JPH0534343A - Test implement - Google Patents
Test implementInfo
- Publication number
- JPH0534343A JPH0534343A JP18874891A JP18874891A JPH0534343A JP H0534343 A JPH0534343 A JP H0534343A JP 18874891 A JP18874891 A JP 18874891A JP 18874891 A JP18874891 A JP 18874891A JP H0534343 A JPH0534343 A JP H0534343A
- Authority
- JP
- Japan
- Prior art keywords
- poly
- test device
- support
- main component
- test
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Biological Depolymerization Polymers (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、ヒトの健康状態をチェ
ックするための血液や尿の試験具に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a blood or urine test device for checking human health.
【0002】[0002]
【従来の技術】従来の試験具は図1に示すように、手で
持つことのできる支持体2はポリスチレンやポリエチレ
ンテレフタレート等の合成樹脂などで短冊状に作られ、
検体中の成分の測定のため試薬を担持して試薬層3と
し、支持体2に試薬層3を接着剤層4にて接着してい
た。そしてそれらは検体中の成分の測定が終了すると、
一般のプラスチックゴミや一般家庭ゴミと同じ様に処理
され、埋め立てや焼却処分されていた。2. Description of the Related Art As shown in FIG. 1, in a conventional test tool, a support 2 which can be held by hand is made of a synthetic resin such as polystyrene or polyethylene terephthalate in a strip shape.
A reagent was carried to form a reagent layer 3 for measuring components in a sample, and the reagent layer 3 was adhered to the support 2 with an adhesive layer 4. And when they finish measuring the components in the sample,
It was treated in the same way as general plastic waste and general household waste, and was landfilled or incinerated.
【0003】また、最近、水溶紙に水溶性樹脂をコート
した水溶性の支持体を用いることにより、試験終了後、
水洗トイレに、廃棄できるものが、開発されている。Further, recently, by using a water-soluble support comprising water-soluble paper coated with a water-soluble resin, after the end of the test,
A flush toilet has been developed that can be discarded.
【0004】ヒトの血液や尿などの検体に触れた試験具
が一般のゴミと混ざって処分されることは不衛生であ
り、また健常人ではない病人からの検体(血液や尿)の場
合には病気の感染のおそれすらある。このため、成分の
測定が終了したら、直ちにこの試験具を衛生的に処分す
ることが望まれていた。[0004] It is unsanitary to dispose of a test device that touches a sample such as human blood or urine mixed with general garbage, and in the case of a sample (blood or urine) from a sick person who is not a healthy person. He may even be infected by a disease. Therefore, it has been desired to dispose of the test tool hygienically immediately after the measurement of the components is completed.
【0005】また、水溶性の支持体を用いた試験具は、
その強度を試験中に維持させておくのが難しく、強度を
上げると溶けにくくなり、また、溶け易くすると強度が
不足し、試験中に折れ曲がったりすることがあり、ほど
よい強度や溶け易さを調整するのは、非常に難しかっ
た。Further, a test device using a water-soluble support is
It is difficult to maintain its strength during the test, increasing the strength makes it difficult to melt, and if it is easy to melt, the strength may be insufficient and it may bend during the test, so it has moderate strength and easy melting. It was very difficult to adjust.
【0006】[0006]
【発明が解決しようとしている課題】本発明の目的は、
この様に衛生的な処分を可能とする試験具を提供するこ
とにある。The object of the present invention is to:
In this way, it is an object to provide a test device that enables hygienic disposal.
【0007】[0007]
【課題を解決するための手段】このような目的は次の構
成により達成される。Such an object is achieved by the following constitution.
【0008】支持体と該支持体の一部分に試薬層を有す
る試験具において、該支持体は、ポリ(ヒドロキシアル
カノエート)を主成分とする基材から構成されることに
よって達成される。In a test device having a support and a reagent layer on a part of the support, the support is achieved by comprising a base material containing poly (hydroxyalkanoate) as a main component.
