How can micelle systems be rebuilt by a heating process?

Int J Nanomedicine. 2012:7:141-50. doi: 10.2147/IJN.S25761. Epub 2012 Jan 12.

Abstract

The aim of this work was to evaluate how an aqueous micellar system containing Amphotericin B (AmB) and sodium deoxycholate (DOC) can be rebuilt after heating treatment. Also, a review of the literature on the physicochemical and biological properties of this new system was conducted. Heated (AmB-DOC-H) and unheated (AmB-DOC) micelles were then diluted at four different concentrations (50 mg · L(-1), 5 mg · L(-1), 0.5 mg · L(-1), and 0.05 mg · L(-1)) to perform physicochemical studies and a pharmacotoxicity assay, in which two cell models were used for the in vitro experiments: red blood cells (RBC) from human donors and Candida parapsilosis (Cp). While potassium (K(+)) and hemoglobin leakage from RBC were the parameters used to evaluate acute and chronic toxicity, respectively, the efficacy of AmB-DOC and AmB-DOC-H were assessed by K(+) leakage and cell survival rate from Cp. The spectral study revealed a slight change in the AmB-DOC aggregate peak from 327 nm to 323 nm, which is the peak for AmB-DOC-H. Although AmB-DOC and AmB-DOC-H exhibited different behavior for hemoglobin leakage, AmB-DOC produced higher leakage than AmB-DOC-H at high concentrations (from 5 mg · L(-1)). For K(+) leakage, both AmB-DOC and AmB-DOC-H showed a similar profile for both cell models, RBC and Cp (P < 0.05). AmB-DOC-H and AmB-DOC also revealed a similar profile of activity against Cp with an equivalent survival rate. In short, AmB-DOC-H showed much less toxicity than AmB-DOC, but remained as active as AmB-DOC against fungal cells. The results highlight the importance of this new procedure as a simple, inexpensive, and safe way to produce a new kind of micelle system for the treatment of systemic fungal infections.

Keywords: micelles; nanotechnology; pre-heated amphotericin B; super-aggregates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amphotericin B / chemistry
  • Amphotericin B / pharmacology
  • Analysis of Variance
  • Candida / drug effects
  • Deoxycholic Acid / chemistry
  • Deoxycholic Acid / pharmacology
  • Dose-Response Relationship, Drug
  • Erythrocytes / drug effects
  • Hemoglobins / analysis
  • Hemolysis / drug effects
  • Hot Temperature
  • Humans
  • Micelles*
  • Microbial Viability / drug effects
  • Models, Biological
  • Nanotechnology / methods*
  • Potassium / analysis
  • Spectrophotometry, Ultraviolet

Substances

  • Hemoglobins
  • Micelles
  • Deoxycholic Acid
  • Amphotericin B
  • Potassium