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Tamoxifen nanostructured lipid carriers: Enhanced in vivo antitumor efficacy with reduced adverse drug effects

机译:他莫昔芬纳米结构脂质载体:增强体内抗肿瘤功效,减少不良药物作用

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摘要

A novel approach of enhancing the Tamoxifen uptake via Intestinal Lymphatic System is executed by developing long chain lipid and oil based nanostructured lipid carrier system (Tmx-NLC). The aim was to achieve improved systemic bioavailability of Tamoxifen, prevent systemic and hepatotoxicity and enhance antitumor efficacy. Following the proof of concept achieved in cell culture experiments and in vivo pharmacokinetic and biodistribution study, the current work focuses on investigation of antitumor efficacy and treatment associated toxicity in murine mammary tumor mice model. The efficacy study demonstrated greater tumor suppression and 100% survival with 1.5 and 3 mg/kg Tmx-NLC compared to 3 mg/kg Tamoxifen suspension and Mamofen? (Khandelwal Pharmaceuticals, Mumbai, India). Tmx-NLC treatment for a month demonstrated improved systemic toxicity profile and no evidences of hepatotoxicity. Thus, developed Tmx-NLC could prove to be a promising delivery strategy to confer superior therapeutic efficacy and ability to address the biopharmaceutical and toxicity associated issues of drug.
机译:通过开发长链脂质和油基纳米结构脂质载体系统(Tmx-NLC),可以执行一种通过肠淋巴系统增强他莫昔芬摄取的新方法。目的是提高他莫昔芬的全身生物利用度,预防全身和肝毒性并增强抗肿瘤功效。继在细胞培养实验以及体内药代动力学和生物分布研究中获得概念验证之后,当前的工作重点是研究鼠乳腺肿瘤小鼠模型的抗肿瘤功效和与治疗相关的毒性。功效研究表明,与3 mg / kg的他莫昔芬混悬液和Mamofen?相比,1.5和3 mg / kg的Tmx-NLC能够更好地抑制肿瘤并100%存活。 (印度孟买的Khandelwal Pharmaceuticals)。 Tmx-NLC治疗一个月显示出改善的全身毒性,没有肝毒性的证据。因此,开发的Tmx-NLC可能被证明是一种有前途的递送策略,可赋予其优异的治疗功效和解决药物的生物药物和毒性相关问题的能力。

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