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Half life / clearance determination using Microsomes /
Hepatocytes / S9 fractions / CYP across species (Human /
microsomes, plasma and tissue
homogenate across various
Rat / Mouse / Dog / monkey) species (Rat / Mouse / Human &
CYP Inhibition (CYP1A2, CYP2C9, CYP2C19, CYP2D6, Dog).
CYP3A4 and 2C8)
Pathway determination (Phase I and Phase II)
Metabolite identification with Microsomes /
Hepatocytes and S9 fraction across species(Human / Rat
/ Mouse / Dog / Monkey)using Light Sight MetId
PAMPA
(Parallel artificial membrane permeability assay)
ADME Services
GVK BIO In vitro ADME screening service offers a portfolio
of automated High throughput assays for investigating:
metabolism, distribution and toxicity, permeability,
solubility & physicochemical properties. We deliver
consistent, accurate compound data with cost-efficiency.
In vitro ADME Capabilities
• Physicochemical studies
Log D/Log P
Solubility(Kinetic/Equilibrium)
Chemical stability
Biological matrix stability (serum / plasma / microsomes /
blood / hepatocytes / tissue homogenates)
• Absorption/Distribution Assays
Caco2 and PAMPA permeability
Tissue permeability studies- Franz Diffusion assay
Pgp substrate / inhibitor assays
Protein binding
Blood/Plasma Partitioning Ratio
• Metabolism/Excretion
software
• Log D/Log P
Log D is determined by the shake-flask method, by
dissolving some of the solute in a volume of octanol and
water/buffer and measure the concentration of the solute
in each solvent. Log D is determined by HPLC-UV with
confirmation by mass.
Solubility
Solubility is one of the most important physicochemical
properties. We determine equilibrium solubility by dried
DMSO method. We can also determine solubility in
aqueous buffer (pH 1-9), organic solvents (DMSO, Ethanol,
etc), formulations and excipients by pION / Multiscreen /
HPLC - UV / MS / MS- MS methods.
Protein Binding
In vitro binding studies with
plasma have proven to be a
valuable tool for predicting In vivo
protein binding. We determine the
protein binding by both ultra
filtration and rapid equilibrium
dialysis. Using RED device we
determine protein binding in
The Parallel Artificial Membrane Permeability Assay
(PAMPA) is used as an in vitro model of passive,
transcellular permeability and also for the prediction of
oral absorption and brain penetration. Effective
permeability (log Pe) may be measured by pION/
Multiscreen/ LCMS.
ADME Services
Microsomal Stability
Metabolic stability plays an
important role in the success of
drug candidates. First pass
metabolism is one of the major
causes of poor oral bioavailability
and short half life and the study
influences both oral bioavailability
and half life. The half life
/clearance/percentage metabolized
can be determined in microsomes/
S9 fractions/hepatocytes.
Hepatocyte metabolic stability
Per orally administered drug may undergo first-pass
metabolism which influences the pharmacokinetic
properties such as the clearance, the half-life or the
bioavailability. Cryopreserved hepatocytes are used to
calculate half life/clearance/percentage parent compound
remaining.
CYP Inhibition
CYP inhibition occurs either as reversible inhibition,
quasi irreversible inhibition or irreversible inhibition. CYP
inhibition is a fluorescent /LCMS based assay. Specific
isoforms of CYP (CYP1A2, CYP2C9, CYP2C19, CYP2D6,
CYP2C8 and CYP3A4) are used to determine the inhibition
(IC50).
Metabolite identification using Light Sight Software
In vitro metabolite identification & characterization of the
test compounds are determined using Q trap with Light
Sight MetId software.
HTS Bioanalysis
The method development for HTS ADME is performed
using Discovery Quant Software.
• LC-MS/MS
3200 QTRAP
API3000
API4000
• HPLC
Agilent 1200 RRLC with PDA
Shimadzu Prominence with UV
Agilent 1200 RRLC with HTS PAL
• Others
Spectramax (Molecular Devices)
BMG Polarstar
Tomtec Quadra4 Liquid Handler
About GVK BIO
GVK Biosciences, India’s premier Contract Research Organization, delivers integrated research services.
The company accelerates the Drug Discovery and Development process of its customers through science and innovation.
