| CPC A61K 31/519 (2013.01) [A61K 9/0019 (2013.01); A61K 9/0092 (2013.01); A61K 9/08 (2013.01); A61K 9/5123 (2013.01); A61K 9/5146 (2013.01); A61K 47/6949 (2017.08); A61K 49/0095 (2013.01); C12Q 1/6881 (2013.01); C12Q 1/6883 (2013.01); C12Q 1/6886 (2013.01); G01N 33/6893 (2013.01); C12N 15/113 (2013.01); C12N 15/1137 (2013.01); C12N 15/1138 (2013.01); C12N 2310/14 (2013.01); C12N 2320/32 (2013.01); C12Q 2600/106 (2013.01); C12Q 2600/158 (2013.01); C12Q 2600/178 (2013.01); C12Y 304/24812 (2013.01); G01N 2800/102 (2013.01); Y02A 50/30 (2018.01)] | 7 Claims |

|
1. A method of treating a disease or disorder of the central nervous system comprising administration of an effective amount of a nanopiece, wherein said nanopiece comprises a compound of Formula I or Formula II or a combination thereof, and a nucleic acid:
![]() wherein,
X is CH or N;
R2 is hydrogen or a linker group;
Y is absent when R2 is hydrogen or is an amino acid side-chain, amino acid or polypeptide; and
R1 is hydrogen or C1 to C10 alkyl; and
wherein the nanopiece has a size in at least one dimension between 1 nm and 30 nm,
wherein a ratio of the compound to nucleic acid ranges from 4.4 to 30 μg compound per to 0.1 nmol of the nucleic acid,
wherein the nanopiece is positively charged at pH 7-7.5.
|