JPH01242514A - Manicure - Google Patents

Manicure

Info

Publication number
JPH01242514A
JPH01242514A JP6796688A JP6796688A JPH01242514A JP H01242514 A JPH01242514 A JP H01242514A JP 6796688 A JP6796688 A JP 6796688A JP 6796688 A JP6796688 A JP 6796688A JP H01242514 A JPH01242514 A JP H01242514A
Authority
JP
Japan
Prior art keywords
silica
nail
montmorillonite
amount
human body
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.)
Granted
Application number
JP6796688A
Other languages
Japanese (ja)
Other versions
JP2554522B2 (en
Inventor
Yoshikazu Soyama
美和 曽山
Atsushi Takahashi
淳 高橋
Yoshiyuki Ogusu
小楠 芳之
Toru Okamoto
亨 岡本
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shiseido Co Ltd
Original Assignee
Shiseido Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Shiseido Co Ltd filed Critical Shiseido Co Ltd
Priority to JP63067966A priority Critical patent/JP2554522B2/en
Priority to PCT/JP1989/000301 priority patent/WO1993012762A1/en
Priority to US07/427,134 priority patent/US5071639A/en
Publication of JPH01242514A publication Critical patent/JPH01242514A/en
Application granted granted Critical
Publication of JP2554522B2 publication Critical patent/JP2554522B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Cosmetics (AREA)

Abstract

PURPOSE:To obtain the title manicure having safety to human body, excellent stability with time, excellent physical properties of coating film and use value free from precipitation of pigment and pearl agent, containing organic modified montmorillonite, silica and a nonaromatic solvent as active ingredients. CONSTITUTION:A manicure containing organic modified montmorillonite (compound obtained by chemically reacting montmorillonite, clay minerals, a cationic activator of quaternary ammonium salt type and a nonionic higher organic polar compound), silica and a nonaromatic solvent as active ingredients. N-Butyl acetate, acetone, etc., may be cited as the nonaromatic solvent and the amount thereof blended is 60-85wt.%. The amount of silica is most preferably 0.5-1.5wt.% and the amount of the montmorillonite is preferably 0.2-3.0wt.%, especially preferably 0.8-2.0wt.%.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は新規な美爪料に関する。ざらに詳しくは有機変
性モンモリロナイト、シリカ及び非芳香族系溶剤を配合
した美爪料に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a novel nail beauty product. More specifically, the present invention relates to a nail polish containing organically modified montmorillonite, silica, and a non-aromatic solvent.

すなわち、本発明は人体に安全で顔料やバール剤の沈降
がなく、経時安定性に優れ、しかも塗膜物性、使用性の
良好な美爪料に関する。
That is, the present invention relates to a nail beauty product that is safe for the human body, does not cause sedimentation of pigments or burl agents, has excellent stability over time, and has good coating film properties and usability.

[従来の技術] 従来から、美爪料において有機変性モンモリロナイトを
配合し、このものの粘土鉱物に由来する良好なチキソト
ロピー付与性を利用して顔料やバール剤の沈降を防ぐこ
とが行われ、そして、この場合に溶剤としてトルエン、
キシレン等の芳香族炭化水素溶剤が使用されてきた。ト
ルエン等の芳香族炭化水素系溶剤は、該クレーを膨潤さ
せ最も良好なゲルを構築し、このようなゲルを含む美爪
料は比較的良好な分散安定性を示し経時的に沈降、分踵
することがないため、トルエン等はこの種美爪料の溶剤
として不可欠なものとされていた。
[Prior Art] Conventionally, organically modified montmorillonite has been blended into nail care preparations to utilize its good thixotropy properties derived from clay minerals to prevent pigments and varnish from settling. In this case, toluene as a solvent,
Aromatic hydrocarbon solvents such as xylene have been used. Aromatic hydrocarbon solvents such as toluene swell the clay and form the best gels, and nail polishes containing such gels exhibit relatively good dispersion stability and do not settle or split over time. For this reason, toluene and the like were considered indispensable as solvents for this type of nail polish.

