Comparison of solventwetted and kneaded l -sulpirideloaded solid dispersions: Powder characterization and in vivo evaluation
2016; Elsevier BV; Volume: 511; Issue: 1 Linguagem: Inglês
10.1016/j.ijpharm.2016.07.006
ISSN1873-3476
AutoresDong Shik Kim, Jong Seo Choi, Dong Wuk Kim, Kyeong Soo Kim, Youn Gee Seo, Kwan Hyung Cho, Jong Oh Kim, Chul Soon Yong, Yu Seok Youn, Soo‐Jeong Lim, Sung Giu Jin, Han‐Gon Choi,
Tópico(s)Microencapsulation and Drying Processes
ResumoThe purpose of this study was to compare the powder properties, solubility, dissolution and oral absorption of solventwetted (SWSD) and kneaded (KNSD) l-sulpirideloaded solid dispersions. The SWSD and KNSD were prepared with silicon dioxide, sodium laurylsulfate and D-α-tocopheryl polyethylene glycol 1000 succinate (TPGS) using a spray dryer and high shear mixer, respectively. Their powder properties, solubility, dissolution and oral absorption were assessed compared to l-sulpiride powder. The drug in SWSD was in the amorphous state; however, in KNSD, it existed in the crystalline state. The SWSD with a drug/sodium laurylsulphate/TPGS/silicon dioxide ratio of 5/1/2/12 gave the higher drug solubility and dissolution compared to the KNSD with the same composition. The oral absorption of drug in the SWSD was 1.4 fold higher than the KNSD and 3.0 fold higher than the l-sulpiride powder (p < 0.05) owing to better solubility and reduced crystallinity. Furthermore, the SWSD at the half dose was bioequivalent of commercial l-sulpirideloaded product in rats. Thus, the SWSD with more improved oral absorption would be recommended as an alternative for the l-sulpirideloaded oral administration.
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