Biodegradable Polymers

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About This Presentation

Biodegradable Polymeric Delivery System
Drug delivery system


Slide Content

Biodegradable Polymeric Delivery System
Presented By:Presented By:
Sunil Kamboj
Roll No: 1211533
DEPARTMENT OF CHEMICAL ENGINEERING
JMIT, Radaur- 135133

 A large number of the carriers have been designed for delivery of
proteins and peptides via liposome, niosome, polymeric nanoparticles,
solid lipid nanoparticles etc.
 Polymer based carriers have taken much attention of the scientific
community for safe and effective delivery of proteins.
 Biodegradable polymers is used through slight modifications of their
structures.
 Biodegradable polymers have a great applications in pharmaceutical,
medical and biomedical engineering.
 Biodegradable polymers are not limited to release of drugs, peptides or
proteins but are also extended to medical devices and wound dressing.

Polymer?
•Large molecule composed of a number of sub-units
-Natural e.g. alginates,
-synthetic e.g. poly(HMPA)
-Function governed by number and arrangement of constitutional repeat
units e.g. –[A-]
n
, -[A-B-]
n
, -[A-A]
n
-[B-B]
m
, --A-A-B-A-B-B-A-
•How are they made?
-Processing of natural products – alginates from seaweeds, celluloses
from plants
-Synthesis from chemical feedstocks – poly(olefins), nylons, poly(esters)
•How can they help?
-Protection of therapeutic compound during passage through body, as
encapsulant or carrier.
-Mediator or activator of controlled release

CHARACTERISTICS OF IDEAL POLYMER
Should be inert and compatible with the
environment.
Should be non-toxic.
Should be easily administered.
Should be easy and inexpensive to
fabricate.
Should have good mechanical strength.

Criteria Followed In Polymer
Selection
It must be soluble and easy to synthesize;
must have a finite molecular wt.
Should provide drug attachment and
release sites for drug polymer linkages.
Should be compatible with biological
environment, i.e. non-toxic and non-
antigenic.
Should be biodegradable or be eliminated
from body after its function is over.

Biodegradable polymers
-Polymer degrades in vivo to release the drug
-Simple release mechanism, but difficult to obtain fine control
over degradation
-Does not invoke an inflammatory or toxic response.
-It is metabolized in the body after fulfilling its purpose, leaving
no trace
•Examples in use
-Resomer (PLGA)
-Vicryl (PLGA)
•Common biodegradable polymers
-Poly(lactide-co-glycolide) (PLGA)
-Poly(hydroxybutyrate-co valerate) (Biopol)

List of Biodegradable Polymers used in Drug Delivery
Natural polymers
Protein-based polymersCollagen, albumin, gelatin
Polysaccharides Agarose, alginate, carrageenan,
hyaluronic acid, dextran,
chitosan,
Cyclodextrins
Synthetic polymers
Polyesters Poly(lactic acid), poly(glycolic
acid),
poly(hydroxy butyrate), poly(ε-
caprolactone),
poly(α-malic acid),
poly(dioxanones)
Polyesters
Polyanhydrides Poly(sebacic acid), poly(adipic
acid),
Continues......

Polyamides Poly(imino carbonates), polyamino acids
Phosphorous-
based polymers
Polyphosphates, polyphosphonates,
polyphosphazenes
Others Poly(cyano acrylates), polyurethanes,
polyortho
esters,
polydihydropyrans, polyacetals

Polymeric DDS devices
Particulate systems
Nanoparticles
Nanocapsules
Nanospheres
Microparticles
Microspheres
Microcapsules

Controlled release implies controlled release of drugs
from polymer drug delivery systems (DDS)
Type of polymer
Non-degradable / Degradable
Type of Design
Reservoir Matrix
Release mechanisms
Diffusion / polymer degradation / combination
Controlled Release Systems

Biodegradable Delivery Systems
Drug is physically incorporated (mixed) into a biocompatible
polymer matrix
Drug is protected by the polymer
Drug migrates from the polymer to the body
Drug is released in a controlled manner
After all drug is released, surgical removal of the polymer is
not necessary
Polymer contains labile bonds
t = 0 t = n
polymer
drug

Mechanism of Biodegradation
A. Hydrolytic Degradation :
Breakdown of polymer by water by cleaving
long chain into monomeric acids. This is done
by two ways :
Bulk eroding polymers
e.g. Polylactic acid (PLA)
Polyglycolic acid (PGA)
Surface Eroding Polymers
e.g. Polyanhydrides
B. Enzymatic Degradation :
 Exact mechanism is not known but may be
due to lysis of long polymer chain by
attaching to it.

Drug delivery from (a) bulk-eroding and (b) surface-eroding biodegradable
systems

Physical incorporation of a drug in a polymer-based
delivery systems are an improvement to conventional
administration
Drawbacks:
Incorporate low percentages of drug
High potential for drug separation (accidental or
intentional)
Drug is released with a burst
Biodegradable Delivery Systems

Plasma drug concentrations
proportional to the dose
Traditional drug dosing requires
repeated administration
Drug is distributed throughout
the body
Maintain therapeutic levels
by a single administration
Drug preservation and
protection
Localize drug delivery
Increase patient comfort and
improve compliance
Drug Delivery Systems

Comparison of Controlled Release System Designs
Polymer Non-degradable Degradable
Design Reservoir Matrix Reservoir Matrix
Release √√√ √√√ √√ √√
Removal √ √
Rupture √ √
Low Mw √ √ √ √
High Mw √ √ √
Duration 5 years 5 years 1-2 years Months
Examples Norplant
®
Jadelle
®
Capronor
TMMicrospheres

References

Neeraj Mishra, Amit Goyal, Kapil Khatri, Bhuvaneshwar Vaidya, Rishi Paliwal,
Shivani Rai, Abhinav Mehta, Shailja Tiwari, Shiva Vyas and Suresh Vyas.
Biodegradable polymer based particulate carrier(s) for the delivery of proteins and
peptides. Anti-Inflammatory and Anti-Allergy Agents in Medicinal Chemistry, 2008, 7:
240-251.
•Gemma Vilar, Judit Tulla-Puche and Fernando Albericio. Polymers and drug delivery
systems. Current Drug Delivery, 2012, 9: 1-28.
•Kumaresh Soppimatha, Tejraj Aminabhavia, Anandrao Kulkarnia and Walter
Rudzinski. Biodegradable polymeric nanoparticles as drug delivery devices. Journal of
Controlled Release, 2001, 70: 1–20.
• Avnesh Kumari, Sudesh Yadav and Subhash Yadav. Biodegradable polymeric
nanoparticles based drug delivery systems. Colloids and Surfaces B: Biointerfaces,
2010, 75: 1–18.
• Yulia Chernysheva, Valery Babak, Natalia Kildeeva, Franck Boury, Jean Benoit,
Nathalie Ubrichd and Philippe Maincent. Effect of the type of hydrophobic polymers
on the size of nanoparticles obtained by emulsification solvent evaporation. Mendeleev
Communication, 2003, 13(2), 65–67.
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