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Liposomal formulations of hydrophobic photosensitizer for photodynamic therapy

机译:用于光动力疗法的疏水性光敏剂的脂质体制剂

摘要

Pharmaceutical liposomal formulations are described for photodynamic therapy comprising a, hydrophobic porphyrin photosensitizer, a monosaccharide and one or more synthetic phospholipids, which are stable in storage especially through freeze-drying process. The liposomal formulations provide therapeutically effective amounts of the photosensitizer for intravenous administration. In particular derivatives of chlorins and bacteriochlorins, such as temoporfin, are, hydrophobic photosensitizers whose efficacy and safety are enhanced by such liposomal formulations. The formulation can be efficiently freeze-dried preserving the size of the liposomal vehicles, and the content of a therapeutically effective amount of the photosensitizer, due to the selection of phospholipids and monosaccharides. The invention also relates to liposome compositions formed upon reconstitution with an aqueous vehicle. The freeze-dried formulation upon reconstitution with a suitable aqueous vehicle forms liposomes that are useful for intravenous administration.
机译:描述了用于光动力疗法的药物脂质体制剂,其包含疏水性卟啉光敏剂,单糖和一种或多种合成磷脂,它们在储存中尤其是通过冷冻干燥过程是稳定的。脂质体制剂为静脉内给药提供了治疗有效量的光敏剂。二氢卟酚和细菌二氢卟酚的衍生物,例如替莫泊芬,是疏水性光敏剂,其疏水性光敏剂的功效和安全性通过此类脂质体制剂得以增强。由于选择了磷脂和单糖,因此可以有效地冻干该制剂,以保持脂质体运载体的大小以及治疗有效量的光敏剂的含量。本发明还涉及用水性赋形剂重构后形成的脂质体组合物。用合适的水性赋形剂重构后的冻干制剂形成了可用于静脉内给药的脂质体。

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