【0009】さらに、前記試薬層はポリ(ヒドロキシア
ルカノエート)を主成分とする不織布に試薬を担持させ
たものであることが好ましい。Further, it is preferable that the reagent layer is a non-woven fabric containing poly (hydroxyalkanoate) as a main component and carrying a reagent.
【0010】支持体と該支持体の一端に試薬層を有する
試験具において、該支持体は、ポリ(ヒドロキシアルカ
ノエート)を主成分とする基材から構成されることによ
り、機械的強度が十分あり、また、試験後水洗トイレな
どに容易に廃棄できる。In a test device having a support and a reagent layer at one end of the support, the support is composed of a base material containing poly (hydroxyalkanoate) as a main component, so that the support has sufficient mechanical strength. Yes, and can be easily discarded in a flush toilet after the test.
【0011】さらに、前記試薬層はポリ(ヒドロキシア
ルカノエート)を主成分とする不織布に試薬を担持させ
たものにすることにより、ほとんど固形物を残すことな
く、分解してしまうことができる。Furthermore, the reagent layer can be decomposed by leaving almost no solid matter by using a non-woven fabric containing poly (hydroxyalkanoate) as a main component and supporting the reagent.
【0012】本発明に適用されるポリ(ヒドロキシアル
カノエート)はヒドロキシアルカノエート繰り返し単位
として炭素数2〜12程度のものが例示され、具体的に
はポリ(2−ヒドロキシアセテート)、ポリ(2−ヒド
ロキシプロピオネート)等のポリ(2−ヒドロキシアル
カノエート)類、ポリ(3−ヒドロキシプロピオネー
ト)、ポリ(3−ヒドロキシブチレート)、ポリ(3−
ヒドロキシバリレート)、ポリ(3−ヒドロキシオクタ
ノエート)等のポリ(3−ヒドロキシアルカノエート)
類、ポリ(4−ヒドロキシブチレート)、ポリ(4-バ
リレート)等のポリ(4−ヒドロキシアルカノエート)
類等が好適に用いられる。Examples of the poly (hydroxyalkanoate) applicable to the present invention include those having about 2 to 12 carbon atoms as a hydroxyalkanoate repeating unit, and specifically, poly (2-hydroxyacetate) and poly (2-hydroxyacetate). Hydroxypropionate) and other poly (2-hydroxyalkanoates), poly (3-hydroxypropionate), poly (3-hydroxybutyrate), poly (3-
Hydroxyvalerate), poly (3-hydroxyoctanoate) and other poly (3-hydroxyalkanoates)
Poly (4-hydroxyalkanoates) such as poly (4-hydroxybutyrate) and poly (4-valerate)
Classes and the like are preferably used.
【0013】本発明においては、ポリヒドロキシアルカ
ノエートは単一なホモポリマーである必要はなく、これ
らの共重合体であってもよい。In the present invention, the polyhydroxyalkanoate need not be a single homopolymer, but may be a copolymer thereof.
【0014】これらの共重合体の具体例としては、2−
ヒドロキシアセテート・2−ヒドロキシプロピオネート
共重合体、3−ヒドロキシプロピオネート・3−ヒドロ
キシブチレート共重合体、3−ヒドロキシブチレート・
3−ヒドロキシバリレート共重合体、3−ヒドロキシブ
チレート・4−ヒドロキシブチレート共重合体、3−ヒ
ドロキシブチレート・4−ヒドロキシバリレート共重合
体、3−ヒドロキシブチレート・3−ヒドロキシオクタ
ノエート共重合体、3−ヒドロキシブチレート・3−ヒ
ドロキシプロピオネート・3−ヒドロキシバリレート共
重合体、3−ヒドロキシブチレート・3−ヒドロキシバ
リレート・4−ヒドロキシブチレート共重合体等が好適
に例示されるが、本発明ではそれらに限定されるもので
はない。Specific examples of these copolymers include 2-
Hydroxyacetate / 2-hydroxypropionate copolymer, 3-hydroxypropionate / 3-hydroxybutyrate copolymer, 3-hydroxybutyrate /
3-hydroxyvalerate copolymer, 3-hydroxybutyrate-4-hydroxybutyrate copolymer, 3-hydroxybutyrate-4-hydroxyvalerate copolymer, 3-hydroxybutyrate-3-hydroxyoctano Aate copolymer, 3-hydroxybutyrate / 3-hydroxypropionate / 3-hydroxyvalerate copolymer, 3-hydroxybutyrate / 3-hydroxyvalerate / 4-hydroxybutyrate copolymer and the like are preferable. However, the present invention is not limited thereto.