又、疎水性シリカを配合し分散安定性、経時安定性を更
に改良した例(特開昭62−174003)があるが、
これらはトルエンが必須のゲル組成物を使用するため、
必然的に美爪料にもトルエンが含有されている。一方ト
ルエン、キシレン等の芳香族炭化水素溶剤を含有しない
美爪料用ゲル組成物として、水酸基含有極性物質とフェ
ニル基含有有機シリコン化合物を特定配合した例(特公
昭31−001044号)があり人体に安全な美爪料に
ついての技術が確立している。
There is also an example (Japanese Unexamined Patent Publication No. 174003/1983) in which hydrophobic silica was added to further improve dispersion stability and stability over time.
These use gel compositions that require toluene, so
Naturally, nail polishes also contain toluene. On the other hand, there is an example (Japanese Patent Publication No. 31-001044) in which a hydroxyl group-containing polar substance and a phenyl group-containing organosilicon compound are specifically blended as a nail beauty gel composition that does not contain aromatic hydrocarbon solvents such as toluene and xylene. The technology for safe nail polish has been established.

[発明が解決しようとしている課MJ トルエン、キシレン等芳香族炭化水素溶剤は人体への安
全性上の聞届があり、特に美爪料を頻繁に使用した場合
、爪に損傷や癌みを与える懸念のあることが知られてい
る。又、トルエン、キシレン等をまったく含有しないと
する特公昭61−001044号は人体に安全でチキソ
トロピー性を付与し、分散安定性、経時安定性もやや良
好ではあったが、安定性面では更なる改良の余地が残さ
れていた。
[The problem that the invention is trying to solve MJ Aromatic hydrocarbon solvents such as toluene and xylene have been reported to be safe for the human body, and they can damage and make nails especially if you use nail polish frequently. Known to be of concern. In addition, Japanese Patent Publication No. 61-001044, which does not contain toluene, xylene, etc., is safe for the human body and has thixotropic properties, and has somewhat good dispersion stability and stability over time, but in terms of stability it is even worse. There was still room for improvement.

本発明者らは、このような状況に鑑み、人体に安全で分
散安定性、経時安定性に非常に優れ、しかも塗膜物性、
使用性に優れた美爪料を開発すべく鋭意検討を重ねた結
果、有機変性モンモリロナイト、シリカ、及び非芳香族
系溶剤を必須に含有する、人体に安全で、顔料やパール
剤の沈降がなく、経時安定性に優れ、しかも塗膜物性、
使用性の良好な美爪料を見出し本発明を完成させるに至
った。
In view of these circumstances, the present inventors have developed a coating film that is safe for the human body, has excellent dispersion stability, and stability over time, and has excellent coating film properties.
As a result of intensive research to develop a nail polish that is easy to use, we have developed a nail polish that is safe for the human body, contains organically modified montmorillonite, silica, and a non-aromatic solvent, and does not cause the settling of pigments or pearlescent agents. , has excellent stability over time, and has good coating film properties.
We have discovered a nail beauty product with good usability and completed the present invention.

[課題を解決するための手段] 即ち、本発明は有機変性モンモリロナイト、シリカ、及
び非芳香族系溶剤を必須として含有する美爪料を提供す
るものである。これまで使用されていたトルエン・キシ
レン等の芳香族炭化水素if剤やフェニル基含有有機シ
リコン等は該クレーを膨潤させ、チキソトロピー性を付
与する物質であった。しかし、本発明はトルエン、キシ
レン等をまったく使用せず、人体に安全な非芳香族系溶
剤を用い有機変性モンモリロナイトとシリカの相互作用
により優れたチキソトリビー性を付与し、大きな目的を
達成している。
[Means for Solving the Problems] That is, the present invention provides a nail polish that essentially contains organically modified montmorillonite, silica, and a non-aromatic solvent. Aromatic hydrocarbon if agents such as toluene and xylene, phenyl group-containing organic silicones, and the like that have been used so far are substances that swell the clay and impart thixotropic properties. However, the present invention does not use toluene, xylene, etc. at all, uses a non-aromatic solvent that is safe for the human body, and provides excellent thixotrivy properties through the interaction of organically modified montmorillonite and silica, achieving a major objective. There is.

以下に本発明の構成についてのべる。The configuration of the present invention will be described below.

