Bio-artificial periosteum based on micropatterning of biomimetic mineralized calcium-phosphorus nanoparticles and method for manufacturing the same

US9821087B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9821087-B2
Application numberUS-201615079872-A
CountryUS
Kind codeB2
Filing dateMar 24, 2016
Priority dateOct 9, 2015
Publication dateNov 21, 2017
Grant dateNov 21, 2017

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  5. First independent claim

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Abstract

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The disclosure relates to a bio-artificial periosteum based on micropatterning of biomimetic mineralized calcium-phosphorus nanoparticles and a method for manufacturing the same. The method includes: first, a micropatterned biomimetic mineralized calcium-phosphorus nanoparticle layer is manufactured on a surface of an inert substrate; then, an organic polymer is cross-linked and solidified on the micropatterned biomimetic mineralized calcium-phosphorus nanoparticle layer; at last, the inert substrate is removed, so that the bio-artificial periosteum based on micropatterning of biomimetic mineralized calcium-phosphorus nanoparticles is obtained. The bio-artificial periosteum not only simulates the composition of natural bone in material components, but also realizes high degree of biomimesis in micro-nano size in structure. Moreover, the distribution of bone marrow mesenchymal stem cells can be regulated by the bio-artificial periosteum, so that the cells can be effectively defined on a surface of calcium-phosphorus particle micropattern and a high degree of ordered alignment thereof can be realized.

