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  • Preparation and evaluation of high dispersion stable nanocrystal formulation of poorly water-soluble compounds by using povacoat.

Preparation and evaluation of high dispersion stable nanocrystal formulation of poorly water-soluble compounds by using povacoat.

Journal of pharmaceutical sciences (2014-09-12)
Kayo Yuminoki, Fuko Seko, Shota Horii, Haruka Takeuchi, Katsuya Teramoto, Yuichiro Nakada, Naofumi Hashimoto
ABSTRACT

In this study, we reported the application of Povacoat®, a hydrophilic polyvinylalcohol copolymer, as a dispersion stabilizer of nanoparticles of poorly water-soluble compounds. In addition, the influence of aggregation of the nanoparticles on their solubility and oral absorption was studied. Griseofulvin (GF) was used as a model compound with poor water solubility and was milled to nanoparticles by wet bead milling. The dispersion stability of GF milled with Povacoat® or the generally used polymers (polyvinylalcohol, hydroxypropylcellulose SSL, and polyvinylpyrrolidone K30) was compared. Milled GF suspended in Povacoat® aqueous solution with D-mannitol, added to improve the disintegration rate of freeze-dried GF, exhibited high dispersion stability without aggregation (D90 = ca. 0.220 μm), whereas milled GF suspended in aqueous solutions of the other polymers aggregated (D90 > 5 μm). Milled GF with Povacoat® showed improved aqueous solubility and bioavailability compared with the other polymers. The aggregation of nanoparticles had significant impact on the solubility and bioavailability of GF. Povacoat® also prevented the aggregation of the various milled poorly water-soluble compounds (hydrochlorothiazide and tolbutamide, etc.) more effectively than the other polymers. These results showed that Povacoat® could have wide applicability to the development of nanoformulations of poorly water-soluble compounds.

MATERIALS
Product Number
Brand
Product Description

Supelco
Griseofulvin, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
Mannitol, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
D-Mannitol, SAJ first grade, ≥99.0%
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Acyclovir, Pharmaceutical Secondary Standard; Certified Reference Material
USP
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USP
Griseofulvin, United States Pharmacopeia (USP) Reference Standard
USP
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Acycloguanosine, ≥99% (HPLC), powder
Sigma-Aldrich
Griseofulvin, from Penicillium griseofulvum, 97.0-102.0%
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Indomethacin, 98.5-100.5% (in accordance with EP)
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D-Mannitol, meets EP, FCC, USP testing specifications
Sigma-Aldrich
D-Mannitol, ≥98% (GC), suitable for plant cell culture
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D-Mannitol, ≥98% (GC)
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Millipore
D-Mannitol, ACS reagent, ≥99.0%, suitable for microbiology
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D-Mannitol, BioUltra, ≥99.0% (sum of enantiomers, HPLC)
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Indomethacin, Pharmaceutical Secondary Standard; Certified Reference Material
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Indomethacin, meets USP testing specifications
USP
Indomethacin, United States Pharmacopeia (USP) Reference Standard
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USP
Griseofulvin Permeability Diameter, United States Pharmacopeia (USP) Reference Standard