Formulation and pharmacokinetics of artemisinin and its derivatives
Identifieur interne : 002F34 ( Main/Exploration ); précédent : 002F33; suivant : 002F35Formulation and pharmacokinetics of artemisinin and its derivatives
Auteurs : H. A. C. Titulaer [Pays-Bas] ; J. Zuidema [Pays-Bas] ; C. B. Lugt [Pays-Bas]Source :
- International Journal of Pharmaceutics [ 0378-5173 ] ; 1991.
English descriptors
- Teeft :
- Absorption rate, Acta pharm, Antimalarial, Antimalarial action, Antimalarial activity, Aqueous suspension, Artemether, Artemisinin, Artemisinin curves, Artesunate, Available literature, Bioavailability, Blood cells, Clinical studies, Derivative, Dosing scheme, Drug absorption, Erythrocyte, Falciparum, Falciparum malaria, Hairless mice, High concentrations, High recrudescence rate, Highest concentrations, Intramuscular administration, Intramuscular injection, Kinetic aspects, Laboratory animals, Liquid chromatography, Malaria, More research, Oral administration, Oral dose, Parasite, Parasite clearances, Peak concentration, Peak concentrations, Pharmacokinetic, Pharmacokinetic parameters, Plasmodium, Plasmodium falciparum, Protein binding, Protein synthesis, Qinghaosu, Qinghaosu antimalaria, Recrudescence, Recrudescence rate, Rectal, Rectal administration, Research group, Rodent malaria, Sesquiterpene lactone, Shen, Shishan zhao, Sodium salt, Suppository, Titulaer, Trans, Warhurst, Zhao.
Abstract
Abstract: Artemisinin, the leading compound of a completely deviant class of drugs, might be of incredible importance in the combat of malaria. Although the herb from which it is isolated has been known for more than 2000 years, and over 2000 patients have been successfully treated in clinical studies, no pharmacokinetic data are available, and thus empirical formulations are used. In this review the available literature on formulation and kinetic aspects of artemisinin and its derivatives is reinterpreted and discussed in order to determine the kinetic requirements for a rational and optimal design of artemisinin formulations.
Url:
DOI: 10.1016/0378-5173(91)90213-8
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 001295
- to stream Istex, to step Curation: 001295
- to stream Istex, to step Checkpoint: 001D05
- to stream Main, to step Merge: 003001
- to stream Main, to step Curation: 002F34
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title>Formulation and pharmacokinetics of artemisinin and its derivatives</title>
<author><name sortKey="Titulaer, H A C" sort="Titulaer, H A C" uniqKey="Titulaer H" first="H. A. C." last="Titulaer">H. A. C. Titulaer</name>
</author>
<author><name sortKey="Zuidema, J" sort="Zuidema, J" uniqKey="Zuidema J" first="J." last="Zuidema">J. Zuidema</name>
</author>
<author><name sortKey="Lugt, C B" sort="Lugt, C B" uniqKey="Lugt C" first="C. B." last="Lugt">C. B. Lugt</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:176BED56FEA16E51E6F89E2DF1E3E401F5B8407A</idno>
<date when="1991" year="1991">1991</date>
<idno type="doi">10.1016/0378-5173(91)90213-8</idno>
<idno type="url">https://api.istex.fr/ark:/67375/6H6-675ZTQMF-4/fulltext.pdf</idno>
<idno type="wicri:Area/Istex/Corpus">001295</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001295</idno>
<idno type="wicri:Area/Istex/Curation">001295</idno>
<idno type="wicri:Area/Istex/Checkpoint">001D05</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">001D05</idno>
<idno type="wicri:doubleKey">0378-5173:1991:Titulaer H:formulation:and:pharmacokinetics</idno>
<idno type="wicri:Area/Main/Merge">003001</idno>
<idno type="wicri:Area/Main/Curation">002F34</idno>
<idno type="wicri:Area/Main/Exploration">002F34</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a">Formulation and pharmacokinetics of artemisinin and its derivatives</title>
<author><name sortKey="Titulaer, H A C" sort="Titulaer, H A C" uniqKey="Titulaer H" first="H. A. C." last="Titulaer">H. A. C. Titulaer</name>
<affiliation wicri:level="1"><country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Pharmaceutics, Croesestraat 79</wicri:regionArea>
<wicri:noRegion>Croesestraat 79</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Zuidema, J" sort="Zuidema, J" uniqKey="Zuidema J" first="J." last="Zuidema">J. Zuidema</name>
<affiliation wicri:level="1"><country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Pharmaceutics, Croesestraat 79</wicri:regionArea>
