Hydroxypropyl Methylcellulose Acetate Succinate-Based Spray-Dried Dispersions: An Overview
Распылительно высушенные дисперсии на основе ацетата сукцината гидроксипропилметилцеллюлозы: обзор
2008-12-01
SCID: 54.1/656k72ua
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amorphous drug/polymer colloidsbioavailabilityhydroxypropyl methylcellulose acetate succinatespray-dried dispersionssupersaturation
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Abstract (AI)
Spray-dried dispersions (SDDs) of low-solubility drugs have been prepared using the polymer hydroxypropyl methylcellulose acetate succinate (HPMCAS). For a variety of drug structures, these SDDs provide supersaturation in in vitro dissolution determinations and large bioavailability increases in vivo. In bile-salt/lecithin in vitro solutions, these SDDs provide amorphous drug/polymer colloids and an increased concentration of free drug and drug in micelles relative to crystalline or amorphous drug. As dry powders, the SDDs are a single amorphous phase in which the drug remains amorphous and dispersed and does not crystallize over storage times relevant for practical drug products. A melting temperature (Tm)/glass-transition temperature (Tg) (K/K) versus log P map for 139 compounds formulated as SDDs provides a perspective on an appropriate formulation strategy for low-solubility drugs with various physical properties.
Key Findings
1
A Tm/Tg versus log P map covering 139 compounds supports formulation-strategy selection for low-solubility drugs with varied properties.
2
HPMCAS-based spray-dried dispersions provide supersaturation during in vitro dissolution across diverse low-solubility drug structures.
3
In bile-salt/lecithin media, HPMCAS dispersions form amorphous drug–polymer colloids and increase free and micellar drug concentrations.
4
The dry dispersions form a single amorphous phase that maintains dispersed, noncrystalline drug during practically relevant storage.
5
These dispersions produce large in vivo bioavailability increases compared with crystalline or amorphous drug forms.
Research Object
Hydroxypropyl methylcellulose acetate succinate-based spray-dried dispersions of low-solubility drugs
Research Subject
The dispersions’ ability to maintain amorphous drug state, prevent crystallization, generate supersaturation and colloidal/micellar drug solubilization, and enhance bioavailability across drugs with different physical properties
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2008-12-01
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