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81 - 97 共 97 條結(jié)果
應(yīng)用的篩選條件
In this application note, the use of the AssayMAP Bravo platform is discussed for protein analysis of antibody drug conjugate Brentuximab Vedotin in monkey plasma, with particular attention to DAR workflow development.
Learn about new technologies that can dramatically reduce the risks around routine pharmaceutical analysis while also reducing the time required from hours and days to minutes.
This application note demonstrates the use of the Agilent 8890 GC system coupled with an FID detector to detect and quantify ethylene glycol and diethylene glycol in propylene glycol, glycerin and syrup samples.
FTIR and chemometrics were used to determine the potency of several forms of cannabis products.
This application note demonstrates the use of the handheld Vaya Raman system, for the identification of mRNA LNPs through transparent and opaque containers.
New limits for elemental impurities in pharmaceutical materials and dietary supplements have been released by the USP and ICH.
Learn about proven workflows for regulatory compliance, enhance drug quality and safety, simplify analysis with cutting-edge technology.
Compares Analytical Instrument Qualification using Agilent ACE with other options using Data Integrity and compliance with USP general chapter as a framework.
The Agilent workflow solution for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
This application note describes the validation of a procedure for the measurement of elemental impurities in sterile artificial tear eye drops (SATED).
Reducing the time and expense of ICP-MS method development and system validation for measuring elemental impurities in pharmaceuticals
Expanded support for USP / and ICH Q3D methods supports compliance with elemental impurity analysis in pharmaceutical materials via ICP-OES
Agilent sample preparation systems, supplies, and reliable triple quadrupole LC/MS systems offer a rapid start-to-finish workflow to confidently achieve EPA Method 8327 and EPA Method 537.1 detection limits for PFAS in waters, while providing...
ASMS 2023 - In this work, the GC column and separation were optimized to obtain the ultimate detection limit for these analytes using a high efficiency ion source and MRM.
This application note demonstrates the benefits of combining helium collision mode and discrete sampling to develop and validate an easy-to-use, polyatomic interference-free method for the determination of 13 elements in tea infusion.
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| 樣品 | 化學(xué)基團 |
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Agilent 8697 ヘッドスペースサンプラ（HSS）と水素炎イオン化検出器（FID）を搭載した 8890 ガスクロマトグラフ（GC）を用いて、窒素および水素キャリアガスにより日本薬局方殘留溶媒試験のクラス 1、2A、2B の溶媒を測定しました。水溶性試料および非水溶性試料について適合性を満たし...
Agilent 8697 ヘッドスペースサンプラ（HSS）と水素炎イオン化検出器（FID）を搭載した 8890 ガスクロマトグラフ（GC）を用いてヘリウムキャリアガスにより日本薬局方殘留溶媒試験のクラス 1、2A、2B の溶媒を測定しました。水溶性試料および非水溶性試料について適合性を満たしました。...