Conjugate of α-amylase and symmetric dimethylarginine, and application thereof
A conjugate of α-amylase and SDMA with a 10 to 17-atom linker using Sulfo-GMBS overcomes the limitations of harmful crosslinking agents, achieving high S/N ratio quantification of SDMA for renal and cardiovascular disease detection.
Patent Information
- Application Number
- PCT/JP2025/011736
- Authority / Receiving Office
- WO · WO
- Patent Type
- Applications
- Current Assignee / Owner
- Priority Date
- 2024-03-26
- Filing Date
- 2025-03-25
- Publication Date
- 2025-10-02
AI Technical Summary
Existing SDMA quantification methods face challenges in achieving a high signal-to-noise (S/N) ratio while using safe and inexpensive materials, as conventional crosslinking agents generate harmful substances and have limited tolerance for the number of atoms in the crosslinking group.
A conjugate of α-amylase and symmetric dimethylarginine (SDMA) is formed using a linker with 10 to 17 atoms, utilizing a safe and commercially available crosslinking agent like Sulfo-GMBS, which does not generate harmful hydrogen halides, enabling high S/N ratio quantification of SDMA.
The conjugate allows for safe, inexpensive, and efficient quantification of SDMA with a high S/N ratio, suitable for early detection of renal and cardiovascular diseases, particularly in veterinary medicine.