JPS6318500B2 - - Google Patents
Info
- Publication number
- JPS6318500B2 JPS6318500B2 JP55049622A JP4962280A JPS6318500B2 JP S6318500 B2 JPS6318500 B2 JP S6318500B2 JP 55049622 A JP55049622 A JP 55049622A JP 4962280 A JP4962280 A JP 4962280A JP S6318500 B2 JPS6318500 B2 JP S6318500B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- gel
- line
- acrylic acid
- agent
- 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.)
- Expired
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 229920002125 Sokalan® Polymers 0.000 claims description 6
- 239000000080 wetting agent Substances 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- 238000002604 ultrasonography Methods 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 239000011550 stock solution Substances 0.000 claims description 3
- 230000003472 neutralizing effect Effects 0.000 claims description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- -1 polyoxyethylene Polymers 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 235000015112 vegetable and seed oil Nutrition 0.000 description 4
- 239000008158 vegetable oil Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 239000002537 cosmetic Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 210000003491 skin Anatomy 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 230000005856 abnormality Effects 0.000 description 2
- 230000036760 body temperature Effects 0.000 description 2
- 238000002592 echocardiography Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 210000002615 epidermis Anatomy 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000001356 surgical procedure Methods 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- RFIMISVNSAUMBU-UHFFFAOYSA-N 2-(hydroxymethyl)-2-(prop-2-enoxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC=C RFIMISVNSAUMBU-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- ODHCTXKNWHHXJC-VKHMYHEASA-M 5-oxo-L-prolinate Chemical compound [O-]C(=O)[C@@H]1CCC(=O)N1 ODHCTXKNWHHXJC-VKHMYHEASA-M 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 208000003174 Brain Neoplasms Diseases 0.000 description 1
- 206010018852 Haematoma Diseases 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 238000002405 diagnostic procedure Methods 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000003670 easy-to-clean Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000001605 fetal effect Effects 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 210000003709 heart valve Anatomy 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 231100000344 non-irritating Toxicity 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000003169 placental effect Effects 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940071139 pyrrolidone carboxylate Drugs 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Landscapes
- Ultra Sonic Daignosis Equipment (AREA)
Description
【発明の詳細な説明】
本発明は超音波診断装置用媒剤に係わる。更に
詳しくは水湿潤性の原液を、中和された架橋型ア
クリル酸系ポリマーでゲル化した、超音波診断装
置用ゲル剤に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a medium for ultrasonic diagnostic equipment. More specifically, the present invention relates to a gel agent for ultrasonic diagnostic equipment, which is obtained by gelling a water-wettable stock solution with a neutralized crosslinked acrylic acid polymer.
超音波診断装置を使用して各種画像を捉える方
法は、病気や異状を発見して人命を救うのに画期
的な方法であり、X線が後遺的な障碍を伴い易い
のに反して全く安全であり、極めて有用な診断方
法として広く使われる傾向にあることは周知であ
る。超音波装置に接続されたトランスジユーサ
(プローブともいう)を人体表皮に密着させ、被
験部全体に動かしながらコンピユーターで焦点を
合せて、像の全体をすべてぴたりと焦点の合つた
状態で捉えるのである。脳腫瘍、血腫、結石、心
蔵弁異常、胎児胎盤の状態等々が、高周波数の音
波が体の組織を貫通してエコー(反響)としては
ね返つて来るのを集めて画像を結ばせることによ
つて、読みとられ診断されるのである。 The method of capturing various images using ultrasound diagnostic equipment is an innovative method for discovering diseases and abnormalities and saving lives. It is well known that it is safe and tends to be widely used as a very useful diagnostic method. A transducer (also called a probe) connected to an ultrasound device is placed in close contact with the human epidermis, and as it is moved over the entire area to be examined, it is focused by a computer and the entire image is captured in perfect focus. be. Brain tumors, hematomas, stones, cardiac valve abnormalities, fetal placental conditions, etc. can be detected by collecting images of high-frequency sound waves that penetrate body tissues and bounce back as echoes. Therefore, it is read and diagnosed.
