Independent education resourceInformation here does not replace care from a qualified health professional.
Peptide Therapy GuideClear peptide education

Educational guide

Targeted LNP Formulation

Targeted LNP Formulation mRNA Delivered Where It Matters Home » IVT RNA Production Services » Targeted Lipid Nanoparticle (LNP) Formulation Services Targeted Lipid Nanoparticle (LNP) Formulation Services At GenScript, we are committed to pushing the boundaries

Written by Peptide Therapy Guide Editorial Team
For education only

This guide cannot diagnose a condition or recommend a personal treatment plan. Discuss medical questions with a qualified professional.

Targeted LNP Formulation

mRNA Delivered Where It Matters

Home » IVT RNA Production Services » Targeted Lipid Nanoparticle (LNP) Formulation Services

Targeted Lipid Nanoparticle (LNP) Formulation Services

At GenScript, we are committed to pushing the boundaries of innovation in the field of lipid nanoparticle (LNP) technology. Building on the success and reliability of our current LNP services, we are thrilled to announce the launch of our Targeted LNP Service—designed to revolutionize the precision and efficacy of therapeutic delivery.

This advanced service leverages cutting-edge lipid formulations and targeting ligands to ensure that therapeutic payloads reach their intended destinations with unparalleled accuracy. Whether you're developing gene therapies, mRNA vaccines, or other innovative treatments, our Targeted LNP Service could offer advanced solutions to your mRNA and LNP projects.

Accuracy

Customizable targeting ligands to direct LNPs to specific cells or tissues.

Improved Efficacy

Increased mRNA expression at the target site

Versatility

A Wide Array of Targeting Options to Optimize Payload Delivery

Rush mRNA Synthesis New!

GMP-like mRNA Manufacturing Services

Catalog IVT mRNA, circRNA, saRNA, LNP products

mRNA QC Analysis

GenScript Cap Technology

Circular RNA Synthesis

Self-Amplifying RNA

LNP Formulation

Targeted LNP Formulation

ReadyEdit LNP Formulation

Targeted LNP Service

Target Options

T Cell Targeted LNP: CD3-Ab/LNP

CD34+ cell targeted LNP: CD34-Ab/LNP

Liver targeted LNP: Tri-GalNac/LNP, 20DODAP LNP

Spleen targeted LNP: SM10218PA LNP

Lung Targeted LNP: 50DOTAP LNP, CD31-Ab/LNP

Macrophage targeted LNP: Mannose/LNP

Kidney enhanced delivery: KKEEE/LNP

Corresponding Case Studies Below

QC Testing

Encapsulation Efficiency: >85%

Size Distribution: POI ±20 nm

Polydispersity Index: <0.2

Zeta potential: ± 15 mV

pH: 7.4 ± 0.5

Endotoxin : <4 EU/ml

Size/Scale Options

Load 20 nt ~ 20 kb mRNA

Load 0.1- gram level mRNA

Administration

Intramuscular (I.M.) for animal use only

Intravenous (I.V.) for animal use only

For in vitro studies

Novel LNP formulation

CX108

CX175

SM-CX712

CX108 LNP exhibited comparable in vivo performance to the benchmark SM102 LNP, and demonstrated enhanced expression in primary T cells after CD3 antibody conjugation, highlighting its potential for in vivo CAR-T applications.

CX175 LNP exhibited comparable in vivo performance to the benchmark SM102 LNP, and demonstrated enhanced expression in primary T cells after CD3 antibody conjugation, highlighting its potential for in vivo CAR-T applications.

SM-CX712 LNP can enhance RNA’s distribution to muscle, and reduce its expression in liver by IM injection

Popular off-the-shelf mRNA_LNP catalogs available now!

Ready-to-use targeted LNPs for specific cell and tissue delivery including T cells, CD34+ stem cells, liver (TriGalNAc, 20DODAP), and spleen (18PA) pre-loaded with mRNAs expressing eGFP or F-Luciferase, available in 5 days

“Not sure which T-cell targeted LNP fits your application? Check our LNP selector tool for guidance.”

