RS-DSC 簡介：一種用於篩選高濃度生物治劑熱穩定性的免稀釋方法
網路研討會 RS-DSC 簡介：一種用於篩選高濃度生物治劑熱穩定性的免稀釋方法 確保短期熱穩定性對於維持抗體藥…
RS-DSC 簡介：一種用於篩選高濃度生物治劑熱穩定性的免稀釋方法
RS-DSC產品演示 高濃度生物製藥之無稀釋熱安定性篩選方法 資源 應用說明： 高濃度生物藥物的快速熱穩定性篩…
Installing and Calibrating the Rheo-Impedance Spectroscopy Accessory for HR Rheometers
Overview In this Tech Tip, we will install and calibrat…
Rheology Theory and Applications
Will my paint coat the wall or drip off? Will my topical pharmaceutical spread on skin or form clumps? Rheology answers vital questions to inform how we create and interact with materials on a daily basis.
流變學，原來這麼簡單！
我喜歡在廚房裡做實驗，尤其是烘焙和製作甜點。為了慶祝圓周率日，讓我們把科學和實驗帶進廚房，用餡餅麵團和餡料……還有流變儀。
透過同時進行流變學和阻抗測量來評估電池漿料
鋰離子電池 (LIB) 由多種活性及非活性材料組成，並經多步驟工藝製造而成。材料選擇和製程條件會極大地影響電池的最終性能。
利用流變學研究改進配方性能
從配方開發到商業配方的進展，皆取決於最終藥物的劑量強度、內在穩定性和蛋白質自結合程度。1 這是因為該藥物的研發已進入最後階段。
Comprehensive Rheological Characterization to Optimize Electrode Manufacturing
Summary Electrode manufacturing for lithium-ion batteri…
Unlocking Data Accessibility with TRIOS JSON Export
Overview We’re excited to introduce a brand-new feature…
TRIOS EasyMass: Unlocking Efficient Experiment Preparation with Automatic Mass Data Transfer
Overview Learn how to use the new TRIOS EasyMass featur…
3 Essential Types of Mechanical Testing for Polymer Development
High-performance polymers are a critical material for manufacturers due to their combination of mechanical, thermal, and chemical properties, but especially their cost. Without adequate testing, manufacturers could run into a slew of issues, from immediate product failure to poor performance or failure after some time in usage.
Unlocking Stability: The Crucial Role of Thermal Analysis in Lyophilization Temperature Optimization
The method of drug delivery significantly influences the final stages of the manufacturing process. Currently, lyophilization—a widely adopted technique—enables drug developers to stabilize formulations and therapeutic molecules using a validated commercial approach. In this process, precise control of pressure and temperature within a lyophilizer facilitates the removal of liquids from formulations containing thermally sensitive or hydrolytically unstable active pharmaceutical ingredients or formulation components.