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公开(公告)号：KR101421537B1
公开(公告)日：2014-07-23
申请号：KR1020120015379
申请日：2012-02-15
Applicant: 목포대학교산학협력단
Abstract: 본 발명은 다시마(
Laminaria
japonica ) 아임계수 추출물을 유효성분으로 포함하는 화장료 조성물을 제공한다. 구체적으로, 본 발명은 유효성분인 다시마 아임계수 추출물은 1 MPa 내지 5 MPa 및 180℃ 내지 240℃의 아임계 조건에서 추출한 다시마 아임계수 추출물일 수 있다.
또한, 본 발명은 다시마로부터 항주름 활성이 가장 우수할 뿐만 아니라 추출수율도 가장 높은 다시마 아임계수 추출물의 제조방법에 관한 것이다. 상기 제조방법은 다시마를 분쇄하여 다시마 분쇄물을 제조하는 단계; 상기 다시마 분쇄물에 물을 첨가하는 단계; 및 상기 다시마 분쇄물 및 물을 3 MPa 및 180℃ 내지 240℃의 조건에서 반응시켜 다시마 아임계수 추출물을 제조하는 단계를 포함하는 주름 예방 또는 개선능을 가진 다시마 아임계수 추출물 제조방법일 수 있다.
본 발명의 제조방법에 의해 제조된 다시마 아임계수 추출물은 에스터라제 저해 활성 및 콜라겐 합성능 즉, 항주름 활성이 우수할 뿐만 아니라, 식품으로 사용되던 해조류와 가장 안전한 용매인 수용매를 이용하는 것으로 부작용 등에 대한 안전성도 보장되며, 우리나라 서해안지역에서 풍부하게 생산되는 해조류를 이용하여 간단한 방법으로 제조될 수 있어 경제적으로도 유리하고, 지역경제 활성화 및 지역 농어민 소득향상에도 이바지할 수 있으므로, 본 발명의 화장료 조성물은 산업적 측면에서 그 효과가 매우 클 것으로 기대된다.-
公开(公告)号：KR1020140080953A
公开(公告)日：2014-07-01
申请号：KR1020120150179
申请日：2012-12-21
Applicant: 목포대학교산학협력단
IPC: A23L29/256 , A23L17/60
CPC classification number: A23L17/60 , A23L29/256 , A23L29/281 , A23V2002/00 , A23V2300/10 , A23V2300/24
Abstract: The present invention relates to gel products using seaweed fulvescens and sea string and gel products thereby. By one embodiment of the present invention, the gel product using seaweed fulvescens and sea string comprises a step for washing the seaweed fulvescens and sea string; a step for drying the washed seaweed fulvescens and sea string in a dryer; a step for crushing the dried seaweed fulvescens and sea string and sieving the seaweed fulvescens and sea string to manufacture powder; a step for preparing jelly by putting the powder into a heated mixture including sediment, agar, and sugar and heating and stirring the mixture; a step for putting the jelly into a molding frame to mold the jelly; a step for drying the molded jelly at room temperature; and a step for cooling the dried jelly. the step for preparing jelly by putting the powder into a heated mixture including sediment, agar, and sugar and heating and stirring the mixture, honey and salt are additionally added. In the step for preparing jelly by putting the powder into a heated mixture including sediment, agar, and sugar and heating and stirring the mixture, based on 100 parts by weight of total jelly, the input amount of the powder is 0.5-2 parts by weight. In the step for preparing jelly by putting the powder into a heated mixture including sediment, agar, and sugar and heating and stirring the mixture, based on 100 parts by weight of total jelly, the input amount of seaweed fulvescens is 0.5 parts by weight and the input amount of the sea string is 1 parts by weight.
