Doxorubicin and paclitaxel co-bound lactosylated albumin nanoparticles having targetability to hepatocellular carcinoma

作者：Thao Le Quang; Lee Changkyu; Kim Bomi; Lee Sungin; Kim Tae Hwan; Kim Jong Oh; Lee Eun Seong; Oh Kyung Taek; Choi Han Gon; Yoo Sun Dong; Youn Yu Seok^*

来源：Colloids and Surfaces B: Biointerfaces , 2017, 152: 183-191.

DOI：10.1016/j.colsurfb.2017.01.017

• Albumin nanoparticles
• Lactose
• Liver targetability
• Hepatocellular carcinoma
• Asialoglycoprotein receptor
• Nab (R) Technology

Anticancer drug targeting to liver asialoglycoprotein receptors (ASGPR) is viewed as a good approach for hepatocellular carcinoma (HCC) treatment. Lactose residue is a promising ASGPR ligand due to its high receptor affinity. Herein, we introduce doxorubicin and paclitaxel co-bound lactosylated albumin (Lac-BSA) nanoparticles (Dox/Pac Lac-BSA NPs) with good liver targetability. Lac-BSA was synthesized by conjugating lactobionic acid to naive BSA then characterized by mass spectrometry. Dox/Pac Lac-BSA NPs were fabricated utilizing high-pressure homogenization and evaporation with Nab (R) (nanoparticle albumin bound) technology. Dox/Pac Lac-BSA NPs were spherical and well-dispersed, with a 148.7 +/- 13.8 nm particle size and -54.1 +/- 0.7 mV zeta potential at a 100% Lac-BSA feed ratio. Combined Dox and Pac synergistic cytotoxicity was confirmed in Hep G2 cells. Specifically, the inhibitory concentration (IC50; 0.21 +/- 0.02 mu g/ml) for Dox/Pac Lac-BSA NPs was 3.2 time lower than plain Dox/Pac BSA NPs (IC50; 0.68 +/- 0.04 mu g/ml). Also, Dox/Pac Lac-BSA NPs exhibited better internalizing in Hep G2 cells (61.8% vs. 14.4% for Dox) and spheroids compared to Dox/Pac BSA NPs. Finally, Dox/Pac Lac-BSA NPs displayed much greater localization into ICR mice livers compared to Dox/Pac BSA NPs. This was indicated by the presence of NP lactose residues revealed by a galactose inhibition study. Based on these results, we suggest that lactose-modified albumin-based nanoparticles fabricated with the Nab (R) technique can be a potential therapeutic vector for treating HCC via hepatocyte targeting.

• 出版日期2017-4-1