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A chemically stable fluorescent marker of the ureter

  1. Author:
    Cha, Jaepyeong
    Nani, Roger R
    Luciano, Michael P
    Kline, Gabriel
    Broch, Aline
    Kim, Kihoon
    Namgoong, Jung-Man
    Kulkarni, Rhushikesh A
    Meier, Jordan L
    Kim, Peter
    Schnermann, Martin J
  2. Author Address

    Sheikh Zayed Institute for Pediatric Surgical Innovation, Children 39;s National Health System, 111 Michigan Ave., NW Washinton, DC 20010, United States. Electronic address: JCHA2@childrensnational.org., Chemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, United States., Sheikh Zayed Institute for Pediatric Surgical Innovation, Children 39;s National Health System, 111 Michigan Ave., NW Washinton, DC 20010, United States; Department of Surgery, Inje University Haeundae Paik Hospital, 875 Haeun-daero, Haeundae-gu, Busan 612-896, South Korea., Sheikh Zayed Institute for Pediatric Surgical Innovation, Children 39;s National Health System, 111 Michigan Ave., NW Washinton, DC 20010, United States; Department of Surgery, Asan Medical Center, 88 Olympic-ro 43-gil, Songpa-gu, Seoul 138-736, South Korea., Chemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, United States. Electronic address: martin.schnermann@nih.gov.,
    1. Year: 2018
    2. Date: Sep 1
    3. Epub Date: 2018 02 24
  1. Journal: Bioorganic & Medicinal Chemistry Letters
    1. 28
    2. 16
    3. Pages: 2741-2745
  2. Type of Article: Article
  1. Abstract:

    Surgical methods guided by exogenous fluorescent markers have the potential to define tissue types in real time. Small molecule dyes with efficient and selective renal clearance could enable visualization of the ureter during surgical procedures involving the abdomen and pelvis. These studies report the design and synthesis of a water soluble, net neutral C4'-O-alkyl heptamethine cyanine, Ureter-Label (UL)-766, with excellent properties for ureter visualization. This compound is accessed through a concise synthetic sequence involving an N- to O-transposition reaction that provides other inaccessible C4'-O-alkyl heptamethine cyanines. Unlike molecules containing a C4'-O-aryl substituent, which have also been used for ureter visualization, UL-766 is not reactive towards glutathione and the cellular proteome. In addition, rat models of abdominal surgery reveal that UL-766 undergoes efficient and nearly exclusive renal clearance in vivo. In total, this molecule represents a promising candidate for visualizing the ureter during a variety of surgical interventions. Published by Elsevier Ltd.

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External Sources

  1. DOI: 10.1016/j.bmcl.2018.02.040
  2. PMID: 29510880
  3. WOS: 000443150500020
  4. PII : S0960-894X(18)30145-8

Library Notes

  1. Fiscal Year: FY2017-2018
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