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LIPID MEMBRANE STRUCTURE 新技術説明会

外国特許コード F120006481
整理番号 S2010-0171-C0
掲載日 2012年5月7日
出願国 世界知的所有権機関(WIPO)
国際出願番号 2011JP053963
国際公開番号 WO 2011135905
国際出願日 平成23年2月23日(2011.2.23)
国際公開日 平成23年11月3日(2011.11.3)
優先権データ
  • 特願2010-103333 (2010.4.28) JP
発明の名称 (英語) LIPID MEMBRANE STRUCTURE 新技術説明会
発明の概要(英語) Disclosed is a lipid membrane structure which fulfils intracellular migration properties, selectivity for target cells and in vivo stability and can be used for the delivery of a substance to a target cell. In the lipid membrane structure, a lipid membrane is modified with (a) polyalkylene glycol having a target-cell-selective ligand bound thereto and (b) a polypeptide containing multiple arginine residues.
従来技術、競合技術の概要(英語) BACKGROUND ART
Drag, delivery, system (DDS) used as is to a membrane structure such as a lipid of the liposome, the ability to retain the drug, in vivo stability, drug should be delivered to a particular cell (target cell) selectivity, a target cell to go, the release of the drug within the target cells and the like various performance are required. In particular, in the nucleus or the cytoplasm of the target for delivery of a drug or nucleic acid in the lipid membrane structure, as well as selectivity to target cells, within the cell, in particular of the specific organelle such as nucleus inside the target cell and thus an excellent migration.
The inventors have found that, previously, such as octaarginine (R8) a peptide having consecutive arginine residues of the lipid membrane by modifying the surface of the structure, transfer from the cells of the lipid membrane structure, in particular nuclear import can be improved are found (International Publication WO2005/032593; Journal of Controlled Release, 98, pp.317-323, 2004). However, modifications can comprise R8, specificity for a particular cell is not provide internalization. In addition, due to a cationic R8, R8 modified lipid membrane structure may be easily and quickly evacuated from the living body, lipid modified R8 film structure is selected to be within the delivery to target cells is thought to be difficult.
On the other hand, the in vivo stability of the lipid membrane structure, particularly as a method of increasing blood stability, polyalkylene glycol, typically polyethylene glycol (PEG) modified the surface of the lipid membrane structure is widely known (for example, JP-1-249717 publication, JP-2-149512 publication, JP-4-346918 publication, JP-2004-10481 are described in Japanese Patent Application). The method, a lipid membrane structure PEG hydration layer covering the carrier particles such as opsonization and serum protein adsorption is suppressed and the like, as a result, phagocytosis by macrophages and uptake by the reticuloendothelial system based on the tissue can be avoided.
However, R8 was modified with the lipid membrane structure for the purpose of enhancing the in vivo stability of the lipid membrane structure further PEG and modify the surface, by modification of R8 internalization ability is lost and there is a problem. That is, lipid membrane structure R8 and simultaneous modifications PEG, modified PEG the lipid membrane structure to improve the in vivo stability of the other hand, that lower the cell transition in a contradicting problem (also referred to as the dilemma PEG) has been altered.
This PEG as an attempt to solve the dilemma, the present inventor et al. further phospholipid PEG residues between residues of the matrix metalloproteinase can be a substrate peptide comprising substrate arranged phospholipid derivatives is created, the lipid membrane structure lipid derivatives are proposed (Japanese Patent Application JP-2007-099750). The lipid membrane structure is a matrix metalloproteinase by cleavage of the peptide portion PEG for a property of being desorbed and, in the blood is stable due to the presence of the site of modification on the other hand, malignant tumor cells secrete matrix metalloprotease in the vicinity of the site of modification in the lipid membrane structure being detached from the characteristic of lowering the stability of the has. Due to this characteristic, the lipid membrane structure held in the anti-tumor agent and a nucleic acid is released at the outside of the malignant tumor cells, or the site of modification in the dissociation of the lipid membrane structure in the malignant tumor cells efficiently taken up by, or nucleic acid of the drug in malignant tumor cells can be introduced efficiently.
However, in Japanese Patent Application Laid-open 2007-099750 the technique, as malignant tumor cells secrete matrix metalloprotease DDS of even though it is effective, other target cells, or that do not secrete matrix metalloprotease in particular, the amount of secretion or less relative to the effectiveness as DDS cannot be hardly expected, other than the malignant tumor cells to improve the selectivity in the cells is not particularly limited.
In addition, the lipid membrane structure as a method of increasing the selectivity towards the target cells, such as the cell membrane surface receptors that are present in a particular cell-specific expression of the living body to the substance or ligand can selectively bind to the lipid membrane structure of the surface-modifying methods have been known. In this method, the in vivo stability of the lipid membrane structure to improve the selectivity for the target cell in order to satisfy at the same time, via PEG ligand is generally arranged on the surface of the lipid membrane structure in many cases. However, the lipid membrane structure is a target cell specific ligand selectivity for the modification of the performance improves, mediated endocytosis into cells of the saturation property due to uptake, intracellular migration property of the lipid membrane structure is the upper limit, the uptake of the drug or the like is expected at the high medicinal effect cannot be enhanced and has a problem. In this way, conventional, intracellular migration, selectivity for target cells, and in vivo stability of the lipid membrane structure is satisfactory at the same time has yet to be provided in.
  • 出願人(英語)
  • ※2012年7月以前掲載分については米国以外のすべての指定国
  • NATIONAL UNIVERSITY CORPORATION HOKKAIDO UNIVERSITY
  • 発明者(英語)
  • HARASHIMA Hideyoshi
  • HATAKEYAMA Hiroto
  • KHALIL Ikramy
  • TAKARA Kazuhiro
国際特許分類(IPC)
指定国 National States: AE AG AL AM AO AT AU AZ BA BB BG BH BR BW BY BZ CA CH CL CN CO CR CU CZ DE DK DM DO DZ EC EE EG ES FI GB GD GE GH GM GT HN HR HU ID IL IN IS JP KE KG KM KN KP KR KZ LA LC LK LR LS LT LU LY MA MD ME MG MK MN MW MX MY MZ NA NG NI NO NZ OM PE PG PH PL PT RO RS RU SC SD SE SG SK SL SM ST SV SY TH TJ TM TN TR TT TZ UA UG US UZ VC VN ZA ZM ZW
ARIPO: BW GH GM KE LR LS MW MZ NA SD SL SZ TZ UG ZM ZW
EAPO: AM AZ BY KG KZ MD RU TJ TM
EPO: AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR
OAPI: BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG
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