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Quinine: Reimagined and Redirected
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Malaria Control & Elimination

ISSN: 2470-6965

Open Access

Perspective - (2024) Volume 13, Issue 3

Quinine: Reimagined and Redirected

Nobuko Tuno*
*Correspondence: Nobuko Tuno, Department of Malaria Immunology, Bernhard Nocht University, Hamburg, Germany, Email:
Department of Malaria Immunology, Bernhard Nocht University, Hamburg, Germany

Received: 02-May-2024, Manuscript No. mcce-24-138438; Editor assigned: 05-May-2024, Pre QC No. P-138438; Reviewed: 16-May-2024, QC No. Q-138438; Revised: 22-May-2024, Manuscript No. R-138438; Published: 29-May-2024 , DOI: 10.37421/2470-6965.2024.13.288
Citation: Tuno, Nobuko. “Quinine: Reimagined and Redirected.” Malar Contr Elimination 13 (2024): 288.
Copyright: © 2024 Tuno N. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.

Introduction

Quinine, a natural compound extracted from the bark of the cinchona tree, has a long history of use in the treatment of malaria. However, its efficacy has been challenged by the emergence of drug-resistant malaria strains and adverse side effects. In recent years, researchers have reimagined and redirected quinine in innovative ways to overcome these challenges and enhance its therapeutic potential. This article explores the novel approaches and applications of quinine, ranging from drug delivery systems to combination therapies, in the fight against malaria and other diseases.

Description

Quinine has been used for centuries as a primary treatment for malaria, with its discovery dating back to the 17th century. Its effectiveness in combating the malaria parasite, Plasmodium, earned it the status of a "wonder drug" and a cornerstone of antimalarial therapy. However, widespread use led to the development of drug-resistant strains of malaria, prompting the search for alternative treatments and strategies. One approach to enhance quinine's efficacy is through redesigned drug delivery systems. Nanotechnologybased formulations, such as liposomes and nanoparticles, offer improved pharmacokinetics and targeted delivery of quinine to infected cells. These systems help overcome the limitations of conventional quinine formulations, such as poor bioavailability and systemic toxicity, while minimizing the risk of drug resistance. Another strategy involves combining quinine with other antimalarial agents to create synergistic effects and prevent the emergence of drug resistance. Artemisinin-based combination therapies which combine quinine derivatives with artemisinin derivatives, have become the first-line treatment for uncomplicated malaria in many regions. These combinations offer rapid parasite clearance and reduced treatment duration, leading to improved patient outcomes and decreased transmission of drug-resistant strains [1].

Beyond malaria, quinine has demonstrated therapeutic potential in various non-malarial diseases. Its antiparasitic properties have been explored in the treatment of conditions such as babesiosis and trypanosomiasis. Additionally, quinine's anti-inflammatory and antiviral activities have shown promise in the management of autoimmune disorders and viral infections, including COVID-19. Despite its potential, quinine faces several challenges, including its limited availability, high cost, and adverse side effects, such as cinchonism. Furthermore, the emergence of quinine-resistant strains of malaria continues to pose a threat to its efficacy. Future research efforts aim to address these challenges by developing novel formulations, exploring alternative delivery routes, and optimizing combination therapies to maximize quinine's therapeutic benefits while minimizing its drawbacks. Quinine, traditionally recognized for its role in combating malaria, has expanded its therapeutic horizon beyond parasitic infections to encompass various nonmalarial diseases. Its multifaceted pharmacological properties have rendered it a valuable asset in the treatment and management of conditions ranging from parasitic diseases to autoimmune disorders and viral infections [2].

