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Evaluation of Safety and Antileishmanial Efficacy of Amine Functionalized Carbon-Based Composite Nanoparticle Appended With Amphotericin B: An in vitro and Preclinical Study

Visceral leishmaniasis (VL) has been a major health concern in the developing world, primarily affecting impoverished people. It is caused by a protozoan parasite Leishmania donovani and is characterized by immune dysfunction that can lead to deadly secondary infections. Several adverse side effects...

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Autores principales: Gedda, Mallikarjuna Rao, Madhukar, Prasoon, Vishwakarma, Alok Kumar, Verma, Vimal, Kushwaha, Anurag Kumar, Yadagiri, Ganesh, Mudavath, Shyam Lal, Singh, Om Prakash, Srivastava, Onkar Nath, Sundar, Shyam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7350933/
https://www.ncbi.nlm.nih.gov/pubmed/32719770
http://dx.doi.org/10.3389/fchem.2020.00510
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author Gedda, Mallikarjuna Rao
Madhukar, Prasoon
Vishwakarma, Alok Kumar
Verma, Vimal
Kushwaha, Anurag Kumar
Yadagiri, Ganesh
Mudavath, Shyam Lal
Singh, Om Prakash
Srivastava, Onkar Nath
Sundar, Shyam
author_facet Gedda, Mallikarjuna Rao
Madhukar, Prasoon
Vishwakarma, Alok Kumar
Verma, Vimal
Kushwaha, Anurag Kumar
Yadagiri, Ganesh
Mudavath, Shyam Lal
Singh, Om Prakash
Srivastava, Onkar Nath
Sundar, Shyam
author_sort Gedda, Mallikarjuna Rao
collection PubMed
description Visceral leishmaniasis (VL) has been a major health concern in the developing world, primarily affecting impoverished people. It is caused by a protozoan parasite Leishmania donovani and is characterized by immune dysfunction that can lead to deadly secondary infections. Several adverse side effects limit the existing treatment options; hence, the need of the hour is some drug option with high efficacy and no toxicity. To make targeted delivery of Amphotericin B (AmB), we have used amine-functionalized versions of carbon nanostructures, namely f-CNT and f-Graphene (f-Grap). The results with f-Grap-AmB, because of a much larger surface area, were expected to be better. However, the results obtained by us showed only marginal improvement (IC50 f-Grap-AmB; 0.0038 ± 0.00119 μg/mL). This is, in all likelihood, due to the agglomeration effect of f-Grap-AmB, which is invariably obtained with graphene. To resolve this issue, we have synthesized a graphene-CNT composite (graphene 70% and CNT 30% by weight). Because CNT is dispersed in between graphene sheets, the agglomeration effect is avoided, and our study suggests that the f-Composite-AmB (f-Comp-AmB) showed no toxicity against the murine J774A.1 macrophage cell line and did not induce any hepatic or renal toxicity in Swiss albino mice. The f-Comp-AmB also showed a remarkable elevation in the in vitro and in vivo antileishmanial efficacy in comparison to AmB and f-CNT-AmB or f-Grap-AmB in J774A.1 and Golden Syrian hamsters, respectively. Additionally, we have also observed that the percentage suppression of parasite replication in the spleen of the hamster was significantly higher in the f-Comp-AmB (97.79 ± 0.2375) treated group in comparison with the AmB (85.66 ± 1.164) treated group of hamsters. To conclude, f-Comp-AmB could be a safe and reliable therapeutic option over the other carbon-based nanoparticles (NPs), i.e., f-CNT-AmB, f-Grap-AmB, and conventional AmB.
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spelling pubmed-73509332020-07-26 Evaluation of Safety and Antileishmanial Efficacy of Amine Functionalized Carbon-Based Composite Nanoparticle Appended With Amphotericin B: An in vitro and Preclinical Study Gedda, Mallikarjuna Rao Madhukar, Prasoon Vishwakarma, Alok Kumar Verma, Vimal Kushwaha, Anurag Kumar Yadagiri, Ganesh Mudavath, Shyam Lal Singh, Om Prakash Srivastava, Onkar Nath Sundar, Shyam Front Chem Chemistry Visceral leishmaniasis (VL) has been a major health concern in the developing world, primarily affecting impoverished people. It is caused by a protozoan parasite Leishmania donovani and is characterized by immune dysfunction that can lead to deadly secondary infections. Several adverse side effects limit the existing treatment options; hence, the need of the hour is some drug option with high efficacy and no toxicity. To make targeted delivery of Amphotericin B (AmB), we have used amine-functionalized versions of carbon nanostructures, namely f-CNT and f-Graphene (f-Grap). The results with f-Grap-AmB, because of a much larger surface area, were expected to be better. However, the results obtained by us showed only marginal improvement (IC50 f-Grap-AmB; 0.0038 ± 0.00119 μg/mL). This is, in all likelihood, due to the agglomeration effect of f-Grap-AmB, which is invariably obtained with graphene. To resolve this issue, we have synthesized a graphene-CNT composite (graphene 70% and CNT 30% by weight). Because CNT is dispersed in between graphene sheets, the agglomeration effect is avoided, and our study suggests that the f-Composite-AmB (f-Comp-AmB) showed no toxicity against the murine J774A.1 macrophage cell line and did not induce any hepatic or renal toxicity in Swiss albino mice. The f-Comp-AmB also showed a remarkable elevation in the in vitro and in vivo antileishmanial efficacy in comparison to AmB and f-CNT-AmB or f-Grap-AmB in J774A.1 and Golden Syrian hamsters, respectively. Additionally, we have also observed that the percentage suppression of parasite replication in the spleen of the hamster was significantly higher in the f-Comp-AmB (97.79 ± 0.2375) treated group in comparison with the AmB (85.66 ± 1.164) treated group of hamsters. To conclude, f-Comp-AmB could be a safe and reliable therapeutic option over the other carbon-based nanoparticles (NPs), i.e., f-CNT-AmB, f-Grap-AmB, and conventional AmB. Frontiers Media S.A. 2020-07-03 /pmc/articles/PMC7350933/ /pubmed/32719770 http://dx.doi.org/10.3389/fchem.2020.00510 Text en Copyright © 2020 Gedda, Madhukar, Vishwakarma, Verma, Kushwaha, Yadagiri, Mudavath, Singh, Srivastava and Sundar. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Gedda, Mallikarjuna Rao
Madhukar, Prasoon
Vishwakarma, Alok Kumar
Verma, Vimal
Kushwaha, Anurag Kumar
Yadagiri, Ganesh
Mudavath, Shyam Lal
Singh, Om Prakash
Srivastava, Onkar Nath
Sundar, Shyam
Evaluation of Safety and Antileishmanial Efficacy of Amine Functionalized Carbon-Based Composite Nanoparticle Appended With Amphotericin B: An in vitro and Preclinical Study
title Evaluation of Safety and Antileishmanial Efficacy of Amine Functionalized Carbon-Based Composite Nanoparticle Appended With Amphotericin B: An in vitro and Preclinical Study
title_full Evaluation of Safety and Antileishmanial Efficacy of Amine Functionalized Carbon-Based Composite Nanoparticle Appended With Amphotericin B: An in vitro and Preclinical Study
title_fullStr Evaluation of Safety and Antileishmanial Efficacy of Amine Functionalized Carbon-Based Composite Nanoparticle Appended With Amphotericin B: An in vitro and Preclinical Study
title_full_unstemmed Evaluation of Safety and Antileishmanial Efficacy of Amine Functionalized Carbon-Based Composite Nanoparticle Appended With Amphotericin B: An in vitro and Preclinical Study
title_short Evaluation of Safety and Antileishmanial Efficacy of Amine Functionalized Carbon-Based Composite Nanoparticle Appended With Amphotericin B: An in vitro and Preclinical Study
title_sort evaluation of safety and antileishmanial efficacy of amine functionalized carbon-based composite nanoparticle appended with amphotericin b: an in vitro and preclinical study
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7350933/
https://www.ncbi.nlm.nih.gov/pubmed/32719770
http://dx.doi.org/10.3389/fchem.2020.00510
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