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Smart Stimuli-responsive Drug Delivery Systems in Spotlight of COVID-19

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Date 2024 Jan 4
PMID 38173712
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Abstract

The world has been dealing with a novel severe acute respiratory syndrome (SARS-CoV-2) since the end of 2019, which threatens the lives of many people worldwide. COVID-19 causes respiratory infection with different symptoms, from sneezing and coughing to pneumonia and sometimes gastric symptoms. Researchers worldwide are actively developing novel drug delivery systems (DDSs), such as stimuli-responsive DDSs. The ability of these carriers to respond to external/internal and even multiple stimuli is essential in creating "smart" DDS that can effectively control dosage, sustained release, individual variations, and targeted delivery. To conduct a comprehensive literature survey for this article, the terms "Stimuli-responsive", "COVID-19″ and "Drug delivery" were searched on databases/search engines like "Google Scholar", "NCBI", "PubMed", and "Science Direct". Many different types of DDSs have been proposed, including those responsive to various exogenous (light, heat, ultrasound and magnetic field) or endogenous (microenvironmental changes in pH, ROS and enzymes) stimuli. Despite significant progress in DDS research, several challenging issues must be addressed to fill the gaps in the literature. Therefore, this study reviews the drug release mechanisms and applications of endogenous/exogenous stimuli-responsive DDSs while also exploring their potential with respect to COVID-19.

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References
1.
Alamdari D, Bagheri Moghaddam A, Amini S, Keramati M, Zarmehri A, Alamdari A . Application of methylene blue -vitamin C -N-acetyl cysteine for treatment of critically ill COVID-19 patients, report of a phase-I clinical trial. Eur J Pharmacol. 2020; 885:173494. PMC: 7440159. DOI: 10.1016/j.ejphar.2020.173494. View

2.
Dou Y, Li C, Li L, Guo J, Zhang J . Bioresponsive drug delivery systems for the treatment of inflammatory diseases. J Control Release. 2020; 327:641-666. PMC: 7476894. DOI: 10.1016/j.jconrel.2020.09.008. View

3.
Poole K, Nelson C, Joshi R, Martin J, Gupta M, Haws S . ROS-responsive microspheres for on demand antioxidant therapy in a model of diabetic peripheral arterial disease. Biomaterials. 2014; 41:166-75. PMC: 4274772. DOI: 10.1016/j.biomaterials.2014.11.016. View

4.
Cui Z, Phoeung T, Rousseau P, Rydzek G, Zhang Q, Bazuin C . Nonphospholipid fluid liposomes with switchable photocontrolled release. Langmuir. 2014; 30(36):10818-25. DOI: 10.1021/la502131h. View

5.
Issa B, Obaidat I, Albiss B, Haik Y . Magnetic nanoparticles: surface effects and properties related to biomedicine applications. Int J Mol Sci. 2013; 14(11):21266-305. PMC: 3856004. DOI: 10.3390/ijms141121266. View