Multifunctional hydrogels based on chitosan, hyaluronic acid and other biological macromolecules for the treatment of inflammatory bowel disease: A review

被引:89
作者
Ouyang, Yongliang [1 ]
Zhao, Jiulong [2 ]
Wang, Shige [1 ]
机构
[1] Univ Shanghai Sci & Technol, Sch Mat & Chem, 516 Jungong Rd, Shanghai 200093, Peoples R China
[2] Naval Med Univ, Changhai Hosp, Dept Gastroenterol, 168 Changhai Rd, Shanghai 200433, Peoples R China
关键词
Multifunctional hydrogels; Inflammatory bowel disease; Chitosan; Hyaluronic acid; Biological macromolecules; MESOPOROUS SILICA NANOPARTICLES; NEGATIVELY CHARGED LIPOSOMES; REGULATORY T-CELLS; DRUG-DELIVERY; ULCERATIVE-COLITIS; OXIDATIVE STRESS; COLONIC-MUCOSA; ORAL DELIVERY; THERAPY; PATHOGENESIS;
D O I
10.1016/j.ijbiomac.2022.12.032
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
Hydrogel is a three-dimensional network polymer material rich in water. It is widely used in the biomedical field because of its unique physical and chemical properties and good biocompatibility. In recent years, the incidence of inflammatory bowel disease (IBD) has gradually increased, and the disadvantages caused by traditional drug treatment of IBD have emerged. Therefore, there is an urgent need for new treatments to alleviate IBD. Hydrogel has become a potential therapeutic platform. However, there is a lack of comprehensive review of functional hydrogels for IBD treatment. This paper first summarizes the pathological changes in IBD sites. Then, the action mechanisms of hydrogels prepared from chitosan, sodium alginate, hyaluronic acid, functionalized polyethylene glycol, cellulose, pectin, and gamma-polyglutamic acid on IBD were described from aspects of drug delivery, peptide and protein delivery, biologic therapies, loading probiotics, etc. In addition, the advanced functions of IBD treatment hydrogels were summarized, with emphasis on adhesion, synergistic therapy, pH sensitivity, particle size, and temperature sensitivity. Finally, the future development direction of IBD treatment hydrogels has been prospected.
引用
收藏
页码:505 / 523
页数:19
相关论文
共 191 条
[11]   Crohn's disease [J].
Baumgart, Daniel C. ;
Sandborn, William J. .
LANCET, 2012, 380 (9853) :1590-1605
[12]   Can inflammatory bowel disease be permanently treated with short-term interventions on the microbiome? [J].
Berg, Dana ;
Clemente, Jose C. ;
Colombel, Jean-Frederic .
EXPERT REVIEW OF GASTROENTEROLOGY & HEPATOLOGY, 2015, 9 (06) :781-795
[13]   Thiomers:: A new generation of mucoadhesive polymers [J].
Bernkop-Schnürch, A .
ADVANCED DRUG DELIVERY REVIEWS, 2005, 57 (11) :1569-1582
[14]   Preclinical Evidence for the Pharmacological Actions of Naringin: A Review [J].
Bharti, Saurabh ;
Rani, Neha ;
Krishnamurthy, Bhaskar ;
Arya, Dharamvir Singh .
PLANTA MEDICA, 2014, 80 (06) :437-451
[15]   OXIDATIVE STRESS: AN ESSENTIAL FACTOR IN THE PATHOGENESIS OF GASTROINTESTINAL MUCOSAL DISEASES [J].
Bhattacharyya, Asima ;
Chattopadhyay, Ranajoy ;
Mitra, Sankar ;
Crowe, Sheila E. .
PHYSIOLOGICAL REVIEWS, 2014, 94 (02) :329-354
[16]   Development and Characterization of a New Endoscopic Drug-Eluting Platform With Proven Efficacy in Acute and Chronic Experimental Colitis [J].
Bon, Ignacio ;
Cano-Sarabia, Mary ;
de la Ossa, Napoleon ;
Bartoli, Ramon ;
Lorenzo-Zuniga, Vicente .
FRONTIERS IN MEDICINE, 2020, 7
[17]   Thiomers - From bench to market [J].
Bonengel, Sonja ;
Bernkop-Schnuerch, Andreas .
JOURNAL OF CONTROLLED RELEASE, 2014, 195 :120-129
[18]   Crohn's disease: Th1, Th17 or both? The change of a paradigm: new immunological and genetic insights implicate Th17 cells in the pathogenesis of Crohn's disease [J].
Brand, S. .
GUT, 2009, 58 (08) :1152-1167
[19]   Lipid mediator-induced expression of bactericidal/permeability-increasing protein (BPI) in human mucosal epithelia [J].
Canny, G ;
Levy, O ;
Furuta, GT ;
Narravula-Alipati, S ;
Sisson, RB ;
Serhan, CN ;
Colgan, SP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (06) :3902-3907
[20]   IGF-1C hydrogel improves the therapeutic effects of MSCs on colitis in mice through PGE2-mediated M2 macrophage polarization [J].
Cao, Xiaocang ;
Duan, Liyun ;
Hou, Huixing ;
Liu, Yue ;
Chen, Shang ;
Zhang, Shuaiqiang ;
Liu, Yuanyuan ;
Wang, Chen ;
Qi, Xin ;
Liu, Na ;
Han, Zhibo ;
Zhang, Dekui ;
Han, Zhong-Chao ;
Guo, Zhikun ;
Zhao, Qiang ;
Li, Zongji .
THERANOSTICS, 2020, 10 (17) :7697-7709