Treatment of esophagitis

a technology for esophagitis and esophagitis, which is applied in the field of therapeutic compositions, can solve the problems of pain, other cell types can be damaged as well, and significant disruption of cellular integrity in mucosal epithelium, so as to prevent or reduce the incidence, severity and/or duration of the diseas

Inactive Publication Date: 2007-01-18
ENDO PHARMA COLORADO
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0011] In one aspect, the present invention provides a therapeutic composition for the treatment of mucositis. By treatment of mucositis, it is meant that the therapeutic composition is effective to prevent or reduce the incidence, severity and / or duration of the disease. The therapeutic composition comprises at least one pharmaceutical substance that, as formulated in the therapeutic composition, presents therapeutic effect in mammalian hosts, typically human hosts, for the treatment of mucositis, together with at least one biocompatible polymer that aids delivery of the pharmaceutical substance to the targeted mucosal site. One preferred embodiment of the therapeutic composition includes N-acetylcysteine as the pharmaceutical substance and a polyoxyalkylene block copolymer as the biocompatible polymer.

Problems solved by technology

Mucositis is a serious and often very painful disorder involving inflammation of the mucous membrane, with the inflammation often accompanied by infection and / or ulceration.
While cancerous cells are the primary targets of cancer therapies, other cell types can be damaged as well.
Exposure to radiation and / or chemotherapeutics often results in significant disruption of cellular integrity in mucosal epithelium, leading to inflammation, infection and / or ulceration at mucosal sites.
As one example, oral mucositis (OM) is a painful and costly complication of some cancer therapies.
The oral cavity is lined with mucosal epithelium, and exposure to radiation and / or chemotherapeutics results in the disruption of cellular integrity leading to the development of ulcerative lesions commonly referred to as oral mucositis.
The risk of developing mucositis is markedly exacerbated when chemotherapeutic agents that typically produce mucosal toxicity are given in high doses, in frequent repetitive schedules, or in combination with ionizing irradiation (e.g., conditioning regimens prior to bone marrow transplant).
These painful lesions often limit a patient's ability to eat and drink and in some cases require hospitalization.
The presence of these lesions can also interrupt scheduled chemotherapy and / or radiation treatments.
Although topical antifungal prophylaxis and treatment may clear superficial oropharyngeal infections, topical agents tend not to be well absorbed and have not been demonstrated to be effective against more deeply invasive fungal infections, which typically involve the esophagus and lower gastrointestinal tract.
Analgesics such as lidocaine mouthwashes are effective for short periods of time but within hours the pain and discomfort usually returns.
Also, studies utilizing nonsteroidal agents and coating agents, such as sucralfate (Carafate), have had conflicting results.
Finally, claims that chlorhexidine (Peridex) reduces mucositis in both irradiated patients and leukemia patients receiving bone marrow transplants have not been verified.
To date, none of these approaches has shown a significant impact.
Esophagitis in this patient population can impede the progress of cancer treatment.

Method used

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Examples

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example

[0084] This example describes the formulation and use of the antioxidant, NAC, within a Pluronic® F127 delivery matrix in the absence and presence of chitosan as a penetration enhancer, for preventing or reducing the clinical outcome of oral mucositis in a hamster model of radiation-induced buccal mucositis.

[0085] Preparation of stock solutions: Pluronic® F127 (poloxamer 407; BASF Corporation, Washington, N.J.) was autoclaved and dissolved in sterile water for injection (Abbott Laboratories, North Chicago, Ill.) at 30% (w / w). Chitosan (medium molecular weight; Sigma-Aldrich, St. Louis, Mo.) was autoclaved and dissolved at 3% (w / w) in sterile filtered water for injection containing 1% (v / v) acetic acid (Fisher Scientific, Fair Lawn, N.J.). NaOH (Fisher Scientific) was prepared in sterile water for injection at 4 M and sterile filtered.

[0086] Preparation of antioxidant formulations: The antioxidant, N-acetyl-L-cysteine (NAC; Sigma-Aldrich), was formulated in the various delivery mat...

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Abstract

A method for treatment of esophagitis is disclosed in which a therapeutic composition is introduced into the esophagus to contact a mucosal surface within the esophagus. The pharmaceutical composition comprises a reverse-thermal gelation polyoxyalkylene block copolymer, a pharmaceutical substance and a pharmaceutical substance selected from the group consisting of glutathione and a precursor for glutathione biosynthesis.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS [0001] This application is a divisional of U.S. patent application Ser. No. 10 / 728,277, filed Dec. 4, 2003, which is a continuation of U.S. patent application Ser. No. 09 / 993,383 filed Nov. 21, 2001, which is a continuation-in-part of U.S. patent application Ser. No. 09 / 721,516 filed Nov. 22, 2000, and the entire contents of each of said applications are incorporated herein by reference as if each and every part of said applications were set forth herein in full.FIELD OF THE INVENTION [0002] This invention relates to a therapeutic composition useful for treatment of mucositis and methods for using the therapeutic composition. BACKGROUND OF THE INVENTION [0003] Mucositis is a serious and often very painful disorder involving inflammation of the mucous membrane, with the inflammation often accompanied by infection and / or ulceration. Mucositis can occur at any of the different mucosal sites in the body. A nonlimiting list of examples of locations...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K9/14A61K9/00A61K31/195A61K31/198A61K31/255A61K38/00A61K45/00A61K47/10A61K47/12A61K47/34A61K47/36A61P1/00A61P1/02A61P11/06A61P13/10A61P27/16A61P29/00
CPCA61K9/0014A61K9/006A61K9/06A61K47/34A61K31/198A61K47/10A61K31/195A61P1/00A61P1/02A61P11/06A61P13/10A61P27/16A61P29/00
Inventor ROSENTHAL, GARY J.ETTER, JEFFREY B.RODELL, TIMOTHY C.SCHAUER, WREN H.SAMANIEGO, ADRIAN
Owner ENDO PHARMA COLORADO
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