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Microneedle-Array-Mediated Transdermal Delivery of GCV-Functionalized Zeolitic Imidazolate Framework-8 Nanoparticles for KSHV Treatment
被引:0
|作者:
Liu, Chengjing
[1
]
Yin, Xiuyuan
[2
]
Xu, Huiling
[1
]
Xu, Jianyu
[1
]
Gong, Mengru
[1
]
Li, Zhenzhong
[1
]
Xu, Qianhe
[2
]
Cao, Dongdong
[1
]
Li, Dongmei
[1
]
机构:
[1] Shihezi Univ, Sch Med, Key Lab Xinjiang Endem & Ethn Dis, NHC Key Lab Prevent & Treatment Cent Asia High Inc, Shihezi 832003, Peoples R China
[2] East China Univ Sci & Technol, Sch Chem & Mol Engn, Shanghai Key Lab Funct Mat Chem, Key Lab Adv Mat, Shanghai 200237, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Kaposi's sarcoma-associated herpesvirus;
ganciclovir;
microneedle;
zeolite imidazolate framework-8;
nano-delivery;
GANCICLOVIR;
D O I:
10.3390/ijms252312946
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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.
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