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Smart nanocrystals of artemether: fabrication, characterization, and comparative in vitro and in vivo antimalarial evaluation
Artemether (ARTM) is a very effective antimalarial drug with poor solubility and consequently low bioavailability. Smart nanocrystals of ARTM with particle size of 161±1.5 nm and polydispersity index of 0.172±0.01 were produced in <1 hour using a wet milling technology, Dena(®) DM-100. The crysta...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5125812/ https://www.ncbi.nlm.nih.gov/pubmed/27920499 http://dx.doi.org/10.2147/DDDT.S114962 |
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author | Shah, Syed Muhammad Hassan Ullah, Farhat Khan, Shahzeb Shah, Syed Muhammad Mukarram de Matas, Marcel Hussain, Zahid Minhas, Muhammad Usman AbdEl-Salam, Naser M Assi, Khaled Hafez Isreb, Mohammad |
author_facet | Shah, Syed Muhammad Hassan Ullah, Farhat Khan, Shahzeb Shah, Syed Muhammad Mukarram de Matas, Marcel Hussain, Zahid Minhas, Muhammad Usman AbdEl-Salam, Naser M Assi, Khaled Hafez Isreb, Mohammad |
author_sort | Shah, Syed Muhammad Hassan |
collection | PubMed |
description | Artemether (ARTM) is a very effective antimalarial drug with poor solubility and consequently low bioavailability. Smart nanocrystals of ARTM with particle size of 161±1.5 nm and polydispersity index of 0.172±0.01 were produced in <1 hour using a wet milling technology, Dena(®) DM-100. The crystallinity of the processed ARTM was confirmed using differential scanning calorimetry and powder X-ray diffraction. The saturation solubility of the ARTM nanocrystals was substantially increased to 900 µg/mL compared to the raw ARTM in water (145.0±2.3 µg/mL) and stabilizer solution (300.0±2.0 µg/mL). The physical stability studies conducted for 90 days demonstrated that nanocrystals stored at 2°C–8°C and 25°C were very stable compared to the samples stored at 40°C. The nanocrystals were also shown to be stable when processed at acidic pH (2.0). The solubility and dissolution rate of ARTM nanocrystals were significantly increased (P<0.05) compared to those of its bulk powder form. The results of in vitro studies showed significant antimalarial effect (P<0.05) against Plasmodium falciparum and Plasmodium vivax. The IC(50) (median lethal oral dose) value of ARTM nanocrystals was 28- and 54-fold lower than the IC(50) value of unprocessed drug and 13- and 21-fold lower than the IC(50) value of the marketed tablets, respectively. In addition, ARTM nanocrystals at the same dose (2 mg/kg) showed significantly (P<0.05) higher reduction in percent parasitemia (89%) against P. vivax compared to the unprocessed (27%), marketed tablets (45%), and microsuspension (60%). The acute toxicity study demonstrated that the LD(50) value of ARTM nanocrystals is between 1,500 mg/kg and 2,000 mg/kg when given orally. This study demonstrated that the wet milling technology (Dena(®) DM-100) can produce smart nanocrystals of ARTM with enhanced antimalarial activities. |
format | Online Article Text |
id | pubmed-5125812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-51258122016-12-05 Smart nanocrystals of artemether: fabrication, characterization, and comparative in vitro and in vivo antimalarial evaluation Shah, Syed Muhammad Hassan Ullah, Farhat Khan, Shahzeb Shah, Syed Muhammad Mukarram de Matas, Marcel Hussain, Zahid Minhas, Muhammad Usman AbdEl-Salam, Naser M Assi, Khaled Hafez Isreb, Mohammad Drug Des Devel Ther Original Research Artemether (ARTM) is a very effective antimalarial drug with poor solubility and consequently low bioavailability. Smart nanocrystals of ARTM with particle size of 161±1.5 nm and polydispersity index of 0.172±0.01 were produced in <1 hour using a wet milling technology, Dena(®) DM-100. The crystallinity of the processed ARTM was confirmed using differential scanning calorimetry and powder X-ray diffraction. The saturation solubility of the ARTM nanocrystals was substantially increased to 900 µg/mL compared to the raw ARTM in water (145.0±2.3 µg/mL) and stabilizer solution (300.0±2.0 µg/mL). The physical stability studies conducted for 90 days demonstrated that nanocrystals stored at 2°C–8°C and 25°C were very stable compared to the samples stored at 40°C. The nanocrystals were also shown to be stable when processed at acidic pH (2.0). The solubility and dissolution rate of ARTM nanocrystals were significantly increased (P<0.05) compared to those of its bulk powder form. The results of in vitro studies showed significant antimalarial effect (P<0.05) against Plasmodium falciparum and Plasmodium vivax. The IC(50) (median lethal oral dose) value of ARTM nanocrystals was 28- and 54-fold lower than the IC(50) value of unprocessed drug and 13- and 21-fold lower than the IC(50) value of the marketed tablets, respectively. In addition, ARTM nanocrystals at the same dose (2 mg/kg) showed significantly (P<0.05) higher reduction in percent parasitemia (89%) against P. vivax compared to the unprocessed (27%), marketed tablets (45%), and microsuspension (60%). The acute toxicity study demonstrated that the LD(50) value of ARTM nanocrystals is between 1,500 mg/kg and 2,000 mg/kg when given orally. This study demonstrated that the wet milling technology (Dena(®) DM-100) can produce smart nanocrystals of ARTM with enhanced antimalarial activities. Dove Medical Press 2016-11-24 /pmc/articles/PMC5125812/ /pubmed/27920499 http://dx.doi.org/10.2147/DDDT.S114962 Text en © 2016 Shah et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Shah, Syed Muhammad Hassan Ullah, Farhat Khan, Shahzeb Shah, Syed Muhammad Mukarram de Matas, Marcel Hussain, Zahid Minhas, Muhammad Usman AbdEl-Salam, Naser M Assi, Khaled Hafez Isreb, Mohammad Smart nanocrystals of artemether: fabrication, characterization, and comparative in vitro and in vivo antimalarial evaluation |
title | Smart nanocrystals of artemether: fabrication, characterization, and comparative in vitro and in vivo antimalarial evaluation |
title_full | Smart nanocrystals of artemether: fabrication, characterization, and comparative in vitro and in vivo antimalarial evaluation |
title_fullStr | Smart nanocrystals of artemether: fabrication, characterization, and comparative in vitro and in vivo antimalarial evaluation |
title_full_unstemmed | Smart nanocrystals of artemether: fabrication, characterization, and comparative in vitro and in vivo antimalarial evaluation |
title_short | Smart nanocrystals of artemether: fabrication, characterization, and comparative in vitro and in vivo antimalarial evaluation |
title_sort | smart nanocrystals of artemether: fabrication, characterization, and comparative in vitro and in vivo antimalarial evaluation |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5125812/ https://www.ncbi.nlm.nih.gov/pubmed/27920499 http://dx.doi.org/10.2147/DDDT.S114962 |
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