1 Flashcards

1
Q

Which type of microneedles don’t have to be removed after application

A

Dissolving microneedles

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2
Q

What type of vaccine can benefit from delivery system

A

Subunit vaccine

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3
Q

Which nanoparticles type/s is/are made of amphiphilic molecules

A

Liposomes

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4
Q

Nanoparticle made of a polymer with many branches

A

Dendrimers

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5
Q

What’s the size of a dendrimers

A

1.5-10nm

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6
Q

Microsphere, Microparticles

A

•can be solid microparticales
Porous microspheres
Hollow in nature microcapsules
•spherical
•made from lipids , polymers , protiens etc
•size 1 - 1000 micro
• PLA /PLGA mostly in market

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7
Q

What’s the mechanism controlling drug release of incorporated drug in Microspheres

A

Degradation rate of matrix in vivo

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8
Q

Which type of contruct have an EPR effect

A

•polymer-drug conjugates: dendrimers
•protein nanoparticles
•polymeric nanoparticles
Micro capsules (no)

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9
Q

Stealth nanoparticles

A

•solid polymeric nanoparticles coated with PEG on surface
•Hydrophilic surface
•less recognized by immune system
•prolonged half life
•Inc plasmas circulation time ,
Inc accumulation at leaky site
•less accumulated in liver and spleen
•achieve active targeting by attaching targeting groups on nanoparticles

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10
Q

Quality control dissolution test

A

•Used to Verify safety and efficacy
•over discrimantory methods are sometimes chosen
•surfactants are not always added:
-in reciprocating cylinder USP apparatus 3 : can’t be added
-in sink condition, added in conc above the CMC “Critical micelle conc”
•sink conditions are generally used
•they are simpler than predictive test
•they do not simulate closely the physiological conditions in the stomach and intestines,

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11
Q

Abraxane, albumin-based nano particles formulation containing paclitaxel/taxol

A

•Inc the overall solubility of the system
Low solubility
•PREVIOUS FORMULATION: solvent (cremophor) a highly toxic castor oil derivative
Abraxane: avoids the toxicity when used with taxol
•abraxane used for treatment of breast cancer
•it accumulates in cancer tissue by active and passive targeting

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12
Q

PEGylated protiens advantages and disadvantages

A

Advantages:
•improve drug delivery ( prolonged half life and less enzymatic degradation)
•low toxicity
•high hydration higher solubility
•ease of use of conjugation with drugs
Disadvantages:
•when it’s conjugated with protien therapeutics, activity can be reduced

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13
Q

Subcutaneous and intramuscular administration of liposomes can?

A

Target drug to reach lymphatic system, lymph nodes (B, T and other immune cells)

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14
Q

Ambisome , liposomal formulation of Amphotericin B

A

•given IV
•in bilayer of liposomes
• they are SUV “small unilamellar vesicles” 80nm
•poorly soluble
•enable to reduce high risk of nephrotoxicity ,associated with Amphotericin B (when not formulated to liposomes)

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15
Q

Sustained release liposomes

A

•MVV(100nm to several micrometers)
“multi vesicles liposomes”
•epidural administration
•multiple bilayers
•slow breakdown and slow clearance controlling the drug release
•form a depot in site of injection

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16
Q

To reduce drug opsonisation?

A

Fatty acid chains within the phospholipidd:
Inc the degree of saturation (single bond) and the length
Long and without double bonds

17
Q

To improve drug retention within the liposomes

A

REDUCE DRUG OPSONISATION

Fatty acid chains within the phospholipidd:
Inc the degree of saturation (single bond) and the length
Long and without double bonds

18
Q

Which type of microneedles are used in liquid vaccine formulation

A

Hollow microneedle

19
Q

What is a nanoparticle that have star-shape

A

Dendrimers

20
Q

Which apparatus CANNOT be used with surfactant in medium

A

3