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JPH085776B2 - Method for producing enzyme-containing facial cleansing powder - Google Patents
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JPH085776B2 - Method for producing enzyme-containing facial cleansing powder - Google Patents

Method for producing enzyme-containing facial cleansing powder

Info

Publication number
JPH085776B2
JPH085776B2 JP60240040A JP24004085A JPH085776B2 JP H085776 B2 JPH085776 B2 JP H085776B2 JP 60240040 A JP60240040 A JP 60240040A JP 24004085 A JP24004085 A JP 24004085A JP H085776 B2 JPH085776 B2 JP H085776B2
Authority
JP
Japan
Prior art keywords
enzyme
facial cleansing
granulated
powder
cleansing powder
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 - Fee Related
Application number
JP60240040A
Other languages
Japanese (ja)
Other versions
JPS6299321A (en
Inventor
忠生 白石
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP60240040A priority Critical patent/JPH085776B2/en
Publication of JPS6299321A publication Critical patent/JPS6299321A/en
Publication of JPH085776B2 publication Critical patent/JPH085776B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof
    • A61K8/66Enzymes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Dermatology (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Description

【発明の詳細な説明】 (イ)産業上の利用分野 本発明は酵素入り洗顔パウダーの製造方法に関するも
のである。
DETAILED DESCRIPTION OF THE INVENTION (a) Field of Industrial Application The present invention relates to a method for producing an enzyme-containing facial cleansing powder.

(ロ)従来技術 従来、酵素入り洗顔パウダーの酵素としてはパパイン
等の植物起源の蛋白分解酵素などが単独で用いられてき
た。
(B) Conventional technology Conventionally, as the enzyme of the facial cleansing powder containing the enzyme, a proteolytic enzyme of plant origin such as papain has been used alone.

(ハ)発明が解決しようとする問題点 しかし、かかる単独の酵素のみでは蛋白分解作用が弱
く、しかも酵素の目的である毛穴につまった蛋白質等の
汚れ及び角質化した皮膚の洗浄を充分に行い難かった。
(C) Problems to be solved by the invention However, such an enzyme alone has a weak proteolytic action, and the purpose of the enzyme is to sufficiently clean dirt such as proteins clogged in pores and keratinized skin. It was difficult.

又、洗顔パウダー自体が湿気を帯び易く、この湿気に
より酵素の安定化が阻害され、経時的に蛋白分解作用等
が低下するという問題があった。また基材としてタルク
を使用している為、使用時にざらつきを生じ、使用感が
悪かった。
Further, there is a problem that the face-washing powder itself is apt to take moisture, and this moisture hinders the stabilization of the enzyme, and the proteolytic action and the like decrease over time. In addition, since talc is used as the base material, it has a rough texture during use and is uncomfortable to use.

本発明はこのような問題点を解決することができる洗
顔パウダーの製造方法を提供することを目的とする。
An object of the present invention is to provide a method for producing a face-washing powder that can solve such problems.

(ニ)問題点を解決するための手段 本発明は、界面活性剤と、酵素成分としての微生物起
源の酵素と、植物起源の酵素とを洗顔パウダーの基剤中
に混合するにあたり、前記酵素成分中の少なくとも1種
以上を造粒したことを特徴とする酵素入り洗顔パウダー
の製造方法に係るものである。
(D) Means for Solving the Problems In the present invention, when a surfactant, an enzyme of microbial origin as an enzyme component, and an enzyme of plant origin are mixed in the base of a facial cleansing powder, The present invention relates to a method for producing an enzyme-containing facial cleansing powder, which is characterized in that at least one of the above is granulated.

なお、ここで微生物起源の酵素とは、枯草菌、麹菌、
放線菌などより得られる蛋白分解作用等を有する酵素を
いう。
The enzymes of microbial origin are Bacillus subtilis, Aspergillus,
An enzyme having a proteolytic action and the like obtained from actinomycetes and the like.

また、植物起源の酵素とは、パパイン、ブロメライ
ン、フィシン、または、大豆、麦芽等より得られる蛋白
分解作用、脂肪分解作用、澱粉分解作用等を有する酵素
をいう。
The enzyme of plant origin refers to an enzyme having a proteolytic action, a lipolytic action, a starch decomposing action, etc. obtained from papain, bromelain, ficin, soybean, malt and the like.

本発明においては、前記各々の酵素の少なくとも1種
以上を造粒し、洗顔パウダーの基剤中における異なる種
類の酵素同士の反応等による著しい酵素活性の低下を防
止する。
In the present invention, at least one kind of each of the above-mentioned enzymes is granulated to prevent a significant decrease in enzyme activity due to a reaction between different kinds of enzymes in the base of the face-washing powder.

前記酵素の造粒化方法としては、各種形態が考えら
れ、押出し造粒、転動式造粒、ブリケッティング等があ
るが、酵素の造粒という観点からは、造粒工程による活
性の低下防止及び配合安定等を考慮して、押出し式によ
る造粒化方法が望ましい。
As the method for granulating the enzyme, various forms are conceivable, and there are extrusion granulation, tumbling granulation, briquetting, and the like, but from the viewpoint of granulation of the enzyme, the activity decrease due to the granulation step. An extrusion-type granulation method is desirable in consideration of prevention and compounding stability.

前記押出し造粒における顆粒の大量生産は、粉体→混
合→加水捍和→造粒→乾燥→篩別の工程で行なう湿式造
粒法により行なうことができる。
Mass production of granules in the extrusion granulation can be carried out by a wet granulation method which is carried out in the steps of powder → mixing → hydrogenation → granulation → drying → sieving.

また、かかる微生物及び植物起源の酵素はともに抗炎
症作用も有する。
In addition, both such microbial and plant-derived enzymes also have anti-inflammatory effects.

さらに、本発明における洗顔パウダーの基剤自体は、
従来から洗顔パウダーの基剤として周知のものであり、
コーンスターチ、タルク、ラウリル硫酸ナトリウム、N
−ラウロイル−L−グルタミン酸ナトリウム、アラント
イン、ヨクイニン油、香料などの成分を適宜組み合わせ
て用いるものである。
Furthermore, the base itself of the face-washing powder in the present invention is
It is well known as the base of facial cleansing powder,
Corn starch, talc, sodium lauryl sulfate, N
-A component such as sodium lauroyl-L-glutamate, allantoin, yochinin oil, and a fragrance is used in an appropriate combination.

更に、ポリアクリル酸ナトリウムの配合、ビタミン
C、ビタミンE等のビタミン類の配合、或いはコウボ
ク、センキュウ、トウヒ、シャクヤク等の生薬末やオオ
バクエキス等の生薬エキス及び種々植物抽出液を配合す
ることもできる。
Further, it is possible to mix sodium polyacrylate, mix vitamins such as vitamin C and vitamin E, or mix crude powders such as pearl syrup, senkyu, spruce, peony and crude drug extracts such as psyllium extract and various plant extracts. .

(ホ)作用及び効果 微生物起源の酵素と植物起源の酵素は、それぞれpH及
び温度に関する活性率において、最高値を示す帯域を相
違しているため、これらの協働によって、かかる最高値
を示す帯域を広くでき、水質の相違や使用温度の相違に
かかわらず、酵素による高い清浄化作用を維持すること
ができる。
(E) Action and effect Since the enzyme of microbial origin and the enzyme of plant origin are different in the bands showing the highest values in the activity rates with respect to pH and temperature, respectively, the band showing the highest value is obtained by their cooperation. Therefore, it is possible to maintain a high cleaning action by the enzyme regardless of the difference in water quality and the difference in use temperature.

また、前記微生物起源の酵素及び植物起源の酵素の少
なくとも1種以上の酵素を造粒化しているので、各々異
なる起源の酵素同士の接触反応による酵素活性の低下を
防止することができ、前記作用効果を長期間維持するこ
とができる。
In addition, since at least one or more kinds of enzymes of microbial origin and plant origin are granulated, it is possible to prevent a decrease in enzyme activity due to a contact reaction between enzymes of different origins. The effect can be maintained for a long time.

さらに、ポリアクリル酸ナトリウムの配合により使用
時に滑らかな泡立ちを実現してタルク等によるざらつき
を緩和し、使用感を良好とし得る。
Furthermore, by blending sodium polyacrylate, smooth foaming can be realized at the time of use, and the roughness due to talc or the like can be mitigated to improve the feeling of use.

