Prompt Description
Applications of Artificial Intelligence in Fixed Tooth-Supported Prosthodontics: A Systematic Review Abstract Background: Artificial intelligence is being increasingly integrated into dental practice, especially within fixed prosthodontics. Its application demonstrates potential for improving diagnostic precision, aiding clinical workflows, and enhancing the quality of dental restorations. Nevertheless, despite its increasing adoption, robust and consolidated evidence concerning its efficacy in essential prosthodontic procedures remains limited. Objective: To thoroughly assess the effectiveness of artificial intelligence-based systems in tooth-supported fixed prosthodontics, emphasizing their applications in automated crown design, margin and finish-line identification, crack detection, and the analysis of retention loss in fixed partial dentures. Methods: A systematic literature search was conducted across several databases, including PubMed, Scopus, Google Scholar, and Web of
![Subject: Experiment Flowchart of Bacterial Activation and Phage Treatment of Biofilm Formation
Style: Concise, scientific experimental flowchart, black lines on a white background, clear icons
Requirements:
Use clear arrows to connect each step.
All key nouns must be represented by icons/pictures, and ensure the icons are easy to understand.
The process layout is from left to right and from top to bottom, with clear logic.
Steps and Icon List:
Start
[Icon: Stock tube] (containing target bacteria)
Use [Icon: Inoculation loop] to pick up bacterial solution from [Icon: Stock tube].
Perform [Icon: Streak plating] on [Icon: 90mm petri dish] (containing solid medium) to activate bacteria.
Incubate in an incubator until [Icon: Single colony] grows.
Use [Icon: Inoculation loop] to pick a [Icon: Single colony].
Inoculate the picked colony into [Icon: Erlenmeyer flask] containing [Icon: 2216E liquid medium] and shake culture.
Measure periodically until [Icon: Spectrophotometer] shows the bacterial solution [Icon: OD600=0.1].
Branch point: Dispense the bacterial solution into two new, sterile [Icon: Erlenmeyer flasks].
Control group: Keep one [Icon: Erlenmeyer flask] as is.
Experimental group: Add [Icon: Bacteriophage] to the other [Icon: Erlenmeyer flask].
Use [Icon: Pipette] to transfer the liquid from the two Erlenmeyer flasks to the wells of 4 [Icon: 24-well plates] respectively (the liquid from each Erlenmeyer flask corresponds to 2 well plates).
Parallel processing: Place these 4 [Icon: 24-well plates] in [Icon: Different environments] (e.g., different temperatures or shakers) and incubate for [Icon: 24 hours].
After incubation, remove all well plates.
Collect the [Icon: Biofilm] formed in each well plate.
Place the collected [Icon: Biofilm] samples in [Icon: 1.5ml centrifuge tube].
End (for subsequent analysis).
Layout: Please ensure that steps 1-7 are arranged vertically, and after step 8 (dispensing), the control group and the experimental group expand downwards in parallel, and steps 9-13 converge again.](/_next/image?url=https%3A%2F%2Fpub-8c0ddfa5c0454d40822bc9944fe6f303.r2.dev%2Fai-drawings%2FtBg6VEIvj0JHqBd0LOLXjlnAkPj8Lpax%2F06996af5-ce83-4761-bc4c-8fa3feecafab%2F4cedc944-94ba-4056-b4c9-a7ad54eefabf.png&w=3840&q=75)
