Erythritol-based dry powder of glucagon for pulmonary administration

被引:27
作者
Endo, K
Amikawa, S
Matsumoto, A
Sahashi, N
Onoue, S
机构
[1] Ito Life Sci Inc, Div Pharmaceut, Ibaraki 3020104, Japan
[2] Toho Univ, Dept Biol, Fac Pharmaceut Sci, Funabashi, Chiba 2748510, Japan
[3] Toho Univ, Fac Pharmaceut Sci, Dept Analyt Chem, Funabashi, Chiba 2748510, Japan
关键词
dry powder inhalant; erythritol; glucagon; carrier; excipient; pulmonary absorption;
D O I
10.1016/j.ijpharm.2004.11.018
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Glucagon, a key regulatory element of glycogen metabolism, is known to be effective in the clinical treatment of hypoglycemia and the maintenance of normal circulating glucose levels in patients with total pancreatectomy, however the clinical use of this gut hormone has been restricted to parenteral administration. In this investigation, we prepared dry powder dosage forms of glucagon, which were formulated by mixing micronized glucagon particles and excipients with larger carrier particles. To achieve alveolar deposition for subsequent systemic absorption, a dry powder inhalant (DPI) of glucagon was size-reduced to a mass median diameter between 1 and 6 mum, as measured by laser diffraction analysis. The use of erythritol as both excipient and carrier in DPI of glucagon resulted in high and reproducible flowability and dispersibility of the powder mixtures, and therefore it provided a low dosing of the active substances. Distinct transpulmonary absorption of glucagon was confirmed after intratracheal administration of the glucagon dry powder to anesthetized rats, as evidenced by the increase in the blood glucagon and blood sugar levels. These results suggested the usefulness of an erythritol-based powder form of glucagon for systemic administration. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:63 / 71
页数:9
相关论文
共 30 条
[1]   FORMATION AND STRUCTURE OF GELS AND FIBRILS FROM GLUCAGON [J].
BEAVEN, GH ;
GRATZER, WB ;
DAVIES, HG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1969, 11 (01) :37-&
[2]   GLUCAGON DEFICIENCY AND HYPERAMINOACIDEMIA AFTER TOTAL PANCREATECTOMY [J].
BODEN, G ;
MASTER, RW ;
REZVANI, I ;
PALMER, JP ;
LOBE, TE ;
OWEN, OE .
JOURNAL OF CLINICAL INVESTIGATION, 1980, 65 (03) :706-716
[3]   Effects of glucagon, insulin, amylin and CGRP on feeding [J].
Geary, N .
NEUROPEPTIDES, 1999, 33 (05) :400-405
[4]   Lower blood glucose, hyperglucagonemia, and pancreatic α cell hyperplasia in glucagon receptor knockout mice [J].
Gelling, RW ;
Du, XQ ;
Dichmann, DS ;
Romer, J ;
Huang, H ;
Cui, L ;
Obici, S ;
Tang, B ;
Holst, JJ ;
Fledelius, C ;
Johansen, PB ;
Rossetti, L ;
Jelicks, LA ;
Serup, P ;
Nishimura, E ;
Charron, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (03) :1438-1443
[6]  
HAGEN JH, 1961, J BIOL CHEM, V236, P1023
[7]   GLUCAGON RECEPTOR MESSENGER-RNA DISTRIBUTION IN RAT-TISSUES [J].
HANSEN, LH ;
ABRAHAMSEN, N ;
NISHIMURA, E .
PEPTIDES, 1995, 16 (06) :1163-1166
[8]   GLUCAGON IN THE METABOLIC AND NUTRITIONAL MANAGEMENT AFTER TOTAL PANCREATECTOMY - A CASE-REPORT [J].
HIROTA, M ;
IKEI, S ;
MISHIMA, M ;
MORI, K ;
SAKAMOTO, K ;
YAMANE, T ;
IDEGAMI, K ;
KATAFUCHI, S ;
KIYOHARA, H ;
NAKASHIMA, Y ;
NAKANO, M ;
AKAGI, M .
JAPANESE JOURNAL OF SURGERY, 1989, 19 (05) :586-592
[9]   Endoproteolysis of glucagon-like peptide (GLP)-1(7-36) amide by ectopeptidases in RINm5F cells [J].
HupeSodmann, K ;
Goke, R ;
Goke, B ;
Thole, HH ;
Zimmerman, B ;
Voigt, K ;
McGregor, GP .
PEPTIDES, 1997, 18 (05) :625-632
[10]   Effects of oral administration of erythritol on patients with diabetes [J].
Ishikawa, M ;
Miyashita, M ;
Kawashima, Y ;
Nakamura, T ;
Saitou, N ;
Modderman, J .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1996, 24 (02) :S303-S308