发明名称 Light-enabled drug delivery
摘要 Conjugates are provided which comprise a membrane permeable drug linked to a moiety that is not membrane permeable. Attachment of the moiety that is not membrane permeable prevents the drug from crossing cell membranes and entering cells. However, exposure to light either i) breaks the linkage, releasing the drug and allowing it to enter cells; or ii) converts the non-membrane permeable moiety to a membrane permeable form, allowing the entire conjugate to enter the cell, where the drug is released from the conjugate by cleavage. The membrane permeable drugs are thus delivered to cells at locations of interest, e.g. cancer cells in a tumor, in a temporally and spatially controlled manner.
申请公布号 US9364551(B2) 申请公布日期 2016.06.14
申请号 US201214347656 申请日期 2012.09.28
申请人 Virginia Commonwealth University 发明人 Hartman Matthew;Dcona Martin Michael;Mitra Deboleena
分类号 A61K38/00;C07K2/00;A61K47/48;A61K41/00;A61K31/704;A61N5/06 主分类号 A61K38/00
代理机构 Whitham, Curtis & Cook, P.C. 代理人 Whitham, Curtis & Cook, P.C.
主权项 1. A conjugate for delivering a membrane permeable drug into cells, consisting of: said membrane permeable drug, and a membrane impermeable moiety chemically attached to said membrane permeable drug, wherein said membrane impermeable moiety comprises a peptide that adopts an α-helical conformation and becomes membrane permeable upon exposure to light.
地址 Richmond VA US