Literature DB >> 23396259

Supersaturatable formulations for the enhanced oral absorption of sirolimus.

Min-Soo Kim1, Jeong-Soo Kim, Wonkyung Cho, Kwang-Ho Cha, Hee-Jun Park, Junsung Park, Sung-Joo Hwang.   

Abstract

The purpose of this study was to develop supersaturatable formulations for the enhanced solubility and oral absorption of sirolimus. Supersaturatable formulations of hydrophilic polymers and/or surfactants were screened by formulation screening, which is based on solvent casting. The solid dispersion particles in the optimized formulations were prepared by spray drying. The particles were characterized in vitro and in vivo. The most effective supersaturatable formulation found in the formulation screening process was hydroxypropylmethyl cellulose (HPMC)-D-α-tocopheryl polyethylene glycol 1000 succinate (TPGS), followed by HPMC-Sucroester. In addition, the supersaturated state generated from HPMC-TPGS and HPMC-Sucroester 15 particles prepared by spray drying significantly improved the oral absorption of sirolimus in rats. Based on the pharmacokinetic parameters and supporting in vitro supersaturated dissolution data, the enhanced supersaturation properties of sirolimus led to enhanced in vivo oral absorption. In addition, the experimental results from the formulation screening used in our study could be useful for enhancing the bioavailability of sirolimus in preformulation and formulation studies.
Copyright © 2013 Elsevier B.V. All rights reserved.

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Year:  2013        PMID: 23396259     DOI: 10.1016/j.ijpharm.2013.01.067

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  7 in total

1.  Preparation and in vivo evaluation of a dutasteride-loaded solid-supersaturatable self-microemulsifying drug delivery system.

Authors:  Min-Soo Kim; Eun-Sol Ha; Gwang-Ho Choo; In-Hwan Baek
Journal:  Int J Mol Sci       Date:  2015-05-13       Impact factor: 5.923

2.  Fabrication and evaluation of valsartan-polymer- surfactant composite nanoparticles by using the supercritical antisolvent process.

Authors:  Min-Soo Kim; In-Hwan Baek
Journal:  Int J Nanomedicine       Date:  2014-11-07

3.  Influence of hydrophilic additives on the supersaturation and bioavailability of dutasteride-loaded hydroxypropyl-β-cyclodextrin nanostructures.

Authors:  Min-Soo Kim
Journal:  Int J Nanomedicine       Date:  2013-05-20

4.  Improving dissolution and oral bioavailability of pranlukast hemihydrate by particle surface modification with surfactants and homogenization.

Authors:  Eun-Sol Ha; In-hwan Baek; Jin-Wook Yoo; Yunjin Jung; Min-Soo Kim
Journal:  Drug Des Devel Ther       Date:  2015-06-24       Impact factor: 4.162

5.  Design of a gelatin microparticle-containing self-microemulsifying formulation for enhanced oral bioavailability of dutasteride.

Authors:  In-hwan Baek; Eun-Sol Ha; Jin-Wook Yoo; Yunjin Jung; Min-Soo Kim
Journal:  Drug Des Devel Ther       Date:  2015-06-23       Impact factor: 4.162

6.  Development of megestrol acetate solid dispersion nanoparticles for enhanced oral delivery by using a supercritical antisolvent process.

Authors:  Eun-Sol Ha; Jeong-Soo Kim; In-Hwan Baek; Jin-Wook Yoo; Yunjin Jung; Hyung Ryong Moon; Min-Soo Kim
Journal:  Drug Des Devel Ther       Date:  2015-08-04       Impact factor: 4.162

7.  Development and Evaluation of Raloxifene-Hydrochloride-Loaded Supersaturatable SMEDDS Containing an Acidifier.

Authors:  Jong-Hwa Lee; Hak Hyung Kim; Young Ho Cho; Tae-Sung Koo; Gye Won Lee
Journal:  Pharmaceutics       Date:  2018-06-29       Impact factor: 6.321

  7 in total

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