JP2005027930A - Bone substitute - Google Patents

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JP2005027930A
JP2005027930A JP2003271800A JP2003271800A JP2005027930A JP 2005027930 A JP2005027930 A JP 2005027930A JP 2003271800 A JP2003271800 A JP 2003271800A JP 2003271800 A JP2003271800 A JP 2003271800A JP 2005027930 A JP2005027930 A JP 2005027930A
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tcp
bone
collagen
slurry
bone substitute
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Takashi Miyazaki
隆 宮崎
Akira Shibata
陽 柴田
Kiyohiro Fujiwara
聖裕 藤原
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Ishifuku Metal Industry Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To easily and inexpensively ensure bone substitute at a defective part at a bone of a human body. <P>SOLUTION: In a pseudo body liquid 2 adjusted to an original component, β-TCP is settled by discharging in liquid. When the supernatant of the slurry of β-TCP is removed, β-TCP of the slurry which is alkali of PH 11 etc is generated. It is added with collagen solution treated with hydrochloric acid and mixed, thereby curing is started by neutralization reaction. Finally, compound material of hydroxyapatite is formed in the state of agar to obtain the bone anaplerotic material. Curing occurs early only by β-TCP obtained by polymerization reaction of phosphoric acid, and hydrogen bond of collagen, and uniform bone replenishment is realized by utilizing β-TCP. In addition. Since the bone substitute is easily cured even when including water, anaplerosis is possible even at a bleeding site, and the material can be utilized also as the carrier of another drug. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

開示技術は、人体中の顎骨等の骨の破損部分を自然な骨の状態にする骨補填の製作技術分野に属する。   The disclosed technology belongs to the field of production technology for bone replacement in which a damaged portion of a bone such as a jawbone in a human body is in a natural bone state.

人体内部には顎骨等の重要な成分を成す骨体があるが、当該骨体は医学・治療中における余分な切削や交通事故等により著しく欠けるところが生じる場合があり、当該欠損部に対する自然発生的な骨部分を充填して周囲の骨部分と一体化するような次の如き骨補填技術がさまざまに開発されるようになってきた。
Soichiro Ito他著「Development of an artificial vertebralbody using a novel biomaterial,hydroxyapatite/collagen composite」 BiomaterialsVolume 23 Issue 19 P3919- 3926(October 2002) Myung Chui Chang他著「FT-IR study forhydroxyapatite/collagen nanocomposite cross-linked by glutaraldehyde」Biomaterials Volume 23,Issue 24 P4811-4818 (December 2002) Myung Chui Chang他著「XPS study for the microstructuredevelopment of hydroxyapatite-collagen nanocomposites cross-linked using glutaraldehyde」 Biomaterials Volume 23 Isuue 18 P3879-3885(October 2002) Yong Zhang他著「Calcium phosphate/chitosanc compositescaffolds for controlled in vitro antibiotic drug release」 Journal ofBiomedical Materials Research Volume 62 Issue 3 P378-386(December 2002) 而して、人体の骨成分は無機成分のハイドロキシアパタイトと有機成分としてのコラーゲンの複合体からなるものであるにもかかわらず、これまで他の研究者等によって研究されているものはハイドロキシアパタイトとコラーゲン溶液を単に混合したものに過ぎず、これらのものは単なる混合体であり、又、水酸化カルシウムとリン酸溶液、及びコラーゲンを混合したものであってもゾル化するのみであり、複合体としてまた固まらないために交互にグルタールアルデヒド等の添加をしたり、紫外線を照射したりしなければならず、著しくコスト高になるという不利点があり複合体とはなりえず、β−TCPに関しては全く検討されていないデメリットがあった。
There are bones that form important components such as the jawbone inside the human body, but the bones may be significantly missing due to excessive cutting or traffic accidents during medical treatment, etc. Various bone filling techniques have been developed as follows, which fill a bone portion and integrate it with the surrounding bone portion.
Soichiro Ito et al. `` Development of an artificial vertebralbody using a novel biomaterial, hydroxyapatite / collagen composite '' BiomaterialsVolume 23 Issue 19 P3919-3926 (October 2002) Myung Chui Chang et al. “FT-IR study for hydroxyapatite / collagen nanocomposite cross-linked by glutaraldehyde” Biomaterials Volume 23, Issue 24 P4811-4818 (December 2002) Myung Chui Chang et al. “XPS study for the microstructure development of hydroxyapatite-collagen nanocomposites cross-linked using glutaraldehyde” Biomaterials Volume 23 Isuue 18 P3879-3885 (October 2002) Yong Zhang et al., Calcium phosphate / chitosanc composite scaffolds for controlled in vitro antibiotic drug release, Journal of Biomedical Materials Research Volume 62 Issue 3 P378-386 (December 2002). Despite being composed of a complex of collagen, what has been studied by other researchers so far is merely a mixture of hydroxyapatite and a collagen solution. Even if it is a mixture of calcium hydroxide, phosphoric acid solution, and collagen, it will only be solated, so that it does not harden as a complex, and glutaraldehyde etc. may be added alternately. , It must be irradiated with ultraviolet rays, and it has the disadvantage of being extremely expensive, so it cannot be a composite , Β-TCP has a demerit that has not been studied at all.

