Department of Medical Biotechnology, Chettinad Academy of Research and Education, Kelambakkam 603 103, Tamil Nadu, India.
Department of Endocrinology, Dr. ALM PG Institute of Basic Medical Sciences, University of Madras, Taramani Campus, Chennai 600 113, Tamil Nadu, India.
IET Nanobiotechnol. 2018 Sep;12(6):727-732. doi: 10.1049/iet-nbt.2017.0106.
Research dealing with early diagnosis and efficient treatment in colon cancer to improve patient's survival is still under investigation. Chemotherapeutic agent result in high systemic toxicity due to their non-specific actions on DNA repair and/or cell replication. Traditional medicine such as (LC) has been claimed to have therapeutic potentials against cancer. The present study focuses on targeted drug delivery of cationic liposomal nanoformulated LC (CL-LC) in colon cancer cells (HCT15) and comparing the efficacy with an anti-colon cancer drug, 7-ethyl-10-hydroxy-camptothecin (SN38) along with its nanoformulated form (CL-SN38). The colloidal suspension of LC was made using thin film hydration method. The drugs were characterised using ultraviolet, dynamic light scattering, scanning electron microscopy, energy, dispersive X-ray spectroscopy. drug release showed kinetics of 49 and 89% of SN38 and LC, whereas CL-SN38 and CL-LC showed 73 and 74% of sustained drug release, respectively. Studies on morphological changes, cell viability, cytotoxicity, apoptosis, cancer-associated gene expression analysis of Bcl-2, Bax, p53 by real-time polymerase chain reaction and western blot analysis of Bad and p53 protein were performed. Nanoformulated LC significantly inhibited growth and increased the apoptosis of colon cancer cells indicating its potential anti-cancer activity against colon cancer cells.
研究旨在通过早期诊断和有效治疗结肠癌,提高患者的生存率,目前仍在探索中。化疗药物由于对 DNA 修复和/或细胞复制的非特异性作用,导致全身性毒性高。传统药物如(LC)已被声称具有抗癌潜力。本研究专注于阳离子脂质体纳米制剂 LC(CL-LC)在结肠癌细胞(HCT15)中的靶向药物传递,并将其与抗癌药物 7-乙基-10-羟基喜树碱(SN38)及其纳米制剂(CL-SN38)的疗效进行比较。LC 的胶体悬浮液采用薄膜水化法制备。采用紫外分光光度法、动态光散射、扫描电子显微镜、能量色散 X 射线光谱法对药物进行了表征。药物释放显示 SN38 和 LC 的动力学分别为 49%和 89%,而 CL-SN38 和 CL-LC 的持续药物释放动力学分别为 73%和 74%。进行了形态变化、细胞活力、细胞毒性、细胞凋亡、Bcl-2、Bax、p53 癌相关基因表达分析以及 Bad 和 p53 蛋白的实时聚合酶链反应和 Western blot 分析。纳米制剂 LC 显著抑制结肠癌细胞的生长并增加其凋亡,表明其具有针对结肠癌细胞的潜在抗癌活性。