WO2007147297A1 - The use of derviate of pyridone for preventing and treating radioactive injury of lungs - Google Patents
The use of derviate of pyridone for preventing and treating radioactive injury of lungs Download PDFInfo
- Publication number
- WO2007147297A1 WO2007147297A1 PCT/CN2006/002504 CN2006002504W WO2007147297A1 WO 2007147297 A1 WO2007147297 A1 WO 2007147297A1 CN 2006002504 W CN2006002504 W CN 2006002504W WO 2007147297 A1 WO2007147297 A1 WO 2007147297A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- radiotherapy
- radiation
- formula
- compound
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4418—Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7028—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
- A61K31/7034—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
- A61K31/704—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N5/00—Radiation therapy
- A61N5/10—X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- This invention relates to the field of pharmaceuticals, and more particularly to the novel use of pyridone derivatives for the prevention and treatment of radiation-induced lung injury. Background technique
- Radiotherapy is a commonly used treatment for malignant tumors. After radiotherapy in lung cancer, breast cancer, esophageal cancer, malignant lymphoma or other malignant tumors of the chest, the normal lung tissue in the radiation field is damaged, causing an inflammatory reaction, that is, radiation-induced lung injury, an acute radiation pneumonitis.
- Radioactive pneumonia is a more harmful side effect in radiation therapy, divided into early changes (radioactive pneumonia) and late changes (radioactive pulmonary fibrosis). Every patient exposed to the lungs has this change, but most do not develop symptoms. At this time, if there is an infection, the symptoms are called acute radiation pneumonitis. If symptoms do not occur, after the end of the irradiation, the inflammation gradually absorbs and dissipates, gradually forming different degrees of fibrosis of the lung parenchyma. Pulmonary fibrosis occurs about 6 months after irradiation and gradually increases, reaching the most severe point in one year.
- the pathological changes in the acute phase of radiation pneumonitis occur mostly from 1 to 2 months after radiotherapy, and are also found as late after the end of treatment. It is characterized by congestion, edema and cell infiltration of pulmonary vessels, especially capillary lesions, low alveolar type II cell regeneration, lymphatic vessel expansion and transparent membrane formation. Acute changes may dissipate on their own, but often cause pulmonary connective tissue hyperplasia, fibrosis and glassy changes. The chronic phase often occurs after 9 months of radiation therapy.
- the pathology is extensive alveolar fibrosis, lung contraction, capillary intimal thickening, sclerosis, stenosis or obstruction leading to increased pulmonary circulation resistance and pulmonary hypertension.
- the pleura can also be thickened by inflammation and fibrosis.
- the epithelial changes of the bronchioles and the secondary infection of the lungs can promote radioactive fibrosis.
- radiation pneumonitis has the greatest relationship with the irradiation area, and it is also related to the dose and segmentation, the body factors, individual differences, the presence or absence of chronic lung disease and radiation pneumonitis.
- anti-cancer drugs such as ADM, PYM, VCR and smoking in radiotherapy is also likely to promote the occurrence of radiation pneumonitis.
- the severity of lung injury is closely related to radiation dose, lung irradiation area, and irradiation speed.
- Pathological changes manifested as an exudative inflammatory response in the acute phase and extensive lung tissue fibrosis in the chronic phase.
- the greater the dose received (more than 20 Gy) the more severe the degree of radiation pneumonitis, and further develop into extensive fibrosis of the lung.
- the occurrence of radiation pneumonitis has caused great obstacles to the treatment of common and rapidly progressing chest malignancies, seriously affecting patients' life treatment, and even life-threatening. Its incidence rate is different at home and abroad, about 8.25%-58%.
- Conventional treatment methods include:
- Adrenal cortex hormones control inflammation.
- Anticoagulant therapy is effective in preventing small blood vessel embolism.
- the principles of medication are: 1. Patients with general radiation pneumonitis can choose oral prednisone or dexamethasone. 2. Severe cases of intravenous dexamethasone. 3. When combined with pulmonary infection, add antibiotics. However, there is still a question about the efficacy of hormone therapy, and studies have shown that hormones have no effect on radiation-induced lung injury.
- Radiotherapy in the treatment of malignant tumors is very significant, but it is also necessary to see the existence of radiation reactions and injuries.
- High-dose radiation kills cancer cells and also damages normal cells, and patients will have certain adverse reactions. If the dose is not limited, it will kill the tumor but kill normal cells.
- Radiotherapy can only kill tumor cells to the maximum extent possible if normal tissues can tolerate them.
- the dose of cancer cells will not damage normal tissues around the tumor, and radiation therapy can cure the tumor.
