Self-Assembling Lipid Formulations

  • Tiberg F
  • Johnsson M
  • Nistor C
  • et al.
N/ACitations
Citations of this article
17Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Encapsulation of drugs into lipid-based liquid crystalline (LC) phases offers a broadly applicable approach for the in vivo stabilization and sustained release delivery of peptides and proteins as well as small molecule drug substances. This is exemplified by the FluidCrystal (R) Injection depot, an adaptive drug delivery system, combining ease of manufacturing, handling, and injection, with long acting release. The system exploits specific liquid mixtures of naturally occurring polar lipids and small amounts of solvents, which upon contact with minute quantities of aqueous tissue fluids self-assemble into reversed LC phases. The resulting encapsulation of dissolved or dispersed active pharmaceutical ingredients provides a release duration from a small volume injection, which is tunable from days to months.

Cite

CITATION STYLE

APA

Tiberg, F., Johnsson, M., Nistor, C., & Joabsson, F. (2012). Self-Assembling Lipid Formulations. In Long Acting Injections and Implants (pp. 315–333). Springer US. https://doi.org/10.1007/978-1-4614-0554-2_16

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free