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以磷脂聚合物作为维替泊芬纳米转运体的光动力疗法对前哨淋巴结转移的无创治疗

The Noninvasive Treatment for Sentinel Lymph Node Metastasis by Photodynamic Therapy Using Phospholipid Polymer as a Nanotransporter of Verteporfin.

作者信息

Shimada Kyosuke, Matsuda Sachiko, Jinno Hiromitsu, Kameyama Noriaki, Konno Tomohiro, Arai Tsunenori, Ishihara Kazuhiko, Kitagawa Yuko

机构信息

Department of Breast Surgery, Kawasaki Municipal Ida Hospital, 2-27-1 Ida, Nakahara, Kawasaki, Kanagawa 211-0035, Japan.

Department of Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, Tokyo 160-8582, Japan.

出版信息

Biomed Res Int. 2017;2017:7412865. doi: 10.1155/2017/7412865. Epub 2017 Apr 3.

Abstract

. The usefulness of photodynamic therapy (PDT) for treating sentinel lymph node (SLN) metastasis was evaluated. . Verteporfin, a hydrophobic photosensitizer, forms a soluble aggregate with poly(2-methacryloyloxyethyl phosphorylcholine---butyl methacrylate) (PMB). The concentrations of verteporfin were determined by measuring the fluorescence emitted at 700 nm. Seven days after the inoculation of A431 cells at the forearm of BALB/c nude mice, PMB-verteporfin was injected at dorsum manus and 75 J of light energy was delivered for 1 minute. Fifty-three mice were randomly assigned to the combination of PMB-verteporfin injection and light exposure, light exposure alone, PMB-verteporfin injection alone, and no treatment groups. Ten days after PDT, brachial lymph nodes, which were considered as SLNs, were harvested and evaluated. . The concentration of verteporfin in SLN was significantly higher than other organs. The combination of PMB-verteporfin injection and light exposure group significantly reduced the SLN metastasis (13%) comparing with no treatment group (52%), light exposure alone group (57%), and PMB-verteporfin injection alone group (46%). . These data suggested that PDT using PMB as a nanotransporter of verteporfin could be a minimally invasive treatment of SLN metastasis in breast cancer and represent a potential alternative procedure to SLNB.

摘要

评估了光动力疗法(PDT)治疗前哨淋巴结(SLN)转移的有效性。维替泊芬是一种疏水性光敏剂,它与聚(2-甲基丙烯酰氧基乙基磷酰胆碱-甲基丙烯酸丁酯)(PMB)形成可溶性聚集体。通过测量在700nm处发射的荧光来测定维替泊芬的浓度。在BALB/c裸鼠前臂接种A431细胞7天后,在手部背部注射PMB-维替泊芬,并在1分钟内给予75J光能。53只小鼠被随机分配到PMB-维替泊芬注射联合光照、单纯光照、单纯PMB-维替泊芬注射和不治疗组。PDT后10天,收集并评估被认为是SLN的肱淋巴结。SLN中维替泊芬的浓度显著高于其他器官。与不治疗组(52%)、单纯光照组(57%)和单纯PMB-维替泊芬注射组(46%)相比,PMB-维替泊芬注射联合光照组显著降低了SLN转移(13%)。这些数据表明,使用PMB作为维替泊芬的纳米转运体的PDT可能是乳腺癌SLN转移的微创治疗方法,并且是SLNB的潜在替代方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08c7/5394349/82b62b584275/BMRI2017-7412865.001.jpg

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