Encapsulated superparamagnetic particles

Claim 2

Encapsulated superparamagnetic particles having a narrow particle size distribution, the mean diameter of the particles being within the range of from about 70 Å to about 450 Å, said particles comprising particles of magnetite having a narrow particle size distribution, the mean diameter of the magnetite particles being between about 50 Å and about 350 Å, said magnetite particles having a magnetization of greater than about 30 emu/gm and a coercive force of less than about 30 Oe, said magnetite particles being encapsulated with a coating of a crosslinked coacervate of gelatin and a polymeric acid and wherein the weight ratio of magnetite to coacervate in said encapsulated particles on a dry basis is from 4:1 to 1:1.

Claim 3

The superparamagnetic particles of claim 1 wherein said polymeric acid comprises recurring acid groups selected from the group consisting of carboxylic acid groups and sulfonic acid groups.

Claim 4

The encapsulated particles of claim 1 wherein at least 80% of the magnetite particles have diameters in the range of between about 100 Å and about 300 Å.

Claim 5

The encapsulated particles of claim 1 wherein the magnetite particles have a magnetization greater than 40 emu/gm.

Claim 6

The encapsulated particles of claim 1 wherein the magnetite particles have a coercive force less than about 25 Oe.

Claim 7

The encapsulated particles of claim 1 which have mean diameters within the range of from about 100 Å to about 400 Å.

Claim 8

The encapsulated particles of claim 1 wherein at least 80% of the particles have mean diameters within the range of from about 150 Å to about 350 Å.

Claim 9

The encapsulated particles of claim 1 wherein the magnetite particles have a magnetization greater than about 50 emu/gm and a coercive force less than about 25 Oe.

Claim 10

The encapsulated particles of claim 1 which have a magnetization greater than about 30 emu/gm and a coercive force less than about 25 Oe.

Claim 11

The encapsulated particles of claim 1 wherein the coacervate coating has an average thickness of between about 30 Å and about 100 Å.

Claim 12

A method for preparing the stable, coated, superparamagnetic magnetite particles of claim 1 having a narrow particle size distribution which consists essentially of forming an equeous solution of ferric and ferrous salts by adding a mixture of ferric and ferrous salts to water in amounts that provide a molar ratio of ferric to ferrous ion in the range of from about 1.6 to 2.4 and in concentrations in the range of from about 0.1 to 1 molar; adding to the solution concentrated hydroxide in an amount in excess of 8 moles of OH - per mole of ferrous ion present in the solution to form a dispersion of fine particles of magnetite; washing the resultant magnetite particles with water until the pH of the magnetite dispersion is within the range of about 10-11; depositing a coating of gelatin and a polymeric acid on the particles by removing excess water from the magnetite dispersion that had been washed to said pH of 10-11; to form a concentrated dispersion of magnetite particles, then coating the thus produced particles by adding the resulting magnetite dispersion to an aqueous solution, having a temperature of at least about 40° C., said aqueous solution consisting essentially of gelatin having an isoelectric point greater than about 8 and a polymeric acid comprising at least one recurring acid group; and adjusting to coacervation conditions comprising a pH in the range of between about 4.0 and 5.5 and a concentration of the gelatin/polymeric acid mixture of less than about 2% (wt/vol); and then crosslinking to form and produce.

Claim 13

The method of claim 11 wherein the molar ratio of ferric to ferrous ions is about 2.

Claim 14

The method of claim 11 wherein the ferric and ferrous salts are sulfates.

Claim 15

The method of claim 11 wherein the concentration of the salts is about 0.1 molar.

Claim 16

The method of claim 11 which further comprises adding sufficient acid to the aqueous mixture of ferric and ferrous salts to adjust the pH to less than about 1.5.

Claim 17

The method of claim 15 wherein the acid is sulfuric acid.

Claim 18

The method of claim 11 which further comprises adding from about 0.1 to about 5% (wt/vol) of a surfactant to the salt solution.

Claim 19

The method of claim 17 wherein the surfactant is sodium dodecyl sulfate.

Claim 20

The method of claim 11 which further comprises purging the solution of oxygen by bubbling therethrough an inert gas for a period of at least about 10 minutes.

Claim 21

The method of claim 19 wherein said bubbling is continued for at least about 30 minutes.

Claim 22

The method of claim 11 wherein the concentrated hydroxide comprises NaOH in an amount equivalent to about 10 moles per mole of ferrous ion present in the salt solution.

Claim 23

The method of claim 11 wherein each of said gelatin and polymeric acid are present in a concentration of from about 1% to about 10% (w/vol) and the ratio of magnetite to the gelatin/polymeric acid mixture on a dry basis being from about 4:1 to about 1:1.

Claim 24

The method of claim 11 wherein said recurring acid group is selected from the group consisting of carboxylic acid groups and sulfonic acid groups.

Claim 25

The method of claim 11 wherein the coacervate is crosslinked with a suitable crosslinking agent for gelatin.

Claim 26

The method of claim 11 wherein the gelatin has an isoelectric point of at least about 8.5.

Claim 27

The method of claim 11 wherein the polymeric acid is gum arabic.

Claim 28

The method of claim 11 wherein said adjusting to coacervating conditions comprises adding to the dispersion of magnetite containing gelatin and polymeric acid sufficient concentrated acid solution to provide said pH within the range of from about 4.0 to 5.5.

Claim 29

The method of claim 27 which further comprises adding the resulting suspension slowly, with stirring, to a large excess of cold water maintained at a temperature below about 5° C. and stirring to stabilize the coacervate coated particles.

Claim 30

The method of claim 24 wherein said crosslinking agent is a gelatin hardener.

Claim 31

The method of claim 29 wherein the gelatin hardener is glutaraldehyde.

Claim 32

The method of claim 30 wherein said glutaraldehyde is added in a concentrated solution containing sufficient glutaraldehyde to provide at least about 2 gms. of glutaraldehyde per 100 gm. of gelatin on a dry basis.

Claim 33

The method of claim 24 wherein said crosslinking step includes stirring for a sufficient time to assure completion of the crosslinking reaction, raising the pH to above 7, increasing the temperature to about 20-25° C., and washing with water to remove unreacted crosslinking agent.

Claim 34

The method of claim 32 wherein said pH is raised to at least about 10.