November 2019

Mass Balance Studies: What You Need and Why You Need It

Author:  Jolanta Golec, Madison Knapp
Posted:  15 November 2019

In vivo mass balance studies are an important element of nonclinical drug development, to inform first in-human (FIH) studies and to understand the pharmacokinetic (PK) profile of a drug. Elucidating PK properties can help bridge activity and toxicity data to paint a full picture of a drug’s behavior in patient populations.
 

Regulatory Expectations

According to the US FDA, “Pharmacokinetic studies are intended to define the time course of a drug and, where appropriate, major metabolite concentrations in blood…” and “[…] the most critical information is that showing […] the route of elimination by metabolic or excretory pathways.”1 Mass balance studies provide information to demonstrate primary mechanisms of elimination and excretion from the body and proportion of parent drug converted to metabolite, shedding light on clearance mechanisms of a drug and its metabolites. While clinical mass balance studies in humans provide the best predictive data for effect on patient populations, animal mass balance data is a necessary step in preliminary risk assessment and study design planning before administration to human volunteers.
  Mass-Balance-Analysis.jpg

Why You Need It

You need both animal mass balance and QWBA data for dosimetry calculations to determine appropriate radiolabeled dose in human absorption, metabolism, and excretion (hAME) studies in Phase I clinical trials. Data from these nonclinical studies can also provide evidence needed when human mass balance studies yield low recovery: “Total recovery should be at least 90% of the dose. Lower recoveries must be explained by biological factors like long elimination half-life, irreversible binding to tissue components or loss through expirations. Animal (tissue distribution and excretion) data can support such explanations.”2 Typical animal mass balance (excretion) studies measure excretion of radiolabeled parent compound and metabolites in urine, feces, and expired air, and if necessary can measure biliary excretion and residual radioactivity in the carcass.
 

Mass Balance Studies with Us

Mass balance is one part of our standard in vivo ADME package, and our sister lab in Tokai, Japan, has over 50 years’ experience performing radiolabeled (RI) experimentation, synthesis, and purity checks for pharmaceutical companies as the leading in vivo ADME CRO in Japan. The facilities are AAALAC-accredited to meet compliance with ethical requirements upheld by FDA, EMA, and PMDA for all animal studies. Their capabilities allow for flexibility in study design elements, such as:
 
Routes of Administration Radionuclides Animal Species
Oral 14C Rats
Intravenous (administration or infusion) 3H Mouse (including chimeric with humanized liver)
Percutaneous 125I Rabbit
Subcutaneous 33P Dog
Intramuscular 35S Monkeys
Intracheal 51Cr Miniature pig
Opthalmic 111In Animal models of human disease (knockout models)
Colorectal 55,59Fe  
Intraduodenal 65Zn  
Nasal 75Se  
Intraocular 90Y  
Sublingual 153Gd  
Intrauterine    
Intracerebral    
Intravesical    
Knee Joint    
Mass-Balance-Researcher.jpg 

Standard Mass Balance Data Analysis

After collection at each time point, analysists use a liquid scintillation counter (LCS) to measure radioactivity in each biomaterial. Typically, mass balance studies run in tandem with other in vivo ADME and clients choose to run metabolite identification (MetID) on materials as well, in which case advanced LC-MS/MS is used to elucidate metabolic profiles in excreta over time.
 

Bile Duct Cannulation (BDC)

Bile duct cannulation is necessary to examine biliary excretion when more than 20% of radioactivity is seen in feces after oral dosing, normally in rats.
 
The free-moving cannulation method is a complex surgical procedure that requires a highly-skilled and experienced hand to perform properly. Our surgeons at the Drug Development Solutions Center each have extensive experience and training; this ensures that each study is conducted accurately and smoothly, without delays from having to repeat procedures due to improper implantation.
 
Mass-Balance-Services.jpgIn a typical BDC study concurrent with mass balance, bile is collected from cannulated animals up to 48 hours, but the collection window can be extended if necessary by supplying treated animals with electrolytes and dextrose water or untreated bile (after IACUC (Institutional Animal Care and Use Committee) review). Reabsorption through enterohepatic circulation can be investigated if a drug shows extensive excretion into the bile.
 
Get in touch with a SEKISUI XenoTech representative about getting your mass balance study started today!
 
More about our in vivo ADME services:
Find more information about QWBA or other components in our standard in vivo ADME package, or find out more about the history, experience, and expertise of the Drug Development Solutions Center.
 
About the Authors
Jolanta Golec has been with the SEKISUI Drug Development Solutions Center, our sister lab in Tokai, Japan, since 2013. She has experience serving in both scientific research and sales promotional capacities. Jolanta holds a M.Eng. in Agriculture from the University of Agriculture in Krakow (Poland), M.Sc. in Pharmaceutical Biotechnology from the University College Cork (Ireland) and is working on her MBA from the University of Manchester (UK).

Madison Knapp received her BS from the University of Missouri – Columbia and became SEKISUI XenoTech’s Scientific Communications Coordinator in 2019 after serving in similar positions at CropLife America, Bond Life Sciences Center and the CAFNR Office of Communications.
 
[1] Center for Drugs and Biologics, Food and Drug Administration, Department of Health and Human Services Center for Drug Evaluation and Research. Guideline for the format and content of the human pharmacokinetics and bioavailability section of an application.
[2] Beumer et al 2006. “Mass Balance Studies, with a Focus on Anticancer Drugs.”

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