JP2022100464A - Agent for increasing collagen - Google Patents
Agent for increasing collagen Download PDFInfo
- Publication number
- JP2022100464A JP2022100464A JP2020214443A JP2020214443A JP2022100464A JP 2022100464 A JP2022100464 A JP 2022100464A JP 2020214443 A JP2020214443 A JP 2020214443A JP 2020214443 A JP2020214443 A JP 2020214443A JP 2022100464 A JP2022100464 A JP 2022100464A
- Authority
- JP
- Japan
- Prior art keywords
- collagen
- extract
- orengedokuto
- increasing agent
- amount
- 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
Links
- 102000008186 Collagen Human genes 0.000 title claims abstract description 43
- 108010035532 Collagen Proteins 0.000 title claims abstract description 43
- 229920001436 collagen Polymers 0.000 title claims abstract description 43
- 230000001965 increasing effect Effects 0.000 title claims abstract description 26
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 36
- 239000000284 extract Substances 0.000 claims description 55
- 239000009289 huang-lien-chieh-tu-tang Substances 0.000 claims description 37
- 210000004207 dermis Anatomy 0.000 claims description 12
- 210000003491 skin Anatomy 0.000 claims description 4
- 230000000694 effects Effects 0.000 abstract description 9
- 239000004480 active ingredient Substances 0.000 abstract description 5
- 239000000463 material Substances 0.000 abstract description 5
- 239000009441 oren gedoku to Substances 0.000 abstract 1
- 239000000843 powder Substances 0.000 description 12
- 229940079593 drug Drugs 0.000 description 10
- 239000003814 drug Substances 0.000 description 10
- 241000037740 Coptis chinensis Species 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 239000000654 additive Substances 0.000 description 7
- 240000004534 Scutellaria baicalensis Species 0.000 description 6
- 235000017089 Scutellaria baicalensis Nutrition 0.000 description 6
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- SHGAZHPCJJPHSC-YCNIQYBTSA-N all-trans-retinoic acid Chemical compound OC(=O)\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C SHGAZHPCJJPHSC-YCNIQYBTSA-N 0.000 description 4
- 210000004027 cell Anatomy 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 229960001727 tretinoin Drugs 0.000 description 4
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 3
- 241001336887 Lilium rubellum Species 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 235000012041 food component Nutrition 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000000144 pharmacologic effect Effects 0.000 description 3
- 229930002330 retinoic acid Natural products 0.000 description 3
- 229960003471 retinol Drugs 0.000 description 3
- 235000020944 retinol Nutrition 0.000 description 3
- 239000011607 retinol Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000003463 adsorbent Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000000739 antihistaminic agent Substances 0.000 description 2
- 229940125715 antihistaminic agent Drugs 0.000 description 2
- -1 brighteners Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 235000012054 meals Nutrition 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 210000000056 organ Anatomy 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 210000001519 tissue Anatomy 0.000 description 2
- 239000005526 vasoconstrictor agent Substances 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- 238000002965 ELISA Methods 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102000010834 Extracellular Matrix Proteins Human genes 0.000 description 1
- 108010037362 Extracellular Matrix Proteins Proteins 0.000 description 1
- 241000191998 Pediococcus acidilactici Species 0.000 description 1
- 206010036790 Productive cough Diseases 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 238000000692 Student's t-test Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 230000000954 anitussive effect Effects 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000003474 anti-emetic effect Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000002921 anti-spasmodic effect Effects 0.000 description 1
- 239000002111 antiemetic agent Substances 0.000 description 1
- 229940125683 antiemetic agent Drugs 0.000 description 1
- 229940030600 antihypertensive agent Drugs 0.000 description 1
- 239000002220 antihypertensive agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 229940124575 antispasmodic agent Drugs 0.000 description 1
- 239000003434 antitussive agent Substances 0.000 description 1
- 229940124584 antitussives Drugs 0.000 description 1
- 239000003212 astringent agent Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical class CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 230000003177 cardiotonic effect Effects 0.000 description 1
- 210000000845 cartilage Anatomy 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 230000037319 collagen production Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000012228 culture supernatant Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229940124568 digestive agent Drugs 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000002934 diuretic Substances 0.000 description 1
- 229940030606 diuretics Drugs 0.000 description 1
- 239000013583 drug formulation Substances 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 210000002744 extracellular matrix Anatomy 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000001605 fetal effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000004503 fine granule Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 239000007902 hard capsule Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 239000003589 local anesthetic agent Substances 0.000 description 1
- 229960005015 local anesthetics Drugs 0.000 description 1
- 210000003141 lower extremity Anatomy 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000010330 ougon Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 230000004799 sedative–hypnotic effect Effects 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 230000009759 skin aging Effects 0.000 description 1
- 210000001626 skin fibroblast Anatomy 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007901 soft capsule Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 208000024794 sputum Diseases 0.000 description 1
- 210000003802 sputum Anatomy 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 210000000434 stratum corneum Anatomy 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 238000012353 t test Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000017423 tissue regeneration Effects 0.000 description 1
- 210000001364 upper extremity Anatomy 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 230000029663 wound healing Effects 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Images
Landscapes
- Medicines Containing Plant Substances (AREA)
Abstract
Description
本発明は、コラーゲン増加剤に関する。 The present invention relates to a collagen increasing agent.
