Pregled bibliografske jedinice broj: 1081626
A CGRP receptor antagonist peptide formulated for nasal administration to treat migraine
A CGRP receptor antagonist peptide formulated for nasal administration to treat migraine // Journal of pharmacy and pharmacology, 72 (2020), 10; 1352-1360 doi:10.1111/jphp.13317 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1081626 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
A CGRP receptor antagonist peptide formulated for
nasal administration to treat migraine
Autori
Mentzer, Bengt ; Russo, Andrew F. ; Zhang, Zhongming ; Kuburas, Adisa ; Killoran, Patrick M. ; D’Aloisio, Vera ; Nizic, Laura ; Capel, Vicky ; Kendall, David A. ; Coxon, Christopher R. ; Hutcheon, Gillian A.
Izvornik
Journal of pharmacy and pharmacology (0022-3573) 72
(2020), 10;
1352-1360
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
aCGRP (8-37) ; aCGRP (27-37) ; cAMP ; plasma extravasation ; SK-N-MC
Sažetak
Objectives To investigate the formulation of the peptide- based antagonist (34Pro, 35Phe)CGRP27–37, of the human calcitonin gene-related peptide (CGRP) receptor as a potential nasally delivered migraine treatment. Methods Peptide sequences were prepared using automated methods and purified by preparative HPLC. Their structure and stability were determined by LCMS. Antagonist potency was assessed by measuring CGRP-stimulated cAMP accumulation in SK-N-MC, cells and in CHO cells overexpressing the human CGRP receptor. In vivo activity was tested in plasma protein extravasation (PPE) studies using Evans blue dye accumulation. Peptide-containing chitosan microparticles were prepared by spray drying. Key findings (34Pro, 35Phe)CGRP27–37 exhibited a 10- fold increased affinity compared to aCGRP27–37. Administration of (34Pro, 35Phe)CGRP27–37 to mice led to a significant decrease in CGRP-induced PPE confirming antagonistic properties in vivo. There was no degradation of (34Pro, 35Phe)CGRP27–37 and no loss of antagonist potency during formulation and release from chitosan microparticles. Conclusions (34Pro, 35Phe)CGRP27–37 is a potent CGRP receptor antagonist both in vitro and in vivo, and it can be formulated as a dry powder with no loss of activity indicating its potential as a nasally formulated anti-migraine medicine.
Izvorni jezik
Engleski
Znanstvena područja
Farmacija, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)
POVEZANOST RADA
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb
Profili:
Laura Nižić Nodilo
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE