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Journal ArticleDOI

Development of solid self-emulsifying drug delivery systems: preparation techniques and dosage forms.

TLDR
An overview of the recent advances in the study of S-SEDDS, especially the related solidification techniques and the development of solid SE dosage forms is given.
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This article is published in Drug Discovery Today.The article was published on 2008-07-01. It has received 358 citations till now. The article focuses on the topics: Drug delivery.

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Citations
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Journal ArticleDOI

Strategies to Address Low Drug Solubility in Discovery and Development

TL;DR: The article provides an integrated and contemporary discussion of current approaches to solubility and dissolution enhancement but has been deliberately structured as a series of stand-alone sections to allow also directed access to a specific technology where required.
Journal ArticleDOI

Pharmaceutical particle technologies: An approach to improve drug solubility, dissolution and bioavailability

TL;DR: A review of solid particle technologies available for improving solubility, dissolution, and bioavailability of drugs with poor aqueous solubilities is presented in this article, where the authors highlight the solid particle technology available to improve the bioavailability.
Journal ArticleDOI

Oral delivery of anticancer drugs: Challenges and opportunities

TL;DR: Various emerging trends to tackle the challenges associated with oral delivery of anticancer drugs are reviewed, which invariably include efflux transporter based-, functional excipient- and nanocarrier based-approaches.
Journal ArticleDOI

Lyotropic liquid crystal systems in drug delivery

TL;DR: An overview of recent advances and current status of reversed cubic and hexagonal mesophases, especially with respect to their preparation methods and applications in the field of drug delivery is given.
Journal ArticleDOI

Lipid-based formulations for oral administration of poorly water-soluble drugs.

TL;DR: The aim of this review is to provide an overview of the different lipid-based dosage forms from a biopharmaceutical point of view and to describe effects of lipid dosage forms and lipid excipients on drug solubility, absorption and distribution.
References
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Journal ArticleDOI

Solid dispersion of poorly water‐soluble drugs: Early promises, subsequent problems, and recent breakthroughs

TL;DR: Commercial use of solid dispersion systems during the past four decades has been very limited, primarily because of manufacturing difficulties and stability problems, but this has been changing in recent years because of the availability of surface-active and self-emulsifying carriers and the development of technologies to encapsulate solid dispersions directly into hard gelatin capsules as melts.
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Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs.

TL;DR: Self-emulsifying drug delivery systems (SEDDS), which are isotropic mixtures of oils, surfactants, solvents and co-solvents/surfactants, can be used for the design of formulations in order to improve the oral absorption of highly lipophilic drug compounds as discussed by the authors.
Journal ArticleDOI

Lipid microemulsions for improving drug dissolution and oral absorption: physical and biopharmaceutical aspects

TL;DR: This review highlights the state-of-the-art in pharmaceutical microemulsions with emphasis on self-emulsifying systems, from both a physical and biopharmaceutical perspective, primarily focused on their potential for oral drug delivery and intestinal absorption improvement.
Journal ArticleDOI

Oral lipid-based formulations

TL;DR: This commentary provides a comprehensive summary of the development, characterization, and utilization of oral lipid-based formulations, from both physicochemical and biopharmaceutical perspectives.
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