Erdogan Suna, Roby Aruna, Torchilin Vladimir P
Department of Pharmaceutical Sciences, School of Pharmacy, Northeastern University, Boston, Massachusetts 02115, USA.
Mol Pharm. 2006 Sep-Oct;3(5):525-30. doi: 10.1021/mp060055t.
Here, we have prepared long-circulating PEGylated liposomes heavily loaded with 111In via the liposome-incorporated polylysine-based (PLL-based) polychelating amphiphilic polymer (PAP) and additionally modified with the monoclonal antibody 2C5 (mAb 2C5) possessing the nucleosome-restricted (NS-restricted) specificity and capable of specific recognition of a broad variety of live cancer cells via the cancer cell surface bound NSs. These liposomes have been tested as a tumor-specific contrast agent for the gamma-scintigraphic visualization of model tumors in mice. The tumor accumulation of mAb 2C5 modified liposomes prepared in this study was significantly (3-to-5-fold) higher than in the neighboring muscle tissue at all times after administration (6, 24, and 48 h) in mice bearing murine Lewis lung carcinoma (LLC) and human HT-29 tumors. The whole body direct gamma-imaging of LLC tumor bearing mice at different times has demonstrated the superior in vivo tumor accumulation of the targeted mAb 2C5 modified PAP-containing PEGylated liposomes compared to nontargeted liposomal control formulations, which resulted in better and faster tumor imaging as shown with LLC-bearing mice.
在此,我们通过基于脂质体掺入的聚赖氨酸(PLL)的多螯合两亲聚合物(PAP)制备了大量负载111In的长循环聚乙二醇化脂质体,并另外用具有核小体限制(NS限制)特异性且能够通过癌细胞表面结合的NS特异性识别多种活癌细胞的单克隆抗体2C5(mAb 2C5)进行修饰。这些脂质体已作为肿瘤特异性造影剂用于小鼠模型肿瘤的γ闪烁显像。在携带小鼠Lewis肺癌(LLC)和人HT - 29肿瘤的小鼠中,本研究制备的mAb 2C5修饰脂质体在给药后所有时间点(6、24和48小时)在肿瘤中的蓄积均显著高于邻近肌肉组织(高3至5倍)。对携带LLC肿瘤的小鼠在不同时间进行的全身直接γ成像表明,与非靶向脂质体对照制剂相比,靶向mAb 2C5修饰的含PAP的聚乙二醇化脂质体在体内肿瘤蓄积方面具有优势,这导致携带LLC的小鼠显示出更好、更快的肿瘤成像效果。