DNA-Based Nanomaterials as Drug Delivery Platforms for Increasing the Effect of Drugs in Tumors

被引:19
作者
Shishparenok, Anastasiya N. N. [1 ]
Furman, Vitalina V. V. [2 ]
Zhdanov, Dmitry D. D. [1 ,3 ]
机构
[1] Inst Biomed Chem, Lab Med Biotechnol, Pogodinskaya St 10-8, Moscow 119121, Russia
[2] ITMO Univ, Ctr Chem Engn, Kronverkskiy Prospekt 49A, St Petersburg 197101, Russia
[3] Peoples Friendship Univ Russia, RUDN Univ, Dept Biochem, Miklukho Maklaya St 6, Moscow 117198, Russia
关键词
DNA-based nanomaterials; tetrahedron; origami; nanotube; aptamer; drug delivery; endocytosis; MESOPOROUS SILICA NANOPARTICLES; APTAMER-CONJUGATED LIPOSOME; IRON-OXIDE NANOPARTICLES; PROSTATE-CANCER CELLS; BREAST-CANCER; TARGETED DELIVERY; IN-VITRO; RNA APTAMER; CD133; APTAMERS; ORIGAMI NANOSTRUCTURES;
D O I
10.3390/cancers15072151
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
DNA nanotechnology has significantly advanced and might be used in biomedical applications, drug delivery, and cancer treatment during the past few decades. DNA nanomaterials are widely used in biomedical research involving biosensing, bioimaging, and drug delivery since they are remarkably addressable and biocompatible. Gradually, modified nucleic acids have begun to be employed to construct multifunctional DNA nanostructures with a variety of architectural designs. Aptamers are single-stranded nucleic acids (both DNAs and RNAs) capable of self-pairing to acquire secondary structure and of specifically binding with the target. Diagnosis and tumor therapy are prospective fields in which aptamers can be applied. Many DNA nanomaterials with three-dimensional structures have been studied as drug delivery systems for different anticancer medications or gene therapy agents. Different chemical alterations can be employed to construct a wide range of modified DNA nanostructures. Chemically altered DNA-based nanomaterials are useful for drug delivery because of their improved stability and inclusion of functional groups. In this work, the most common oligonucleotide nanomaterials were reviewed as modern drug delivery systems in tumor cells.
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页数:58
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