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Related Concept Videos

Modified-Release Drug Delivery Systems: Site-Targeted01:24

Modified-Release Drug Delivery Systems: Site-Targeted

Site-targeted drug delivery systems enhance therapeutic efficacy while minimizing systemic toxicity and treatment costs. Unlike conventional methods, these systems ensure precise drug delivery, improving bioavailability and reducing side effects. Targeted drug delivery is classified into three levels. First-order targeting directs drugs to the capillary beds of specific organs or tissues. Second-order targets specific cell types, such as tumor cells, using receptor-mediated interactions.
In Vitro Drug Dissolution: Compendial Testing Models II01:09

In Vitro Drug Dissolution: Compendial Testing Models II

Various dissolution methods are utilized to assess a drug’s dissolution rate, including the flow-through cell, paddle-over-disk, cylinder, and reciprocating disk methods.The flow-through cell apparatus (USP (United States Pharmacopeia) method 4) comprises a reservoir for the dissolution medium and a pump that propels the medium through the cell containing the test sample. This method is crucial for assessing modified-release dosage forms with minimally soluble active ingredients, maintaining...
Bioavailability Enhancement: Drug Solubility Enhancement01:16

Bioavailability Enhancement: Drug Solubility Enhancement

Bioavailability is a critical factor in determining a drug's effectiveness. It refers to the proportion of a drug that enters the circulation when introduced into the body and is, as a result, able to have an active effect. Enhancing bioavailability is essential for drugs with poor solubility, as it can significantly impact their therapeutic efficacy. Various methods are employed to increase the solubility of drugs, thereby enhancing their bioavailability.Micronization and nanonization are...
Modified-Release Drug Delivery Systems: Rate-Programmed II01:19

Modified-Release Drug Delivery Systems: Rate-Programmed II

Rate-programmed drug delivery systems release drugs in a controlled manner to maintain therapeutic levels. Three main designs include reservoir, matrix, and hybrid systems.Reservoir systems consist of a drug core enclosed within a membrane that controls drug release. In non-swelling reservoir systems, polymers like ethyl cellulose or polymethacrylates are used. These do not hydrate in aqueous media and control release through membrane thickness, porosity, or insolubility. This type includes...
In Vitro Drug Dissolution: Alternative Methods01:17

In Vitro Drug Dissolution: Alternative Methods

Alternative drug dissolution methods include the rotating bottle, intrinsic dissolution test, peristalsis, and the Franz diffusion cell method. The rotating bottle method involves meticulously rotating tightly capped controlled-release beads in a temperature-controlled bath. Periodic decanting of samples allows for residue assay, followed by refilling with fresh medium and testing at various pH levels to emulate the gastrointestinal tract conditions.In contrast, the intrinsic dissolution test...
Oral Drug Delivery Systems: Continuous-Release Systems01:26

Oral Drug Delivery Systems: Continuous-Release Systems

Continuous-release drug delivery systems offer a strategic approach to maintaining therapeutic drug levels over extended periods following oral administration. By modulating the release rate of active pharmaceutical ingredients, these systems minimize fluctuations in plasma concentrations, which enhances clinical efficacy and reduces the need for frequent dosing. Such characteristics make them particularly advantageous in managing chronic diseases where patient adherence and stable drug...

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Updated: Jun 22, 2026

Self-Nanoemulsification of Healthy Oils to Enhance the Solubility of Lipophilic Drugs
08:18

Self-Nanoemulsification of Healthy Oils to Enhance the Solubility of Lipophilic Drugs

Published on: July 27, 2022

High-throughput formulation screening system for self-microemulsifying drug delivery.

Kenichi Sakai1, Hiroyuki Maeda, Takayuki Yoshimori

  • 1Formulation Technology Research Department, Chugai Pharmaceutical Co., Ltd., Kita-Ku, Tokyo, Japan. sakaikni@chugai-pharm.co.jp

Drug Development and Industrial Pharmacy
|June 12, 2009
PubMed
Summary

A new high-throughput formulation screening (HTFS) system rapidly identifies optimal self-microemulsifying drug delivery system (SMEDDS) formulations and surfactant combinations with minimal resources.

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Last Updated: Jun 22, 2026

Self-Nanoemulsification of Healthy Oils to Enhance the Solubility of Lipophilic Drugs
08:18

Self-Nanoemulsification of Healthy Oils to Enhance the Solubility of Lipophilic Drugs

Published on: July 27, 2022

Microfluidic Production of Lysolipid-Containing Temperature-Sensitive Liposomes
09:51

Microfluidic Production of Lysolipid-Containing Temperature-Sensitive Liposomes

Published on: March 3, 2020

Area of Science:

  • Pharmaceutical Sciences
  • Drug Delivery Systems
  • Formulation Development

Background:

  • Self-microemulsifying drug delivery systems (SMEDDS) enhance oral bioavailability of poorly soluble drugs.
  • Efficient screening methods are crucial for optimizing SMEDDS formulations.
  • Traditional screening methods can be time-consuming and resource-intensive.

Purpose of the Study:

  • To develop a high-throughput formulation screening (HTFS) system for SMEDDS.
  • To enable rapid and efficient selection of optimal SMEDDS formulations.
  • To identify the most suitable hydrophilic surfactant (HS)/lipophilic surfactant (LS) combinations for SMEDDS.

Main Methods:

  • Utilized a robotic liquid dispenser for formulation preparation.
  • Employed a turbidity assay for screening emulsion particle size and phase stability.
  • Developed a SMEDDS-HTFS system for rapid evaluation.

Main Results:

  • Formulations were prepared rapidly (40 min/96 formulations).
  • Screenings for particle size and stability were highly efficient (1 min/96 formulations).
  • The system identified optimal SMEDDS formulations and HS/LS combinations with minimal manpower and compound usage.

Conclusions:

  • The developed SMEDDS-HTFS system allows for rapid and efficient selection of SMEDDS formulations.
  • This system facilitates the identification of optimal hydrophilic and lipophilic surfactant combinations.
  • The HTFS approach significantly reduces time, manpower, and compound consumption in SMEDDS development.