その場合トランスジユーサと人体表皮の間に空
隙が介在すると、超音波は遮断されて伝達率がゼ
ロになつて必要な画像が得られない。この介在空
間を填めるために水、生体電極用ペースト、鉱植
物油などが使用されている。第1図に示す通りそ
の伝達率は植物油及び水が好ましい値を与える。
即ち第1図に於いて線1は空気、線2は鉱物油、
線3は市販の生体電極用ペースト、線4は水、線
5は植物油の場合の伝達率を示す。 In that case, if a gap exists between the transducer and the human body epidermis, the ultrasonic waves are blocked and the transmission rate becomes zero, making it impossible to obtain the necessary image. Water, bioelectrode paste, mineral vegetable oil, etc. are used to fill this intervening space. As shown in FIG. 1, vegetable oil and water give preferable transmissibility values.
That is, in Figure 1, line 1 is air, line 2 is mineral oil,
Line 3 shows the transmissivity in the case of commercially available bioelectrode paste, line 4 shows the transmissibility in water, and line 5 shows the transmissivity in the case of vegetable oil.
しかし好ましい伝達率を示しても、植物油は温
度によつて粘度の変化があつたり酸敗のおそれが
あつたりして扱い難い上に、皮膚に塗布した場合
に術後の清拭に多大の難点があり、水は体温によ
つて蒸発倍加して短時間で乾燥して直ちに空隙の
介在を許すことになり、且つそれらは何れも体温
程度の温度に於いて易流動性であるために流れて
必要部位に留めること極めて困難であること明白
である。生体電極用ペーストは導電性を良好なら
しめるために食塩など電解質の他種々のものを溶
解して成り、従つて当初から、更に蒸発が若干で
も進むと尚一層濁度が上昇してこれが伝達率急低
下の原因になる。 However, even though they exhibit favorable transmissibility, vegetable oils are difficult to handle because their viscosity changes depending on temperature and there is a risk of rancidity, and when applied to the skin, it is very difficult to clean it after surgery. Water evaporates twice as much as it evaporates due to body temperature, dries in a short time, and immediately allows the formation of voids, and since both of them are free-flowing at temperatures around body temperature, they flow and are necessary. It is clear that it is extremely difficult to keep it in place. The paste for bioelectrodes is made by dissolving various substances such as electrolytes such as common salt in order to improve its conductivity. Therefore, if evaporation progresses even slightly, the turbidity will increase even more, and this will affect the transmittance. This will cause a sudden decline.
即ち超音波診断装置用媒剤は、(1)超音波の伝達
(反響の場合も含む)効率が水と同等以上、(2)皮
膚面で流れたり垂れたりしない、(3)乾燥し難い、
(4)トランスジユーサーの動きに適した粘性を有し
且つその粘度変化がない、(5)透明であつて結晶析
出などによる濁りがない、(6)毒性乃至皮膚刺戟が
ない、(7)使用後拭きとりが容易、などの性質を具
備していなければならない。 In other words, the medium for ultrasonic diagnostic equipment has the following properties: (1) The transmission efficiency of ultrasonic waves (including the case of echoes) is equal to or higher than that of water, (2) it does not run or drip on the skin surface, and (3) it does not dry easily.
(4) It has a viscosity suitable for the movement of the transducer and does not change in viscosity, (5) It is transparent and does not have turbidity due to crystal precipitation, (6) It is not toxic or irritates the skin, (7) It must have properties such as being easy to wipe off after use.
本発明者は上記必須要件に適合した超音波診断
装置用媒剤を提供すべく鋭意研究し、水湿潤性の
原液を、中和された架橋型アクリル酸系ポリマー
でゲル化した、超音波診断装置用ゲル剤の発明を
完成した。 The present inventor has conducted extensive research to provide a medium for ultrasound diagnostic equipment that meets the above-mentioned essential requirements. Completed invention of gel for equipment.
