tableting

简明释义

英[ˈteɪblɪŋ]美[ˈteɪblɪŋ]

n. 制锭

英英释义

单词用法

同义词

反义词

例句

1.Disintegration of solid forms may be retarded by excessive pressure applied during the tableting procedure or by special coatings applied to protect the tablet from the digestive processes of the gut.

在制片过程中压片压力过大，或为了使药片免受肠道消化作用的影响而使用特殊的包衣，可延缓固体剂型的崩解。

2.Super Cleanse For Your Colon (with its aqueous coating) utilizes a special tableting process to promote the rapid release of its ingredients.

超级净化你的结肠(水性涂料)采用了特殊的压片过程中，以促进其成分快速释放。

3.Because it equipped with an excellent compactibility and a low chemical reactivity, it makes the MCC to become one of the most useful excipient of direct compression tableting.

由于其具备良好的压锭性，以及低化学反应活性，使得微晶纤维素被认为是目前最有用的直接压锭赋形剂之一。

4.RESULTS Tableting strength, humidity in granules and granule strength were the leading factors which affect tensile strength, fragility, dissolution percentage of tablets.

结果压片力、颗粒含水量和颗粒强度是影响片剂抗张强度、脆碎度及释放度的主要因素。

5.This compression tableting machine is capable of producing a multilayer tablet of configuration that despite multilayer structure, is not limited to cylindrical form.

根据该压缩制片机，能够制造具有多层结构并且不限制为圆柱状的形状的多层片。

6.Compressible starch can be used as fillers and dry binder in ta-blets directly compressed with commonly tableting machines.

可压性淀粉的试用表明，可在普通压片机上顺利地进行粉末直接压片。

7.Disintegration of solid forms may be retarded by excessive pressure applied during the tableting procedure or by special coatings applied to protect the tablet from the digestive processes of the gut.

在制片过程中压片压力过大，或为了使药片免受肠道消化作用的影响而使用特殊的包衣，可延缓固体剂型的崩解。

8.Hydraulic lift cylinder achieves lifting feeding mechanism up and down with limit switch to control the position, and interlocks with the feeding, tableting and sorting.

升降部分由液压升降油缸实现送料机构上升、下降，用限位开关控制位置，并与送料、压片、整粒联锁。

9.The process of tableting is essential in the pharmaceutical industry for creating solid dosage forms.

在制药行业中，tableting（压片）过程对于制造固体剂型至关重要。

10.During tableting, it is important to control the pressure applied to ensure uniform tablets.

在进行tableting（压片）时，控制施加的压力以确保片剂均匀性非常重要。

11.Quality control is critical during the tableting process to prevent defects.

在tableting（压片）过程中，质量控制至关重要，以防止缺陷。

12.Innovations in tableting technology have led to faster production rates and improved tablet quality.

在tableting（压片）技术上的创新导致了更快的生产速度和更好的片剂质量。

13.The formulation of the drug must be optimized for effective tableting.