コラーゲンは細胞外マトリックスの一種であり、組織及び臓器形態の保持に必須であるだけでなく、創傷治癒及び組織の修復過程等の生理的条件下においても重要な役割を果たしている。中でも、皮膚におけるコラーゲンは老化及び光刺激等によって減少し、皮膚老化の減少であるしわ及びたるみ等を引き起こす一因となる。 Collagen is a type of extracellular matrix and is not only essential for the maintenance of tissue and organ morphology, but also plays an important role in physiological conditions such as wound healing and tissue repair processes. Among them, collagen in the skin is reduced by aging and light stimulation, which is one of the causes of wrinkles and sagging, which is a decrease in skin aging.
皮膚に弾力を与える働きをもつコラーゲンの生成を促進するため配合される成分としての代表例がレチノイン酸及びレチノールである。レチノイン酸はしわ改善医薬品の有効成分として用いられているが、刺激が高いため医師の処方せんが必要である。レチノールによる生理活性の強さは、レチノイン酸の約100分の1であり、安全性が高いことから化粧品に配合されて用いられている。 Typical examples of ingredients to be blended to promote the production of collagen having a function of giving elasticity to the skin are retinoic acid and retinol. Tretinoin acid is used as an active ingredient in wrinkle-relieving medicines, but it is highly irritating and requires a doctor's prescription. The strength of the physiological activity of retinol is about 1/100 of that of retinoic acid, and since it is highly safe, it is used in cosmetics.
近年では、コラーゲンを増加させる作用を持つ他の素材の研究が行われている。例えば、特許文献1には、ペディオコッカス・アシディラクティシ(Pediococcus acidilactici)の菌体又はその処理物を含有するコラーゲン産生促進用組成物が開示されており、特許文献2には、オトメユリ(Lilium rubellum)水抽出物を有効成分とすることを特徴とするコラーゲン産生促進剤が開示されている。 In recent years, research has been conducted on other materials that have the effect of increasing collagen. For example, Patent Document 1 discloses a collagen production-promoting composition containing a cell of Pediococcus acidilactici or a processed product thereof, and Patent Document 2 discloses Lilium rubellum (Lilium rubellum). Lilium rubellum) A collagen production promoter characterized by containing a water extract as an active ingredient has been disclosed.
上述の通り、レチノイン酸には刺激の問題があり、レチノールは効果がさほど高くないという問題がある。また、特許文献1及び2に記載される素材は、細胞レベルで効果が確認されたに過ぎず、実際に生体に適用した場合にどの程度の効果が奏されるかについては示されていない。 As mentioned above, retinoic acid has a problem of irritation, and retinol has a problem that the effect is not so high. Further, the materials described in Patent Documents 1 and 2 have only been confirmed to have an effect at the cellular level, and do not show how much the effect is exhibited when actually applied to a living body.
そこで、本発明は、生体に適用した場合でもコラーゲンの増加効果が認められる新たな素材を提供することを目的とする。 Therefore, an object of the present invention is to provide a new material which has an effect of increasing collagen even when applied to a living body.
本発明者は、鋭意検討した結果、黄連解毒湯エキスが、生体に適用した場合でもコラーゲンの増加作用を示すことを見出した。本発明は、かかる知見に基づいて、更に検討を重ねることにより完成したものである。 As a result of diligent studies, the present inventor has found that orengedokuto extract exhibits an increasing effect on collagen even when applied to a living body. The present invention has been completed by further studies based on such findings.
