JPS63188610A - Cosmetic - Google Patents

Cosmetic

Info

Publication number
JPS63188610A
JPS63188610A JP2154087A JP2154087A JPS63188610A JP S63188610 A JPS63188610 A JP S63188610A JP 2154087 A JP2154087 A JP 2154087A JP 2154087 A JP2154087 A JP 2154087A JP S63188610 A JPS63188610 A JP S63188610A
Authority
JP
Japan
Prior art keywords
organic
cosmetic
acid
properties
antimicrobial
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.)
Pending
Application number
JP2154087A
Other languages
Japanese (ja)
Inventor
Masashi Fujii
政志 藤井
Minoru Ito
実 伊藤
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.)
NOEBIA KK
Noevir Co Ltd
Original Assignee
NOEBIA KK
Noevir 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 NOEBIA KK, Noevir Co Ltd filed Critical NOEBIA KK
Priority to JP2154087A priority Critical patent/JPS63188610A/en
Publication of JPS63188610A publication Critical patent/JPS63188610A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain a safe cosmetic having synergistically increased antimicrobial activity and sufficient antisepticizing power free from a feeling of skin irritation, by using specific amounts of 1,3-butylene glycol, a surface active agent having a specific ratio of inorganic properties and organic properties and an organic acid. CONSTITUTION:A cosmetic is blended with (A) 0.5-10wt.% calculated as antimicrobial component of a surface active agent such as monopalmitic acid sucrose ester, monomyristic acid decaglycerin, etc., having antimicrobial activity and a ratio of inorganic properties and organic properties of 1.20-2.00, (B) 0.05-0.5wt.% one or more organic acids, preferably citric acid, lactic acid, etc., as an antimicrobial component and (C) 3-20wt.% 1,3-butylene glycol to give a cosmetic having enhanced antimicrobial actions of the components A and B, showing sufficient antimicrobial activity without adding an antiseptic such as parahydroxybenzoic ester, etc., providing an unfavorable irritating feeling and high safety.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明は、1.3−ブチレングリコール3〜20重量
%と、1.0.8が1.20〜2.00の界面活性剤お
よび有機酸の、1種又は2種以上を配合した防腐力を有
し皮膚刺激感のない安全な化粧料に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention is directed to the use of 1.3-butylene glycol in an amount of 3 to 20% by weight, a surfactant in which 1.0.8 is 1.20 to 2.00, and an organic The present invention relates to a safe cosmetic containing one or more acids, which has antiseptic properties and does not cause skin irritation.

〔従来の技術〕[Conventional technology]

従来、化粧料には微生物汚染を防ぐために、表1に挙げ
たような防腐剤または防腐効果を有する香料を配合して
いる。 化粧料に配合する防腐剤としては、抗菌スペク
トルが広いこと、少量で有効であること、処方系で安定
でありpl+や他成分の影響によって効力の低下を生じ
ないこと、溶解性。
Conventionally, cosmetics have been formulated with preservatives or fragrances having a preservative effect as listed in Table 1 in order to prevent microbial contamination. Preservatives to be added to cosmetics must have a broad antibacterial spectrum, be effective in small amounts, be stable in formulations and not have their efficacy reduced by the influence of PL+ or other ingredients, and have solubility.

分散性に優れ、製品の機能9色、匂いなどを阻害しない
こと、生体に対してなるべく無害、無刺激で感作性、光
毒性、光感作性、変異原性がなく安全性が高いこと等が
望まれ、これらの点を満たす防腐剤が探究され検討され
てきた。 その結果、多種の防腐剤が化粧料に使用でき
るものと認められているが、それ°らの中でも、バラヒ
ドロキシ安息香酸エステル類は安全性が高いとされ、最
も汎用されている。
It has excellent dispersibility, does not interfere with the product's nine colors, odors, etc., is as harmless to living organisms as possible, is non-irritating, has no sensitization, phototoxicity, photosensitization, or mutagenicity, and is highly safe. etc., and preservatives that meet these requirements have been sought and studied. As a result, a wide variety of preservatives have been recognized as being usable in cosmetics, and among them, rose hydroxybenzoic acid esters are considered to be highly safe and are the most commonly used.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

