Multiple analytes are evaluated during ADC PK studies to characterize systemic exposure, payload retention, and in vivo stability.
|
Analyte |
Measurement |
Application |
|---|---|---|
|
Total Antibody |
Conjugated and unconjugated antibody (DAR ≥0) |
Evaluate overall antibody exposure and clearance |
|
Conjugated Antibody |
Payload-conjugated antibody (DAR ≥1) |
Evaluate ADC exposure and payload retention |
|
Total Payload |
Conjugated and released payload forms |
Evaluate overall payload exposure |
|
Free Payload |
Unconjugated payload in circulation |
Assess payload release and systemic exposure |
Combined analysis of Total Antibody and Conjugated Antibody enables evaluation of ADC exposure, payload retention, and in vivo deconjugation.
Quantification of conjugated antibody is essential for evaluating ADC exposure and payload retention in PK studies.
ACROBiosystems ADC Quantification ELISA Kits enable payload-specific measurement of MMAE-, MMAF-, and Exatecan-conjugated ADCs in preclinical serum and plasma samples. These kits support ADC PK studies, linker stability evaluation, and assessment of payload retention.
|
Application |
Purpose |
|---|---|
|
PK Studies |
Quantify ADC exposure and support PK parameter analysis, including half-life (t1/2), clearance (CL), and AUC |
|
Toxicokinetic (TK) Studies |
Monitor systemic ADC exposure during nonclinical safety studies |
|
Tissue Distribution Studies |
Characterize ADC biodistribution profiles and evaluate in vivo distribution patterns |
|
Linker Evaluation |
Assess payload retention and evaluate linker stability |
|
Candidate Selection & Developability Assessment |
Compare ADC candidates with different payloads, linkers, DAR values, and conjugation strategies |
Validated in cynomolgus monkey serum and plasma matrices.
Example: MMAE-ADC Quantification ELISA Kit(Cat. No. PKA-A001)
|
ID |
Components |
Size |
|---|---|---|
|
PKA001-C01 |
Pre-coated Anti-MMAE Antibody Microplate |
1 plate (8×12 strips) |
|
PKA001-C02 |
MMAE-ADC Standard |
20 μg |
|
PKA001-C03 |
HRP-Anti-Human-IgG-Fc Antibody |
20 μg |
|
PKA001-C04 |
10×Washing Buffer |
50 mL |
|
PKA001-C05 |
2×Dilution Buffer |
50 mL |
|
PKA001-C06 |
Substrate Solution |
12 mL |
|
PKA001-C07 |
Stop Solution |
7 mL |
Beyond ADC Quantification ELISA Kits, ACROBiosystems provides reagents and services to support ADC PK assay development, PK characterization, and immunogenicity assessment.
ACROBiosystems anti-payload antibodies enable payload-specific detection and support assay development across ADC programs.
Anti-idiotypic antibodies specifically recognize the variable region of therapeutic antibodies and are valuable tools for drug-specific PK assays and immunogenicity assessment.
ACROBiosystems provides highly specific anti-idiotypic antibodies and customized development services to support ADC PK assay development throughout the drug development process.
Applications
|
Scenario |
Application |
|---|---|
| PK Assay Development | Support drug-specific concentration measurement and in vivo exposure evaluation. |
| Immunogenicity Assessment | Support ADA assay development and immunogenicity assessment. |
| Bioanalytical Method Development | Enable the development and optimization of analytical platforms, including bridging assays, sandwich ELISAs, and related formats. |
Customized services are available from antigen preparation through monoclonal and polyclonal anti-idiotypic antibody generation and PK/ADA assay kit development.
Service
Payload-specific antibodies selectively detect ADCs containing the corresponding payload, with minimal cross-reactivity toward ADCs bearing alternative payload classes.
Anti-MMAE/MMAF antibody (Cat. No. MME-M5252) demonstrates specific recognition of MMAE- and MMAF-conjugated ADCs, with no significant cross-reactivity observed toward DXd-, SN-38-, or DM1-conjugated ADCs.
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The Exatecan-ADC Quantification ELISA Kit (Cat. No. PKA-A003) demonstrates excellent linearity across the validated concentration range, supporting quantitative analysis of ADC samples.
For each experiment, a standard curve should be generated for each microplate. The absolute OD values may vary depending on the laboratory, operator, or equipment. The example data provided below are for reference only.
Quantitative PK assays for RC48 and trastuzumab deruxtecan in serum samples.
Immobilized Mouse Anti-MMAE&MMAF Antibody, Mouse IgG1 (Cat. No. MME-M5252) at 5 μg/mL, add Disitamab Vedotin (RC48) in the 50% Mouse serum and then add Biotinylated Human Her2, His,Avitag, premium grade (Cat. No. HE2-H82E2) at 0.5 μg/mL. Detection was performed using HRP-conjugated Streptavidin (Acro, Cat. No. STN-NH913) (Routinely tested).
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Immobilized Human Her2, His Tag (Cat. No. HE2-H5225) at 1 μg/mL, add Trastuzumab Deruxtecan in the 100% Human Serum and then add Biotinylated Anti-DXD Antibody, Mouse IgG1, Avitag (Cat. No. DXD-BVM807) at 0.05 μg/mL. Detection was performed using HRP-conjugated Streptavidin (Acro, Cat. No. STN-NH913) (QC tested).
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Immobilized ADC-DXD at 1 μg/mL (100 μL/well) can bind Mouse Anti-DXD&Exatecan Antibody, Mouse IgG1, mAb (Cat. No. DXD-M684) with a linear range of 0.1-4 ng/mL (Routinely tested).
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Immobilized Disitamab Vedotin (RC48) at 0.2 μg/mL (100 μL/well) can bind Monoclonal Anti-MMAE&MMAF Antibody, Mouse IgG1 (Cat. No. MME-M5252) with a linear range of 0.1-2 ng/mL (QC tested).
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Custom Anti-Idiotypic Antibody Enables Sensitive ADC PK Quantification
Naked F(ab′)₂ was used for immunization to generate anti-idiotypic antibodies. The selected anti-idiotypic antibody was paired with Mouse Anti-MMAE Antibody, Mouse IgG1 (MALS verified; Cat. No. MME-M5252) to establish a drug-specific ADC PK assay. Detection was performed using HRP-conjugated streptavidin, achieving a sensitivity of 0.69 ng/mL.
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‘ADC Potency Analysis and Quality Control Technology Breakthrough’ Webinar Series
ACROBiosystems proudly presents the flagship 'ADC Potency Analysisand Quality Control Technology Breakthrough' live webinar series. This series will systematicallydeconstruct critical aspects ofADC drug development through five coremodules-from potency analysis to quality control technologiesempowering breakthroughs in ADC therapeutics by overcoming keytechnical bottlenecks.
Watch NowAddressing Challenges in Antibody-Drug Conjugate Development
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