multi‐dimensional chromatography · multi‐dimensional chromatography 29th october 2019...
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MULTI‐DIMENSIONAL CHROMATOGRAPHY
29TH OCTOBER 2019
Jealott’s Hill International Research Centre
Jealott's Hill International Research Centre
Bracknell, Berkshire
RG42 6EX, United Kingdom
A one‐day symposium that explores the latest techniques in multi‐dimensional chromatography.
Leading specialists from industry and academia will explain how they apply
the latest 2‐D techniques to achieve very difficult separations in the liquid,
supercritical fluid, and gas phases.
Instrumentation and consumables will be displayed in a comprehensive
supporting exhibition from relevant manufacturers.
INVITED LECTURE PRESENTATIONS “Multi‐dimensional liquid chromatography: from small molecules to large particles and from method development to data analysis” - Bob Pirok (Van ‘t Hoff Institute for Molecular Sciences University of Amsterdam) "Development of two‐dimensional high‐performance liquid‐chromatography for the separation and characterisation of therapeutic oligonucleotides and associated manufacturing impurities" ‐ Christina J Vanhinsbergh (Uni Sheffield) “The Investigation of 2D Separation Techniques for the Analysis of Agrochemical Formulations and Co‐formulants” ‐ Pablo Navarro (Syngenta, Jealott’s Hill, UK) “2D‐LC coupled with radio‐detection: applications for chiral agrochemical analysis” ‐ Dr Mark Garrod (Syngenta, Jealott’s Hill, UK) “Development of a screening method for peak purity assessment by 2D‐LC”. ‐ Jeorg Weber (Syngenta, Münchwilen, Switzerland) “2D‐LC in Pharmaceutical R&D. Applications beyond increasing peak capacity” Adrian Clarke TRD and CHAD Analytical Network Leader, Novartis Pharmaceuticals, Basel, Switzerland Lecturers and Exhibitors will be updated and timings and abstracts added to
the programme as they are received. ‐‐‐‐‐‐‐‐‐‐‐‐‐‐
REGISTRATION
The Chromatographic Society SAS Event & Association Management
The Old George Brewery Rollestone Street
Salisbury SP1 1DX UK T: +44 (0)1722 339811 F: +44 (0)1722 331313 www.chromsoc.com
Stephne Graham: [email protected]
Event Registration: [email protected]
Delegate Admission Prices
Member of the Chromatographic Society or one of its affiliated societies
(BMSS, ELRIG or RSC) ‐ £150 + VAT = £180
Non‐member rate ‐ £180 + VAT = £216
Bona fide student/Retired rate £75 + VAT = £90
CHROMSOC Industrial and student bursaries are available, for more
information and to apply, visit our website.
http://www.chromsoc.com/academic‐support.aspx
Please find below the link to register online for the meeting.
If you are attending the conference as a paying delegate, an exhibitor,
or as a complimentary delegate (Chromatographic Society Committee,
organiser or invited speaker)
please CLICK HERE to register.
Please note that Syngenta employee scientists are admitted free of charge to lectures and
exhibition.
The Chromatographic Society thanks Dr David Portwood, Lisa Asuncion and Syngenta
management for inviting us to run this symposium at their site at Jealott’s Hill and assisting
and supporting us in so many ways.
Refreshments will be provided throughout the day for paying delegates, exhibitors and
speakers.
SPONSORSHIP AND EXHIBITION COSTS
GOLD LEVEL SPONSORSHIP ‐ £1750 + VAT = £2100
This includes a table top exhibition stand plus 20 mins lecture time integrated
into the programme and 3 free delegate admission places.
SILVER LEVEL SPONSORSHIP ‐ £1250 + VAT = £1500
This includes a table top exhibition stand plus 10 mins lecture time integrated
into the programme and 2 free delegate admission places.
BRONZE LEVEL SPONSORSHIP ‐ £750 plus VAT = £900
This includes a table top exhibition stand and 1 free delegate admission place.
SPEAKERS & EXHIBITORS:
To discuss your sponsorship level and/or your lecture content please contact
Dr. Chris Bevan on [email protected]
To book your exhibition stand and sponsorship please click on the registration
link HERE.
Delivery of equipment to Syngenta from exhibiting companies
Syngenta will accept deliveries of table top size equipment & marketing
materials a few days before the event, but you MUST let them know the
approximate size and weight of all packages sent to:
SYNGENTA, Building 121, c/o Concierge (Oct29th ChromSoc meeting)
Jealots Hill International Research Centre, Bracknell, Berks RG42 6EY
Phone= 01344 424701
Exhibiting companies are invited to set up on their allocated exhibit tables in
the afternoon of 28th October if they wish, please inform Lisa Asuncion.
