Department of Biopharmaceutical Sciences, University of Illinois at Chicago.
Drug Deliv Transl Res. 2012 Dec 1;2(6):454-62. doi: 10.1007/s13346-012-0107-x.
Cancer chemotherapy is hampered by serious toxicity to healthy tissues. Conceivably, encapsulation of cytotoxic drugs in actively-targeted, biocompatible nanocarriers could overcome this problem. Accordingly, we used sterically stabilized mixed micelles (SSMM) composed of biocompatible and biodegradable phospholipids to solubilize paclitaxel (P), a hydrophobic model cytotoxic drug, and deliver it to breast cancer in rats. To achieve active targeting, the surface of SSMM was grafted with a ligand, human vasoactive intestinal peptide (VIP) that selectively interacts with its cognate receptors overexpressed on breast cancer cells. We found that even in vitro cytotoxicity of P-SSMM-VIP was 2-fold higher that that of free paclitaxel (p<0.05). Given the unique attributes of P-SSMM and P-SSMM-VIP, most notable small hydrodynamic diameter (~15nm) and stealth properties, biodistribution of paclitaxel was significantly altered. Accumulation of paclitaxel in breast tumor was highest for P-SSMM-VIP, followed by P-SSMM and Cremophor based paclitaxel (PTX). Importantly, bone marrow accumulation of paclitaxel encapsulated in both SSMM-VIP and SSMM was significantly less than that of PTX. Administration of clinically-relevant dose of paclitaxel (5mg/kg) as P-SSMM-VIP and P-SSMM eradicated carcinogen-induced orthotopic breast cancer in rats, whereas PTX decreased tumor size by only 45%. In addition, a 5-fold lower dose (1mg/kg) of paclitaxel in actively targeted P-SSMM-VIP was associated with ~80% reduction in tumor size while the response to PTX and P-SSMM was significantly less. Hypotension was not observed when VIP was grafted onto SSMM. Based on our findings, we propose further development of effective and safe VIP-grafted phospholipid micelle nanomedicines of anti-cancer drugs for targeted treatment of solid tumors in humans.
癌症化疗受到严重的健康组织毒性的阻碍。可以想象,将细胞毒性药物封装在主动靶向、生物相容的纳米载体中可以克服这个问题。因此,我们使用由生物相容和可生物降解的磷脂组成的空间稳定混合胶束(SSMM)来溶解紫杉醇(P),一种疏水性模型细胞毒性药物,并将其递送到大鼠的乳腺癌中。为了实现主动靶向,SSMM 的表面接枝了一种配体,即与人血管活性肠肽(VIP)选择性相互作用的配体,该配体在乳腺癌细胞上过表达其同源受体。我们发现,即使在体外,P-SSMM-VIP 的细胞毒性也比游离紫杉醇高 2 倍(p<0.05)。鉴于 P-SSMM 和 P-SSMM-VIP 的独特属性,尤其是小的水动力直径(~15nm)和隐身特性,紫杉醇的生物分布发生了显著改变。紫杉醇在乳腺癌肿瘤中的积累最高的是 P-SSMM-VIP,其次是 P-SSMM 和基于 Cremophor 的紫杉醇(PTX)。重要的是,SSMM-VIP 和 SSMM 中包裹的紫杉醇在骨髓中的积累明显少于 PTX。以 P-SSMM-VIP 和 P-SSMM 形式给予临床相关剂量的紫杉醇(5mg/kg)可根除大鼠致癌原诱导的原位乳腺癌,而 PTX 仅使肿瘤缩小 45%。此外,主动靶向的 P-SSMM-VIP 中低 5 倍剂量(1mg/kg)的紫杉醇与肿瘤大小减少约 80%相关,而对 PTX 和 P-SSMM 的反应明显减少。当 VIP 接枝到 SSMM 上时,没有观察到低血压。基于我们的发现,我们建议进一步开发有效的和安全的 VIP 接枝磷脂胶束纳米药物用于癌症药物的靶向治疗,以治疗人类的实体肿瘤。