- Some tumor cells have a radiation lethal dose similar to that of normal surrounding tissue cells, and killing cancer cells can also seriously damage normal tissues.
- U.S. Patent 5,789,426 discloses a method of treating a fibrotic disease by administering a protein hydroxylation inhibitor wherein the inhibitor is an N-substituted hydroxypyridone derivative.
- U.S. Patent 6,090,822 discloses the use of N-substituted 2(1H)pyridone or N-substituted 3(1H)pyridone for the treatment of diseases caused by cell growth factors.
- WO00/44381 discloses the use of N-substituted 2(1H)pyridone or N-substituted 3(1 ⁇ )pyridone for the treatment of cancers such as lymphoma and leukemia.
- ⁇ 1138329 discloses the use of 5-methyl-1-phenyl-2-(1 ⁇ )-pyridone for the treatment of fibrous damage.
- Pirfenidone is a pharmacologically active compound invented in the 1970s. The original patent for Pirfenidone was granted in 1976 (US3974281), and the researchers subsequently discovered that it can be used to treat interstitial lung disease (AU5427080) and prevent tissue fibrosis (WO9426249). The clinical trial of idiopathic pulmonary fibrosis (IPF) is currently underway in the United States. The initial study found that it has a certain anti-inflammatory effect.
- IPF idiopathic pulmonary fibrosis
- a novel medicament for alleviating or treating the symptoms of radiation-induced lung injury, and in particular for the use of the medicament for preventing radiation-induced lung injury.
- R 2 is a hydroxyl group at the 2, 3 or 4 position, a mercapto group, a C 6 alkoxy group (such as a methoxy group, an ethoxy group), or a C 6 thio group (such as a methylthio group or an ethylthio group); no,
- the radiation damage is caused by radiation treatment of lung cancer, breast cancer, esophageal cancer, malignant lymphoma or other malignant tumors of the chest.
- the compound is pirfenidone.
- R 2 is a hydroxyl group, a mercapto group, a ( ⁇ . 6 alkoxy group, or a 6 alkylthio group) at the 2, 3 or 4 position; or a no, wherein it is used for the preparation of a drug for increasing the radioactive dose of radiotherapy.
- the radiotherapy is radiotherapy for lung cancer, breast cancer, esophageal cancer, malignant lymphoma or other malignant tumors of the chest.
- the compound is pirfenidone.
- a method of preventing radiation lung injury in a mammal comprising the steps of:
- R 2 is a hydroxyl group at the 2, 3 or 4 position, a mercapto group, a C 6 anthracene group, or a C 6 alkylthio group; or R: is none;
- the mammal is then subjected to radiotherapy.
- the radiotherapy is radiotherapy for lung cancer, breast cancer, esophageal cancer, malignant lymphoma or other malignant tumors of the chest.
- a method of increasing radiation dose for radiotherapy in a mammal comprising the steps of:
- R 2 is a hydroxyl group at the 2, 3 or 4 position, a fluorenyl group, a ( ⁇ -6 alkoxy group, or a 6 alkylthio group; or none;
- the original radiation dose of the radiotherapy of the suckling animal is D Q ;
- the radiation doses are 0! and 0. Satisfy the following formula:
- the compound is pirfenidone.
- the radiotherapy is for the treatment of lung cancer, breast cancer, esophageal cancer, malignant lymphoma or other malignant tumors of the chest.
- the dose of the compound of formula I is administered from 1 to 50 mg/kg body weight per day.
- Figure 1 shows the alveolar lavage cytometer of pirfenidone (PF) in a radiotherapy model mouse. The impact of the number.
- Figure 2 shows the effect of pirfenidone (PF) on lung hydroxyproline content in radiotherapy model mice.
- pyridone compounds such as pirfenidone have extremely significant preventive effects against radiation-induced lung injury. Therefore, by applying such a pyridone compound in advance, it is also possible to increase the radiation dose in the radiotherapy treatment, thereby achieving a more effective anti-therapeutic effect.
- the present invention has been completed on this basis. Although the mechanism of action of the present invention is not clear, the zoological experiments of the present application clearly show that pirfenidone can effectively alleviate or cure radiation-induced lung injury. Therefore, pirfenidone is particularly suitable for the prevention or treatment of radiation-induced lung injury.
- the active ingredient of the pharmaceutical composition of the present invention is pirfenidone and a pyridone compound of a similar structure.
- the pirfenidone which can be used in the present invention is not particularly limited and includes a pharmaceutically acceptable salt, ester or the like. Pirfenidone can be administered alone or in combination with any pharmaceutically acceptable pharmaceutical excipient or carrier.
