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Updated: Sep 23, 2025

Self-Nanoemulsification of Healthy Oils to Enhance the Solubility of Lipophilic Drugs
Published on: July 27, 2022
Spray Drying as an Effective Method in the Development of Solid Self- Emulsifying Drug Delivery Systems
Mohit Kumar1, Pooja A Chawla2, Abdul Faruk1
1Department of Pharmaceutical Sciences, HNB Garhwal University, Srinagar, Garhwal, Uttarakhand, India.
Solidifying self-emulsifying drug delivery systems (SEDDS) using spray drying enhances stability and bioavailability for lipophilic drugs. This review details the spray drying method for solid SEDDS (S-SEDDS) and their conversion into tablets.
Area of Science:
- Pharmaceutical Sciences
- Drug Delivery Systems
Background:
- Lipophilic drug candidates often exhibit low bioavailability due to poor water solubility.
- Self-emulsifying drug delivery systems (SEDDS) are effective for enhancing the solubility and absorption of such drugs.
- Challenges with liquid SEDDS, including low drug loading and handling difficulties, necessitate formulation solidification.
Approach:
- This review focuses on the solidification of SEDDS using spray drying, a scalable and stable technique.
- It examines the critical role of adsorbent carriers in the formulation and drug compatibility.
- The review details the advantages, development methods, spray drying parameters, and characterization of solid SEDDS (S-SEDDS).
Key Points:
- Spray drying offers significant advantages for SEDDS, including improved scalability and stability.
- The choice of adsorbent carrier is crucial for the performance and compatibility of S-SEDDS.
- Solidified SEDDS can be further processed into tablet dosage forms, potentially increasing bioavailability and stability.
Conclusions:
- Spray drying is a viable method for producing stable and handleable solid SEDDS (S-SEDDS).
- Conversion of S-SEDDS into tablets presents a promising approach to overcome limitations of liquid SEDDS and enhance therapeutic efficacy.
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