Welcome to HitGen

Chemistry

HitGen's chemistry business adheres to the philosophy of high quality, efficiency and continuous innovation, providing global partners with effective and competitively cost-efficient chemical solutions.

  1. Chemistry
  2. Analytical Chemistry and Quality Research

Analytical Chemistry and Quality Research

Capabilities:

 

The analytical capabilities at HitGen is comprised of two parts, including the analytical chemistry for R&D, and quality control. Each part is performed by an experienced and dedicated team.

 

Analytical chemistry for R&D: An experienced team with capabilities of characterization and purification of various analytes for DEL synthesis, oligonucleotides production, and chiral analysis for diverse analytical needs in the process of drug discovery. 

 

Ø  Platform for DEL Synthesis

      UPLC-MS based high throughput analysis for DNA reactions

      Prep-HPLC purification for DEL materials and products

      Affinity Selection Mass Spectrometry (ASMS) for DEL on DNA Validation

 

Ø  Characterization and Purification of Nucleotides, Nucleosides Nucleic Acids

      Purity determination using HPLC, LC-MS and NMR

      Prep-HPLC purification for mg to g samples

      siRNA characterization

 

Ø  Analysis and preparation of Chiral and Achiral Compounds

      Chiral analysis and separation with SFC and prep-SFC

      Achiral analysis and separation with HPLC and LC-MS

      Structural elucidation using NMR, HR LC-MS, and GC-MS

 

Ø Other Analyses

      Native MS analysis

      Impurity isolation and analysis

      qNMR for absolute purity determination

      Water content determination

      Residual solvent determination

 

 

Quality Research  :An experienced team with capabilities of physicochemical analysis, method development and validation, quality control testing, and stability study systems.


 Ø  Physicochemical Characterization

      Lipophilicity (logP, logD)

      pKa

      Solubility (K.S, and T.S.)

      Stability (solid and in solution)


Ø  Analytical Method Development & Validation

      Purity determination

      Quantitative Method development

      Method validation


Ø  Quality Analysis and Control

      Purity determination

      Organic impurity and genotoxicity analysis

      Elemental analysis

      Residual solvent analysis


Ø  Stability Study

      In-house stability chambers for stress testing, accelerated studies, and real time studies for Packing material selection and container closure system

      Degradation profile study

      Designed stability protocols with proper intervals


Analytical Instruments:

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