Abstract translation: 本发明涉及使用海藻玻璃菌和海绳和凝胶产品的凝胶产品。 通过本发明的一个实施方案，使用海藻和海绳的凝胶产品包括用于洗涤海藻和海绳的步骤; 在干燥机中干燥洗涤的海藻和海绳的步骤; 破碎海藻和海绳并筛分海藻和海绳以制造粉末的步骤; 通过将粉末放入含有沉淀物，琼脂和糖的加热混合物中并加热和搅拌混合物来制备果冻的步骤; 将果冻放入模制框架以模制果冻的步骤; 在室温下干燥模制果冻的步骤; 以及冷却干果冻的步骤。 通过将粉末放入含有沉淀物，琼脂和糖的加热混合物中并加热搅拌混合物，蜂蜜和盐来制备果冻的步骤。 在通过将粉末放入含有沉淀物，琼脂和糖的加热混合物中并加热搅拌混合物的步骤中，基于100重量份的总果冻，粉末的投入量为0.5-2份 重量。 在通过将粉末放入含有沉淀物，琼脂和糖的加热混合物中并加热和搅拌该混合物的步骤中，基于100重量份的总果冻，海藻黄酮的投入量为0.5重量份， 海绳的输入量为1重量份。
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公开(公告)号：KR101403396B1
公开(公告)日：2014-06-11
申请号：KR1020120015565
申请日：2012-02-15
Applicant: 목포대학교산학협력단
Abstract: 본 발명은 개꼬시래기 아임계수 추출물을 유효성분으로 포함하는 항염 조성물에 관한 것이다. 본 발명의 개꼬시래기 아임계수 추출물은 식용으로 사용되는 식물 및 가장 안전한 추출용매인 수용매를 이용한 추출물로서 부작용이나 안전성에 대한 문제가 없고, 염증과 관련된 NO 분비량 및 세포 생존률을 통하여 확인한 결과, 효과적으로 염증을 저해할 수 있는 것으로 확인되었다. 따라서, 상기 개꼬시래기 아임계수 추출물을 유효성분으로 포함하는 항염 조성물은 염증을 억제하여 염증과 관련된 질병을 치료 또는 예방하기 위한 항염증제 및 특정 제형 등과 관련하여 화장품 제조에 필수적으로 사용되는 성분 또는 외부환경으로 인한 피부의 염증을 효과적으로 억제할 수 있는 특징을 갖는 화장료 조성물 등에 응용될 수 있다.
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公开(公告)号：KR1020090010471A
公开(公告)日：2009-01-30
申请号：KR1020070073588
申请日：2007-07-23
Applicant: 목포대학교산학협력단
Abstract: A method for mass production of zoospores of Ecklonia stolonifera is provided to more stably perform the seed production of Ecklonia stolonifera and control the seed production period of Ecklonia stolonifera more freely by inducing the artificial maturation and apothecium formation of the immature Ecklonia stolonifera mummy. The zoospores of Ecklonia stolonifera is mass produced by culturing the immature Ecklonia stolonifera lobe or the lobe fraction cut therefrom, wherein the immature Ecklonia stolonifera is the biennial or greater; the lobe fraction is prepared by cutting the growing zone or the tip of Ecklonia stolonifera lobe, and is cultured under the conditions of the temperature of 19-21 deg. C, illuminance of 25-35 mumol m-2s-1 and illumination period of 10:14h(L:D); and the lobe or the lobe fraction cut therefrom is cultured for 90-110 days.
Abstract translation: 提供了大量生产Ecklonia stolonifera的游动孢子的方法，以更稳定地进行Ecklonia stolonifera的种子生产，并通过诱导未成熟的Ecklonia stolonifera木乃伊的人工成熟和apohecium形成，更自由地控制Ecklonia stolonifera的种子生产期。 Ecklonia stolonifera的游动孢子是通过培养未成熟的Ecklonia stolonifera叶或从其切割的叶片部分大量产生的，其中未成熟的Ecklonia stolonifera是两年一次或更长时间; 通过切割Ecklonia stolonifera叶的生长区域或尖端来制备叶部分，并在19-21℃的温度条件下培养。 C，照度为25-35 mumol m-2s-1，照度为10：14h（L：D）; 并将从其切下的叶或叶分数培养90-110天。
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公开(公告)号：KR1020090010470A
公开(公告)日：2009-01-30
申请号：KR1020070073586
申请日：2007-07-23
Applicant: 목포대학교산학협력단
Abstract: A cultivation method of Ecklonia stolonifera is provided to simplify the cultivation method by eliminating an outdoor seedling process and to increase the productivity. A cultivation method of Ecklonia stolonifera comprises a seed collection step for obtaining zoospore from the matured Ecklonia stolonifera dummy formed with apothecium; a step for obtaining the young leaf by cultivating zoospore; a step for cultivating young leaf; and a step for transplanting the cultivated young leaf in sea.