<wicri:noRegion>Croesestraat 79</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Lugt, C B" sort="Lugt, C B" uniqKey="Lugt C" first="C. B." last="Lugt">C. B. Lugt</name>
<affiliation wicri:level="1"><country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>ACF-Chemie BV</wicri:regionArea>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">International Journal of Pharmaceutics</title>
<title level="j" type="abbrev">IJP</title>
<idno type="ISSN">0378-5173</idno>
<imprint><publisher>ELSEVIER</publisher>
<date type="published" when="1991">1991</date>
<biblScope unit="volume">69</biblScope>
<biblScope unit="issue">2</biblScope>
<biblScope unit="page" from="83">83</biblScope>
<biblScope unit="page" to="92">92</biblScope>
</imprint>
<idno type="ISSN">0378-5173</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0378-5173</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Absorption rate</term>
<term>Acta pharm</term>
<term>Antimalarial</term>
<term>Antimalarial action</term>
<term>Antimalarial activity</term>
<term>Aqueous suspension</term>
<term>Artemether</term>
<term>Artemisinin</term>
<term>Artemisinin curves</term>
<term>Artesunate</term>
<term>Available literature</term>
<term>Bioavailability</term>
<term>Blood cells</term>
<term>Clinical studies</term>
<term>Derivative</term>
<term>Dosing scheme</term>
<term>Drug absorption</term>
<term>Erythrocyte</term>
<term>Falciparum</term>
<term>Falciparum malaria</term>
<term>Hairless mice</term>
<term>High concentrations</term>
<term>High recrudescence rate</term>
<term>Highest concentrations</term>
<term>Intramuscular administration</term>
<term>Intramuscular injection</term>
<term>Kinetic aspects</term>
<term>Laboratory animals</term>
<term>Liquid chromatography</term>
<term>Malaria</term>
<term>More research</term>
<term>Oral administration</term>
<term>Oral dose</term>
<term>Parasite</term>
<term>Parasite clearances</term>
<term>Peak concentration</term>
<term>Peak concentrations</term>
<term>Pharmacokinetic</term>
<term>Pharmacokinetic parameters</term>
<term>Plasmodium</term>
<term>Plasmodium falciparum</term>
<term>Protein binding</term>
<term>Protein synthesis</term>
<term>Qinghaosu</term>
<term>Qinghaosu antimalaria</term>
<term>Recrudescence</term>
<term>Recrudescence rate</term>
<term>Rectal</term>
<term>Rectal administration</term>
<term>Research group</term>
<term>Rodent malaria</term>
<term>Sesquiterpene lactone</term>
<term>Shen</term>
<term>Shishan zhao</term>
<term>Sodium salt</term>
<term>Suppository</term>
<term>Titulaer</term>
<term>Trans</term>
<term>Warhurst</term>
<term>Zhao</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Abstract: Artemisinin, the leading compound of a completely deviant class of drugs, might be of incredible importance in the combat of malaria. Although the herb from which it is isolated has been known for more than 2000 years, and over 2000 patients have been successfully treated in clinical studies, no pharmacokinetic data are available, and thus empirical formulations are used. In this review the available literature on formulation and kinetic aspects of artemisinin and its derivatives is reinterpreted and discussed in order to determine the kinetic requirements for a rational and optimal design of artemisinin formulations.</div>
</front>
</TEI>
<affiliations><list><country><li>Pays-Bas</li>
</country>
</list>
<tree><country name="Pays-Bas"><noRegion><name sortKey="Titulaer, H A C" sort="Titulaer, H A C" uniqKey="Titulaer H" first="H. A. C." last="Titulaer">H. A. C. Titulaer</name>
</noRegion>
<name sortKey="Lugt, C B" sort="Lugt, C B" uniqKey="Lugt C" first="C. B." last="Lugt">C. B. Lugt</name>
<name sortKey="Zuidema, J" sort="Zuidema, J" uniqKey="Zuidema J" first="J." last="Zuidema">J. Zuidema</name>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Sante/explor/ChloroquineV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002F34 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 002F34 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Sante |area= ChloroquineV1 |flux= Main |étape= Exploration |type= RBID |clé= ISTEX:176BED56FEA16E51E6F89E2DF1E3E401F5B8407A |texte= Formulation and pharmacokinetics of artemisinin and its derivatives }}
This area was generated with Dilib version V0.6.33. |