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基于 - 乙酰神经氨酸的合成两亲分子的自组装选择性抗癌材料。

Selective Anticancer Materials by Self-Assembly of Synthetic Amphiphiles Based on -Acetylneuraminic Acid.

机构信息

KU-KIST Graduate School of Converging Science and Technology, Department of Integrative Energy Engineering, Korea University, Seoul 02841, Republic of Korea.

Pohang Accelerator Laboratory, Postech, Gyeongbuk 790-784, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2022 Apr 13;14(14):16100-16107. doi: 10.1021/acsami.2c02922. Epub 2022 Apr 4.

Abstract

-Acetylneuraminic acid (Neu5Ac), one of the abundant types of sialic acid, is an emerging anticancer agent owing to its ability to target selectins in the plasma membrane of cancer cells. Considering the functionality of Neu5Ac, obtaining novel Neu5Ac-conjugated materials with a selective and an enhanced antitumor activity has remained a challenge. Herein, we report the supramolecular materials of three novel amphiphiles composed of Neu5Ac as a hydrophilic segment and pyrene or adamantane as a hydrophobic segment. The synthetic amphiphiles , , and self-assembled into ribbons, vesicles, and irregular aggregates in an aqueous solution, respectively. Among the materials, vesicles of amphiphile showed the most substantial selectivity toward cancer cells, followed by cell death due to the production of reactive oxygen species by the pyrene group. The dual advantage of Neu5Ac-selectivity and the pyrene-cytotoxicity of vesicles of amphiphile can provide a strategy for effective anticancer materials.

摘要

乙酰神经氨酸(Neu5Ac)是唾液酸的丰富类型之一,由于其能够靶向癌细胞质膜中的选择素,因此成为一种新兴的抗癌药物。考虑到 Neu5Ac 的功能,获得具有选择性和增强抗肿瘤活性的新型 Neu5Ac 缀合物材料仍然是一个挑战。在此,我们报告了三种新型两亲物的超分子材料,它们由 Neu5Ac 作为亲水部分和芘或金刚烷作为疏水部分组成。在水溶液中,合成的两亲物 、 和 分别自组装成带状物、囊泡和不规则聚集体。在这些材料中,两亲物 的囊泡对癌细胞表现出最强的选择性,随后由于芘基团产生活性氧而导致细胞死亡。两亲物囊泡的 Neu5Ac 选择性和芘细胞毒性的双重优势可为有效抗癌材料提供一种策略。

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