(ヘ)実施例 以下、本発明に係わる酵素配合洗顔パウダーの製造方
法を比較例及び実施例に基づき詳説する。
(F) Example Hereinafter, a method for producing the enzyme-containing facial cleansing powder according to the present invention will be described in detail based on Comparative Examples and Examples.

〔第1比較例〕 まず、微生物起源の酵素であるASPプロテアーゼ(5
万単位/g)と、植物起源の酵素であるパパイン(3万単
位/g)を、基剤であるタルク、コーンスターチと、ラウ
リル硫酸ナトリウム、アラントイン、ヨクイニン油等を
撹拌混合し、同混合物に香料を加え、比較品1とする。
[First Comparative Example] First, ASP protease (5
10,000 units / g) and the plant-derived enzyme papain (30,000 units / g) are mixed with the bases such as talc, corn starch, sodium lauryl sulfate, allantoin, and yochinin oil with stirring, and the mixture is used as a fragrance. To make Comparative Product 1.

〔第1実施例〕 本実施例に係わる洗顔パウダーは、酵素の安定化を図
るため、微生物起源の酵素及び植物起源の酵素の少なく
ともいずれかを造粒化したものである。
[First Example] The face-washing powder according to this example is formed by granulating at least one of an enzyme of microbial origin and an enzyme of plant origin in order to stabilize the enzyme.

上記第1表において、比較品1は、微生物起源の酵素
及び植物起源の酵素がともに造粒化されていない場合で
あり、発明品1は植物起源の酵素のみ造粒化した場合で
あり、発明品2は微生物起源の酵素のみが造粒化されて
いる場合であり、発明品3は植物起源及び微生物起源の
酵素がいずれも造粒化されている場合である。
In Table 1 above, Comparative product 1 is a case where both the enzyme of microbial origin and the enzyme of plant origin are not granulated, and the invention product 1 is a case where only the enzyme of plant origin is granulated. The product 2 is a case where only the enzyme of microbial origin is granulated, and the invention product 3 is a case where both the enzyme of plant origin and the enzyme of microbial origin are granulated.

かかる洗顔パウダー(発明品1〜3及び比較品1)
も、第1実施例と同様な工程で製造するものである。
Such face-washing powder (Invention products 1 to 3 and Comparative product 1)
Also, it is manufactured by the same process as in the first embodiment.

また、上記発明品1〜3及び比較品1内に含有する酵
素の残存活性率を、恒温室ではない室内における室温
(20℃〜27℃)と保存温度40℃とした場合について調
べ、その結果を第1図及び第2図のグラフに示す。
In addition, the residual activity ratios of the enzymes contained in the invention products 1 to 3 and the comparative product 1 were examined when the room temperature (20 ° C to 27 ° C) and the storage temperature 40 ° C were used in a room that was not a thermostatic chamber, and the results were obtained. Is shown in the graphs of FIG. 1 and FIG.

第1図から明らかなように、室温保存では、100日経
過した時点で、植物起源の酵素及び微生物起源の酵素の
いずれも造粒化していない洗顔パウダー(比較品1)の
残存活性率が22%となっているのに対して、いずれかの
酵素を造粒化したもの(発明品1及び2)は、72%及び
42%の残存活性率を示しており、さらに両方の酵素とも
造粒化したもの(発明品3)は、95%の残存活性率を示
している。
As is clear from FIG. 1, after 100 days of storage at room temperature, the residual activity ratio of the facial cleansing powder (Comparative Product 1) in which neither the plant-derived enzyme nor the microbial-derived enzyme was granulated was 22. %, Whereas those granulated with either enzyme (invention products 1 and 2) had 72% and
The residual activity rate of 42% is shown, and the granulated product of both enzymes (Invention Product 3) shows a residual activity rate of 95%.