【0015】さらに本発明では、上記のポリ(ヒドロキ
シアルカノエート)類やそれらの共重合体の混合物、あ
るいはポリ(ヒドロキシアルカノエート)類とそれらの
共重合体の混合物であってもよい。Further, in the present invention, a mixture of the above poly (hydroxyalkanoates) and their copolymers, or a mixture of poly (hydroxyalkanoates) and their copolymers may be used.
【0016】本発明のポリヒドロキシアルカノエートが
主成分とする基材のポリヒドロキシアルカノエート成分
の含率は50wt%以上が好ましい。水溶性のポリマーと
組み合わせることは効果的ではあるが、ポリヒドロキシ
アルカノエート成分の含率が50wt%以下では浄化槽内
の活性汚泥中での分解が不十分となる可能性があるた
め、ポリヒドロキシアルカノエート成分の含率は50wt
%以上が好ましい。また、本発明の基材が浄化漕に至る
前に形態的の崩壊するように上述の水溶性ポリマーや水
溶性物質を混合することも可能である。The content of the polyhydroxyalkanoate component of the base material containing the polyhydroxyalkanoate as the main component of the present invention is preferably 50 wt% or more. Although it is effective to combine it with a water-soluble polymer, if the content of the polyhydroxyalkanoate component is 50 wt% or less, the decomposition in the activated sludge in the septic tank may be insufficient. Content of ate component is 50wt
% Or more is preferable. Further, it is also possible to mix the above-mentioned water-soluble polymer or water-soluble substance so that the base material of the present invention disintegrates morphologically before reaching the purification tank.
【0017】本発明のポリヒドロキシアルカノエートの
作り方は、微生物を用いた発酵合成から得る方法でも、
化学合成から得る方法でもよい。前者の方法としては特
願平2−076585、特開昭57−150393、ジ
ャーナル オブ ジェネラルマイクロバイオロジー
(J.General.Microbiology),
115,185〜192(1979)、ジャーナル オ
ブ ザ ソサエティー,ケミカル コミニケーションズ
(J.Chm.Soc.,Chem.Commun.)
1635〜1636(1987)、ポリマー コミニケ
ーションズ(Polymer Commun.)30,
169〜171(1989)、アプライドマイクロバイ
オロジー アンドバイオテクノロジー(Appl.Mi
crobiol.Biotech.)30,569〜5
73(1989)などに記載された方法があるが、もち
ろんこれ以外の培養条件、菌株を用いても構わない。ま
た後者の方法としては、β−ブチロラクトンやγ−バレ
ロラクトンなどの開環重合する方法、3−ヒドロキシ酪
酸やその誘導体、4−ヒドロキシ吉草酸やその誘導体な
どを重縮合する方法などがあり、その一例として高分子
学会予稿集(Polymer Preprints,J
apan)39,NO.7,2265〜2267(19
90)がある。The polyhydroxyalkanoate of the present invention can be produced by a method obtained by fermentation synthesis using a microorganism,
The method obtained from chemical synthesis may also be used. Examples of the former method include Japanese Patent Application No. 2-076585, JP-A-57-150393, and Journal of General Microbiology,
115 , 185-192 (1979), Journal of the Society, Chemical Communications (J. Chm. Soc., Chem. Commun.).
