IP Library Granted Patent US 7,223,600
Granted Patent B2
US 7,223,600 · App. 10/433,136 · Granted May 29, 2007

Photochemical internalization for delivery of molecules into the cytosol

Assignee: The Norwegian Radium Hospital Research Foundation
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Quick Facts
Patent No.
US 7,223,600
App. No.
10/433,136
Granted
May 29, 2007
Kind
B2
Abstract

The present invention provides a method for introducing a molecule into the cytosol of a cell in which the cell is contacted with a photosentistising agent, the cell is irradiated with light of a wavelength effective to activate the photosentisitising agent and, substantially at the same time or after the irradiation, the cell is contacted with the molecule to be introduced, particularly for use in cancer treatment, gene therapy and vaccination.

Claims (29)

1. A method for introducing a nucleic acid transfer molecule into the cytosol of a cell, said method comprising

contacting said cell with a photosensitising agent,

contacting said cell with said nucleic acid transfer molecule and

irradiating said cell with light of a wavelength effective to activate the photosensitising agent,

wherein said nucleic acid transfer molecule is taken up by the cell and

wherein as a consequence of said irradiation said nucleic acid transfer molecule is released into the cytosol of said cell, wherein said irradiation is performed prior to the cellular uptake of said nucleic acid transfer molecule into any intracellular compartment.

2. A method for introducing a nucleic acid transfer molecule into the cytosol of a cell, said method comprising

contacting said cell with a photosensitising agent,

irradiating said cell with light of a wavelength effective to activate the photosensitising agent and,

at the same time or at a time after the irradiation, contacting said cell with said nucleic acid transfer molecule, wherein said nucleic acid transfer molecule is taken up by the cell and wherein as a consequence of said irradiation is released into the cytosol of the cell.

3. A method as claimed in claim 1 wherein the cell is contacted with the transfer molecule at a time point after irradiation has taken place.

4. A method as claimed in claim 1 wherein the cell is contacted with said transfer molecule 0 to 4 hours after irradiation has taken place.

5. A method as claimed in claim 1 wherein the cell is contacted with the transfer molecule at the same time as the irradiation.

6. A method as claimed in claim 1 wherein the transfer molecule is contacted with said cell for 30 minutes to 6 hours.

7. A method as claimed in claim 1 wherein said method is performed on cells in vitro or in vivo.

8. A method as claimed in claim 1 wherein said cell is an antigen-presenting cell.

9. A method as claimed in claim 1 wherein said nucleic acid molecule is incorporated into a vector, preferably an adenovirus.

10. A method as claimed in claim 1 wherein the photosensitising agent is selected from the group consisting of meso-tetraphenyl porphine with 4 sulfonate groups (TPPS 4 ), tetraphenyl porphine with 2 sulfonate groups on adjacent phenyl groups (TPPS 2a ), aluminum phthalocyanine with 2 sulfonate groups on adjacent phenyl rings (AlPcS 2a ) and other amphiphilic photosensitizers.

11. A method as claimed in claim 1 wherein said photosensitizing agent is a compound being 5-aminolevulinic acid or an ester of 5-aminolevulinic acid or a pharmaceutically acceptable salt thereof.

12. A method as claimed in claim 1 wherein said photosensitizing agent is contacted with said cells for 4 to 24 hours prior to irradiation, preferably for that period immediately prior to irradiation.

13. A method as claimed in claim 1 wherein said photosensitizing agent is removed after contact with said cell for 1 to 4 hours prior to irradiation.

14. A method as claimed in claim 1 wherein one or both of the photosensitising agent and the transfer molecule is affached to, associated with, or conjugated to, one or more carrier molecules, targeting molecules or vectors.

15. A method as claimed in claim 14 wherein the carrier, targeting molecule or vector to which or with which, the transfer molecule is attached, associated, or conjugated, is an adenovirus, a polycation, a cationic lipid or a peptide or targeted vector.

16. A method as claimed in claim 15 wherein said transfer molecule is attached to, associated with, or conjugated to an adenovirus vector.

17. A method as claimed in claim 15 wherein said polycation is poly-L-lysine or poly-D-lysine.

18. A method as claimed in claim 15 wherein said cationic lipid is 1,2-bis(oleoyloxy)-3-(trimethylamino)propane (DOTAP).

19. A method as claimed in claim 14 wherein said one or more carrier molecules are a liposome or lipid based construct, preferably containing at least one cationic lipid.

20. A method as claimed in claim 1 wherein the method is performed in a plurality of cells, and at least 50% of said cells into which said transfer molecule is introduced are not killed.

21. A method as claimed in claim 1 wherein the irradiation step is 1 to 10 minutes in length.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 10, 2003
From: NORWEGIAN RADIUM HOSPITAL RESEARCH FOUNDATION, THE
To: PCI BIOTECH AS
Reel/Frame 014667/0987 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 10, 2003
From: BERG, KRISTIAN; PRASMICKAITE, LINA; HOGSET, ANDERS; SELBO, PAL KRISTIAN
To: NORWEGIAN RADIUM HOSPITAL RESEARCH FOUNDATION, THE
Reel/Frame 014668/0296 →
Priority Claims (3)
GB 0029134.4 · Nov 29, 2000 · national
GB 0029404.1 · Dec 1, 2000 · national
GB 0114695.0 · Jun 15, 2001 · national
Continuity (1)
Related Publication 20050075268A1 · Apr 7, 2005