しかし、バラヒドロキシ安息香酸エステル類をはじめと
して、これら防腐剤には、今日まで化粧料による皮膚の
炎症や黒皮症といった問題に隠れてほとんど取り上げら
れなかった「皮膚刺激感」という問題点があった。(現
在、日本化粧品技術者会誌投稿中) この皮膚刺激感は
、ヒトパンチテストにおいて炎症性刺激が認められない
、実際に使用される防腐剤濃度ででも皮膚塗布時に感じ
られる「痛み」、「かゆみ」、「ひりひり感」といった
不快感で、炎症性あるいは感作性刺激と同様に化粧料の
使用時に重大な゛問題となる。 いくつかの防腐剤につ
いて、それらによる皮膚刺激感を表1に示した。
However, these preservatives, including rose hydroxybenzoic acid esters, have the problem of ``skin irritation,'' which has been largely ignored until now due to problems such as skin irritation and melasma caused by cosmetics. Ta. (Currently being submitted to the journal of the Japan Society of Cosmetic Technologists) This skin irritation is caused by the pain and itchiness felt when applied to the skin, even at the preservative concentration actually used, where no inflammatory irritation was observed in the human punch test. It causes unpleasant sensations such as ``burning'' and ``tingling,'' and, like inflammatory or sensitizing irritation, is a serious problem when using cosmetics. Table 1 shows the skin irritation caused by some preservatives.

表1.防腐剤による皮膚刺激感 防腐剤      濃度a) 皮膚刺激感b)オイゲノ
ール     0.05    2.9a)カルボキシ
メチルセルロース(C,M、C)1.0%水溶液中重量
% b)被験者30名に対し、塗布時の刺激感を次の4段階
評価させたときの、評点の平均値で示す。
Table 1. Skin irritation caused by preservative Preservative Concentration a) Skin irritation b) Eugenol 0.05 2.9a) Carboxymethyl cellulose (C, M, C) 1.0% aqueous solution weight % b) Applied to 30 subjects It is shown as the average value of the ratings when the feeling of stimulation is evaluated on the following four levels.

評 価    刺激感 0    刺激を感じない 1    やや痛い 2    痛い 3    非常に痛い しかし、この皮膚刺激感を抑制するためにこれら防腐剤
の使用を控えると、化粧料の微生物汚染という問題が生
じるため、化粧料の形態についても検討が必要となる他
、無菌製造を強いられることになり、重大な設備投資と
工程の厳密な管理が必要となる。
Evaluation: 0 Irritation No irritation 1 Somewhat painful 2 Painful 3 Very painful However, if we refrain from using these preservatives to suppress this skin irritation, the problem of microbial contamination of cosmetics will arise, so cosmetics should not be used. In addition to the need to consider the form of the material, it also requires aseptic manufacturing, which requires significant capital investment and strict control of the process.

〔問題点を解決するための手段〕[Means for solving problems]

以上の問題点を解決するため、種々の検討を行っていっ
たところ、我々は、1,3−ブチレングリコールを添加
すると系の防腐力が向上することがあることを知った(
US特許37321)2.英国特許1409024゜K
、八cott  ら ;  J、Food  Sci、
、41(31541−546(1976))。 また、
従来の防腐剤以外にも抗菌活性を有する界面活性剤や有
機酸が存在することがわかってきた(加藤信行ら;防菌
防黴3(sl 355−361 (1975)、内掘毅
;表面21(4t 182−193 (1983) 、
衛生技術会;天然物利用による食品の保存技術pp、5
−1)(1981) )。 これらを組み合わせて使用
すると、個々の抗菌活性の相剰効果により実用的な抗菌
活性を期待することができる。
In order to solve the above problems, we conducted various studies and found that adding 1,3-butylene glycol can improve the preservative power of the system (
US Patent 37321)2. British patent 1409024°K
, 8cott et al.; J. Food Sci.
, 41 (31541-546 (1976)). Also,
In addition to conventional preservatives, it has been found that there are surfactants and organic acids that have antibacterial activity (Nobuyuki Kato et al.; Antibacterial and Antifungal 3 (sl 355-361 (1975); Takeshi Uchibori; Surface 21). (4t 182-193 (1983),
Sanitation Technology Society; Food preservation technology using natural products pp, 5
-1) (1981)). When these are used in combination, practical antibacterial activity can be expected due to the additive effect of the individual antibacterial activities.

