Literature DB >> 32589055

Vesicular drug delivery systems as theranostics in COVID-19.

Saurabh Satija1,2, Meenu Mehta1,2,3, Mousmee Sharma4, Parteek Prasher5, Gaurav Gupta6, Dinesh K Chellappan7, Kamal Dua1,3,8,9.   

Abstract

Entities:  

Keywords:  COVID-19; theranostics; vesicular drug delivery

Mesh:

Substances:

Year:  2020        PMID: 32589055      PMCID: PMC7319496          DOI: 10.4155/fmc-2020-0149

Source DB:  PubMed          Journal:  Future Med Chem        ISSN: 1756-8919            Impact factor:   3.808


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The World Health Organization (WHO) had announced the outbreak of coronavirus disease 2019 (COVID-19) as a pandemic on 11 March 2020. With the entire world reeling under the prodigious attack of the pandemic in collosal proportions, various strategies were designed to nullify the transmission, but with little success. Preventive measures, namely social distancing, sealing off large towns, closing borders and confining people to their homes were strategically implemented. Inspite of these, the transmission rates grew unabated. Adding fuel to fire, the lack of effective antiviral drugs and vaccine further worsened the scenario. Although, therapeutic strategies, namely repurposing drugs, adopting alternative or complementary systems and providing symptomatic treatment have, to a lesser extent helped, but the menace is largely rampant [1-3]. These factors have made it imperative for the urgent need of developing an effective ‘all-in-one package’ option having both diagnostics and therapeutics as a combined treatment approach. Such a theranostic approach could be a promising tool in combating the novel corona virus. Theranostics is a diagnostic imaging technique that determines the target receptors that are present on a cell, and subsequently allows the receptors to be treated with an effective radiation therapy. In the antiviral theranostic approach, radiopharmaceuticals are largely used to identify and diagnose combination therapies that may prevent virus replication [4,5]. Recent data have revealed that theranostic drug therapies with chloroquine have effectively inhibited the 2019 novel coronavirus in vitro. Wang et al. tested the virus inhibition potential with another notable theranostic antiviral agent, penciclovir which demonstrated potent antiviral behavior. These findings have further strengthened and supported the need to develop newer technologies such as theranostics. This technology will also allow viral cell interaction monitoring and evaluation, employing clinical imaging when using its therapeutic potential alone or in combination with other antiviral drugs [6-8] as a co-delivery strategy. A study involving fast, responsive lateral flow immunoassay was conducted by Chen et al. to detect the anti-SRV-CoV-2 IgG in human serum using lanthanide-doped polysterene nanoparticles that could be further helpful in tracking the COVID-19 progression. Moreover, this assay will also help in assessing patient's treatment response [9]. Vesicular drug-delivery systems have been progressively employed as co-delivery tools for personalized theranostics that combine diagnostic, prognostic therapeutic and image-guided therapeutic effects [10]. Multifunctional- and multimodality-based theranostic techniques that employ vesicular drug-delivery systems are urgently needed to be developed for simultaneous imaging of the COVID-19 etiology. Vesicular-delivery systems provide a flexible framework in which different diagnostic agent types could be effectively transported. These nanostructures composed of liposomes, polymersomes, nanoparticles such as gold nanoparticles and peptide-based vesicles have potential therapeutic properties that are essential for the development of effective nanomedicines [11-14]. In addition, it is well reported that nanomedicine formulations such as extracellular vesicles might improve the activity of antiviral medicines. The fate of such encapsulated drugs may also be affected by nanoparticles, which allow controlled release kinetics, enhanced bioavailability, improved pharmacokinetics, reduced side effects and maximal patient compliance [15]. Furthermore, the unique physicochemical properties of nanocarriers could assist in targeting specific sites that could enable interaction with viral structures. Nanomedicines are also reported to possess the ability to enhance the antiviral therapeutic index [16,17]. To introduce this innovative approach at the clinical level, certain factors namely quality, impact on health and manufacturing issues have to be carefully evaluated [16]. In the medical sector, the applications of vesicular-delivery systems will prove to be very promising, especially in the development of new therapeutic and diagnostic approaches to COVID-19 [18]. Theranostics with vesicular-delivery systems can further offer innovative solutions to combat future coronavirus outbreak. Currently, there are no specific antiviral treatments that are available for COVID-19. However, previously developed medicines for the treatment of other viral infections along with several anti-malarial drugs are being tested for their efficacy against COVID-19 virus. As stated earlier, clinical studies are underway to determine the effectiveness and safety of several drugs such as chloroquine, arbidol, remdesivir and favipiravir [19]. As a futuristic approach, these drugs can be used with vesicular-delivery systems with a theranostic strategy in developing novel COVID-19 treatment regimens.

