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Phase homogeneity in ternary amorphous solid dispersions and its impact on solubility, dissolution and supersaturation - Influence of processing and hydroxypropyl cellulose grade
被引:2
作者:

Postges, Florian
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机构:
Univ Bonn, Dept Pharmaceut Technol & Biopharmaceut, Gerhard Domagk Str 3, D-53121 Bonn, Germany Univ Bonn, Dept Pharmaceut Technol & Biopharmaceut, Gerhard Domagk Str 3, D-53121 Bonn, Germany

Lenhart, Jonas
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机构:
Univ Tubingen, Fac Sci, Dept Pharmaceut Technol, Morgenstelle 8, D-72076 Tubingen, Germany Univ Bonn, Dept Pharmaceut Technol & Biopharmaceut, Gerhard Domagk Str 3, D-53121 Bonn, Germany

Stoyanov, Edmont
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机构:
Nisso Chem Europe GmbH, Berliner Allee 42, D-40212 Dusseldorf, Germany Univ Bonn, Dept Pharmaceut Technol & Biopharmaceut, Gerhard Domagk Str 3, D-53121 Bonn, Germany

Lunter, Dominique J.
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Univ Tubingen, Fac Sci, Dept Pharmaceut Technol, Morgenstelle 8, D-72076 Tubingen, Germany Univ Bonn, Dept Pharmaceut Technol & Biopharmaceut, Gerhard Domagk Str 3, D-53121 Bonn, Germany

Wagner, Karl G.
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Univ Bonn, Dept Pharmaceut Technol & Biopharmaceut, Gerhard Domagk Str 3, D-53121 Bonn, Germany Univ Bonn, Dept Pharmaceut Technol & Biopharmaceut, Gerhard Domagk Str 3, D-53121 Bonn, Germany
机构:
[1] Univ Bonn, Dept Pharmaceut Technol & Biopharmaceut, Gerhard Domagk Str 3, D-53121 Bonn, Germany
[2] Univ Tubingen, Fac Sci, Dept Pharmaceut Technol, Morgenstelle 8, D-72076 Tubingen, Germany
[3] Nisso Chem Europe GmbH, Berliner Allee 42, D-40212 Dusseldorf, Germany
关键词:
Ternary amorphous solid dispersions;
Supersaturation;
Polymer mixing;
Hydroxypropyl cellulose;
Confocal Raman spectroscopy;
Dissolution;
HOT-MELT EXTRUSION;
POLYMER BLEND;
DRUG;
STABILITY;
BEHAVIOR;
STABILIZATION;
FORMULATIONS;
MISCIBILITY;
PERFORMANCE;
IMPROVEMENT;
D O I:
10.1016/j.ijpx.2023.100222
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
As performance of ternary amorphous solid dispersions (ASDs) depends on the solid-state characteristics and polymer mixing, a comprehensive understanding of synergistic interactions between the polymers in regard of dissolution enhancement of poorly soluble drugs and subsequent supersaturation stabilization is necessary. By choosing hot-melt extrusion (HME) and vacuum compression molding (VCM) as preparation techniques, we manipulated the phase behavior of ternary efavirenz (EFV) ASDs, comprising of either hydroxypropyl cellulose (HPC)-SSL or HPC-UL in combination with Eudragit (R) L 100-55 (EL 100-55) (50:50 polymer ratio), leading to single-phased (HME) and heterogeneous ASDs (VCM). Due to higher kinetic solid-state solubility of EFV in HPC polymers compared to EL 100-55, we visualized higher drug distribution into HPC-rich phases of the phase separated ternary VCM ASDs via confocal Raman microscopy. Additionally, we observed differences in the extent of phase-separation in dependence on the selected HPC grade. As HPC-UL exhibited decisive lower melt viscosity than HPC-SSL, formation of partially miscible phases between HPC-UL and EL 100-55 was facilitated. Consequently, as homogeneously mixed polymer phases were required for optimal extent of solubility improvement, the manufacturing-dependent differences in dissolution performances were smaller using HPC-UL, instead of HPC-SSL, i.e. using HPC-UL was less demanding on shear stress provided by the process.
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