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拓扑异构酶I抑制剂在功能化碳纳米管中的包封与增强递送

Encapsulation and Enhanced Delivery of Topoisomerase I Inhibitors in Functionalized Carbon Nanotubes.

作者信息

Chae Sieun, Kim Dahee, Lee Kyung-Jin, Lee Dasol, Kim Young-O, Jung Yong Chae, Rhee Sang Dal, Kim Kwang Rok, Lee Jeong-O, Ahn Sunjoo, Koh Byumseok

机构信息

Advanced Materials Division and Bio and Drug Discovery Division, Korea Research Institute of Chemical Technology, 141 Gajeong-ro, Yuseong-gu, Daejeon 34114, Republic of Korea.

Institute of Advanced Composite Materials, Korea Institute of Science and Technology, 92 Chudong-ro, Bongdong-eup, Wanju-gun, Jeollabuk-do 55324, Republic of Korea.

出版信息

ACS Omega. 2018 Jun 30;3(6):5938-5945. doi: 10.1021/acsomega.8b00399. Epub 2018 Jun 1.

Abstract

The topoisomerase I inhibitors SN-38 and camptothecin (CPT) have shown potent anticancer activity, but water insolubility and metabolic instability limits their clinical application. Utilizing carbon nanotubes as a protective shell for water-insoluble SN-38 and CPT while maintaining compatibility with aqueous media via a carboxylic acid-functionalized surface can thus be a strategy to overcome this limitation. Through hydrophobic-hydrophobic interactions, SN-38 and CPT were successfully encapsulated in carboxylic acid functionalized single-walled carbon nanotubes and dispersed in water. The resulting cell proliferation inhibition and drug distribution profile inside the cells suggest that these drug-encapsulated carbon nanotubes can serve as a promising delivery strategy for water-insoluble anticancer drugs.

摘要

拓扑异构酶I抑制剂SN-38和喜树碱(CPT)已显示出强大的抗癌活性,但水不溶性和代谢不稳定性限制了它们的临床应用。利用碳纳米管作为水不溶性SN-38和CPT的保护壳,同时通过羧酸官能化表面保持与水性介质的兼容性,因此可以成为克服这一限制的策略。通过疏水-疏水相互作用,SN-38和CPT成功地包裹在羧酸官能化的单壁碳纳米管中并分散在水中。由此产生的细胞增殖抑制和细胞内药物分布情况表明,这些药物包裹的碳纳米管可以作为一种很有前景的水不溶性抗癌药物递送策略。

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