本発明で用いられる有機変性モンモリロナイトは、粘土
鉱物であるモンモリロナイトに第4級アンモニウム塩型
のカチオン活性剤、及び非イオン性の高級有機極性化合
物を化学的に結合させた物質であって、市販品として例
えばベントン(ナショナルレッド社製のベントン27、
ベントン34、ベントン38等)が挙げられ、何れも利
用できる。これらは必要に応じて任意に選択でき、1種
または2種以上を配合することができる。これら成分の
好ましい配合量は0.2〜3.0重量%であり、ざらに
好まし′くは0.2〜2.0重量%である。0.2重量
%未満では良好なチキソトロピー性が得られず、3.0
重量%を趣えると美爪料の塗膜の光沢や経時のも′?3
(ハガレ)が悪くなる。
The organically modified montmorillonite used in the present invention is a substance in which a quaternary ammonium salt type cation activator and a nonionic higher organic polar compound are chemically bonded to montmorillonite, which is a clay mineral, and is a commercially available product. For example, Benton (Benton 27 manufactured by National Red Co., Ltd.)
Bentone 34, Bentone 38, etc.), any of which can be used. These can be arbitrarily selected as required, and one or more types can be blended. The preferred amount of these components is 0.2 to 3.0% by weight, more preferably 0.2 to 2.0% by weight. If it is less than 0.2% by weight, good thixotropy cannot be obtained;
When you look at the weight percentage, does it affect the gloss and age of the nail polish coating? 3
(Peeling) gets worse.

本発明で用いられるシリカは周知のものでよく例えば、
市販品としてはアエロジル#200、アエロジル廿30
0、アエロジル#380、或はアエロジルR972等が
挙げられる。これらの中でもアエロジルit 200、
アエロジル#300、アエロジルR972等の粒径が0
.01μ未満のものがチキソトロピー性の点で好ましい
The silica used in the present invention may be well-known, for example,
Commercially available products include Aerosil #200 and Aerosil #30.
0, Aerosil #380, or Aerosil R972. Among these, Aerosil IT 200,
The particle size of Aerosil #300, Aerosil R972, etc. is 0.
.. It is preferable to have a particle diameter of less than 0.01 μm from the viewpoint of thixotropy.

これら成分の好ましい配合量は0.1〜2.0重量%で
あり、ざらに好ましくは0.5〜1.5重量%である。
The preferred amount of these components is 0.1 to 2.0% by weight, more preferably 0.5 to 1.5% by weight.

0.1重量%未満では良好なチキソトロピー性が得られ
ず経時安定性が悪くなる。2.0重量%を越えると、使
用性においてエナメル塗膜の光沢が悪く経時の持ちも劣
ってくる。
If it is less than 0.1% by weight, good thixotropy will not be obtained and stability over time will deteriorate. If it exceeds 2.0% by weight, the enamel coating will have poor gloss and poor durability over time.

本発明で用いられる非芳香族系溶剤とは、トルエン、キ
シレン等の芳香族炭化水素以外の有機溶剤を広く指称し
、例えば酢酸nブチル、酢酸イソブチル、酢酸エチル、
メチルエチルケトン、アセトン、nブタノール、イソプ
ロピルアルコール、エチルアルコール等である。これら
溶剤の1種または2種以上を配合できる。これら成分の
好ましい配合量は60〜85重量%である。
The non-aromatic solvent used in the present invention broadly refers to organic solvents other than aromatic hydrocarbons such as toluene and xylene, such as n-butyl acetate, isobutyl acetate, ethyl acetate,
Examples include methyl ethyl ketone, acetone, n-butanol, isopropyl alcohol, and ethyl alcohol. One or more of these solvents can be blended. The preferred amount of these components is 60 to 85% by weight.

更に本発明の美爪料には、上記必須成分以外に通常美爪
料に使用される皮膜形成剤、樹脂、可塑剤、顔料、パー
ル剤等が配合され、また、紫外線吸収剤、保湿剤、薬剤
、香料、そして水分等も適量配合することがで苦る。も
ちろん、これらは本発明の目的を損なわない質的、量的
条件下で使用されなければならない。
Furthermore, in addition to the above-mentioned essential ingredients, the nail beauty preparation of the present invention contains film-forming agents, resins, plasticizers, pigments, pearlescent agents, etc. that are usually used in nail beauty preparations, and also contains ultraviolet absorbers, humectants, It is difficult to mix drugs, fragrances, and water in appropriate amounts. Of course, these must be used under qualitative and quantitative conditions that do not impair the purpose of the present invention.

