Atomisation vs lyophilisation pour la microencapsulation: compréhension mécanistique des relations formulation-procédé-microstructure à l'échelle moléculaire pour maîtriser stabilité et libération // Spray-drying vs freeze-drying for microencapsulation:
|
ABG-136173
ADUM-71457 |
Sujet de Thèse | |
| 03/03/2026 | Contrat doctoral |
Université Claude Bernard Lyon 1
VILLEURBANNE Cedex - Auvergne-Rhône-Alpes - France
Atomisation vs lyophilisation pour la microencapsulation: compréhension mécanistique des relations formulation-procédé-microstructure à l'échelle moléculaire pour maîtriser stabilité et libération // Spray-drying vs freeze-drying for microencapsulation:
- Chimie
Microencapsulation, spray-drying, lyophilisation, modélisation
Microencapsulation, spray-drying, freeze-drying, modelling
Microencapsulation, spray-drying, freeze-drying, modelling
Description du sujet
Microencapsulation is widely used to protect sensitive compounds and to tailor their release, yet the choice
between spray-drying and freeze-drying is still largely empirical. These two processes generate markedly
different dried architectures (skin formation and internal gradients vs porous networks shaped by freezing and
sublimation), resulting in distinct stability and release behaviours. This PhD project aims to establish a
mechanistic and quantitative comparison between spray-drying and freeze-drying, linking molecular/colloidal
interactions in the feed formulation to process-driven microstructure, and ultimately to stability and release
kinetics. The work will deliver robust descriptors (e.g., water activity, sorption, glass transition temperature,
plasticization, porosity, internal distribution) and provide predictive guidelines to rationally select and design
drying routes for microencapsulation across applications.
------------------------------------------------------------------------------------------------------------------------------------------------------------------------
------------------------------------------------------------------------------------------------------------------------------------------------------------------------
Microencapsulation is widely used to protect sensitive compounds and to tailor their release, yet the choice
between spray-drying and freeze-drying is still largely empirical. These two processes generate markedly
different dried architectures (skin formation and internal gradients vs porous networks shaped by freezing and
sublimation), resulting in distinct stability and release behaviours. This PhD project aims to establish a
mechanistic and quantitative comparison between spray-drying and freeze-drying, linking molecular/colloidal
interactions in the feed formulation to process-driven microstructure, and ultimately to stability and release
kinetics. The work will deliver robust descriptors (e.g., water activity, sorption, glass transition temperature,
plasticization, porosity, internal distribution) and provide predictive guidelines to rationally select and design
drying routes for microencapsulation across applications.
------------------------------------------------------------------------------------------------------------------------------------------------------------------------
------------------------------------------------------------------------------------------------------------------------------------------------------------------------
Début de la thèse : 01/10/2026
between spray-drying and freeze-drying is still largely empirical. These two processes generate markedly
different dried architectures (skin formation and internal gradients vs porous networks shaped by freezing and
sublimation), resulting in distinct stability and release behaviours. This PhD project aims to establish a
mechanistic and quantitative comparison between spray-drying and freeze-drying, linking molecular/colloidal
interactions in the feed formulation to process-driven microstructure, and ultimately to stability and release
kinetics. The work will deliver robust descriptors (e.g., water activity, sorption, glass transition temperature,
plasticization, porosity, internal distribution) and provide predictive guidelines to rationally select and design
drying routes for microencapsulation across applications.
------------------------------------------------------------------------------------------------------------------------------------------------------------------------
------------------------------------------------------------------------------------------------------------------------------------------------------------------------
Microencapsulation is widely used to protect sensitive compounds and to tailor their release, yet the choice
between spray-drying and freeze-drying is still largely empirical. These two processes generate markedly
different dried architectures (skin formation and internal gradients vs porous networks shaped by freezing and
sublimation), resulting in distinct stability and release behaviours. This PhD project aims to establish a
mechanistic and quantitative comparison between spray-drying and freeze-drying, linking molecular/colloidal
interactions in the feed formulation to process-driven microstructure, and ultimately to stability and release
kinetics. The work will deliver robust descriptors (e.g., water activity, sorption, glass transition temperature,
plasticization, porosity, internal distribution) and provide predictive guidelines to rationally select and design
drying routes for microencapsulation across applications.
------------------------------------------------------------------------------------------------------------------------------------------------------------------------
------------------------------------------------------------------------------------------------------------------------------------------------------------------------
Début de la thèse : 01/10/2026
Nature du financement
Contrat doctoral
Précisions sur le financement
Concours pour un contrat doctoral
Présentation établissement et labo d'accueil
Université Claude Bernard Lyon 1
Etablissement délivrant le doctorat
Université Claude Bernard Lyon 1
Ecole doctorale
206 Chimie de Lyon
Profil du candidat
Candidate profile
Master's degree (or equivalent) in Chemistry / Chemical Engineering / Physical Chemistry / Soft matter /
Formulation science. Strong interest in mechanistic reasoning and quantitative experimentation. Experience
(or
motivation) in drying processes, thermal analysis (DSC/Tg), water activity/sorption, particle
characterisation, microscopy and statistical modelling (DoE) is appreciated.
Candidate profile Master's degree (or equivalent) in Chemistry / Chemical Engineering / Physical Chemistry / Soft matter / Formulation science. Strong interest in mechanistic reasoning and quantitative experimentation. Experience (or motivation) in drying processes, thermal analysis (DSC/Tg), water activity/sorption, particle characterisation, microscopy and statistical modelling (DoE) is appreciated.
Candidate profile Master's degree (or equivalent) in Chemistry / Chemical Engineering / Physical Chemistry / Soft matter / Formulation science. Strong interest in mechanistic reasoning and quantitative experimentation. Experience (or motivation) in drying processes, thermal analysis (DSC/Tg), water activity/sorption, particle characterisation, microscopy and statistical modelling (DoE) is appreciated.
24/04/2026
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