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相关概念视频

Cis-regulatory Sequences02:02

Cis-regulatory Sequences

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Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
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Formulation and Manufacturing Process: Physical Attributes of Generic Tablets and Capsules01:18

Formulation and Manufacturing Process: Physical Attributes of Generic Tablets and Capsules

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Bioequivalence in generic drugs, such as tablets and capsules, refers to their pharmaceutical equivalence to the brand-name counterparts. However, for therapeutic equivalence, manufacturers must also consider physical attributes like size, shape, and weight (FDA Guidance for Industry, December 2003). Discrepancies in these aspects could impact patient compliance and cause medication errors. For instance, swallowing difficulties, often experienced with larger tablets or capsules, can lead to...
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Design Consideration01:22

Design Consideration

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Designing a structure involves a series of considerations, primarily the material's ultimate strength, calculated through tests that measure changes under increased force until the material reaches its breaking point or limit. The ultimate load, where the material breaks, is divided by its original cross-sectional area, resulting in the ultimate normal stress or strength. The ultimate shearing stress is another significant factor taken into account.
The factor of safety is another key...
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Tensile Strength Considerations of Concrete01:16

Tensile Strength Considerations of Concrete

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Considering the tensile strength of concrete involves recognizing that the theoretical strength of cement paste can be up to a thousand times higher than what is observed in practical applications. This significant discrepancy is largely attributed to the presence of microscopic cracks within the concrete. These cracks tend to amplify stress at their tips when a load is applied, a phenomenon explained by Griffith's theory of brittle fracture.
The dimensions and shape of a concrete specimen...
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Global Regulatory Systems01:28

Global Regulatory Systems

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Global regulatory systems in bacteria enable rapid and coordinated responses to environmental changes by integrating sensory inputs with gene expression, ensuring efficient adaptation to fluctuating conditions. Key global regulatory mechanisms include regulons, two-component systems, sigma factors, and secondary messengers.Regulons and Global RegulatorsA regulon is a collection of genes and operons controlled by a common global regulator. These regulators enable bacteria to prioritize resource...
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Planar and Three-Dimensional Printing of Conductive Inks
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三维打印的儿科药物:配方,过程和监管考虑

Krisztina Petrinca1, Zsófia Németh1, Ildikó Csóka1

  • 1Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Eötvös Street 6, 6720 Szeged, Hungary.

Pharmaceutics
|January 28, 2026
PubMed
概括

开发个性化的3D打印药物为儿科患者提供了有前途的解决方案,解决了剂量准确性,可口性和保证更安全,更有效的药理疗法的挑战.

科学领域:

  • 制药科学 制药科学
  • 生物医学工程 生物医学工程
  • 儿科医学 儿科医学

背景情况:

  • 儿科配方面临挑战,因为儿童的生理和药理动力学变化取决于年龄.
  • 修改成人药物用于儿科可以导致剂量错误,污染和降低疗效.
  • 现有的挑战需要创新的方法来安全有效的儿科药物输送.

研究的目的:

  • 审查开发3D打印儿科药物的生理,技术和监管方面.
  • 讨论3D打印儿科剂型的关键质量和性能属性.
  • 探索3D打印药品不断变化的监管环境.

主要方法:

  • 关于儿科配方和3D打印技术的当前文献的综述.
  • 对3D打印药物的关键质量和性能属性的分析.
  • 讨论儿童3D打印药物的监管考虑和良好制造实践 (GMP).

主要成果:

  • 3D打印使得个性化的儿科用药剂形式具有可调强度和可控释放.
  • 儿童友好的形状和改善的口感可以提高药物的接受和坚持.
  • 剂量准确性,稳定性和可重复性等关键属性对于3D打印的儿科药物至关重要.
关键词:
通过3D打印打印3D打印.通过3D打印打印的药物.个性化治疗是个性化的治疗.儿科用药剂型 儿科用药剂型儿科 儿科 儿科

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结论:

  • 3D打印具有个性化儿科药物治疗的变革潜力.
  • 解决技术和监管因素对于成功实施至关重要.
  • 这项技术为为儿童提供了更安全,更有效和更为定制的药物的途径.