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US5314905A Expired / Lapsed US ⏱️ 0.0 years remaining

Pyropheophorbides conjugates and their use in photodynamic therapy

Assignee: Health Research Inc
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Filing: 1992-11-09
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Granted: 1994-05-24
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Expires: 2012-11-09
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Abstract

Abstract Conjugate are formed by covalently linking a target-specific compound to pyropheophorbide compound which conjugated are injected into a host and accumulate in tumor tissue to a higher degree than surrounding normal tissues. When the pyropheophorbide compound component of the conjugate is exposed to a particular wavelength of light the compound becomes cytotoxic destroying the tumor or diseased tissue without causing irreversible normal tissue damage. The pyropheophorbide compounds have been shown to have a variety of characteristics when used in photodynamic therapy. These characteristics are further improved when the compounds are bound to a target specific component such as a ligand capable of binding to a specific cellular receptor (e.g. growth hormones and growth factors) or an antibody capable of binding to a particular antigen.

Inventors

  • 👤 Ravindra K. Pandey
  • 👤 Thomas J. Dougherty

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 21:27
CPC Classifications
C; C07; C07D; C07D487/00; C07D487/22; A; A61; A61K; A61K41/00; A61K41/0057; A61K41/0071; A61K51/00; A61K51/02; A61K51/04; A61K51/0474; A61K51/0485; A61P; A61P31/00; A61P31/12; A61P35/00; C07D519/00; A61K2123/00

