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载熊果酸的聚乙二醇化脂质体的抗肿瘤疗效评价。

An evaluation of the anti-tumor efficacy of oleanolic acid-loaded PEGylated liposomes.

机构信息

Applied Chemical Key Lab of Hebei Province, College of Environmental and Chemical Engineering, Yanshan University, No. 438 Hebei Street, Qinhuangdao 066004, People's Republic of China.

出版信息

Nanotechnology. 2013 Jun 14;24(23):235102. doi: 10.1088/0957-4484/24/23/235102. Epub 2013 May 13.

Abstract

The effective delivery of oleanolic acid (OA) to the target site has several benefits in therapy for different pathologies. However, the delivery of OA is challenging due to its poor aqueous solubility. The study aims to evaluate the tumor inhibition effect of the PEGylated OA nanoliposome on the U14 cervical carcinoma cell line. In our previous study, OA was successfully encapsulated into PEGylated liposome with the modified ethanol injection method. Oral administration of PEGylated OA liposome was demonstrated to be more efficient in inhibiting xenograft tumors. The results of organ index indicated that PEG liposome exhibited higher anti-tumor activity and lower cytotoxicity. It was also found that OA and OA liposomes induced tumor cell apoptosis detected by flow cytometry. Furthermore, effects of OA on the morphology of tumor and other tissues were observed by hematoxylin and eosin staining. The histopathology sections did not show pathological changes in kidney or liver in tested mice. In contrast, there was a significant difference in tumor tissues between treatment groups and the negative control group. These observations imply that PEGylated liposomes seem to have advantages for cancer therapy in terms of effective delivery of OA.

摘要

齐墩果酸(OA)递送至靶部位在治疗多种疾病方面具有多种益处。然而,由于其水溶性差,OA 的递送具有挑战性。本研究旨在评估 PEG 化 OA 纳米脂质体对 U14 宫颈癌细胞系的肿瘤抑制作用。在我们之前的研究中,OA 已成功通过改良乙醇注入法包封入 PEG 化脂质体中。口服 PEG 化 OA 脂质体在抑制异种移植瘤方面更有效。器官指数的结果表明,PEG 脂质体表现出更高的抗肿瘤活性和更低的细胞毒性。还通过流式细胞术检测到 OA 和 OA 脂质体诱导肿瘤细胞凋亡。此外,通过苏木精和伊红染色观察 OA 对肿瘤和其他组织形态的影响。组织病理学切片显示,在受试小鼠中,肾脏或肝脏没有观察到病理变化。相比之下,治疗组与阴性对照组之间的肿瘤组织有显著差异。这些观察结果表明,PEG 化脂质体在 OA 的有效递送上似乎具有癌症治疗的优势。

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