Lecture 11 Platforms Particulate systems Flashcards

1
Q

Describe liposomes.

A

Microscopic vesicles made of lipid bilayers, typically composed of phospholipids and cholesterol, that self-assemble into spherical structures with an aqueous core.

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2
Q

What are some advantages of particulate systems?

A

Enhanced therapeutic efficacy, minimization of side effects, improved patient compliance, optimization of biopharmaceutical properties, enablement of novel therapies, tailored treatment approaches, facilitation of personalized medicine.

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3
Q

How do liposomes serve as carriers for therapeutic agents?

A

Liposomes encapsulate drugs in their lipid core, lipid bilayers, or both.

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4
Q

Define the application areas of liposomes.

A

Vaccination, cancer therapy, gene therapy, photodynamic therapy, transdermal delivery, pulmonary delivery, imaging, and oral drug delivery.

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5
Q

List some advantages of liposomes.

A

Broad spectrum of agents, organ targeting, potential for long-acting effects, drug protection, overcoming biological barriers, enhancing immune response, improved pharmacokinetics, decreased toxicity.

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6
Q

What are some disadvantages of liposomes?

A

High production cost, leakage and fusion of encapsulated drugs/molecules, susceptibility to oxidation and hydrolysis, short half-life, low solubility.

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7
Q

Describe PLGA micro/nanoparticles.

A

PLGA micro/nanoparticles are composed of a biodegradable and biocompatible polymer designed to encapsulate therapeutic agents for targeted delivery. They break down into non-toxic components and are eliminated from the body naturally.

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8
Q

Do PLGA microspheres have any advantages?

A

Yes, advantages of PLGA microspheres include biodegradability, biocompatibility, controlled release, versatility, targeted delivery, protection of encapsulated drugs, tunable properties, reduced toxicity, and enhanced pharmacokinetics.

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9
Q

Define burst release in the context of PLGA micro/nanoparticles.

A

Burst release refers to the rapid and immediate release of the encapsulated drug from PLGA micro/nanoparticles, which can lead to potential issues in drug delivery.

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10
Q

How is PLGA utilized in Vivitrol® formulation?

A

Vivitrol® is an extended-release formulation of naltrexone for alcohol and opioid dependence that uses PLGA microspheres for sustained drug release.

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11
Q

Describe the disadvantages of PLGA micro/nanoparticles.

A

Disadvantages of PLGA micro/nanoparticles include burst release, acidic microenvironment, polymer degradation, incomplete release, particle aggregation, manufacturing complexity, size limitations, immunogenicity, and cost implications.

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12
Q

Describe the importance of particle size in nanocrystal technology.

A

Particle size plays a crucial role in nanocrystal technology as smaller size leads to a bigger A factor, impacting factors like adhesion, concentration gradient, and drug delivery.

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13
Q

What are the advantages of long-acting nanosuspensions in drug delivery?

A

Advantages include prolonged release, enhanced bioavailability, targeted delivery, stability, reduced side effects, flexibility in formulation, ease of administration, and manufacturing scalability.

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14
Q

How does milling impact drug delivery in nanocrystal technology?

A

Milling helps in delivering drug nano particles orally, leading to finely dispersed nano-crystals that exhibit pronounced adhesion, reproducibility, and a high concentration gradient.

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15
Q

Define the Noyes-Whitney equation and its relevance in drug formulation.

A

The Noyes-Whitney equation relates the rate of dissolution of a solid material to its surface area and solubility. In drug formulation, it signifies that smaller particle size results in a larger surface area, affecting dissolution and bioavailability.

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16
Q

What are the disadvantages of long-acting nanosuspensions in drug delivery?

A

Disadvantages include stability challenges, formulation and manufacturing complexity, potential toxicity, regulatory hurdles, risk of incompatibility, limitations in administration routes, and increased cost.