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Title: Powdered pharmaceutical formulations having
improved dispersibility
United States Patent: 6,187,344
Inventors: Eljamal; Mohammed (Tripoli, CA); Patton; John S.
(Portola, CA); Foster; Linda C. (Sunnyvale, CA); Platz; Robert M. (Half
Moon Bay, CA)
Assignee: Inhale Therapeutic Systems (San Carlos, CA)
Appl. No.: 903658
Filed: July 31, 1997
Abstract
Dispersibility of a respirable powder, administrable by inhalation, is
increased by including a pharmaceutically acceptable water-soluble
polypeptide.
SUMMARY OF THE INVENTION
One aspect of this invention is a dispersible dry power composition that
is suitable for administration to a subject by inhalation, and that
comprises a pharmaceutically-acceptable excipient, a therapeutically
effective amount of an active agent suitable for treating a condition
susceptible to treatment by oral inhalation, and a dispersibility-enhancing
amount of a pharmaceutically acceptable polypeptide, e.g., HSA.
Alternatively, an aspect of this invention can be viewed as an improvement
over existing powdered pharmaceutical compositions suitable for inhalation
therapy, in that the improvement comprises the presence of a
dispersibility-enhancing amount of a pharmaceutically acceptable
polypeptide in the powdered pharmaceutical composition.
Another aspect of this invention is a method of administering a
therapeutically effective amount of a powdered composition of this
invention to a human subject in need thereof by dispersing said powdered
composition as an aerosol into a chamber having a delivery outlet suitable
for inhalation therapy, e.g., a mouthpiece and having said subject inhale,
preferably orally, said dispersed powder into the subject's lungs.
Another aspect of this invention is an improvement in a process for
preparing a respirable powdered pharmaceutical composition. In a process
for preparing a respirable powdered pharmaceutical composition by (a)
forming a homogeneous aqueous composition comprising water, a
pharmaceutically acceptable excipient and an active agent suitable for
treating a disease state by inhalation, (b) removing the water from the
aqueous composition to form a solid and (c) transforming the resulting
solid into a respirable powdered pharmaceutical composition, the
improvement of this invention comprises adding a water-soluble,
physiologically-acceptable protein (e.g., HSA) to the aqueous composition
in an amount sufficient to enhance the dispersibility of the resulting
respirable powdered pharmaceutical composition.
Another, more specific, aspect of this invention is a method for preparing
a spray-dried, dispersible powdered pharmaceutical composition that
comprises spray drying a homogeneous aqueous mixture comprising water, a
pharmaceutically acceptable excipient, an active agent suitable for
treating a disease state by inhalation, and a dispersibility-enhancing
amount of a physiologically acceptable, water-soluble protein under
conditions sufficient to provide a dispersible powdered pharmaceutical
composition having a particle size less than about ten microns.
Alternatively, this aspect may be viewed as an improvement in a method for
preparing a spray-dried, dispersible, powdered pharmaceutical composition
by spray drying a homogeneous aqueous mixture comprising water, a
pharmaceutically acceptable excipient and an active agent suitable for
treating a disease state by inhalation under conditions sufficient to
provide a dispersible powder, wherein the improvement comprises including
a dispersibility-enhancing amount of a physiologically acceptable,
water-soluble protein in the aqueous mixture.
Claim 1 of 17 Claims
The claimed subject matter is:
1. A spray-dried dispersible powdered composition suitable for inhalation
by a human subject, comprising:
(a) a therapeutically effective amount of an active agent suitable for
treating a condition in said subject by inhalation;
(b) a pharmaceutically-acceptable excipient selected from the group
consisting of carbohydrates, amino acids, and mixtures thereof, wherein
said excipient is present in an amount sufficient to uniformly distribute
the active agent throughout the composition, and
(c) about 1% by weight to about 15% by weight of a dispersibility-enhancing,
physiologically-acceptable, water-soluble polypeptide, whereby the
presence of said polypeptide in the composition is effective to increase
the dispersibility of the composition over the dispersibility of the
composition in the absence of said polypeptide.
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