また、第2図から明らかなように、40℃保存では、植
物起源の酵素及び微生物起源の酵素のいずれも造粒化し
ていない洗顔パウダー(比較品1)は、70日経過した時
点で、残存活性率が零になっているのに対して、いずれ
かの酵素を造粒化した洗顔パウダー(発明品1,2)は、
それぞれ100日経過した時点で、残存活性率を34%と17
%としており、さらに両方の酵素とも造粒化した洗顔パ
ウダー(発明品3)は、100日経過した時点で、66%の
残存活性率を示している。このように、本発明品は、少
なくともいずれかの酵素を造粒化させることによって、
室温及び40℃のいずれにおいても、酵素の高い活性を保
持することができる。
Further, as is clear from FIG. 2, the facial cleansing powder (Comparative Product 1) in which neither the plant-derived enzyme nor the microbial-derived enzyme had been granulated after storage at 40 ° C. remained after 70 days. Whereas the activity rate is zero, the facial cleansing powder (invention products 1 and 2) granulated with one of the enzymes
After 100 days, the residual activity rate was 34% and 17%, respectively.
%, And the facial cleansing powder (invention product 3) in which both enzymes were granulated showed a residual activity rate of 66% after 100 days. Thus, the product of the present invention, by granulating at least one of the enzyme,
The high activity of the enzyme can be retained at both room temperature and 40 ° C.

〔第2実施例及び第2比較例〕 第1実施例と同様な造粒化による酵素の安定化試験
を、植物起源の酵素としてブロメライン(3万単位/g)
を、微生物起源の酵素として放線菌プロテアーゼ(5万
単位/g)を混合した洗顔パウダー(発明品4〜6及び比
較品2)について行った。
[Second Example and Second Comparative Example] A stabilization test of an enzyme by granulation similar to that of the first example was carried out by using bromelain (30,000 units / g) as an enzyme of plant origin.
Was performed on the face-washing powder (Invention Products 4 to 6 and Comparative Product 2) in which actinomycete protease (50,000 units / g) was mixed as an enzyme of microbial origin.

かかる洗顔パウダーの成分構成を第2表に示すととも
に、第3図及び第4図に試験結果を示す。なお、第2表
中の比較品2は、いずれの酵素も造粒していない比較品
である。
The composition of components of such face-washing powder is shown in Table 2, and the test results are shown in FIGS. 3 and 4. Comparative product 2 in Table 2 is a comparative product in which neither enzyme was granulated.

第3図及び第4図から明らかなように、本実施例も、
植物起源及び微生物起源の酵素の少なくともいずれかの
酵素を造粒化させることによって、室温及び40℃のいず
れにおいても、酵素の高い活性を保持することができる
ことを示している。
As is apparent from FIGS. 3 and 4, this embodiment also
It is shown that the high activity of the enzyme can be retained at both room temperature and 40 ° C. by granulating the enzyme of plant origin and / or microbial origin.

〔第3実施例及び第3比較例〕 また、発明品1〜3及び比較品1については、さらに
含有する酵素量を測定した。
[Third Example and Third Comparative Example] Further, regarding the invention products 1 to 3 and the comparative product 1, the amount of the enzyme further contained was measured.

なお、測定法は、チロジン−フオリン法を用い、1分
間に1μgのチロジン相当量フオリン呈色を1プロテア
ーゼ単位とした。
The tyrosin-fluorin method was used as the measuring method, and 1 μg of thyrozine equivalent amount of phosphorin per minute was defined as 1 protease unit.

その結果を第3表に示す。 The results are shown in Table 3.

第3表から明らかなように、植物起源の酵素及び微生
物起源の酵素のいずれも造粒化していない比較品1につ
いては、合計力価のみが測定できたが、酵素成分が他の
成分と同一剤型であるため、活性測定の前処理ができ
ず、どのような酵素がどの位の活性量含有されているか
については測定できなかった。即ち、比較品1について
は、分離定量が不可能であった。
As is clear from Table 3, only the total titer of the comparative product 1 in which neither the plant-derived enzyme nor the microbial-derived enzyme was granulated, but the enzyme component was the same as the other components. Since it is a dosage form, pretreatment for activity measurement was not possible, and it was not possible to measure what kind of enzyme and what amount of activity was contained. That is, it was impossible to separate and quantify the comparative product 1.