Abstract translation: 提供了Ecklonia stolonifera的栽培方法，通过消除户外幼苗过程并提高生产率来简化栽培方法。 Ecklonia stolonifera的栽培方法包括从成熟的Ecklonia stolonifera虚拟物形成的酵母菌获得游动孢子的种子收集步骤; 通过培育动物园获得幼叶的步骤; 培育幼叶的一步; 并在海上移植栽培的幼叶的步骤。
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Patent Agency Ranking
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公开(公告)号：KR101576269B1
公开(公告)日：2015-12-10
申请号：KR1020130150561
申请日：2013-12-05
Applicant: 목포대학교산학협력단
Abstract: 본발명은개꼬시래기아임계수추출물을유효성분으로포함하는비만치료, 개선또는예방용조성물에관한것이다. 특히, 본발명의유효성분인개꼬시래기아임계수추출물은지방전구세포(3T3-L1)의분화를저해하고, 지방세포의증식을억제하며, 지방대사물질의축적을억제할수 있으므로, 비만의치료, 개선및 예방효과가우수할뿐만아니라, 세포독성이없고, 천연물질로부터유래된것이므로부작용도문제되지아니하여비만의치료, 개선또는예방을위해널리사용할수 있다.
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8.发明授权
公开(公告)号：KR101264383B1
公开(公告)日：2013-05-14
申请号：KR1020110062259
申请日：2011-06-27
Applicant: 대한민국(관리부서:국립수산과학원) , 목포대학교산학협력단
Abstract: 본발명은대형갈조류인넓미역의대량생산방법에관한것으로서, 보다구체적으로넓미역으로부터분리된암수유리배우체각각수거하고, 세포수, 온도, 조도및 광주기를조절함으로써생장률이우수한최적의조건을설정하고, 상기조건에서유리배우체의성숙을유도함으로써, 넓미역을생산하는방법에관한것으로서, 이러한방법을통하여넓미역인공채묘기법을개발하고대량양식에이용될수 있다.
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公开(公告)号：KR1020130094043A
公开(公告)日：2013-08-23
申请号：KR1020120015379
申请日：2012-02-15
Applicant: 목포대학교산학협력단
CPC classification number: A61K8/9706 , A61K36/03 , A61K2236/37 , A61Q19/08
Abstract: PURPOSE: Subcritical water extracts of laminaria japonica is provided to improve an esterase inhibition activity, a collagen synthesis capability and an anti-wrinkle activity and prevent side effects by using marine algae and an aqueous solvent, thereby having a marked effect in an industrial aspect. CONSTITUTION: A cosmetic composition for wrinkle protection or wrinkle improvement includes the subcritical water extracts of laminaria japonica which are extracted with the subcritical water of 3 MPa and 180-240°C. The cosmetic composition for wrinkle protection or wrinkle improvement adds water in crushed laminaria japonica and includes the subcritical water extracts of laminaria japonica which are characterized by being extracted under 3 MPa and 180-240°C as an active ingredient. A manufacturing method of the subcritical water extracts of laminaria japonica having a wrinkle protection activity and a wrinkle improvement activity comprises: a step of manufacturing crushed laminaria japonica by pulverizing laminaria japonica; a step of adding water in the crushed laminaria japonica; and a step of manufacturing the subcritical water extract of laminaria japonica by reacting the crushed laminaria japonica with water at a condition of 3 MPa and 180-240°C.
Abstract translation: 目的：提供aria粳亚临界水提取物，以提高酯酶抑制活性，胶原合成能力和抗皱活性，并通过使用海藻和水性溶剂防止副作用，从而在工业方面具有显着的效果。 构成：用于皱纹保护或皱纹改善的化妆品组合物包括用3MPa和180-240℃的亚临界水提取的lamin粳亚临界水提取物。 用于皱纹保护或皱纹改善的化妆品组合物在粉碎的lamin粳中添加水，并且包括以3MPa和180-240℃作为活性成分提取的aria粳亚临界水提取物。 具有皱纹保护作用和皱纹改善活性的aria粳亚临界水提取物的制造方法包括：通过粉碎lamin粳制造粉碎的lamin粳的步骤; 在粉碎的lamin粳中加水的步骤; 并且在3MPa和180-240℃的条件下，通过使粉碎的j粳与水反应来制造aria粳亚临界水提取物的步骤。
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公开(公告)号：KR1020130001479A
公开(公告)日：2013-01-04
申请号：KR1020110062259
申请日：2011-06-27
Applicant: 대한민국(관리부서:국립수산과학원) , 목포대학교산학협력단
