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Co-hybridized composite nanovesicles for enhanced transdermal eugenol and cinnamaldehyde delivery and their potential efficacy in ulcerative colitis.

Abstract
Percutaneous absorption of drugs can be enhanced by ethosomes, which are nanocarriers with excellent deformability and drug-loading properties. However, the ethanol within ethosomes increases phospholipid membrane fluidity and permeability, leading to drug leakage during storage. Here, we developed and characterized a new phospholipid nanovesicles that is co-hybridized with hyaluronic acid (HA), ethanol and the encapsulated volatile oil medicines (eugenol and cinnamaldehyde [EUG/CAH]) for transdermal administration. In comparison with EUG/CAH-loaded ethosomes (ES), the formulation stability and percutaneous drug absorption of EUG/CAH-loaded HA-immobilized ethosomes (HA-ES) were significantly improved. After transdermal administration of HA-ES, the interstitial cells of Cajal in the colon of rats with trinitrobenzene sulfonate-induced ulcerative colitis (UC) were significantly increased, and the stem cell factor/c-kit signaling pathway was partly repaired. Overall, HA-ES possesses excellent deformability and showed improved efficacy against UC compared with ES, which is demonstrated as a promising transdermal delivery vehicle for volatile oil medicines.
AuthorsYongtai Zhang, Hongyu Zhang, Kai Zhang, Zhe Li, Teng Guo, Tong Wu, Xuefeng Hou, Nianping Feng
JournalNanomedicine : nanotechnology, biology, and medicine (Nanomedicine) Vol. 28 Pg. 102212 (08 2020) ISSN: 1549-9642 [Electronic] United States
PMID32334099 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2020 Elsevier Inc. All rights reserved.
Chemical References
  • Liposomes
  • Phospholipids
  • Eugenol
  • Acrolein
  • cinnamaldehyde
Topics
  • Acrolein (administration & dosage, analogs & derivatives, therapeutic use)
  • Administration, Cutaneous
  • Animals
  • Cell Line, Tumor
  • Cell Survival (drug effects)
  • Colitis, Ulcerative (drug therapy)
  • Eugenol (administration & dosage, therapeutic use)
  • Humans
  • Inflammatory Bowel Diseases (drug therapy)
  • Liposomes (chemistry)
  • Nanoparticles (chemistry)
  • Phase Transition
  • Phospholipids (chemistry)
  • Rats
  • Skin (metabolism)

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