水湿潤性原液とは、水、水と湿潤剤の混合液、
或は湿潤剤の何れかをいう。湿潤剤は乾燥抑制剤
として医薬品とか化粧品に通常使用される例えば
アルコール類、グリコール類など、好ましくは化
粧品原料基準に適合する品種品質のものでそれ自
身が乾燥し難く、水と混合可能であつて水と混合
したとき乾燥を抑制するもの、例えばエチレング
リコールモノブチルエーテル、ブチレングリコー
ル、ポリオキシエチレンアルキルフエニルエーテ
ル、ポリオキシエチレンアルキルエーテル、プロ
ピレングリコール、グリセリン、ポリエチレング
リコールなどがある。またピロリドンカルボン酸
塩、乳酸など水溶性固体で乾燥抑制効果のあるも
の、湿潤力あるスルホコハク酸塩エステル、ラウ
リル硫酸塩エステルなどの界面活性剤類も使用で
きる。 A water-wetting stock solution is water, a mixture of water and a wetting agent,
or a wetting agent. The humectant is a drying agent that is commonly used in pharmaceuticals and cosmetics, such as alcohols and glycols, and is preferably of a variety quality that meets cosmetic raw material standards, is difficult to dry by itself, and can be mixed with water. There are substances that suppress drying when mixed with water, such as ethylene glycol monobutyl ether, butylene glycol, polyoxyethylene alkyl phenyl ether, polyoxyethylene alkyl ether, propylene glycol, glycerin, and polyethylene glycol. Furthermore, water-soluble solids such as pyrrolidone carboxylate and lactic acid that have a drying suppressing effect, and surfactants such as sulfosuccinate ester and lauryl sulfate ester that have wetting properties can also be used.
架橋型アクリル酸系ポリマーとは、アクリル酸
または(及び)メタアクリル酸を、ジビニルベン
ゼン、ペンタエリスリトールアリルエーテル、シ
アヌル酸アリル、リン酸または亜リン酸類のアリ
ル系エステル、ポリアルキレングリコールジアリ
ル類エーテル、ビスアクリル酸アルキレン、アル
キレンジカルボン酸メタアクリルなど共重合可能
な複数個の完能基をもつ、所謂架橋剤と共に共重
合して得られた水膨潤性をもつ架橋型ポリマーを
いい、アクリル酸系モノマーと共に無水マレイン
酸などの共重合性モノマーを併用したものを含
む。これら水膨潤性ポリマーは、無機または有機
のアルカリで中和することによつて増粘効果を発
揮するものである。中和剤として使用されるアル
カリも、炭酸ナトリウム、重炭酸ナトリウム、ア
ンモニヤ水、水酸化ナトリウム、トリエタノール
アミン、ジエタノールアミンなどが化粧品原料基
準に収載されている。 Crosslinked acrylic acid polymers include acrylic acid or (and) methacrylic acid, divinylbenzene, pentaerythritol allyl ether, allyl cyanurate, phosphoric acid or phosphorous acid allyl esters, polyalkylene glycol diallyl ethers, A water-swellable crosslinked polymer obtained by copolymerizing with a so-called crosslinking agent, which has multiple copolymerizable fully functional groups such as alkylene bisacrylate and methacrylic alkylene dicarboxylate, and is an acrylic acid monomer. It also includes copolymerizable monomers such as maleic anhydride. These water-swellable polymers exhibit a thickening effect when neutralized with an inorganic or organic alkali. Alkali used as neutralizing agents include sodium carbonate, sodium bicarbonate, aqueous ammonia, sodium hydroxide, triethanolamine, and diethanolamine, which are listed in the Cosmetic Raw Materials Standards.
