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首页> 外文期刊>Journal of Materials Chemistry, B. materials for biology and medicine >Hyaluronic acid-conjugated graphene oxide/ photosensitizer nanohybrids for cancer targeted photodynamic therapy
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Hyaluronic acid-conjugated graphene oxide/ photosensitizer nanohybrids for cancer targeted photodynamic therapy

机译:透明质酸共轭氧化石墨烯/光敏剂纳米杂化物用于癌症的光动力疗法

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摘要

Hyaluronic acid (HA)-graphene oxide (GO) conjugates, with a high loading of photosensitizers (PS; Ce6), were developed as a cancer cell targeted and photoactivity switchable nanoplatform for photodynamic therapy (PDT). HA-GO conjugates with size below 100 nm were first prepared by the chemical conjugation between ADH-modified HA and fractionated GO sheets with size relevant for drug delivery. Before evaluating the drug delivery efficacies, their chemical structure, morphology, and biocompatibility were characterized by ~1H NMR, UV, TGA, AFM, DLS and MTT assays. The physical adsorption of Ce6 onto HA-GO nanocarriers was mainly due to the π-π stacking as well as hydrophobic interactions. It was demonstrated by CLSM and FACS that the cellular internalization of the HA-GO/Ce6 nanohybrids was much more effective when compared with free Ce6, which was also found to be significantly influenced by the co-treatment with an excess amount of HA polymers, illustrating their active targeting to HA receptors overexpressed on cancer cells. The photoactivity of Ce6 adsorbed on HA-GO nanocarriers was mostly quenched in aqueous solution to ensure biocompatibility, but was quickly recovered after the release of Ce6 from HA-GO nanocarriers upon cellular uptake. As a result, the PDT efficiency of the HA-GO/Ce6 nanohybrids was remarkably improved ~10 times more than that of free Ce6, as well demonstrated in both MTT and LIVE/DEAD assays.
机译:具有高负载光敏剂(PS; Ce6)的透明质酸(HA)-氧化石墨烯(GO)共轭物被开发为靶向癌细胞和光活性可切换的纳米平台,用于光动力疗法(PDT)。首先通过ADH修饰的HA和大小与药物传递相关的GO分馏片之间的化学偶联,制备尺寸小于100 nm的HA-GO缀合物。在评估药物传递效率之前,通过〜1H NMR,UV,TGA,AFM,DLS和MTT分析表征了它们的化学结构,形态和生物相容性。 Ce6在HA-GO纳米载体上的物理吸附主要是由于π-π堆积以及疏水相互作用。 CLSM和FACS证明,与游离Ce6相比,HA-GO / Ce6纳米杂化物的细胞内在化更为有效,而游离Ce6也受到过量的HA聚合物的共同处理的影响,说明它们主动靶向癌细胞上过表达的HA受体。吸附在HA-GO纳米载体上的Ce6的光活性大多在水溶液中淬灭以确保生物相容性,但在细胞摄取后从HA-GO纳米载体上释放Ce6后很快恢复。结果,HA-GO / Ce6纳米杂交体的PDT效率比游离Ce6显着提高了约10倍,这在MTT和LIVE / DEAD分析中均得到证明。

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