关非瑟酮作为抗癌治疗潜在候选物的深入信息、其特性以及各种制剂策略。