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The application of hyaluronic acid-derivatized carbon nanotubes in hematoporphyrin monomethyl ether-based photodynamic therapy for in vivo and in vitro cancer treatment.

Abstract
Carbon nanotubes (CNTs) have shown great potential in both photothermal therapy and drug delivery. In this study, a CNT derivative, hyaluronic acid-derivatized CNTs (HA-CNTs) with high aqueous solubility, neutral pH, and tumor-targeting activity, were synthesized and characterized, and then a new photodynamic therapy agent, hematoporphyrin monomethyl ether (HMME), was adsorbed onto the functionalized CNTs to develop HMME-HA-CNTs. Tumor growth inhibition was investigated both in vivo and in vitro by a combination of photothermal therapy and photodynamic therapy using HMME-HA-CNTs. The ability of HMME-HA-CNT nanoparticles to combine local specific photodynamic therapy with external near-infrared photothermal therapy significantly improved the therapeutic efficacy of cancer treatment. Compared with photodynamic therapy or photothermal therapy alone, the combined treatment demonstrated a synergistic effect, resulting in higher therapeutic efficacy without obvious toxic effects to normal organs. Overall, it was demonstrated that HMME-HA-CNTs could be successfully applied to photodynamic therapy and photothermal therapy simultaneously in future tumor therapy.
AuthorsJinjin Shi, Rourou Ma, Lei Wang, Jing Zhang, Ruiyuan Liu, Lulu Li, Yan Liu, Lin Hou, Xiaoyuan Yu, Jun Gao, Zhenzhong Zhang
JournalInternational journal of nanomedicine (Int J Nanomedicine) Vol. 8 Pg. 2361-73 ( 2013) ISSN: 1178-2013 [Electronic] New Zealand
PMID23843694 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Drug Carriers
  • Hematoporphyrins
  • Nanotubes, Carbon
  • hematoporphyrin monomethyl ether
  • Hyaluronic Acid
Topics
  • Animals
  • Antineoplastic Agents (chemistry, pharmacokinetics, pharmacology)
  • Apoptosis (drug effects)
  • Cell Line, Tumor
  • Cell Survival (drug effects)
  • Drug Carriers (chemistry, pharmacokinetics, radiation effects, toxicity)
  • Hematoporphyrins (chemistry, pharmacokinetics, pharmacology)
  • Hot Temperature
  • Hyaluronic Acid (chemistry)
  • Infrared Rays
  • Mice
  • Microscopy, Fluorescence
  • Nanotubes, Carbon (chemistry, radiation effects, toxicity)
  • Photochemotherapy (methods)
  • Xenograft Model Antitumor Assays

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