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Nanoparticulation improves bioavailability of Erlotinib

Authors
 Kyung Mi Yang  ;  In Chul Shin  ;  Joo Won Park  ;  Kab-Sig Kim  ;  Dae Kyong Kim  ;  Kyungmoon Park  ;  Kunhong Kim 
Citation
 Drug Development and Industrial Pharmacy, Vol.43(9) : 1557-1565, 2017 
Journal Title
 Drug Development and Industrial Pharmacy 
Issue Date
2017
MeSH
Animals ; Antineoplastic Agents/chemistry ; Antineoplastic Agents/pharmacokinetics* ; Biological Availability* ; Chemistry, Pharmaceutical ; Erlotinib Hydrochloride/chemistry ; Erlotinib Hydrochloride/pharmacokinetics* ; Erlotinib Hydrochloride/pharmacology ; Excipients/chemistry* ; Humans ; Lung Neoplasms/drug therapy* ; Mice, Nude ; Nanoparticles/chemistry* ; Solubility
Keywords
Bioavailability ; Erlotinib ; NUFS-Ert ; fed-fasted variance ; pharmacokinetics
Abstract
OBJECTIVES: Nanoparticulation using fat and supercritical fluid (NUFSTM) is a drug delivery platform technology enabling efficient and effective formulation of poorly soluble drugs. We performed experiments to examine whether NUFS™ could improve poor bioavailability and reduce fed-fasted bioavailability variances of erlotinib (Ert). METHODS: NUFS-Ert was prepared using NUFS™ technology; its physical properties were characterized, and drug release was measured. Furthermore, in vitro and in vivo efficacy tests and pharmacokinetic analysis were performed. RESULTS: NUFS-Ert nanoparticles had an average size of 250 nm and were stable for 2 months at 40 °C, 4 °C, and room temperature. The dissolution rate of NUFS-Ert increased in bio-relevant dissolution media. NUFS-Ert was more potent in inhibiting EGF signaling and in suppressing the proliferation of A549, a human non-small cell lung cancer cell line. Furthermore, A549 xenografts in BALB/c nude mice treated with NUFS-Ert regressed more efficiently than those in the mice treated with vehicle or Tarceva®. In addition, experimental lung metastasis was more efficiently inhibited by NUFS-Ert than by Tarceva®. The relative bioavailability of NUFS-Ert compared with that of Tarceva® was 550% and the ratio of the area under the concentration-time curve (AUC) of fed state to the AUC of fasted state was 1.8 for NUFS-Ert and 5.8 for Tarceva®. CONCLUSIONS: NUFS-Ert could improve poor bioavailability and reduce fed-fasted bioavailability variances of Ert. NUFS-Ert was more efficacious than Tarceva®.
URI
http://ir.ymlib.yonsei.ac.kr/handle/22282913/161293
DOI
10.1080/03639045.2017.1326931
Appears in Collections:
1. Journal Papers (연구논문) > 1. College of Medicine (의과대학) > Dept. of Biochemistry and Molecular Biology (생화학-분자생물학교실)
Yonsei Authors
김건홍(Kim, Kun Hong) ; 양경미(Yang, Kyung Mi)
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Full Text
https://www.tandfonline.com/doi/full/10.1080/03639045.2017.1326931
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