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含氯铝酞菁的脂质体和纳米胶囊对人黑色素瘤细胞系的体外光毒性

In vitro phototoxicity of liposomes and nanocapsules containing chloroaluminum phthalocyanine on human melanoma cell line.

作者信息

Barbugli Paula A, Siqueira-Moura Marigilson P, Espreafico Enilza M, Tedesco Antonio C

机构信息

Programa de Pós-Graduação em Ciências Farmacêuticas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Av. do Café s/n, 14040-903, Ribeirão Preto-SP, Brasil.

出版信息

J Nanosci Nanotechnol. 2010 Jan;10(1):569-73. doi: 10.1166/jnn.2010.1741.

Abstract

In this study, the photodynamic action of liposomes (LP) and nanocapsules (NC) containing Chloroaluminum phthalocyanine (CIAIPc), on the human melanoma cell (WM 1552C), was assessed. The light source was setup at 672 nm, which corresponds to the maximum absorption wavelength of the CIAIPc. Both colloidal carriers presented size in nanometric scale as well as negative zeta potential. The cellular damage was light dose dependent ranging from 30% of cell death at 70 mJ x cm-2 to 90% of death at 700 mJ x cm(-2). However, the photocytotoxic effect of LP at 70 mJ x cm(-2) was slightly more efficient to induce cellular death than NC formulation. At 140 mJ x cm(-2), and 700 mJ x cm(-2) both nanocarriers were equally efficient to induce cellular damage. Therefore, in the present work, the maximum phototoxic effect was obtained with 700 mJ x cm(-2) of light dose, in combination with 0.29 microg x mL(-1) of CIAIPc encapsulated into LP and NC. The cells were also positive to annexin V, after the PDT treatment with LP and NC, showing that one of the mechanisms of cellular death involved is apoptosis. In summary, the potential of LP and NC as a drug delivery system, in Photodynamic Therapy (PDT) against melanoma, has been confirmed using a lower concentration of the photosensitizer and lower light doses than that applied in current protocols. This is an innovative proposal to treat melanoma cell lines that until now have not received the benefit of the PDT protocol for treatment.

摘要

在本研究中,评估了含有氯铝酞菁(CIAIPc)的脂质体(LP)和纳米胶囊(NC)对人黑色素瘤细胞(WM 1552C)的光动力作用。光源设置在672 nm,这对应于CIAIPc的最大吸收波长。两种胶体载体均呈现纳米级尺寸以及负的zeta电位。细胞损伤呈光剂量依赖性,从70 mJ·cm⁻²时30%的细胞死亡到700 mJ·cm⁻²时90%的死亡。然而,70 mJ·cm⁻²时LP的光细胞毒性作用诱导细胞死亡的效率略高于NC制剂。在140 mJ·cm⁻²和700 mJ·cm⁻²时,两种纳米载体诱导细胞损伤的效率相同。因此,在本研究中,700 mJ·cm⁻²的光剂量与封装在LP和NC中的0.29 μg·mL⁻¹的CIAIPc组合可获得最大光毒性作用。在用LP和NC进行光动力疗法(PDT)治疗后,细胞对膜联蛋白V也呈阳性,表明所涉及的细胞死亡机制之一是凋亡。总之,使用比当前方案更低浓度的光敏剂和更低的光剂量,已证实LP和NC作为药物递送系统在光动力疗法(PDT)治疗黑色素瘤方面的潜力。这是一种创新的治疗黑色素瘤细胞系的方案,而这些细胞系至今尚未从PDT治疗方案中获益。

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