Characterization and pharmacokinetic study of itraconazole solid dispersions prepared by solvent-controlled precipitation and spray-dry methods. (5th September 2017)
- Record Type:
- Journal Article
- Title:
- Characterization and pharmacokinetic study of itraconazole solid dispersions prepared by solvent-controlled precipitation and spray-dry methods. (5th September 2017)
- Main Title:
- Characterization and pharmacokinetic study of itraconazole solid dispersions prepared by solvent-controlled precipitation and spray-dry methods
- Authors:
- Sim, Taehoon
Lim, Chaemin
Lee, Jun Won
Kim, Dong Wuk
Kim, Youngsam
Kim, Minsoo
Choi, Seungmok
Choi, Han-Gon
Lee, Eun Seong
Kim, Kil-Soo
Kang, Wonku
Oh, Kyung Taek - Abstract:
- Abstract: Objectives: Solid dispersion formulations have attracted attention to improve solubility and bioavailability of water-insoluble drugs. In this study, the variation of solubility and bioavailability by different preparation methods were studied using itraconazole (ITZ) solid dispersions. Methods: Itraconazole solid dispersions were prepared by a solvent-controlled precipitation method (SCPM) using HPMCAS-LF, HCl antisolvent or a spray-drying method (SDM) for comparison. Dissolution tests by pH transition and pharmacokinetic study using male Sprague Dawley rats were conducted. Key findings: Itraconazole solid dispersion dissolution tests by pH transition exhibited better dissolution compared to naive ITZ, limited dissolution in acidic conditions and a burst release at neutral pH. The ITZ solid dispersions by SCPM indicated a smaller-sized particle dispersion, limited dissolution at acidic pH and a higher release at neutral pH compared to those by SDM, suggesting that the increased protonation of anionic polymers and HPMCAS-LF by acidic antisolvent could form a tighter hydrophobic aggregation with ITZ in solid dispersions. ITZ solid dispersion prepared by SCPM also showed improved ITZ absorption in male Sprague Dawley rats compared to SDM and naïve ITZ. Conclusions: This study suggests that the SCPM method can be widely used for solid dispersion preparations due to improved dissolution and PK profile.
- Is Part Of:
- Journal of pharmacy and pharmacology. Volume 69:Number 12(2017:Dec.)
- Journal:
- Journal of pharmacy and pharmacology
- Issue:
- Volume 69:Number 12(2017:Dec.)
- Issue Display:
- Volume 69, Issue 12 (2017)
- Year:
- 2017
- Volume:
- 69
- Issue:
- 12
- Issue Sort Value:
- 2017-0069-0012-0000
- Page Start:
- 1707
- Page End:
- 1715
- Publication Date:
- 2017-09-05
- Subjects:
- biological evaluation of dosage forms -- controlled- and sustained-release systems -- dosage form design and characterization -- pharmaceutics and drug delivery
Pharmacy -- Periodicals
Pharmacology -- Periodicals
615.1 - Journal URLs:
- https://academic.oup.com/jpp ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)2042-7158 ↗
http://onlinelibrary.wiley.com/ ↗
http://www.ingentaconnect.com/content/rpsgb/jpp ↗ - DOI:
- 10.1111/jphp.12805 ↗
- Languages:
- English
- ISSNs:
- 0022-3573
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5034.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 16558.xml