Hyaluronic Acid Receptor-Mediated Nanomedicines and Targeted Therapy

被引:8
作者
Ouyang, Qiuhong [1 ,2 ]
Zhao, Ying [1 ,2 ]
Xu, Kunyao [3 ]
He, Yuechen [1 ,2 ]
Qin, Meng [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Lung Canc Ctr, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Ctr Preclin Safety Evaluat Drugs, Chengdu 610041, Peoples R China
[3] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Beijing 100029, Peoples R China
来源
SMALL METHODS | 2024年 / 8卷 / 10期
关键词
hyaluronic acid; nanomedicines; receptor-targeted delivery; HEPATIC STELLATE CELLS; EXTRACELLULAR-MATRIX; KNEE OSTEOARTHRITIS; MOLECULAR-WEIGHT; DRUG-DELIVERY; NANOPARTICLES; CD44; PROGRESSION; INHIBITION; IMMUNE;
D O I
10.1002/smtd.202400513
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hyaluronic acid (HA) is a naturally occurring polysaccharide found in the extracellular matrix with broad applications in disease treatment. HA possesses good biocompatibility, biodegradability, and the ability to interact with various cell surface receptors. Its wide range of molecular weights and modifiable chemical groups make it an effective drug carrier for drug delivery. Additionally, the overexpression of specific receptors for HA on cell surfaces in many disease states enhances the accumulation of drugs at pathological sites through receptor binding. In this review, the modification of HA with drugs, major receptor proteins, and the latest advances in receptor-targeted nano drug delivery systems (DDS) for the treatment of tumors and inflammatory diseases are summarized. Furthermore, the functions of HA with varying molecular weights of HA in vivo and the selection of drug delivery methods for different diseases are discussed. Hyaluronic acid with multiple modifying groups can be modified by different methods and assembled with drugs to form various types of nanomedicines. Through the targeted binding of HA to receptors overexpressed on the cell surface in inflammatory and tumor microenvironments, the drugs can be delivered precisely to the target site, improving therapeutic efficacy and in vivo safety. image
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页数:30
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共 203 条
  • [1] Endogenous inspired biomineral-installed hyaluronan nanoparticles as pH-responsive carrier of methotrexate for rheumatoid arthritis
    Alam, Md. Mahmudul
    Han, Hwa Seung
    Sung, Shijin
    Kang, Jin Hee
    Sa, Keum Hee
    Al Faruque, Hasan
    Hong, Jungwan
    Nam, Eon Jeong
    Kim, In San
    Park, Jae Hyung
    Kang, Young Mo
    [J]. JOURNAL OF CONTROLLED RELEASE, 2017, 252 : 62 - 72
  • [2] Layer-by-Layer Encapsulation of Probiotics for Delivery to the Microbiome
    Anselmo, Aaron C.
    McHugh, Kevin J.
    Webster, Jamie
    Langer, Robert
    Jaklenec, Ana
    [J]. ADVANCED MATERIALS, 2016, 28 (43) : 9486 - +
  • [3] LYVE-1, a new homologue of the CD44 glycoprotein, is a lymph-specific receptor for hyaluronan
    Banerji, S
    Ni, J
    Wang, SX
    Clasper, S
    Su, J
    Tammi, R
    Jones, M
    Jackson, DG
    [J]. JOURNAL OF CELL BIOLOGY, 1999, 144 (04) : 789 - 801
  • [4] Structures of the Cd44-hyaluronan complex provide insight into a fundamental carbohydrate-protein interaction
    Banerji, Suneale
    Wright, Alan J.
    Noble, Martin
    Mahoney, David J.
    Campbell, Iain D.
    Day, Anthony J.
    Jackson, David G.
    [J]. NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2007, 14 (03) : 234 - 239
  • [5] Distinctive Properties of the Hyaluronan-binding Domain in the Lymphatic Endothelial Receptor Lyve-1 and Their Implications for Receptor Function
    Banerji, Suneale
    Hide, Branwen R. S.
    James, John R.
    Noble, Martin E. M.
    Jackson, David G.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (14) : 10724 - 10735
  • [6] TLR4 signalling
    Bell, Elaine
    [J]. NATURE REVIEWS IMMUNOLOGY, 2008, 8 (04) : 241 - 241
  • [7] Bhattacharya DS, 2017, J MATER CHEM B, V5, P8183, DOI [10.1039/C7TB01895A, 10.1039/c7tb01895a]
  • [8] Layilin, a cell surface hyaluronan receptor, interacts with merlin and radixin
    Bono, P
    Cordero, E
    Johnson, K
    Borowsky, M
    Ramesh, V
    Jacks, T
    Hynes, RO
    [J]. EXPERIMENTAL CELL RESEARCH, 2005, 308 (01) : 177 - 187
  • [9] Macrophage-Targeted Sonodynamic/Photothermal Synergistic Therapy for Preventing Atherosclerotic Plaque Progression Using CuS/TiO2 Heterostructured Nanosheets
    Cao, Zhengyu
    Yuan, Guotao
    Zeng, Lingli
    Bai, Lu
    Liu, Xiao
    Wu, Maoxiong
    Sun, Runlu
    Chen, Zhiteng
    Jiang, Yuan
    Gao, Qingyuan
    Chen, Yangxin
    Zhang, Yuling
    Pan, Yue
    Wang, Jingfeng
    [J]. ACS NANO, 2022, 16 (07) : 10608 - 10622
  • [10] Caruso R, 2020, NAT REV IMMUNOL, V20, P411, DOI [10.1038/s41577-019-0268-7, 10.4161/gmic.20228]