Compositions comprising salbutamol sulphate

US10039828B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10039828-B2
Application numberUS-201615357279-A
CountryUS
Kind codeB2
Filing dateNov 21, 2016
Priority dateOct 12, 2011
Publication dateAug 7, 2018
Grant dateAug 7, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A pharmaceutical composition is described that is suitable for delivery from a pressurised container. The composition is free of polar excipients and comprises: (a) a propellant component that consists essentially of 1,1-difluoroethane (R-152a); (b) a surfactant component that comprises oleic acid; and (c) a drug component that consists of salbutamol sulphate. The pharmaceutical composition can be delivered using a metered dose inhaler (MDI).

First claim

Opening claim text (preview).

The invention claimed is: 1. A pharmaceutical composition that is free of polar excipients and 1,1,1,2-tetrafluoroethane (R-134a), said composition comprising: (a) a propellant component comprising 1,1-difluoroethane (R-152a), (b) a surfactant component comprising oleic acid; and (c) a drug component consisting of salbutamol sulphate. 2. The pharmaceutical composition of claim 1 which consists essentially of components (a), (b) and (c). 3. A pharmaceutical composition that is free of 1,1,1,2-tetrafluoroethane (R-134a) for delivery from a pressurised container, said composition consisting essentially of: (a) a propellant component consisting essentially of 1,1-difluoroethane (R-152a), (b) a surfactant component comprising oleic acid; and (c) a drug component consisting of salbutamol sulphate. 4. The pharmaceutical composition of claim 1 or claim 3 which consists entirely of components (a), (b) and (c). 5. The pharmaceutical composition of claim 1 , wherein the propellant component consists entirely of 1,1-difluoroethane (R-152a). 6. The pharmaceutical composition of claim 1 , wherein the surfactant component consists entirely of oleic acid. 7. The pharmaceutical composition of claim 1 , wherein the surfactant component consists of oleic acid and at least one additional surfactant compound selected from polyethylene glycols, polyvinylpyrrolidone, and lecithin. 8. The pharmaceutical composition of claim 1 , wherein the surfactant component consists of oleic acid and at least one additional surfactant compound selected from ethyl oleate, sorbitan trioleate, isopropyl myristate, polyethylene glycol 300, polyoxyethylene 20 sorbitan monooleate and monolaurate, propoxylated polyethyleneglycol, polyvinylpyrrolidone, and lecithin. 9. A sealed container that contains the pharmaceutical composition as claimed in claim 1 . 10. The sealed container of claim 9 which is a pressurized container for use with a metered dose inhaler (MDI). 11. A metered dose inhaler (MDI) fitted with a pressurized container as claimed in claim 10 . 12. A method for treating a patient suffering or likely to suffer from a respiratory disorder which comprises administering to the patient a therapeutically or prophylactically effective amount of the pharmaceutical composition as claimed in claim 1 . 13. The method of claim 12 , wherein the respiratory disorder is asthma. 14. The method of claim 12 , wherein the pharmaceutical composition is delivered to the patient using a metered dose inhaler (MDI). 15. A method for manufacturing the pharmaceutical composition as claimed in claim 1 , said method comprising the steps of: introducing a weighed amount of the drug component into an open container from which the drug component will ultimately be released as an aerosol spray using a medication delivery device; fitting a valve device onto the container; introducing the propellant component, in liquid form, through the valve into the container under pressure; and introducing the surfactant component through the valve into the container under pressure. 16. The method of claim 15 , wherein the propellant component is mixed together with the surfactant component and the resulting liquid mixture introduced into the container under pressure via the valve.

Assignees

Inventors

Classifications

  • Antiasthmatics · CPC title

  • Drugs for disorders of the respiratory system · CPC title

  • A61K47/06Primary

    Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite · CPC title

  • Arylalkylamines, e.g. amphetamine, epinephrine, salbutamol, ephedrine {or methadone} · CPC title

  • A61K9/008Primary

    comprising drug dissolved or suspended in liquid propellant for inhalation via a pressurized metered dose inhaler [MDI] · CPC title

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Frequently asked questions

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What does patent US10039828B2 cover?
A pharmaceutical composition is described that is suitable for delivery from a pressurised container. The composition is free of polar excipients and comprises: (a) a propellant component that consists essentially of 1,1-difluoroethane (R-152a); (b) a surfactant component that comprises oleic acid; and (c) a drug component that consists of salbutamol sulphate. The pharmaceutical composition can…
Who is the assignee on this patent?
Mexichem Amanco Holding Sa
What technology area does this patent fall under?
Primary CPC classification A61K47/06. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Aug 07 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).