Abstract: PURPOSE: A undaria peterseniana mass production method by inducing the regeneration and aging of undaria peterseniana free-living gametophytes is provided by securing the optimal condition for the regeneration and aging of the Undaria peterseniana free-living gametophytes. CONSTITUTION: Zoospores are released from an apothecium site of Undaria peterseniana. The released zoospores are cultured, and form gametophytes. Separate the gametophytes formed into female and male gametophytes. Culture the separated female and male gametophytes until the gametophytes reach the respective diameter of 3-10mm. Cut the cultured female and male gametophytes in the respective size of 50-400 micrometers. Culture the excised female and male gametophytes under the cell count of 3-25 cell/ind., the temperature condition of 5-20deg. C , the illumination of 5-40micromolm-2s-1, and the photoperiod of 10:14(Light:Dark)-14:10(L:D). Cross-fertilize the cultivated female and male gametophytes. Culture the gametophytes in a liquid culture medium of PESI(Provasoli`s enriched seawater media). Culture the female and male gametophytes until the gametophytes reach the diameter size of 5-6mm. Excise the female gametophytes in the size of 50-100 micrometers. Excise the male gametophytes in the size of 60-150 micrometers. Culture the female gametophytes under the cell count of 3-8 cell/ind., the temperature condition of 10-20 deg. C, the illumination of 15-30 micromolm-2s-1, and the photoperiod of 10:14(Light:Dark). Culture the male gametophytes under the cell count of 8-12 cell/ind., the temperature condition of 5-20 deg. C, the illumination of 15-25 micromolm-2s-1, and the photoperiod of 14:10(Light:Dark). [Reference numerals] (AA) Matured thallus of Undaria peterseniana; (BB) Rinsing the matured thallus, cut after washing, with sterilized seawater and ABM solution; (CC) Releasing zoospores at 10°C, 20umolm^-2s^-1, and 10:14h(L:D); (DD) 0.1ml zoospore solution; (EE) Separating the zoospores by dilution; (FF) Female gametophyte; (GG) Male gametophyte; (HH) Mass-producing clone gametophyte; (I1,I2) Cutting and regenerating every 20 days at 15°C, 20umolm^-2s^-1, and 10:14h(L:D); (JJ) Mixing the cut female and male gametophyte at the ratio of 1:1; (KK) Forming gamete for at least 15 days at 15°C, 20umolm^-2s^-1, and 14:10h(L:D); (LL) Forming young sporophyte for 40 days at 15°C, 60umolm^-2s^-1, and 14:10h(L:D)
Abstract translation: 目的：通过诱导无花果自由生存配子体的再生和衰老，通过确保无花果种子自由生存配子体的再生和衰老的最佳条件，提供了一种不育种的大量生产方法。 构成：动物孢子从黑腹果蝇的药膳部位释放出来。 释放的游动孢子被培养，形成配子体。 将形成的配子体分成雌雄配子体。 培养分离的雌雄配子，直到配子体达到3-10mm的相应直径。 切割培养的雌雄配子体大小为50-400微米。 培养切除的雌雄配子体细胞计数为3-25细胞/ ind，温度条件为5-20度。 C，5-40微摩尔-2s -1的照射，光照时间为10:14（Light：Dark）-14：10（L：D）。 对栽培的雌性和雄性配子进行交叉施肥。 在PESI（Provasoli富集海水培养基）的液体培养基中培养配子体。 培养雌雄配子，直到配子体直径达到5-6mm。 消除50-100微米尺寸的雌配子体。 消除大小为60-150微米的雄性配子体。 在3-8细胞/ ind的细胞计数下培养雌配子体，温度条件为10-20度。 C，照度为15-30微摩尔-2s -1，光周期为10:14（Light：Dark）。 培养雄性配子体细胞计数为8-12个细胞/ ind，温度条件为5-20度。 C，照射15-25微摩尔-2s -1，光周期为14:10（Light：Dark）。 （AA）成熟Un of属（Undaria peterseniana）; （BB）冲洗成熟的沙门氏菌，洗涤后切除，用灭菌海水和ABM溶液洗涤; （CC）在10℃，20umol ^ -2s ^ -1和10：14h（L：D）释放游动孢子; （DD）0.1ml游动液溶液; （EE）通过稀释分离游动孢子; （FF）雌配子体; （GG）雄配子体; （HH）大量生产克隆配子体; （I1，I2）在15℃，20umol ^ -2s ^ -1和10：14h（L：D）每20天切割和再生; （JJ）以1：1的比例混合切割的雌性和雄性配子体; （KK）在15℃，20umol ^ -2s ^ -1和14：10h（L：D）下成型配子至少15天; （LL）在15℃，60umol ^ -2s ^ -1和14：10h（L：D）形成年轻孢子体40天，
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