即ち、本発明は、下記に掲げる態様の発明を提供する。
項1. 黄連解毒湯エキスを含む、コラーゲン増加剤。
項2. 皮膚真皮層におけるコラーゲン量を増加させるために用いられる、項1に記載のコラーゲン増加剤。
項3. 目尻のコラーゲン量を増加させるために用いられる、項1又は2に記載のコラーゲン増加剤。
That is, the present invention provides the inventions of the following aspects.
Item 1. Collagen increasing agent containing orengedokuto extract.
Item 2. Item 2. The collagen increasing agent according to Item 1, which is used to increase the amount of collagen in the dermis layer of the skin.
Item 3. Item 2. The collagen increasing agent according to Item 1 or 2, which is used to increase the amount of collagen in the outer corner of the eye.
本発明によれば、生体に適用した場合でもコラーゲンの増加効果が認められる新たな素材が提供される。 According to the present invention, there is provided a new material which has an effect of increasing collagen even when applied to a living body.
本発明のコラーゲン増加剤は、黄連解毒湯エキスを含むことを特徴とする。以下、本発明のコラーゲン増加剤について詳述する。 The collagen-increasing agent of the present invention is characterized by containing orengedokuto extract. Hereinafter, the collagen-increasing agent of the present invention will be described in detail.
黄連解毒湯エキス
本発明のコラーゲン増加剤は、有効成分として黄連解毒湯エキスを含む。黄連解毒湯は、「外台秘要方」を原典とする、オウゴン、オウレン、サンシシ、オウバクからなる混合生薬である。
Orengedokuto extract The collagen-increasing agent of the present invention contains orengedokuto extract as an active ingredient. Orengedokuto is a mixed crude drug consisting of Scutellaria baicalensis, Coptis chinensis, Scutellaria baicalensis, and Scutellaria baicalensis, which is based on "Scutellaria baicalensis".
本発明において、黄連解毒湯を構成する生薬の混合比については特に制限されないが、通常、オウゴン1.5~4重量部、好ましくは2~3重量部;オウレン0.5~3重量部、好ましくは0.75~2重量部;サンシシ0.5~4重量部、好ましくは1~3重量部;オウバク0.5~4重量部、好ましくは0.75~3重量部が挙げられる。 In the present invention, the mixing ratio of the crude drugs constituting Orengedokuto is not particularly limited, but is usually 1.5 to 4 parts by weight, preferably 2 to 3 parts by weight of Ougon; 0.5 to 3 parts by weight of Ouren. It is preferably 0.75 to 2 parts by weight; 0.5 to 4 parts by weight of Sanshishi, preferably 1 to 3 parts by weight; 0.5 to 4 parts by weight of Oubaku, preferably 0.75 to 3 parts by weight.
本発明で使用される黄連解毒湯エキスの製造に供される生薬調合物の好適な例としては、オウゴン3重量部、サンシシ2重量部、オウレン1.5重量部、オウバク1.5重量部が挙げられる。 Suitable examples of the crude drug formulation used for producing the orengedokuto extract used in the present invention are 3 parts by weight of Scutellaria baicalensis, 2 parts by weight of Coptis chinensis, 1.5 parts by weight of Coptis chinensis, and 1.5 parts by weight of Scutellaria baicalensis. Can be mentioned.
黄連解毒湯のエキスの形態としては、流エキス、軟エキス等の液状のエキス、又は固形状の乾燥エキス末のいずれであってもよい。 The form of the extract of Orengedokuto may be any of a liquid extract such as a flowing extract and a soft extract, or a solid dry extract powder.
