Open AccessMaltotriose–Chlorin e6 Conjugate Linked via Tetraethyleneglycol as an Advanced Photosensitizer for Photodynamic Therapy. Synthesis and Antitumor Activities against Canine and Mouse Mammary Carcinoma Cells
Author(s) -
Atsushi Narumi,
Rioko Rachi,
Hiromi Yamazaki,
Seigou Kawaguchi,
Moriya Kikuchi,
Hiroyuki Konno,
Tomohiro Osaki,
Yoshiharu Okamoto,
Xiande Shen,
Toyoji Kakuchi,
Hiromi Kataoka,
Akihiro Nomoto,
Tomokazu Yoshimura,
Shigenobu Yano
Publication year - 2021
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.0c06316
Subject(s) - photodynamic therapy , chemistry , photosensitizer , conjugate , cancer research , reactive oxygen species , apoptosis , biochemistry , biology , photochemistry , mathematical analysis , mathematics , organic chemistry
Glycoconjugated chlorins represent a promising class of compounds that meet the requirements for the third-generation photosensitizer (PS) for photodynamic therapy (PDT). We have focused on the use of glucose (Glc) to improve the performance of the PS based on the Warburg effect-a phenomenon where tumors consume higher Glc levels than normal cells. However, as a matter of fact, Glc-conjugation has a poor efficacy in hydrophilic modification; thus, the resultant PS is not suitable for intravenous injection. In this study, a Glc-based oligosaccharide, such as maltotriose (Mal 3 ), is conjugated to chlorin e6 (Ce6). The conjugation is assisted by two additional molecular tools, such as propargyl amine and a tetraethylene glycol (TEG) derivative. This route produced the target Mal 3 -Ce6 conjugate linked via the TEG spacer (Mal 3 -TEG-Ce6), which shows the required photoabsorption properties in the physiological media. The PDT test using canine mammary carcinoma (SNP) cells suggested that the antitumor activity of Mal 3 -TEG-Ce6 is extremely high. Furthermore, in vitro tests against mouse mammary carcinoma (EMT6) cells have been demonstrated, providing insights into the photocytotoxicity, subcellular localization, and analysis of cell death and reactive oxygen species (ROS) generation for the PDT system with Mal 3 -TEG-Ce6. Both apoptosis and necrosis of the EMT6 cells occur by ROS that is generated via the photochemical reaction between Mal 3 -TEG-Ce6 and molecular oxygen. Consequently, Mal 3 -TEG-Ce6 is shown to be a PS showing the currently desired properties.