IP Library Granted Patent US 10,201,609
Granted Patent B2
US 10,201,609 · App. 15/805,664 · Granted Feb 12, 2019

Method for the production of a formulation of a hypericin salt

Inventors: Stefan Welzig (Vienna, AT); Gregor Medinger (Sag Harbor, NY); Beate Kälz (Steinbrunn, AT); József Gungl (Agfalva, HU); Klaus Gerdes (Dusseldorf, DE); Werner Frantsits (Vienna, AT); Christina Abrahamsberg (Vienna, AT)
Assignee: SANOCHEMIA PHARMAZEUTIKA AG
A61K41/0057A61K9/0009A61K9/08A61K9/19A61K47/32A61K47/58A61K47/60A61N5/062A61N2005/0663
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Quick Facts
Patent No.
US 10,201,609
App. No.
15/805,664
Granted
Feb 12, 2019
Kind
B2
Abstract

Photodynamic therapy of tumors such as bladder tumors includes photosensitizing with a photosensitizer that is a complex or a compound of hypericin and a polymeric complexing agent. The photosensitizer is formed from an alkali salt of hypericin and the polymeric complexing agent. The alkali salt of hypericin is a sodium salt or a potassium salt. The complexing agent is a polyethylene glycol or a poly-N-vinyl amide.

Claims (22)

1. A method for the production of a formulation of a hypericin salt, comprising:

bonding or complexing the hypericin salt to a polyethylene glycol, a poly-N-vinyl amide, or polyvinylpyrrolidone (PVP);

adding a buffer system comprising a phosphate buffer or a citric acid buffer to obtain a concentration of 0.0225 mg hypericin/g solution; and

lyophilizing the solution to obtain lyophilizate to yield 0.225 mg hypericin.

2. A method for the production of a formulation of a hypericin salt, comprising:

bonding or complexing the hypericin salt to a polyethylene glycol, a poly-N-vinyl amide, or polyvinylpyrrolidone (PVP);

adding a buffer system comprising a phosphate buffer or a citric acid buffer to obtain a concentration of 0.0225 mg hypericin/g solution; and

lyophilizing the solution to obtain lyophilizate to yield 0.225 mg hypericin,

wherein the complexing is performed in aqueous solution.

3. The method according to claim 2 , wherein the aqueous solution is decanted into injection flasks and freeze-dried.

4. The method according to claim 1 , wherein the formulation is prepared for intravenous, intracavity, inhalative, oral, intraperitoneal and topical administration, in hydrophilic or hydrophobic vehicles, or in the form of a solution, a cream, a gel, an aerosol, emulsions or as a patch.

5. A method for the production of a formulation for photodynamic therapy, comprising:

bonding or complexing a hypericin salt to a polymeric complexing agent selected from the group consisting of a polyethylene glycol, a poly-N-vinyl amide, and polyvinylpyrrolidone (PVP), wherein

the formulation is a stable complex or a stable compound of a sodium or potassium salt of hypericin, wherein the photosensitizer is obtained from a lyophilisate obtained from a solution of the sodium or potassium salt of hypericin, containing 0.0225 mg hypericin/g solution, the polymeric complexing agent and a buffer system comprising a phosphate buffer or a citric acid buffer, and

the formulation has been lyophilized to obtain lyophilizate to yield 0.225 mg hypericin in each resulting obtained photosensitizer.

6. The method according to claim 5 , wherein the formulation is prepared for intravenous, intracavity, inhalative, oral, intraperitoneal and topical administration, in hydrophilic or hydrophobic vehicles, or in the form of a solution, a cream, a gel, an aerosol, emulsions or as a patch.

7. A method for the production of a formulation for photodynamic therapy, comprising:

bonding or complexing a hypericin salt to a polymeric complexing agent selected from the group consisting of a polyethylene glycol, a poly-N-vinyl amide, and polyvinylpyrrolidone (PVP), wherein

the formulation is a stable complex or a stable compound of a sodium or potassium salt of hypericin, wherein the photosensitizer is obtained from a lyophilisate obtained from a solution of the sodium or potassium salt of hypericin, containing 0.0225 mg hypericin/g solution, the polymeric complexing agent and a buffer system comprising a phosphate buffer or a citric acid buffer, and

the formulation has been lyophilized to obtain lyophilizate to yield 0.225 mg hypericin in each resulting obtained photosensitizer,

wherein the complexing is performed in aqueous solution.

8. The method according to claim 7 , wherein the aqueous solution is decanted into injection flasks and freeze-dried.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 9, 2020
From: SANOCHEMIA PHARMAZEUTIKA AG
To: SANOCHEMIA PHARMAZEUTIKA GMBH
Reel/Frame 053724/0617 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2017
From: WELZIG, STEFAN; MEDINGER, GREGOR; KALZ, BEATE; GUNGL, JOZSEF; GERDES, KLAUS; FRANTSITS, WERNER; ABRAHAMSBERG, CHRISTINA
To: SANOCHEMIA PHARMAZEUTIKA AG
Reel/Frame 044056/0994 →
Continuity (2)
Division 14878515 · Oct 8, 2015
Related Publication 20180055935A1 · Mar 1, 2018