Bioinspired and self-restorable alginate-tyramine hydrogels with plasma reinforcement for arthritis treatment

被引:9
|
作者
Chen, Yu-Ming [1 ]
Wong, Chin-Chean [2 ,3 ,4 ,5 ]
Weng, Pei-Wei [1 ,2 ,3 ,4 ,5 ]
Chiang, Chih-Wei [6 ]
Lin, Po-Yen [7 ]
Lee, Po-Wei
Jheng, Pei-Ru [1 ]
Hao, Ping-Chien [1 ]
Chen, Yan-Ting [1 ]
Cho, Er-Chen [1 ]
Chuang, Er-Yuan [1 ,8 ]
机构
[1] Taipei Med Univ, Grad Inst Nanomed & Med Engn, Coll Biomed Engn, Int PhD Program Biomed Engn,Grad Inst Biomed Mat &, Taipei 11031, Taiwan
[2] Taipei Med Univ, Shuang Ho Hosp, Dept Orthoped, New Taipei 23561, Taiwan
[3] Taipei Med Univ, Coll Med, Sch Med, Dept Orthoped, Taipei 11031, Taiwan
[4] Taipei Med Univ, Res Ctr Biomed Devices, Taipei 11031, Taiwan
[5] Taipei Med Univ, Coll Med, Int PhD Program Cell Therapy & Regenerat Med, Taipei 11031, Taiwan
[6] Taipei Med Univ, Taipei Med Univ Hosp, Bone & Joint Res Ctr, Dept Orthoped,Sch Med,Coll Med, Taipei, Taiwan
[7] BioGend Therapeut Co, New Taipei 23561, Taiwan
[8] Taipei Med Univ, Wan Fang Hosp, Cell Physiol & Mol Image Res Ctr, Taipei 11696, Taiwan
关键词
Self-restorable alginate-tyramine hydrogel; Immunomodulation; Arthritis treatment; PLATELET-RICH PLASMA; MECHANICAL-PROPERTIES; CARBOXYLIC-ACIDS; THERAPY; PROTEIN; AMINES; TISSUE; GEL;
D O I
10.1016/j.ijbiomac.2023.126105
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
Long-standing administration of disease-modifying antirheumatic drugs confirms their clinical value for managing rheumatoid arthritis (RA). Nevertheless, there are emergent worries over unwanted adverse risks of systemic drug administration. Hence, a novel strategy that can be used in a drug-free manner while diminishing side effects is immediately needed, but challenges persist in the therapy for RA. To this end, herein we conjugated tyramine (TYR) with alginate (ALG) to form ALG-TYR and then treated it for 5 min with oxygen plasma (ALGTYR + P/5 min). It was shown that the ALG-TYR + P/5 min hydrogel exhibited favorable viscoelastic, morphological, mechanical, biocompatible, and cellular heat-shock protein amplification behaviors. A thorough physical and structural analysis was conducted on the ALG-TYR + P/5 min hydrogel, revealing favorable physical characteristics and uniform porous structural features within the hydrogel. Moreover, ALG-TYR + P/5 min not only effectively inhibited inflammation of RA but also potentially regulated lesion immunity. Once ALGTYR + P/5 min was intra-articularly administered to joints of rats with zymosan-induced arthritis, we observed that ALG-TYR + P/5 min could ameliorate syndromes of RA joint. This bioinspired and self-restorable ALG-TYR + P/5 min hydrogel can thus serve as a promising system to provide prospective outcomes to potentiate RA therapy.
引用
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页数:16
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