DC Chemicals

DC67295 · Updated 28 October 2026

MK16

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 mg1.0022 mL0.5011 mL
25 mg2.5054 mL1.2527 mL
50 mg5.0108 mL2.5054 mL
100 mg10.0216 mL5.0108 mL

Literature formulation reference

ComponentDC Chemicals productMolecular weightMolar ratioMass at 1 µmol total lipid (mg)
MK16DC67295997.84600.457900
DOPEDC33634744.03300.170714
CholesterolDCD-041386.65400.118287
DMG-PEG2000DC4016925070.750.014380

MK16/DOPE/cholesterol/DMG-PEG2000 = 60:30:40:0.75 relative molar parts, not mol%. The parts sum to 130.75 and are normalized only for the calculated masses. MK16:mRNA = 12.5:1 by weight; N/P was not disclosed. Source: formulation selection in the main text and Supplementary Fig. 6a.

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

References

  1. Wang C, Xue Y, Markovic T, et al. Blood-brain-barrier-crossing lipid nanoparticles for mRNA delivery to the central nervous system. Nature Materials 24, 1653–1663 (2025). DOI: 10.1038/s41563-024-02114-5.
  2. Author manuscript, Figures 3–6 and associated Supplementary Information.