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3D-Printed Solid Dispersion Drug Products
被引:15
|作者:
Chew, Suet Li
[1
]
de Mohac, Laura Modica
[1
,2
]
Raimi-Abraham, Bahijja Tolulope
[1
]
机构:
[1] Kings Coll London, Fac Life Sci & Med, Inst Pharmaceut Sci, Drug Delivery Grp, Franklin Wilkins Bldg,150 Stamford St, London SE1 9NH, England
[2] Univ Palermo, Dept Sci Hlth Promot & Mother Child Care G DAless, I-90100 Palermo, Italy
关键词:
3D printing;
amorphous solid dispersion;
additive manufacturing;
poor solubility;
fixed dose combination;
SOLUBILITY PARAMETERS;
RELEASE;
FABRICATION;
CRYSTALLIZATION;
FORMULATION;
MECHANISMS;
POLYMERS;
SOLVENT;
IMPROVE;
TABLETS;
D O I:
10.3390/pharmaceutics11120672
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
With the well-known advantages of additive manufacturing methods such as three-dimensional (3D) printing in drug delivery, it is disappointing that only one product has been successful in achieving regulatory approval in the past few years. Further research and development is required in this area to introduce more 3D printed products into the market. Our study investigates the potential of fixed dose combination solid dispersion drug products generated via 3D printing. Two model drugs-fluorescein sodium (FS) and 5-aminosalicyclic acid (5-ASA)-were impregnated onto a polyvinyl alcohol (PVA) filament, and the influence of solvent choice in optimal drug loading as well as other influences such as the physicochemical and mechanical properties of the resultant filaments were investigated prior to development of the resultant drug products. Key outcomes of this work included the improvement of filament drug loading by one- to threefold due to solvent choice on the basis of its polarity and the generation of a 3D-printed product confirmed to be a solid dispersion fixed dose combination with the two model drugs exhibiting favourable in vitro dissolution characteristics.
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页数:12
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