Cargando…

Formulation, process development and evaluation of artemether and lumefantrine soft gelatin capsule

Artemether and Lumefantrine capsules are indicated for the treatment of P. falciparum malaria cases resistant to both chloroquine and sulphadoxine, pyrimethamine combination. Both artemether and lumefantrine act as blood schizontocides. Artemether is a sesquiterpene lactone derived from artemisinin....

Descripción completa

Detalles Bibliográficos
Autores principales: Patel, A., Lodha, A., Chaudhuri, J., Jadia, P., Joshi, T., Dalal, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467843/
https://www.ncbi.nlm.nih.gov/pubmed/23066225
http://dx.doi.org/10.4103/0975-7406.94155
_version_ 1782245882626834432
author Patel, A.
Lodha, A.
Chaudhuri, J.
Jadia, P.
Joshi, T.
Dalal, J.
author_facet Patel, A.
Lodha, A.
Chaudhuri, J.
Jadia, P.
Joshi, T.
Dalal, J.
author_sort Patel, A.
collection PubMed
description Artemether and Lumefantrine capsules are indicated for the treatment of P. falciparum malaria cases resistant to both chloroquine and sulphadoxine, pyrimethamine combination. Both artemether and lumefantrine act as blood schizontocides. Artemether is a sesquiterpene lactone derived from artemisinin. Artemisinin is a compound derived from the sweet wormwood plant and has been used for centuries in traditional Chinese medicine to treat fever. Lumefantrine is a synthetic aryl-amino alcohol antimalarial (quinine, mefloquine and halofantrine are members of the same group). Artemether is absorbed fairly rapidly with peak plasma concentrations reached about 2 hours after dosing. Absorption of lumefantrine, a highly lipophilic compound, starts after a lag period of up to 2 hours, with peak plasma concentration about 6-8 hours after dosing. In order to overcome this problem, we have observed that when the drug is given in the soft gelatin dosage form, the bioavailability of the drug is increased. Thus, increasing the absorption of the drug and peak plasma concentration is reached earlier then the conventional dosage form.
format Online
Article
Text
id pubmed-3467843
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-34678432012-10-12 Formulation, process development and evaluation of artemether and lumefantrine soft gelatin capsule Patel, A. Lodha, A. Chaudhuri, J. Jadia, P. Joshi, T. Dalal, J. J Pharm Bioallied Sci Original/Brief Artemether and Lumefantrine capsules are indicated for the treatment of P. falciparum malaria cases resistant to both chloroquine and sulphadoxine, pyrimethamine combination. Both artemether and lumefantrine act as blood schizontocides. Artemether is a sesquiterpene lactone derived from artemisinin. Artemisinin is a compound derived from the sweet wormwood plant and has been used for centuries in traditional Chinese medicine to treat fever. Lumefantrine is a synthetic aryl-amino alcohol antimalarial (quinine, mefloquine and halofantrine are members of the same group). Artemether is absorbed fairly rapidly with peak plasma concentrations reached about 2 hours after dosing. Absorption of lumefantrine, a highly lipophilic compound, starts after a lag period of up to 2 hours, with peak plasma concentration about 6-8 hours after dosing. In order to overcome this problem, we have observed that when the drug is given in the soft gelatin dosage form, the bioavailability of the drug is increased. Thus, increasing the absorption of the drug and peak plasma concentration is reached earlier then the conventional dosage form. Medknow Publications & Media Pvt Ltd 2012-03 /pmc/articles/PMC3467843/ /pubmed/23066225 http://dx.doi.org/10.4103/0975-7406.94155 Text en Copyright: © Journal of Pharmacy and Bioallied Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original/Brief
Patel, A.
Lodha, A.
Chaudhuri, J.
Jadia, P.
Joshi, T.
Dalal, J.
Formulation, process development and evaluation of artemether and lumefantrine soft gelatin capsule
title Formulation, process development and evaluation of artemether and lumefantrine soft gelatin capsule
title_full Formulation, process development and evaluation of artemether and lumefantrine soft gelatin capsule
title_fullStr Formulation, process development and evaluation of artemether and lumefantrine soft gelatin capsule
title_full_unstemmed Formulation, process development and evaluation of artemether and lumefantrine soft gelatin capsule
title_short Formulation, process development and evaluation of artemether and lumefantrine soft gelatin capsule
title_sort formulation, process development and evaluation of artemether and lumefantrine soft gelatin capsule
topic Original/Brief
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467843/
https://www.ncbi.nlm.nih.gov/pubmed/23066225
http://dx.doi.org/10.4103/0975-7406.94155
work_keys_str_mv AT patela formulationprocessdevelopmentandevaluationofartemetherandlumefantrinesoftgelatincapsule
AT lodhaa formulationprocessdevelopmentandevaluationofartemetherandlumefantrinesoftgelatincapsule
AT chaudhurij formulationprocessdevelopmentandevaluationofartemetherandlumefantrinesoftgelatincapsule
AT jadiap formulationprocessdevelopmentandevaluationofartemetherandlumefantrinesoftgelatincapsule
AT joshit formulationprocessdevelopmentandevaluationofartemetherandlumefantrinesoftgelatincapsule
AT dalalj formulationprocessdevelopmentandevaluationofartemetherandlumefantrinesoftgelatincapsule