首页> 外文会议>Photonic Therapeutics and Diagnostics; Progress in Biomedical Optics and Imaging; vol.6, no.1 >Herbal Tea extract combined with light induced significant in vitro cytotoxicity of human bladder cancer cells
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Herbal Tea extract combined with light induced significant in vitro cytotoxicity of human bladder cancer cells

机译:凉茶提取物与光结合对人膀胱癌细胞具有明显的体外细胞毒性

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The anti-inflammatory, anti-microbial, antiviral, and antidepressant activities of the Greek herb, Hypericum Perforatum L, HP L, have been attributed to the total extract or single constituents. We investigated the use of the extract, specifically of the polar methanolic fraction (PMF) of Epirus'HPL in photodynamic therapy (PDT) alone and in combination with recombinant Interferon-α2b (IFN) and gemcitabine (GCB) in the treatment of human bladder cancer cells. The PMF was extracted from the dry herb with methanol, followed by liquid-liquid extraction with petroleum ether. T-24 bladder cancer cells were plated (10~5 cells/well) and placed in the incubator (37℃, 5%CO) for 24 hours prior to addition of drugs. PMF 60ug/ml was added and incubation continued. After 24 hours, the cells were subjected to laser light (630nm) treatment with 0, 1, 4 and 8 Joules. After reincubation for 24 hours, IFN, (50,000 IU) or GCB, (2ug/ml) was added to the PDT-treated cells. After this incubation cell survival was assessed by the MTT assay. PMF-PDT alone-induced percent cell kill of 0%, 8%, 44% and 80% versus 31%, 64 and 86 % for PMF-PDT and IFN, versus 63%, 80% and 88% for MPF-PDT plus GCB at 1, 2, 4 and 8 Joules respectively. IFN and GCB induced 20% and 53% cell kill respectively. Our data suggest that MPF may be an effective agent for in vitro photodynamic therapy. PMF-PDT combined with Intron A, or gemcitabine achieved improved kill of cultured bladder cancer cells. Confirmation of these results in preclinical studies may lead to clinical trials.
机译:希腊草药贯叶连翘L,HP L的抗炎,抗微生物,抗病毒和抗抑郁活性已归因于总提取物或单一成分。我们研究了提取物,特别是Epirus'HPL的极性甲醇部分(PMF)在单独的光动力疗法(PDT)中以及与重组干扰素-α2b(IFN)和吉西他滨(GCB)联合用于治疗人膀胱的用途癌细胞。用甲醇从干草中提取PMF,然后用石油醚液-液萃取。将T-24膀胱癌细胞铺板(10〜5个细胞/孔),并在加入药物之前在培养箱(37℃,5%CO)中放置24小时。加入60ug / ml的PMF,并继续孵育。 24小时后,以0、1、4和8焦耳对细胞进行激光(630nm)处理。再孵育24小时后,将IFN(50,000 IU)或GCB(2ug / ml)添加到PDT处理的细胞中。孵育后,通过MTT测定评估细胞存活。单独的PMF-PDT诱导的细胞杀伤百分比为0%,8%,44%和80%,而PMF-PDT和IFN分别为31%,64和86%,而MPF-PDT plus分别为63%,80%和88% GCB分别为1、2、4和8焦耳。 IFN和GCB分别诱导20%和53%的细胞杀死。我们的数据表明,MPF可能是体外光动力疗法的有效药物。 PMF-PDT与内含子A或吉西他滨组合可提高对培养的膀胱癌细胞的杀伤力。在临床前研究中证实这些结果可能会导致临床试验。

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