Carrier liquid solutions for the production of gas microbubbles, preparation thereof, and use thereof as contrast medium for ultrasonic diagnostics

Claim 2

A combination adapted when microbubbles are formed therein for use as contrast medium for ultrasonic diagnostics, consisting essentially of (a) an amount from about 0.01% to 10% by weight of at least one tenside, as a solution in an aqueous intravenously injectable physiologically acceptable aqueous carrier liquid, effective to impart a surface tension to the solution of less than 43 dyn/cm; (b) an amount from about 0.5% to 50% by weight of at least one viscosity-raising compound, as a solution in an aqueous intravenously injectable physiologically acceptable aqueous carrier liquid, effective to impart a viscosity to the solution of at least 20 mPa·s; wherein (a) and (b) are present in the combination as a single solution or as separate solutions which, when mixed, form the single solution; and (c) a physiologically acceptable sterile gas for forming microbubbles in a mixture of (a) and (b).

Claim 3

A combination according to claim 1 wherein (a) and (b) are present in the combination as a single solution.

Claim 4

A combination according to claim 1 wherein (a) and (b) are present in the combination as separate solutions.

Claim 5

A combination according to claim 2, produced by mixing together separate solutions of (a) and (b) to form the single solution and the physiologically acceptable sterile gas and wherein one of the separate solutions contains 0.05-5% by weight of a physiologically acceptable salt of carbonic acid, and the other contains an amount of physiologically acceptable acid equivalent to and reactive with the carbonic acid salt.

Claim 6

A combination according to claim 1 wherein the tenside of (a) is non-ionic.

Claim 7

A combination according to claim 5 wherein the nonionic tenside contains a polyoxyethylene-polyoxypropylene polymer.

Claim 8

A combination according to claim 6 wherein the polyoxyethylene-polyoxypropylene polymer has a molecular weight of about 6,000 to 9,000, about 13,000 or about 16,000.

Claim 9

A combination according to claim 5 wherein the nonionic tenside is a polyoxyethylene fatty acid ester or a polyoxyethylene stearate.

Claim 10

A combination according to claim 1 wherein the tenside is an ionic tenside.

Claim 11

A combination according to claim 9 wherein the ionic tenside is sodium lauryl sulfate or sodium dioctylsulfosuccinate.

Claim 12

A combination according to claim 10 wherein the carrier liquid is water, a physiological saline solution or Ringer's solution.

Claim 13

A combination according to claim 1 wherein the viscosity-raising compound is gelatin or oxypolygelatin.

Claim 14

A combination according to claim 1 wherein the viscosity-raising compound is lactose or glucose.

Claim 15

A combination according to claim 1 wherein the physiologically acceptable gas is air, carbon dioxide, oxygen, nitrogen, a noble gas or mixture thereof.

Claim 16

A combination according to claim 14 wherein the physiologically acceptable gas is air.

Claim 17

A combination according to claim 14 wherein the physiologically acceptable gas is carbon dioxide.

Claim 18

A combination according to claim 1 wherein (a) is a 1% solution in water of polyoxyethylene-polypropylene polymer having a molecular weight of about 6,000 to 9,000 and (b) is about a 1% solution of gelatin in water.

Claim 19

In a method for altering the transmission characteristics of blood to an electromagnetic or elastic wave transmitted therethrough by the steps of forming an amount of microbubbles effective to substantially alter such transmission characteristics of blood in the area thereof containing the microbubbles in an intravenously injectable physiologically acceptable aqueous carrier liquid by mechanically agitating the carrier liquid in the presence of a physiologically acceptable gas, and dispersing the microbubble-containing carrier liquid in the blood, the improvement wherein the carrier liquid is substantially free of undissolved solids, has a surface tension of less than 43 dyn/cm and a viscosity of at least 20 mPa·s, and the physiologically acceptable gas is sterile.

Claim 20

In a method for altering the transmission characteristics of blood to an electromagnetic or elastic wave transmitted therethrough by the steps of forming an amount of microbubbles effective to substantially alter such transmission characteristics of blood in the area thereof containing the microbubbles in an intravenously injectable physiologically acceptable aqueous carrier liquid by mechanically agitating the carrier liquid in the presence of a physiologically acceptable gas, and dispersing the microbubble-containing carrier liquid in the blood, the improvement wherein the carrier liquid is substantially free of undissolved solids, has a surface tension of less than 43 dyn/cm and a viscosity of at least 20 mPa·s, and the physiologically acceptable gas is sterile.

Claim 21

A method according to claim 18 wherein at least a portion of the microbubbles are formed by injecting a solution of the tenside in an intravenously injectable, physiologically acceptable carrier liquid into a solution of the viscosity-raising compound in an intravenously injectable, physiologically acceptable carrier liquid under an atmosphere of the physiologically acceptable gas.

