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Ionizable lipids / MP2
MP2 chemical structure
Product imageResearch use only
CAT. NO. DCL0007

MP2

Ionizable lipids for colonic RNA delivery · cationic/ionizable lipids

Research highlights
Methylprednisolone-derived headgroup with a three-tail ionizable scaffold.15-fold colonic luciferase signal versus the SM102 LNP formulation in TNBS mice.IL-35 mRNA LNPs studied in acute and chronic mouse colitis models.mRNA delivery examined in ex vivo human colonic biopsies.

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Product overview

Description & Application

MP2 is a methylprednisolone-derived ionizable lipid with a steroidal headgroup and three acetal-containing C8 tails. In the cited study, MP2 was formulated with DOPE, cholesterol and DMG-PEG2k for rectal mRNA delivery to inflamed colonic tissue. The MP2 formulation produced about 15-fold higher colonic luciferase signal than the study's SM102 formulation in TNBS colitis mice. MP2 LNPs carrying IL-35 mRNA improved disease measures in acute and chronic mouse colitis models; mRNA delivery was also examined in ex vivo human colonic biopsies. These results describe the tested LNP formulations, not isolated lipid efficacy.

CAS No.Not reported
Chemical NameMP2
SMILESCCCCCCCCOCOCCCCN(CCCCCCOC(=O)CCC(=O)OCC(=O)[C@@]1(O)CC[C@H]2[C@@H]3C[C@H](C)C4=CC(=O)C=C[C@]4(C)[C@H]3[C@@H](O)C[C@@]21C)CCCN(CCCCOCOCCCCCCCC)CCCCOCOCCCCCCCC
FormulaC74H132N2O14
M.Wt1273.87
Purity>95% by ELSD-HPLC
StorageRequest batch-specific handling guidance
Product classificationIonizable lipids for colonic RNA delivery; Cationic/Ionizable Lipids
PublicationCao D, et al. Anti-inflammation lipid nanoparticles enable localized mRNA therapy for inflammatory bowel disease. Nature Communications (2026). doi:10.1038/s41467-026-78302-5

Literature-reported MP2 LNP composition

ComponentReported ratioRole
MP220Ionizable lipid
DOPE30Helper phospholipid
Cholesterol40Sterol
DMG-PEG2k0.75PEG lipid
Sum of printed values90.75Confirm with the authors before reproducing
Microfluidic mixing; lipid:mRNA mass ratio 10:1; PBS dialysis
Not reported
Rectal administration; MP2 LNPs mixed with Pluronic F127 hydrogel

Reported study results

Lead selection · mouse colon

In TNBS-induced colitis mice, rectally administered Fluc mRNA MP2 LNPs gave approximately 15-fold higher colonic luminescence than the study's SM102 formulation at 6 hours (0.5 mg/kg mRNA; n = 3 mice per group; Fig. 1g).

Cell delivery · Caco-2

MP2 was among the five three-tail steroid-derived formulations with more than 30-fold higher Fluc mRNA expression than the study's SM102 formulation in Caco-2 cells (0.5 µg/mL mRNA; 18 hours; n = 4 wells per group; Fig. 1f).

Mouse colitis research

IL-35 mRNA-loaded MP2 LNPs improved clinical and colonic inflammation measures in TNBS acute and IL-10 knockout chronic mouse colitis models. The IL-10 knockout study reported disease activity index 0.38 for MP2-IL-35 versus 3.75 for SM102-IL-35 at week 18 (1 mg/kg mRNA rectally each week; Fig. 4).

Human tissue · ex vivo

MP2 LNPs delivered GFP mRNA to immune, epithelial and endothelial cells in human colonic biopsies. IL-35 mRNA-loaded MP2 LNPs were also studied in IBD patient biopsies for cytokine and T-cell readouts (Fig. 5).

Reference: Cao D, Tian M, Yu C, et al. Nature Communications (2026), doi:10.1038/s41467-026-78302-5. Structure and analytical record: Supplementary Fig. 1 and MP2 NMR/MALDI-MS; LNP composition: Methods. The reported molar ratio totals 90.75 and has not been normalized here. Published performance reflects the stated formulation, cargo, dose and model.
SDSMSDSInquire for availability
COACOABatch-specific document on request
Laboratory planning

Solution Calculators

Molecular weight is calculated for the neutral MP2 structure shown in Supplementary Fig. 1. Confirm solvent compatibility and solubility before preparation.

Mass = concentration × volume × molecular weight
Enter any three values to calculate the fourth.
C₁V₁ = C₂V₂
Enter any three values to calculate the fourth.

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