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Marine Drug Development and Delivery

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Marine Drug Development and Delivery Prof. Dr. Basavaraj K. Nanjwade M. Pharm., Ph. D Department of Pharmaceutics KLE University College of Pharmacy – PowerPoint PPT presentation

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Title: Marine Drug Development and Delivery


1
Marine Drug Development and Delivery
  • Prof. Dr. Basavaraj K. Nanjwade M. Pharm., Ph. D
  • Department of Pharmaceutics
  • KLE University College of Pharmacy
  • BELGAUM-590010, Karnataka, India

2
Drug Development
  • Substances produced by living organisms found in
    nature have played a critical role in the
    development of drugs for life-threatening
    conditions.
  • Number of recent breakthroughs have resulted in
    the development and approval of anticancer drugs
    derived from marine sources such as coral and
    sponges.

3
Why Marine Drug Development
  • The marine environment provides a broad range of
    diverse habitats from which novel sources of
    natural products can be derived.
  • Studies from around the world have shown that
    marine organisms produce a diverse array of
    metabolites with novel chemical structures and
    potent biological activities as well as other
    desirable properties.

4
Discovery and Development
5
New Drug Development
6
New Drug Development Stages
  • Natural/Marine product discovery
  • Chemically modified drug
  • Discovery unknown structure of compounds
  • Synthesis, recombinant DNA
  • Source of leads for product development

7
New Drug Development Stages
  • Synthetic compounds based on existing compounds
  • Chemical improvement on drug molecule
  • Drug candidates
  • Pre-clinical and clinical trials
  • Approval process
  • Marketing new drug products

8
Natural/Marine product discovery
  • Natural products, secondary metabolites, isolated
    from plants, animals and microbes are important
    sources for bioactive molecules that in many
    cases have been developed into treatments for
    diseases.
  • Marine natural products for inflammation, cancer,
    infections, and neurological disorders.

9
Chemically modified drug
  • Most therapeutic drugs distribute to the whole
    body, which results in general toxicity and poor
    acceptance of the treatments by patients.
  • The targeted delivery of chemotherapeutics to
    defined cells, either stromal or cancer cells in
    cancer lesions, or defined inflammatory cells in
    immunological disorders, is one of the main
    challenges and a very active field of research in
    the development of treatment strategies to
    minimize side-effects of drugs.

10
Discovery unknown structure of compounds
  • Determining the structure of an unknown compound
    is a time-consuming process which could take
    months, therefore the ability to immediately
    see the structure of a chemical compound simply
    by looking through a microscope is a tremendous
    feat, said Professor Jaspars.
  • This new approach could lead to much faster
    identification of unknown compounds and
    ultimately speed up the process of the
    development of new medicines.

11
Synthesis, recombinant DNA
Recombinant DNA
12
1. Transformation
13
2. Non-bacterial Transformation
14
3. Phage
15
Source of leads for product development
  • The Lead User market research method is built
    around the idea that the richest understanding of
    new product and service needs is held by just a
    few "Lead Users.
  • They can be identified and drawn into a process
    of joint development of new product or service
    concepts with manufacturer personnel.

16
Synthetic compounds based on existing compounds
  • The more stable synthetic compounds, are based on
    the earlier natural and synthetic compounds, but
    differ so markedly from them in properties and
    activity as to constitutes a new class of
    compounds.

17
Chemical improvement on drug molecule
  • Technology can be applied to chemically
    improvement on the drug molecule/bioactive
    molecule.
  • Drug molecule of protein, peptide or small
    molecule drugs, either in development, or
    currently marketed, by other companies.

18
Drug candidates
  • Hits, leads and drug candidates constitute three
    millstones in the course of drug discovery and
    development.
  • The definition of drug candidates is a critical
    point in the value chain of drug innovation,
    which not only differentiates the research and
    development stages, but more importantly,
    determines the perspective and destiny of the
    pre-clinical and clinical studies.

19
Drug candidates
  • All outcomes from the development stage are
    actually attributed to the chemical structure of
    candidates.
  • The quality of candidates, however, is restricted
    by the drug-likeness of lead compounds, which in
    turn is decided by the characteristics of hits

20
Pre-clinical Development
  • In drug development, pre-clinical development is
    a stage of research that begins before clinical
    trials (testing in humans) can begin, and during
    which important feasibility, iterative testing
    and drug safety data is collected.
  • The main goals of pre-clinical studies (also
    named preclinical studies and nonclinical
    studies) are to determine a product's ultimate
    safety profile.
  • Products may include new or iterated or like-kind
    medical devices, drugs, gene therapy solutions,
    etc.

21
Clinical trials
  • Clinical trials are a set of procedures in
    medical research and drug development that are
    conducted to allow safety (or more specifically,
    information about adverse drug reactions and
    adverse effects of other treatments) and efficacy
    data to be collected for health interventions
    (e.g., drugs, diagnostics, devices, therapy
    protocols).
  • These trials can take place only after
    satisfactory information has been gathered on the
    quality of the non-clinical safety, and Health
    Authority/Ethics Committee approval is granted in
    the country where the trial is taking place.

22
Approval Process
23
Approval Process
24
Approval Process
25
Marketing new drug products
  • Test Procedures and Acceptance Criteria for
    Biotechnological/Biological Products addresses
    guideline specifications, tests and procedures
    for biotechnological/biological products.
  • Radiopharmaceuticals, products of fermentation,
    oligonucleotides, herbal products and crude
    products of animal or plant origin are similarly
    not covered.

26
Marine Drug Delivery
27
Marine Drug Delivery
28
(No Transcript)
29
Thank you
E-mail bknanjwade_at_yahoo.co.in Cont. No
00919742431000
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