Claim 22

A method according to claim 19 wherein the thusproduced mixture of microbubble-containing solution of tenside and viscosity-raising compound is mechanically agitated under an atmosphere of the physiologically acceptable gas prior to dispersing the mixture in the blood.

Claim 23

A method according to claim 18 wherein at least a portion of the microbubbles are formed by injecting a portion of the solution of the tenside and viscosity-raising compound into another portion of the solution, under an atmosphere of the physiologically acceptable gas.

Claim 24

A method according to claim 21 wherein the thusproduced mixture of microbubble-containing solution of tenside and viscosity-raising compound is mechanically agitated under an atmosphere of the physiologically acceptable gas prior to dispersing the mixture in the blood.

Claim 25

A method according to claim 18 wherein the carrier liquid is produced immediately prior to being mechanically agitated with the physiologically acceptable gas by mixing (a) a solution of an amount from about 0.01% to 10% by weight of at least one tenside in an aqueous intravenously injectable physiologically acceptable aqueous carrier liquid, effective to impart a surface tension to the solution of less than 43 dyn/cm, with (b) a solution of an amount from about 0.5% to 50% by weight of at least one viscosity-raising compound in an aqueous intravenously injectable physiologically acceptable aqueous carrier liquid, effective to impart a viscosity to the solution of at least 20 mPa·s.

Claim 26

A kit for preparing a liquid suspension of microbubbles suitable for use as a contrast medium for ultrasonic diagnostics, comprising (a) a first sterile sealed container provided with a means for gaining access to the contents thereof with a hypodermic needle under sterile conditions and containing a solution in an intravenously injectable carrier liquid substantially free of undissolved solids, of an amount from 0.02% to 50% by weight of at least one tenside effective to lower the surface tension of the mixture produced when the solution in (a) is mixed with the solution in (b) to less than 43 dyn/cm; and (b) a second sterile sealed container provided with means for gaining access to the contents thereof with a hypodermic needle under sterile conditions and containing an amount of from about 1% to 50% by weight of a solution in an injectable aqueous liquid substantially free of undissolved solids of at least one viscosity-raising compound, effective to impart a viscosity to the mixture produced when the solution in (a) is mixed with the solution in (b) of at least 20 mPa·s; at least one of (a) and (b) also containing a sufficient amount of a sterile physiologically acceptable gas to produce microbubbles in the mixture of the solution in (a) and (b) when the mixture is mechanically agitated.

Claim 27

A kit for preparing a liquid suspension of microbubbles suitable for use as a contrast medium for ultrasonic diagnostics, comprising (a) a first sterile sealed container provided with a means for gaining access to the contents thereof with a hypodermic needle under sterile conditions and containing a solution in an intravenously injectable carrier liquid substantially free of undissolved solids, of an amount from 0.02% to 50% by weight of at least one tenside effective to lower the surface tension of the mixture produced when the solution in (a) is mixed with the solution in (b) to less than 43 dyn/cm; and (b) a second sterile sealed container provided with means for gaining access to the contents thereof with a hypodermic needle under sterile conditions and containing an amount of from about 1% to 50% by weight of a solution in an injectable aqueous liquid substantially free of undissolved solids of at least one viscosity-raising compound, effective to impart a viscosity to the mixture produced when the solution in (a) is mixed with the solution in (b) of at least 20 mPa·s; at least one of (a) and (b) also containing a sufficient amount of a sterile physiologically acceptable gas to produce microbubbles in the mixture of the solution in (a) and (b) when the mixture is mechanically agitated.

Claim 28

A kit according to claim 24 wherein (b) contains a sufficient amount of a physiologically acceptable gas to produce the microbubbles.

Claim 29

A sealed vial containing a solution, in an intravenously injectable, physiologically acceptable aqueous carrier liquid substantially free of undissolved solids, of an amount from about 0.1% to 10% by weight of at least one tenside effective to substantially lower the surface tension of the carrier liquid and an amount of from about 0.5 to 50% by weight of at least one viscosity-raising compound effective to substantially raise the viscosity of the carrier liquid and a volume of a sterile physiologically acceptable gas sufficient to produce microbubbles in the solution when the solution and gas are mixed by mechanical agitation.

Claim 30

A sealed vial containing a solution, in an intravenously injectable, physiologically acceptable aqueous carrier liquid substantially free of undissolved solids, of an amount from about 0.1% to 10% by weight of at least one tenside effective to substantially lower the surface tension of the carrier liquid and an amount of from about 0.5 to 50% by weight of at least one viscosity-raising compound effective to substantially raise the viscosity of the carrier liquid and a volume of a sterile physiologically acceptable gas sufficient to produce microbubbles in the solution when the solution and gas are mixed by mechanical agitation.