尚測定室等に於いて被験者、取扱者に好感を与
えるように着色剤、着香料など、及び保存性を向
上するために防腐剤、防カビ剤などを加えること
は自由である。 In addition, in the measurement room, etc., it is free to add coloring agents, flavoring agents, etc. to give a favorable impression to subjects and handlers, and to add preservatives, antifungal agents, etc. to improve preservability.
水、水と湿潤剤との混合液、または湿潤剤に、
望むならば着色、着香、防腐等の処理をし、これ
を撹拌しながらゆつくりと通常0.2〜3.0重量%量
の架橋型アクリル酸系ポリマーを添加溶解する。
透明に溶解した処で撹拌をゆるやかにしてポリマ
ーに対応する量のアルカリ、作業性良いためには
弱アルカリを添加して中和する。かくて本発明超
音波診断装置用ゲル剤が得られる。本ゲル剤は高
い超音波伝達率を示し、好適な粘度を有して流れ
たり垂れたりすることなく、乾燥し難く、常に透
明で毒性や刺戟性がなく、術後の拭きとりは極め
て容易で布や紙で、或はそれに水を含ませて拭け
ば容易に完全に除去することができ、また粘性の
ゆえにトランスジユーサの細孔へ入り難く、よし
んば入つても水易溶性であるために簡単に掃除が
でき、あらゆる点で極めて好適なすぐれた超音波
診断装置用媒剤として有用である。 In water, a mixture of water and a wetting agent, or a wetting agent,
If desired, the mixture is subjected to treatments such as coloring, flavoring, and preservative treatment, and while stirring, a crosslinked acrylic acid polymer is slowly added and dissolved in an amount of usually 0.2 to 3.0% by weight.
When the polymer is dissolved transparently, stir slowly and neutralize by adding an amount of alkali corresponding to the amount of the polymer, or a weak alkali for better workability. In this way, a gel for an ultrasonic diagnostic apparatus of the present invention is obtained. This gel has a high ultrasound transmission rate, has a suitable viscosity, does not run or drip, is difficult to dry, is always transparent, is non-toxic and non-irritating, and is extremely easy to wipe off after surgery. It can be easily and completely removed by wiping it with a cloth or paper dampened with water, and because of its viscosity, it is difficult to enter the pores of the transducer, and even if it does enter, it is easily water-soluble. It is easy to clean and is extremely suitable in all respects, making it useful as an excellent medium for ultrasonic diagnostic equipment.
以下に実施例を示す。数量を表わす部は重量部
である。 Examples are shown below. Parts expressing quantities are parts by weight.
実施例 1
プロピレングリコール20部と水80部との混合物
に極めて僅量のエンバスブルーを添加して淡い青
色を与え、撹拌のもと市販の架橋型アクリル酸系
ポリマー(和光純薬工業(株)製ハイビスワコー104)
0.5部を添加溶解する。透明な溶液をゆつくり撹
拌しながらモノエタノールアミン0.4部で中和、
B8H型回転粘度計(20rpm、25℃測定)粘度
48000cpsのゲル剤を得る。本例ゲル剤の超音波伝
達率は第1図の線6で示される。Example 1 A very small amount of Embass Blue was added to a mixture of 20 parts of propylene glycol and 80 parts of water to give a pale blue color, and under stirring, a commercially available cross-linked acrylic acid polymer (Wako Pure Chemical Industries, Ltd. ) made by Hibis Wako 104)
Add and dissolve 0.5 part. Neutralize the clear solution with 0.4 part of monoethanolamine while stirring slowly.
B8H type rotational viscometer (20 rpm, 25℃ measurement) viscosity
Obtain 48000cps of gel. The ultrasonic transmittance of the gel of this example is shown by line 6 in FIG.
