TY - JOUR
T1 - Inhalative administration of insulin using a new bubble jet atomization device.
AU - Hisasue, Junko
AU - Fukuyama, Satoru
AU - Nakagaki, Noriaki
AU - Moriwaki, Atsushi
AU - Inoue, Sachiko
AU - Sakurada, Naoko
AU - Kaneko, Hideki
AU - Takayama, Koichi
AU - Inoue, Hiromasa
AU - Nakanishi, Yoichi
N1 - Funding Information:
Acknowledgements The authors are grateful to H.K. Selbmann (Institut für Medizinische Biometrie, Tübingen, Germany) for discussions and critical advice in the planning phase regarding techniques to ensure objectivity of the guidelines. The authors appreciate the help of Dr. S. Nikolaus (Kiel, Germany, for recording the discussion during the guidelines conference and for conducting Medline/abstract searches to obtain evidence generated by clinical trials, experiments and other reports) and of Dr. N. Sfikas (Kiel, Germany, for calculating confidence intervals from the response rates reported in the literature). The generation of guidelines and the expert consensus were financed by public funds (BMBF Competence Network “Inflammatory Bowel Disease”) and through joint contributions of Amgen GmbH, Ares Serono AG, Celltech/Medeva Inc., ISIS Pharmaceuticals and Schering-Plough Research Institute. All industrial contributions were handled through a university trust account without direct contacts between attendees of the guidelines conference and sponsoring institutions/companies.
PY - 2011/6
Y1 - 2011/6
N2 - In this study, we attempted to perform inhalative administration of insulin using a new "bubble jet" atomization device based on ink jet printing technology and developed by Canon Inc. The aim of this study was to confirm the usefulness of the new device for achieving a hypoglycemic effect by insulin inhalation in normal rats. Inhaled insulin (15 U/kg) or a control solution without insulin was administrated to each Wistar rat intratracheally using the bubble-jet atomization device. Blood glucose concentrations were measured at 0, 10, 20, 30, 60, 90 and 120 min after administration of insulin or control solution. The blood glucose concentrations in the inhaled insulin group were 63 +/- 10 mg/dl (20 min), 43 +/- 8 mg/dl (60 min) and 35 +/- 9 mg/dl (120 min), while those in the control solution group were 80 +/- 9 mg/dl (p = 0.016), 75 +/- 10 mg/dl (p < 0.001) and 85 +/- 27 mg/dl (p < 0.001). The blood glucose concentrations after administration of inhaled insulin were significantly lower than those after administration of control solution at all time points (p < 0.05) except 0 and 10 min. We confirmed the hypoglycemic effect of inhaled insulin using the new bubble jet atomization device. These results proved that the new device could atomize insulin while maintaining its bioactivity.
AB - In this study, we attempted to perform inhalative administration of insulin using a new "bubble jet" atomization device based on ink jet printing technology and developed by Canon Inc. The aim of this study was to confirm the usefulness of the new device for achieving a hypoglycemic effect by insulin inhalation in normal rats. Inhaled insulin (15 U/kg) or a control solution without insulin was administrated to each Wistar rat intratracheally using the bubble-jet atomization device. Blood glucose concentrations were measured at 0, 10, 20, 30, 60, 90 and 120 min after administration of insulin or control solution. The blood glucose concentrations in the inhaled insulin group were 63 +/- 10 mg/dl (20 min), 43 +/- 8 mg/dl (60 min) and 35 +/- 9 mg/dl (120 min), while those in the control solution group were 80 +/- 9 mg/dl (p = 0.016), 75 +/- 10 mg/dl (p < 0.001) and 85 +/- 27 mg/dl (p < 0.001). The blood glucose concentrations after administration of inhaled insulin were significantly lower than those after administration of control solution at all time points (p < 0.05) except 0 and 10 min. We confirmed the hypoglycemic effect of inhaled insulin using the new bubble jet atomization device. These results proved that the new device could atomize insulin while maintaining its bioactivity.
UR - http://www.scopus.com/inward/record.url?scp=80052074599&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=80052074599&partnerID=8YFLogxK
M3 - Article
C2 - 21823515
AN - SCOPUS:80052074599
SN - 0016-254X
VL - 102
SP - 215
EP - 222
JO - Fukuoka igaku zasshi = Hukuoka acta medica
JF - Fukuoka igaku zasshi = Hukuoka acta medica
IS - 6
ER -