[発明の効果] 本発明は人体に安全で顔料やパール剤の沈降がな(経時
安定性に優れ、しかも、塗膜物性、使用性の良好な美爪
料に関する。従来技術のトルエン、キシレン等の芳香族
炭化水素系溶剤を使用したものに比べて、人体に対する
安全性が高く爪の損傷や痛を与えることが極めて少なく
、経時のもちの点でも優れている。また、トルエン、キ
シレン等の芳香族炭化水素系溶剤を含有しない美爪fx
Iに比べてもバール剤の沈澱、経時安定性、塗膜物性、
使用性の点で更に優れた品質となっている。
[Effects of the Invention] The present invention relates to a nail beauty product that is safe for the human body, does not cause sedimentation of pigments or pearlescent agents (has excellent stability over time, and has good coating film properties and usability. Compared to aromatic hydrocarbon solvents such as toluene and xylene, they are safer for the human body, cause very little damage or pain to nails, and have superior durability over time. Beautiful nail fx that does not contain aromatic hydrocarbon solvents
Compared to I, the precipitation of Burr agent, stability over time, physical properties of coating film,
The quality is even better in terms of usability.

[実施例] 以下、実施例によって本発明の詳細な説明する配合量は
重量%である。
[Examples] Hereinafter, the present invention will be explained in detail with reference to Examples, and the blending amounts are expressed in % by weight.

実施例に先立ち、効果試験方法及び評価方法について詳
述する。
Prior to Examples, effectiveness testing methods and evaluation methods will be described in detail.

猫度 BL型粘度計ローターt(o、2.6 rpm、30℃
、1分間測定。
Cat degree BL type viscometer rotor t (o, 2.6 rpm, 30℃
, measured for 1 minute.

毛」L宏」L性− 美爪料を容器に充填し経時の沈澱、及び分離を肉眼で観
察する。
Hair "L-Hiroshi" L properties - Fill a container with nail polish and visually observe precipitation and separation over time.

O沈澱、分離が全く認められない。No O precipitation or separation was observed.

O沈澱、分離が僅かに認められる。A slight amount of O precipitate and separation is observed.

■ 沈澱、分離が認められる。■ Precipitation and separation are observed.

△ 沈澱、分離が非常に認められる。△ Sedimentation and separation are significantly observed.

±1夏光沢 実際の使用において官能で評価 0 非常に光沢がある O やや光沢がある O やや光沢がない △ 光沢がない X 全く光沢がない !■ の  ち  ハ  し 実際の使用(3日間)において官能で評価。±1 summer gloss Sensory evaluation in actual use 0 Very shiny O: Slightly shiny O: Slightly lackluster △ Lack of luster X Not shiny at all ! ■ No Chi Ha Sensory evaluation during actual use (3 days).

0 非常にもちが良い Oややもちが良い Oややもちが悪い △ ももが悪い × 非常にもちが悪い −への−轡 実際の使用において官能で評価。 n=500 爪の異
常を認めた人 3未満 O爪の異常を認めた人 3〜5 0 爪の異常を認めた人 6〜10 △ 爪の異常を認めた大 11〜15 × 爪の異常を認めた大 16以上 実施例1.2、比較例1 表−1に示す組成で常法により、美爪料を製造し、それ
ぞれの品質評価を行なった。
0 Very sticky O Good sticky O Poor sticky △ Poor thigh × Very poor sticky - to - 轡 Sensory evaluation in actual use. n=500 People with nail abnormalities Less than 3O People with nail abnormalities 3-5 0 People with nail abnormalities 6-10 △ Large with nail abnormalities 11-15 × Nail abnormalities Recognized size: 16 or more Example 1.2, Comparative Example 1 Nail beauty products were produced using the compositions shown in Table 1 in a conventional manner, and the quality of each product was evaluated.

アエロジル R972”−1・・・粒径0.016μア
エロジル380°−2・・・粒径0.007μ表−1か
ら明らかなように実施例1.2は人体に安全で顔料やバ
ール剤の沈降がなく経時安定性に優れ、しかも、塗膜物
性、使用性が良好であることが判る。これに対しトルエ
ン及びシリカを配合した美爪料(比較例1)は安定性面
では優れているものの、経時のもち、人体への安全性の
点で劣り、爪への異常が認められている。
Aerosil R972''-1...particle size 0.016μAerosil 380°-2...particle size 0.007μAs is clear from Table-1, Example 1.2 is safe for the human body and precipitates pigments and bur agents. It can be seen that the nail polish containing toluene and silica (Comparative Example 1) has excellent stability over time, and also has good coating properties and usability. It is inferior in terms of durability over time, safety to the human body, and abnormalities to nails have been observed.

