Title: Nanotechnology in Drug Discovery- Development and Delivery
1Nanotechnology in Drug Discovery- Development and
Delivery
- Dr. Basavaraj K. Nanjwade
- KLE University College of Pharmacy
- Belgaum-590010
- E-mail bknanjwade_at_yahoo.co.in
- Cell No 00919742431000
2Nanotechnology
- Nanotechnology breakthrough research in
Pharmaceutical Biopharmaceutical Industry. - Nanotechnology, a field of science and technology
that aims to control matter at the atomic and
molecular level.
3Drug Discovery and Development
- Validate specific targets
- Discover the right molecule (potential drug) to
interact with the target chosen - Test the new compound in the lab and clinic for
safety and efficacy and - Gain approval and get the new drug into the hand
of doctors and patients.
4Drug Discovery and Development
- Success requires immense resources
- The best scientist minds, highly
sophisticated technology and complex project
management. -
- It is also takes persistence and sometimes luck.
-
- Ultimately the process of drug discovery
brings hope and relief to millions of patients
5Drug Development and Delivery
- The multi-disciplinary field of nanotechnology is
making small device, closer and closer to
reality. - Manipulate and organize matter on the nano-scale.
6Drug Development and Delivery
- Drug filled nano-capsules, release their
biological compounds on contact with cancers
only. - Nanotechnology will be applied at all stages of
drug development, from formulations for optimal
delivery to diagnostic applications in clinical
trials.
7Discovery
8Development
9Pre-Discovery
10Pre-Discovery
- Before any potential new medicine can be
discovered, scientist work to understand the
disease to be treated as well as possible. - Try to understand how the genes are altered, how
that affects the proteins.
11Target Identification
- Once have enough understanding of the underlying
cause of a disease, pharmaceutical researchers
select a target for a potential new medicine. - A target is generally a single molecule, such as
gene or protein, which is involved in a
particular disease. - Early stage in drug discovery it is critical to
researchers pick a target that is drugable.
12Target Validation
- After choosing a potential target, scientist must
show that it actually is involved in the disease
and can be acted upon by a drug. - Target validation is crucial to help scientists
avoid research paths that look promising, but
ultimately lead to dead ends. - Researchers demonstrate that a particular target
is relevant to the disease being studied through
complicated experiments in both living and in
animal models of disease
13Drug Discovery and Development Activities
14Drug Discovery and Development
15Lead Compound
- Nature
- De Novo
- High-throughput screening
- Biotechnology
16Early Safety Tests
- Absorbed into the bloodstream
- Distributed to the proper site of action in the
body - Metabolized efficiently and effectively
- Successfully excreted from the body and
- Demonstrated to be not toxic
17Lead Optimization
- Lead compounds that survive the initial screening
are then optimized or altered to make them more
effective and safer. - Hundreds of different variations or analogues
of the initial leads are made and tested. - Early stage, researchers begin to think about how
the drug will be made, considering formulation,
delivery mechanism and large-scale manufacturing
18Preclinical Testing
- Scientist carry out in vitro and in vivo test
- In vitro test are experiments conducted in the
lab, usually carried out in the test tube and
beakers (vitro is glass in Latin) - In vivo studies are those in living cell cultures
and animal models (vivo is life in Latin)
19Development of IND (Investigational New drug)
- IND application contains information in three
broad areas - 1.Animal Pharmacology and Toxicology Studies
- 2.Manufacturing Information of drug including
manufacturer, composition, stability and controls - 3.Clinical Protocols and Investigator Information
20Phase 1 Clinical Trial
- Phase I studies are carried out in healthy
volunteers, which are small in number usually
20 to 100. - The purpose of phase I studies is to mainly
determine safety profile.
21Phase 2 Clinical Trial
- Phase 2 includes the early controlled clinical
studies conducted to obtain some preliminary data
on the effectiveness of the drug. - Phase 2 studies are typically well-controlled,
closely monitored, and conducted in a relatively
small number of patients, usually involving
several hundred people
22Phase 3 Clinical Trial
- The additional information about effectiveness
and safety that is needed to evaluate the overall
benefit-risk relationship of the drug. - Phase 3 studies usually include several hundred
to several thousand people.
23Manufacturing
- Going from small-scale to large-scale
manufacturing is a major undertaking. - In many cases, companies must build a new
manufacturing facility or reconstruct an old one
because the manufacturing process is different
from drug to drug. - Each facility must meet strict FDA guidelines for
Good Manufacturing Practices (GMP)
24Ongoing Studies Phase 4 Trial
- Phase IV, also known as Post Marketing
Surveillance is also carried out once the drug is
approved and marketed. - The aim of Phase IV is to find out safety profile
in large patient pool across the world and to
establish the safety profile of the drug.
25NDA Review Process
26ANDA/AADA Review Process
27OTC Drug Monograph Process
28Successful Therapy Combines Drug Discovery and
Delivery
29Nanotech Components
30Nanotechnology Regulatory
31Nanotechnology Collaboration
32Research Priorities
33 Suggested Topics and Modules
34Nanoparticles in the context of Biopharmaceuticals
35Current Nanoparticle Products
36 Current Nanoparticle Products
37Nanoparticles As Emulsion
38Nanoparticles Reduce Size
39Nanoparticles Grow Them
40Nanoparticles Emulsion/Diffusion
41Structure
42Release
43Drug Delivery Carriers
44Methods of Drug Delivery
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46- THANKING YOU
- E-mail bknanjwade_at_yahoo.co.in
- Cell No 0091 9742431000