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
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页数:21
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