Artemisinin Cocrystals for Bioavailability Enhancement. Part 1: Formulation Design and Role of the Polymeric Excipient.


Journal

Molecular pharmaceutics
ISSN: 1543-8392
Titre abrégé: Mol Pharm
Pays: United States
ID NLM: 101197791

Informations de publication

Date de publication:
06 12 2021
Historique:
pubmed: 2 11 2021
medline: 15 3 2022
entrez: 1 11 2021
Statut: ppublish

Résumé

Artemisinin (ART) is a most promising antimalarial agent, which is both effective and well tolerated in patients, though it has therapeutic limitations due to its low solubility, bioavailability, and short half-life. The objective of this work was to explore the possibility of formulating ART cocrystals, i.e., artemisinin-orcinol (ART-ORC) and artemisinin-resorcinol (ART

Identifiants

pubmed: 34723557
doi: 10.1021/acs.molpharmaceut.1c00384
doi:

Substances chimiques

Artemisinins 0
Excipients 0
Polymers 0
artemisinin 9RMU91N5K2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4256-4271

Auteurs

Manreet Kaur (M)

Leicester School of Pharmacy, De Montfort University, Leicester LE1 9BH, U.K.

Vanessa Yardley (V)

Department of Infection & Immunity, Faculty of Infectious & Tropical Diseases, London School of Hygiene and Tropical Medicine, London WC1E 7HT, U.K.

Ke Wang (K)

Leicester School of Pharmacy, De Montfort University, Leicester LE1 9BH, U.K.

Jinit Masania (J)

Leicester School of Pharmacy, De Montfort University, Leicester LE1 9BH, U.K.

Adolfo Botana (A)

JEOL (U.K.) LTD., Welwyn Garden City AL7 1LT, U.K.

Randolph R J Arroo (RRJ)

Leicester School of Pharmacy, De Montfort University, Leicester LE1 9BH, U.K.

Mingzhong Li (M)

Leicester School of Pharmacy, De Montfort University, Leicester LE1 9BH, U.K.

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Classifications MeSH