Literature DB >> 16370943

Development of supersaturatable self-emulsifying drug delivery system formulations for improving the oral absorption of poorly soluble drugs.

Ping Gao1, Walter Morozowich.   

Abstract

The supersaturatable self-emulsifying drug delivery system (S-SEDDS) represents a new thermodynamically stable formulation approach wherein it is designed to contain a reduced amount of a surfactant and a water-soluble cellulosic polymer (or other polymers) to prevent precipitation of the drug by generating and maintaining a supersaturated state in vivo. The S-SEDDS formulations can result in enhanced oral absorption as compared with the related self-emulsifying drug delivery systems (SEDDS) formulation and the reduced surfactant levels may minimise gastrointestinal surfactant side effects.

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Year:  2006        PMID: 16370943     DOI: 10.1517/17425247.3.1.97

Source DB:  PubMed          Journal:  Expert Opin Drug Deliv        ISSN: 1742-5247            Impact factor:   6.648


  21 in total

Review 1.  Characterization of supersaturatable formulations for improved absorption of poorly soluble drugs.

Authors:  Ping Gao; Yi Shi
Journal:  AAPS J       Date:  2012-07-14       Impact factor: 4.009

Review 2.  Current Status of Supersaturable Self-Emulsifying Drug Delivery Systems.

Authors:  Heejun Park; Eun-Sol Ha; Min-Soo Kim
Journal:  Pharmaceutics       Date:  2020-04-16       Impact factor: 6.321

3.  Lipid absorption triggers drug supersaturation at the intestinal unstirred water layer and promotes drug absorption from mixed micelles.

Authors:  Yan Yan Yeap; Natalie L Trevaskis; Christopher J H Porter
Journal:  Pharm Res       Date:  2013-06-21       Impact factor: 4.200

4.  Intestinal mucus is capable of stabilizing supersaturation of poorly water-soluble drugs.

Authors:  Yan Yan Yeap; Jaclyn Lock; Sean Lerkvikarn; Tanner Semin; Nicholas Nguyen; Rebecca L Carrier
Journal:  J Control Release       Date:  2018-12-06       Impact factor: 9.776

5.  Enhanced solubility and oral bioavailability of γ-tocotrienol using a self-emulsifying drug delivery system (SEDDS).

Authors:  Saeed Alqahtani; Alaadin Alayoubi; Sami Nazzal; Paul W Sylvester; Amal Kaddoumi
Journal:  Lipids       Date:  2014-06-17       Impact factor: 1.880

6.  Targeted intestinal delivery of supersaturated itraconazole for improved oral absorption.

Authors:  Dave A Miller; James C DiNunzio; Wei Yang; James W McGinity; Robert O Williams
Journal:  Pharm Res       Date:  2008-06       Impact factor: 4.200

7.  Novel cationic supersaturable nanomicellar systems of raloxifene hydrochloride with enhanced biopharmaceutical attributes.

Authors:  Atul Jain; Rajpreet Kaur; Sarwar Beg; Varun Kushwah; Sanyog Jain; Bhupinder Singh
Journal:  Drug Deliv Transl Res       Date:  2018-06       Impact factor: 4.617

Review 8.  Tocotrienols: the emerging face of natural vitamin E.

Authors:  Chandan K Sen; Savita Khanna; Cameron Rink; Sashwati Roy
Journal:  Vitam Horm       Date:  2007       Impact factor: 3.421

9.  Nonlinear absorption kinetics of self-emulsifying drug delivery systems (SEDDS) containing tocotrienols as lipophilic molecules: in vivo and in vitro studies.

Authors:  Saeed Alqahtani; Alaadin Alayoubi; Sami Nazzal; Paul W Sylvester; Amal Kaddoumi
Journal:  AAPS J       Date:  2013-04-10       Impact factor: 4.009

Review 10.  Tocotrienols in health and disease: the other half of the natural vitamin E family.

Authors:  Chandan K Sen; Savita Khanna; Sashwati Roy
Journal:  Mol Aspects Med       Date:  2007-03-27
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