Abstract:
PURPOSE: A manufacturing method of interpenetrating polymer network scaffold for cell delivery which includes hyaluronic acid and alginate are provided to provide porous hyaluronic acid-alginate supporter which recycles chondrocyte and enoughly delivers nutrients. CONSTITUTION: A manufacturing method of interpenetrating polymer network scaffold for cell delivery which includes hyaluronic acid and alginate comprises the following steps: melting hyaluronic acid and alginate into a sodium hydroxide aqueous solution; adding an epoxy-based cross linking agent and homogenizing the hyaluronic acid-alginate solution; hydrogelizing the homogenized hyaluronic acid-alginate solutions; washing the hydrogel with a calcium chloride aqueous solution; obtaining porosity by expanding the washed hyaluronic acid-alginate in a calcium chloride aqueous solution; eliminating calcium chloride remaining in the hyaluronic acid - alginate supporter using distilled water; and obtaining a porous hyaluronic acid supporter by freeze-drying the hydrogel.
Abstract:
The present invention relates to multi-layered proliposome and a method for preparing the same. The multi-layered prolipsome can significantly increase the content of a bioactive ingredient in a lipid layer when compared with existing proliposome; maintain the stability of the bioactive ingredient; promote the absorption into the intestinal tract; and control the release rate, the release amount, and the release site of the bioactive ingredient. Particularly, a multi-layered coating is performed while the amount of sugar used in the preparation of the proloposome is reduced, thereby producing the multi-layered proliposome capable of increasing the release rate and the release amount of a poorly water-soluble drug and significantly reducing the amount of vehicle. The multi-layered proliposome can be useful to develop medicines for treatment or prevention, cosmetics, or food additives.
Abstract:
PURPOSE: A liquid phase formulation for nasal administration containing antiallergic A drug is provided to easily administrate and to minimize side effects. CONSTITUTION: A liquid phase formulation for nasal administration contains 0.1-5 weight% of antiallergic drug, 2-10 weight% of oil, 20-70 weight aprts of% surfactant. The antiallergic drug is anti-histamin agent, steroid drug. The liquid phase formulation is microemulsion.
Abstract:
본발명은다층프로리포솜및 이의제조방법에관한것으로, 상기다층프로리포솜은기존의프로리포솜에비해지질층중 생리활성성분의함유량을크게증가시킬뿐 아니라, 생리활성성분의안정성을유지시켜주며, 장관내흡수를증진시키며, 사용된고분자특성에따라생리활성성분의방출속도, 방출량및 방출장소를조절할수 있다. 특히프로리포솜의제조에사용되는당류의양을줄여서다층코팅을함으로써난용성약물의방출속도와방출량을높이면서도부형제의양을획기적으로줄일수 있는다층프로리포솜을제조할수 있다. 상기다층프로리포솜은치료또는예방용약제, 화장품또는식품첨가제의개발에유용하게사용될수 있다.
Abstract:
본 발명은 가공인삼 성분을 국소 피부에 적용할 수 있는 마이크로이멀젼계 하이드로겔에 관한 것으로, 가공인삼, 이소프로필 미리스테이트, 라브라솔, 프로필렌 글리콜 및 인지질을 유효성분으로 함유하는 100nm 이하의 마이크로이멀젼을 제조하고 상기 마이크로이멀젼에 겔화제를 첨가하여 얻어진 마이크로이멀젼계 하이드로겔은 피부 미백, 재생 및 항주름 효과 등 피부개선 효과가 기대되지만 난용성이고 분자량이 500Da 이상으로 피부흡수가 어려운 가공인삼을 피부내로 잘 투과시키고 국재시킬 수 있을 수 있기 때문에 가공인삼을 유효성분으로 함유하는 피부개선용 피부외용제로 유용하게 사용할 수 있다.
Abstract:
PURPOSE: A micro emulsion hydro gel which contains processed ginseng as an active ingredient is provided to be used as external preparation of skin for skin improvement by penetrating and localizing processed ginseng within skin. CONSTITUTION: A micro emulsion hydro gel comprises 0.02-3.0 wt% of processed ginseng, 5.0-15.0 wt% of Isopropyl myristate, 15.0-60.0 wt% of surfactant, 0.5-5.0 wt% of gelling agent, and residual water. Processed ginseng is steamed and is dried at 110 to 130>= for two to four hours.