Preclinical Research
ISSUE NO. 16 — Microsampling in Drug Development

Microsampling significantly lessens the volume of blood and plasma/serum that is collected and analyzed to determine circulating concentrations of therapeutic drugs, metabolites, and biomarkers in preclinical and clinical research.
In preclinical research, microsampling technology supports the 3Rs of animal research, and allows for less intrusive blood collection procedures.
By definition, clinical microsampling reduces sample volume to less than or equal to 50 microlitres (μL) compared to conventional venipuncture wherein millilitres (mL) of blood volume is collected. In Altasciences’ experience, microsample volumes being analyzed are less than or equal to 20 μL, with some microsampling techniques as low as 5 μL.
In Issue 16 of The Altascientist, we explore the benefits, applications, and considerations of microsampling in preclinical, clinical, and bioanalytical research, including:
- Regulatory considerations
- Case study: Anti-Epileptic Drug Monitoring – Sample Preparation Using Impact-Assisted Extraction
- Case study: Large Molecule – Determination of Rituximab Using a Surrogate Peptide Approach
Benefits of Microsampling in Preclinical Research
Microsampling addresses two of the 3Rs (replacement and reduction) of preclinical research. By eliminating or greatly reducing the use of satellite animals, microsampling can reduce the number of rodents in certain preclinical studies by 30 to 40 percent. Decreasing the number of animals required can have an added benefit of reducing R&D costs related to animals and housing, particularly for toxicokinetic (TK) studies that use satellite animals to minimize repeated conventional blood sampling procedures.
Lower-volume blood draws, from both rodents and non-rodents, taken from less disruptive locations, allow lab animals to recover more quickly, and have fewer sampling-related adverse events compared to conventional sampling. Refinement of the bleeding technique also translates to less animal handling, minimizing stress.
The elimination of satellite animals improves the quality of research data, as scientists conduct all TK analysis using main study animals. This enables direct correlation of exposure with pharmacodynamic and toxicological outcomes.
Benefits of Microsampling in Clinical Research
Microsampling in clinical research reduces patient burden, improves enrollment and engagement, and reduces drop-out. Self-administration facilitates the data collection during studies related to unpredictable clinical episodes, such as acute migraine or epilepsy attacks, and allows episodic sampling to relate efficacy with bioavailability. The dried blood samples can be stored and transported at ambient temperature, eliminating the costly cryopreservation and shipment that conventional wet blood samples demand.
Microsampling also provides a convenient, low-cost way to collect blood and plasma/serum from patients remotely. Individuals in remote geographic locations are able to participate in clinical trials, as they can conduct their blood draws at home.
Bioanalytical Considerations for Microsampling
The accurate analysis of dried blood microsamples requires equipment with high sensitivity and specificity, such as that offered by triple-stage quadrupole mass spectrometry systems paired with liquid chromatography front ends to optimize signal-to-noise ratio. When additional selectivity is required, this can be addressed by accurate mass filtering (e.g., time-of-flight or orbitrap mass spectrometer) or the use of differential ion mobility spectrometry to separate analyte from interference prior to mass selection.
Is Microsampling the Right Option for Your Preclinical or Clinical Study?
Microsampling is not appropriate for all studies and should be considered on a case-by-case basis. In a microsampling drug development program, it is critical to establish the appropriate pharmacokinetic/ statistical considerations to enable correlation/concordance between microsampling and standard blood sampling techniques.
How Altasciences Can Help
Altasciences’ scientific acumen and experience with different microsampling devices, supporting numerous programs, has led to unparalleled expertise in the development of assays and processes for all your drug candidates, from the straightforward to the most complex.
Explore all issues of The Altascientist in our Resource Center. And don’t forget to subscribe to “The Altascientist: Audiobooks” on Spotify, Apple Podcasts, or wherever you get your audio content.
2020 Year in Review
2020 has been quite a year! Each year, we strive to provide you with a more innovative, simplified, and seamless early phase drug development journey. And the past 12 months have been no exception.
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ISSUE NO. 14 — Central Nervous System
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As you work towards a successful New Drug Application (NDA) submission, there are In Issue 14 of The Altascientist, we look into the complex considerations of CNS-active drugs, including:
THE IMPORTANCE OF CLINICAL STUDIES FOR CNS-ACTIVE DRUGSCNS-active drugs have unique attributes that necessitate additional specialized study, such as:
Because CNS-active drugs can have unintended effects in the critical neural system that influences so many aspects of human health, the required preclinical and clinical studies are typically more detailed and rigorous than for other types of drugs. In addition, the results of such studies will have a material impact on your development program going forward, both in terms of timelines and budget, so you will want the answers for yourself as much as for the regulatory bodies. One of the key considerations in evaluating a CNS-active drug molecule (or its metabolites), is the evaluation of abuse potential. Such data is integral in determining whether or not a new drug approved for medical use may need to be a controlled substance. The FDA uses an eight-factor format for NDA submissions of CNS-active molecules. A controlled substance is assigned a schedule based on whether it has a currently accepted medical use in treatment in the United States, and its relative abuse potential and likelihood of causing dependence. Physical dependence is a neuroadaptive process that can occur in the absence of abuse potential. The ability of a drug to produce physical or psychological dependence plays a role in the scheduling placement of an abusable drug under the CSA. DRUG SCHEDULING AND THE CONTROLLED SUBSTANCES ACTThe Controlled Substances Act, enacted in 1970, provides a framework for appropriate labelling and controlled distribution of medications with certain attributes. Scheduling of a medication impacts market availability and prescribing behavior. For planning and development purposes, it is important to act on early signals that suggest scheduling will be necessary. Drugs and other substances that are considered ‘controlled substances’ are classified into five schedules. As the schedule progresses from I through V, the abuse potential reduces and thereby the limitations on prescribing practices are lessened. Schedules I and II both represent drug molecules with the highest known abuse potential. Schedule I drugs are not approved for medical use in the United States, whereas Schedule II drugs are. Explore all issues of The Altascientist in our Resource Center. And don’t forget to subscribe to “The Altascientist: Audiobooks” on Spotify, Apple Podcasts, or wherever you get your audio content. Download publicationDetermination of Pirfenidone and Metabolites in Rat Plasma by Coupling On-Line Fractionation with LC-MS-MS
Microsampling - Making a Difference in Drug Development
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Microsampling volumeBlood microsampling is a less invasive and simplified alternative to traditional venipuncture, and provides significant ad Up Close and Personal with Francis Douville
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Francis Douville joined the Altasciences team in 2018, as Senior Vice President, Technical Operations, for our preclinical services. |