ADME of Biologics—What Have We Learned from Small Molecules?

Journal Title: The AAPS Journal - Year 2012, Vol 14, Issue 3

Abstract

Thorough characterization and in-depth understanding of absorption, distribution, metabolism, and elimination (ADME) properties of a drug candidate have been well recognized as an important element in small molecule (SM) drug discovery and development. This has been the area of focus for drug metabolism and pharmacokinetics (DMPK) scientists, whose role has been evolving over the past few decades from primarily being involved in the development space after a preclinical candidate was selected to extending their involvement into the discovery stage prior to candidate selection. This paradigm shift has ensured the entry into development of the best candidates with optimal ADME properties, and thus has greatly impacted SM drug development through significant reduction of the failure rate for pharmacokinetics related reasons. In contrast, the sciences of ADME and DMPK have not been fully integrated into the discovery and development processes for large molecule (LM) drugs. In this mini-review, we reflect on the journey of DMPK support of SM drug discovery and development and highlight the key enablers that have allowed DMPK scientists to make such impacts, with the aim to provide a perspective on relevant lessons learned from SM drugs that are applicable to DMPK support strategies for LMs.

Authors and Affiliations

Thomayant Prueksaritanont, Cuyue Tang

Keywords

Related Articles

In vivo microdialysis for PK and PD studies of anticancer drugs

In vivo microdialysis technique has become one of the major tools to sample endogenous and exogenous substances in extracellular spaces. As a well-validated sampling technique, microdialysis has been frequently employed...

Examination of Gossypol-Pluronic Micelles as Potential Radiosensitizers

Chemoradiotherapy, the combination of chemotherapy and radiotherapy to treat cancer, has the potential to enhance local therapeutic effects and simultaneously treat systemic disease. However, chemoradiotherapy may also e...

Simultaneous population optimal design for pharmacokinetic-pharmacodynamic experiments

Multiple outputs or measurement types are commonly gathered in biological experiments. Often, these experiments are expensive (such as clinical drug trials) or require careful design to achieve the desired information co...

Modeling, Simulation, and Translation Framework for the Preclinical Development of Monoclonal Antibodies

The industry-wide biopharmaceutical (i.e., biologic, biotherapeutic) pipeline has been growing at an astonishing rate over the last decade with the proportion of approved new biological entities to new chemical entities...

Download PDF file
  • EP ID EP681245
  • DOI  10.1208/s12248-012-9353-6
  • Views 58
  • Downloads 0

How To Cite

Thomayant Prueksaritanont, Cuyue Tang (2012). ADME of Biologics—What Have We Learned from Small Molecules?. The AAPS Journal, 14(3), -. https://europub.co.uk./articles/-A-681245