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Transcript
Drug
Metabolism
It is important to understand the key role that drug metabolism
and drug-drug interactions play in the efficacy and safety
elements of the drug discovery and development process. At
Charles River, we can help you identify the metabolic pathways,
potential interactions and routes of elimination of your compound
at an early stage.
candidate optimization. Development studies are designed to
satisfy the requirements of international regulatory authorities and
to provide safety data to assess the validity of laboratory species
as appropriate toxicological models for humans. Our drug
metabolism facilities are networked and utilize validated data
management systems for data capture, storage and evaluation.
We have scientists dedicated to both discovery and development,
allowing lead candidate selection to flow seamlessly into the
development phase. Our discovery and research specialists offer
customized screening programs to ensure early and late lead
We offer a comprehensive range of drug metabolism services.
With our scientific depth, regulatory knowledge and technical
expertise, we can help you accelerate the development of safe
and effective therapies.
FPO
Areas of expertise include:
• Discovery and Research Services
• Mass Balance
• Biotransformation
• In Vitro Metabolism
• Labeled and Label-Free
Tissue/Whole-Body Imaging
• Laboratory Sciences
• Absorption, Distribution,
Metabolism and Excretion (ADME)
• Pharmacokinetics
• Surgical Services
• Clinical Metabolism Support
• Humane Care
Discovery and Research Services
Early attrition of unsuitable drug candidates is key to the
successful development of a new therapeutic. In vitro ADME-Tox
(ADMET) and in vivo pharmacokinetic (PK)/ADME screening
provide valuable information to help you prioritize and accelerate
your drug discovery process from compound ranking to lead
candidate selection. These services are just part of a full range of
discovery and research services offered at Charles River.
• In vitro ADMET
• PK/ADME screening
• Lead optimization toxicology
• Pharmacology models of disease
Absorption, Distribution, Metabolism
and Excretion
Charles River offers a complete range of in vivo metabolism
studies in support of lead candidate selection, preclinical testing
and clinical development programs. The studies are designed
to investigate the ADME properties of novel compounds in
laboratory animal species and man. Our experienced scientists
routinely conduct mass balance and tissue distribution studies
to determine tissue half-life, clearance rates and potential
sites of toxicity after systemic exposure. Individual protocols
are developed collaboratively with our clients to satisfy the
appropriate international regulatory requirements.
• Plasma kinetics
• Phenotyping services
• Excretion balance
• Biomarker services
• Biliary excretion
• Formulation development
• Tissue distribution
In Vitro Metabolism
By providing critical information early in the drug development
process, our ADMET screening assays help you identify and
focus efforts on compounds that have the greatest likelihood
of success. Once a lead candidate is selected, both qualitative
and quantitative analyses of radiolabeled and nonradiolabeled
compounds are provided in a range of in vitro test systems.
Studies are designed to complement the metabolism,
toxicokinetic (TK) and bioanalytical investigations undertaken
in pharmaceutical product development. Other laboratory
assays that balance our in vitro metabolism services include cell
proliferation, cytotoxicity, hERG blockade and protein binding.
• Drug-drug interaction
• Reaction phenotyping
• Metabolic stability
• Intestinal permeability
• Aqueous solubility
• Quantitative whole-body autoradiography (QWBA)
• Placental and milk transfer
• Biotransformation
• Early-phase clinical trial support
• DEBRA® data management system
Pharmacokinetics
We excel in conducting discovery and developmental PK studies.
This service includes discrete or cassette dosing studies for
screening multiple compounds and conventional GLP PK and TK
studies designed for product registration purposes. Our scientists
have direct access to our world-renowned research models,
unique surgical models and colonies of nonrodent species.
Bioanalysis of the collected samples is available, and qualified
pharmacokineticists are on hand to assist in study design, PK
modeling, statistical analysis and data interpretation.
• Discovery screening
• Bioanalysis
• Bioavailability
• Bioequivalence
• Dose proportionality
• Data evaluation and interpretation
Preclinical Services
Mass Balance
Surgical Services
Our scientists design and conduct mass balance studies in a
variety of species. Studies routinely use radiolabeled compounds
to fully describe the rate and routes of elimination of the
administered radioactivity. The samples generated are also used
to provide information on the biotransformation of the parent
drug. We have expertise in a wide range of preclinical laboratory
species and dose routes, allowing us to fully meet the needs of
your development programs.