药物的配方必须优化，以便有效进行tableting（压片）。

作文

In the pharmaceutical industry, the process of tableting plays a crucial role in the production of solid dosage forms. Tableting refers to the method of compressing powdered substances into tablets, which are one of the most common forms of medication. This process not only ensures accurate dosing but also enhances the stability and shelf-life of the drugs. Understanding the intricacies of tableting is essential for anyone involved in the field of pharmaceuticals, as it directly impacts the efficacy and safety of medications.The tableting process begins with the formulation of the tablet, which involves selecting the appropriate active pharmaceutical ingredients (APIs) and excipients. Excipients are inactive substances that serve as the vehicle for the API, aiding in the tablet's formation, stability, and absorption. The choice of excipients can significantly affect the tableting process, influencing factors such as flowability, compressibility, and dissolution rate.Once the formulation is established, the next step in tableting is the granulation process. Granulation involves agglomerating the powder mixture to improve its flow properties and ensure uniformity in tablet weight and content. There are two primary methods of granulation: wet granulation and dry granulation. Wet granulation uses a liquid binder to form granules, while dry granulation compresses the powder directly into larger particles without the use of solvents. Each method has its advantages and limitations, and the choice depends on the specific formulation requirements.After granulation, the granules undergo drying to remove excess moisture, which can affect the stability of the final product. Once dried, the granules are milled to achieve the desired particle size before proceeding to the tableting stage. This milling process is crucial, as it ensures that the granules are of uniform size, which is necessary for consistent tablet quality.The actual tableting is performed using a tablet press, a machine that compresses the prepared granules into tablets. Tablet presses can produce thousands of tablets per hour, making them an efficient choice for large-scale production. During this process, several parameters must be carefully controlled, including compression force, tablet thickness, and punch speed. These factors can greatly influence the hardness, disintegration time, and overall performance of the tablets.Once the tablets are formed, they undergo various quality control tests to ensure they meet the required specifications. These tests include assessing the hardness, friability, dissolution rate, and content uniformity of the tablets. Quality control is a critical aspect of the tableting process, as it ensures that the final product is safe and effective for patient use.In conclusion, tableting is a vital process in the pharmaceutical manufacturing industry that requires careful consideration of formulation, granulation, and compression techniques. By understanding the complexities of tableting, professionals can contribute to the development of high-quality medications that improve patient outcomes. As the pharmaceutical industry continues to evolve, advancements in tableting technology will likely lead to even more efficient and effective drug delivery systems, ultimately enhancing the healthcare landscape.

在制药行业中，tableting过程在固体剂型的生产中发挥着至关重要的作用。Tableting指的是将粉状物质压缩成片剂的方法，片剂是最常见的药物形式之一。这个过程不仅确保了准确的剂量，还增强了药物的稳定性和保质期。了解tableting的复杂性对于任何参与制药领域的人来说都是至关重要的，因为它直接影响到药物的功效和安全性。Tableting过程始于片剂的配方，这涉及选择合适的活性药物成分（API）和赋形剂。赋形剂是作为API载体的非活性物质，有助于片剂的形成、稳定性和吸收。赋形剂的选择可以显著影响tableting过程，影响流动性、可压缩性和溶解速率等因素。一旦配方确定，tableting的下一个步骤是颗粒化过程。颗粒化涉及将粉末混合物团聚在一起，以改善其流动性并确保片剂的重量和含量均匀。颗粒化有两种主要方法：湿法颗粒化和干法颗粒化。湿法颗粒化使用液体粘合剂形成颗粒，而干法颗粒化则直接将粉末压缩成较大的颗粒，而不使用溶剂。每种方法都有其优缺点，选择取决于具体的配方要求。颗粒化后，颗粒会进行干燥，以去除多余的水分，这可能会影响最终产品的稳定性。一旦干燥，颗粒会被研磨，以达到所需的颗粒大小，然后才能进入tableting阶段。这个研磨过程至关重要，因为它确保颗粒的均匀大小，这是确保片剂质量一致性所必需的。实际的tableting是通过片剂压机进行的，这是一种将准备好的颗粒压缩成片剂的机器。片剂压机每小时可以生产数千片片剂，成为大规模生产的高效选择。在这个过程中，必须仔细控制多个参数，包括压缩力、片剂厚度和冲头速度。这些因素可能会极大地影响片剂的硬度、崩解时间和整体性能。一旦片剂形成，它们会经过各种质量控制测试，以确保它们符合所需的规格。这些测试包括评估片剂的硬度、脆碎性、溶解速率和含量均匀性。质量控制是tableting过程中的关键方面，因为它确保最终产品对患者使用是安全和有效的。总之，tableting是制药制造行业中的一个重要过程，需要仔细考虑配方、颗粒化和压缩技术。通过理解tableting的复杂性，专业人员可以为开发高质量的药物做出贡献，从而改善患者的治疗效果。随着制药行业的不断发展，tableting技术的进步可能会导致更高效和有效的药物递送系统，最终改善医疗保健领域。