DC Chemicals

DC67567 · Updated 28 October 2026

ARV-T1

Instructions for Use

Before use

Check the supplied lot number, batch COA, approved SDS, quantity and retest date. Pure form: −20 °C, 1 year; In solvent: −80 °C, 6 months; −20 °C, 1 month. Sealed and protected from light.

For small quantities of viscous or oily lipid, volumetric transfer can reduce weighing losses. Confirm solvent compatibility and solubility before preparing a stock; calculated volumes do not establish solubility.

Stock-solution planning

Volume (mL) = mass (mg) × 1000 / [molecular weight × concentration (mM)].

Mass10 mM20 mM
10 mg1.0983 mL0.5491 mL
25 mg2.7457 mL1.3729 mL
50 mg5.4914 mL2.7457 mL
100 mg10.9829 mL5.4914 mL

Literature formulation reference

ComponentDC Chemicals productMolecular weightMolar ratioMass at 1 µmol total lipid (mg)
ARV-T1DC67567910.51500.455255
DSPCDC57005790.15100.079015
CholesterolDCD-041386.6538.50.148860
DMG-PEG2000DC4016925071.50.037605

ARV-T1/DSPC/cholesterol/DMG-PEG2000 = 50:10:38.5:1.5 mol%; reported N/P = 4. Source: Methods, LNP formulation. DMG-PEG2000 uses 2507 for calculated component masses. A lipid:RNA mass ratio is not inferred from N/P.

Read the complete study conditions, biological results, tolerability and figures →

References

  1. Jeon JH, et al. Lipid Nanoparticles Formulated with a Novel Cholesterol-Tailed Ionizable Lipid Markedly Increase mRNA Delivery Both in vitro and in vivo. International Journal of Nanomedicine 20, 9389–9405 (2025). DOI: 10.2147/IJN.S527822.
  2. Full text: formulation Methods and Figures 2–7.