そして、単なる混合物をフリーズドライ後ブロックにして成形して適宜に充填するに過ぎず、治療中においてチェアーサイドにて行うに充填することが不可能である難点があった。   Then, the simple mixture is simply made into a block after freeze-drying and then molded and filled appropriately, and there is a difficulty that it is impossible to fill the chair side during treatment.

又、紫外線を用いたりしてコスト的に高くなって実用性が低い不利点があるものであった。   In addition, there is a disadvantage that the cost becomes high due to the use of ultraviolet rays and the practicality is low.

そして、これらの混和物をフリーズドライして充填するには形態的にもワーク等の板体を用いる等の拘束する条件があり、実用性に乏しいという不都合さがあった。   In order to freeze-dry and fill these admixtures, there are restraining conditions such as the use of a plate such as a work in terms of form, and there is a disadvantage that the practicality is poor.

この出願の発明の目的は上述従来技術に基づくハイドロキシアパタイトとコラーゲン溶液を単に混合するだけでは複合体に出来ない、又、実際の生態に適用出来ない点に鑑みて自在に骨補填が出来、コスト的にも安く、操作がし易いように医療衛生産業における加工技術利用技術分野に益する優れた骨補填材を提供せんとするものである。   The object of the invention of this application is that it cannot be made into a complex by simply mixing the hydroxyapatite and collagen solution based on the above-mentioned prior art, and it can be bone-filled freely in view of the fact that it cannot be applied to actual biology, and the cost In particular, it is intended to provide an excellent bone prosthetic material that is beneficial to the technical field of processing technology in the medical hygiene industry so that it is cheap and easy to operate.

上述目的に沿い先述特許請求の範囲を要旨とするこの出願の発明の構成は、前述課題を解決するために、擬似体液とコラーゲン溶液の混合体から得られるβ−TCPを有する骨補填材において、オリジナル成分に調整した該擬似体液から得られるβ−TCPとコラーゲンよりなる複合体であるようにすることを基幹とし、そして、上記β−TCPが上記擬似体液中で液中放電により得られたものであるようにし、そして、上記β−TCPがアルカリスラリーであるようにもし、そして、上記複合体がチェアーサイドで形成されるようにもした技術的手段を講じたものである。   In order to solve the above-mentioned problems, the composition of the invention of the present application, which is summarized in the scope of the above-mentioned claims along the above-mentioned object, is a bone grafting material having β-TCP obtained from a mixture of a simulated body fluid and a collagen solution. The basis is to be a complex composed of β-TCP and collagen obtained from the simulated body fluid adjusted to the original component, and the β-TCP is obtained by submerged discharge in the simulated body fluid And β-TCP is an alkaline slurry, and technical measures are taken to allow the composite to be formed on the chair side.

この出願の発明の効果として、従来の如くブロック状に成形したものを用いる等の形態状の拘束条件がなく適宜に混練して、充填することが出来、治療時にあってチェアーサイドでの操作が容易に行われるという実用性が高い効果がある。   As an effect of the invention of this application, there is no constraint condition of the form such as using a block shaped like the conventional one, it can be appropriately kneaded and filled, and it can be operated at the chair side at the time of treatment There is an effect of high practicality that it is easily performed.

単に、β−TCPとコラーゲン溶液を混合するだけで極めて短い時間で早急に硬化することが出来るという効果がある。   There is an effect that it can be hardened rapidly in a very short time by simply mixing β-TCP and a collagen solution.

