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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >Evaluating the photodynamic therapy efficacy using 5-aminolevulinic acid and folic acid-conjugated bismuth oxide nanoparticles on human nasopharyngeal carcinoma cell line
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Evaluating the photodynamic therapy efficacy using 5-aminolevulinic acid and folic acid-conjugated bismuth oxide nanoparticles on human nasopharyngeal carcinoma cell line

机译:使用5-氨基乙酰丙烯酸和叶酸 - 缀合的氧化铋氧化物纳米粒子在人鼻咽癌细胞上评价光动力治疗疗效

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Selective accumulation of photosensitizers (PSs) into cancerous cells is one of the most important factors affecting photodynamic therapy (PDT) efficacy. 5-Aminolevulinic acid (5-ALA) is precursor of a strong PS, protoporphyrin-IX (Pp-IX); but it has poor permeability in lipophilic membrane of the cells due to its hydrophilic property. Therefore, establishment of an improved delivery strategy could highly affect on treatment outcome. Moreover, folate receptors (FRs) are overexpressed on the surface of many tumor cells. In the present work, targeting ligand folic acid (FA) and 5-ALA conjugated bismuth oxide nanoparticles (FA-5ALA-Bi2O3 NPs) were synthesized; and used in PDT against human nasopharyngeal carcinoma cells (KB cell line). The KB cells incubated with the synthesized NPs for 2h; then illuminated using a custom-made red light LED lamp at the light dose of 26J/cm(2). MTT and caspase-3 activity assays were performed to evaluate the efficacy of treatment. Results showed that FR targeting ligand enables selective endocytosis of FA-5-ALA-conjugated NPs into KB cells. Improved internalization of 5-ALA into cells decreased the cell viability to about 50%, 65%, and 85% in the groups receiving FA-5ALA-Bi2O3 NPs, 5ALA-Bi2O3 NPs, free 5-ALA and subsequent PDT, respectively. Therefore, FA-5ALA-Bi2O3 NPs can significantly increase the cell killing effect of PDT.
机译:光敏剂(PSS)的选择性积累癌细胞是影响光动力治疗(PDT)功效的最重要因素之一。 5-氨基乙酰丙烯酸(5-ALA)是强PS的前体,PROPOROPORMYRIN-IX(PP-IX);但由于其亲水性,它具有细胞的亲脂膜的渗透性差。因此,建立改善的交付策略可能会影响治疗结果影响。此外,叶酸受体(FRS)在许多肿瘤细胞的表面上过表达。在本作工作中,合成靶向配体叶酸(FA)和5-ALA缀合的氧化物纳米颗粒(FA-5ALA-BI2O3 NPS);并用于针对人鼻咽癌细胞(KB细胞系)的PDT。将KB细胞与合成的NPS一起温育2小时;然后在26J / cm(2)的光剂量下使用定制的红光LED灯照亮。进行MTT和Caspase-3活性测定以评估治疗的疗效。结果表明,FR靶向配体使得FA-5-ALA缀合的NPS的选择性内吞作物进入KB细胞。将5 Ala进入细胞的改善的内化在接受Fa-5Ala-Bi2O3 NPS,5Ala-Bi2O3 NPS,Free 5-Ala和随后的PDT的基团中,细胞活力降低至约50%,65%和85%。因此,FA-5ALA-BI2O3 NPS可以显着增加PDT的细胞杀伤效果。

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