Literature DB >> 29248606

Comparison of a revaprazan-loaded solid dispersion, solid SNEDDS and inclusion compound: Physicochemical characterisation and pharmacokinetics.

Jong Hyuck Park1, Dong Shik Kim1, Omer Mustapha2, Abid Mehmood Yousaf3, Jung Suk Kim1, Dong Wuk Kim4, Chul Soon Yong5, Yu Seok Youn6, Kyung Taek Oh7, Soo-Jeong Lim8, Jong Oh Kim9, Han-Gon Choi10.   

Abstract

The aim of this research was to compare three strategies for enhancing the solubility of poorly water-soluble revaprazan hydrochloride: solid dispersion, solid SNEDDS and inclusion compound. The influence of polymers, surfactants and oils on the drug solubility was assessed, and via the chosen carriers, the three types of formulations were prepared utilising spray drying technique. Their physicochemical properties, solubility, dissolution and pharmacokinetics in rats were performed compared with revaprazan powder. Among the liquid SNEDDS formulations assessed, the compositions of revaprazan, peceol, Tween 80 and Labrasol (10:15:55:30, weight ratio) provided the smallest emulsion size. Moreover, this liquid SNEDDS and dextran were suspended/dissolved in distilled water, and spray-dried, producing an optimal revaprazan-loaded solid SNEDDS. The appropriate solid dispersion and inclusion compound were composed of revaprazan, hydroxypropylmethylcellulose and cremophor A25 (5:1.4:5.6) and drug and hydroxyl-β-cyclodextrin (2.5:8.77), respectively. The crystalline drug was converted to an amorphous state in all formulations. In the solid dispersion, the drug was attached to the hydrophilic carrier. The solid SNEDDS and inclusion compound contained aggregate microspheres and separate microspheres, respectively. All formulations significantly increased the drug solubility, dissolution, plasma concentration and AUC compared with revaprazan powder. These properties were ranked in the order solid dispersion ≥ solid SNEDDS > inclusion compound. Particularly, the solid dispersion improved about 9500-fold drug solubility and 10-fold oral bioavailability. Thus, the improved properties were considerably dependent upon these techniques, although all of the techniques employed similar mechanisms. Among the strategies checked, the solid dispersion system would be recommended as an oral revaprazan-loaded pharmaceutical product.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Bioavailability; Crystallinity; Inclusion compound; Revaprazan hydrochloride; Solid SNEDDS; Solid dispersion; Solubility

Mesh:

Substances:

Year:  2017        PMID: 29248606     DOI: 10.1016/j.colsurfb.2017.12.017

Source DB:  PubMed          Journal:  Colloids Surf B Biointerfaces        ISSN: 0927-7765            Impact factor:   5.268


  7 in total

Review 1.  Advances in the use of functional composites of β-cyclodextrin in electrochemical sensors.

Authors:  Xiaohui Niu; Zunli Mo; Xing Yang; Mingyuan Sun; Pan Zhao; Zhenliang Li; Meixuan Ouyang; Zhenyu Liu; Huhu Gao; Ruibin Guo; Nijuan Liu
Journal:  Mikrochim Acta       Date:  2018-06-16       Impact factor: 5.833

2.  Development of a Solid Supersaturable Micelle of Revaprazan for Improved Dissolution and Oral Bioavailability Using Box-Behnken Design.

Authors:  Yoon Tae Goo; Cheol-Ki Sa; Ji Yeh Choi; Min Song Kim; Chang Hyun Kim; Hyeon Kyun Kim; Young Wook Choi
Journal:  Int J Nanomedicine       Date:  2021-02-17

3.  Preparation and evaluation of tacrolimus-loaded thermosensitive solid lipid nanoparticles for improved dermal distribution.

Authors:  Ji-Hyun Kang; Jinmann Chon; Young-Il Kim; Hyo-Jung Lee; Dong-Won Oh; Hong-Goo Lee; Chang-Soo Han; Dong-Wook Kim; Chun-Woong Park
Journal:  Int J Nanomedicine       Date:  2019-07-18

4.  A Solid Ultra Fine Self-Nanoemulsifying Drug Delivery System (S-SNEDDS) of Deferasirox for Improved Solubility: Optimization, Characterization, and In Vitro Cytotoxicity Studies.

Authors:  Alaa Alghananim; Yıldız Özalp; Burcu Mesut; Nedime Serakinci; Yıldız Özsoy; Sevgi Güngör
Journal:  Pharmaceuticals (Basel)       Date:  2020-07-24

5.  Comparison of Three Different Aqueous Microenvironments for Enhancing Oral Bioavailability of Sildenafil: Solid Self-Nanoemulsifying Drug Delivery System, Amorphous Microspheres and Crystalline Microspheres.

Authors:  Jung Suk Kim; Fakhar Ud Din; Sang Min Lee; Dong Shik Kim; Mi Ran Woo; Seunghyun Cheon; Sang Hun Ji; Jong Oh Kim; Yu Seok Youn; Kyung Taek Oh; Soo-Jeong Lim; Sung Giu Jin; Han-Gon Choi
Journal:  Int J Nanomedicine       Date:  2021-08-24

Review 6.  Mechanisms of increased bioavailability through amorphous solid dispersions: a review.

Authors:  Andreas Schittny; Jörg Huwyler; Maxim Puchkov
Journal:  Drug Deliv       Date:  2020-12       Impact factor: 6.419

7.  Electrospun Gelatin Nanocontainers for Enhanced Biopharmaceutical Performance of Piroxicam: In Vivo and In Vitro Investigations.

Authors:  Lin Zhao; Omer Mustapha; Shumaila Shafique; Talha Jamshaid; Fakhar Ud Din; Yasir Mehmood; Khaleeq Anwer; Qurrat Ul Ain Yousafi; Talib Hussain; Ikram Ullah Khan; Muhammad Usman Ghori; Yasser Shahzad; Abid Mehmood Yousaf
Journal:  Int J Nanomedicine       Date:  2020-11-10
  7 in total

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