Quality Control and Specification

Appearance

Visual Inspect

Clear and free of foreign particles​

Final Concentration

RiboGreen assay

0.05 – 0.4 mg/mL

Encapsulation Efficiency

> 85%

Encapsulated RNA Integrity

Bioanalyzer

> 75%

Particle size

Dynamic light scattering

Particle sizes differ with different LNP formulations

Poly Dispersity Index

< 0.2

Zeta Potential

Zetasizer by dynamic light scattering

Zeta potential varies with different LNP formulations

pH​

pH paper

7.4 ± 0.5​

Endotoxin​

Quantitative

<4 EU/ml

Bioburden​

Direct inoculation

No Growth after 72 hrs

Lipid Composition

LC-CAD

as detected

Upon Request

Antibody conjugation efficiency

Bradford assay

CD3-Ab/LNP

T Cells

Ligand decorated

Up to 4 payloads

65-165 nm

±20mV

CD34-Ab/LNP

CD34+ Cells

Tri-GalNac/LNP

Liver

65-125 nm

±15mV

CD31-Ab/LNP

Lung

Mannose/LNP

Macrophage

KKEEE/LNP

Kidney

20DODAP LNP

Formulation optimized

SM10218PA LNP

Spleen

-30 ~ +10 mV

50DOTAP LNP

-10 ~ +30 mV

Case Studies

Fluc mRNA(N1-methyl-pseU) was encapsulated with SM102-LNP or SM102-LNP decorated with anti-Human CD3 Antibody (Clone: OKT3, mAb, Mouse, GenScript, A02199), 100ng of mRNA encapsulated in LNP were incubated with jurkat cells in RPMI140 +10%FBS at 37C for 24 hrs. The expression of Fluc was detected using Luciferase Assay (Promega, E4030).

eGFP mRNA(N1-methyl-pseU) was encapsulated with SM102-LNP or SM102-LNP decorated with anti-Human CD3 Antibody (Clone OKT3, mAb, Mouse, GenScript), 10-150ng of mRNA encapsulated in LNP were incubated with primary T cells for 24 hrs. The expression of eGFP was detected using flow cytometry. W1, W2 and W3 indicate different wash conditions.

Fluc mRNA(N1-methyl-pseU) was encapsulated with SM102-LNP or SM102-LNP decorated with anti-mouse CD3 Antibody, 0.3mg/kg of mRNA encapsulated in LNP were injection through tail vein into mice, after 24 hrs, mice were sacrificed, and the expression of Fluc mRNA was measured with whole body imaging with different organs.

*Not sure which T-cell targeted LNP fits your application? Check our LNP selector tool for guidance >>

Resting primary T cells were seeded at 1 × 10⁶ cells per well in a 24-well plate and transfected with 500 ng of generic LNP, CD3Ab-LNP, or CD5Ab-LNP. The anti-human CD3 antibody (OKT3, mAb, mouse, GenScript) and anti-human CD5 antibody (mAb, Rabbit, GenScript) were used for LNP surface decoration. T-cell expression was assessed by flow cytometry (FACS) at 48 h post-transfection. Because CD3Ab (OKT3) is known to activate primary T cells, CD3Ab-LNP exhibited a higher expression level compared with CD5Ab-LNP. Notably, despite the intrinsic difficulty of transfecting resting T cells, CD5Ab-LNP still achieved over 80% transfection-positive cells.

Resting primary T cells were seeded at 1 × 10⁶ cells per well in a 24-well plate and transfected with 500 ng of generic LNP, CD3Ab-LNP, CD4Ab-LNP, or CD8Ab-LNP. The anti-human CD3 antibody (OKT3, mAb, mouse, GenScript), anti-human CD4 antibody (F001, mAb, mouse, GenScript), and anti-human CD8 antibody (F002, mAb, mouse, GenScript) were used for LNP surface decoration. T-cell expression was assessed by flow cytometry (FACS) at 48 h post-transfection. CD4Ab-LNP and CD8Ab-LNP exhibited selective delivery to CD4⁺ and CD8⁺ T cells, respectively, with minimal off-target expression.

EGFP mRNA(N1-methyl-pseU) was encapsulated with SM102-LNP or SM102-LNP decorated with anti-Human CD34 Antibody (Purified anti-human CD34 antibody(Anti-Human CD34 Antibody, mAb, Mouse, GenScript, CP0001) 100ng of mRNA encapsulated in LNP were incubated with Kasumi-1 cells for 24 hrs. The expression of eGFP was detected using flow cytometry.

EGFP mRNA(N1-methyl-pseU) was encapsulated with ALC0315-LNP or ALC0315-LNP decorated with anti-Human CD34 Antibody (Purified anti-human CD34 antibody(Anti-Human CD34 Antibody, mAb, Mouse, GenScript, CP0001) 100ng of mRNA encapsulated in LNP were incubated with primary human CD34+ cells for 24 hrs. The expression of eGFP was detected using flow cytometry.

Fluc mRNA(N1-methyl-pseU) was encapsulated with LNP , 0.3mg/kg of mRNA encapsulated in LNP were injection through tail vein into mice, after 24 hrs, mice were sacrificed, and the expression of Fluc mRNA was measured with whole body imaging with different organs.