- R 2 is a hydroxyl group at the 2, 3 or 4 position, a mercapto group, a 6 alkoxy group, or a ( ⁇ 6 alkylthio group; or R: none.
- 1 is methyl and none.
- 1 ⁇ is methyl and R: It is a hydroxyl group. More preferably, it is a methyl group at the 5-position, and R 2 is a hydroxyl group at the 4-position.
- a particularly preferred compound is pirfenidone.
- Another particularly preferred compound is 5-methyl-1-(4-hydroxyphenyl)-2-(1 ⁇ )-pyridone, and the compound is referred to as F351.
- the compounds of the invention also include the form of a salt derived from a pharmaceutically or physiologically acceptable acid or base.
- These salts include, but are not limited to, salts formed with inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, and salts with organic acids, while organic acids refer to acetic acid, oxalic acid, succinic acid, tartaric acid, and methanesulfonic acid. Acid and maleic acid.
- Other salts include those formed with alkali or alkaline earth metals such as sodium, potassium, calcium or magnesium, in the form of esters, carbamates or other conventional "prodrugs" (when administered in this form) , can be converted into active part in the body).
- the invention further encompasses pharmaceutical compositions and methods of treatment comprising administering to a mammal a pharmaceutically effective amount of a compound of formula I.
- the compound of the present invention when used in the above-mentioned use, it may be mixed with one or more pharmaceutically acceptable carriers or excipients, such as a solvent, a diluent, etc., and may be orally administered in the form of tablets, pills, Capsules, dispersible powders, granules or suspensions (containing, for example, about 0.05-5% suspension), syrups (containing, for example, about 10-50% sugar), and elixirs (containing about 20-50% ethanol), or by external means. Administration: Ointment, gel, medicated tape, etc., or parenteral administration in the form of a sterile injectable solution or suspension (containing about 0.05-5% suspending agent in an isotonic medium).
- these pharmaceutical preparations may contain from about 0.01% to about 99%, more preferably from about 0.1% to about 90% by weight of the active ingredient in admixture with the carrier.
- the effective dose of the active ingredient employed will vary depending upon the compound employed, the mode of administration, and the severity of the condition being treated. However, generally, when the compound of the present invention is administered at a dose of about 0.25 to 1000 mg/kg of animal body weight per day, a satisfactory effect can be obtained, preferably administered in 2-4 divided doses per day, or in a sustained release form. Dosing. For most large mammals, the total daily dose is about 1-100 mg/kg, preferably about 2-80 mg/kg. Dosage forms suitable for internal administration comprising from about 0.25 to 500 mg of active compound in intimate admixture with a solid or liquid pharmaceutically acceptable carrier Things. This dosage regimen can be adjusted to provide an optimal therapeutic response. For example, several separate doses may be administered per day, or the dose may be proportionally reduced, as is critical to the condition of the treatment.
- Solid carriers include: starch, lactose, dicalcium phosphate, microcrystalline cellulose, sucrose, and kaolin
- liquid carriers include: sterile water, polyethylene glycol, nonionic surfactants, and edible oils (such as corn oil, Peanut oil and sesame oil), as long as it is suitable for the characteristics of the active ingredient and the particular mode of administration desired.
- Adjuvants which are usually used in the preparation of pharmaceutical compositions may also be advantageously included, for example, flavoring agents, coloring agents, preservatives and antioxidants such as vitamin E, vitamin C, BHT and BHA.
- compositions are solid compositions, especially tablets and solid filled or liquid filled capsules. Oral administration of the compound is preferred.
- active compounds can also be administered parenterally or intraperitoneally. Solutions or suspensions of these active compounds (as free bases or pharmaceutically acceptable salts) may also be prepared in water suitably mixed with a surfactant such as hydroxypropylcellulose or polyvinylpyrrolidone. Dispersions can also be prepared in glycerol, liquids, polyethylene glycols, and mixtures thereof in oils. These preparations contain preservatives to prevent microbial growth under normal conditions of storage and use.
- the pharmaceutical forms suitable for injection include sterile aqueous solutions or dispersions and sterile powders (for the temporary preparation of sterile injectable solutions or dispersions). In all cases, these forms must be sterile and must be fluid to facilitate fluid discharge from the syringe. It must be stable under the conditions of manufacture and storage and must be able to prevent the growth of microorganisms (such as bacteria and fungi).
- the carrier may be a solvent or dispersion medium containing, for example, water, an alcohol (e.g., glycerol, propylene glycol, and a liquid, polyethylene glycol), a suitable mixture thereof, and a vegetable oil.
- the compounds of the present invention can be used in combination with other drugs such as ⁇ -interferon, ⁇ -interferon, ⁇ -interferon, corticosteroid, and methotrexate.
