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Biomedical Microdevices

Volumn 13, Issue 6, 2011, Pages 1015-1025

Cyclodextrin/poly(anhydride) nanoparticles as drug carriers for the oral delivery of atovaquone

(4) Calvo, Javier a Lavandera, José Luis a Agüeros, Maite b Irache, Juan M b

a GLAXOSMITHKLINE (Spain)

b UNIVERSITY OF NAVARRA (Spain)

Author keywords

Atovaquone; Bioadhesion; Cyclodextrin; Nanoparticles; Oral delivery

Indexed keywords

ATOVAQUONE; BIOADHESION; BIOADHESIVES; DESOLVATION; DRUG CARRIER; DRUG LOADING; IN-VIVO; LIPOPHILIC DRUGS; LOADING CAPACITIES; METHYLCELLULOSE; NANOPARTICLE FORMULATION; ORAL DELIVERY; PHARMACOKINETIC STUDIES; PHYSICOCHEMICAL PROPERTY; RELATIVE BIOAVAILABILITY; SUSPENSION CONTROL;

BIOCHEMISTRY; CYCLODEXTRINS; ETHERS;

NANOPARTICLES;

2 HYDROXYPROPYL BETA CYCLODEXTRIN; 2,6 O DIMETHYL BETA CYCLODEXTRIN; ATOVAQUONE; BETA CYCLODEXTRIN; BETA CYCLODEXTRIN DERIVATIVE; BETA CYCLODEXTRIN SULFOBUTYL ETHER; DRUG CARRIER; METHYLCELLULOSE; NANOPARTICLE; POLYANHYDRIDE;

ANIMAL EXPERIMENT; AREA UNDER THE CURVE; ARTICLE; COMPLEX FORMATION; CONTROLLED STUDY; DRUG BIOAVAILABILITY; DRUG BLOOD LEVEL; DRUG CLEARANCE; DRUG DELIVERY SYSTEM; DRUG DISTRIBUTION; DRUG HALF LIFE; DRUG SOLUBILITY; IN VIVO STUDY; LIPOPHILICITY; MALE; MAXIMUM PLASMA CONCENTRATION; MEAN RESIDENCE TIME; NANOANALYSIS; NANOENCAPSULATION; NANOFABRICATION; NANOPHARMACEUTICS; NONHUMAN; PARTICLE SIZE; PHYSICAL CHEMISTRY; PRIORITY JOURNAL; RAT; TIME TO MAXIMUM PLASMA CONCENTRATION; ZETA POTENTIAL;

ADMINISTRATION, ORAL; ANIMALS; ATOVAQUONE; BETA-CYCLODEXTRINS; BIOLOGICAL AVAILABILITY; DRUG CARRIERS; DRUG DESIGN; MALE; NANOPARTICLES; PHYSICOCHEMICAL PHENOMENA; POLYANHYDRIDES; RATS; RATS, WISTAR;

RATTUS;

EID: 84855417564 PISSN: 13872176 EISSN: 15728781 Source Type: Journal
DOI: 10.1007/s10544-011-9571-1 Document Type: Article

Times cited : (21)

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