黄連解毒湯の液状のエキスは、黄連解毒湯に従った混合生薬を抽出処理し、得られた抽出液を必要に応じて濃縮することにより得ることができる。抽出処理に使用される抽出溶媒としては、特に限定されず、水又は含水エタノール、好ましくは水が挙げられる。また、黄連解毒湯の乾燥エキス末は、液状のエキスを乾燥処理することにより得ることができる。乾燥処理の方法としては特に限定されず、例えば、スプレードライ法や、エキスの濃度を高めた軟エキスに適当な吸着剤(例えば無水ケイ酸、デンプン等)を加えて吸着末とする方法等が挙げられる。 The liquid extract of Orengedokuto can be obtained by extracting and treating a mixed crude drug according to Orengedokuto and concentrating the obtained extract as necessary. The extraction solvent used in the extraction treatment is not particularly limited, and examples thereof include water or hydrous ethanol, preferably water. Further, the dried extract powder of Orengedokuto can be obtained by drying a liquid extract. The method of the drying treatment is not particularly limited, and for example, a spray-drying method, a method of adding an appropriate adsorbent (for example, anhydrous silicic acid, starch, etc.) to a soft extract having an increased concentration of the extract to obtain an adsorbed powder, and the like are used. Can be mentioned.
本発明において、黄連解毒湯エキスとしては、前述の方法で調製したエキスを使用してもよいし、市販されるものを使用してもよい。例えば、黄連解毒湯の乾燥エキス末としては、黄連解毒湯乾燥エキス-AT(日本粉末薬品株式会社製)、黄連解毒湯乾燥エキス-F(アルプス薬品株式会社製)等が商品として知られており、商業的に入手することもできる。 In the present invention, as the orengedokuto extract, the extract prepared by the above-mentioned method may be used, or a commercially available extract may be used. For example, as the dried extract powder of orengedokuto, orengedokuto dried extract-AT (manufactured by Nippon Powder Chemicals Co., Ltd.), orengedokuto dried extract-F (manufactured by Alps Pharmaceutical Co., Ltd.), etc. are known as products. It is available and can be obtained commercially.
本発明のコラーゲン増加剤において、黄連解毒湯エキスの含有量としては、本発明の効果を奏する限り、特に限定されないが、黄連解毒湯エキスの乾燥エキス末量換算で、通常10~100重量%、好ましくは20~90重量%、より好ましくは40~80重量%、更に好ましくは60~70重量%が挙げられる。なお、本発明において、黄連解毒湯の乾燥エキス末量換算とは、黄連解毒湯の乾燥エキス末を使用する場合にはそれ自体の量であり、黄連解毒湯の液状のエキスを使用する場合には、溶媒を除去した残量に換算した量である。また、黄連解毒湯の乾燥エキス末が、製造時に添加される吸着剤等の添加剤を含む場合は、当該添加剤を除いた量である。 In the collagen-increasing agent of the present invention, the content of the orengedokuto extract is not particularly limited as long as the effect of the present invention is exhibited, but it is usually 10 to 100% by weight in terms of the dry extract powder amount of the orengedokuto extract. %, Preferably 20 to 90% by weight, more preferably 40 to 80% by weight, still more preferably 60 to 70% by weight. In the present invention, the dry extract powder conversion of orengedokuto is the amount of the dried extract powder of orengedokuto itself, and the liquid extract of orengedokuto is used. If so, it is the amount converted into the remaining amount after removing the solvent. When the dried extract powder of Orengedokuto contains an additive such as an adsorbent added at the time of production, the amount is the amount excluding the additive.
その他の成分
本発明のコラーゲン増加剤は、黄連解毒湯エキス単独からなるものであってもよく、製剤形態に応じた添加剤や基剤を含んでいてもよい。このような添加剤及び基剤としては、薬学的に許容されることを限度として特に制限されないが、例えば、賦形剤、結合剤、崩壊剤、滑沢剤、等張化剤、可塑剤、分散剤、乳化剤、溶解補助剤、湿潤化剤、安定化剤、懸濁化剤、粘着剤、コーティング剤、光沢化剤、水、油脂類、ロウ類、炭化水素類、脂肪酸類、高級アルコール類、エステル類、水溶性高分子、界面活性剤、金属石鹸、低級アルコール類、多価アルコール、pH調整剤、緩衝剤、酸化防止剤、紫外線防止剤、防腐剤、矯味剤、香料、粉体、増粘剤、色素、キレート剤等が挙げられる。これらの添加剤は、1種単独で使用してもよく、また2種以上を組み合わせて使用してもよい。また、これらの添加剤及び基剤の含有量については、使用する添加剤及び基剤の種類、コラーゲン増加剤の製剤形態等に応じて適宜設定される。
Other Ingredients The collagen-increasing agent of the present invention may consist of orengedokuto extract alone, or may contain additives or bases according to the pharmaceutical form. Such additives and bases are not particularly limited as long as they are pharmaceutically acceptable, but for example, excipients, binders, disintegrants, lubricants, tonicity agents, plasticizers, etc. Dispersants, emulsifiers, solubilizers, wetting agents, stabilizers, suspending agents, pressure-sensitive agents, coating agents, brighteners, water, fats and oils, waxes, hydrocarbons, fatty acids, higher alcohols , Esters, water-soluble polymers, surfactants, metal soaps, lower alcohols, polyhydric alcohols, pH adjusters, buffers, antioxidants, UV inhibitors, preservatives, emulsifiers, fragrances, powders, Examples include thickeners, pigments, chelating agents and the like. These additives may be used alone or in combination of two or more. The contents of these additives and bases are appropriately set according to the types of additives and bases to be used, the form of the collagen-increasing agent, and the like.