EGFP mRNA(N1-methyl-pseU) was encapsulated with SM102-LNP or SM102-LNP decorated with TriGalNac, 0.3mg/kg of mRNA encapsulated in LNP were injection through tail vein into mice, after 24 hrs, mice were sacrificed, and liver organs were lysed. The eGFP expression in lysate was detected using western blot method.

Fluc mRNA (m1Ψ) was encapsulated with LNP, 0.3mg/kg of mRNA encapsulated in LNP were injection through tail vein into mice. Conjugation of anti-CD31 antibodies to LNPs can enhance mRNA expression levels in the lungs of mice. FACS analysis of lung cells revealed that CD31-Ab/LNPs exhibit clear targeting specificity toward CD31⁺ cells.

Fluc mRNA (m1Ψ) was encapsulated with LNP, 0.3mg/kg of mRNA encapsulated in LNP were injection through tail vein into mice. Mannose/LNP improved Fluc mRNA expression in spleen and lymph node system.

Mannose/LNPs delivering sgRNA targeting Zeb2 achieved efficient gene editing in Cas9⁺ BMDM cells and significantly suppressed tumors in a Cas9-GFP mouse model.

Fluc mRNA (m1Ψ) was encapsulated with LNP, 0.3mg/kg of mRNA encapsulated in LNP were injection through tail vein into mice. KKEEE/SM102 LNP enhanced Fluc mRNA expression in kidney organ ~4.6 times comparing undecorated LNP.

FAQs

We accept various antibody formats for targeted LNP conjugation, including:

Full-length antibodies (IgG)

scFv (single-chain variable fragments)

Fab fragments

VHH (nanobodies)

Other antibody formats

If you have questions about a specific antibody format, please contact our technical team to discuss compatibility.

Antibody-Decorated LNP Platforms for Targeted T-Cell Delivery

Antibody-decorated lipid nanoparticles (LNPs) enable non-viral, cell-specific nucleic acid delivery to immune cell subsets. By selecting antibodies against well-characterized T-cell surface markers, LNPs can be tuned for broad immune engagement, precision immunomodulation, or selective cytotoxic enhancement, supporting applications from in vivo CAR-T to autoimmune and infectious disease therapies.

CD3-LNP

Primary Target Cell Population

Best-Fit Disease Applications

Key Cons / Limitations

CD3 engagement may activate T cells (risk of cytokine release)

Limited cell-type specificity

Requires careful antibody density/affinity tuning

CD4-LNP

Does not target cytotoxic CD8+ T cells

Risk of altering helper/Treg balance

Potential off-target immune modulation

CD5-LNP

Expression on both T and B cells reduces specificity

Biological role in signaling is complex

Weaker targeting signal than CD3/CD7

CD7-LNP

Broad expression on normal T/NK cells

Potential on-target toxicity

Less suitable for non-oncology indications

CD8-LNP

Excludes CD4+ helper/Treg populations

Lower total T-cell reach than CD3-LNP

May require combination strategies

REQUEST A QUOTE

EMAIL

[email protected]

PHONE

1-877-436-7274

ONLINE FORM

Online Quote Submission

FAX

1-732-210-0262

Connected reading

Helpful context for this guide

Source-derived material selected through this article’s indexed topics.

Research context

Read sources and limitations before applying a claim.

Case Studies

Espcas9 mRNA/sgRNA targeting TARC (GenScript) were formulated in LP01-LNP formulation at 1:1 mass ratio achieved 97% editing efficiency, comparing to 61% by lipofectamine. 2.4 ug of RNA/LNP formulation were incubated with HEK293T cells, cell were lysed at day 3 and day 5 for PCR and sanger sequencing. Transfection efficiency was compared by delivering eGFP mRNA (100% N1-methyl-pseU modified, GenScript) into Jurkat and THP-1 immune cells using SM102-LNP (GenScript), Lipofectamine™ MessengerMAX™ (ThermoFisher Scientific) and TransIT® (Mirus). 100ng of mRNA were transfected into cells in 24 well plates. Starvation medium (OptiMEM) was used for lipofectamine and TransIT per the manufacturer’s instruction, and complete medium was used for LNP. The expression of eGFP was measured by flow cytometry after 48 hours. GS-MC3 LNP formulation has strong mRNA expression GS-MC3 LNP as generic formulation for customers’ mRNA screening project In vivo delivery efficiency of four different LNP formulations was compared by delivering Fluc mRNA (100% N1-methyl-pseU modified, GenScript) into Balb-C mice via IM injection at a dose of 0.25mg/kg. The expression of Fluc mRNA was measured by whole-body bioluminescence imaging. Fluc mRNA delivered by MC3-LNP showed the highest expression level after 8 and 48 hours by imaging at both Dorsal and Ventral pose of mice. To evaluate the biodistribution profile of different formulations, the heart, liver, lung, spleen, kidney, and brain of the mice were collected and imaged after 48 hours, MC3 -LNP formulation showed the strongest liver accumulation compared to others after 48 hours. Both LNP formulations are safe for IV injection SM102 has stronger liver accumulation among the two tested formulations In vivo delivery efficiency of two different LNP formulations was compared by delivering Fluc mRNA (100% N1-methyl-pseU modified, GenScript) into Balb-C mice via IV injection at a dose of 0.3mg/kg. The expression of Fluc mRNA was measured by whole-body bioluminescence imaging. In imaging analysis, Fluc-mRNA delivered by SM102-LNP showed higher expression efficiency than MC3 after 8 and 48 hours. To evaluate the biodistribution profile of different formulations, heart, liver, lung, spleen, kidney, and brain of the mice were collected and imaged after 48 hours, SM102 -LNP showed stronger liver accumulation compared to MC3-LNP after 48 hours. MC3-LNP showed stronger spleen accumulation after 48 hrs. Neither formulation caused significant body weight loss during the experiment period for 3 days.

