Emulsion-electrospun polyvinyl alcohol nanofibers as a solid dispersion system to improve solubility and control the release of probucol, a poorly water-soluble drug

被引:36
|
作者
Shibata, Takato [1 ]
Yoshimura, Nobuyoshi [2 ]
Kobayashi, Ayaka [2 ]
Ito, Takaaki [1 ]
Hara, Kouji [3 ]
Tahara, Kohei [1 ]
机构
[1] Gifu Pharmaceut Univ, Lab Pharmaceut Engn, 1-25-4 Daigaku Nishi, Gifu 5011196, Japan
[2] Mitsubishi Chem Corp, Osaka R&D Ctr, 2-13-1 Muroyama, Ibaraki, Osaka 5670052, Japan
[3] Mitsubishi Chem Corp, Healthcare Solut Unit, Chiyoda Ku, 1-1 Marunouchi 1 Chome, Tokyo 1008251, Japan
关键词
Nanofibers; Electrospinning; Emulsion; Solid dispersion; Poorly water-soluble drug; Polyvinyl alcohol; PHARMACEUTICAL APPLICATIONS; FORMULATION;
D O I
10.1016/j.jddst.2021.102953
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We attempted to improve the solubility of poorly water-soluble drugs by preparing drug-loaded polyvinyl alcohol (PVA) nanofibers as a solid dispersion system via emulsion electrospinning. Probucol (PBC), a poorly water-soluble drug, was used as a model drug. Nanofibers were electrospun using an oil/water (o/w) emulsion consisting of PBC dissolved in an immiscible solvent, such as ethyl acetate, and an aqueous PVA phase. PBC-containing PVA nanofibers with diameters ranging from 300 to 600 nm were obtained by electrospinning from o/w emulsions. The physical properties of the nanofibers were affected by the degrees of polymerization and hydrolysis of the PVA grades. In PVA nanofibers prepared without a surfactant, PBC existed in an amorphous state, and the dissolution of PBC was greatly improved. PBC dissolution was lower in PVA nanofibers with 30% PBC content compared to those with 11% or 20% PBC. In PVA nanofibers prepared using the surfactant polysorbate 80 as an emulsifier, PBC was partially crystallized; however, the PBC was homogenously dispersed, and dissolution was improved, even in PVA nanofibers containing 30% PBC. PVA nanofibers produced by o/w emulsion electrospinning were demonstrated to be suitable solid dispersion systems enabling robust controlled release of poorly water-soluble drugs.
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页数:10
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