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DC60856 · Updated 24 October 2026

DMA4-H228
Formulation & Performance

This edition organizes the previously reviewed, source-linked product record. It is not a new independent review of every paper or supporting file. Reported and calculated values retain their original labels.

Literature-reported formulation composition

Componentmol%Role
DMA4-H22866.67Ionizable lipid
Cholesterol25.67Sterol
DSPC6.67Helper phospholipid
DMG-PEG20001PEG lipid
Reported total100.01Source values retained

Component molecular weights and calculated amounts

Composition retained from the cited study below. Research planning aid only. Results cover lipid component weights and do not include RNA, buffer, solvent, process loss or an N/P ratio.

ComponentMolecular weightMolar partsNormalized mol%Amount (µmol)Weight (mg)
DMA4-H22866.66378.553779.1420
Cholesterol25.66730.245611.6944
DSPC6.6697.85896.2097
DMG-PEG20001.0001.17822.9539

Calculated total: 100.0000 mg lipid.

Calculated catalog planning quantities; RNA, solvent and process loss are excluded. DMG-PEG2000 uses 2507. Component mass = total lipid mass × molar parts × molecular weight / sum(parts × molecular weight). This conversion does not infer N/P.

Not reported in the cited article
10:1
25 mM sodium acetate, pH 5.2.
FLuc mRNA; separate OVA mRNA vaccine studies
Intravenous tail vein
FLuc 0.25 mg/kg in Fig.1; OVA 10 micrograms/mouse per dose in separate studies
BALB/c reporter screening; C57BL/6 tumor studies
Dropwise addition of ethanolic lipid solution to acetate; dialyse blank LNPs against PBS; combine blank LNPs with RNA by pipetting.

Literature-reported performance for the cited formulation

Literature-reported97.9% in the representative Fig.1E readout0.25 mg/kg FLuc mRNA IV; screen n=2; not percent injected dose · 6 hMain PDF p.4, Fig.1D-E
Literature Data DisclaimerAll formulation parameters and performance values shown in this section are derived from the cited publication and are provided for reference only. These results were obtained using the specific materials, formulation process, cargo, dose, analytical method, model and administration route described in that study. Unless otherwise stated, the data were not generated or independently verified by DC Chemicals. DC Chemicals supplies the lipid compound only and does not guarantee that customers will reproduce the reported LNP properties or biological performance.

The administration route shown above was used in the cited study and is not a clinical-use instruction or recommendation by DC Chemicals.
Cited literature for this formulation and performance datasetDimethylamino-based synthetic lipidoid nanoparticles for selective mRNA delivery to splenic antigen-presenting cells. DOI: 10.1016/j.jconrel.2025.113737 DOI: 10.1016/j.jconrel.2025.113737
Main article supplied; SI not supplied. 10:1 is ionizable-lipid:RNA by weight, not total-lipid:RNA or N/P. Rounded component values total 100.01.

Primary article