Therapeutic gas-releasing nanomedicines with controlled release: Advances and perspectives

被引:67
作者
Opoku-Damoah, Yaw [1 ]
Zhang, Run [1 ]
Ta, Hang T. [1 ,2 ,3 ]
Xu, Zhi Ping [1 ]
机构
[1] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Brisbane, Qld 4072, Australia
[2] Griffith Univ, Sch Environm & Sci, Brisbane, Qld, Australia
[3] Griffith Univ, Queensland Micro & Nanotechnol Ctr, Brisbane, Qld, Australia
来源
EXPLORATION | 2022年 / 2卷 / 05期
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
gas-releasing molecules; gas-releasing nanomedicines; nanoparticle delivery systems; stimulus-triggered gas release; therapeutic gases; MESOPOROUS SILICA NANOPARTICLES; EXPEDITES METABOLIC EXHAUSTION; UP-CONVERSION NANOPARTICLES; CARBON-MONOXIDE RELEASE; DRUG-DELIVERY SYSTEMS; NITRIC-OXIDE DONORS; HYDROGEN-SULFIDE; SULFUR-DIOXIDE; CATALYTIC GENERATION; PHOTOTHERMAL THERAPY;
D O I
10.1002/EXP.20210181
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nanoparticle-based drug delivery has become one of the most popular approaches for maximising drug therapeutic potentials. With the notable improvements, a greater challenge hinges on the formulation of gasotransmitters with unique challenges that are not met in liquid and solid active ingredients. Gas molecules upon release from formulations for therapeutic purposes have not really been discussed extensively. Herein, we take a critical look at four key gasotransmitters, that is, carbon monoxide (CO), nitric oxide (NO), hydrogen sulphide (H2S) and sulphur dioxide (SO2), their possible modification into prodrugs known as gas-releasing molecules (GRMs), and their release from GRMs. Different nanosystems and their mediatory roles for efficient shuttling, targeting and release of these therapeutic gases are also reviewed extensively. This review thoroughly looks at the diverse ways in which these GRM prodrugs in delivery nanosystems are designed to respond to intrinsic and extrinsic stimuli for sustained release. In this review, we seek to provide a succinct summary for the development of therapeutic gases into potent prodrugs that can be adapted in nanomedicine for potential clinical use.
引用
收藏
页数:21
相关论文
共 192 条
[111]   Macromolecular and Inorganic Nanomaterials Scaffolds for Carbon Monoxide Delivery: Recent Developments and Future Trends [J].
Nguyen, Diep ;
Boyer, Cyrille .
ACS BIOMATERIALS SCIENCE & ENGINEERING, 2015, 1 (10) :895-913
[112]   A glutathione responsive nitric oxide release system based on charge-reversal chitosan nanoparticles for enhancing synergistic effect against multidrug resistance tumor [J].
Niu, Xiaoyan ;
Cao, Jing ;
Zhang, Yapei ;
Gao, Xuefeng ;
Cheng, Mingbo ;
Liu, Yang ;
Wang, Wei ;
Yuan, Zhi .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2019, 20
[113]   Spontaneous catalytic generation of nitric oxide from S-nitrosothiols at the surface of polymer films doped with lipophilic copper(II) complex [J].
Oh, BK ;
Meyerhoff, ME .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (32) :9552-9553
[114]   Vitamin E-facilitated carbon monoxide pro-drug nanomedicine for efficient light-responsive combination cancer therapy [J].
Opoku-Damoah, Yaw ;
Zhang, Run ;
Ta, Hang T. ;
Xu, Zhi Ping .
BIOMATERIALS SCIENCE, 2021, 9 (18) :6086-6097
[115]   Lipid-encapsulated upconversion nanoparticle for near-infrared light-mediated carbon monoxide release for cancer gas therapy [J].
Opoku-Damoah, Yaw ;
Zhang, Run ;
Ta, Hang T. ;
Jose, D. Amilan ;
Sakla, Rahul ;
Xu, Zhi Ping .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2021, 158 :211-221
[116]   Functional Diagnostic and Therapeutic Nanoconstructs for Efficient Probing of Circulating Tumor Cells [J].
Opoku-Damoah, Yaw ;
Assanhou, Assogba G. ;
Sooro, Mopa A. ;
Baduweh, Cynthia A. ;
Sun, Chunmeng ;
Ding, Yang .
ACS APPLIED MATERIALS & INTERFACES, 2018, 10 (17) :14231-14247
[117]   Versatile Nanosystem-Based Cancer Theranostics: Design Inspiration and Predetermined Routing [J].
Opoku-Damoah, Yaw ;
Wang, Ruoning ;
Zhou, Jianping ;
Ding, Yang .
THERANOSTICS, 2016, 6 (07) :986-1003
[118]   Carbon monoxide has anti-inflammatory effects involving the mitogen-activated protein kinase pathway [J].
Otterbein, LE ;
Bach, FH ;
Alam, J ;
Soares, M ;
Lu, HT ;
Wysk, M ;
Davis, RJ ;
Flavell, RA ;
Choi, AMK .
NATURE MEDICINE, 2000, 6 (04) :422-428
[119]   Core-shell materials bearing iron(II) carbonyl units and their CO-release via an upconversion process [J].
Ou, Jun ;
Zheng, Weihua ;
Xiao, Zhiyin ;
Yan, Yuping ;
Jiang, Xiujuan ;
Dou, Yong ;
Jiang, Ran ;
Liu, Xiaoming .
JOURNAL OF MATERIALS CHEMISTRY B, 2017, 5 (41) :8161-8168
[120]   NITRIC-OXIDE RELEASE ACCOUNTS FOR THE BIOLOGICAL-ACTIVITY OF ENDOTHELIUM-DERIVED RELAXING FACTOR [J].
PALMER, RMJ ;
FERRIGE, AG ;
MONCADA, S .
NATURE, 1987, 327 (6122) :524-526