Interpreting non-linear drug diffusion data: Utilizing Korsmeyer-Peppas model to study drug release from liposomes

The aim of this work was to clarify the dynamics behind the influence of ionic strength on the changes in drug release from large unilamellar vesicles (LUVs). For this purpose, we have investigated the transport of two different model drugs (caffeine and hydrocortisone) formulated into liposomes thr...

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Vydané v:European journal of pharmaceutical sciences Ročník 138; s. 105026
Hlavní autori: Wu, Iren Yeeling, Bala, Sonali, Škalko-Basnet, Nataša, di Cagno, Massimiliano Pio
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Netherlands Elsevier B.V 01.10.2019
Predmet:
Cholesterol
Cholesterol - metabolism
Diffusion
Drug Delivery Systems - methods
Drug Liberation - physiology
Drug release kinetics
Kinetics
Korsmeyer-Peppas model
Large unilamellar vesicles
Liposomes - chemistry
Membranes - metabolism
Osmotic stress
Permepad
Pharmaceutical Preparations - metabolism
RT
iso
LUVs
SPC
K
Osmotic stress
SD
R2adj
Large unilamellar vesicles
Korsmeyer-Peppas model
hyper
EE
PBS
hypo
Mt/M
Cholesterol
n
RB
Drug release kinetics
t
Permepad
ZP
PI
RL
PL
ISSN:0928-0987, 1879-0720, 1879-0720
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Shrnutí:The aim of this work was to clarify the dynamics behind the influence of ionic strength on the changes in drug release from large unilamellar vesicles (LUVs). For this purpose, we have investigated the transport of two different model drugs (caffeine and hydrocortisone) formulated into liposomes through different types of barriers with different retention properties (regenerated cellulose and the newly introduced biomimetic barrier, Permeapad®). Drug release from liposomes was studied utilizing the standard Franz diffusion cells. LUV dispersions were exposed to the isotonic, hypotonic and hypertonic environment (difference of 300 mOsm/kg between the initial LUVs and the environment) and experimental data treated with both linear and non-linear (Korsmeyer-Peppas) regression models. To alter the rigidity of the liposomal membranes, cholesterol was introduced in the liposomal barriers (up to 25% w/w). Korsmeyer-Peppas model was proven to be suited to analyse experimental data throughout the experimental time frame, providing important additive information in comparison to standard linear approximation. The obtained results are highly relevant as they improve the interpretation of drug release kinetics from LUVs under osmotic stress. Moreover, the findings can be utilized in the development of liposomal formulations intended for nose-to-brain targeted drug delivery. [Display omitted]
Bibliografia:ObjectType-Article-1
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content type line 23
ISSN:0928-0987
1879-0720
1879-0720
DOI:10.1016/j.ejps.2019.105026