Challenges with Developing In Vitro Dissolution Tests for Orally Inhaled Products (OIPs)

T Riley, D Christopher, J Arp, A Casazza… - Aaps Pharmscitech, 2012 - Springer
The purpose of this article is to review the suitability of the analytical and statistical
techniques that have thus far been developed to assess the dissolution behavior of particles …

[HTML][HTML] In vitro dissolution and permeability testing of inhalation products: Challenges and advances

A Nokhodchi, S Chavan, T Ghafourian - Pharmaceutics, 2023 - mdpi.com
In vitro dissolution and permeability testing aid the simulation of the in vivo behavior of
inhalation drug products. Although the regulatory bodies have specific guidelines for the …

[PDF][PDF] The inhalation ad hoc advisory panel for the USP performance tests of inhalation dosage forms

VP Shah, MJ Smurthwaite, JM Veranth… - Pharmaceutical …, 2008 - researchgate.net
ABSTRACT The US Pharmacopeia (USP) contains standards for tests, procedures, and
acceptance criteria for inhalation dosage forms that are administered orally and intranasally …

[PDF][PDF] Towards standardized dissolution techniques for in vitro performance testing of dry powder inhalers

A Floroiu, M Klein, J Krämer, CM Lehr - Dissolution Technol, 2018 - dissolutiontech.com
The pulmonary route of administration is used for both locally and systemically acting drugs.
However, knowledge gaps about the fate of aerosol particles after deposition in the lung …

Dry powder inhalers: An overview of the in vitro dissolution methodologies and their correlation with the biopharmaceutical aspects of the drug products

SP Velaga, J Djuris, S Cvijic, S Rozou, P Russo… - European Journal of …, 2018 - Elsevier
In vitro dissolution testing is routinely used in the development of pharmaceutical products.
Whilst the dissolution testing methods are well established and standardized for oral dosage …

Development of a standardized dissolution test method for inhaled pharmaceutical formulations

YJ Son, JT McConville - International journal of pharmaceutics, 2009 - Elsevier
The aim of this research was to investigate a potential standardized test method to
characterize the dissolution properties of formulations intended for pulmonary delivery. A …

Dissolution Techniques for In Vitro Testing of Dry Powders for Inhalation

S May, B Jensen, M Wolkenhauer, M Schneider… - Pharmaceutical …, 2012 - Springer
Purpose To evaluate different dissolution testing methods and subsequently develop a
simple to perform but reproducible and discriminating dissolution technique for inhalative …

[HTML][HTML] RespiCellTM: An Innovative Dissolution Apparatus for Inhaled Products

F Sonvico, V Chierici, G Varacca, E Quarta, D D'angelo… - Pharmaceutics, 2021 - mdpi.com
To overcome some of the shortfalls of the types of dissolution testing currently used for
pulmonary products, a new custom-built dissolution apparatus has been developed. For …

[HTML][HTML] Development of an Aerosol Dose Collection Apparatus for In Vitro Dissolution Measurements of Orally Inhaled Drug Products

R Price, J Shur, W Ganley, G Farias, N Fotaki… - The AAPS journal, 2020 - Springer
The aim of the study was to develop a robust and standardized in vitro dissolution
methodology for orally inhaled drug products (OIDPs). An aerosol dose collection (ADC) …

[PDF][PDF] Optimization of an in vitro dissolution test method for inhalation formulations

YJ Son, M Horng, M Copley, JT McConville - Dissolution Technol, 2010 - researchgate.net
The aim of this research project was to investigate a potential standardized test method to
characterize the dissolution properties of numerous formulation types available for …