我々の検討の結果からは、1.3−ブチレングリコール
は他の物質の抗菌作用を増強する効果を有し、有機酸は
その添加によるpHの低下によって抗菌的に作用するも
のと考察した。 抗菌活性を有する界面活性剤について
は、無機性対有機性比(Inor−ganic−Org
anic balance、 1.O,B)を用いて説
明することができた。 すなわち、ある物質が抗菌活性
を有するためには、その物質がある程度親水性で水相に
有効量が移行して水相中の微生物と接触する必要がある
。 一方、微生物と接触した物質が、微生物の細胞膜を
透過して抗菌活性を発揮するためにはある程度の親油性
が要求される。 つまり、親水性および親油性の両方を
兼ね備える必要がある。 こういった性質を有機概念図
を用いて表現した。 有機概念図とは有機化合物の性状
をひとつの理論の下に体系的にまとめようとしたもので
、有機化合物のいくつかの基本的な物理的性状を基礎と
して系統的に組み立てられている。
From the results of our study, we considered that 1,3-butylene glycol has the effect of enhancing the antibacterial effects of other substances, and that organic acids act antibacterially by lowering the pH due to the addition of 1,3-butylene glycol. For surfactants with antimicrobial activity, the inorganic-to-organic ratio (Inor-ganic-Org
anic balance, 1. This could be explained using O, B). That is, in order for a certain substance to have antibacterial activity, the substance must be hydrophilic to some extent and an effective amount must be transferred to the aqueous phase and come into contact with microorganisms in the aqueous phase. On the other hand, in order for a substance that has come into contact with a microorganism to permeate the cell membrane of the microorganism and exhibit antibacterial activity, a certain degree of lipophilicity is required. In other words, it is necessary to have both hydrophilicity and lipophilicity. These properties were expressed using an organic conceptual diagram. An organic conceptual diagram is an attempt to systematically summarize the properties of organic compounds under one theory, and is systematically assembled based on some basic physical properties of organic compounds.

そして個々の物性値による以外に、全範囲の化合物につ
いである程度の化学構造から大体の輪郭を予見すること
ができるように、性状の起源に基づ(一定の基準を数値
として求め、それによって任意の化合物をグラフ上に示
す方法を考えて全有機化合物の概念的把握に役立てよう
とするものである。 この有R概念図において、有機化
合物の性状を表すために、無機性対有機性比(Inor
ganic−Organic balance、1.0
.B )を用いる。 !、0.8は簡単にいえば、有機
化合物の構造中、無機性を示す部分と有機性を示す部分
の比率である。 本発明において、我々の目的にかなう
界面活性剤のI。
In addition to individual physical property values, it is also possible to predict the general outline of a wide range of compounds from a certain degree of chemical structure, based on the origin of the properties (determining a certain standard as a numerical value, and then This paper aims to help conceptually understand all organic compounds by considering a method of showing the compounds of Inor
ganic-organic balance, 1.0
.. B) is used. ! , 0.8 is simply the ratio of the inorganic part to the organic part in the structure of an organic compound. In the present invention, surfactants I which serve our purposes.

0.8は、1.20〜2.00の範囲にあった。0.8 was in the range of 1.20-2.00.

1.0.8が1.20〜2.00の界面活性剤の配合量
は、抗菌活性発現のための有効量で刺激を生じない程度
の量を考えて、0.5〜10重量%とした。
The blending amount of the surfactant with 1.0.8 of 1.20 to 2.00 is 0.5 to 10% by weight, considering the amount that is effective for expressing antibacterial activity and does not cause irritation. did.

有機酸の配合量は皮膚刺激感のない0.05〜0.5重
量%とした。  1,3−ブチレングリコールについて
は、有効量と使用感を考えて3〜20重量%配合するこ
とにした。
The amount of organic acid blended was 0.05 to 0.5% by weight, which does not cause skin irritation. Regarding 1,3-butylene glycol, it was decided to incorporate 3 to 20% by weight in consideration of the effective amount and feeling of use.