1635 to 1636 (1987), Polymer Communications 30 ,
169-171 (1989), Applied Microbiology and Biotechnology (Appl. Mi
crobiol. Biotech. ) 30 , 569-5
73 (1989) and the like, but other culture conditions and strains may of course be used. The latter method includes a method of ring-opening polymerization of β-butyrolactone or γ-valerolactone, a method of polycondensing 3-hydroxybutyric acid or a derivative thereof, 4-hydroxyvaleric acid or a derivative thereof, and the like. As an example, the Polymer Society of Japan Proceedings (Polymer Preprints, J
apan) 39 , NO. 7, 2265-2267 (19
90).
【0018】本発明の試験具の支持体に成形するには、
ポリヒドロキシアルカノエートを主成分とする材料を射
出成形、押出し成形、熱プレスなどの熱成形によってシ
ート化し、作ることができる。また、ポリヒドロキシア
ルカノエートの溶剤、例えばクロロホルム、ジクロロメ
タン、ジオキサンなどを用いて溶媒キャスト法にてシー
ト化することができる。これらのシートを必要な大きさ
にカットして試験具の支持体とすることができる。To form the support of the test device of the present invention,
A material containing polyhydroxyalkanoate as a main component can be formed into a sheet by thermoforming such as injection molding, extrusion molding, and hot pressing. Further, it can be formed into a sheet by a solvent casting method using a solvent of polyhydroxyalkanoate, such as chloroform, dichloromethane, dioxane and the like. These sheets can be cut to a required size to provide a support for the test device.
【0019】本発明の試験具の支持体上に接着する試薬
層はポリヒドロキシアルカノエートを主成分とする不織
布からなり、ポリヒドロキシアルカノエートを主成分と
する材料を溶融押出し成形し、また必要に応じて延伸処
理をした糸を不規則にまとめることにより得られる。こ
れらは、水溶性の薬品を載せやすくするため、不織布表
面をアルコール処理したり、プラズマ処理することも可
能である。また、糸状に押出し成形する前に親水性物
質、例えばグリセロールトリアテレートなどを混合して
おくことも効果的である。The reagent layer adhered to the support of the test device of the present invention comprises a non-woven fabric containing polyhydroxyalkanoate as a main component, and a material containing polyhydroxyalkanoate as a main component is melt-extruded and, if necessary, It is obtained by randomly gathering the yarns that have been stretched accordingly. In order to facilitate the placement of water-soluble chemicals, it is possible to subject the nonwoven fabric surface to alcohol treatment or plasma treatment. It is also effective to mix a hydrophilic substance such as glycerol triatelate before extruding into a thread form.
【0020】本発明の試験具支持体と試薬層を接着する
には得に何の制限もなく通常の接着剤を用いて良い。For adhering the test device support of the present invention to the reagent layer, any ordinary adhesive may be used without any particular limitation.
【0021】本発明の試験具に用いることのできる検査
項目は特に何の制限もなく、通常測定される項目が適用
出来る。例えば、血液試験具ではpH、ブドウ糖など、
尿試験具では、pH、ブドウ糖、蛋白質、ウロビリノー
ゲン、ケトン体、ビリルビン、潜血、亜硝酸塩などの項
目が適用できる。また、妊娠の判定する項目にも適用可
能である。There are no particular restrictions on the inspection items that can be used in the test device of the present invention, and normally measured items can be applied. For example, for blood test devices, pH, glucose, etc.
With the urine test device, items such as pH, glucose, protein, urobilinogen, ketone bodies, bilirubin, occult blood, and nitrite can be applied. It can also be applied to items for determining pregnancy.
【0022】[0022]
【実施例】以下、本発明の実施例を図面を参照して具体
的に説明する。Embodiments of the present invention will be specifically described below with reference to the drawings.
【0023】[実施例1]3−ヒドロキシブチレート・3
−ヒドロキシバリレート共重合体(3−ヒドロキシ吉草
酸含率17モル%、Aldrich社より購入)を成形
温度170℃にてTダイより押出し成形して厚み0.5
mmのシートとし、70×7mmの長方形にカットして
支持体とした。[Example 1] 3-hydroxybutyrate-3
-Hydroxyvalerate copolymer (3-hydroxyvaleric acid content 17 mol%, purchased from Aldrich) is extruded from a T-die at a molding temperature of 170 ° C and molded to a thickness of 0.5.
mm sheet and cut into a 70 × 7 mm rectangle to obtain a support.