- the pharmaceutical compositions of the invention comprise a pharmaceutically acceptable carrier and a compound of formula I (e.g., pirfenidone).
- a compound of formula I e.g., pirfenidone
- the content of the compound of the formula I is from 0.01 to 99.99% by weight, preferably from 0.1 to 95% by weight, more preferably from 0.5 to 90% by weight.
- it may contain a substance selected from the group consisting of protease inhibitors such as Sivelestat Sodium, anti-inflammatory drugs such as Ibuprofen, various types of interferons and other novel non-solids.
- Alcohol anti-inflammatory drugs such as pentoxifylline, cytoprotective agent Amifostine, antioxidant N-acetylcysteine (Acetylcysteine against inflammatory cells and their mediators and Anti-endotoxin monoclonal antibodies, IL-1 receptor antagonists (IL-lm), TGF and its receptor antagonists, TNFGC and its receptor antagonists, and EGF/PDGF and its receptor antagonists
- IL-1 receptor antagonists IL-1 receptor antagonists
- TGF and its receptor antagonists TNFGC and its receptor antagonists
- EGF/PDGF and its receptor antagonists the following Chinese medicines or their extracts may also be included: Salvia miltiorrhiza, Astragalus, armor, or a mixture thereof.
- the dosage form of the pharmaceutical composition of the present invention is not particularly limited and may be in the form of a solid, a semi-solid or a liquid.
- the pharmaceutical preparations of the invention may be administered by intravenous, subcutaneous, and other suitable routes.
- a preferred mode is effective orally.
- Another preferred mode is parenteral administration, such as intravenous injection, which reduces the time during which the drug works in the body.
- the subject to be treated by the pharmaceutical compositions and methods of the invention is a mammal, especially a human.
- the daily dose typically used in the prophylaxis is about 0.1-500 mg/kg, preferably 0.1-200 mg/kg, more preferably 0.5-100 mg/kg, more It is preferably 1-80 mg/kg.
- the number of administrations can be once a day, or several times.
- the present invention provides a method of preventing radiation lung injury.
- the method comprises pre-administering a prophylactically effective amount of pirfenidone to a patient in need of radiation therapy, followed by radiotherapy.
- the invention also provides a method of increasing the radiation dose of a radiotherapy.
- the method includes pressing D as originally planned. Radiation therapy patient radiation dose previously administered prophylactically effective amount of pirfenidone, and then emitted radiation therapy at a dose D, where D ⁇ D ⁇ D Q ratio is preferably 20% larger, more preferably 50% larger.
- prophylactically effective amount is an amount that can be administered to prevent the effects of radiation-induced lung injury. Generally, the prophylactically effective amount is from 1 to 50 mg/kg body weight per day.
- pirfenidone may be used singly or in combination with a prodrug.
- the main advantages of the invention are:
- Pirfenidone has a significant preventive effect on radiation-induced lung injury, and the drug has less toxic side effects and is safe to use.
- Source of illumination Varian 600C linac, 6 MV X-ray. 4
- Irradiation method 6 babies in a conscious state were fixed in a special plexiglass container, covered with a 1.5 cm thick plexiglass plate to compensate for the dose-building effect, source skin distance 100 cm, field 2.5 X 18 cm, The straight lead door blocks the head and abdomen and only illuminates the chest of the mouse. A single shot of 1200 cGy. Experimental mice were placed in a clean animal room using a dedicated sealed transfer box with air filtration.
- Model control group 60 rats: Only radiation was given and no treatment was given.
- Prophylactic administration group 60 rats: A certain dose of the drug was administered for 2 weeks from the 2 days before the irradiation. The radiation treatment method and dose were the same as the model control group. Pirfenidone was administered once a day (dose of 200 mg/kg, dissolved in 0.5% CMC-Na and then administered in an amount of 0.1 ml/10 g) for a total of 3 months.
- Therapeutic administration group 60 rats: A certain dose of the drug was administered from the day of irradiation to intervene. Radiotherapy treatment and dose were the same as the model control group, single irradiation. Pirfenidone was administered by gavage (diluent 200 mg/kg, dissolved in 0.5% CMC-Na and administered as 0.1 ml/10 g) once daily for 3 months.
- Blank control group 60 rats: 0.5% CMC-Na was administered daily for 3 months without irradiation. Each group of mice was observed once a day after the irradiation to observe whether or not death occurred. After the experimental treatment, the cell count and count of the lavage fluid, the determination of collagen content (hydroxyproline), and pathological morphology were observed regularly.
