Co-reporter:Tao Gao;Bik Ee Lau;Tadashi Yamaguchi;Naoyuki Hanari;Hisashi Gunji;Masayuki Kano;Hisahiro Matsubara;Hideki Hayashi
Surgery Today 2017 Volume 47( Issue 1) pp:122-129
Publication Date(Web):2017/01/01
DOI:10.1007/s00595-016-1345-1
Recently, the incidence of postoperative pancreatic leakage has been reported to have significantly increased after laparoscopic gastrectomy for gastric cancers in comparison to open surgery. Although their lateral thermal spread has been shown to be smaller than that of other electrosurgical devices, ultrasonically activated surgical devices (USADs) have been suggested as one of the causes. We therefore hypothesized that cavitation generated by USADs could cause injuries to pancreatic tissue. Our retrospective study showed that the amylase activity in the drainage fluid of patients in whom surgery was performed using a USAD with a curved blade was significantly higher than that in patients in whom surgery was performed using a USAD with a straight blade. We therefore focused on the effects of straight and curved USAD blades.The distribution of microbubbles generated in degassed water, which produce mechanical and biological tissue destructive forces, was measured and compared between the two types of USAD.More microbubbles were found to be generated from the side aspect of the curved blade, and the mechanical and biological destructive forces were found to be significantly higher than those generated by the side aspect of the straight blade.These findings strongly suggest that cavitation generated by USADs could injure pancreatic tissues in the clinical cases. Surgeons should be aware of these properties of devices to achieve safe and secure surgeries.
Co-reporter:Taro Toyota, Hiromichi Fujito, Akiko Suganami, Tomoki Ouchi, Aki Ooishi, Akira Aoki, Kazutaka Onoue, Yutaka Muraki, Tomoyuki Madono, Masanori Fujinami, Yutaka Tamura, Hideki Hayashi
Bioorganic & Medicinal Chemistry 2014 Volume 22(Issue 2) pp:721-727
Publication Date(Web):15 January 2014
DOI:10.1016/j.bmc.2013.12.026
Liposomally formulated indocyanine green (LP-ICG) has drawn much attention as a highly sensitive near-infrared (NIR)-fluorescence probe for tumors or lymph nodes in vivo. We synthesized ICG derivatives tagged with alkyl chains (ICG-Cn), and we examined NIR-fluorescence imaging for lymph nodes in the lower extremities of mice by using liposomally formulated ICG-Cn (LP-ICG-Cn) as well as conventional liposomally formulated ICG (LP-ICG) and ICG. Analysis with a noninvasive preclinical NIR-fluorescence imaging system revealed that LP-ICG-Cn accumulates in only the popliteal lymph node 1 h after injection into the footpad, whereas LP-ICG and ICG accumulate in the popliteal lymph node and other organs like the liver. This result indicates that LP-ICG-Cn is a useful NIR-fluorescence probe for noninvasive in vivo bioimaging, especially for the sentinel lymph node.We synthesized ICG derivatives tagged with alkyl chains (ICG-Cn), and we examined NIR-fluorescence imaging for lymph nodes in the lower extremities of mice by using liposomally formulated ICG-Cn (LP-ICG-Cn).
Co-reporter:Akiko Suganami, Taro Toyota, Shigetoshi Okazaki, Kengo Saito, Katsuhiko Miyamoto, Yasunori Akutsu, Hiroshi Kawahira, Akira Aoki, Yutaka Muraki, Tomoyuki Madono, Hideki Hayashi, Hisahiro Matsubara, Takashige Omatsu, Hiroshi Shirasawa, Yutaka Tamura
Bioorganic & Medicinal Chemistry Letters 2012 Volume 22(Issue 24) pp:7481-7485
Publication Date(Web):15 December 2012
DOI:10.1016/j.bmcl.2012.10.044
We have rationally designed and synthesized a novel near-infrared (NIR) photoactivating probe, designated by iDOPE, in which an indocyanine green (ICG) fluorophore is covalently conjugated with a phospholipid moiety, 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), to incorporate into liposome bilayers. NIR irradiation showed that iDOPE retained the optical and fluorescence properties of ICG and demonstrated photoactivator characteristics: fluorescence emission at around 820 nm in a solvent, singlet oxygen production, and concentration-dependent heat generation. Additionally, iDOPE was incorporated into liposome bilayers and maintained stable liposomally formulated iDOPE (LP-iDOPE) over 1 week under physiological conditions. We also observed the tumor-specific biodistribution of LP-iDOPE of in vivo xenografts. These findings suggest that LP-iDOPE might be a promising tool for NIR optical imaging, photodynamic therapy, and photothermal therapy.