Scientific Library: results

Publications & Application notes

Robustness evaluation of weak anion exchange chromatography method for the purity analysis of therapeutic oligonucleotides

Authors
Lara Nercessian
Dilhan Ozturk
Claire I. Butré
Vincent Bertholet
Sébastien Patiny
Damien Mouvet
Arnaud Delobel
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Analysis of Oligonucleotides by Size-Exclusion Chromatography: SEC-UV, SEC-MS, SEC-MALS

Authors
Jennifer Bouchenna
Claire Butré
Arnaud Delobel
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Validation of a Monocyte Activation Test (MAT) using the PyroMAT™ kit

Authors
Sara Hully
Fabian Vandermeers
Vincent Bertholet
Géry Van Vyncht
Arnaud Delobel
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Development of orthogonal chromatographic methods for the purity analysis of therapeutic oligonucleotides

Authors
Arnaud Delobel
Claire Butré
Morgane Lescut
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Absolute Quantification of Oligonucleotides by ICP-MS/MS

Authors
Arnaud Delobel
Juliusz Bianga
Magali Perez
Damien Mouvet
Caroline Cajot
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Innovative ICP-MS/MS approach for the determination of phosphodiester to phosphorothioate ratio in phosphorothioate oligonucleotides

Authors
Juliusz Bianga
Caroline Cajot
Philippe De Raeve
Arnaud Delobel
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Webinar

App video_SEC Oligo

Analysis of Oligonucleotides by Size-Exclusion Chromatography: SEC-UV, SEC-MS, SEC-MALS

The field of therapeutic oligonucleotides has seen remarkable progress over the last years.

Authors
Jennifer Bouchenna
Claire Butré
Arnaud Delobel
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OLIGONUCLEOTIDES: absolute quantification and P=O/P=S ratio in a single ICP-MS/MS run

Access this 20 minutes webcast to learn how Quality Assistance developed an ICP-MS/MS method based on the quantification of P and S after microwave digestion to determine the P=O/P=S ratio in oligonucleotide samples.
Authors
Philippe De Raeve
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Excipient & API suppliers: ICH Q3D is also for you!

Access this 30 minute webinar to learn how the Q3D guideline for EIs can be efficiently implemented for all drug substances, excipients and drug products.
Authors
Philippe De Raeve, Scientific Director
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Elemental Impurities: How to be compliant with Q3D ?

Access this webinar which presented how the Q3D guideline for EIs can be efficiently implemented for all drug substances, excipients and drug products.
Authors
Philippe De Raeve, Scientific Director
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Conference

TIDES Europe Damien Mouvet Oligos ICP-MS

ICP MS/MS: An innovative approach for the characterisation of therapeutic oligonucleotides

ICP-MS/MS: An Innovative Approach for the Characterisation of Therapeutic Oligonucleotides


ICP-MS/MS methodologies were developed for the characterisation of therapeutic oligonucleotides:

Authors
Damien Mouvet
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Oligonucleotide

Characterisation of therapeutic oligonucleotides by ICP-MS/MS

Quality Assistance developed an innovative method for the absolute quantification of therapeutic oligonucleotides, as well as for the determination of phosphodiester-to-phosphorothioate (PO/PS) ratio by ICP-MS.MS.

Authors
Juliusz Bianga
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Quality Assistance Oligonucleotide

Oligonucleotides : absolute quantification and P=O/P=S ratio in a single ICP-MS/MS run

ICP-MS can be a solution for a fast and accurate generic method for oligonucleotides quantification without the reference oligo !
Authors
Philippe De Raeve, Scientific Director
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Q3D - Elemental Impurities

What implications for APIs & excipients suppliers?
Authors
Philippe De Raeve, Scientific Director
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Scientific poster

Development of orthogonal chromatographic methods for the purity analysis of therapeutic oligonucleotides

Authors
Morgane Lescut
Claire Butré
Arnaud Delobel
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Oligonucleotides: Absolute quantification and P=O/P=S in a single ICP-MS/MS run

Authors
Juliusz Bianga
Philippe De Raeve
Arnaud Delobel
Caroline Cajot
Location
TIDES 2018
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Elemental impurities: how to be compliant with ICH Q3D guideline?

Authors
Philippe De Raeve
Pascal Brichart
Julius Bianga
Géry Van Vyncht
Arnaud Delobel
Location
CPhI ISCE 2015
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