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叶酸偶联瓜尔胶纳米粒靶向递送至结肠癌的甲氨蝶呤

Folic acid conjugated guar gum nanoparticles for targeting methotrexate to colon cancer.

机构信息

Pharmaceutics Division, CSIR-Central Drug Research Institute, Chattar Manzil Palace, Lucknow 226001, India.

出版信息

J Biomed Nanotechnol. 2013 Jan;9(1):96-106. doi: 10.1166/jbn.2013.1474.

Abstract

It was envisaged to develop surface modified Guar Gum Nanoparticles (GGNP) with Folic acid (FA) charged with methotrexate (MTX) to target the colon specifically. The MTX loaded FA functionalized GGNP (MTX-FA-GGNP) have been prepared by emulsion crosslinking method. These surface modified nanoparticles were compared with unmodified MTX loaded GGNP (MTX-GGNP). The developed formulations were evaluated for size and size distribution, zeta potential, Differential Scanning Calorimetry (DSC), release profile and uptake studies. The nanoparticles have been found to have average size of 325 nm in diameter having polydispersity index (PDI) 0.177 indicating mono-disperse particles. The zeta potential of the particles was found to be -36.9 mV. The percent growth inhibition of Caco 2 cells with MTX-FA-GGNP was found to be better than MTX-GGNP indicating folate receptor mediated uptake. The MTX-GGNP protects the release of MTX in upper gastrointestinal tract while maximum release of MTX occurred in simulated colonic fluids of pH 6.8. The in vivo uptake studies revealed preferential uptake of nanoparticles formulation in the colon. These studies provide evidences that MTX-FA-GGNP holds promise to address colorectal cancer over-expressing folate receptors. This prototype formulation enjoys dual advantage of having propensity to release the drug in the colon and in the conditions of colorectal carcinoma; it could be better localized and targeted with improved therapy due to over-expression of folate receptors.

摘要

预计开发表面修饰的瓜尔胶纳米颗粒(GGNP),用叶酸(FA)负载甲氨蝶呤(MTX),以专门靶向结肠。通过乳化交联法制备负载 MTX 的 FA 功能化 GGNP(MTX-FA-GGNP)。将这些表面修饰的纳米颗粒与未修饰的负载 MTX 的 GGNP(MTX-GGNP)进行了比较。对开发的制剂进行了粒径和粒径分布、Zeta 电位、差示扫描量热法(DSC)、释放曲线和摄取研究。发现这些纳米颗粒的平均粒径为 325nm,多分散指数(PDI)为 0.177,表明为单分散颗粒。颗粒的 Zeta 电位为-36.9mV。与 MTX-GGNP 相比,Caco2 细胞的 MTX-FA-GGNP 的细胞抑制率百分比更高,表明叶酸受体介导的摄取。MTX-GGNP 可保护 MTX 在胃肠道上部的释放,而在 pH6.8 的模拟结肠液中则释放最大量的 MTX。体内摄取研究表明,纳米颗粒制剂在结肠中的摄取具有优先性。这些研究提供了证据,表明 MTX-FA-GGNP 有望用于治疗表达叶酸受体的结直肠癌。该原型制剂具有双重优势,即在结肠中释放药物的倾向,以及在结直肠癌细胞癌的条件下;由于叶酸受体的过度表达,它可以更好地定位和靶向,从而改善治疗效果。

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