Session Details
[SS09]Young Pharmaceutical Scientists Pioneer Future Oligonucleotide Therapeutics
Fri. Mar 28, 2025 1:15 PM - 2:45 PM JST
Fri. Mar 28, 2025 4:15 AM - 5:45 AM UTC
Fri. Mar 28, 2025 4:15 AM - 5:45 AM UTC
Room 5 (Fukuoka International Congress Center: 202 [2F])
Sponsored by Transformative Research Area (B) “Cell Membrane Permeation of Oligonucleotides Controlled by Membrane Modulator Molecules”
Organizer: Takashi Osawa, (Grad. Sch. Pharm., Osaka Univ.) Yuuya Kasahara (NIBIOHN)
Organizer: Takashi Osawa, (Grad. Sch. Pharm., Osaka Univ.) Yuuya Kasahara (NIBIOHN)
Antisense oligonucleotides (ASOs) and siRNAs have attracted attention as a drug discovery modality following small molecule and antibody drugs, and their development research is becoming more active every year. As a result of numerous attempts to improve the efficacy of oligonucleotide therapeutics by utilizing chemically modified nucleic acids, it is now possible to easily obtain oligonucleotides with high efficacy required for clinical application. In addition, the delivery of oligonucleotide therapeutics to target tissues, which had been an issue until recently, is being overcome by the fusion of state-of-the-art DDS using lipid nanoparticles and nucleic acid science. However, to further accelerate their practical application, there are still many issues that cannot be solved by conventional technologies, such as the extremely low cell membrane permeability of oligonucleotides. Furthermore, for oligonucleotide therapeutics to continue to develop in the future, it is essential to develop new modalities following ASO and siRNA. In this symposium, six young pharmaceutical scientists who are taking up the challenge of overcoming such situations will present some of their latest research. In addition, some of the symposiasts will introduce the latest results of the ongoing Transformative Research Area (B) project, "Cell Membrane Permeation of Oligonucleotides Controlled by Membrane Modulator Molecules" which aims to improve the membrane permeability of oligonucleotide therapeutics.
オーガナイザー挨拶・趣旨説明:大澤 昂志(阪大院薬)
[SS09-1]In vitro screening for the discovery of dipeptide ligands that enhance the activity of antisense oligonucleotides
○Takashi Osawa1, Ryosuke Kita1, Harumi Yamaguma2, Yuuya Kasahara1,2, Satoshi Obika1,3 (1. Grad. Sch. Pharm. Sci., Osaka Univ., 2. NIBIOHN, 3. OTRI, Osaka Univ.)
[SS09-2]Synthesis ofP-modified chimeric oligonucleotides for the development of oligonucleotide therapeutics having high safety and potency
○Kazuki Sato1, Yuhei Takahashi1, Takeshi Wada1 (1. Sch. Pharm. Sci., Tokyo University of Science)
[SS09-3]Technological improvements for antisense nucleic acid-loaded LNP preparation
○Hiroki Tanaka1,2, Hidetaka Akita1,2 (1. Grad. Sch. Pharm. Sci., Tohoku Univ., 2. CAMaD, Osaka Univ.)
[SS09-4]Development of oligonucleotide therapeutics for the radical cure for retro virus-related diseases
○Yu Mikame1, Haruki Toyama1, Chikara Dohno2, Takehiko Wada3, Asako Yamayoshi1,4 (1. Grad. Sch. Biomed. Sci., Nagasaki Univ., 2. SANKEN, Osaka Univ., 3. IMRAM, Tohoku Univ., 4. Dept. Life Sci. Tech., Science Tokyo)
[SS09-5]Promotion of membrane permeation of biopharmaceuticals using coacervates
○Yoshimasa Kawaguchi1, Shiroh Futaki1 (1. Inst. Chem. Res., Kyoto Univ.)
[SS09-6]Establishment of a platform for the development of gapmer-type antisense oligonucleotides and the application of drug discovery for the intractable diseases
○Yuuya Kasahara1,2 (1. NIBIOHN, 2. Grad. Sch. Pharm. Sci., Osaka Univ.)