1、O,Bが1.20〜2.00の界面活性剤としては
、モノパルミチン酸ショ糖エステル、モノミリスチン酸
デカグリセリル等を用いる。 また有機酸としては、ク
エン酸、乳酸が好ましい結果を与える。
1. As the surfactant having O and B of 1.20 to 2.00, sucrose monopalmitate, decaglyceryl monomyristate, etc. are used. Furthermore, as the organic acid, citric acid and lactic acid give preferable results.

〔作用および効果〕[Action and effect]

本発明の作用および効果を、実施例により詳細に説明す
る。
The functions and effects of the present invention will be explained in detail with reference to Examples.

(実施例1) クレンジングクリーム 以下に比較例とともに処方を示す。(Example 1) Cleansing cream The prescription is shown below along with comparative examples.

■〜■を混合し85〜90℃に加熱溶解した後、同じく
混合加熱した0〜[相]、■を添加して乳化させる。 
乳化後攪拌しながら冷却し、45℃で■を添加する。
After mixing ① to ② and heating and dissolving at 85 to 90°C, 0 to [phases] and ①, which were mixed and heated in the same manner, are added and emulsified.
After emulsification, cool while stirring, and add ① at 45°C.

(実施例2) 化粧水 以下に比較例とともに、処方を示す。(Example 2) lotion The prescription is shown below along with comparative examples.

■〜■を混合溶解する。 ■を添加する際には、あらか
じめ■の1部に加熱溶解させ、冷却してから混合する。
Mix and dissolve ■~■. When adding (2), heat and dissolve part of (2) in advance, cool and mix.

上記実施例1お°よび2.比較例1〜4について、皮膚
刺激感と抗菌活性の検討を行った。
Examples 1 and 2 above. Comparative Examples 1 to 4 were examined for skin irritation and antibacterial activity.

皮膚刺激感は被験者30人に実施例および比較例の化粧
料を使用させ、その随感じた刺激感を次のように4段階
評価させた。
Regarding the sensation of skin irritation, 30 subjects used the cosmetics of Examples and Comparative Examples and evaluated the sensation of irritation on a four-point scale as follows.

評 価   刺激感 0    刺激を感じない 1    やや痛い 2    痛い 3    非常に痛い 結果は各試料について、評価O〜3をつけた被験者の人
数(割合)で示し、表2にまとめた。
Evaluation Sensation of irritation 0 No irritation 1 Slightly painful 2 Painful 3 Very painful The results are shown as the number (percentage) of subjects who gave ratings of O to 3 for each sample, and are summarized in Table 2.

抗菌活性は、大腸菌(Escherichia  co
l i) 。
Antibacterial activity was determined by Escherichia coli (Escherichia coli).
l i).

緑MiA苗(Pseudomonas  aerugi
nosa) 、シュードモナス・セパ−シャ(Pseu
domonas  エμμハエ) 。
Green MiA seedling (Pseudomonas aerugi)
nosa), Pseudomonas cepasia (Pseu
domonas eμμ flies).

黄色ブドウ球菌(Sta hylococcus  a
ureus)を各々単独に培養した後混合し、試料20
gに植菌数が約5.0X10  個/gとなるように植
菌して凹べた。
Staphylococcus aureus (Staphylococcus a)
ureus) were cultured individually and then mixed, sample 20
The bacteria were inoculated to approximately 5.0 x 10 cells/g in a well.

植菌後試料を37℃で静置し、2週間後の各試料1gあ
たりの生菌数を表3に示した。
After inoculation, the samples were allowed to stand at 37°C, and the number of viable bacteria per gram of each sample after 2 weeks is shown in Table 3.

表2.皮膚刺激感 表3.抗菌活性 表22表3から、防腐剤(パラヒドロキシ安息香酸メチ
ルおよびプロピル)を用いた化粧料、すなわち比較例1
.比較例3では、抗菌活性は植菌後2週間で試験菌が死
滅するので十分満足できるが、皮膚刺激感については良
い結果を得ていないことが示される。 つまり、比較例
1では被験者の80%が、比較例3では被験者の60%
が何らかの皮膚刺激感を訴えている。
Table 2. Skin irritation table 3. Antibacterial activity Table 22 From Table 3, cosmetics using preservatives (methyl and propyl parahydroxybenzoate), namely Comparative Example 1
.. In Comparative Example 3, the antibacterial activity was sufficiently satisfactory as the test bacteria were killed two weeks after inoculation, but it was shown that good results were not obtained regarding skin irritation. In other words, 80% of the subjects in Comparative Example 1 and 60% of the subjects in Comparative Example 3
complains of some kind of skin irritation.

