首页> 外文会议>Conference on optical methods for tumor treatment and detection: mechanisms and techniques in photodynamic therapy XXVI >Phototoxic effects of free phthalocyanine and phthalocyanine conjugated to gold nanoparticles for targeted photodynamic therapy of melanoma cancer
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Phototoxic effects of free phthalocyanine and phthalocyanine conjugated to gold nanoparticles for targeted photodynamic therapy of melanoma cancer

机译:黑硝基氰酮和酞菁缀合金纳米粒子靶向光动力治疗黑素瘤癌的光毒性效应

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Photodynamic therapy (PDT) has emerged as an effective treatment modality for various malignant neoplasia and diseases. In PDT, the photochemical interaction of photosensitizer (PS), light and molecular oxygen produces singlet oxygen which can lead to tumour cell apoptosis, necrosis or autophagy. The success of PDT is limited by the hydrophobic characteristic of the PS which hinders treatment administration and efficiency. To circumvent this limitation, PS can be incorporated in nanostructured drug delivery systems such as gold nanoparticles (AuNPs). In this study, we investigated the effectiveness of free zinc monocarboxyphenoxy phthalocyanine (ZnMCPPc) and ZnMCPPc conjugated to AuNPs. Commercially purchased melanoma cancer cells cultured as cell monolayers were used in this study. Changes in cellular response were evaluated using cellular morphology, viability, proliferation and cytotoxicity. Untreated cells showed no changes in cellular morphology, proliferation and cytotoxicity. However, photoactivated free ZnMCPPc and ZnMCPPc conjugated to AuNPs showed changes in cellular morphology and a dose dependent decrease in cellular viability and proliferation as well as an increase in cell membrane. ZnMCPPc conjugated to AuNPs showed an improved efficiency in PDT as compared to free ZnMCPPc, which might be as a result of the vehicle effect of AuNPs. Both PSs used in this study were effective in inducing cell death with ZnMCPPc conjugated to AuNPs showing great potential as an effective PS for PDT.
机译:光动力疗法(PDT)已成为各种恶性肿瘤和疾病的有效治疗方式。在PDT中,光敏剂(PS),光和分子氧的光化学相互作用产生单线氧,其可导致肿瘤细胞凋亡,坏死或自噬。 PDT的成功受到PS的疏水性的限制,妨碍治疗给药和效率。为了避免这种限制,PS可以掺入纳米结构化药物递送系统中,例如金纳米颗粒(AUNP)。在这项研究中,我们研究了游离锌单羧基苯氧基(ZnMCPPC)和ZnMCPPC缀合的自由锌单羧基苯氧基酞菁(ZnMCPPC)和ZnMCPPC的有效性。在本研究中使用了作为细胞单层培养的商业购买的黑色素瘤癌细胞。使用细胞形态,活力,增殖和细胞毒性评估细胞反应的变化。未处理的细胞显示细胞形态,增殖和细胞毒性没有变化。然而,光活化的游离ZnMCPPC和ZnMCPPC与AUNP共轭显示细胞形态的变化和细胞活力和增殖的剂量依赖性降低以及细胞膜的增加。与自由ZnMCPPC相比,ZnMCPPC与AUNP的缀合出的效率为PDT,这可能是AUNP的车辆效果。本研究中使用的PSS两种PSS都是有效地诱导细胞死亡与ZnMCPPC缀合,与AUNPS缀合,显示出PDT的有效PS的巨大潜力。

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