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载 UCNPs 的磷脂酶 A2 响应性磷酸胶束用于前列腺癌细胞的生物成像。

Phospholipase A2-Responsive Phosphate Micelle-Loaded UCNPs for Bioimaging of Prostate Cancer Cells.

机构信息

Department of Chemistry, Changwon National University, Changwon, 641-773, Korea.

出版信息

Sci Rep. 2017 Nov 22;7(1):16073. doi: 10.1038/s41598-017-16136-4.

Abstract

We report the effective synthesis of biocompatible upconversion nanoparticles (UCNP)-loaded phosphate micelles and successful delivery of UCNPs to prostate cancer cells via secreted phospholipase A2 (sPLA-2) enzyme cleavage of the loaded micelles for the first time. The activity of the (sPLA-2) enzyme toward the synthesized micelles was investigated and confirmed by LC-MS. TEM results showed that the micelles have a size distribution of 80 to 150 nm, whereas UCNP-loaded micelles range from 200 to 350 nm, indicating the successful loading of UCNPs. The selective release of UCNPs to prostate cancer cells rather than other cells, specifically cervical cancer cells, was observed and confirmed by a range of bioimaging studies. Moreover, cytotoxicity assays confirmed the biocompatibility of the UCNP-loaded micelles.

摘要

我们首次报道了生物相容性上转换纳米粒子(UCNP)负载的磷酸胶束的有效合成,并通过负载胶束中分泌型磷脂酶 A2(sPLA-2)酶的裂解,成功地将 UCNP 递送至前列腺癌细胞。通过 LC-MS 对合成胶束中 sPLA-2 酶的活性进行了研究和验证。TEM 结果表明,胶束的粒径分布在 80 至 150nm 之间,而负载 UCNP 的胶束粒径在 200 至 350nm 之间,表明 UCNP 的成功负载。通过一系列生物成像研究观察到并证实了 UCNP 优先递送至前列腺癌细胞而不是其他细胞,特别是宫颈癌细胞。此外,细胞毒性试验证实了负载 UCNP 的胶束的生物相容性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc38/5700164/b71d94665412/41598_2017_16136_Fig1_HTML.jpg

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