首页> 外文会议>Nano Science and Technology Institute(NSTI) Nanotechnology Conference and Trade Show(NSTI Nanotech 2006) vol.2 >Shell Cross-Linked Nanoparticle Based on Poly(ε-caprolactone)-Poly(ethylene glycol) for Photosensitizer Delivery
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Shell Cross-Linked Nanoparticle Based on Poly(ε-caprolactone)-Poly(ethylene glycol) for Photosensitizer Delivery

机译:基于聚(ε-己内酯)-聚(乙二醇)的壳交联纳米粒子用于光敏剂的递送

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Polymeric micelles as drug carriers attract highly concern recent years for their ability to incorporate hydrophobic drugs. Photodynamic therapy (PDT) is a promising new cancer treatment that involves the combination of visible light and a photosensitizer. In this study, protoporphyrin IX (PpIX) was encapsulated into shell crosslinked nanoparticles (SCKs) for photosensitizer delivery to reduce the side effects of PDT.The particle size of the SCKs without drug was about 140 nm, and the size of the SCKs with PpIX were about 240 nm. The cytotoxicity reveals that SCKs/PpIX have some toxicity to normal cell line. As shown in the results of fluorescence microscopy and flow cytometry, the uptake of SCKs with PpIX reach the maximum at the incubation time of 12-24 hours. The PDT effects of SCKs/PpIX show no significant differences with free PpIX.In summary, in vitro characterization and in vitro PDT effect of SCKs encapsulated with PpIX were studies. These results may lead to more successful development on the application of SCKs for photodynamic therapy.
机译:高分子胶束作为药物载体,由于其结合疏水性药物的能力而引起了近年来的高度关注。光动力疗法(PDT)是一种有前途的新型癌症疗法,涉及可见光和光敏剂的组合。在这项研究中,原卟啉IX(PpIX)被封装在壳交联的纳米颗粒(SCKs)中用于光敏剂的递送以减少PDT的副作用。无药物的SCKs的粒径约为140 nm,具有PpIX的SCKs的粒径约240nm。细胞毒性表明,SCKs / PpIX对正常细胞系具有一定的毒性。如荧光显微镜和流式细胞术的结果所示,在12-24小时的孵育时间,PpIX对SCK的吸收达到最大。 SCKs / PpIX的PDT效应与游离PpIX没有显着差异。总之,研究了用PpIX封装的SCK的体外表征和体外PDT效应。这些结果可能导致SCKs在光动力治疗中的应用获得更成功的发展。

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