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Implantable Drug Delivery
System
PAWAN TIKTE
Introduction
 Lafarge introduced the implantable system concept for
sustained release drug administration in 1861.
 It was first introduced to produce steroid hormones -
containing solid implants for long-term delivery.
 Implants are very small pellets composed of drug
without excipients.
Definition.....
 Implants are small sterile solid masses consisting of a
highly purified drug made by compression or moulding.
 Implants are DDS which provides CDDS over period of
time at site of implantation.
 Implants are intended for implantation in the body’s
subcutaneous or intramuscular tissue by a minor surgical
incision or injected through a large bore needle.
Ideal Properties of an - IDDS
 Environmentally stable.
 Bio compatible.
 Easy to manufacture and sterilize.
 Enable rate controlled drug release.
 Relatively inexpensive.
 A good mechanical strength.
 Free from surgical procedure.
Advantages
 Controlled drug delivery for a longer period.
 Decrease frequency of dose.
 Avoid first pass metabolism.
 Minimize drug side effects.
 Improve drug stability and bioavailability.
Disadvantages
 Small surgery needed for large implantation and painful .
 Therapy cannot be discontinued easily.
 Bio compatabillity issue.
 Reaction between host and implants.
 Implants infection, inflammatory reactions.
 Device failure and implants dislocation.
 The osmotic pumps can be implanted
subcutaneously or intraperitoneally depending on
the size of animal.
 For targeted drug delivery system , a catheter can
be attached to the osmotic pump to gain access to
the tissues of interest.
 Subcutaneous implantation is technically the easiest
and least intrusive procedure.
Concepts of implants & osmotic pumps
 The implantable osmotic pump employ
osmotic gradient inside the lumen called the
salt sleeve and the tissue condition in which
the pump is implanted.
 A high osmalarity of the salt sleeve make
water flow into the pump through a
semipermeable film which encases the
external surfaces of the pump
Principle
Alzet osmotic pump
 In cross section, the implantable osmotic release
pump are composed of ..
1. A drug core (reserviour)
2. The diffusion agent
3. The tissue layer ( rate controller)
4. A flow moderator is inserted into the body of the
diffusion pump.
Apparatus and equipment
Main components of or implantable osmotic release pump
include :
 drug compound ( water soluble / insoluble)
 Osmogens or osmotic agents ( ionic compound / inorganic salt
 A stable semipermeable membrane.
 Plasticizers.
 Flux regulators.
 Pore forming agent
 Coating solvents.
 Ex : alzet osmotic pump
Implantable drug delivery system

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Implantable drug delivery system

  • 2. Introduction  Lafarge introduced the implantable system concept for sustained release drug administration in 1861.  It was first introduced to produce steroid hormones - containing solid implants for long-term delivery.  Implants are very small pellets composed of drug without excipients.
  • 3. Definition.....  Implants are small sterile solid masses consisting of a highly purified drug made by compression or moulding.  Implants are DDS which provides CDDS over period of time at site of implantation.  Implants are intended for implantation in the body’s subcutaneous or intramuscular tissue by a minor surgical incision or injected through a large bore needle.
  • 4. Ideal Properties of an - IDDS  Environmentally stable.  Bio compatible.  Easy to manufacture and sterilize.  Enable rate controlled drug release.  Relatively inexpensive.  A good mechanical strength.  Free from surgical procedure.
  • 5. Advantages  Controlled drug delivery for a longer period.  Decrease frequency of dose.  Avoid first pass metabolism.  Minimize drug side effects.  Improve drug stability and bioavailability.
  • 6. Disadvantages  Small surgery needed for large implantation and painful .  Therapy cannot be discontinued easily.  Bio compatabillity issue.  Reaction between host and implants.  Implants infection, inflammatory reactions.  Device failure and implants dislocation.
  • 7.
  • 8.  The osmotic pumps can be implanted subcutaneously or intraperitoneally depending on the size of animal.  For targeted drug delivery system , a catheter can be attached to the osmotic pump to gain access to the tissues of interest.  Subcutaneous implantation is technically the easiest and least intrusive procedure. Concepts of implants & osmotic pumps
  • 9.  The implantable osmotic pump employ osmotic gradient inside the lumen called the salt sleeve and the tissue condition in which the pump is implanted.  A high osmalarity of the salt sleeve make water flow into the pump through a semipermeable film which encases the external surfaces of the pump Principle
  • 11.  In cross section, the implantable osmotic release pump are composed of .. 1. A drug core (reserviour) 2. The diffusion agent 3. The tissue layer ( rate controller) 4. A flow moderator is inserted into the body of the diffusion pump. Apparatus and equipment
  • 12. Main components of or implantable osmotic release pump include :  drug compound ( water soluble / insoluble)  Osmogens or osmotic agents ( ionic compound / inorganic salt  A stable semipermeable membrane.  Plasticizers.  Flux regulators.  Pore forming agent  Coating solvents.  Ex : alzet osmotic pump