- Cell count of alveolar lavage fluid Inject a certain amount of normal saline into the right lung, slowly aspirate, and collect 1.5 ⁇ 2.0ml of lavage fluid into the centrifuge tube. Immediately after collecting the alveolar lavage fluid, the inflammatory cell content was manually counted using a cell counting plate.
- Determination of pulmonary hydroxyproline content Take lung tissue and measure according to the procedure of the hydroxyproline kit. Histopathological examination: The lung tissue was fixed with formalin, dehydrated and paraffin-embedded, HE stained and Masson trichrome stained. Evaluation criteria: Refer to Ashcroft interstitial pulmonary fibrosis semi-quantitative scoring criteria to assess radiation-induced lung injury
- Pirfenidone can increase the tolerance to radiotherapy doses
- Prevention group 60 rats: A certain dose of drug was administered from 2 days before the irradiation. The drug treatment was divided into two groups, and pirfenidone was administered by gavage (dose of 200 mg/kg, dissolved in 0.5% of CMC-Na and then administered in an amount of 0.1 ml/10 g) for a total of 3 months.
- mice A total of 60 animals in each group. Each group of mice was observed once a day after irradiation to observe whether there was difficulty in breathing and death. After the experimental treatment, the lung weight, the lavage fluid cell count, the collagen content (hydroxyproline), the plasma cytokine assay (ACE, TGF- ⁇ , TNF- ⁇ , etc.), pathological morphology, etc. were observed regularly.
- pirfenidone and sodium chloride were weighed, prepared into a solution, filled in a 10 ml injection bottle, and packaged after sterilization. For injection.
- Stearyl magnesium 2-10m g According to the dosage of 1000 tablets (formulation as above), weigh pirfenidone, lactose, hydroxypropyl methylcellulose and sodium alginate separately after grinding through 80 mesh sieve, mix the hook, and then with microcrystalline cellulose. Mix well, wet with water, granulate with 16-18 mesh sieve, dry at 60 °C, whole grain, add stearyl magnesium and mix and compress to make tablets.
- Example 5 According to the dosage of 1000 capsules, weigh the above excipients separately and sieve them, then mix them evenly, then add the pirfenidone and salvia miltiorrhiza extracts by equal addition method, fully grind them to make them evenly dispersed, and then pass through 80 mesh sieve. And then into a capsule.
- Example 5 According to the dosage of 1000 capsules, weigh the above excipients separately and sieve them, then mix them evenly, then add the pirfenidone and salvia miltiorrhiza extracts by equal addition method, fully grind them to make them evenly dispersed, and then pass through 80 mesh sieve. And then into a capsule.
- Example 5 Example 5
- Example 1 was repeated except that 5-methyl-1-(4-hydroxyphenyl)-2-(m)-pyridone (F351) was used. The pirfenidone was replaced, and 20 animals per group.
- F351 5-methyl-1-(4-hydroxyphenyl)-2-(m)-pyridone
- Lung injury is a common problem in chest tumors undergoing radiotherapy, divided into early and late stage radioactive lung injury.
- Early lung injury (radioactive pneumonia) often occurs during radiotherapy, often causing serious consequences.
- Lighter treatment leads to interruption of treatment and affects the efficacy of tumor treatment. In severe cases, it can directly lead to death.
- Pulmonary infection also aggravates fibrosis of the lungs, and late radiation damage in the lungs is mainly prevented.
- pirfenidone has the effect of inhibiting tissue fibrosis. It can improve lung function, anti-inflammatory and anti-fibrosis.
