Amirkhanov R N, Zarytova V F, Amirkhanov N V
Bioorg Khim. 2014 May-Jun;40(3):286-92. doi: 10.1134/s1068162014030030.
When delivering peptide nucleic acids (PNA) to the cells in the nanocomposites TiO2 · PL · DNA/PNA, containing titanium dioxide nanoparticles coated with polylysine (PL) and immobilized DNA/PNA duplexes, it is important not only to transport them to the cell, but also ability to control the release rate of the PNA-drug from the carrier. PNA desorption from TiO2 · PL · DNA/PNA nanocomposite in time has been shown. Desorption is caused by dissociation of immobilized DNA/PNA duplex while the DNA remains on the carrier and PNA goes away in solution. It has been found that the half-retention times of PNA on TiO2 · PL · DNA/PNA nanocomposites containing DNA/PNA duplexes with overlapping complementary base pairs equal to 10, 12, 14, and 16 are 10, 14, 22 and 70 minutes, respectively. Thus, it has been shown that the release rate of the PNA-drug from nanocomposites can be adjusted by varying the overlap of complementary base pairs in the immobilized DNA/PNA duplex. This method of PNA immobilization may be used for designing of nanocomposites with optimum release time of the PNA-drugs. Created TiO2 · PL · DNA/PNA nanocomposites can be used to efficiently deliver therapeutically significant drug PNA and their selective effect on the pathogenic nucleic acid in the cell.
在将肽核酸(PNA)递送至纳米复合材料TiO₂·PL·DNA/PNA中的细胞时,该纳米复合材料包含涂有聚赖氨酸(PL)的二氧化钛纳米颗粒以及固定化的DNA/PNA双链体,不仅要将它们转运至细胞,而且要能够控制PNA药物从载体中的释放速率。已证明PNA会及时从TiO₂·PL·DNA/PNA纳米复合材料中解吸。解吸是由固定化的DNA/PNA双链体解离引起的,而DNA仍保留在载体上,PNA则进入溶液中。已发现,含有互补碱基对重叠数分别为10、12、14和16的DNA/PNA双链体的TiO₂·PL·DNA/PNA纳米复合材料上PNA的半衰期分别为10、14、22和70分钟。因此,已表明可以通过改变固定化DNA/PNA双链体中互补碱基对的重叠来调节PNA药物从纳米复合材料中的释放速率。这种PNA固定化方法可用于设计具有最佳PNA药物释放时间的纳米复合材料。所制备的TiO₂·PL·DNA/PNA纳米复合材料可用于高效递送具有治疗意义的药物PNA及其对细胞中致病核酸的选择性作用。