Controlled release compositions for administration of therapeutic agents to ruminants

Claim 2

A controlled release composition for administering a therapeutic agent to a ruminant comprising the therapeutic agent and a carrier material in the form of a coherent tablet or bolus in solid form, wherein said carrier material is formed from a non-tacky free flowing powder which forms a gel in contact with an aqueous medium in which 90% of the particles are less than 100 μm (200 mesh sieve) and which can be mixed with the therapeutic agent to give a uniform, intimate and reproducible mixture such that when the tablet or bolus contacts an aqueous medium a fluid from the aqueous medium is absorbed at the tablet/aqueous medium interface into the body of the tablet to a predetermined depth of penetration so as to produce a gelled volume contiguous with the interface corresponding to the depth of penetration of the fluid, said gel hindering further penetration of the fluid into the tablet beyond the prearranged depth in order to maintain the rate of fluid penetration constant and the integrity of the tablet beyond the prearranged depth of penetration of the fluid to prevent release of therapeutic agent therefrom and said gel having a yield stress which is substantially less than the yield stress of the corresponding volume of the tablet before gelling and which sharply declines with increasing water content up to a preselected critical water content thereby permitting controlled release of therapeutic agent from the gel in use.

Claim 3

A controlled release composition according to claim 1 further comprising a bonding and/or slip agent.

Claim 4

A controlled release composition according to claim 1 in which the tablet or bolus is formed in a die under pressure.

Claim 5

A controlled release composition according to claim 1 in which the yield stress of the gel declines gradually as the water content is increased above the critical water content.

Claim 6

A controlled water release composition according to claim 1 in which the fluid is an aqueous solution from the rumen of the ruminant.

Claim 7

A controlled release composition according to claim 1 in which the carrier material has a softening point greater than 39° C. when in the rumen of a ruminant.

Claim 8

A controlled release composition according to claim 1 in which the critical water content is greater than 4%.

Claim 9

A controlled release composition according to claim 1 in which the critical water content is in the range from greater than 4% to about 40%.

Claim 10

A controlled release composition according to claim 1 in which the carrier material is a surface active material or an emulsifying agent.

Claim 11

A controlled release composition according to claim 1 in which the carrier material is selected from the group comprising a sucrose ester, polyglyceryl stearate, and milk powder.

Claim 12

A controlled release composition according to claim 10 in which the sucrose ester is a monosteorate ester.

Claim 13

A controlled release composition according to claim 1 in which the yield stress of the gelled area of the tablet or bolus is less than 2500 G.

Claim 14

An intraruminal device for administering a therapeutic agent to a ruminant comprising a hollow body having an opening located at one end, a solid tablet or bolus comprising the therapeutic agent and a carrier material contained within the body, a driving means for urging the tablet or bolus towards the opening, restricting means adjacent the opening for preventing expulsion of ungelled tablet or bolus from the device by said drving means, and retaining means connected to the body for retaining the device in the rumen of the ruminant after location therein, said carrier material being in the form of a coherent tablet or bolus in solid form, wherein said carrier material is formed from a non-tacky free flowing powder which forms a gel in contact with an aqueous medium in which 90% of the particles are less than 100 μm (200 mesh sieve) and which can be mixed with the therapeutic agent to give a uniform, intimate and reproducible mixture such that when the tablet or bolus contacts an aqueous medium a fluid from the aqueous medium is absorbed at the tablet/aqueous medium interface into the body of the tablet to a predetermined depth of penetration so as to produce a gelled volume contiguous with the interface corresponding to the depth of penetration of the fluid, said gel hindering further penetration of the fluid into the tablet beyond the prearranged depth in order to maintain the rate of fluid penetration constant and the integrity of the tablet beyond the prearranged depth of penetration of the fluid to prevent release of therapeutic agent therefrom and said gel having a yield stress which is substantially less than the yield stress of the corresponding volume of the tablet before gelling and which sharply declines with increasing water content up to a preselected critical water content thereby permitting controlled release of therapeutic agent from the gel in use.

