High Throughput Screening Assay Flashcards

1
Q

Bioassay

A

It is any qualitative or quantitative analysis of a substance that uses a living system, such as an intact cell, as a component

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2
Q

Bioassay broad categories

A

-Virtual screening
-Primary Bioassays
-Secondary Bioassays
-Preclinical Trials
-Clinical Trials

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3
Q

Virtual and In Silicon Screening

A

-Ligand based or target based
-Target selection
-Screening of libraries of compounds virtually
-lead identification
-Prediction of structure-activity relationships
-it saves Time, money and efforts

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4
Q

Primary Bioassays

A

-Non-physiological assays
-Biochemical or Mechanism based Assays
-Microorganism-based bioassays
-Cell-based or tissue based assays
-A hit rate of less than 1% is reasonable

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5
Q

Secondary Bioassays

A

-Animal based assays
-Toxicological assessments in whole animals
-ADME studies
-Behaviour studies ( you can’t study effects on neurological activity on only one cell)
-Preclinical studies

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6
Q

In Vitro Bioassays

A

-Experiment occurs outside the organism
-Biological or chemical work is done in test tube rather than in living systems
-It includes Toxicity Assays like MTT assay and cancer cell line assay

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7
Q

In Vivo screenings

A

The test is performed in a living system such as antidiabetic assays, CNS assays and antihypertensive assays
-It includes:
animal toxicity( acute and chronic toixicity)
-Pre-clinical trials
-clinical trials

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8
Q

HIT

A

A hit is a compound which has the desired activity in a compound screen and whose activity is a confirmed upon retesting

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9
Q

Primary assay

A

Just checks if the drug works

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10
Q

Secondary assays

A

Determine how drug works

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11
Q

assay development

A

-Relevant
-Robust
-Reliability/Reproducibility
-Practicality/Feasibility
-cost
-Automation

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12
Q

HTS technology

A

-Robotics
-Miniaturisation
-sophisticated assay chemistry
-sophisticated software and database

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13
Q

Recent advances for HTs

A

‘Organ-on-a-chip’
Microchips lined by living human cells that could revolutionise drug development, disease modeling and personalized medicine.
If we can integrate all these chips in a system, we can imitate a physiological response

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