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Aminolevulinic Acid Derivatives and Liposome Delivery as Strategies for Improving 5-Aminolevulinic Acid- Mediated Photodynamic Therapy

机译:氨基乙酰丙酸衍生物和脂质体递送作为改善5-氨基乙酰丙酸介导的光动力疗法的策略

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摘要

Photodynamic Therapy employing 5-aminolevulinic acid (ALA) as a precursor of the photosensitizer Protoporphyrin IX has become a promising approach to treat superficial cancers. However, the hydrophilic nature of the ALA molecule somewhat limits the penetration through the skin as well as all cell membranes. Different attempts are currently under investigation to enhance ALA penetration, such as the development of new synthetic and more lipophilic molecules derived from ALA and the incorporation of ALA into lipophilic vehicles such as liposomes. Among the new synthesized molecules, we can find ALA esters, ALA aminoacid derivatives and ALA dendrimers. In general, there is consensus that the promising results obtained in vitro with ALA esters cannot be reproduced in vivo. However, ALA methyl ester (1) has been widely used for treatment of skin malignancies and ALA hexyl ester (15) proved to be more powerful than ALA in bladder imaging. ALA aminoacid derivatives have been designed to use specific cellular aminopeptidases to targeting tumors, and it was shown that they can be metabolized to ALA with some specificity.
机译:使用5-氨基乙酰丙酸(ALA)作为光敏剂原卟啉IX的前体的光动力疗法已成为治疗浅表癌症的一种有前途的方法。但是,ALA分子的亲水性在某种程度上限制了通过皮肤以及所有细胞膜的渗透。目前正在研究增强ALA渗透性的各种尝试,例如开发新的合成的和衍生自ALA的更具亲脂性的分子,以及将ALA掺入亲脂性载体(如脂质体)中。在新合成的分子中,我们可以找到ALA酯,ALA氨基酸衍生物和ALA树状聚合物。通常,已经达成共识,用ALA酯在体外获得的有希望的结果不能在体内复制。但是,ALA甲酯(1)已被广泛用于治疗皮肤恶性肿瘤,并且在膀胱成像中,ALA己基酯(15)被证明比ALA更强大。已经设计了ALA氨基酸衍生物以使用特定的细胞氨基肽酶靶向肿瘤,并且显示它们可以以某些特异性代谢为ALA。

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