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Welcome to Alfa Cytology's Peptide Design and Synthesis Services, dedicated to revolutionizing cancer therapy through innovative peptide-based treatments. Our cutting-edge services are tailored to meet the unique challenges of cancer treatment, offering customized peptide design and synthesis solutions to target specific tumor biomarkers and signaling pathways. With a commitment to excellence and a focus on precision medicine, we aim to empower researchers and clinicians with advanced peptide therapeutics that hold the promise of improved patient outcomes in the fight against cancer.
Peptide Drug Conjugates represent a groundbreaking approach in cancer therapy, combining the selectivity of peptides with the cytotoxic potency of small-molecule drugs. At Alfa Cytology, our peptide drug conjugates development service aims to overcome the limitations of conventional chemotherapy by precisely delivering therapeutic payloads to cancer cells while sparing healthy tissues. Through strategic conjugation strategies and innovative drug delivery systems, we seek to maximize therapeutic efficacy and minimize adverse effects, ushering in a new era of targeted cancer treatment.
Fig.1 Peptide-Drug Conjugates. (Alas, M., et al., 2021)
Common functional groups in the linker region can be broadly classified into four groups: enzyme-cleavable (esters, amides, and carbamates), acid-cleavable (hydrazones and carbonates), reducible disulfides, and non-cleavable (thioethers, oximes, and triazoles). The classification is based on how these functional groups behave after cellular uptake or under in vivo conditions. Linkage group chemistry plays an important role in the success of PDCs in improving efficacy.
Linker Chemistries of the ADCs Approved for Therapeutic Use
ADC | Linker Chemistry | Year approved |
---|---|---|
Enzyme cleavable | ||
Brentuximab vedotin (Adcetris) | carbamate, dipeptide, thioether | 2011 |
Polatuzumab vedotin (Polivy) | carbamate, dipeptide, thioether | 2019 |
Enfortumab vedotin (Padcev) | carbamate, dipeptide, thioether | 2019 |
Trastuzumab deruxtecan (Enhertu) | amide, tripeptide, thioether | 2019 |
Trastuzumab emtansine (Kadcyla) | thioether, amide | 2013 |
Enzyme or acid cleavable/ Reducible disulfide | ||
Gemtuzumab ozogamicin (Mylotarg) | disulfide, hydrazone, amide | 2000* |
Inotuzumab ozogamicin (Besponza) | disulfide, hydrazone, amide | 2017 |
Acid cleavable | ||
Sacituzumab govitecan (Trodelvy) | carbonate, triazole, thioether | 2020 |
Our peptide drug conjugates development service combines peptides with therapeutic agents to create targeted cancer treatments, improving precision and minimizing side effects.
Targeted Drug Delivery Systems
Conjugation Chemistry
Choose Alfa Cytology for peptide drug conjugates development service, and embark on a journey towards innovative cancer therapy solutions that prioritize precision, efficacy, and patient-centered care. Contact us today, and get started with out innovative service.
Reference
For research use only.