体液とオリジナル的に略同一の成分を有するナトリウムやリンやカルシウム,カリウムイオン等を有している擬似体液(m・SBF−)を液中放電により当該擬似体液中の成分を沈殿させ擬似体液を沈殿させる。   Pseudo body fluids (m · SBF-) containing sodium, phosphorus, calcium, potassium ions, etc., which have essentially the same components as the body fluids, are precipitated in the body by discharging the pseudo body fluids. Precipitate.

当該電気分解した液の上澄を捨てることによりアルカリのβ−TCPのスラリーが得られる。
当該アルカリのβ−TCPのスラリーに対し、予め塩酸により酸化したコラーゲン溶液を添加して混和することにより中和反応を成し、硬化が開始され最終的に寒天状のハイドロキシアパタイトとコラーゲンの複合体が得られて、30秒程度の短い時間で硬化し、リン酸の重合反応とコラーゲンの水素結合による架橋反応が進行して骨補填が全体的に形成されることになる。
By discarding the supernatant of the electrolyzed solution, an alkaline β-TCP slurry is obtained.
The alkali β-TCP slurry is neutralized by adding a collagen solution previously oxidized with hydrochloric acid and mixing, and then the hardening is started and finally agar-like hydroxyapatite and collagen complex Is cured in a short time of about 30 seconds, and the bone grafting is formed as a result of the progress of the polymerization reaction of phosphoric acid and the crosslinking reaction by hydrogen bonding of collagen.

この際、当該水溶液が水を含んでいても硬化するので当該充填部位が出血部位であっても充填することが出来、他の薬剤のキャリアとしも利用出来るようなものである。   At this time, since the aqueous solution hardens even if it contains water, it can be filled even if the filling site is a bleeding site, and can be used as a carrier for other drugs.

次にこの出願の発明の実施しようとする形態を実施例の態様として図面を参照して説明すれば以下の通りである。   Next, embodiments of the invention of this application will be described as embodiments of the present invention with reference to the drawings.

Figure 2005027930
表1に示す通りに、枠内でオリジナル成分に調整した水分を有する当該表1のm・SBF-で
示す擬似体液2を作成し、図1に示す様に、電気分解槽1内に擬似体液2を所定量収納し、該擬似体液2中にプラチナの陰極4とその対面にプラチナの陽極5を浸漬させて電源3より100ボルトで2アンペアで液中放電を行い液中の成分を沈殿させると、底部分にβ−TCPリン酸カルシウムのβ型6が沈殿する。そして当該溶液分の上澄部分を除去すると、アルカリの(PH11程度の)β−TCPのスラリー6が沈殿分として出来る。
Figure 2005027930
As shown in Table 1, a simulated body fluid 2 indicated by m · SBF- in Table 1 having moisture adjusted to the original component within the frame is prepared, and the simulated body fluid is stored in the electrolysis tank 1 as shown in FIG. 2 is stored, and a platinum cathode 4 and a platinum anode 5 are immersed in the simulated body fluid 2 and discharged from the power source 3 at 100 volts at 2 amps to precipitate components in the liquid. Then, β-TCP calcium phosphate β-type 6 precipitates at the bottom. When the supernatant portion of the solution is removed, an alkaline (about PH11) β-TCP slurry 6 can be formed as a precipitate.

そして、当該沈殿6に対し、図示しないコラーゲン液を予め塩酸を添加して酸化させておいたものを混合すると中和反応が始まり、液化硬化が始まり、寒天状のハイドロキシアパタイトとコラーゲンの複合体が得られる。   When the collagen solution (not shown) previously oxidized with hydrochloric acid is mixed with the precipitate 6, a neutralization reaction begins, liquefaction hardening begins, and an agar-like hydroxyapatite / collagen complex is formed. can get.

実験のデーターによればその硬化時間は約30秒であり、充分に実用性に耐えるものであった。   According to experimental data, the curing time was about 30 seconds, and it was sufficiently practical.

結果的には当該複合体は骨補填として充分に実用に耐えることがわかった。   As a result, it was found that the composite sufficiently withstands practical use as bone replacement.

そして、複合体は水を含んでも固まるので実用上は出血部位においても充分に充填することが出来るものである。   And since a composite_body | complex is solid even if it contains water, it can be filled enough also in a bleeding site practically.

以上、この発明の骨補填によれば水を含んでも固まるので人体の出血部位でも充分に補填することが出来る。   As described above, according to the bone filling of the present invention, even if it contains water, it hardens, so that it is possible to sufficiently fill even the bleeding site of the human body.

