siRNA Conjugate Delivery Systems

被引:282
作者
Jeong, Ji Hoon [2 ]
Mok, Hyejung [1 ]
Oh, Yu-Kyoung [3 ]
Park, Tae Gwan [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
[2] Sungkyunkwan Univ, Coll Pharm, Suwon 440746, South Korea
[3] Korea Univ, Sch Life Sci & Biotechnol, Seoul, South Korea
关键词
POLYELECTROLYTE COMPLEX MICELLES; CELL-PENETRATING PEPTIDES; SMALL INTERFERING RNA; POLY(ETHYLENE GLYCOL)-SIRNA CONJUGATE; TAT-DEPENDENT TRANSACTIVATION; CATIONIC FUSOGENIC PEPTIDE; CULTURED-MAMMALIAN-CELLS; INNATE IMMUNE-RESPONSE; TARGETING IN-VIVO; INTRACELLULAR DELIVERY;
D O I
10.1021/bc800278e
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Small interfering RNA (siRNA) has been chemically conjugated to a variety of bioactive molecules, lipids, polymers, peptides, and inorganic nanostructured materials to enhance their pharmacokinetic behavior, cellular uptake, target specificity, and safety. To efficiently deliver siRNAs to the target cells and tissues, many different siRNA bioconjugates were synthesized and characterized, and their gene silencing efficiencies were tested in vitro and in vivo. In this review, recent developments of siRNA bioconjugates are summarized.
引用
收藏
页码:5 / 14
页数:10
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