Literature DB >> 16107306

Trials of clear aceclofenac-loaded soft capsules with accelerated oral absorption in human subjects.

Chul Soon Yong1, Yu-Kyoung Oh, Kyung Hee Lee, Sang-Man Park, Young-Joon Park, Young Sig Gil, Chang Hun Yu, Bong-Kyu Yoo, Jong Soo Woo, Jong Oh Kim, Jong-Dal Rhee, Chong-Kook Kim, Han-Gon Choi.   

Abstract

To develop an effective oral drug delivery system with accelerated absorption in human subjects for a poorly water-soluble acelofenac, five aceclofenac-loaded soft capsule preparations containing various ratios of different solubilizers were prepared and their dissolution tests were carried out. Among five preparations tested, a preparation with ethanolamine was selected as a formula of aceclofenac soft capsule (Korea United Pharm. Co. Ltd., Clanza S, since it was clear in appearance and showed the fastest dissolution rate due to the solubility-enhancing effect of aceclofenac. To evaluate and compare the pharmacokinetics of acelofenac-loaded soft capsules with the conventional aceclofenac tablets (Dae-Woong Pharm. Co. Ltd., Airtal) in human subjects; 14 normal healthy male volunteers (age 20-25 years old) were divided into two groups and a randomized 2 x 2 cross-over study was performed. Following oral administration of one tablet or capsule, each containing 100mg of aceclofenac, blood samples were collected at the predetermined time intervals and the concentration of aceclofenac in plasma was determined by HPLC method using UV detector. The AUC, Cmax, MRT, t1/2 and Kel of aceclofenac delivered from soft capsule were not significantly different from those from aceclofenac-loaded conventional tablet. However, soft capsule gave significantly higher initial concentration and significantly faster Tmax of aceclofenac than did conventional tablet, suggesting that the soft capsule with ethanolamine showed the faster absorption of aceclofenac in human subjects. Thus, the clear aceclofenac-loaded soft capsule with ethanolamine was a more effective oral dosage form with fast absorption for poorly water-soluble aceclofenac.

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Year:  2005        PMID: 16107306     DOI: 10.1016/j.ijpharm.2005.06.008

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


  4 in total

1.  Pharmacokinetics of a new once-daily controlled-release formulation of aceclofenac in Korean healthy subjects compared with immediate-release aceclofenac and the effect of food: a randomized, open-label, three-period, crossover, single-centre study.

Authors:  Soo Kyung Bae; Soo-Hwan Kim; Hae Won Lee; Sook Jin Seong; Su-Yeon Shin; Sang Hun Lee; Mi-Sun Lim; Young-Ran Yoon; Hye Jung Lee
Journal:  Clin Drug Investig       Date:  2012-02-01       Impact factor: 2.859

2.  Development and characterization of enteric-coated immediate-release pellets of aceclofenac by extrusion/spheronization technique using kappa-carrageenan as a pelletizing agent.

Authors:  Vaishali A Kilor; Nidhi P Sapkal; Jasmine G Awari; Bharti D Shewale
Journal:  AAPS PharmSciTech       Date:  2010-03-03       Impact factor: 3.246

3.  Development of fast dispersible aceclofenac tablets: effect of functionality of superdisintegrants.

Authors:  C Mallikarjuna Setty; D V K Prasad; V R M Gupta; B Sa
Journal:  Indian J Pharm Sci       Date:  2008 Mar-Apr       Impact factor: 0.975

4.  Preparation and In Vivo Pharmacokinetics of the Tongshu Suppository.

Authors:  Guoqiang Liu; Leilei Dong; Kuan Lu; Sisi Liu; Yingying Zheng
Journal:  Biomed Res Int       Date:  2016-08-16       Impact factor: 3.411

  4 in total

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