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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Enhanced transdermal lymphatic delivery of doxorubicin via hyaluronic acid based transfersomes/microneedle complex for tumor metastasis therapy
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Enhanced transdermal lymphatic delivery of doxorubicin via hyaluronic acid based transfersomes/microneedle complex for tumor metastasis therapy

机译:通过透明酸基转移晶体/微针络合物增强多柔枯蛋白的透皮淋巴递送,用于肿瘤转移治疗

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Tumor-draining lymph nodes (TDLN) are major metastatic sites for many solid tumor to support tumor progression and metastasis. Lymphatic delivery is regarded as a desirable route to promote adoptive immune response via vaccination, or to achieve efficient chemotherapy for tumor metastasis. In this study, a novel dissolving microneedle was fabricated using hyaluronic acid, integrated with transfersome (T) to break the limit of trans dermal cargo transit. In virtue of the insertion capacity of microneedle and the lymphatic delivering ability of transfersomes, such transfersome/microneedles complex (T/MNs) was expected to enhance lymphatic delivery. The results revealed that the microneedles were able to efficiently insert into rat skin and release the doxorubicin loaded transfersome (DOX-T) in dermis via self-dissolution. DOX-T would maintain their multilayer structure as released from dissolved microneedles. DOX-T/MN could significantly promote accumulation of DOX in lymph nodes compared to epidermal diffusion, and increased its transdermal bioavailability in plasma The results not only are promising for chemo-therapy of tumor through lymphatic drug delivery, especially for killing the metastasized tumor cells appeared in draining lymph nodes, they also provide an efficient strategy for tumor immune therapy using transdermal administration. (C) 2018 Elsevier B.V. All rights reserved.
机译:肿瘤排出的淋巴结(TDLN)是许多实体瘤的主要转移位点,以支持肿瘤进展和转移。淋巴递送被认为是一种理想的途径,以通过疫苗接种促进过养类免疫应答,或实现肿瘤转移的有效化疗。在该研究中,使用透明质酸制造一种新的溶解微针,与透明质酸一体化,与转噬物组(t)集成,以破坏反式皮质货物运输的极限。借助于微针的插入能力和转移晶体的淋巴输送能力,预期这种椎体组/微针复合物(T / MNS)增强淋巴递送。结果表明,微针能够通过自解溶出将微针能够有效地插入大鼠皮肤中并在真皮中释放多柔比蛋白负载的转移体(DOX-T)。 DOX-T将维持其从溶解的微针释放的多层结构。与表皮扩散相比,DOX-T / MN可以显着促进DOX在淋巴结中的积累,并增加了血浆中的透皮生物利用度,结果不仅对淋巴药物递送进行了化学治疗肿瘤,特别是用于杀死转移肿瘤细胞出现在排出淋巴结中,他们还提供了使用透皮给药的肿瘤免疫治疗的有效策略。 (c)2018年elestvier b.v.保留所有权利。

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