また、本発明のコラーゲン増加剤は、黄連解毒湯エキスの他に、必要に応じて、他の栄養成分や薬理成分を含有していてもよい。このような栄養成分や薬理成分としては、薬学的に許容されることを限度として特に制限されないが、例えば、制酸剤、健胃剤、消化剤、整腸剤、鎮痙剤、粘膜修復剤、抗炎症剤、収れん剤、鎮吐剤、鎮咳剤、去痰剤、消炎酵素剤、鎮静催眠剤、抗ヒスタミン剤、カフェイン類、強心利尿剤、抗菌剤、血管収縮剤、血管拡張剤、局所麻酔剤、生薬エキス、ビタミン類、メントール類等が挙げられる。これらの栄養成分や薬理成分は、1種単独で使用してもよく、また2種以上を組み合わせて使用してもよい。また、これらの成分の含有量については、使用する成分の種類等に応じて適宜設定される。 In addition to the orengedokuto extract, the collagen-increasing agent of the present invention may contain other nutritional components and pharmacological components, if necessary. Such nutritional components and pharmacological components are not particularly limited as long as they are pharmaceutically acceptable, but for example, antihypertensive agents, stomachic agents, digestive agents, intestinal regulators, antispasmodics, mucosal repair agents, antihistamines, and astringents. Agents, antiemetics, antitussives, sputum, anti-inflammatory enzyme agents, sedative hypnotics, antihistamines, caffeines, cardiotonic diuretics, antibacterial agents, vasoconstrictors, vasoconstrictors, local anesthetics, crude drug extracts, vitamins, menthol Kind and the like. These nutritional components and pharmacological components may be used alone or in combination of two or more. Further, the content of these components is appropriately set according to the type of the component to be used and the like.
製剤形態
本発明のコラーゲン増加剤の製剤形態については、経口投与が可能であることを限度として特に制限されないが、例えば、散剤、細粒剤、顆粒剤、錠剤、トローチ剤、チュアブル剤、カプセル剤(軟カプセル剤、硬カプセル剤)、丸剤等の固形状製剤;ゼリー剤等の半固形状製剤;液剤、懸濁剤、シロップ剤等の液状製剤が挙げられ、好ましくは顆粒剤又は錠剤が挙げられる。
Pharmaceutical form The pharmaceutical form of the collagen-increasing agent of the present invention is not particularly limited as long as it can be orally administered, and is, for example, a powder, a fine granule, a granule, a tablet, a troche, a chewable agent, or a capsule. (Soft capsules, hard capsules), solid formulations such as rounds; semi-solid formulations such as jelly; liquid formulations such as liquids, suspensions and syrups, preferably granules or tablets. Can be mentioned.
製造方法
本発明のコラーゲン増加剤の製造方法は、上記生薬成分を用いて、医薬分野で採用されている通常の製剤化手法に従って製剤化すればよい。
Production method The method for producing the collagen-increasing agent of the present invention may be formulated by using the above-mentioned crude drug components according to a usual formulation method adopted in the pharmaceutical field.
用途
本発明のコラーゲン増加剤は、コラーゲン量を増加することを目的として用いられる。
Use The collagen-increasing agent of the present invention is used for the purpose of increasing the amount of collagen.