【0024】また、同じ材料を用い、ダイの内径0.3
mmから押出し、延伸操作は行わず自重のみにより延伸
された糸を得た。その糸の外径は約0.1〜0.3mm
であった。これを集めて、圧縮するとことにより不織布
とし、試薬層を形成した。この基材と不織布を少量のエ
ポキシ系接着剤(チバガイギ社製アラルダイト)で接着
した。そして不織布部分をエチルアルコール(試薬特
級)で処理したのち、pH測定用の浸漬液に約10秒漬
浸して尿試験具を作成した。Further, using the same material, the inner diameter of the die is 0.3.
A yarn was obtained by extruding from mm and drawing only by its own weight without performing a drawing operation. The outer diameter of the thread is about 0.1 to 0.3 mm
Met. This was collected and compressed into a nonwoven fabric to form a reagent layer. The base material and the non-woven fabric were bonded with a small amount of an epoxy adhesive (Araldite manufactured by Ciba-Geigy). Then, the non-woven fabric portion was treated with ethyl alcohol (special grade reagent), and then immersed in a dipping solution for pH measurement for about 10 seconds to prepare a urine test device.
【0025】なお、pH測定用浸漬液はメチルレッド
(東京化成工業社製特級)20mg/dlエタノール溶
液17.6mlと、ブロムチモールブルー(和光純薬社
製特級)200mg/dlエタノール溶液25mlと、
ポリビニリピロリドン(東京化成工業社製K−30)1
2g/dlエタノール溶液50mlを混合し、さらに全
量を100mlになる様にエタノールを加えて作製し
た。この尿試験具を用いて健常人の尿のPHを測定した
ところ、通常通り使用でき、また、市販品(テルモ社製
尿試験紙ウリエース)の測定結果と一致した。測定終了
後、神奈川県伊勢原市の下水最終処理場から採取した活
性汚泥を好気的培養している坂口フラスコに使用後の尿
試験紙を入れ、1カ月後に観察したところ、活性汚濁中
の微生物に資化されたために基材および不織布部分は残
っていなかった。このため、通常の水洗トイレに本発明
の尿試験紙を廃棄しても、浄化槽内の活性汚泥によって
完全に分解され、問題ないものといえる。The dipping solution for pH measurement was methyl red (special grade manufactured by Tokyo Kasei Kogyo Co., Ltd.) 20 mg / dl ethanol solution 17.6 ml, bromthymol blue (special grade manufactured by Wako Pure Chemical Industries, Ltd.) 200 mg / dl ethanol solution 25 ml,
Polyvinylpyrrolidone (K-30 manufactured by Tokyo Chemical Industry Co., Ltd.) 1
A 2 g / dl ethanol solution (50 ml) was mixed, and ethanol was added so that the total amount became 100 ml. When the pH of urine of a healthy person was measured using this urine test tool, it was used as usual, and it was in agreement with the measurement result of a commercial product (urine test paper Uriace manufactured by Terumo Corp.). After the measurement, put the used urine test paper in the Sakaguchi flask that aerobically cultures the activated sludge collected from the sewage final treatment plant in Isehara City, Kanagawa Prefecture, and observe it one month later. The base material and the non-woven fabric portion did not remain because it was assimilated into. Therefore, even if the urine test strip of the present invention is discarded in an ordinary flush toilet, it can be said that there is no problem because it is completely decomposed by the activated sludge in the septic tank.
【0026】[実施例2]基材と試薬層の成形材料にポリ
3−ヒドロキシブチレート(Aldrich社より購
入)にグリセロールトリアセテート(東京化成工業社
製)を20wt%混合したものを用いた以外実施例1と
同様にしてpH測定用の尿試験具を作成した。健常人の
尿のpH測定は市販品と同じ結果を示した。また、活性
汚泥中での分解も1カ月後には完全に起きていた。Example 2 Other than using 20% by weight of poly-3-hydroxybutyrate (purchased from Aldrich) and glycerol triacetate (manufactured by Tokyo Chemical Industry Co., Ltd.) as a molding material for the base material and the reagent layer. A urine test device for pH measurement was prepared in the same manner as in Example 1. The pH measurement of urine of a healthy person showed the same result as the commercially available product. Decomposition in activated sludge was completely caused after 1 month.
