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PRODUCT USE GUIDE · DC99010

CICL-1 (L829)

Instructions for Use

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Product information

CICL-1, identified in the cited study as Lipid 829 (L829), is an ionizable lipid used in targeted lipid nanoparticles for in vivo delivery of CAR mRNA to T cells. CD8-targeted L829 tLNPs preferentially engineered CD8-positive T cells in the reported models, produced rapid B-cell depletion, and controlled a humanized leukemia xenograft. In cynomolgus monkeys, anti-CD20 CAR mRNA tLNPs produced deep peripheral and tissue B-cell depletion, followed by repopulation dominated by naïve B cells; the authors described this finding as suggestive of immune reset. The supplied main article does not include Supplementary Table S1, so the complete five-lipid composition and N/P ratio are not presented as verified formulation values. All performance statements below are literature-reported study results, not product specifications or guaranteed outcomes.

CAS No.Not available
Chemical NameCICL-1 (L829)
FormulaC55H100O14N2
M.Wt1,013.40
Purity>98%
StorageOriginal product: up to 1 year under the storage conditions stated on the vial, kept tightly sealed. Stock solutions: aliquots at -20°C, generally up to one month.
Shipping conditionShips from Shanghai. Pure lipid is stable during ice-pack transport.

Formulation & study context

Literature information refers to the cited study and its particular formulation. Administration routes are research context, not clinical instructions or a guarantee of performance.

Componentmol%Role
L829 (CICL-1)Not reportedIonizable lipid
Anti-CD8 targeting-moiety lipid conjugate (lipid identity not reported in supplied main article)Not reportedTargeting-lipid conjugate
Three additional lipid components (identities not reported in supplied main article)Not reportedAdditional lipid components
Reported totalNot reportedSource values retained
N/P ratioNot reported in the cited article
Total lipid:cargo weight ratioNot reported in the supplied main article
Buffer & pHNot reported in the supplied main article; formulation details are assigned to Supplementary Table S1
CargoAnti-CD20 CAR mRNA
Administration routeIntravenous injection
Dose0.1-2.0 mg/kg every 72 h for three doses
Animal modelCynomolgus monkeys; 22 animals across three studies
Formulation processNot reported in the supplied main article; Materials and Methods and Supplementary Table S1 were not included in the uploaded PDF

N/P is the molar ratio of specified lipid nitrogen groups to nucleic-acid phosphate groups. A lipid:cargo mass ratio is a different quantity and must not be used as N/P.

Stock-solution preparation table

Calculated from the product-page molecular weight: 1013.4 g/mol. Volumes are final solution volumes.

Lipid mass1 mM5 mM10 mM
10 mg9.868 mL1.974 mL0.987 mL
25 mg24.669 mL4.934 mL2.467 mL
50 mg49.339 mL9.868 mL4.934 mL
100 mg98.678 mL19.736 mL9.868 mL
250 mg246.694 mL49.339 mL24.669 mL

Volume (mL) = mass (mg) × 1000 / [MW (g/mol) × concentration (mM)]. These are mathematical conversions, not measured solubility or validated solvent recommendations. Confirm solvent compatibility and the molecular weight of the exact material before use.

Open editable solution calculators →

Handling & storage

Provided that storage conditions are as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 1 year.

Wherever possible, prepare and use solutions on the same day. If stock solutions must be prepared in advance, store them as aliquots in tightly sealed vials at -20°C. Generally, these will be usable for up to one month.

Before use, and prior to opening the vial, allow the product to equilibrate to room temperature for at least 1 hour.

References

Cited literature for this formulation and performance dataset Hunter TL, Bao Y, Zhang Y, et al. In vivo CAR T cell generation to treat cancer and autoimmune disease. Science. 2025;388(6753):1311-1317. DOI: 10.1126/science.ads8473 Identity and performance: supplied Science main article, Figures 1 and 3-5. The complete five-lipid composition, preparation method and particle-characterization details are assigned by the article to Supplementary Table S1 and Materials and Methods, which were not present in the uploaded PDF.