Your browser doesn't support javascript.
loading
Formulation and Characterization of Bioactive Agent Containing Nanodisks.
Lethcoe, Kyle; Fox, Colin A; Moh, Isabel; Swackhamer, Matthew; Karo, Michael; Lockhart, Ryan; Ryan, Robert O.
Affiliation
  • Lethcoe K; Department of Biochemistry and Molecular Biology, University of Nevada.
  • Fox CA; Department of Biochemistry and Molecular Biology, University of Nevada.
  • Moh I; Department of Biochemistry and Molecular Biology, University of Nevada.
  • Swackhamer M; Department of Biochemistry and Molecular Biology, University of Nevada.
  • Karo M; Department of Biochemistry and Molecular Biology, University of Nevada.
  • Lockhart R; Department of Biochemistry and Molecular Biology, University of Nevada.
  • Ryan RO; Department of Biochemistry and Molecular Biology, University of Nevada; robertryan@unr.edu.
J Vis Exp ; (193)2023 03 17.
Article in En | MEDLINE | ID: mdl-37010309
ABSTRACT
The term nanodisk refers to a discrete type of nanoparticle comprised of a bilayer forming lipid, a scaffold protein, and an integrated bioactive agent. Nanodisks are organized as a disk-shaped lipid bilayer whose perimeter is circumscribed by the scaffold protein, usually a member of the exchangeable apolipoprotein family. Numerous hydrophobic bioactive agents have been efficiently solubilized in nanodisks by their integration into the hydrophobic milieu of the particle's lipid bilayer, yielding a largely homogenous population of particles in the range of 10-20 nm in diameter. The formulation of nanodisks requires a precise ratio of individual components, an appropriate sequential addition of each component, followed by bath sonication of the formulation mixture. The amphipathic scaffold protein spontaneously contacts and reorganizes the dispersed bilayer forming lipid/bioactive agent mixture to form a discrete, homogeneous population of nanodisk particles. During this process, the reaction mixture transitions from an opaque, turbid appearance to a clarified sample that, when fully optimized, yields no precipitate upon centrifugation. Characterization studies involve the determination of bioactive agent solubilization efficiency, electron microscopy, gel filtration chromatography, ultraviolet visible (UV/Vis) absorbance spectroscopy, and/or fluorescence spectroscopy. This is normally followed by an investigation of biological activity using cultured cells or mice. In the case of nanodisks harboring an antibiotic (i.e., the macrolide polyene antibiotic amphotericin B), their ability to inhibit the growth of yeast or fungi as a function of concentration or time can be measured. The relative ease of formulation, versatility with respect to component parts, nanoscale particle size, inherent stability, and aqueous solubility permits myriad in vitro and in vivo applications of nanodisk technology. In the present article, we describe a general methodology to formulate and characterize nanodisks containing amphotericin B as the hydrophobic bioactive agent.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amphotericin B / Nanoparticles Limits: Animals Language: En Journal: J Vis Exp Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amphotericin B / Nanoparticles Limits: Animals Language: En Journal: J Vis Exp Year: 2023 Document type: Article