Claims Analysis

Total Claims: 23
Claim 1
Independent Claim 58 words
A conjugate comprising a target-specific component covalently bound to a compound of formula I: ##STR7## wherein R 1 is CH 2 OR 2 where R 2 is a primary or secondary alkyl containing 1 to 20 carbons; and R 3 is --CO 2 R 4 where R 4 is H or an alkyl containing 1 to 20 carbons.
Claim 2
Dependent Claim 58 words
A conjugate comprising a target-specific component covalently bound to a compound of formula I: ##STR7## wherein R 1 is CH 2 OR 2 where R 2 is a primary or secondary alkyl containing 1 to 20 carbons; and R 3 is --CO 2 R 4 where R 4 is H or an alkyl containing 1 to 20 carbons.
Claim 3
Dependent Claim 36 words
The conjugate of claim 1, wherein the target-specific component is selected from the group consisting of a ligand capable of binding to a specific cellular receptor, and an antibody capable of binding to a particular antigen.
Claim 4
Dependent Claim 12 words
The conjugate of claim 2, wherein the antibody is a monoclonal antibody.
Claim 5
Dependent Claim 20 words
The conjugate of claim 2, wherein the ligand is selected from the group consisting of steroid hormones, and growth factors.
Claim 6
Dependent Claim 15 words
The conjugate of claim 2, wherein the conjugate is further attached to a detectable label.
Claim 7
Dependent Claim 29 words
The conjugate as claimed in claim 1, wherein R 1 is CH 2 --O--hexyl, R 2 is --CH 3 , and R 3 is --CO 2 CH 3 .
Claim 8
Dependent Claim 35 words
A method to effect the destruction of a target virus, cell or tissue, comprising: contacting said target with an effective amount of the conjugate of claim 1; and irradiating with light absorbed by said conjugate.
Claim 9
Dependent Claim 30 words
A pharmaceutical composition useful in treatment of a target virus, cells or tissue, comprising: an effective amount of the conjugate of claim 1 in admixture with a pharmaceutically acceptable excipient.
Claim 10
Dependent Claim 56 words
A conjugate comprising a target-specific component covalently bound to a compound of formula II: ##STR8## wherein R 5 is --OR 6 where R 6 is a primary or secondary alkyl containing 1 to 20 carbons and R 7 is --CO 2 R 8 where R 8 is H or an alkyl containing 1 to 20 carbons.
Claim 11
Dependent Claim 56 words
A conjugate comprising a target-specific component covalently bound to a compound of formula II: ##STR8## wherein R 5 is --OR 6 where R 6 is a primary or secondary alkyl containing 1 to 20 carbons and R 7 is --CO 2 R 8 where R 8 is H or an alkyl containing 1 to 20 carbons.
Claim 12
Dependent Claim 36 words
The conjugate of claim 9, wherein the target-specific component is selected from the group consisting of a ligand capable of binding to a specific cellular receptor, and an antibody capable of binding to a particular antigen.
Claim 13
Dependent Claim 12 words
The conjugate of claim 10, wherein the antibody is a monoclonal antibody.
Claim 14
Dependent Claim 20 words
The conjugate of claim 10, wherein the ligand is selected from the group consisting of steroid hormones, and growth factors.
Claim 15
Dependent Claim 15 words
The conjugate of claim 10, wherein the conjugate is further attached to a detectable label.
Claim 16
Dependent Claim 21 words
The compound as claimed in claim 9, wherein R 5 is --O--hexyl and R 7 is --CO 2 CH 3 .
Claim 17
Dependent Claim 35 words
The compound as claimed in claim 9, wherein R 5 is --O--(CH 2 ) 5 CH 3 and R 7 is selected from the group consisting of CO 2 CH 3 and --CO 2 H.
Claim 18
Dependent Claim 34 words
A method to effect the destruction of target virus, cells or tissue, comprising: contacting said target with an effective amount of the conjugate of claim 9; and irradiating with light absorbed by said conjugate.
Claim 19
Dependent Claim 30 words
A pharmaceutical composition useful in treatment of a target virus, cells or tissue, comprising: an effective amount of the compound of claim 9 in admixture with a pharmaceutically acceptable excipient.
Claim 20
Independent Claim 139 words
A method of treating a human with abnormal cells which replicate at an abnormally high rate, comprising the steps of: administering to the human therapeutically effective amount of a conjugate comprising a target-specific component covalently bound to a compound of formula II ##STR9## wherein R 5 is OR 6 where R 6 is a primary or secondary alkyl containing 5 to 20 carbons and R 7 is --CO 2 R 8 where R 8 is H or --CH 3 ; allowing the conjugate to accumulate on the abnormal cells; and irradiating the conjugate with a wavelength of light which is absorbed by the compound of formula II and thereby generating a cytotoxic effect with respect to the abnormal cells, wherein the conjugate is administered in an amount in the range of 0.01 mg/kg to 1.0 mg/kg of body weight.
Claim 21
Independent Claim 139 words
A method of treating a human with abnormal cells which replicate at an abnormally high rate, comprising the steps of: administering to the human therapeutically effective amount of a conjugate comprising a target-specific component covalently bound to a compound of formula II ##STR9## wherein R 5 is OR 6 where R 6 is a primary or secondary alkyl containing 5 to 20 carbons and R 7 is --CO 2 R 8 where R 8 is H or --CH 3 ; allowing the conjugate to accumulate on the abnormal cells; and irradiating the conjugate with a wavelength of light which is absorbed by the compound of formula II and thereby generating a cytotoxic effect with respect to the abnormal cells, wherein the conjugate is administered in an amount in the range of 0.01 mg/kg to 1.0 mg/kg of body weight.
Claim 22
Dependent Claim 54 words
The method as claimed in claim 18 wherein the conjugate is administered at timed intervals in the range of from every 3 hours to every 72 hours for over a period of from 1 day to 30 days and wherein the wavelength of the light is in the range of 600 to 700 nm.
Claim 23
Dependent Claim 30 words
The method as claimed in claim 18, wherein R 5 is --O--hexyl and R 7 is --CO 2 H and wherein the wavelength of the light is about 660 nm.

References Cited (Backward Citations)

US4649191A Cited
US4883790A Cited
US4920143A Cited
US5002962A Cited
US5093349A Cited
US5198460A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1997-05-23 1997-11-22 1998-05-24 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2001-05-23 2001-11-22 2002-05-24 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2005-05-23 2005-11-22 2006-05-24 $7700.00 Window Closed / Lapsed

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