Liu Chengjing, Yin Xiuyuan, Xu Huiling, Xu Jianyu, Gong Mengru, Li Zhenzhong, Xu Qianhe, Cao Dongdong, Li Dongmei
Key Laboratory of Xinjiang Endemic and Ethnic Diseases, NHC Key Laboratory of Prevention and Treatment of Central Asia High Incidence Diseases, School of Medicine, Shihezi University, Shihezi 832003, China.
Shanghai Key Laboratory of Functional Materials Chemistry, Key Laboratory for Advanced Materials, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, China.
Int J Mol Sci. 2024 Dec 2;25(23):12946. doi: 10.3390/ijms252312946.
Kaposi's sarcoma-associated herpesvirus (KSHV) is a variety of the human gamma-herpesvirus that often leads to the occurrence of malignant tumors. In addition, the occurrence of Kaposi's sarcoma is a major cause of death among AIDS patients. Ganciclovir (GCV) is the most widely used drug against KSHV infection in the clinic. GCV can restrict the in vivo synthesis of DNA polymerase in KSHV, thereby inhibiting the replication of the herpesvirus. However, GCV still suffers from poor specificity and transmembrane capabilities, leading to many toxic side effects. Therefore, developing a drug delivery system that increases GCV concentrations in target cells remains a significant clinical challenge. In this study, zeolite imidazole salt framework-8 (ZIF-8), a biocompatible porous material constructed by coordinating zinc ions and 2-methylimidazole, was used to load GCV. A nano-delivery system with a microneedle structure was also constructed using a polydimethylsiloxane (PDMS) microneedle mold to fabricate MN/GCV@ZIF-8 arrays. These arrays not only offered good skin-piercing capabilities but also significantly inhibited the cleavage and replication of the virus in vivo, exerting an anti-KSHV function. For these reasons, the arrays were able penetrate the skin's stratum corneum at the tumor site to deliver GCV and play an anti-KSHV role.
卡波西肉瘤相关疱疹病毒(KSHV)是人类γ-疱疹病毒的一种,常导致恶性肿瘤的发生。此外,卡波西肉瘤的发生是艾滋病患者死亡的主要原因之一。更昔洛韦(GCV)是临床上治疗KSHV感染最常用的药物。GCV可抑制KSHV中DNA聚合酶的体内合成,从而抑制疱疹病毒的复制。然而,GCV的特异性和跨膜能力仍然较差,导致许多毒副作用。因此,开发一种能提高靶细胞内GCV浓度的药物递送系统仍然是一项重大的临床挑战。在本研究中,采用锌离子与2-甲基咪唑配位构建的生物相容性多孔材料沸石咪唑盐骨架-8(ZIF-8)来负载GCV。还使用聚二甲基硅氧烷(PDMS)微针模具构建了具有微针结构的纳米递送系统,以制备MN/GCV@ZIF-8阵列。这些阵列不仅具有良好的皮肤穿刺能力,而且能显著抑制体内病毒的裂解和复制,发挥抗KSHV功能。基于这些原因,该阵列能够穿透肿瘤部位皮肤的角质层来递送GCV并发挥抗KSHV作用。