Jung Joohee, Matsuzaki Takashi, Tatematsu Kenji, Okajima Toshihide, Tanizawa Katsuyuki, Kuroda Shun'ichi
Department of Structural Molecular Biology, Institute of Scientific and Industrial Research, Osaka University, Ibaraki, Osaka 567-0047, Japan.
J Control Release. 2008 Mar 20;126(3):255-64. doi: 10.1016/j.jconrel.2007.12.002. Epub 2007 Dec 14.
Bio-nanocapsules (BNCs) consisting of hepatitis B virus (HBV) surface antigen (HBsAg) are approximately 50-nm hollow particles displaying a human hepatocyte-recognizing molecule (pre-S1 peptide). They have been used as an HB vaccine for the last two decades. Original BNC can incorporate various payloads (e.g., drugs, genes) by electroporation and deliver them to human hepatocytes specifically by utilizing the HBV infection mechanism. Here, we developed a new BNC conjugated with liposomes and succeeded in incorporating large materials (100-nm fluorescence-labeled polystyrene beads and >30 kbp plasmids) into the BNC-liposome complex. The complex delivered these large materials to human hepatocytes specifically ex vivo and in vivo. The transfection efficiency of the BNC-liposome complex was significantly higher than that of the original BNC. These results indicated that BNC confers the tissue- and cell-specificity on the conventional liposomes and raises new possibilities for drug delivery systems, gene delivery systems, and bio-imaging systems in vivo.
由乙肝病毒(HBV)表面抗原(HBsAg)组成的生物纳米胶囊(BNCs)是直径约50纳米的空心颗粒,表面展示有人类肝细胞识别分子(前S1肽)。在过去二十年中,它们一直被用作乙肝疫苗。原始的BNC可通过电穿孔包封各种有效载荷(如药物、基因),并利用HBV感染机制将其特异性递送至人类肝细胞。在此,我们开发了一种与脂质体偶联的新型BNC,并成功地将大尺寸物质(100纳米荧光标记的聚苯乙烯珠和大于30千碱基对的质粒)包封进BNC-脂质体复合物中。该复合物能在体外和体内将这些大尺寸物质特异性递送至人类肝细胞。BNC-脂质体复合物的转染效率显著高于原始的BNC。这些结果表明,BNC赋予了传统脂质体组织和细胞特异性,为体内药物递送系统、基因递送系统和生物成像系统带来了新的可能性。