Liposomes coloaded with iopamidol/lipiodol as a res-targeted contrast agent for computed tomography imaging

Soonjae Kweon, Ho Joon Lee, Woo Jin Hyung, Jinsuk Suh, Joon Seok Lim, Soo Jeong Lim

Research output: Contribution to journalArticlepeer-review

50 Citations (Scopus)


Purpose: The need for computed tomography (CT) of reticuloendothelial system (RES)-rich organs such as the liver is increasing, particularly in patients with suspected hepatic metastasis. CT images of the liver have been improved by encapsulating currently used, water-soluble iodine contrast agent in liposomes. The present study was performed to investigate a possibility to overcome the limitations of entrapped iodine in liposomes by preparing liposomes co-loaded with iopamidol, a water-soluble iodinated compound, and lipiodol, an iodized oil. Methods: Iopamidol and lipiodol were simultaneously loaded in liposomes by modified reverse-phase evaporation method. The entrapped iodine concentration, mean particle size and polydispersity index of resulting liposomes were evaluated. Following intravenous injection of these liposomes into rats, CT scanning was performed. Results: Simultaneous loading of iopamidol and lipiodol into liposomes resulted in entrapped iodine concentrations as high as 49.2 iodine mg/ml. The mean particle size was 280 nm, and the mean polydispersity index was 0.230. CT scanning with these iopamidol/lipiodol (I/L) liposomes into rats resulted in more pronounced and more persistent increases in RES-rich organs, liver and spleen, compared with free liposomes or liposomes loaded with iopamidol alone. Conclusions: These findings indicate that I/L liposomes have the potential to allow thorough CT examination of RES-rich organs.

Original languageEnglish
Pages (from-to)1408-1415
Number of pages8
JournalPharmaceutical Research
Issue number7
Publication statusPublished - 2010 Jul

Bibliographical note

Funding Information:
This study was supported by a faculty research grant of Yonsei University College of Medicine (6-2008-225) to J.S. Lim.

All Science Journal Classification (ASJC) codes

  • Biotechnology
  • Molecular Medicine
  • Pharmacology
  • Pharmaceutical Science
  • Organic Chemistry
  • Pharmacology (medical)


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