比較例2および比較例4については、前者が被験者の1
0%がやや刺激感があると答えた程度で、後者では誰も
刺激感を訴えなかったが(表2)、表3に示すように、
植菌後2週間経過しても多数の生菌が認められ(各々8
X 10’個/g、lXl0’個/g)、抗菌活性は全
く認められなかった。
Regarding Comparative Example 2 and Comparative Example 4, the former was subject 1.
0% answered that it was somewhat irritating, and no one in the latter group complained of irritating sensation (Table 2), but as shown in Table 3,
Even after 2 weeks after inoculation, many viable bacteria were observed (8
X10' cells/g, lXl0' cells/g), and no antibacterial activity was observed.

実施例1および実施例2については、前者においてただ
ひとりの被験者の3%がやや刺激感があると訴えただけ
で(表2)、抗菌活性も植菌後2週間で試験菌が死滅し
ており(表3)、十分なものであった。すなわち、本発
明の実施例は、十分な抗菌活性を有しており、しかもほ
とんど皮膚刺激感を与えない安全性の高い化粧料であっ
た。
Regarding Examples 1 and 2, only 3% of the test subjects in the former complained of slight irritation (Table 2), and the antibacterial activity also showed that the test bacteria died two weeks after inoculation. (Table 3) and was sufficient. That is, the examples of the present invention were highly safe cosmetics that had sufficient antibacterial activity and hardly caused skin irritation.

以上述べたように、本発明により、使用に際し好ましく
ない皮膚刺激感を与える原因となる防腐剤を配合しなく
ても、十分な抗菌活性を有し安全性の高い化粧料を提供
することができた。
As described above, the present invention makes it possible to provide cosmetics with sufficient antibacterial activity and high safety without the need to incorporate preservatives that cause undesirable skin irritation upon use. Ta.

Claims (3)

【特許請求の範囲】[Claims] (1)1,3−ブチレングリコール3〜20重量%と、
無機性対有機性比(Inorganic−Organi
c balance、I.O.B)が1.20〜2.0
0の界面活性剤および、有機酸の1種又は2種以上を配
合した化粧料。
(1) 3 to 20% by weight of 1,3-butylene glycol;
Inorganic-Organic Ratio
c balance, I. O. B) is 1.20 to 2.0
A cosmetic containing 0 surfactant and one or more organic acids.
(2)I.O.Bが1.20〜2.00の界面活性剤の
配合量が0.5〜10重量%である、特許請求の範囲第
1項に記載の化粧料。
(2) I. O. The cosmetic according to claim 1, wherein the amount of the surfactant having B of 1.20 to 2.00 is 0.5 to 10% by weight.
(3)有機酸の配合量が0.05〜0.5重量%である
、特許請求の範囲第1項又は第2項に記載の化粧料。
(3) The cosmetic according to claim 1 or 2, wherein the amount of organic acid blended is 0.05 to 0.5% by weight.
JP2154087A 1987-01-30 1987-01-30 Cosmetic Pending JPS63188610A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2154087A JPS63188610A (en) 1987-01-30 1987-01-30 Cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2154087A JPS63188610A (en) 1987-01-30 1987-01-30 Cosmetic

Publications (1)

Publication Number Publication Date
JPS63188610A true JPS63188610A (en) 1988-08-04

Family

ID=12057804

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2154087A Pending JPS63188610A (en) 1987-01-30 1987-01-30 Cosmetic

Country Status (1)

Country Link
JP (1) JPS63188610A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0920630A (en) * 1995-07-06 1997-01-21 Nippon Zetotsuku Kk Cosmetic material
JPH10203955A (en) * 1997-01-20 1998-08-04 Noevir Co Ltd Antimicrobial low-irritating cosmetic

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0920630A (en) * 1995-07-06 1997-01-21 Nippon Zetotsuku Kk Cosmetic material
JPH10203955A (en) * 1997-01-20 1998-08-04 Noevir Co Ltd Antimicrobial low-irritating cosmetic

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