Source: genscript.com ↗

Case Studies

1 SM102-LNP espCas9 TRAC HEK293T 97%, Jurkat 82%, T cells72% , HepG2 86% 2 ALC0315-LNP HEK293T 87%, Jurkat 80%, T cells 61% 3 LP01-LNP HEK293T 63%, Jurkat 75% 4 20DODAP-LNP PCSK9 HepG2 87% 5 SM102-SOPC LNP HepG2 90% 6 HifiCas9 HEK293T 97%, T cells 61% , HepG2 88% 7 8 SM102 LNP Cas12a Ultra HEK293T 63% 9 SM102-Mod LNP PEmax HEK3 pegRNA Nicking guide RNA HEK293T 62% 10 CXM2-LNP CBE HEK293T 34% 11 HEK293T 42% ReadyEdit LNP formulations demonstrate robust delivery of prime editing PE6g mRNA and HEK3 pegRNA across multiple cell types. Using optimized lipid compositions, CXM-2 LNP and SM102-Mod LNP achieved editing efficiencies of up to 80% in HEK293T cells, 36% in HepG2 cells, and 43.5% in Jurkat cells. These results highlight that CXM-2 LNP and SM102-Mod LNP enable efficient prime editing in cells. A breakthrough co-delivery platform using two lipid nanoparticles (LNPs): One delivers Cas9 mRNA + sgRNA for precise cutting at RAB11 The other delivers HDR donor template (circular-ssDNA) optimized for stability & integration Advantages: Achieves high-efficiency knock-in Enables robust tagging, reporter insertion, or functional studies at the endogenous RAB11 locus Scalable, non-viral, and suitable for both in vitro and in vivo applications Dual-LNP Delivery System for Highly Efficient Cas9 mRNA-Based Gene Knock-In at the RAB11 Locus Method: SM102-LNP1 loaded with Cas9mRNA and RAB11gRNA, SM102-LNP2 loaded with EGFP coding css-DNA or linear ss-DNA were co-delivered into HEK293T cells at different doses, the knock in efficiency were measured by flow cytometry after 72hrs . Result: higher knock in efficiency was observed using 200ng of circular ss-donor DNA Result: More than 80% editing observed at the TRAC locus Method: espCas9-mRNA : SafeEdit TRAC sgRNA were co-encapsulated in LNP at a molar ratio of 1:10 , 2.4 ug of RNA loaded LNP were incubated with cells for 72 hours, the gene editing efficiency for knocking out TRAC locus was sanger sequenced and editing efficiency was analyzed by ICE Analysis tool Software Result: More than 70% editing and 80% editing observed in 3A9 and Jurkat Cells Method: espCas9-mRNA : SafeEdit TRAC sgRNA were co-encapsulated in LNP at a molar ratio of 1:10 , 2.4 ug of RNA loaded LNP were incubated with cells for 72 hours, the gene editing efficiency for knocking out TRAC locus was sanger sequenced and editing efficiency was analyzed by ICE Analysis tool Software. sgRNA-1 to sgRNA-6 were designed to target different spacer sequence in TRAC gene in mice. Result: 27% knock in observed with the LNP formulation Result: 80% editing efficiency observed in HEK Cells Method: Cas12a mRNA/ SafeEdit TRAC sgRNA (GenScript) were packaged in LNP at 5:1 mass ratio and a serum dependent effect on editing was observed, RNA with SM102-LNP or ALC0315-LNP formulation were incubated with HEK293T cells, cell were lysed at day3 for NGS

Source: genscript.com ↗
P

About the author

Peptide Therapy Guide Editorial Team

Editorial team for Peptide Therapy Guide.

View all articles →