First claim

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What is claimed is: 1. A bio-artificial periosteum based on micropatterning of biomimetic mineralized calcium-phosphorus nanoparticles, comprising a micropatterned biomimetic mineralized calcium-phosphorus nanoparticle layer and an organic polymer that is cross-linked and solidified on the micropatterned biomimetic mineralized calcium-phosphorus nanoparticle layer. 2. The bio-artificial periosteum according to claim 1 , wherein a micropattern is one selected from a group consisting of straight stripe, annular stripe, and mesh stripe. 3. The bio-artificial periosteum according to claim 1 , wherein in addition to biomimetic mineralized calcium-phosphorus nanoparticles, raw material ingredients of the micropatterned biomimetic mineralized calcium-phosphorus nanoparticle layer further comprise macromolecules which would facilitate cell adhesion, bone growth factor, and/or anti-inflammatory drug. 4. The bio-artificial periosteum according to claim 1 , wherein the organic polymer is one selected from a group consisting of collagen, gelatin, chitosan, hyaluronic acid, polylactic acid, polycaprolactone, polyglycolic acid, poly(lactic-co-glycolic acid), polyurethane, and polycarbonate. 5. A method for manufacturing the bio-artificial periosteum based on micropatterning of biomimetic mineralized calcium-phosphorus nanoparticles according to any one of claims 1 to 4 , comprising the steps of: (1) manufacturing a micropatterned biomimetic mineralized calcium-phosphorus nanoparticle layer, comprising the sub-steps of: taking protein, polysaccharide, or synthetic molecule as a mineralization template, adding calcium-phosphorus salt to the mineralization template, and obtaining biomimetic mineralized calcium-phosphorus nanoparticles after codeposition and self-assembly in a biomimetic mineralization manner; dispersing the biomimetic mineralized calcium-phosphorus nanoparticles into water so as to prepare biomimetic mineralized calcium-phosphorus nanoparticle aqueous suspension; photoetching negative photoresist on a silicon wafer so as to prepare a micropattern array, forming a secondary seal through reversed moulding with PDMS adhesive, and forming a hydrophilic and soft agarose micropattern seal through reversed moulding with agarose; and dropwise adding or coating the biomimetic mineralized calcium-phosphorus nanoparticle aqueous suspension on a surface of the agarose micropattern seal so as to form a uniform thin layer, airing the layer to semidry, printing the layer on a surface of the inert substrate through a micro-contact method, and removing agarose gel so as to obtain the micropatterned biomimetic mineralized calcium-phosphorus nanoparticle layer; or taking protein, polysaccharide, or synthetic molecule as a mineralization template, and dispersing the mineralization template into water so as to prepare mineralization template aqueous suspension; photoetching negative photoresist on a silicon wafer so as to prepare a micropattern array, forming a secondary seal through reversed moulding with PDMS adhesive, and forming a hydrophilic and soft agarose micropattern seal through reversed moulding with agarose; and dropwise adding or coating the mineralization template aqueous suspension on a surface of the agarose micropattern seal so as to form a uniform thin layer, airing the layer to semidry, printing the layer on a surface of the inert substrate through a micro-contact method, removing agarose gel so as to obtain a micropatterned mineralization template layer, and manufacturing biomimetic mineralized calcium-phosphorus nanoparticles on the mineralization template through codeposition in a biomimetic mineralization manner, so as to obtain the micropatterned biomimetic mineralized calcium-phosphorus nanoparticle layer; and (2) covering the micropatterned biomimetic mineralized calcium-phosphorus nanoparticle layer with a polymer solution, and removing the inert substrate after sufficient cross-linking and solidification so as to obtain the bio-artificial periosteum based on micropatterning of biomimetic mineralized calcium-phosphorus nanoparticles. 6. The method according to claim 5 , wherein the inert substrate is one selected from a group consisting of slide, silicon wafer, quartz plate, and polydimethylsiloxane (PDMS) adhesive. 7. The method according to claim 5 , wherein the protein serving as the mineralization template is one or more selected from a group consisting of collagen, bone morphogenetic protein, fibronectin, laminin, bone sialoprotein, silk fibroin, and serum protein; wherein the polysaccharide serving as the mineralization template is one or more selected from a group consisting of glycosaminoglycan, proteoglycan, and chitosan; and wherein the synthetic molecule serving as the mineralization template is one or more selected from a group consisting of synthetic amphoteric peptide molecule and synthetic amphoteric self-assembling molecule. 8. The method according to claim 5 , wherein the cross-linking and solidification in step (2) can be carried out through ultraviolet irradiation for 5 to 20 minutes or reaction at a temperature of 40° C. for 10 to 120 minutes after cross linker being added. 9. The method according to claim 5 , wherein the sub-step of obtaining biomimetic mineralized calcium-phosphorus nanoparticles after codeposition and self-assembly in a biomimetic mineralization manner in step (1) is specifically: adding a solution containing calcium ions to a mineralization template solution, mixing the solution uniformly, dropwise adding a solution containing phosphate ions, dropwise adding alkali solution simultaneously to adjust a pH value to a range between 7 and 8, stirring the solution in water bath with a temperature of 37° C. and aging it, suction filtrating or centrifugally cleaning obtained precipitation with ultra-pure water, lyophilizing and grinding so as to obtain biomimetic mineralized calcium-phosphorus nanoparticles. 10. The method according to claim 5 , wherein the sub-step of manufacturing biomimetic mineralized calcium-phosphorus nanoparticles on the micropatterned mineralization template through codeposition in a biomimetic mineralization manner, so as to obtain the micropatterned biomimetic mineralized calcium-phosphorus nanoparticle layer in step (1) is specifically: dropwise adding simulated body fluid or Dulbecco's Phosphate Buffered Saline (DPBS) containing calcium chloride on a surface of the micropatterned mineralization template layer, covering and immersing the layer in water bath with a temperature of 37° C. and aging it, and removing DPBS by washing with ultra-pure water after biomimetic mineralized calcium-phosphorus nanoparticles are deposited on the mineralization template in a biomimetic mineralization manner, so as to obtain the micropatterned biomimetic mineralized calcium-phosphorus nanoparticle layer.

Assignees

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Classifications

  • which are at least partially destroyed, e.g. broken, molten, before demoulding; Moulding surfaces or spaces shaped by, or in, the ground, or sand or soil, whether bound or not; Cores consisting at least mainly of sand or soil, whether bound or not · CPC title

  • Moulds characterised by special surfaces for producing a desired surface of a moulded article, e.g. profiled or polished moulding surfaces (B28B7/36 takes precedence; producing decorative effects B44C; designs of stone surfaces B44F) · CPC title

  • Phosphorus-containing materials, e.g. apatite · CPC title

  • Biologically active materials, e.g. therapeutic substances {(A61L27/227 takes precedence)} · CPC title

  • by simple casting, the material being neither forcibly fed nor positively compacted (for molten material B28B1/54) · CPC title

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What does patent US9821087B2 cover?
The disclosure relates to a bio-artificial periosteum based on micropatterning of biomimetic mineralized calcium-phosphorus nanoparticles and a method for manufacturing the same. The method includes: first, a micropatterned biomimetic mineralized calcium-phosphorus nanoparticle layer is manufactured on a surface of an inert substrate; then, an organic polymer is cross-linked and solidified on t…
Who is the assignee on this patent?
Univ Huazhong Science Tech
What technology area does this patent fall under?
Primary CPC classification A61L27/24. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Nov 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).