Claim 15

An intraruminal device for administering a therapeutic agent to a ruminant comprising a hollow body having an opening located at one end, a solid tablet or bolus comprising the therapeutic agent and a carrier material contained within the body, a driving means for urging the tablet or bolus towards the opening, restricting means adjacent the opening for preventing expulsion of ungelled tablet or bolus from the device by said drving means, and retaining means connected to the body for retaining the device in the rumen of the ruminant after location therein, said carrier material being in the form of a coherent tablet or bolus in solid form, wherein said carrier material is formed from a non-tacky free flowing powder which forms a gel in contact with an aqueous medium in which 90% of the particles are less than 100 μm (200 mesh sieve) and which can be mixed with the therapeutic agent to give a uniform, intimate and reproducible mixture such that when the tablet or bolus contacts an aqueous medium a fluid from the aqueous medium is absorbed at the tablet/aqueous medium interface into the body of the tablet to a predetermined depth of penetration so as to produce a gelled volume contiguous with the interface corresponding to the depth of penetration of the fluid, said gel hindering further penetration of the fluid into the tablet beyond the prearranged depth in order to maintain the rate of fluid penetration constant and the integrity of the tablet beyond the prearranged depth of penetration of the fluid to prevent release of therapeutic agent therefrom and said gel having a yield stress which is substantially less than the yield stress of the corresponding volume of the tablet before gelling and which sharply declines with increasing water content up to a preselected critical water content thereby permitting controlled release of therapeutic agent from the gel in use.

Claim 16

An intraruminal device as claimed in claim 13 wherein the force exerted on the tablet or bolus by the driving means is sufficient to extrude the therapeutic agent from the gel through the opening of the body.

Claim 17

An intraruminal device as claimed in claim 13 wherein the force exerted by the driving means is insufficient to extrude an ungelled composition through the opening of the device.

Claim 18

An intraruminal device as claimed in claim 13 in which the rate of release of the therapeutic agent is up to about 20 mm per day.

Claim 19

An intraruminal device as claimed in claim 13 in which the rate of release is in the range of 0.1 to 10 mm per day.

Claim 20

An intraruminal device as claimed in claim 13 in which force of the driving means is less than 2500 G.

Claim 21

An intraruminal device as claimed in claim 13 in which the force of the driving means is in the range of 100 to 1000 G.

Claim 22

An intraruminal device as claimed in claim 13 in which the release rate of the therapeutic agent is substantially independent of the force of the driving means.

Claim 23

An intraruminal device according to claim 13 in which the retaining means in a resilient member connected to the body of the device so as to be capable of two different configurations, a first configuration in which the resilient member is relatively close to the body so that the device is capable of being administered to the ruminant and a second configuration in which the resilient member extends from the body so as to be retained the rumen after location therein.

Claim 24

In combination a therapeutic composition comprising a therapeutic agent and carrier material in the form of a coherent tablet or bolus in solid form, wherein said carrier material is formed from a non-tacky free flowing powder which forms a gel in contact with an aqueous medium in which 90% of the particles are less than 100 μm (200 mesh seive) and which can be mixed with the therapeutic agent to give a uniform, intimate and reproducible mixture such that when the tablet or bolus contacts an aqueous medium a fluid from the aqueous medium is absorbed at the tablet/aqueous medium interface into the body of the tablet to a predetermined depth of penetration so as to produce a gelled volume contiguous with the interface corresponding to the depth of penetration of the fluid, said gel hindering further penetration of the fluid into the tablet beyond the prearranged depth in order to maintain the rate of fluid penetration constant and the integrity of the tablet beyond the prearranged depth of penetration of the fluid to prevent release of therapeutic agent therefrom and said gel having a yield stress which is substantially less than the yield stress of the corresponding volume of the tablet before gelling and which sharply declines with increasing water content up to a preselected critical water content thereby permitting controlled release of therapeutic agent from the gel in use and a device for administering the therapeutic agent.

Claim 25

In combination a therapeutic composition comprising a therapeutic agent and carrier material in the form of a coherent tablet or bolus in solid form, wherein said carrier material is formed from a non-tacky free flowing powder which forms a gel in contact with an aqueous medium in which 90% of the particles are less than 100 μm (200 mesh seive) and which can be mixed with the therapeutic agent to give a uniform, intimate and reproducible mixture such that when the tablet or bolus contacts an aqueous medium a fluid from the aqueous medium is absorbed at the tablet/aqueous medium interface into the body of the tablet to a predetermined depth of penetration so as to produce a gelled volume contiguous with the interface corresponding to the depth of penetration of the fluid, said gel hindering further penetration of the fluid into the tablet beyond the prearranged depth in order to maintain the rate of fluid penetration constant and the integrity of the tablet beyond the prearranged depth of penetration of the fluid to prevent release of therapeutic agent therefrom and said gel having a yield stress which is substantially less than the yield stress of the corresponding volume of the tablet before gelling and which sharply declines with increasing water content up to a preselected critical water content thereby permitting controlled release of therapeutic agent from the gel in use and a device for administering the therapeutic agent.