コラーゲン量を増加させるべき組織又は臓器としては特に限定されず、皮膚真皮層、歯茎、軟骨等が挙げられ、好ましくは皮膚真皮層が挙げられる。また、本発明のコラーゲン増加剤が皮膚真皮層におけるコラーゲン量を増加させるために用いられる場合、体表における当該皮膚真皮層の場所としては特に限定されず、顔、首、体幹、上肢、下肢のいずれであってもよいが、好ましくは顔が挙げられ、より好ましくは目尻が挙げられる。 The tissue or organ in which the amount of collagen should be increased is not particularly limited, and examples thereof include a skin dermis layer, gums, and cartilage, and a skin dermis layer is preferable. Further, when the collagen increasing agent of the present invention is used to increase the amount of collagen in the skin dermis layer, the location of the skin dermis layer on the body surface is not particularly limited, and the face, neck, trunk, upper limbs, and lower limbs are not particularly limited. However, the face is preferably mentioned, and the outer corners of the eyes are more preferably mentioned.
用量・用法
本発明のコラーゲン増加剤は、経口投与によって使用される。本発明のコラーゲン増加剤の用量については、投与対象者の年齢、体質、症状の程度等に応じて適宜設定されるが、例えば、ヒト1人に対して1日当たり、黄連解毒湯エキス量(乾燥エキス換算量)として500~2000mg、好ましくは800~1800mgとなる量で、1日1~4回、好ましくは2~3回の頻度で服用すればよい。
Dosage and Usage The collagen-increasing agent of the present invention is used by oral administration. The dose of the collagen-increasing agent of the present invention is appropriately set according to the age, constitution, degree of symptoms, etc. of the administration subject, and for example, the amount of orengedokuto extract per human per day ( The dry extract equivalent amount) may be 500 to 2000 mg, preferably 800 to 1800 mg, and may be taken 1 to 4 times a day, preferably 2 to 3 times a day.
一日の中での服用タイミングについては、特に制限されず、食前、食後、又は食間のいずれであってもよいが、好ましくは食前又は食間が挙げられる。また、コラーゲン増加効果をより一層高める観点から、本発明のコラーゲン増加剤は、例えば3日以上、好ましくは5日以上、更に好ましくは10日以上継続して服用することが好ましい。 The timing of administration during the day is not particularly limited and may be pre-meal, post-meal, or inter-meal, but pre-meal or inter-meal is preferable. Further, from the viewpoint of further enhancing the collagen increasing effect, the collagen increasing agent of the present invention is preferably taken continuously for, for example, 3 days or more, preferably 5 days or more, and more preferably 10 days or more.
以下、本発明を実施例により具体的に説明するが、本発明はこれらの実施例に限定されるものではない。 Hereinafter, the present invention will be specifically described with reference to Examples, but the present invention is not limited to these Examples.
[試験例1]
(1)コラーゲン増加剤の調製
原料生薬として、オウゴン3重量部、サンシシ2重量部、オウレン1.5重量部、オウバク1.5重量部を用い、これらを刻んだ後、水10倍重量を用いて約100℃で1時間抽出し、遠心分離して抽出液を得た。抽出液を減圧下で濃縮してスプレードライヤーを用いて乾燥し、黄連解毒湯エキス末を得た。なお、スプレードライヤーによる乾燥は、抽出液を回転数10000rpmのアトマイザーに落下させ、150℃の空気の熱風を供給して行った。その後、造粒して製錠し、コラーゲン増加剤を得た。コラーゲン増加剤の1日当たりの用量は、黄連解毒湯エキス量(乾燥エキス換算量)で1600mgとした。
[Test Example 1]
(1) Preparation of collagen-increasing agent As raw material crude drugs, 3 parts by weight of Ogon, 2 parts by weight of Sanshishi, 1.5 parts by weight of Ouren, and 1.5 parts by weight of Oubaku were used, and after chopping these, 10 times the weight of water was used. The mixture was extracted at about 100 ° C. for 1 hour and centrifuged to obtain an extract. The extract was concentrated under reduced pressure and dried using a spray dryer to obtain orengedokuto extract powder. The drying with a spray dryer was carried out by dropping the extract onto an atomizer having a rotation speed of 10000 rpm and supplying hot air with air at 150 ° C. Then, granulation was performed and tablets were formed to obtain a collagen increasing agent. The daily dose of the collagen-increasing agent was 1600 mg in terms of the amount of orengedokuto extract (dry extract equivalent amount).
