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33 Cards in this Set

  • Front
  • Back
Slowly releases active ingredient SC or IM
Depot Injection
Act as bioerodible matrix systems to prolong drug release
Bioerodible Microspheres
Example of Bioerodible Microspheres
Prepared as a copolymer that breaks down to lactic acid and glycolic acid
Lupron Depot
Slowly releases active ingredient SC
Implants
Diffusion of saturated solution (reservoir) is controlled by polymer membrane as zero-order release
Require surgical removal and are not bioerodible
Membrane-Controlled (Reservoir)
Membrane-matrix hybrid
One implant containing etonogestrel crystals (birth control) embedded in a solid ethylene vinyl acetate (EVA) polymer matrix surrounded by rate controlling EVA
Zero order release that lasts up to three years
Implanon
Non-biodegradable diffusion controlled Hydron polymer reservoir containing histrelin acetate
Zero-order release that lasts up to a year
Histone Acetate Implant
Histone Acetate Implant Examples
Suprellin LA (central precocious puberty)
Vantas (palliative treatment of advanced prostate cancer)
Composed of bioerodible polymers with uniformly dispersed drug
Dose not have to be removed
Bioerodible Matrix Implant
Bioerodible Matrix Implant
Prepared as copolymer of poly(lactic acid) and poly(glycolic acid) that break down to lactic acid and glycolic acid
Inserted SC in abdomen
Water penetrates and slowly hydrolyzes (breaks down) the polymer
Zoladex
Bioerodible matrix implant
Intracranial implant of carmustine homogeneously dispersed in bioerodible polymer matrix
Contains wafer made of microspheres in a disk shape
The wafer composition allows slow release of the drug as the polymer degrades at the surface and protects the drug from too much degradation
Several wafers can be implanted after brain tumor resection
Gliadel wafer
Bioerodible matrix implant
Two-syringe product mixed prior to SC injection. One syringe contains Atrigel Delivery System and the other contains leuprolide acetate. Atrigel is a polymer delivery system consisting of biodegradable poly(DL-lactide-co-glycolide) (PLG) formulation in a biocompatible solvent
Tissue water causes polymer to precipitate and trap the drug in a solid implant
Eligard
Mechanical implant - Implantable infusion pump
Drug solution is pumped from a reservoir into a catheter by a peristaltic mechanism
SynchroMed
Self-contained units of a pumping mechanism, drug reservoir and catheter that can be surgically implanted in a subcutaneous pocket (subclavian fossa or abdomen)
Usually made of titanium (goo biocompatibility)
Used for both spatial and temporal control of drug delivery
Mechanical Implants - Implantable infusion pump
Uses a piston to force fluid out, thus is gentler on insulin
Refilled every 3 months with formulated insulin for improved stability
A particular site can be catetherized
Certain models can be programmed externally (telometry) for constant infusion or circadian patterns
Minimed
Use positive pressure to deliver medication either as continuous infusion, intermittent infusion, or bolus dosing, and single or multiple solution delivery
Ambulatory (External) Infusion Pump
Ambulatory (External) Infusion Pump
Patient can deliver own pain medicine with the click of a button
Can program bolus dose, dose limits, background infusion rate, and lockout interval
Mainly IV
Patient-Controlled Analgesia
For glucose control in diabetes
Can deliver basal insulin throughout the day and bolus doses as needed
Five brands of insulin pumps available
Disetronic
Animas
Minimed
Nipro
Omnipod
Continuous SC insulin infusion
In contact with water, phospholipids will assemble to form an enclosed lipid bilayer known as this.
Liposome
Liposome drug delivery
IV for Kaposi's sarcoma
Drug is water-soluble (contained in aqueous interior)
Improved parameters (increased half-life and localized to tumor-site)
Doxil
Liposome Spatial Drug Delivery
IV antifungal
Drug is lipid soluble (incorporated in lipid bilayer)
Improved parameters (Decreased renal accumulation of amphotericin B so less nephrotoxicity)
Ambisome
Albumin Nanoparticles Drug Delivery
Albumin nanoparticles are coated with drug (no need for surfactant and 50% alcohol which causes significant hypersensitivity)
Suspension that is injected IV
Achieves targeting due to albumin receptors on neoplasm endothelia. Receptor mediated uptake plus binding to tumor protein.
Abraxane Injectable Suspension
Adhesive matrix
Applied to the scrotum (very permeable)
Testoderm
Adhesive matrix
Relatively largepatch for post-herpatic (shingles) neuralgia for a local action and size can be adjusted
Lidoderm
Square-root of time release that have the drug uniformly mixed in with the matrix
Usually the skin controls drug input
Matrix
Matrix system with drug uniformly mixed in with the adhesive matrix
Fewer layers mean a very thin patch
Adhesive matrix
Drug is a saturated solution and the membrane controls the release and entry into circulation
Zero-order release
Leaking of patch is possible
Membrane-Controlled (Reservoir)
Gelled reservoir of estrogen and ethanol (penetration enhancer)
Estroderm
Ethanol
Penetration enhancer
Combination system in which rate-controlling membrane gives a zero-order release to a matrix system
Drug in adhesive gives a burst effect or saturates skin binding sites
Membrane-Matrix Hybrid
Membrane-Matrix Hybrid
Drug-in-adhesive saturates binding sites
Therapeutic levels in 2-3 days
Catapres TTS
Membrane-Matrix Hybrid
Placed behind the ear (thinner SC and more shunts)
Durg-in-adhesive to saturate skin binding sites and give burst effect
Therapeutic levels in 4 hours
Transderm Scop
Uses electricity to drive drug molecules contained in reservoirs through the skin
Iontophoresis (Electrotransport)