実施例3〜5 表−2に示す組成で常法により、美爪料を製造し、それ
ぞれの品質評価を行なった。
Examples 3 to 5 Nail cosmetics were produced using the compositions shown in Table 2 by a conventional method, and their quality was evaluated.

(以下余白) 表−2から明らかなように実施例3〜5の美爪料は、人
体に安全で、顔料やバール剤の沈降がなく・経時安定性
に優れ、しかも塗膜物性、使用性が非常に優れてぃた。
(The following is a blank space) As is clear from Table 2, the nail polishes of Examples 3 to 5 are safe for the human body, do not cause sedimentation of pigments or burl agents, have excellent stability over time, and have excellent coating film properties and ease of use. was very good.

特許出願人  株式会社 資生霊 手続補正書(自発) 昭和63年8月チ日 特許庁長官 吉 1)文 毅 殿 事件との関係 特許出願人 住 所 東京都中央区銀座7丁目5番5号明細書の「発
明の詳細な説明」の欄 5、補正の内容 (11明♀(■害第5頁第1行の「0.2〜」を「0.
8〜」と補正する。
Patent Applicant: Shiseirei Co., Ltd. Written Amendment to Procedures (Voluntary) August 1986, Commissioner of the Japan Patent Office Yoshiki 1) Relationship to the Moon Tsuyoshi Case Patent Applicant Address: 7-5-5, Ginza, Chuo-ku, Tokyo Details Column 5 of the "Detailed Description of the Invention" of the book, contents of the amendment (11)
8~” is corrected.

(2)明細書第6頁第19行の「痛」の次に「み」を加
入する。
(2) Add ``mi'' next to ``pain'' on page 6, line 19 of the specification.

(3)明細書第7頁第2行のrRJを「降」と補正する
(3) rRJ on page 7, line 2 of the specification is corrected to "fall".

以上that's all

Claims (1)

【特許請求の範囲】[Claims] 有機変性モンモリロナイト、シリカおよび非芳香族系の
溶剤を含有することを特徴とする美爪料。
A nail beauty product characterized by containing organically modified montmorillonite, silica, and a non-aromatic solvent.
JP63067966A 1988-03-22 1988-03-22 Nail polish Expired - Lifetime JP2554522B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP63067966A JP2554522B2 (en) 1988-03-22 1988-03-22 Nail polish
PCT/JP1989/000301 WO1993012762A1 (en) 1988-03-22 1989-03-22 Manicuring preparation
US07/427,134 US5071639A (en) 1988-03-22 1989-03-22 Nail cosmetic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63067966A JP2554522B2 (en) 1988-03-22 1988-03-22 Nail polish

Publications (2)

Publication Number Publication Date
JPH01242514A true JPH01242514A (en) 1989-09-27
JP2554522B2 JP2554522B2 (en) 1996-11-13

Family

ID=13360221

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63067966A Expired - Lifetime JP2554522B2 (en) 1988-03-22 1988-03-22 Nail polish

Country Status (1)

Country Link
JP (1) JP2554522B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07187958A (en) * 1993-12-27 1995-07-25 Co-Op Chem Co Ltd Nail polish

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54160753A (en) * 1978-06-08 1979-12-19 Shiseido Co Ltd Nail enamel
JPS6016910A (en) * 1983-07-07 1985-01-28 Shiseido Co Ltd Nail enamel
JPS61210020A (en) * 1985-03-15 1986-09-18 Shiseido Co Ltd Manicure
JPS62174003A (en) * 1986-01-24 1987-07-30 Kobayashi Kooc:Kk Nail enamel

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54160753A (en) * 1978-06-08 1979-12-19 Shiseido Co Ltd Nail enamel
JPS6016910A (en) * 1983-07-07 1985-01-28 Shiseido Co Ltd Nail enamel
JPS61210020A (en) * 1985-03-15 1986-09-18 Shiseido Co Ltd Manicure
JPS62174003A (en) * 1986-01-24 1987-07-30 Kobayashi Kooc:Kk Nail enamel

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07187958A (en) * 1993-12-27 1995-07-25 Co-Op Chem Co Ltd Nail polish

Also Published As

Publication number Publication date
JP2554522B2 (en) 1996-11-13

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