(2)実験方法
20代の男女9名に、上記のコラーゲン増加剤を10日間(1日2回)服用させた。服用の前後における左目尻部のコラーゲンスコアを、超音波真皮画像装置(装置名:DermaLab(登録商標)、型番:DermaLab、Cortex Technology社製、測定項目:コラーゲンスコア)を用いて測定した。測定は各々3回行い、その平均値を測定値とした(2回のコラーゲンスコア測定値が±5以内になるようにした。室温は20℃、湿度は65%とし、測定は15分の馴化後に行った。
(2) Experimental method Nine men and women in their twenties were allowed to take the above collagen-increasing agent for 10 days (twice a day). The collagen score of the outer corner of the left eye before and after administration was measured using an ultrasonic dermis imaging device (device name: DermaLab (registered trademark), model number: DermaLab, manufactured by Cortex Technology, measurement item: collagen score). The measurement was performed 3 times each, and the average value was used as the measured value (the two collagen score measurements were set to be within ± 5. The room temperature was 20 ° C., the humidity was 65%, and the measurement was acclimatized for 15 minutes. I went later.
得られた超音波真皮画像の一例(服用前及び服用後)を図1に示す。図1に示すそれぞれの画像において、左側が角質層側、左側が真皮層側を示す。この超音波真皮画像では、真皮コラーゲン線維の密度の高い所は黄色に、低い所は緑で表示される。図1に示される通り、服用後にコラーゲン量が顕著に増加していることが確認できた。 An example of the obtained ultrasonic dermis image (before and after taking) is shown in FIG. In each image shown in FIG. 1, the left side shows the stratum corneum side and the left side shows the dermis layer side. In this ultrasonic dermis image, high density areas of dermal collagen fibers are displayed in yellow and low density areas are displayed in green. As shown in FIG. 1, it was confirmed that the amount of collagen increased remarkably after taking the drug.
また、図2に、コラーゲンスコアの測定結果の平均値±標準誤差を算出し、Microsoft(登録商標)Excel(統計解析ソフトウェア:エクセル統計)にて対応のあるt検定で検定を行った(有意水準は両側検定で5%とした)結果を示す。図2に示すとおり、コラーゲンスコアの有意な(*:p<0.05)増加が確認できた。この結果からも、服用後にコラーゲン量が増加していることが確認できた。 In addition, in FIG. 2, the mean value ± standard error of the measurement result of the collagen score was calculated, and the test was performed by the corresponding t-test using Microsoft (registered trademark) Excel (statistical analysis software: Excel statistics) (significance level). Is 5% in the two-sided test). As shown in FIG. 2, a significant (*: p <0.05) increase in collagen score was confirmed. From this result, it was confirmed that the amount of collagen increased after taking the drug.
(3)オウレンエキス及びオウバクエキスからなる混合物によるコラーゲン増加能との対比
本発明のコラーゲン増加剤はコラーゲン増加効果に優れており、黄連解毒湯エキスが有効成分として作用する。このことは、黄連解毒湯の構成生薬であるオウレン及びオウバクそれぞれのエキスの混合物(オウレンエキス及びオウバクエキスからなる混合物)と黄連解毒湯エキスとがそれぞれ以下の細胞試験に供された場合に、黄連解毒湯エキスのほうで優れたコラーゲン増加効果を奏することで確認することができる。
(3) Comparison with collagen increasing ability by a mixture of Coptis chinensis extract and Coptis chinensis extract The collagen increasing agent of the present invention has an excellent collagen increasing effect, and Orengedokuto extract acts as an active ingredient. This is the case when a mixture of Coptis chinensis and Coptis chinensis extracts (a mixture of Coptis chinensis extract and Coptis chinensis extract) and Orengedokuto extract, which are the constituent crude drugs of Orengedokuto, are subjected to the following cell tests, respectively. , Orengedokuto extract can be confirmed to have a better collagen-increasing effect.
