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Title: Propofol composition
United States Patent: 6,140,374
Inventors: May; Thomas (Grayslake, IL); Hofstetter; John
(Vernon Hills, IL); Olson; Kathleen L. (Chicago, IL); Menon; Sukumaran K.
(Gurnee, IL); Mikrut; Bernard A. (Lake Bluff, IL); Ovenshire; Clayton S.
(Park Ridge, IL); Rhodes; Lawrence John (Lindenhurst, IL); Speicher; Earl
R. (Buffalo Grove, IL); Waterson; James R. (Gurnee, IL)
Assignee: Abbott Laboratories (Abbott Park, IL)
Appl. No.: 354017
Filed: July 15, 1999
Abstract
The present invention is directed to a sterile pharmaceutical
composition comprising a propofol containing oil-in-water emulsion
formulation having as an antimicrobial agent, a member selected from the
group consisting of benzyl alcohol and sodium ethylene diamine
tetraacetate; benzethonium chloride; and benzyl alcohol and sodium
benzoate.
DETAILED DESCRIPTION OF THE INVENTION
The term "antimicrobial" means an agent which
delays onset or retards rate of growth to less than 1 logarithmic increase
over a 24 hour period as compared to an unpreserved formulation.
The composition of the present invention comprises an oil-in-water
emulsion in which the 2,6-diisopropylphenol, either alone or dissolved in
a water immiscible solvent, for example a vegetable oil, is emulsified
with water by means of surfactant.
Typically the solvent is an oil such as soybean oil, safflower oil,
cottonseed oil, corn oil, sunflower oil, arachis oil, castor oil, or olive
oil. Preferably the oil is soybean oil. Alternatively the solvent can be
an ester of a medium or long chain fatty acid, for example a mono-,di-, or
triglyceride; or a compound such as ethyl oleate, isopropyl myristate,
isopropyl palmitate, a glycerol ester or a polyoxyl hydrogenated castor
oil. Other suitable solvents may be marine oils, for example cod liver or
other fish derived oils, or fractionated oils, such as fractionated
coconut oil or modified soybean oil. The composition of present invention
may also comprise a mixture of two or more of the above water immiscible
solvents.
The 2,6-diisopropylphenol, either alone or dissolved in the water
immiscible solvent, is emulsified in an aqueous medium with the aid of a
surfactant. Suitable surfactants include synthetic non-ionic surfactants,
for example ethoxylated ethers and ethoxylated esters, polypropylene
polyethylene block copolymers, and phosphatides, as for example egg and
soy phosphatides. Preferably, the surfactant is egg phosphatide.
Preferred compositions of the present invention comprise from 0.1 to 5.0%
by weight, preferably 1 to 2% by weight, and most preferably 1% by weight
of 2,6-diisopropylphenol; from to 1 to 30% by weight, preferably 10 to 20%
by weight of a water immiscible solvent; and from about 0.2 to 2.0% by
weight, preferably 1.2% by weight of a surfactant. The compositions of the
present invention can also contain pH adjusting agents such as sodium
hydroxide or hydrochloric acid so they can be formulated at a
physiologically neutral pH.
The compositions of the present invention may also be made isotonic by the
incorporation of a suitable additive such as glycerol.
The balance of the composition is made up with water.
The antimicrobial systems utilized in the compositions of the present
invention are selected from the group consisting of benzyl alcohol; benzyl
alcohol and disodium ethylenediamine tetraacetate; benzethonium chloride;
and benzyl alcohol and sodium benzoate. The concentration of the
antimicrobial agents in the final composition will vary depending on the
particular agent or agents selected. For instance in a preferred
composition of the invention the amount of benzyl alcohol is in the range
of about 0.0175% to 0.9% (w/v), more preferably about 0.07% to about
0.45%, most preferred in the range of 0.15%. In an alternate preferred
composition of the invention, the amount of benzyl alcohol is about 0.07%
to about 0.9%, optionally including an amount of disodium EDTA of about
0.005%. Yet another embodiment provides a composition including an amount
of benzethonium chloride of about 0.01% to about 0.1%. Optionally, the
composition of the present invention includes 0.07% sodium benzoate. The
most preferred compositions of the present invention include benzyl
alcohol and sodium benzoate. The compositions of the present invention may
be prepared by conventional processes as for example that disclosed in
U.S. Pat. No. 5,714,520.
A particularly preferred composition of the present invention is as set
forth below.
TABLE 1
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(weight percent)
Broad Preferred
Particularly Preferred
Component Range Range Amount
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2,6- 0.1-5.0 1.0-2.0 1.0
diisopropylphenol
Soybean Oil 1.0-30.0 10.0-30.0 10.0
Egg Phosphatide 0.2-2.0 0.7-2.0 1.2
Benzyl alcohol 0.0175-0.9 0.07-0.45 0.15
Sodium benzoate 0-0.07 0.07 0.07
Glycerol 2.0-3.0 2.35-2.75 2.25
Sodium Hydroxide q.s. q.s. q.s.
Water for Injection to 100 to 100 to 100
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The compositions of the present invention may be used as is conventional
in the art, e.g., for the induction of anesthesia prior to maintenance
with a conventional inhalation anesthetic; as a sole anesthetic agent for
short duration, by repeated administration, or by continuous infusion. The
compositions of the invention may be used as a sole anesthetic agent of
longer duration.
Claim 1 of 27 Claims
What is claimed is:
1. A sterile pharmaceutical composition comprising a propofol containing
oil-in-water emulsion having as an antimicrobial agent, a member selected
from the group consisting of:
benzyl alcohol and sodium ethylene diamine tetraacetate;
benzethonium chloride; and
benzyl alcohol and sodium benzoate.
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