Development of therapeutic polymeric nanoparticles for the resolution of inflammation

Advanced Healthcare Materials

Volumn 3, Issue 9, 2014, Pages 1448-1456

  Gadde, Suresh ^a   Even Or, Orli ^b   Kamaly, Nazila ^a   Hasija, Apoorva ^a   Gagnon, Philippe G ^a   Adusumilli, Krishna H ^a   Erakovic, Andrea ^a   Pal, Anoop K ^a   Zhang, Xue Qing ^a   Kolishetti, Nagesh ^a   Shi, Jinjun ^a   Fisher, Edward A ^b   Farokhzad, Omid C ^a,c  

^a HARVARD MEDICAL SCHOOL   (United States)

^b NEW YORK UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c KING ABDULAZIZ UNIVERSITY   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

DISEASES; DRUG DELIVERY; GENE EXPRESSION; MACROPHAGES; NANOPARTICLES; PATHOLOGY;

COMBINATORIAL LIBRARY; INFLAMMATORY DISEASE; INFLAMMATORY GENES; INFLAMMATORY MEDIATORS; PERITONEAL MACROPHAGE; PHYSICOCHEMICAL PARAMETERS; POLYMERIC NANOPARTICLES; THERAPEUTIC INTERVENTION;

FUNCTIONAL POLYMERS;

3 [3 [[2 CHLORO 3 (TRIFLUOROMETHYL)BENZYL](2 DIPHENYLETHYL)AMINO]PROPOXY]PHENYLACETIC ACID; ABC TRANSPORTER A1; DEXAMETHASONE; MONOCYTE CHEMOTACTIC PROTEIN 1; NANOPARTICLE; POLYMER; STEROL REGULATORY ELEMENT BINDING PROTEIN 1C; TUMOR NECROSIS FACTOR ALPHA; ANTIINFLAMMATORY AGENT; BENZOIC ACID DERIVATIVE; BENZYLAMINE DERIVATIVE; LIVER X RECEPTOR; ORPHAN NUCLEAR RECEPTOR;

ABCA1 GENE; ACUTE DISEASE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANTIINFLAMMATORY ACTIVITY; ARTICLE; CONTROLLED STUDY; DRUG DELIVERY SYSTEM; DRUG DETERMINATION; DRUG EFFICACY; DRUG MECHANISM; DRUG STRUCTURE; DRUG SYNTHESIS; GENE EXPRESSION; IN VITRO STUDY; MALE; MOUSE; NEUTROPHIL; NONHUMAN; PERITONEUM MACROPHAGE; PERITONITIS; PHYSICAL CHEMISTRY; PROCESS DEVELOPMENT; PROTEIN SECRETION; SREBP1C GENE; ANIMAL; C57BL MOUSE; CHEMISTRY; DISEASE MODEL; INFLAMMATION; METABOLISM;

ANIMALS; ANTI-INFLAMMATORY AGENTS; BENZOATES; BENZYLAMINES; DISEASE MODELS, ANIMAL; INFLAMMATION; MALE; MICE; MICE, INBRED C57BL; NANOPARTICLES; ORPHAN NUCLEAR RECEPTORS; PERITONITIS; POLYMERS;

EID: 84908025202     PISSN: 21922640     EISSN: 21922659     Source Type: Journal    
DOI: 10.1002/adhm.201300688     Document Type: Article

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