- pirfenidone If pirfenidone is used before pulmonary fibrosis, it can inhibit collagen synthesis, prevent fibroblast proliferation, and down-regulate the production of many cytokines, thereby preventing the development of radiation pneumonitis and radiation-induced pulmonary fibrosis.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pathology (AREA)
- Radiology & Medical Imaging (AREA)
- Toxicology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2006800549309A CN101484167B (zh) | 2006-06-15 | 2006-09-25 | 吡啶酮类衍生物预防和治疗放射性肺损伤的用途 |
CA2656017A CA2656017C (en) | 2006-06-15 | 2006-09-25 | Use of pyridone derivatives in the prevention and treatment of radiation-induced lung injuries |
JP2009514614A JP5213852B2 (ja) | 2006-06-15 | 2006-09-25 | 放射線肺障害の予防及び治療のためのピリドン系誘導体の使用 |
EP06791093A EP2036555B1 (en) | 2006-06-15 | 2006-09-25 | The use of pyridone derivatives for preventing and treating radiation injury of lungs |
AT06791093T ATE533486T1 (de) | 2006-06-15 | 2006-09-25 | Verwendung von pyridonderivaten zur vorbeugung und behandlung von strahlungsbedingter lungenverletzung |
US11/958,353 US8765726B2 (en) | 2006-06-15 | 2007-12-17 | Use of pyridone derivatives in the prevention or treatment of tissue or organ toxicity induced by cytotoxic agents and radiation |
US14/275,562 US20140249347A1 (en) | 2006-06-15 | 2014-05-12 | Use of pyridone derivatives in the prevention or treatment of tissue or organ toxicity induced by cytotoxic agents and radiation |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US80491406P | 2006-06-15 | 2006-06-15 | |
US60/804,914 | 2006-06-15 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/958,353 Continuation-In-Part US8765726B2 (en) | 2006-06-15 | 2007-12-17 | Use of pyridone derivatives in the prevention or treatment of tissue or organ toxicity induced by cytotoxic agents and radiation |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2007147297A1 true WO2007147297A1 (en) | 2007-12-27 |
Family
ID=38833053
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CN2006/002504 WO2007147297A1 (en) | 2006-06-15 | 2006-09-25 | The use of derviate of pyridone for preventing and treating radioactive injury of lungs |
Country Status (7)
Country | Link |
---|---|
US (2) | US8765726B2 (zh) |
EP (1) | EP2036555B1 (zh) |
JP (1) | JP5213852B2 (zh) |
CN (1) | CN101484167B (zh) |
AT (1) | ATE533486T1 (zh) |
CA (1) | CA2656017C (zh) |
WO (1) | WO2007147297A1 (zh) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8969347B2 (en) | 2008-06-03 | 2015-03-03 | Intermune, Inc. | Compounds and methods for treating inflammatory and fibrotic disorders |
US9359379B2 (en) | 2012-10-02 | 2016-06-07 | Intermune, Inc. | Anti-fibrotic pyridinones |
US10233195B2 (en) | 2014-04-02 | 2019-03-19 | Intermune, Inc. | Anti-fibrotic pyridinones |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2882956T3 (es) * | 2006-12-18 | 2021-12-03 | Intermune Inc | Método para proporcionar una terapia de pirfenidona a un paciente |
CN102292124A (zh) * | 2009-01-26 | 2011-12-21 | 英特芒尼公司 | 用于治疗急性心肌梗死和相关疾患的方法 |
MX2011007675A (es) * | 2011-07-19 | 2012-07-11 | Cell Therapy And Technology S A De C V | Procedimiento para la fabricacion de una composicion farmaceutica en forma de tabletas de liberacion prolongada conteniendo pirfenidona y su aplicacion en la regresion de la insuficiencia renal cronica, contractura capsular mamaria y fibrosis hepatica humanas. |
US9682071B2 (en) | 2013-03-15 | 2017-06-20 | Intermune, Inc. | Methods of improving microvascular integrity |
US9763992B2 (en) | 2014-02-13 | 2017-09-19 | Father Flanagan's Boys' Home | Treatment of noise induced hearing loss |
AU2016215173B2 (en) * | 2015-02-05 | 2019-11-21 | Memorial Sloan Kettering Cancer Center | Compositions and methods for treatment of edema |
MX2021013944A (es) * | 2019-05-13 | 2022-04-01 | Bio Medical Sciences Inc | Productos para el tratamiento de heridas y cicatrices con ingredientes activos, procedimiento de fabricacion y articulos utiles. |
