Author:
Sheikhpour Mojgan,Delorme Vincent,Kasaeian Alibakhsh,Amiri Vahid,Masoumi Morteza,Sadeghinia Mohammad,Ebrahimzadeh Nayereh,Maleki Mobina,Pourazar Shahin
Abstract
AbstractDrug resistance in tuberculosis is exacerbating the threat this disease is posing to human beings. Antibiotics that were once effective against the causative agent, Mycobacterium tuberculosis (Mtb), are now no longer usable against multi- and extensively drug-resistant strains of this pathogen. To address this issue, new drug combinations and novel methods for targeted drug delivery could be of considerable value. In addition, studies have shown that the use of the antidepressant drug fluoxetine, a serotonin reuptake inhibitor, can be useful in the treatment of infectious diseases, including bacterial infections. In this study, an isoniazid and fluoxetine-conjugated multi-walled carbon nanotube nanofluid were designed to increase drug delivery efficiency alongside eliminating drug resistance in vitro. The prepared nanofluid was tested against Mtb. Expression levels of inhA and katG mRNAs were detected by Real-time PCR. ELISA was applied to measure levels of cytokine secretion (TNF-α, and IL-6) from infected macrophages treated with the nano delivery system. The results showed that these nano-drug delivery systems are effective for fluoxetine at far lower doses than for free drugs. Fluoxetine also has an additive effect on the effect of isoniazid, and their concomitant use in the delivery system can have significant effects in treating infection of all clinical strains of Mtb. In addition, it was found that the expression of isoniazid resistance genes, including inhA, katG, and the secretion of cytokines TNFα and IL6 under the influence of this drug delivery system is well regulated. It was shown that the drug conjugation can improve the antibacterial activity of them in all strains and these two drugs have an additive effect on each other both in free and conjugated forms. This nano-drug delivery method combined with host targeted molecules could be a game-changer in the development of a new generation of antibiotics that have high therapeutic efficiencies, low side effects, and the potential to overcome the problem of drug resistance.
Publisher
Springer Science and Business Media LLC
Reference43 articles.
1. WHO. Global Tuberculosis Report. 2020. (2020).
2. Mabhula, A. & Singh, V. Drug-resistance in Mycobacterium tuberculosis: where we stand. MedChemComm 10, 1342–1360 (2019).
3. Saifullah, B., Hussein, M. Z. B. & Al Ali, S. H. H. Controlled-release approaches towards the chemotherapy of tuberculosis. Int. J. Nanomed. 7, 5451 (2012).
4. Tafazoli, S., Mashregi, M. & O’Brien, P. J. Role of hydrazine in isoniazid-induced hepatotoxicity in a hepatocyte inflammation model. Toxicol. Appl. Pharmacol. 229, 94–101 (2008).
5. Saifullah, B. et al. Development of a biocompatible nanodelivery system for tuberculosis drugs based on isoniazid-Mg/Al layered double hydroxide. Int. J. Nanomed. 9, 4749 (2014).
Cited by
18 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献