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NANOPARTICLE CARRIER SYSTEMS BASED ON POLY(DL LACTIC CO GLYCOLIC ACID) (PLGA) FOR PHOTODYNAMIC THERAPY (PDT)

机译:基于聚(DL乳酸乙醇酸)(PLGA)的光动力疗法(PDT)纳米颗粒载体系统

摘要

mmmCompositions which are stable in storage and a method of production of pharmaceutical based nanoparticutate formulations for clinical use in photodynamic therapy comprising a hydrophobic photosensitizer poly(lactic co glycolic) acid and stabilizing agents are provided. These nanoparticulate pharmaceutical formulations provide therapeutically effective amounts of photosensitizer for parenteral administration. In particular tetrapyrrole derivatives can be used as photosensitizers whose efficacy and safety are enhanced by such nanoparticulate formulations. It also leaches the method of preparing PLGA based nanoparticles under sterile conditions. In one of the preferred embodiments of the present invention PLGA based nanoparticles have a mean particle size less than 500nm and the photosensitizer is temoporf?n 5 10 15 20 tetrakis(3 hydroxyphenyl) chlorin (THPC). In another embodiment the photosensitizer 2 3 dihydroxy 5 10 15 20 tetrakis(3 hydroxyphenyl) chlorin (THPD OH) is formulated as a nanoparticle for parenteral administration. Yet in another embodiment preferred photosensitizer is 5 10 15 20 tetrakis(3 hydroxyphenyl) porphyrin (THPP). The formulations can be used for treating hyperptasic and neoplasia conditions inflammatory problems and more specifically to target tumor cells.
机译:提供了在贮存中稳定的mmm组合物和用于临床的用于光动力疗法的临床用途的基于药物的纳米颗粒制剂的制备方法,所述纳米颗粒制剂包含疏水性光敏剂聚(乳酸共乙醇酸)和稳定剂。这些纳米颗粒药物制剂为肠胃外给药提供了治疗有效量的光敏剂。特别地,四吡咯衍生物可以用作光敏剂,通过这种纳米颗粒制剂可以提高其功效和安全性。它还提出了在无菌条件下制备基于PLGA的纳米颗粒的方法。在本发明的优选实施方案之一中,基于PLGA的纳米颗粒的平均粒径小于500nm,并且光敏剂为替莫泊芬5 10 15 20四(3羟苯基)二氢卟酚(THPC)。在另一个实施方案中,将光敏剂2 3二羟基5 10 15 20四(3羟苯基)二氢卟酚(THPD OH)配制为用于肠胃外施用的纳米颗粒。在另一个实施方案中,优选的光敏剂是5 10 15 20四(3羟苯基)卟啉(THPP)。所述制剂可用于治疗肥大和瘤形成状况的炎症问题,更具体地用于靶向肿瘤细胞。

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