CN115429802A (zh) * | 2021-06-04 | 2022-12-06 | 北京康蒂尼药业股份有限公司 | 包含羟尼酮与右美沙芬的药物组合物及其治疗肺纤维化的应用 |
CN113274389B (zh) * | 2021-07-09 | 2022-11-08 | 中南大学 | 氟非尼酮在制备治疗急性肺损伤药物中的应用 |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3974281A (en) | 1972-12-18 | 1976-08-10 | Affiliated Medical Research, Inc. | 5-Methyl-1-phenyl-2-(1H)-pyridone compositions and methods of use |
AU5427080A (en) | 1979-01-08 | 1980-07-17 | Margolin, B. | Pirfenidone in the treatment of pulmonary interstitial fibrosis |
WO1994026249A1 (en) | 1993-05-07 | 1994-11-24 | Margolin Solomon B | Compositions and methods for reparation and prevention of fibrotic lesions |
US5789426A (en) | 1995-01-20 | 1998-08-04 | Cornell Research Foundation, Inc. | Method for the treatment of fibroproliferative disorders by application of inhibitors of protein hydroxylation |
US6090822A (en) | 1995-03-03 | 2000-07-18 | Margolin; Solomon B. | Treatment of cytokine growth factor caused disorders |
EP1138329A2 (en) | 1989-02-15 | 2001-10-04 | Yamauchi, Shitotomo | Composition containing 5-Methyl-1-phenyl-2-(1 H)-pyridone for reparation and prevention of fibrotic lesions |
CN1701793A (zh) * | 2004-05-24 | 2005-11-30 | 上海睿星基因技术有限公司 | 吡非尼酮治疗肝损伤坏死和急性肺损伤的用途 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6114353A (en) * | 1995-03-03 | 2000-09-05 | Margolin; Solomon B. | Compositions and method for treatment of lymphomas, leukemias, and leiomyomas |
DE60029246D1 (de) * | 2000-01-24 | 2006-08-17 | Solomon B Margolin | Behandlung von brustkarzinomen, astrozytomen, melanomen und verwandten tumoren |
WO2001058448A1 (fr) * | 2000-02-09 | 2001-08-16 | Shionogi & Co., Ltd. | Inhibiteur d'apoptose |
WO2004019863A2 (en) * | 2002-08-28 | 2004-03-11 | Intermune, Inc. | Combination therapy for treatment of fibrotic disorders |
WO2005000227A2 (en) * | 2003-06-06 | 2005-01-06 | Intermune, Inc. | Methods of treating tnf-mediated disorders |
WO2005040758A2 (en) * | 2003-10-24 | 2005-05-06 | Intermune, Inc. | Use of pirfenidone in therapeutic regimens |
AU2003284808B2 (en) * | 2003-11-14 | 2009-01-22 | Catalyst Biosciences, Inc. | The derivatives of pyridone and the use of them |
-
2006
- 2006-09-25 CA CA2656017A patent/CA2656017C/en active Active
- 2006-09-25 JP JP2009514614A patent/JP5213852B2/ja active Active
- 2006-09-25 CN CN2006800549309A patent/CN101484167B/zh active Active
- 2006-09-25 AT AT06791093T patent/ATE533486T1/de active
- 2006-09-25 EP EP06791093A patent/EP2036555B1/en active Active
- 2006-09-25 WO PCT/CN2006/002504 patent/WO2007147297A1/zh active Application Filing
-
2007
- 2007-12-17 US US11/958,353 patent/US8765726B2/en active Active
-
2014
- 2014-05-12 US US14/275,562 patent/US20140249347A1/en not_active Abandoned
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3974281A (en) | 1972-12-18 | 1976-08-10 | Affiliated Medical Research, Inc. | 5-Methyl-1-phenyl-2-(1H)-pyridone compositions and methods of use |
AU5427080A (en) | 1979-01-08 | 1980-07-17 | Margolin, B. | Pirfenidone in the treatment of pulmonary interstitial fibrosis |
EP1138329A2 (en) | 1989-02-15 | 2001-10-04 | Yamauchi, Shitotomo | Composition containing 5-Methyl-1-phenyl-2-(1 H)-pyridone for reparation and prevention of fibrotic lesions |
WO1994026249A1 (en) | 1993-05-07 | 1994-11-24 | Margolin Solomon B | Compositions and methods for reparation and prevention of fibrotic lesions |
US5789426A (en) | 1995-01-20 | 1998-08-04 | Cornell Research Foundation, Inc. | Method for the treatment of fibroproliferative disorders by application of inhibitors of protein hydroxylation |
US6090822A (en) | 1995-03-03 | 2000-07-18 | Margolin; Solomon B. | Treatment of cytokine growth factor caused disorders |
CN1701793A (zh) * | 2004-05-24 | 2005-11-30 | 上海睿星基因技术有限公司 | 吡非尼酮治疗肝损伤坏死和急性肺损伤的用途 |
Non-Patent Citations (5)
Title |
---|
DATABASE CA [online] BENTON H.P. ET AL.: "Modulation of articular chondrocyte activity by pirfenidone", XP008101706, Database accession no. (142:190640) * |