Services
• Chemistry Services
• Process R&D and Custom Synthesis
• Biology
• Informatics
• Clinical Research
• Clinical Pharmacology
Contact: bdbio@gvkbio.com Visit: www.gvkbio.com

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GVK BIO High Throughput Capabilities of In vitro ADME Services

  • 1. Half life / clearance determination using Microsomes / Hepatocytes / S9 fractions / CYP across species (Human / microsomes, plasma and tissue homogenate across various Rat / Mouse / Dog / monkey) species (Rat / Mouse / Human & CYP Inhibition (CYP1A2, CYP2C9, CYP2C19, CYP2D6, Dog). CYP3A4 and 2C8) Pathway determination (Phase I and Phase II) Metabolite identification with Microsomes / Hepatocytes and S9 fraction across species(Human / Rat / Mouse / Dog / Monkey)using Light Sight MetId PAMPA (Parallel artificial membrane permeability assay) ADME Services GVK BIO In vitro ADME screening service offers a portfolio of automated High throughput assays for investigating: metabolism, distribution and toxicity, permeability, solubility & physicochemical properties. We deliver consistent, accurate compound data with cost-efficiency. In vitro ADME Capabilities • Physicochemical studies Log D/Log P Solubility(Kinetic/Equilibrium) Chemical stability Biological matrix stability (serum / plasma / microsomes / blood / hepatocytes / tissue homogenates) • Absorption/Distribution Assays Caco2 and PAMPA permeability Tissue permeability studies- Franz Diffusion assay Pgp substrate / inhibitor assays Protein binding Blood/Plasma Partitioning Ratio • Metabolism/Excretion software • Log D/Log P Log D is determined by the shake-flask method, by dissolving some of the solute in a volume of octanol and water/buffer and measure the concentration of the solute in each solvent. Log D is determined by HPLC-UV with confirmation by mass. Solubility Solubility is one of the most important physicochemical properties. We determine equilibrium solubility by dried DMSO method. We can also determine solubility in aqueous buffer (pH 1-9), organic solvents (DMSO, Ethanol, etc), formulations and excipients by pION / Multiscreen / HPLC - UV / MS / MS- MS methods. Protein Binding In vitro binding studies with plasma have proven to be a valuable tool for predicting In vivo protein binding. We determine the protein binding by both ultra filtration and rapid equilibrium dialysis. Using RED device we determine protein binding in The Parallel Artificial Membrane Permeability Assay (PAMPA) is used as an in vitro model of passive, transcellular permeability and also for the prediction of oral absorption and brain penetration. Effective permeability (log Pe) may be measured by pION/ Multiscreen/ LCMS.
  • 2. ADME Services Microsomal Stability Metabolic stability plays an important role in the success of drug candidates. First pass metabolism is one of the major causes of poor oral bioavailability and short half life and the study influences both oral bioavailability and half life. The half life /clearance/percentage metabolized can be determined in microsomes/ S9 fractions/hepatocytes. Hepatocyte metabolic stability Per orally administered drug may undergo first-pass metabolism which influences the pharmacokinetic properties such as the clearance, the half-life or the bioavailability. Cryopreserved hepatocytes are used to calculate half life/clearance/percentage parent compound remaining. CYP Inhibition CYP inhibition occurs either as reversible inhibition, quasi irreversible inhibition or irreversible inhibition. CYP inhibition is a fluorescent /LCMS based assay. Specific isoforms of CYP (CYP1A2, CYP2C9, CYP2C19, CYP2D6, CYP2C8 and CYP3A4) are used to determine the inhibition (IC50). Metabolite identification using Light Sight Software In vitro metabolite identification & characterization of the test compounds are determined using Q trap with Light Sight MetId software. HTS Bioanalysis The method development for HTS ADME is performed using Discovery Quant Software. • LC-MS/MS 3200 QTRAP API3000 API4000 • HPLC Agilent 1200 RRLC with PDA Shimadzu Prominence with UV Agilent 1200 RRLC with HTS PAL • Others Spectramax (Molecular Devices) BMG Polarstar Tomtec Quadra4 Liquid Handler About GVK BIO GVK Biosciences, India’s premier Contract Research Organization, delivers integrated research services. The company accelerates the Drug Discovery and Development process of its customers through science and innovation. Services • Chemistry Services • Process R&D and Custom Synthesis • Biology • Informatics • Clinical Research • Clinical Pharmacology Contact: bdbio@gvkbio.com Visit: www.gvkbio.com