Drug delivery vehicles with improved encapsulation efficiency: Taking advantage of specific drug-carrier interactions

Expert Opinion on Drug Delivery

Volumn 8, Issue 3, 2011, Pages 329-342

  Kita, Katarzyna ^a,b   Dittrich, Christian ^c  

^a UNILEVER RESEARCH   (United Kingdom)

^b UNIVERSITY OF LEEDS   (United Kingdom)

^c HARVARD MEDICAL SCHOOL   (United States)

Author keywords

drug encapsulation; drug carrier interactions; encapsulation efficiency; specific interactions

Indexed keywords

7 ETHYL 10 HYDROXYCAMPTOTHECIN; ACETYLCHOLINESTERASE; AMPHOLYTE; BETAMETHASONE VALERATE; BOVINE SERUM ALBUMIN; CISPLATIN; COPOLYMER; CYCLOSPORIN A; DNA; DOXORUBICIN; DRUG CARRIER; FLUOROURACIL; LEUPRORELIN; LIPID; LIPOSOME; METHOTREXATE; MITOXANTRONE; OLIGONUCLEOTIDE; OXAPROZIN; PACLITAXEL; PLASMID DNA; PROPRANOLOL; QUERCETIN; RAPAMYCIN; RETINOIC ACID; TAXANE DERIVATIVE; TESTOSTERONE ENANTATE; UNINDEXED DRUG; VERAPAMIL; VINCRISTINE SULFATE;

COVALENT BOND; DNA DEGRADATION; DRUG DELIVERY SYSTEM; DRUG FORMULATION; DRUG INTERACTION; DRUG STABILITY; ENCAPSULATION; GENE TARGETING; HYDROGEN BOND; HYDROPHOBICITY; MOLECULAR INTERACTION; NUCLEAR MAGNETIC RESONANCE; PROTEIN BINDING; REVIEW; TEMPERATURE;

CHEMISTRY, PHARMACEUTICAL; DOSAGE FORMS; DRUG DELIVERY SYSTEMS;

EID: 79951918587     PISSN: 17425247     EISSN: None     Source Type: Journal    
DOI: 10.1517/17425247.2011.553216     Document Type: Review

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