DATABASE CA [online] SPOND J. ET AL.: "Inhibition of experimental acute pulmonary inflammation by pirfenidone", XP008101704, Database accession no. (140:416) * |
PULMONARY, PHARMACOLOGY & THERAPEUTICS, vol. 16, no. 4, 2005, pages 207 - 214 * |
RESEARCH COMMUNICATIONS IN MOLECULAR PATHOLOGY AND PHARMACOLOGY, 2003, pages 113 - 114, 275 - 288 * |
XUE K.-Y. ET AL.: "A new antifibrotic tissue growth antagonist:pirfenidone", CHINESE JOURNAL OF NEW DRUGS, vol. 14, no. 8, 2005, pages 1070 - 1072, XP008102025 * |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8969347B2 (en) | 2008-06-03 | 2015-03-03 | Intermune, Inc. | Compounds and methods for treating inflammatory and fibrotic disorders |
US9290450B2 (en) | 2008-06-03 | 2016-03-22 | Intermune, Inc. | Compounds and methods for treating inflammatory and fibrotic disorders |
USRE47142E1 (en) | 2008-06-03 | 2018-11-27 | Intermune, Inc. | Compounds and methods for treating inflammatory and fibrotic disorders |
US9359379B2 (en) | 2012-10-02 | 2016-06-07 | Intermune, Inc. | Anti-fibrotic pyridinones |
US9675593B2 (en) | 2012-10-02 | 2017-06-13 | Intermune, Inc. | Anti-fibrotic pyridinones |
US10376497B2 (en) | 2012-10-02 | 2019-08-13 | Intermune, Inc. | Anti-fibrotic pyridinones |
US10898474B2 (en) | 2012-10-02 | 2021-01-26 | Intermune, Inc. | Anti-fibrotic pyridinones |
US10233195B2 (en) | 2014-04-02 | 2019-03-19 | Intermune, Inc. | Anti-fibrotic pyridinones |
US10544161B2 (en) | 2014-04-02 | 2020-01-28 | Intermune, Inc. | Anti-fibrotic pyridinones |
Also Published As
Publication number | Publication date |
---|---|
CA2656017C (en) | 2014-02-04 |
JP2009539887A (ja) | 2009-11-19 |
EP2036555A1 (en) | 2009-03-18 |
CN101484167A (zh) | 2009-07-15 |
CN101484167B (zh) | 2012-07-04 |
CA2656017A1 (en) | 2007-12-27 |
EP2036555A4 (en) | 2009-11-11 |
EP2036555B1 (en) | 2011-11-16 |
US8765726B2 (en) | 2014-07-01 |
JP5213852B2 (ja) | 2013-06-19 |
US20140249347A1 (en) | 2014-09-04 |
US20080161361A1 (en) | 2008-07-03 |
ATE533486T1 (de) | 2011-12-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2007147297A1 (en) | The use of derviate of pyridone for preventing and treating radioactive injury of lungs | |
US20060177444A1 (en) | Concomitant drug as therapeutic agent for inflammatory bowel disease | |
CN111035640B (zh) | 喹啉衍生物用于治疗甲状腺癌的方法和用途 | |
US10736902B2 (en) | Method of treating triple negative breast cancer | |
WO2008016633A2 (en) | Combination therapy | |
UA123401C2 (uk) | Комбінована терапія для лікування злоякісних пухлин | |
WO2020211860A1 (zh) | 用于治疗尤因肉瘤的喹啉类化合物或其药学上可接受的盐 | |
US11419862B2 (en) | Quinoline derivative for treatment of nasopharyngeal carcinoma | |
WO2020224609A1 (zh) | 激酶抑制剂的用途 | |
US20080207644A1 (en) | Therapeutic materials and methods | |
CN107137417B (zh) | 一种用于治疗恶病质的药物组合物及其应用 | |
KR20210084442A (ko) | 포도막 흑색종 치료를 위한 병용 요법 | |
KR20200131265A (ko) | 비인두암을 치료하기 위한 퀴놀린 유도체 | |
CN112826820B (zh) | Nlrp3抑制剂及其应用 | |
WO2024008138A1 (zh) | 1,3,5-三嗪衍生物的药物组合 | |
WO2022199656A1 (zh) | 药物组合、包含其的试剂盒及其用途 | |
US20230029336A1 (en) | Combination Therapy for Treating a Hematological Malignancy | |
CN115645437A (zh) | 富勒烯制剂在制备治疗肠道癌症的药物中的应用 | |
TW202042810A (zh) | 一種含cdk4/6抑制劑的組合物與阿那曲唑聯合在製備治療腫瘤疾病的藥物中的用途 | |
CN117956999A (zh) | 杂芳基氧基萘类化合物的用途 | |
WO2023220396A1 (en) | Methods of treatment using a dual specificity tyrosine-phosphorylation-regulated kinase 1a (dyrk1a) inhibitor | |
WO2023281413A1 (en) | Methods and dosing regimens comprising pf-06873600 for the treatment of cancer | |
WO2021224494A1 (en) | New treatments of viral infections | |
CN111419853A (zh) | 一种治疗乳腺癌的葫芦素与依鲁替尼组合物 | |
WO2020057539A1 (zh) | 用于治疗小细胞肺癌的喹啉衍生物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200680054930.9 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 06791093 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2009514614 Country of ref document: JP |
|
ENP | Entry into the national phase |
Ref document number: 2656017 Country of ref document: CA |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2006791093 Country of ref document: EP |