Suppression of SARS replication by SARS helicase inhibitors
US-9266844-B2 · Feb 23, 2016 · US
US11446254B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11446254-B2 |
| Application number | US-201916538109-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 12, 2019 |
| Priority date | Jul 23, 2014 |
| Publication date | Sep 20, 2022 |
| Grant date | Sep 20, 2022 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention relates to a molecule delivery technology and a carrier technology, which may selectively deliver a material to a desired specific cell and living tissue. The present invention may be utilized in the field of a drug carrier which effectively delivers an imaging probe and a therapeutic agent to an affected part.
Opening claim text (preview).
The invention claimed is: 1. A method of in vivo delivering a pharmaceutically active ingredient to cancer tissue, comprising: administering a self-assembled 3-D nucleic acid nanostructure as a pharmaceutically active ingredient carrier to a subject in need thereof, wherein the self-assembled 3-D nucleic acid nanostructure comprises: double strand nucleic acids; and single strands form the sides of the self-assembled 3-D nucleic acid nanostructure, wherein the pharmaceutically active ingredient carrier has an L-DNA triangular prism structure composed of 5 strands of L-DNA self-assembled from the combination of: i) a single strand of an L-DNA nucleotide sequence of SEQ ID NO:15; ii) a single strand of an L-DNA nucleotide sequence of SEQ ID NO:16; iii) a single strand of an L-DNA nucleotide sequence of SEQ ID NO:17; iv) a single strand of an L-DNA nucleotide sequence of SEQ ID NO:18; and v) a single strand of an L-DNA nucleotide sequence of SEQ ID NO:19, and wherein the pharmaceutically active ingredient carrier does not comprise a targeting ligand for the tissue. 2. The method of claim 1 , wherein the pharmaceutically active ingredient is an anticancer agent. 3. The method of claim 1 , wherein the pharmaceutically active ingredient encapsulated is within the nucleic acid nanostructure or bonded to the backbone of the nucleic acid nanostructure, and thereby delivered to the tissue. 4. A method of in vivo delivering an anticancer agent comprising: administering a pharmaceutical composition comprising: a self-assembled 3-D nucleic acid nanostructure as an anticancer agent carrier to carry the anticancer agent to a subject in need thereof, wherein the self-assembled 3-D nucleic acid nanostructure comprises: double strand nucleic acids; and single strands form the sides of the self-assembled 3-D nucleic acid nanostructure, wherein the anticancer agent carrier has an L-DNA triangular prism structure composed of 5 strands of L-DNA self-assembled from the combination of: i) a single strand of an L-DNA nucleotide sequence of SEQ ID NO:15; ii) a single strand of an L-DNA nucleotide sequence of SEQ ID NO:16; iii) a single strand of an L-DNA nucleotide sequence of SEQ ID NO:17; iv) a single strand of an L-DNA nucleotide sequence of SEQ ID NO:18; and v) a single strand of an L-DNA nucleotide sequence of SEQ ID NO:19, and wherein the anticancer agent carrier does not comprise a targeting ligand for the tissue. 5. The method of claim 1 , wherein each single strand is connected by linker. 6. The method of claim 2 , wherein the anticancer agent is doxorubicin. 7. The method of claim 4 , wherein the anticancer agent is doxorubicin. 8. The method of claim 1 , the self-assembled 3-D nucleic acid nanostructure is mixed with a pharmaceutical acceptable carrier selected from the group consisting of gum acacia, methyl hydroxybenzoate, and propyl hydroxybenzoate. 9. The method of claim 4 , the self-assembled 3-D nucleic acid nanostructure is mixed with a pharmaceutical acceptable carrier selected from the group consisting of gum acacia, methyl hydroxybenzoate, and propyl hydroxybenzoate.
attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin {(digitoxin A61K31/7048)} · CPC title
Fluorescein, used in vivo · CPC title
Antineoplastic agents · CPC title
Double-stranded nucleic acids or oligonucleotides · CPC title
Methine dyes, e.g. cyanine dyes · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.