|
The
Institute's capability in drug R&D; is vested in its
research facilities, infrastructure and expertise. The research
facilities are distributed in 17 R&D; divisions which
cover almost all disciplines required for drug research:
|
-
Biochemistry
- Botany
- Chemical Technology
- Clinical & Experimetal Medicine
- Endocrinology
- Fermentation Technology
- Medical Mycology
- Medicinal Chemistry
|
-
Molecular & Structural Biology
- Microbiology
- Parasitology
- Pharmaceutics
- Pharmacokinetics & Metabolism
- Pharmacology
- Physiology
- Toxicology |
New
Facilities Created
To
strengthen the Institute's capability in targeted drug research,
molecular biology, structural biology, genomics, combinatorial
chemistry, medium/ high throughput screening, molecular modelling,
etc., facilities have recently been created and their further
stengthening is being carried out.
X-ray
crystallography
A
new facility for structural biology research has been created
at CDRI. It comprises a wet laboratory housed with state-of-the-art
equipments for cloning/expression and purification of proteins,
a modern x-ray laboratory with P4 single crystal x-ray diffractometer
system
for small molecule crystallography, a MAR 345 image-plate
detector on RU-300 rotating anode x-ray generator
with cryo-cooling system for macromolecule crystallography,
a precision camera on a FR590 x-ray generator for preliminary
diffraction work and a computer graphics laboratory for molecular
modelling and crystallographic
computations.
The facility will be used for atomic level structure determination
of proteins and small molelcules of biological and structural
importance required for knowledge-based drug design through
molecular modelling.
Combinatorial synthesis & High throughput screening
The
generation of molecular diversity and its potential to facilitate
the drug discovery process has recently attracted enormous
attention. The institute has made an endeavour in this direction
by setting up in-house facilities for both Combinatorial chemistry
and High throughput screening (HTS)
as tools in the Institute's drug discovery programme. This
central facility comprise a Multiple organic synthesizer 496
MOSA for combinatorial synthesis and an Automated Robotics
High Throughput Screening system BMG Polar Star Galaxy with
optional accessories.
The
technical infrastructure comprises of the national level facilities,
viz. National Laboratory Animal Centre (NLAC), Regional Sophisticated
Instrumentation Centre (RSIC) and National Information Centre
for Drugs & Pharmaceuticals (NICDAP). These facilities had
been created at CDRI with financial support from Departments
of Science & Technology, Biotechnology or Scientific & Industrial
Research in recognition of the fact that this Institute already
had the required expertise in these areas. These facilities
cater to the needs of individual researchers, as well as academia,
research institutions and industry.
The
other technical infrastructure comprises specialised facilities
viz Biometry and statistics, Instruments maintenance, Glass
blowing, R&D; planning, IPR protection, Licensing, International
coordination, etc.
The R&D; Capability
Chemical synthesis, Extraction from natural products and Structure
elucidation.
Synthesis
of novel molecules of known and new structural types exhibiting
biological activity.
Laboratory and large scale extraction of ethanolic extracts
of plant material and isolation of active principle(s).
Synthesis of novel structures, and structure elucidation of
active compound(s) by sophisticated techniques.
Biological
Screening
Facilities
are available for 170 in vitro/in vivo test systems
(antifertility, antifilarial, antiamoebic, antileishmanial,
antiviral, antifungal, antibacterial, hepatoprotective, immunomodulator,
CNS & CVS and other pharmacological activities).
Plant Collection and Authentication.
Collection, authentication and supply of plants for biological
screening. The Institute has a specialised herbarium of medicinal
plants containing about 6000 species representing about 1/3
of Indian flora for reference purpose.
Drugs Standardisation
Standardisation of synthetic and plant based drugs by monitoring
through HPTLC and HPLC of active constituents as marker vis-a-vis
their biological activity.
Chemical finger printing of herbal drugs is carried out by
LC-MS to have a complete picture of different organic constituents.
Standardization of candidate drugs is carried out as per ICH
guidelines.
Regulatory Toxicity,
Pharmacokinetics &
Clinical Trials
Facilities for preclinical toxicity evaluation and pharmacokinetics
and phase-I clinical finds are available.
Chemical & Fermentation Technology Development
Pilot
plant scale facilities exist for the synthetic and natural
products. The facilities for natural products include grinding,
extraction and concentration.
Fermentation
technology facilities cover culture isolation to improvement,
bench-scale optimization of process parameters and scaling-up
of the bioprocesses to laboratory/pilot fermenter level. Fermenters
available from 5 to 1500 L alongwith downstream processing
facilities such a centrifugation, extraction, concentration,
drying, etc. Studies carried out on various biotransformation
processes at bench level in novel bioreactor systems using
free as well as immobilized biocatalysts.
The
Institute also undertakes training in 17 specialised areas
relevant to drug research, on payment basis.
|