Formulation and delivery mode affect disposition and activity of tyrphostin-loaded nanoparticles in the rat carotid model

Arteriosclerosis, Thrombosis, and Vascular Biology

Volumn 21, Issue 9, 2001, Pages 1434-1439

  Fishbein, Ilia ^a   Chorny, Michael ^a   Banai, Shmuel ^b   Levitzki, Alexander ^c   Danenberg, Haim D ^d   Gao, Jianchuan ^a   Chen, Xing ^a   Moerman, Evgeny ^a   Gati, Irith ^a   Goldwasser, Victoria ^a   Golomb, Gershon ^a  

^a HEBREW UNIVERSITY OF JERUSALEM   (Israel)

^b BIKUR CHOLIM HOSPITAL   (Israel)

^c HEBREW UNIVERSITY OF JERUSALEM   (Israel)

^d HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

Author keywords

Controlled release; Local delivery; Nanoparticles; Restenosis; Tyrphostins

Indexed keywords

6,7 DIMETHYL 2 PHENYLQUINOXALINE; NANOPARTICLE; POLYLACTIC ACID; TYRPHOSTIN;

ADSORPTION; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CAROTID ARTERY INJURY; CONTROLLED STUDY; DRUG DELIVERY SYSTEM; DRUG DISPOSITION; DRUG EFFICACY; DRUG ELIMINATION; DRUG FORMULATION; ENCAPSULATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MALE; NONHUMAN; PARTICLE SIZE; PRIORITY JOURNAL; RAT; RESTENOSIS;

EID: 0035572882     PISSN: 10795642     EISSN: None     Source Type: Journal    
DOI: 10.1161/hq0901.095567     Document Type: Article

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