相关实验视频

Updated: May 12, 2026

3D Printing of Preclinical X-ray Computed Tomographic Data Sets
11:06

3D Printing of Preclinical X-ray Computed Tomographic Data Sets

Published on: March 22, 2013

40.5K

在不同存储条件下的四个3D打印模型的维度稳定性的体外比较

Vanessa Knode, Björn Ludwig, Sinan Hamadeh

    The Angle orthodontist
    |April 19, 2024
    PubMed
    概括

    评估了3D打印模型的维度稳定性. 所有模型都出现了收缩,白天曝光增加了收缩,这表明需要立即使用正牙器械.

    关键词:
    通过3D打印打印3D打印.维度稳定性 维度稳定性ортодонтический ортодонтические ортодонтические ортодонтические ортодонтические ортодонтические ортодонтические ортодонтические树脂树脂是一种树脂.收缩 收缩 收缩 收缩

    更多相关视频

    Design of an Open-Source, Low-Cost Bioink and Food Melt Extrusion 3D Printer08:01

    Design of an Open-Source, Low-Cost Bioink and Food Melt Extrusion 3D Printer

    Published on: March 2, 2020

    9.9K
    Characterizing Dissipative Elastic Metamaterials Produced by Additive Manufacturing09:39

    Characterizing Dissipative Elastic Metamaterials Produced by Additive Manufacturing

    Published on: June 28, 2024

    914

    相关概念视频

    In Vitro Drug Dissolution: Compendial Testing Models I01:13

    In Vitro Drug Dissolution: Compendial Testing Models I

    Compendial dissolution methods are standardized procedures defined by pharmacopeias to evaluate the rate at which a drug dissolves in a specific medium. These methods ensure batch-to-batch consistency, enable quality control, and support the prediction of drug bioavailability. They are critical for both immediate and modified-release drug products.The apparatuses used for dissolution testing differ in their design and mechanical function, but all aim to simulate the physiological environment of...
    In Vitro Drug Dissolution: Compendial Testing Models II01:09

    In Vitro Drug Dissolution: Compendial Testing Models II

    Various dissolution methods are utilized to assess a drug’s dissolution rate, including the flow-through cell, paddle-over-disk, cylinder, and reciprocating disk methods.The flow-through cell apparatus (USP (United States Pharmacopeia) method 4) comprises a reservoir for the dissolution medium and a pump that propels the medium through the cell containing the test sample. This method is crucial for assessing modified-release dosage forms with minimally soluble active ingredients, maintaining...