TY - JOUR
T1 - Influence of formulation on jet nebulisation quality of α1 protease inhibitor
AU - Flament, M. P.
AU - Leterme, P.
AU - Burnouf, T.
AU - Gayot, A.
PY - 1999/2/1
Y1 - 1999/2/1
N2 - As foam appears during solution constitution and nebulisation of α1 protease inhibitor (α1 PI), we selected in a previous work, antifoams likely to be associated with an α1 PI solution to be nebulised: span 65 at a 0.025% concentration and cetyl alcohol at a 0.05% concentration associated with tyloxapol at 0.025% concentration. The purpose of this study was, on the one hand to study the influence of the formulation on nebulisation quality by relating physicochemical properties and nebulisation capacity, and on the other hand, to define the α1 PI that will be retained for a clinical study. The properties of the different α1 PI formulations are compared: surface tension, viscosity, time required to constitute the protein solution and pH. Nebulisation quality is evaluated under different operating conditions by measuring the droplet size, the quantity of α1 PI nebulised, nebulisation time and the quantity of α1 PI likely to reach the lungs which was subjected to statistical analysis. The statistical analysis of results indicates that the addition of the cetyl alcohol/tyloxapol mixture improves nebulisation effectiveness by significantly increasing the quantity of drug nebulised and therefore the quantity of α1 PI likely to reach the lungs. It is this formulation that will be retained for clinical trials. We check that the nebuliser and operating conditions influence all the parameters, that is to say the respirable fraction, the quantity nebulised and the nebulisation time. Although there is no interaction between the nebuliser and the formulation, nebulisation quality is the combined result of the formulation, the nebuliser and the operating conditions. Copyright (C) 1999 Elsevier Science Ireland Ltd.
AB - As foam appears during solution constitution and nebulisation of α1 protease inhibitor (α1 PI), we selected in a previous work, antifoams likely to be associated with an α1 PI solution to be nebulised: span 65 at a 0.025% concentration and cetyl alcohol at a 0.05% concentration associated with tyloxapol at 0.025% concentration. The purpose of this study was, on the one hand to study the influence of the formulation on nebulisation quality by relating physicochemical properties and nebulisation capacity, and on the other hand, to define the α1 PI that will be retained for a clinical study. The properties of the different α1 PI formulations are compared: surface tension, viscosity, time required to constitute the protein solution and pH. Nebulisation quality is evaluated under different operating conditions by measuring the droplet size, the quantity of α1 PI nebulised, nebulisation time and the quantity of α1 PI likely to reach the lungs which was subjected to statistical analysis. The statistical analysis of results indicates that the addition of the cetyl alcohol/tyloxapol mixture improves nebulisation effectiveness by significantly increasing the quantity of drug nebulised and therefore the quantity of α1 PI likely to reach the lungs. It is this formulation that will be retained for clinical trials. We check that the nebuliser and operating conditions influence all the parameters, that is to say the respirable fraction, the quantity nebulised and the nebulisation time. Although there is no interaction between the nebuliser and the formulation, nebulisation quality is the combined result of the formulation, the nebuliser and the operating conditions. Copyright (C) 1999 Elsevier Science Ireland Ltd.
KW - Antifoam
KW - Formulation
KW - Nebulisation quality
KW - Surface tension
KW - α Protease inhibitor
UR - https://www.scopus.com/pages/publications/0033044720
UR - https://www.scopus.com/pages/publications/0033044720#tab=citedBy
U2 - 10.1016/S0378-5173(98)00354-8
DO - 10.1016/S0378-5173(98)00354-8
M3 - Article
C2 - 10205630
AN - SCOPUS:0033044720
SN - 0378-5173
VL - 178
SP - 101
EP - 109
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
IS - 1
ER -