(細胞試験方法)
正常ヒト皮膚線維芽細胞(NHDF)を、24ウェルカルチャープレート中で培養する。より詳細には、1.0×104細胞/ウェルの密度でプレートに播種し、37℃で、5体積%炭酸ガス及び95体積%空気の環境下で72時間培養する。培養液には、Dulbecco’s Modified Eagle Medium(DMEM)に牛胎児血清(FBS)を2質量%の濃度で含有した培地を使用し、黄連解毒湯エキスの濃度と、オウレンエキス及びオウバクエキスからなる混合物(オウレンエキス及びオウバクエキスの混合重量比=1:1)の濃度(つまり、オウレンエキス及びオウバクエキスの総量)とは、それぞれ0.01質量%になるように添加する。培養終了後、培養上清中のコラーゲン量をELISAにて測定する。
(Cell test method)
Normal human skin fibroblasts (NHDF) are cultured in 24-well culture plates. More specifically, the plates are seeded at a density of 1.0 × 10 4 cells / well and cultured at 37 ° C. for 72 hours in an environment of 5% by volume carbon dioxide and 95% by volume air. For the culture medium, a medium containing Dulvecco's Modified Eagle Medium (DMEM) at a concentration of 2% by mass of bovine fetal serum (FBS) was used, and the concentration of Orengedokuto extract and the concentration of Oulen extract and Oubaku extract were used. The concentration (that is, the total amount of the orengedokuto and the orengedokuto extract) of the mixture (mixed weight ratio of the orengedokuto extract and the orengedokuto extract = 1: 1) is added so as to be 0.01% by mass, respectively. After completion of the culture, the amount of collagen in the culture supernatant is measured by ELISA.
Claims (3)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2020214443A JP2022100464A (en) | 2020-12-24 | 2020-12-24 | Agent for increasing collagen |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2020214443A JP2022100464A (en) | 2020-12-24 | 2020-12-24 | Agent for increasing collagen |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2022100464A true JP2022100464A (en) | 2022-07-06 |
Family
ID=82271497
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2020214443A Pending JP2022100464A (en) | 2020-12-24 | 2020-12-24 | Agent for increasing collagen |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2022100464A (en) |
-
2020
- 2020-12-24 JP JP2020214443A patent/JP2022100464A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104666621B (en) | A Chinese medicinal composition with hemostatic, antiinflammatory and antibacterial effects, and toothpaste containing the same | |
JP2009179625A (en) | Composition or preparation for internal use having anti-stress/fatigue-preventive effect and skin texture-ameliorating or wrinkle-ameliorating/preventive effect | |
CN102512344A (en) | Blumea balsamifera extract, preparation method and application thereof in oral care and clean product | |
CN106924378B (en) | Chinese herbal medicine lipstick for preventing and/or treating chronic cheilitis | |
WO2013176351A1 (en) | Composition comprising extract of mixture of undaria pinnatifida sporophylls and ascidian shells for treating atopic dermatitis | |
CN115381848A (en) | Anti-aging composition and preparation method and application thereof | |
CN100473394C (en) | Compound preparation of baikal skullcap root | |
JP2003146895A (en) | Tablet including ephippium | |
CN108686023A (en) | A kind of antipruritic moisturizing essential oil for treating geroderma itch | |
JP2022100464A (en) | Agent for increasing collagen | |
CN109453169A (en) | The purposes of bulleyaconitine A | |
WO2018164221A1 (en) | Composition for inhibiting myofibrosis | |
CN104825835A (en) | Preparation method of dendrobium nobile oral ulcer buccal tablet | |
JP2007031302A (en) | Adiponectin production accelerator and metabolic syndrome preventive | |
KR101273027B1 (en) | Composition for inhibiting sebum secretion and anti-obesity comprising kaempferol | |
CN106176510A (en) | A kind of oral thing for aesthetic health care and corresponding beautifying health composition | |
JP2008037770A (en) | Anti-aging agent | |
JP7385990B2 (en) | Hypersomnia treatment | |
CN111838669B (en) | Nano composition for treating and improving vulnerable viscera, preparation method and application | |
JP2023019817A (en) | Agent for enhancing healing power of skin | |
CN106983776A (en) | Silk gum Chinese patent drug | |
JP2023503844A (en) | Chinese herbal composition for treating psoriasis, method of preparation and use thereof | |
WO2021048961A1 (en) | Agent for suppressing/improving bad skin caused by fatigue and/or stress and screening method for agents for suppressing/improving bad skin caused by fatigue and/or stress | |
JP2021187802A (en) | Agent for improving abnormal blood vessel | |
WO2023041803A1 (en) | Formulations and uses of resveratrol |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20231128 |