これに対して、発明品1〜3については、それぞれ植
物起源の酵素及び微生物起源の酵素の少なくとも一方を
造粒化したので、これら酵素をどれだけ含有するかの分
離定量を正確に行うことができる。
On the other hand, with regard to Inventions 1 to 3, since at least one of the enzyme of plant origin and the enzyme of microbial origin was granulated, respectively, it is possible to accurately separate and quantify how much these enzymes are contained. it can.

これによって、複数の酵素が含有されていること、及
びそれらの活性量が幾らであるか明示することができ、
使用者に安心感を与えることができる。〔第4実施例及
び第4比較例〕 第3実施例における酵素量の測定を、第2実施例にお
ける比較品2及び発明品4〜6についても行い、その結
果を第4表に示す。
This makes it possible to demonstrate that multiple enzymes are contained and how much their activity is,
It is possible to give the user a sense of security. [Fourth Example and Fourth Comparative Example] The amount of enzyme in the third example was also measured for Comparative Product 2 and Invention Products 4 to 6 in the second Example, and the results are shown in Table 4.

本実施例も、本発明にかかる洗顔パウダーには、複数
の酵素が含有されていること、及びそれらの活性量がい
くらであるかを明示することができ、使用者に安心感を
与えることができる。
Also in this example, the face-washing powder according to the present invention can clearly show that a plurality of enzymes are contained and how much their active amount is, and give the user a sense of security. it can.

【図面の簡単な説明】[Brief description of drawings]

第1図及び第2図は、第1実施例及び第1比較例の室温
及び40℃における洗顔パウダー中の酵素の残存活性率を
示すグラフ、第3図及び第4図は、第2実施例及び第2
比較例の室温及び40℃における洗顔パウダー中の酵素の
残存活性率を示すグラフである。
FIG. 1 and FIG. 2 are graphs showing the residual activity rate of the enzyme in the face-washing powder at room temperature and 40 ° C. of the first example and the first comparative example, and FIGS. 3 and 4 are the second example. And the second
It is a graph which shows the residual activity rate of the enzyme in the face-washing powder at room temperature and 40 ° C of Comparative Example.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】界面活性剤と、酵素成分としての微生物起
源の酵素と、植物起源の酵素とを洗顔パウダーの基剤中
に混合するにあたり、前記酵素成分中の少なくとも1種
以上を造粒したことを特徴とする酵素入り洗顔パウダー
の製造方法。
1. When a surfactant, an enzyme of microbial origin as an enzyme component, and an enzyme of plant origin are mixed in a base of a facial cleansing powder, at least one or more of the enzyme components are granulated. A method for producing a facial cleansing powder containing an enzyme, which comprises:
JP60240040A 1985-10-25 1985-10-25 Method for producing enzyme-containing facial cleansing powder Expired - Fee Related JPH085776B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60240040A JPH085776B2 (en) 1985-10-25 1985-10-25 Method for producing enzyme-containing facial cleansing powder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60240040A JPH085776B2 (en) 1985-10-25 1985-10-25 Method for producing enzyme-containing facial cleansing powder

Publications (2)

Publication Number Publication Date
JPS6299321A JPS6299321A (en) 1987-05-08
JPH085776B2 true JPH085776B2 (en) 1996-01-24

Family

ID=17053575

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60240040A Expired - Fee Related JPH085776B2 (en) 1985-10-25 1985-10-25 Method for producing enzyme-containing facial cleansing powder

Country Status (1)

Country Link
JP (1) JPH085776B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003027094A (en) * 2001-07-12 2003-01-29 Kanebo Ltd Cleaning sheet and method of using the same
JP2009091299A (en) * 2007-10-10 2009-04-30 Asuka Corporation:Kk Face washing powder composition
JP2017165664A (en) * 2016-03-15 2017-09-21 株式会社ツツミプランニング Cleaning agent and method for producing the same

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50111107A (en) * 1974-02-14 1975-09-01
JPS60109518A (en) * 1983-11-16 1985-06-15 Tadao Shiraishi Production of bath agent containing enzyme
JPS60120810A (en) * 1983-12-01 1985-06-28 Tadao Shiraishi Production of face washing powder containing enzyme

Also Published As

Publication number Publication date
JPS6299321A (en) 1987-05-08

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