実施例 2
グリセリン100部に防腐剤としてオキシ安息香
酸プロピル0.05部を添加、撹拌しながら市販の架
橋型アクリル酸系ポリマー0.2部を溶解、得られ
た透明液をゆつくり撹拌しながらトリエタノール
アミン0.3部で中和する。同じく粘度56000cpsの
ゲル剤を得る。同型のシヤーレに同重量ずつ容れ
て同時に37±1℃で比較測定した乾燥曲線を第2
図に示すが、線1は水、線2は市販の生体電極用
ペースト、線3は実施例1のゲル剤でプロピレン
グリコールを使用しなかつた場合、線4は実施例
1のゲル剤、線5は実施例2のゲル剤の、夫々乾
燥曲線であり、4及び5が大差を以て他にすぐ
れ、3がそれに次ぐことが知られる。Example 2 Add 0.05 part of propyl oxybenzoate as a preservative to 100 parts of glycerin, dissolve 0.2 part of a commercially available cross-linked acrylic acid polymer while stirring, and gently stir the resulting transparent liquid to dissolve 0.3 part of triethanolamine. Neutralize in the section. Similarly, a gel with a viscosity of 56,000 cps is obtained. The drying curve obtained by comparing and measuring the same weight in the same type of shear dish at the same time at 37 ± 1℃ is the second
As shown in the figure, line 1 is water, line 2 is commercially available bioelectrode paste, line 3 is the gel of Example 1 without using propylene glycol, line 4 is the gel of Example 1, line 4 is the gel of Example 1, and line 4 is the gel of Example 1. 5 is the drying curve of the gel of Example 2, and it is known that 4 and 5 are superior to the others by a large difference, and 3 is the second best.
第1図は超音波出力に対応した超音波伝達率の
特性を示すグラフであり、第2図は経時乾燥度の
特性を示すグラフである。
FIG. 1 is a graph showing the characteristics of ultrasonic transmissivity corresponding to the ultrasonic output, and FIG. 2 is a graph showing the characteristics of dryness over time.
Claims (1)
り選択される水湿潤性の原液を、架橋型アクリル
酸系ポリマーと中和剤とでゲル化して成る、超音
波診断装置用ゲル剤。1. A gel for ultrasound diagnostic equipment, which is made by gelling a water-wettable stock solution selected from water, a mixture of water and a wetting agent, or a wetting agent with a crosslinked acrylic acid polymer and a neutralizing agent. agent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4962280A JPS56148341A (en) | 1980-04-17 | 1980-04-17 | Gel agent for ultrasonic diagnosis apparatus |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4962280A JPS56148341A (en) | 1980-04-17 | 1980-04-17 | Gel agent for ultrasonic diagnosis apparatus |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS56148341A JPS56148341A (en) | 1981-11-17 |
JPS6318500B2 true JPS6318500B2 (en) | 1988-04-19 |
Family
ID=12836323
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4962280A Granted JPS56148341A (en) | 1980-04-17 | 1980-04-17 | Gel agent for ultrasonic diagnosis apparatus |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS56148341A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5944247A (en) * | 1982-09-06 | 1984-03-12 | 株式会社富士通ゼネラル | Ultrasonic transmitting liquid |
JPS63302834A (en) * | 1987-06-04 | 1988-12-09 | Yotsukaichi Gosei Kk | Contact medium of probe for ultrasonic diagnosis and preparation thereof |
EP0628284B1 (en) * | 1992-12-02 | 2001-06-06 | Shiseido Company Limited | Contact medium for probe of ultrasonic diagnostic apparatus |
JP2013056100A (en) * | 2011-09-09 | 2013-03-28 | Canon Inc | Photoacoustic matching material |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5563636A (en) * | 1978-11-06 | 1980-05-13 | Koyo Sangyo Co | High molecular gel containing water for ultrasoniccwave diagnosis |
-
1980
- 1980-04-17 JP JP4962280A patent/JPS56148341A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5563636A (en) * | 1978-11-06 | 1980-05-13 | Koyo Sangyo Co | High molecular gel containing water for ultrasoniccwave diagnosis |
Also Published As
Publication number | Publication date |
---|---|
JPS56148341A (en) | 1981-11-17 |
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