Quinine's potent antiparasitic properties extend beyond malaria and have been investigated in the treatment of other parasitic infections, such as babesiosis and trypanosomiasis. Babesiosis, caused by Babesia parasites transmitted through tick bites, has shown susceptibility to quinine-based therapies, particularly in cases of severe or drug-resistant infections. Similarly, quinine has exhibited efficacy against trypanosomiasis, a group of diseases caused by Trypanosoma parasites, primarily transmitted by tsetse flies. While further research is needed to optimize dosing regimens and evaluate long-term efficacy, quinine holds promise as a therapeutic option for these parasitic diseases. In addition to its antiparasitic activity, quinine possesses notable anti-inflammatory properties that have implications for the management of autoimmune disorders. Autoimmune diseases, characterized by immune system dysfunction and aberrant inflammation, often require immunosuppressive therapy to alleviate symptoms and prevent disease progression. Quinine's ability to modulate inflammatory responses by inhibiting pro-inflammatory cytokines and cellular pathways makes it a potential adjunctive therapy in autoimmune conditions such as rheumatoid arthritis, systemic lupus erythematosus, and inflammatory bowel disease. While further clinical studies are warranted to elucidate its efficacy and safety profile, quinine represents a promising avenue for addressing the unmet needs of patients with autoimmune disorders [3].

The recent emergence of viral infections, including the COVID-19 pandemic caused by the novel coronavirus (SARS-CoV-2), has spurred interest in repurposing existing drugs with potential antiviral properties. Quinine, with its established safety profile and broad-spectrum antiviral activity, has garnered attention as a candidate for the management of viral infections. In vitro studies have demonstrated quinine's ability to inhibit viral replication and reduce viral load in various RNA and DNA viruses, including respiratory viruses like influenza and coronaviruses. While clinical data on quinine's efficacy against COVID-19 are limited and inconclusive, ongoing research endeavors aim to explore its role as a therapeutic agent in viral infections, either as monotherapy or in combination with other antiviral drugs. The expanding repertoire of quinine's therapeutic applications underscores its versatility and potential in addressing a spectrum of diseases beyond malaria. From parasitic infections to autoimmune disorders and viral illnesses, quinine's diverse pharmacological properties offer new avenues for therapeutic intervention and disease management. While further research is needed to elucidate its efficacy, safety, and optimal dosing regimens in non-malarial diseases, quinine represents a valuable asset in the quest for innovative treatments against a wide range of medical conditions [4,5].

Conclusion

Quinine, once hailed as a miracle cure for malaria, continues to play a vital role in the fight against this deadly disease. Through innovative approaches and strategic redirection, quinine's therapeutic potential extends beyond malaria to encompass a range of parasitic and non-malarial diseases. By reimagining quinine and exploring new applications, researchers aim to overcome existing challenges and pave the way for enhanced treatment options in the battle against infectious diseases.

Acknowledgement

None.

Conflict of Interest

There are no conflicts of interest by author.

References

  1. Borea, Pier Andrea, Stefania Gessi, Stefania Merighi and Fabrizio Vincenzi, et al. "Pharmacology of adenosine receptors: The state of the art."Physiol Rev 98 (2018): 1591-1625.

    Google Scholar, Crossref, Indexed at

  2. Kulkarni, Shashank, Klaus Urbahns and Thomas Spangenberg. "Targeted covalent inhibitors for the treatment of malaria?."ACS Infect Dis 6 (2020): 2815-2817.

    Google Scholar, Crossref, Indexed at

  3. Cullia, Gregorio, Stefano Bruno, Silvia Parapini and Marilena Margiotta, et al. "Covalent inhibitors of Plasmodium falciparum glyceraldehyde 3-phosphate dehydrogenase with antimalarial activity in vitro."ACS Med Chem Lett 10 (2019): 590-595.

    Google Scholar, Crossref, Indexed at

  4. Bruns, Robert F. "Adenosine receptor activation by adenine nucleotides requires conversion of the nucleotides to adenosine."Arch Pharmacol 315 (1980): 5-13.

    Google Scholar, Crossref, Indexed at

  5. Kerr, Iain D., Ji H. Lee, Christopher J. Farady and Rachael Marion, et al. "Vinyl sulfones as antiparasitic agents and a structural basis for drug design."J Biol Chem 284 (2009): 25697-25703.

    Google Scholar, Crossref, Indexed at

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