| Literature DB >> 28429938 |
Jintang He1, Dian Su1, Carl Ng1, Luna Liu1, Shang-Fan Yu1, Thomas H Pillow1, Geoffrey Del Rosario1, Martine Darwish1, Byoung-Chul Lee1, Rachana Ohri1, Hongxiang Zhou2, Xueji Wang2, Jiawei Lu2, Surinder Kaur1, Keyang Xu1.
Abstract
Antibody-drug conjugates (ADCs) represent a promising class of therapeutics for the targeted delivery of highly potent cytotoxic drugs to tumor cells to improve bioactivity while minimizing side effects. ADCs are composed of both small and large molecules and therefore have complex molecular structures. In vivo biotransformations may further increase the complexity of ADCs, representing a unique challenge for bioanalytical assays. Quadrupole-time-of-flight mass spectrometry (Q-TOF MS) with electrospray ionization has been widely used for characterization of intact ADCs. However, interpretation of ADC biotransformations with small mass changes, for the intact molecule, remains a limitation due to the insufficient mass resolution and accuracy of Q-TOF MS. Here, we have investigated in vivo biotransformations of multiple site-specific THIOMAB antibody-drug conjugates (TDCs), in the intact form, using a high-resolution, accurate-mass (HR/AM) MS approach. Compared with conventional Q-TOF MS, HR/AM Orbitrap MS enabled more comprehensive identification of ADC biotransformations. It was particularly beneficial for characterizing ADC modifications with small mass changes such as partial drug loss and hydrolysis. This strategy has significantly enhanced our capability to elucidate ADC biotransformations and help understand ADC efficacy and safety in vivo.Entities:
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Year: 2017 PMID: 28429938 DOI: 10.1021/acs.analchem.7b00408
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986