US2012172997A1PendingUtilityA1
Self-Detaching Layer for Easy Implant Removal
Est. expiryJul 9, 2030(~4 yrs left)· nominal 20-yr term from priority
A61F 2/3094A61L 27/34A61B 2017/00004A61L 27/32A61F 2002/3093A61F 2210/0004A61L 27/58A61L 27/28A61B 17/842A61L 27/306A61B 17/80A61F 2310/00023A61F 2/30767A61F 2002/30672A61L 2430/02A61F 2310/00976A61L 2420/08A61F 2002/30064A61F 2002/30932A61F 2002/30929A61F 2002/30971A61F 2/30A61F 2002/2817A61F 2310/00796A61F 2002/30067A61B 17/848A61B 17/72A61L 2420/02A61L 2400/18
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Claims
Abstract
A bone implant includes (a) a first layer provided over a first outer surface of the bone implant and being formed of a first material which is one of water-soluble and degradable in body fluids, the first layer having a first thickness and (b) a second layer provided over an outer periphery of the first layer and being formed of a biocompatible material, the second layer having a second thickness smaller than the first thickness.
Claims
exact text as granted — not AI-modified1 . A bone implant, comprising:
a first layer provided over a first outer surface of the bone implant and including a first material which is one of water-soluble and degradable in body fluids, the first layer having a first thickness; and a second layer provided over an outer surface of the first layer and formed of a second, biocompatible material, the second layer having a second thickness smaller than the first thickness.
2 . The implant according to claim 1 , wherein the second layer includes a bioresorbable or bio-dissolving material.
3 . The implant according to claim 1 , wherein the second layer includes a non-resorbable or non-dissolving material.
4 . The implant according to claim 3 , wherein the second thickness is between 1 nm and 100 nm.
5 . The implant according to claim 2 , wherein a resorption/dissolution rate of the second layer is smaller than a resorption/dissolution rate of the first layer.
6 . The implant according to claim 5 , wherein the resorption/dissolution rate of the second layer is between two weeks and three months after implantation in vivo.
7 . The implant according to claim 1 , wherein the first layer is made of a resorbable material.
8 . The implant according to claim 1 , wherein the first thickness of the first layer is between approximately 10 μm and 1000 μm, the ratio of the first thickness to the second thickness being in the range of 10,000:1 and 1,000:1.
9 . The implant according to claim 1 , wherein the first layer is formed of one of polyvinyl alcohol (PVA) and a polylactide.
10 . The implant according to claim 9 , wherein the second layer is formed of a non-resorbable metal, preferably titanium or a titanium alloy with a maximum second thickness of 100 nm.
11 . The implant according to claim 9 , wherein the second layer is formed of hydroxyapatite and has a maximum second thickness of 10 μm.
12 . The implant according to claim 1 , wherein at least one of the first and second layers comprises at least one biodegradable metal or metal alloy selected from a group comprising magnesium, iron and alloys thereof.
13 . The implant according to claim 1 , further comprising an intermediary layer interposed between the first layer and the second layer, the intermediary layer being formed of a mixture of the materials of the first and second layers.
14 . The implant according to claim 1 , further comprising a third layer provided over an outer surface of the second layer, the third layer being formed of a material which is one of water-soluble and degradable in body fluids.
15 . The implant according to claim 14 , further comprising a fourth layer provided over an outer surface of the third layer, the fourth layer being formed of a biocompatible material.
16 . The implant according to claim 15 , wherein the number of alternating layers comprising a material which is water-soluble or degradable in body fluids and a biocompatible material is 2 x; x being 3 or larger.
17 . The implant according to claim 1 , wherein the material of the first layer is different from the material of the second layer.
18 . A method for manufacturing a bone implant, comprising:
applying a first layer of a first material over a first surface of the bone implant, the first material being one or both of water-soluble and degradable in body fluids; and applying a second layer of a second material over an outer surface of the first layer, the second material being biocompatible.
19 . The method according to claim 18 , further comprising the step of applying an intermediary layer over the first layer prior to applying the second layer, the intermediary layer being formed of a mixture of the first and second materials.
20 . The method according to claim 18 , wherein the first and second layers are applied by one of dip coating and spray coating.Join the waitlist — get patent alerts
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