Literature DB >> 16650738

Bioavailability of seocalcitol II: development and characterisation of self-microemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglycerides.

Mette Grove1, Anette Müllertz, Jeanet Løgsted Nielsen, Gitte Pommergaard Pedersen.   

Abstract

By constructing ternary phase diagrams it was possible to identify two self-microemulsifying drug delivery systems (SMEDDS) containing either medium chain triglycerides (MC-SMEDDS) or long chain triglycerides (LC-SMEDDS), with the same ratio between lipid, surfactant and co-surfactant. The SMEDDS ended up having a composition of 25% lipid, 48% surfactant and 27% co-surfactant, MC-SMEDDS: viscoleo, cremophor RH40, akoline MCM and LC-SMEDDS: sesame oil, cremophor RH40, peceol. Upon dilution with water both SMEDDS resulted in clear to bluish transparent microemulsions with a narrow droplet size of 30nm. The industrial usefulness of the developed SMEDDS was evaluated with regard to bioavailability and chemical stability using the vitamin D analogue, seocalcitol, as model compound. The absorption and bioavailability of seocalcitol in rats were approximately 45% and 18%, respectively, from both the MC-SMEDDS and LC-SMEDDS indicating similar in vivo behavior of the two formulations, despite the difference in nature of lipid component. There was no improvement in bioavailability by the use of SMEDDS, compared to the bioavailability achieved from simple MCT and LCT solutions (22-24%) (Grove, M., Pedersen, G.P., Nielsen, J.L., Mullertz, A., 2005. Bioavailability of seocalcitol. I. Relating solubility in biorelevant media with oral bioavailability in rats-effect of medium and long chain triglycerides. J. Pharm. Sci. 94, 1830-1838.). After 3 months' storage at accelerated conditions (40 degrees C/75% RH), a decrease in concentration of seocalcitol of 10-11% was found in MC-SMEDDS and LC-SMEDDS compared with a degradation of less than 3% for the simple lipid solutions of MCT and LCT. In this study the simple lipid solutions seem to be a better choice compared with the developed SMEDDS due to a slightly higher bioavailability and a better chemical stability of seocalcitol.

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Year:  2006        PMID: 16650738     DOI: 10.1016/j.ejps.2006.02.005

Source DB:  PubMed          Journal:  Eur J Pharm Sci        ISSN: 0928-0987            Impact factor:   4.384


  15 in total

1.  Self-microemulsifiyng suppository formulation of β-artemether.

Authors:  Dalapathi Gugulothu; Sulabha Pathak; Shital Suryavanshi; Shobhona Sharma; Vandana Patravale
Journal:  AAPS PharmSciTech       Date:  2010-07-27       Impact factor: 3.246

2.  Development of silymarin self-microemulsifying drug delivery system with enhanced oral bioavailability.

Authors:  Xinru Li; Quan Yuan; Yanqing Huang; Yanxia Zhou; Yan Liu
Journal:  AAPS PharmSciTech       Date:  2010-04-20       Impact factor: 3.246

3.  Feasibility of capsule endoscopy for direct imaging of drug delivery systems in the fasted upper-gastrointestinal tract.

Authors:  Pernille Barbre Pedersen; Daniel Bar-Shalom; Stefania Baldursdottir; Peter Vilmann; Anette Müllertz
Journal:  Pharm Res       Date:  2014-02-19       Impact factor: 4.200

4.  Rice germ oil as multifunctional excipient in preparation of self-microemulsifying drug delivery system (SMEDDS) of tacrolimus.

Authors:  Smita K Pawar; Pradeep R Vavia
Journal:  AAPS PharmSciTech       Date:  2012-01-10       Impact factor: 3.246

5.  A Self-microemulsifying Drug Delivery System (SMEDDS) for a Novel Medicative Compound Against Depression: a Preparation and Bioavailability Study in Rats.

Authors:  Lan Wu; Yanli Qiao; Lina Wang; Jiahua Guo; Guocheng Wang; Wei He; Lifang Yin; Jinhua Zhao
Journal:  AAPS PharmSciTech       Date:  2015-02-06       Impact factor: 3.246

6.  Preparation and evaluation of self-nanoemulsifying tablets of carvedilol.

Authors:  Enas A Mahmoud; Ehab R Bendas; Magdy I Mohamed
Journal:  AAPS PharmSciTech       Date:  2009-02-24       Impact factor: 3.246

7.  Chemical drug stability in lipids, modified lipids, and polyethylene oxide-containing formulations.

Authors:  Valentino J Stella
Journal:  Pharm Res       Date:  2013-05-02       Impact factor: 4.200

8.  Preparation and evaluation of Vinpocetine self-emulsifying pH gradient release pellets.

Authors:  Mengqi Liu; Shiming Zhang; Shuxia Cui; Fen Chen; Lianqun Jia; Shu Wang; Xiumei Gai; Pingfei Li; Feifei Yang; Weisan Pan; Xinggang Yang
Journal:  Drug Deliv       Date:  2017-11       Impact factor: 6.419

9.  Lipid-based nanosystem of edaravone: development, optimization, characterization and in vitro/in vivo evaluation.

Authors:  Ankit Parikh; Krishna Kathawala; Chun Chuan Tan; Sanjay Garg; Xin-Fu Zhou
Journal:  Drug Deliv       Date:  2017-11       Impact factor: 6.419

10.  In situ formation of nanocrystals from a self-microemulsifying drug delivery system to enhance oral bioavailability of fenofibrate.

Authors:  You-Meei Lin; Jui-Yu Wu; Ying-Chen Chen; Yu-Der Su; Wen-Tin Ke; Hsiu-O Ho; Ming-Thau Sheu
Journal:  Int J Nanomedicine       Date:  2011-10-19
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