【0027】[比較例1]ポリヒドロキシアルカノエート
を用いずに作製されている市販品(テルモ社製尿試験紙
ウリエース)を前述の活性汚泥中に入れたところ1カ月
後にも原形をそのまま確認することができた。[Comparative Example 1] A commercially available product (urine test paper Uriace manufactured by Terumo Co., Ltd.) prepared without using polyhydroxyalkanoate was put in the above-mentioned activated sludge, and the original shape was confirmed as it was even after one month. I was able to.
【0028】[0028]
【発明の効果】以上、詳述したように本発明の試験具
は、ポリヒドロキシアルカノエートを主成分とする生分
解性の基材から構成されているので、測定終了後に本発
明の試験具をトイレや排水溝に廃棄しても、下水処理工
程中の活性汚濁で微生物によって完全に分解、資化され
るため、下水系に悪影響を与えない。このため、下水系
に悪影響を与えずに試験具を簡単に処理できるという効
果がある。また、試験具に付着している検体尿や血液に
よる感染なども防止することができるという効果があ
る。As described above in detail, since the test device of the present invention is composed of a biodegradable base material containing polyhydroxyalkanoate as a main component, the test device of the present invention can be used after the measurement. Even if it is discarded in the toilet or drain, it does not adversely affect the sewage system because it is completely decomposed and assimilated by microorganisms due to active pollution during the sewage treatment process. Therefore, there is an effect that the test device can be easily treated without adversely affecting the sewage system. Further, there is an effect that it is possible to prevent an infection caused by the urine of the sample or blood attached to the test device.
【図1】 図1は本発明の試験具を示す斜視図である。FIG. 1 is a perspective view showing a test device of the present invention.
1…尿試験具 2…基材 3…試薬層 4…接着層 1 ... Urine test tool 2 ... Base material 3 ... Reagent layer 4 ... Adhesive layer
Claims (2)
る試験具において、該支持体は、ポリ(ヒドロキシアル
カノエート)を主成分とする基材から構成されることを
特徴とする試験具。1. A test device having a support and a reagent layer on a part of the support, wherein the support is composed of a base material containing poly (hydroxyalkanoate) as a main component. Ingredient
ート)を主成分とする不織布に試薬を担持させたもので
あることを特徴とする請求項(1)に記載の試験具。2. The test device according to claim 1, wherein the reagent layer is formed by supporting a reagent on a nonwoven fabric containing poly (hydroxyalkanoate) as a main component.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18874891A JPH0534343A (en) | 1991-07-29 | 1991-07-29 | Test implement |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18874891A JPH0534343A (en) | 1991-07-29 | 1991-07-29 | Test implement |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0534343A true JPH0534343A (en) | 1993-02-09 |
Family
ID=16229086
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18874891A Pending JPH0534343A (en) | 1991-07-29 | 1991-07-29 | Test implement |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0534343A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5489470A (en) * | 1994-01-28 | 1996-02-06 | The Procter & Gamble Company | Biodegradable copolymers and plastic articles comprising biodegradable copolymers |
US5498692A (en) * | 1994-01-28 | 1996-03-12 | The Procter & Gamble Company | Biodegradable copolymers and plastic articles comprising biodegradable copolymers |
US5502116A (en) * | 1994-01-28 | 1996-03-26 | The Procter & Gamble Company | Biodegradable copolymers and plastic articles comprising biodegradable copolymers of 3-hydroxyhexanoate |
US5990271A (en) * | 1994-01-28 | 1999-11-23 | The Procter & Gamble Company | Films and absorbent articles comprising a biodegradable polyhydroxyalkanoate comprising 3-hydroxybutyrate and 3-hydroxyhexanoate comonomer units |