Conclusion

As the epidemic continues to spread, researchers worldwide are actively researching on drugs that could be successful in the battle against COVID-19. Currently, there are no clinically confirmed antiviral treatment options. However, several drugs are now being clinically tested like chloroquine, arbidol, remdesivir and favipiravir that can be targeted with the application of theranostics embedded into vesicular-delivery systems. The effectiveness, preciseness and safety of such advanced technologies have been documented before, nevertheless, further preclinical and clinical trials would validate the applications of these techniques in the treatment of COVID-19.
  6 in total

1.  Biomarking and Induction of Apoptosis in Ovarian Cancer Using Bifunctional Polyethyleneimine-Caged Platinum Nanoclusters.

Authors:  Mengjun Zhang; Haodi Yue; Yuan Liu; Hao Li; Yue Yin; Zhenxing Sun; Ping Cui; Fei Li; Xiuwei Chen; Xin Huang
Journal:  Front Oncol       Date:  2022-06-03       Impact factor: 5.738

2.  Advanced drug delivery systems can assist in targeting coronavirus disease (COVID-19): A hypothesis.

Authors:  Meenu Mehta; Parteek Prasher; Mousmee Sharma; Madhur D Shastri; Navneet Khurana; Manish Vyas; Harish Dureja; Gaurav Gupta; Krishnan Anand; Saurabh Satija; Dinesh Kumar Chellappan; Kamal Dua
Journal:  Med Hypotheses       Date:  2020-09-10       Impact factor: 1.538

3.  Advanced drug delivery systems can assist in managing influenza virus infection: A hypothesis.

Authors:  Yinghan Chan; Sin Wi Ng; Meenu Mehta; Krishnan Anand; Sachin Kumar Singh; Gaurav Gupta; Dinesh Kumar Chellappan; Kamal Dua
Journal:  Med Hypotheses       Date:  2020-09-24       Impact factor: 1.538

Review 4.  Mesenchymal stem cell alongside exosomes as a novel cell-based therapy for COVID-19: A review study.

Authors:  Meruyert Dauletova; Hafsan Hafsan; Negah Mahhengam; Angelina Olegovna Zekiy; Majid Ahmadi; Homayoon Siahmansouri
Journal:  Clin Immunol       Date:  2021-03-06       Impact factor: 10.190

Review 5.  Concepts of advanced therapeutic delivery systems for the management of remodeling and inflammation in airway diseases.

Authors:  Daljeet Singh Dhanjal; Parvarish Sharma; Meenu Mehta; Murtaza M Tambuwala; Parteek Prasher; Keshav R Paudel; Gang Liu; Shakti D Shukla; Philip M Hansbro; Dinesh Kumar Chellappan; Kamal Dua; Saurabh Satija
Journal:  Future Med Chem       Date:  2022-01-12       Impact factor: 3.808

Review 6.  Nanotechnology: A Promising Approach for Cancer Diagnosis, Therapeutics and Theragnosis.

Authors:  Mesfin Dessale; Getachew Mengistu; Hylemariam Mihiretie Mengist
Journal:  Int J Nanomedicine       Date:  2022-08-26
  6 in total

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