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Supramolecular Functionalization of Graphitic Nanoparticles for Drug Delivery

机译:Graphitic纳米粒子的超分子功能化的药物输送。

摘要

Disclosed are nanoparticles, such as carbon nanotubes or other materials having extended aromatic surfaces (e.g., graphene sheet or nanotube), which are used to deliver active agents such as drugs, labels or dyes (termed for convenience a “drug”) to the interior of cells. The nanoparticles are functionalized by a hydrophilic polymer to render them stable in suspension. This molecule may be covalently attached to the nanoparticle, or may be adsorbed thereto as an amphiphilic molecule. The nanoparticles are coupled to the drug through supramolecular bonding i.e., binding to the exterior of the nanoparticle through π-stacking. The drug may also be covalently bonded to the hydrophilic polymer, which is coupled to the nanoparticle through supramolecular bonding. The drug is therefore capable of release in the cell exterior. The drug is more rapidly released at lower pH, as found e.g., in tumor cells. The drug-coupled, functionalized nanoparticles may also be targeted to specific cells through modification of the hydrophilic polymer, e.g., by adding an RGD peptide, or an antibody, which is targeted to cells expressing integrins, or an antibody directed to a cell surface marker. The drug may also be linked to a branched chain hydrophilic polymer, so that each polymer molecule carries more than one drug bound by a cleavable linker.
机译:公开了纳米颗粒,例如碳纳米管或具有延伸的芳族表面的其他材料(例如,石墨烯片或纳米管),其用于将活性剂例如药物,标记或染料(为方便起见称为“药物”)递送至内部细胞。纳米颗粒被亲水性聚合物官能化以使其在悬浮液中稳定。该分子可以共价附于纳米颗粒,或者可以作为两亲性分子被吸附到纳米颗粒上。纳米颗粒通过超分子键合即与药物相互作用,即通过π堆积与纳米颗粒的外部结合。药物也可以与亲水聚合物共价键合,该亲水聚合物通过超分子键合而与纳米颗粒偶联。因此,该药物能够在细胞外部释放。如在肿瘤细胞中发现的那样,该药物在较低的pH下更快地释放。药物偶联的功能化纳米颗粒也可以通过修饰亲水性聚合物而靶向特定细胞,例如通过添加RGD肽或靶向表达整联蛋白的细胞的抗体或针对细胞表面标记的抗体。药物也可以与支链亲水性聚合物连接,使得每个聚合物分子携带不止一种由可裂解的接头结合的药物。

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