そして、他の薬剤の、例えば、抗生物質等の薬剤などのキャリアとしても利用することが出来る利点がある。   And there exists an advantage which can be utilized also as carriers of other chemical | medical agents, such as medicines, such as antibiotics.

そしてコスト的にも極めて安くつくために迅速性からも実用性が極めて高いものである。   And since it is very cheap in terms of cost, it is extremely practical in terms of speed.

そして、リン酸の重合反応とコラーゲンの水素結合による架橋反応はβ−TCPのみで生ずることが出来る優れた効果が奏される。   And the superposition | polymerization reaction of phosphoric acid and the crosslinking reaction by the hydrogen bond of collagen show the outstanding effect which can arise only by (beta) -TCP.

そして、治療中にチェアーサイドを利用することが出来る利点がある   And there is an advantage that you can use the chair side during treatment

液中放電の透視斜視図である。It is a perspective view of the submerged discharge.

符号の説明Explanation of symbols

1 電気分解槽
2 擬似体液
3 電源
4 プラチナ(陰極)
5 プラチナ(陽極)
6 沈殿
1 Electrolysis tank 2 Simulated body fluid 3 Power supply 4 Platinum (cathode)
5 Platinum (Anode)
6 Precipitation

Claims (4)

擬似体液とコラーゲン溶液の混合体から得られるβ−TCPを有する骨補填材において、オリジナル成分に調整した該擬似体液から得られるβ−TCPとコラーゲンよりなる複合体であることを特徴とする骨補填材。 A bone filling material having β-TCP obtained from a mixture of a simulated body fluid and a collagen solution, wherein the bone filling material is a composite comprising β-TCP and collagen obtained from the simulated body fluid adjusted to the original component. Wood. 上記β−TCPが上記擬似体液中で液中放電により得られたものであることを特徴とする請求項1記載の骨補填材。 The bone grafting material according to claim 1, wherein the β-TCP is obtained by submerged discharge in the simulated body fluid. 上記β−TCPがアルカリスラリーであることを特徴とする請求項1記載の骨補填材。 The bone grafting material according to claim 1, wherein the β-TCP is an alkaline slurry. 上記複合体がチェアーサイドで形成されるものであることを特徴とする請求項1記載の骨補填材。 2. The bone grafting material according to claim 1, wherein the composite is formed on a chair side.
JP2003271800A 2003-07-08 2003-07-08 Bone substitute Pending JP2005027930A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8043426B2 (en) * 2008-05-13 2011-10-25 Abdel-Mohsen Onsy Mohamed Method for treating cement kiln dust

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0464362A (en) * 1990-07-05 1992-02-28 Kiyoshi Inoue Surface treatment for material buried in vivo
JPH05285212A (en) * 1991-11-19 1993-11-02 Ishifuku Metal Ind Co Ltd Method of treating surface of implantation material
JPH05285213A (en) * 1992-01-29 1993-11-02 Ishifuku Metal Ind Co Ltd Method of treating surface of implantation material
JP2001137328A (en) * 1999-11-11 2001-05-22 Olympus Optical Co Ltd Bone prosthesis
JP2003038635A (en) * 2002-06-10 2003-02-12 Olympus Optical Co Ltd Osteochondroimplant material
JP2003111831A (en) * 2001-07-30 2003-04-15 Olympus Optical Co Ltd Cartilage implant

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0464362A (en) * 1990-07-05 1992-02-28 Kiyoshi Inoue Surface treatment for material buried in vivo
JPH05285212A (en) * 1991-11-19 1993-11-02 Ishifuku Metal Ind Co Ltd Method of treating surface of implantation material
JPH05285213A (en) * 1992-01-29 1993-11-02 Ishifuku Metal Ind Co Ltd Method of treating surface of implantation material
JP2001137328A (en) * 1999-11-11 2001-05-22 Olympus Optical Co Ltd Bone prosthesis
JP2003111831A (en) * 2001-07-30 2003-04-15 Olympus Optical Co Ltd Cartilage implant
JP2003038635A (en) * 2002-06-10 2003-02-12 Olympus Optical Co Ltd Osteochondroimplant material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8043426B2 (en) * 2008-05-13 2011-10-25 Abdel-Mohsen Onsy Mohamed Method for treating cement kiln dust

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