US6077931A (en) * | 1998-12-21 | 2000-06-20 | The Procter & Gamble Company | Biodegradable PHA copolymers |
US6143947A (en) * | 1996-01-29 | 2000-11-07 | The Procter & Gamble Company | Fibers, nonwoven fabrics and absorbent articles comprising a biodegradable polyhydroxyalkanoate comprising 3-hydroxybutyrate and 3-hydroxyhexanoate |
US6160199A (en) * | 1998-12-21 | 2000-12-12 | The Procter & Gamble Company | Absorbent articles comprising biodegradable PHA copolymers |
US6174990B1 (en) | 1998-12-21 | 2001-01-16 | The Procter & Gamble Company | Films comprising biodegradable PHA copolymers |
US6221316B1 (en) | 1997-12-16 | 2001-04-24 | Urs J. Hänggi | Use of blends of water-resistant and biodegradable polymers made from renewable feedstocks with increased binding affinity for the production of carriers for analytic systems |
-
1991
- 1991-07-29 JP JP18874891A patent/JPH0534343A/en active Pending
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6013590A (en) * | 1994-01-28 | 2000-01-11 | The Procter & Gamble Company | Fibers, nonwoven fabrics, and absorbent articles comprising a biodegradable polyhydroxyalkanoate comprising 3-hydroxybutyrate and 3-hydroxyhexanoate |
US6027787A (en) * | 1994-01-28 | 2000-02-22 | The Procter & Gamble Company | Films and absorbent articles comprising a biodegradable polyhydroxyalkanoate comprising 3-hydroxybutyrate and 3-hydroxyhexanoate comonomer units |
US5502116A (en) * | 1994-01-28 | 1996-03-26 | The Procter & Gamble Company | Biodegradable copolymers and plastic articles comprising biodegradable copolymers of 3-hydroxyhexanoate |
US5602227A (en) * | 1994-01-28 | 1997-02-11 | The Procter & Gamble Company | Biodegradable copolymers |
US5618855A (en) * | 1994-01-28 | 1997-04-08 | The Procter & Gamble Company | Biodegradable copolymers and plastic articles comprising biodegradable copolymers |
US5990271A (en) * | 1994-01-28 | 1999-11-23 | The Procter & Gamble Company | Films and absorbent articles comprising a biodegradable polyhydroxyalkanoate comprising 3-hydroxybutyrate and 3-hydroxyhexanoate comonomer units |
US5498692A (en) * | 1994-01-28 | 1996-03-12 | The Procter & Gamble Company | Biodegradable copolymers and plastic articles comprising biodegradable copolymers |
USRE36548E (en) * | 1994-01-28 | 2000-02-01 | The Procter & Gamble Company | Biodegradable copolymers |
US5489470A (en) * | 1994-01-28 | 1996-02-06 | The Procter & Gamble Company | Biodegradable copolymers and plastic articles comprising biodegradable copolymers |
US6143947A (en) * | 1996-01-29 | 2000-11-07 | The Procter & Gamble Company | Fibers, nonwoven fabrics and absorbent articles comprising a biodegradable polyhydroxyalkanoate comprising 3-hydroxybutyrate and 3-hydroxyhexanoate |
US6221316B1 (en) | 1997-12-16 | 2001-04-24 | Urs J. Hänggi | Use of blends of water-resistant and biodegradable polymers made from renewable feedstocks with increased binding affinity for the production of carriers for analytic systems |
US6077931A (en) * | 1998-12-21 | 2000-06-20 | The Procter & Gamble Company | Biodegradable PHA copolymers |
US6160199A (en) * | 1998-12-21 | 2000-12-12 | The Procter & Gamble Company | Absorbent articles comprising biodegradable PHA copolymers |
US6174990B1 (en) | 1998-12-21 | 2001-01-16 | The Procter & Gamble Company | Films comprising biodegradable PHA copolymers |
US6569990B1 (en) | 1998-12-21 | 2003-05-27 | The Procter & Gamble Company | Plastic articles comprising biodegradable PHA copolymers |
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