Kulandaivelu Karikalan, Mandal Abul Kalam Azad
School of Bio Sciences and Technology, VIT University, Vellore 632014, Tamil Nadu, India.
IET Nanobiotechnol. 2016 Dec;10(6):419-424. doi: 10.1049/iet-nbt.2015.0113.
Tea polyphenols (TPPs) comprise preventive and therapeutic potentials against cancer, cardiovascular and neurological disorders. Chemical instability of TPP which leads to low bioavailability is the major constrain to its use as therapeutic agent. The authors prepared TPP encapsulated solid lipid nanoparticles (TPP-SLNs) to increase its stability and bioefficacy. Comparison of Fourier transformed infrared spectra of unloaded SLN, free TPP and TPP-SLN indicated encapsulation of TPP. Sustained release of TPP from TP-SLN was observed. TPP-SLN showed prolonged free radical scavenging activity compared with free TPP indicating protection of TPP. TPP-SLN showed activation of Caspases-9 and -3 cascades in breast cancer cell line (Michigan cancer foundation (MCF)-7) at conditions. Biochemical parameters were altered in Ehrlich ascetic carcinoma (EAC) cell bearing mice compared with normal (uninduced) mice which were ameliorated significantly by oral feeding of TPP-SLN. Oral administration (pre- and post-treated) of TPP-SLN in EAC bearing mice resulted in significant increase of plasma haemoglobin, glucose, superoxide dismutase and catalase when compared with EAC bearing control mice. Other biochemical parameters (cholesterol, bilirubin, triglyceride, urea, total protein, alanine aminotransferase, alkaline phosphatase and aspertate transaminase were significantly decreased on oral administration (pre- and post-treated) of TPP-SLN in EAC bearing mice.
茶多酚(TPPs)具有预防和治疗癌症、心血管疾病及神经紊乱的潜力。TPP的化学不稳定性导致其生物利用度较低,这是其作为治疗剂应用的主要限制因素。作者制备了包封TPP的固体脂质纳米粒(TPP-SLNs)以提高其稳定性和生物疗效。对未负载的SLN、游离TPP和TPP-SLN的傅里叶变换红外光谱进行比较,表明TPP被包封。观察到TPP从TP-SLN中持续释放。与游离TPP相比,TPP-SLN显示出延长的自由基清除活性,表明TPP得到了保护。在特定条件下,TPP-SLN在乳腺癌细胞系(密歇根癌症基金会(MCF)-7)中显示出半胱天冬酶-9和-3级联的激活。与正常(未诱导)小鼠相比,荷艾氏腹水癌(EAC)细胞的小鼠的生化参数发生了改变,口服TPP-SLN可显著改善这些参数。与荷EAC对照小鼠相比,在荷EAC小鼠中口服(预处理和后处理)TPP-SLN导致血浆血红蛋白、葡萄糖、超氧化物歧化酶和过氧化氢酶显著增加。在荷EAC小鼠中口服(预处理和后处理)TPP-SLN后,其他生化参数(胆固醇、胆红素、甘油三酯、尿素、总蛋白、丙氨酸转氨酶、碱性磷酸酶和天冬氨酸转氨酶)显著降低。