• Multiple species
Charles River offers a diverse range of surgical models and
services developed in accordance with the most recent advances
in surgical procedures and animal welfare. Our research surgeons
have extensive experience in the development of sophisticated
surgical procedures in a variety of rodent and large animal
species, and are available to assist in the creation of the most
relevant animal model for an enhanced understanding of your
compound.
• Vascular access ports
• Radioanalysis
• Intravenous infusion
• Broad spectrum of radioisotopes
• Cannulation
• Metabolite synthetic chemistry
• Cerebrospinal fluid sampling
• Lymph collection
Labeled and Label-Free Tissue/Whole-Body
Imaging
QWBA is a powerful tool used to evaluate the tissue distribution
of drug candidates. As well as supporting development studies,
this technique is utilized in drug discovery to assess target tissue
penetration of potential drug candidates. QWBA is suitable for use
with all rodent species, as well as some nonrodent species (such
as minipigs and nonhuman primates of body weight < 10 kg),
and the technique can be used with a variety of radioisotopes.
• Localization of tissue exposure
• CNS penetration and distribution
• Placental transfer
• Bone marrow exposure for in vivo mutagenicity
• Urinary catheter
Clinical Metabolism Support
An early understanding of the metabolism of a drug candidate
in human subjects is increasingly being considered by the
pharmaceutical industry as a critical step in the development
process. We recommend that these studies be conducted during
early Phase II clinical development to ensure confidence in the
safety profile of a drug candidate before testing the drug in a
wider patient population. We can support the specific metabolism
study requirements related to sample custody analysis and
accountability.
• Carbon-14 and tritium
• Tumor targeting
• Radioactive sample analysis
• Dosimetry studies
• Radio-HPLC and LC-MS
• Biometrics
Offered in collaboration with ImaBiotech, MALDI-MSI (Matrix
Assisted Laser Desorption/Ionization Mass Spectrometry Imaging)
provides a label-free imaging alternative for the detection
and localization of drugs and drug metabolites. Ideally suited
to assessing the intra-organ distribution of drugs and their
metabolites, MALDI-MSI can be successfully adapted to provide
whole-body images in small rodent species. Furthermore, using
proprietary software, quantitative data can be produced.
Preclinical Services
Biotransformation
Humane Care
Isolation, analysis, identification and stability of metabolites in
biological matrices can be critical to the understanding and
interpretation of ADME studies. Characterization of metabolites
in biological samples can be undertaken either as part of other
metabolism or kinetic studies performed at our facilities, or as a
stand-alone study using samples or sample extracts provided by
our clients.
Each of our facilities is committed to scientific excellence, highquality service and ethical business practices. At Charles River,
ethical conduct extends to the humane care of research animals
through uncompromising animal welfare standards, as directed
by our Humane Care Initiative.
Additionally, a synthetic chemistry service is available to undertake
synthesis of metabolites, reference standards and internal
standards to assist with method development and metabolite
identification.
• Radiometric profiling
The use of laboratory animals furthers our knowledge of living
systems and contributes to the discovery of life-saving drugs and
procedures. Therefore, as animal caregivers and researchers,
we are responsible to our clients and the public for the health
and well-being of the animals in our care. We believe that good
medicine is the result of good science, and at Charles River we
provide and accept no less.
• HPLC
• LC-MS and LC-MS/MS
• GC-MS and ion trap MS
• CE for oligonucleotides
• TOF and MALDI-TOF
• Organic chemistry metabolite synthesis
Laboratory Sciences
Each well-designed in vitro and in vivo study must have the
appropriate analytical tools to obtain meaningful data, and we
understand that high-quality, up-to-date laboratory technology is
vital to the success of your program. We have made significant
investments over the years in highly trained scientists and stateof-the-art facilities and instrumentation to increase our capabilities
and capacity to produce rapid and reliable results.
• Formulation development
• Analytical chemistry
• Bioanalysis
• Immunology
• Radioanalysis
[email protected]
www.criver.com
© 2013, Charles River Laboratories International, Inc.