DNA/Tannic Acid Hybrid Gel Exhibiting Biodegradability, Extensibility, Tissue Adhesiveness, and Hemostatic Ability

被引:304
作者
Shin, Mikyung [1 ]
Ryu, Ji Hyun [1 ,2 ]
Park, Joseph P. [1 ]
Kim, Keumyeon [3 ]
Yang, Jae Wook [4 ]
Lee, Haeshin [1 ,2 ]
机构
[1] Korea Adv Inst Sci & Technol, Grad Sch Nanosci & Technol, Taejon 305701, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Chem, Taejon 305701, South Korea
[3] InnoTherapy, R&D Ctr, Taejon 305731, South Korea
[4] Inje Univ, Coll Med, Pusan Paik Hosp, Dept Ophthalmol, Pusan 614735, South Korea
基金
新加坡国家研究基金会;
关键词
HYALURONIC-ACID; DNA; HYDROGELS; CATECHOL; POLYPHOSPHATE; COAGULATION; COMPLEXES; NETWORKS; POLYMERS; RELEASE;
D O I
10.1002/adfm.201403992
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
DNA has emerged as a novel material in many areas of materials science due to its programmability. Especially, DNA hydrogels have been studied to incorporate new functions into gels. To date, only a few methods have been developed for fabricating DNA hydrogels, such as the use of complementary sequences or covalent bond. Herein, it is demonstrated that one of the most well-known plant-derived polyphenols, tannic acid (TA), can form a DNA hydrogel which is named TNA hydrogel (TA + DNA). TA plays a role as a "molecular glue" by a new mode of action reversibly connecting between phosphodiester bonds, which is different from the crosslinking utilizing complementary sequences. TA intrinsically degrades due to ester bonds connecting between pyrogallol groups, causing a degradable DNA hydrogel. Furthermore, TNA gel is multifunctional in that the gel is extensible upon pulling and adhesive to tissues because of the rich polyphenol groups in TA (ten phenols per TA). Unexpectedly, TNA gel exhibits superior in vivo hemostatic ability that can be useful for biomedical applications. This new DNA hydrogel preparation method represents a new technique for fabricating a large amount of DNA-based hemostatic hydrogel without chemically modifying DNA or requiring the crosslinking by complementary sequences.
引用
收藏
页码:1270 / 1278
页数:9
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