Implant injection device

Claim 2

An injection device for injecting a controlled drug release implant beneath a subject's skin, comprising: a housing, said housing having an injection needle mounted on one end thereof and collinearly therewith to form a single unit, both said housing and needle having hollow, communicating centers: an implant being disposed within the hollow center of the housing and needle unit, and a plunger disposed within the hollow center of said housing and displaceable in an axial direction toward said needle to interact with said implant and provided with an actuating element, said actuating element including means extending axially on opposite sides of said element for alternately supporting and pressing said element against or on skin to be treated so as to maintain said plunger in a steady position with respect to said implant despite collinear relative movement of said housing and needle unit.

Claim 3

Device according to claim 1, wherein the actuating element comprises a supporting surface for pressing and supporting against the skin of the subject having a surface area of about 1 to 10 cm 2 .

Claim 4

Device according to claim 2, wherein the supporting surface is elongated and extends in the longitudinal direction and at some radial distance from the plunger.

Claim 5

Device according to claim 3, wherein the supporting surface is situated at an acute angle (α) with respect to the longitudinal direction of the plunger.

Claim 6

Device according to claim 2, comprising a pressing element disposed on the plunger opposite the supporting surface.

Claim 7

Device according to claim 1, wherein the housing has an outside surface with one or more essentially flat surfaces.

Claim 8

Device according to claim 6, wherein the flat surfaces are disposed in a manner such that the housing has a polygonal cross section.

Claim 9

Device according to claim 1, wherein the housing and the plunger are provided with stop elements which interact with each other and which are constructed in a manner such that the distance over which the plunger can be displaced in the hollow needle toward the extremity thereof is limited.

Claim 10

Device according to claim 1, wherein said housing and said plunger are linked to each other via a coupling which, in a closed state, links said housing and said plunger immovably to each other and, in an open state, permits collinear movement of said plunger within said housing and said hollow needle.

Claim 11

Device according to claim 9, wherein one half of the coupling is formed at the end of a supporting surface for the plunger.

Claim 12

Device according to claim 1, wherein the housing, is moulded from a thermoplastic material, is provided with a cylindrical axial bore adjoining the hollow metal needle, the plunger is moulded from a thermoplastic material, is disposed so as to be axially displaceable in the bore of the housing and in the hollow needle, and the actuating element of the plunger is provided with pressing and supporting surfaces situated opposite each other in a diametrically oblique manner with respect to the plunger axis.

Claim 13

Device according to claim 11, wherein the plunger has, at the actuating end, a first section with a large diameter which fits into the bore of the housing and, at the injection end, a second section with a smaller diameter which fits into the hollow needle.

Claim 14

Device according to claim 7 wherein the device is provided with an implant which can release a drug in a controlled manner.

Claim 15

Device according to claim 13, wherein the implant is formed by a polymer in which the drug is dispersed or which encases the drug.

Claim 16

Device according to claim 1, wherein the device is sterilized and is disposed in a closed packaging that is inaccessible to bacteria.

Claim 17

Device according to claim 1, wherein the supporting surface has transverse ribs formed in the surface thereof that is placed against the skin of the subject to be treated.

Claim 18

Device according to claim 5, wherein the surface of the pressing element has transverse ribs formed therein.

Claim 19

Device according to claim 11, wherein the thermoplastic material is a polyacetal polymer.

Claim 20

Device according to claim 14, wherein the polymer is selected from the group consisting of polysiloxane, polyalkylene and polylactide.

Claim 21

Injection device for injecting a controlled drug release implant beneath a subject's skin, comprising a housing having an injection needle mounted on one end thereof and collinearly therewith to form a single housing and needle unit, both the housing and needle having hollow, communicating centers; an implant being disposed within the hollow center of the housing and needle unit; a plunger extending in a longitudinal direction within the hollow center of the housing, being displaceable in an axial direction toward said needle to interact with the implant and including an actuating element, said actuating element comprising a supporting surface for pressing and supporting against the skin of the subject having and a pressing element disposed on the plunger opposite said supporting surface, said housing and said plunger being linked to each other via coupling means which, in a closed state, links said housing and said plunger immovably to each other and, in an open state, permits collinear movement of said plunger within said housing and said hollow needle.

Claim 22

Injection device for injecting a controlled drug release implant beneath a subject's skin, comprising a housing having an injection needle mounted on one end thereof and collinearly therewith to form a single housing and needle unit, both the housing and needle having hollow, communicating centers; an implant being disposed within the hollow center of the housing and needle unit; a plunger extending in a longitudinal direction within the hollow center of the housing, being displaceable in an axial direction toward said needle to interact with the implant and including an actuating element, said actuating element comprising a supporting surface for pressing and supporting against the skin of the subject having and a pressing element disposed on the plunger opposite said supporting surface, said housing and said plunger being linked to each other via coupling means which, in a closed state, links said housing and said plunger immovably to each other and, in an open state, permits collinear movement of said plunger within said housing and said hollow needle.

Claim 23

Device according to claim 22, wherein said supporting surface for pressing and supporting against the skin of the subject has a surface area of about 1 to 10 cm 2 .

Claim 24

Device according to claim 20, wherein said supporting surface is elongated and extends in said longitudinal direction and at a given radial distance from said plunger.

Claim 25

Device according to claim 22, wherein the supporting surface is situated at an actue angle (α) with respect to the longitudinal direction of the plunger.

Claim 26

Device according to claim 20, wherein said housing has an outside surface with one or more essentially flat surfaces.

Claim 27

Device according to claim 24, wherein said flat surfaces are disposed in a manner such that said housing has a polygonal cross section.

Claim 28

Device according to claim 20, wherein the housing and the plunger are provided with stop elements which interact with each other and which are constructed in a manner such that the distance over which the plunger can be displaced in the hollow needle toward the extremity thereof is limited.

Claim 29

Device according to claim 20, wherein one half the coupling is formed at the end of a supporting surface for the plunger.

Claim 30

Device according to claim 20, wherein the housing is moulded from a thermoplastic material, is provided with a cylindrical axial bore adjoining the hollow metal needle, the plunger is moulded from a thermoplastic material, is dispossed so as to be axially displaceable in the bore of the housing and in the hollow needle, and the actuating element of the plunger is provided with pressing and supporting surfaces situated opposite each other in a diamterically oblique manner with respect to the plunger axis.

Claim 31

Device according to claim 20, wherein the plunger has, at the actuating end a first section with a large diameter which fits into the hollow needle.

Claim 32

Device according to claim 25, wherein the device is provided with an implant adapted to release a drug in a controlled manner.

Claim 33

Device according to claim 30, wherein the implant is formed by a polymer in which the drug is dispersed or which encases the drug.

Claim 34

Device according to claim 20, wherein the device is sterilized and is disposed in a closed packaging that is inaccessible to bacteria.

Claim 35

Device according to claim 20, wherein the supporting surface has transverse ribs formed in the surface thereof that is placed against the skin of the subject to be treated.

Claim 36

Device according to claim 20, wherein the surface of the pressing element has transverse ribs formed therein.

Claim 37

Device according to claim 28, wherein the thermoplastic material is polyactetal polymer.

Claim 38

Device according to claim 31, wherein the polymer is selected from the group consisting of polysiloxane, polyalkylene and polyactide.