TY - JOUR
T1 - Novel Strategy for Optimized Nanocatalytic Tumor Therapy
T2 - From an Updated View
AU - Li, Zhen Li
AU - Wu, Han
AU - Zhu, Jia Qi
AU - Sun, Li Yang
AU - Tong, Xiang Min
AU - Huang, Dong Sheng
AU - Yang, Tian
N1 - Publisher Copyright:
© 2022 The Authors. Small Science published by Wiley-VCH GmbH.
PY - 2022/7
Y1 - 2022/7
N2 - Nanozyme has been experiencing rapid development in biomedical applications involving biosensors, immunoassays, and antitumor agents in recent years due to its tunable catalytic performance and desirable biocompatibility. Since the first exploration of nanozyme-based Fenton reaction for nanocatalytic therapy (NCT) against tumor, a variety of Fenton (and Fenton-like) nanozymes, such as Fe3O4, transition metal ions (Co2+, Cu2+, and Mn2+), and metal–organic frameworks (MOFs), have been proved as desirable candidates for tumor therapy, and the modulation of the tumor microenvironment (TME) is determined to be a feasible approach to improve the catalytic efficiency for in situ tumor suppression. At present, increasing studies have focused on improving the therapeutic efficiency of NCT by formulating multifunctional nanozyme-based systems to satisfy the demand for versatile and optimized applications. Herein, updated insights into the novel strategies of 1) achieving highly effective nanocatalytic reactions, including the modification of nanocatalysts and TME-modulating approaches, are provided and 2) the design and formulation of multifunctional nanozyme-based systems which achieve targeted, synergistic therapy, and theranostic applications are analyzed and concluded. Concise and concentrated comments and outlooks are illuminated at the end to outline the perspectives and the remaining challenges for the next-step explorations on further biomedical translation of NCT.
AB - Nanozyme has been experiencing rapid development in biomedical applications involving biosensors, immunoassays, and antitumor agents in recent years due to its tunable catalytic performance and desirable biocompatibility. Since the first exploration of nanozyme-based Fenton reaction for nanocatalytic therapy (NCT) against tumor, a variety of Fenton (and Fenton-like) nanozymes, such as Fe3O4, transition metal ions (Co2+, Cu2+, and Mn2+), and metal–organic frameworks (MOFs), have been proved as desirable candidates for tumor therapy, and the modulation of the tumor microenvironment (TME) is determined to be a feasible approach to improve the catalytic efficiency for in situ tumor suppression. At present, increasing studies have focused on improving the therapeutic efficiency of NCT by formulating multifunctional nanozyme-based systems to satisfy the demand for versatile and optimized applications. Herein, updated insights into the novel strategies of 1) achieving highly effective nanocatalytic reactions, including the modification of nanocatalysts and TME-modulating approaches, are provided and 2) the design and formulation of multifunctional nanozyme-based systems which achieve targeted, synergistic therapy, and theranostic applications are analyzed and concluded. Concise and concentrated comments and outlooks are illuminated at the end to outline the perspectives and the remaining challenges for the next-step explorations on further biomedical translation of NCT.
KW - cancer therapy
KW - nanocatalytic therapy
KW - nanozymes
UR - http://www.scopus.com/inward/record.url?scp=85162231157&partnerID=8YFLogxK
U2 - 10.1002/smsc.202200024
DO - 10.1002/smsc.202200024
M3 - Review article
AN - SCOPUS:85162231157
SN - 2688-4046
VL - 2
JO - Small Science
JF - Small Science
IS - 7
M1 - 2200024
ER -