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Increased dissolution and oral absorption of itraconazole/Soluplus extrudate compared with itraconazole nanosuspension.
Eur J Pharm Biopharm. 2013 Nov; 85(3 Pt B):1285-92.EJ

Abstract

The purpose of this article was to compare the in vitro and in vivo profiles of itraconazole (ITZ) extrudates and nanosuspension separately prepared by two different methods. And it was proved truly to form nanocrystalline and amorphous ITZ characterized by differential scanning calorimetry (DSC), X-ray powder diffraction (XRD) analysis, Fourier transform infrared spectrum (FTIR), transmission electron microscope (TEM), and scanning electron microscope (SEM). The release of ITZ/Soluplus solid dispersions with amorphous ITZ was almost complete while only 40% release was obtained with ITZ nanocrystals. The amorphous state need not to cross over the crystal lattice energy upon dissolution while the crystalline need to overcome it. In the in vivo assay, the AUC(0-t) and C(max) of ITZ/Soluplus were 6.9- and 11.6-time higher than those of pure ITZ. The formulation of the extrudate had an AUC(0-t) and C(max) similar to those of ITZ and also OH-ITZ compared with the commercial capsule (Sporanox®). The relative bioavailability values with their 95% confidence limit were calculated to be 98.3% (92.5-104.1%) and 101.3% (97.9-104.1%), respectively. The results of this study showed increased dissolution and bioavailability of the solid dispersion of Soluplus-based carrier loading ITZ prepared by HME compared with the ITZ nanosuspension prepared by wet milling.

Authors+Show Affiliations

School of Pharmacy, Shenyang Pharmaceutical University, China. Electronic address: zhangkeru89@126.com.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

23562534

Citation

Zhang, Keru, et al. "Increased Dissolution and Oral Absorption of itraconazole/Soluplus Extrudate Compared With Itraconazole Nanosuspension." European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V, vol. 85, no. 3 Pt B, 2013, pp. 1285-92.
Zhang K, Yu H, Luo Q, et al. Increased dissolution and oral absorption of itraconazole/Soluplus extrudate compared with itraconazole nanosuspension. Eur J Pharm Biopharm. 2013;85(3 Pt B):1285-92.
Zhang, K., Yu, H., Luo, Q., Yang, S., Lin, X., Zhang, Y., Tian, B., & Tang, X. (2013). Increased dissolution and oral absorption of itraconazole/Soluplus extrudate compared with itraconazole nanosuspension. European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V, 85(3 Pt B), 1285-92. https://doi.org/10.1016/j.ejpb.2013.03.002
Zhang K, et al. Increased Dissolution and Oral Absorption of itraconazole/Soluplus Extrudate Compared With Itraconazole Nanosuspension. Eur J Pharm Biopharm. 2013;85(3 Pt B):1285-92. PubMed PMID: 23562534.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Increased dissolution and oral absorption of itraconazole/Soluplus extrudate compared with itraconazole nanosuspension. AU - Zhang,Keru, AU - Yu,Hongxia, AU - Luo,Qing, AU - Yang,Shenshen, AU - Lin,Xia, AU - Zhang,Yu, AU - Tian,Bin, AU - Tang,Xing, Y1 - 2013/04/03/ PY - 2012/12/05/received PY - 2013/02/26/revised PY - 2013/03/05/accepted PY - 2013/4/9/entrez PY - 2013/4/9/pubmed PY - 2014/8/13/medline KW - Amorphous state KW - Bioavailability KW - Dissolution KW - Hot melt extrude KW - Itraconazole KW - Nanocrystal KW - Wet milling SP - 1285 EP - 92 JF - European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V JO - Eur J Pharm Biopharm VL - 85 IS - 3 Pt B N2 - The purpose of this article was to compare the in vitro and in vivo profiles of itraconazole (ITZ) extrudates and nanosuspension separately prepared by two different methods. And it was proved truly to form nanocrystalline and amorphous ITZ characterized by differential scanning calorimetry (DSC), X-ray powder diffraction (XRD) analysis, Fourier transform infrared spectrum (FTIR), transmission electron microscope (TEM), and scanning electron microscope (SEM). The release of ITZ/Soluplus solid dispersions with amorphous ITZ was almost complete while only 40% release was obtained with ITZ nanocrystals. The amorphous state need not to cross over the crystal lattice energy upon dissolution while the crystalline need to overcome it. In the in vivo assay, the AUC(0-t) and C(max) of ITZ/Soluplus were 6.9- and 11.6-time higher than those of pure ITZ. The formulation of the extrudate had an AUC(0-t) and C(max) similar to those of ITZ and also OH-ITZ compared with the commercial capsule (Sporanox®). The relative bioavailability values with their 95% confidence limit were calculated to be 98.3% (92.5-104.1%) and 101.3% (97.9-104.1%), respectively. The results of this study showed increased dissolution and bioavailability of the solid dispersion of Soluplus-based carrier loading ITZ prepared by HME compared with the ITZ nanosuspension prepared by wet milling. SN - 1873-3441 UR - https://www.unboundmedicine.com/medline/citation/23562534/Increased_dissolution_and_oral_absorption_of_itraconazole/Soluplus_extrudate_compared_with_itraconazole_nanosuspension_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0939-6411(13)00084-2 DB - PRIME DP - Unbound Medicine ER -