Literature DB >> 11033431

Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems.

C W Pouton1.   

Abstract

'Lipid' formulations for oral administration of drugs generally consist of a drug dissolved in a blend of two or more excipients, which may be triglyceride oils, partial glycerides, surfactants or co-surfactants. The primary mechanism of action which leads to improved bioavailability is usually avoidance, or partial avoidance, of the slow dissolution process which limits the bioavailability of hydrophobic drugs from solid dosage forms. Ideally the formulation allows the drug to remain in a dissolved state throughout its transit through the gastrointestinal tract. The availability of the drug for absorption can be enhanced by presentation of the drug as a solubilizate within a colloidal dispersion. This objective can be achieved by formulation of the drug in a self-emulsifying system or alternatively by taking advantage of the natural process of triglyceride digestion. In practice 'lipid' formulations range from pure oils, at one extreme, to blends which contain a substantial proportion of hydrophilic surfactants or cosolvents. Knowledge of the efficiency of emulsification of these formulations, the nature of the colloidal system formed by dispersion, their susceptibility to digestion, and the subsequent fate of the drug is desirable for formulation. Yet the literature on this subject is limited, so this article represents part review and part commentary on current status of lipid formulations. A simple classification system for lipid formulations, based on the polarity of the blend and reviewed here, will help comparison of data between laboratories. Priorities for future work are discussed. More data is needed on the solubility of drugs in various types of formulations, and in particular, on the relationship between the physical chemistry of the drug and its fate, subsequent to dilution and digestion of the formulation in the lumen of the gastrointestinal tract. The mechanisms of action and practical uses of each type of lipid formulation are discussed.

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Year:  2000        PMID: 11033431     DOI: 10.1016/s0928-0987(00)00167-6

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


  153 in total

1.  Response surface methodology for the optimization of ubiquinone self-nanoemulsified drug delivery system.

Authors:  Sami Nazzal; Mansoor A Khan
Journal:  AAPS PharmSciTech       Date:  2002       Impact factor: 3.246

2.  Release profile and characteristics of electrosprayed particles for oral delivery of a practically insoluble drug.

Authors:  Adam Bohr; Jakob Kristensen; Mark Dyas; Mohan Edirisinghe; Eleanor Stride
Journal:  J R Soc Interface       Date:  2012-04-25       Impact factor: 4.118

3.  Microstructural elucidation of self-emulsifying system: effect of chemical structure.

Authors:  Sharvil S Patil; Edakkal Venugopal; Suresh Bhat; Kakasaheb R Mahadik; Anant R Paradkar
Journal:  Pharm Res       Date:  2012-04-04       Impact factor: 4.200

4.  The studies of phase equilibria and efficiency assessment for self-emulsifying lipid-based formulations.

Authors:  Ahmad Abdul-Wahhab Shahba; Kazi Mohsin; Fars Kaed Alanazi
Journal:  AAPS PharmSciTech       Date:  2012-03-23       Impact factor: 3.246

5.  Novel self-nanoemulsifying drug delivery systems (SNEDDS) for oral delivery of cinnarizine: design, optimization, and in-vitro assessment.

Authors:  Ahmad Abdul-Wahhab Shahba; Kazi Mohsin; Fars Kaed Alanazi
Journal:  AAPS PharmSciTech       Date:  2012-07-04       Impact factor: 3.246

6.  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

7.  A new in vitro lipid digestion - in vivo absorption model to evaluate the mechanisms of drug absorption from lipid-based formulations.

Authors:  Matthew F Crum; Natalie L Trevaskis; Hywel D Williams; Colin W Pouton; Christopher J H Porter
Journal:  Pharm Res       Date:  2015-12-24       Impact factor: 4.200

8.  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

9.  Glyceride lipid formulations: molecular dynamics modeling of phase behavior during dispersion and molecular interactions between drugs and excipients.

Authors:  Dallas B Warren; Dylan King; Hassan Benameur; Colin W Pouton; David K Chalmers
Journal:  Pharm Res       Date:  2013-10-03       Impact factor: 4.200

10.  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

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