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摘要

5-氨基乙酰丙酸(5-ALA)是由甘氨酸和琥珀酰辅酶a产生的线粒体代谢物,通过8个自身分子偶联在卟啉环上形成“血红素”基团,转化为原卟啉IX (PpIX)(图1)[1]。PpIX被用作光敏剂(PS),吸收波长为410 nm, 5-ALA在光动力治疗(PDT)中作为PpIX的前体或前药。外源性给药过量的5-ALA增加血红素生物合成过程中PpIX的产生。24-48 h后消除,长期光敏性风险较低[2]。然而,ALA/PDT有几个缺点。例如,ALA的浓度受到其吸收和药代动力学的影响,而这些吸收和药代动力学并没有完全覆盖治疗区域[3-5]。它还限制了肿瘤的渗透深度并引起疼痛[6]。
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Effectiveness of 5-aminolevulinic Acid-mediated Photodynamic Therapy Combined With Curcumin
5-Aminolevulinic acid (5-ALA) is the mitochondria metabolite produced from glycine and succinyl-CoA, which is converted to protoporphyrin IX (PpIX) by the conjugation of eight itself molecules forming the “heme” group in the porphyrin ring (Figure 1) [1]. The PpIX is used as a photosensitizer (PS) with an absorption wavelength of 410 nm, and 5-ALA acts as a precursor or prodrug for PpIX in photodynamic therapy (PDT). Exogenous administration of excessive amounts of 5-ALA increases the production of PpIX during heme biosynthesis. It is eliminated after 24-48 h with a lower risk of long-term photosensitivity [2]. However, ALA/PDT has several disadvantages. For instance, the concentration of ALA is affected by its absorption and pharmacokinetics that do not fully cover the treatment area [3-5]. It also limits the depth of tumor penetration and causes pain [6].
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