Abstract:
The present invention relates to low-density lipoprotein like cationic lipid nanoparticles in solid form which target liver cells including parenchyma cells and non-parenchyma cells forming the liver tissue; and a composition comprising the same for liver-targeted delivery of a composition for diagnosing and/or treating liver diseases.
Abstract:
The present invention relates to a liver targetted drug delivery system using metal nanoparticles and a method for preparing the same. More specifically, the present invention relates to a method for preparing hyaluronic acid-gold nanoparticle / protein composites which surface-modify gold nanoparticles with enhanced in vivo stability using hyaluronic acid which has biocompatibility, biodegradability, and specific delivery properties for liver tissues and attaches various protein medicines for treating liver complaint to the surfaces of residual gold nanoparticles in order to be used as the liver targetted drug delivery system, and to a composition. In addition, the present invention relates to applications of an agent for treating liver complaint which can be safely applied in human body using the hyaluronic acid-gold nanoparticle / protein composites and increases medicinal effect time and is effectively delivered to liver.
Abstract:
PURPOSE: A method for preparing a self-assembled drug and a cell delivery system is provided to easily synthesize a polymer composite and to prepare a drug and cell delivery system. CONSTITUTION: A method for preparing a self-assembled drug and a cell delivery system comprises a step of mixing: a compound of chemical formula I([B]m-[H]n); a drug, fluorescent substance, radioactive isotope, target oriented material, or imaging material which interacts with the compound of chemical formula I; and a functional group which interacts with the compound of chemical formula I in a solvent. The solvent is water, saline solution, buffer solution, or ethanol. The self-assembled delivery system is a hydrogel.
Abstract:
본 발명은 핵산 전달용 고분자의 제조방법 및 상기 고분자를 함유하는 핵산 전달용 조성물에 관한 것으로, 구체적으로 핵산을 세포 내로 효과적으로 전달하고 독성이 거의 없는 핵산 전달용 고분자의 제조방법 및 상기 고분자를 함유하는 핵산 전달용 조성물에 관한 것이다. 본 발명의 핵산 전달용 고분자의 제조방법 및 상기 고분자를 함유하는 핵산 전달용 조성물은 핵산을 세포 내로 효과적으로 전달할 수 있고 독성이 거의 없어, 핵산의 효과적인 전달 시스템으로 활용할 수 있으며, 특히 저 분자량으로 분해되는 폴리에틸렌이민과 생체적합성이 우수한 히알루론산이 함유되어 주사 제형 및 비강 등을 통해 효과적으로 핵산을 전달할 수 있다. 핵산, 전달, 히알루론산, 폴리에틸렌이민, 스퍼민
Abstract:
PURPOSE: A method for controlling target-specificity of a drug delivery system containing a hyaluronic acid derivative is provided to control carboxyl group substitution rate. CONSTITUTION: A target specificity of a drug delivery system containing hyaluronic acid derivatives is controlled by regulating carboxyl group substitution rate of hyaluronic acid derivatives. A target receptor of the drug delivery system is CD44, LYVE-1, RHAMM, or HARE. The drug delivery system contains hyaluronic acid derivatives in which 5 mole%-45mole% of substituted carboxyl group. The drug delivery system contains encapsulated or sealed drug for preventing or treating liver diseases.
Abstract:
PURPOSE: A method for preparing polymers for nucleic acid delivery is provided to transfer nucleic acid through injection or nasal cavity. CONSTITUTION: A polymer for nucleic acid delivery is prepared by binding hyaluronic acid and disulfide bond-introduced polyethyleneimine. A method for preparing the polymers comprises: a step of adding 1-ethyl-3- [3-(dimethylamino)-propyl]carbodiimide, N, N'-dicyclohexylcarbodiimide(DCC), 1-hydroxy bentriazole monohydrate(HOBt), or N-hydroxysuccinimide(NHS) compound to hyaluronic acid; and a step of binding polyethylene imine in disulfide bond is introduce. A composition for nucleic acid delivery contains polymer of chemical formula 1 or 2.
Abstract:
PURPOSE: A method for preparing hyaluronic acid-peptide conjugate is provided to apply to a drug delivery system of various peptide active ingredients with safety to human body. CONSTITUTION: A method for preparing hyaluronic acid-peptide conjugate comprises: a step of reacting tetra-n-butyl ammonium hydroxide(TBA-OH) with hyaluronic acid(HA), salt thereof, derivative thereof to form HA-TBA; a step of preparing water-insoluble peptide with terminal amino group; and a step of reacting the water-insoluble peptide with HA-TBA and terminal amino group under the presence of organic solvent.
Abstract:
PURPOSE: An X-ray ablation method of hyaluronan hydrogel is provided to obtain a new protocol for manufacturing HA-system hydrogel by the short light X-ray irradiation. CONSTITUTION: An X-ray ablation method of hyaluronan hydrogel comprises the following steps: preparing hyaluronan hydrogel; and irradiating X-rays to the hyaluronan hydrogel for inducing the decomposition of the hyaluronan hydrogel through the gel-sol transition. The decomposition speed of the hyaluronan hydrogel is determined by the dose of the X-ray irradiation.
Abstract:
PURPOSE: A silicon nanowire biosensor for diagnosing cancer is provided to selectively detect vascular endothelial growth factor(VEGF) and early diagnose various kinds of cancer. CONSTITUTION: A silicon nanowire transistor biosensor contains source, drain, gate, a field effect transistor having a channel area between the source and drain, and an RAN aptamer which selectively binds with fixed VEGF on the surface of silicon nano wire. The RNA aptamer is Pegaptanib Sodium.
Abstract:
PURPOSE: A hyaluronate bone filling complex and a method for fabricating the same are provided, which obtain excellent reproduction capacity. CONSTITUTION: A hyaluronate bone filling complex comprises a matrix including hyaluronic acid derivative of the hydrogel form and a bone reproduction derivative which is filled in the matrix. The bone reproduction derivative is bone reproduction derivative synthesized by megagen. The bone reproduction derivative is chemical deposition reactant of biphasic calcium phosphate which includes tricalcium phosphate and hydroxyapatite or calcium nitrate tetrahydrate and dibasic ammonium phosphate.