NOTES: SYNGENTA Meeting rooms booked are – Eagle, Eider, Egret 1&2 and Euphonia. The exhibition tables available to use are approximately 1 m 50 cm long x 75 cm deep. Lisa Asuncion at SYNGENTA will advise and help you with exhibition queries: E‐Mail: [email protected]
TIMETABLE OF EVENTS FOR 28th & 29TH OCTOBER 2019
28TH October 2019 afternoon From 2pm to 5pm SET UP OF 11 EXHIBITORS’ TABLES [ROOMS Egret 1&2 (GOLD), Eider (SILVER), Rear Foyer (BRONZE)] & delivery/placement of equipment from exhibitors. Car parking is in a reserved area of BARLEY car park or as advised by Syngenta. SATNAV POSTAL CODE FOR FRONT GATE ENTRANCE= RG42 6EX ================================================================ 29th October 2019 9am to 10am Registration desk in RECEPTION AREA, ELEMENTS BLDNG open: Tea and Coffee available Audio‐visual equipment is in 90 seat lecture room at SYNGENTA 10 to 10:15am Introduction and welcome from Syngenta and the Chromatographic Society David Portwood and Chris Bevan 10:15 to 10:30am “GC2 Made simple ‐ Comprehensive two dimensional GC using a Thermoelectrically cooled modulator Kathy Ridgway ANATUNE 10:30 to 10:45am “The latest innovations in multidimensional GC software: What can ChromSpace do for you?” Dr Laura McGregor Product Marketing Manager, SepSolve Analytical Ltd 10:45 to 11:15am “Development of Two‐Dimensional Supercritical Fluid Chromatography for highly polar aqueous samples” Raymond Wong, Shimadzu 11:15 to 11:30am Coffee & Tea break, Exhibition open. 11:30 to 12.15pm “Multi‐dimensional liquid chromatography: from small molecules to large particles and from method development to data analysis” ‐ Bob Pirok (Van ‘t Hoff Institute for Molecular Sciences University of Amsterdam) 12:15 to 1:00pm “2D‐LC in Pharmaceutical R&D. Applications beyond increasing peak capacity” Adrian Clarke, TRD and CHAD Analytical Network Leader Novartis Pharmaceuticals, Basel, Switzerland
1pm to 2:00pm Lunch and Exhibition Open in Egret,Eider & Foyer 2:00 to 2:30pm “2D‐LC coupled with radio‐detection: applications for chiral agrochemical analysis” ‐ Dr Mark Garrod (Syngenta, Jealott’s Hill, UK) 2:30 to 3.00pm “Development of a screening method for peak purity assessment by 2D‐LC”. ‐ Jeorg Weber (Syngenta, Münchwilen, Switzerland) 3:00 to 3:30pm “The Investigation of 2D Separation Techniques for the Analysis of Agrochemical Formulations and Co‐formulants” ‐ Pablo Navarro (Syngenta, Jealott’s Hill, UK) 3:30 to 3:45pm Tea break, Exhibition open 3:45 to 4:15 "Development of two‐dimensional high‐performance liquid‐chromatography for the separation and characterisation of therapeutic oligonucleotides and associated manufacturing impurities" ‐ Christina J Vanhinsbergh (Uni Sheffield) 4:15 to 4:35pm “Capillary Electrophoresis hyphenated to mass spectrometry (CESI‐MS) for the analysis of polar analytes such as pesticides and metabolites” Karsten Hendriks, SCIEX 4:35 to 4:50pm “Novel Applications in Enantioseparations” Brian Freer, DAICEL; HICHROM, VWR International Limited 4:50 to 5:05pm “A comparison of GC modulators. Dispelling the Myths” Bryan White, GC product specialist AGILENT 5:05 to 5:25pm “Recent 2D applications developed on the Vanquish Duo LC system” Norman Ramsey, Thermo Fisher Scientific 5:25 to 5:30pm “Summing Up, Thanks and Farewell” Chris Bevan, The Chromatographic Society
EXHIBITING AND LECTURING COMPANIES
ATG Scientific Ltd
representing IonBench, MS Noise, Reichert Inc.
and other specialist manufacturers
ABSTRACTS
UPDATED AS RECEIVED
Multidimensional Liquid Chromatography: a growing addition to separation science technology.
By Christina Jayne Vanhinsbergh, PhD researcher in 2D‐LC, University of Sheffield.
Many industries rely heavily on liquid chromatographic separations for the analysis of
molecular products, active pharmaceutical ingredients, reaction components and toxic
substances. Improvements in stationary phase chemistry, along with reduction in particle
size has helped to increase selectivity and peak capacity dramatically over the past decade.
A drawback for many separations, however, is that molecular species analysed today are
structurally and physicochemically closely related. This, along with biased separation
mechanisms, can lead to co‐elution or reduced resolution of analytes.
Multidimensional chromatography couples orthogonal modes of separations to overcome
challenging analyses. Orthogonal separations can pre‐treat samples, simplify complex
chromatography, as well as resolve co‐eluting species. The technique is developing into both
comprehensive and selective approaches, suited to the analytical drivers of separation.
Multidimensional liquid chromatography also has the potential for reducing reliance on
technologies requiring highly skilled analysts, such as mass spectrometry ‐ as separation of
critical species reduces the requirement for targeted mass detection over a peak. In
workflows where mass spectrometry is utilised, increases in peak capacity and resolution
can improve quantitative analysis.
Multidimensional liquid chromatography presents challenges to the analyst, which require a
detailed understanding of the mobile and stationary phase chemistries, potential analyte
interactions and what factors can detrimentally effect separation (such as miscibility of
mobile phases, dilution and sensitivity). The challenges described, indicate that optimisation
of the technique must be approached with due diligence to achieve the benefits of peak
capacities ranging into the thousands. Multidimensional liquid chromatography could be
applied for food, cosmetic, pharmaceutical, chemical and environmental analysis. A search
for available literature documents evidence of its growing use in aforementioned industries,
as is the growing number of chromatographic conferences dedicating presentation space to
researchers in the field.
Multi‐dimensional liquid chromatography: from small molecules to large
particles and from method development to data analysis
By Dr. Bob Pirok (Van ‘t Hoff Institute for Molecular Sciences University of Amsterdam)
In the MANIAC project, completely different and (seemingly) incompatible separation mechanisms
are compared into a single highly efficient and extensively optimized instrument. Hence the name
“Making Analytically Incompatible Approaches Compatible”. In MANIAC, various chemical,
physical and microbial processes are integrated with (multi‐dimensional) separation systems.
Amongst the investigated applications is the characterization of complex polymeric nanoparticles
encountered in coating formulations and drug‐delivery systems. These complex samples feature a
multitude of sample dimensions, such as the particle‐size distribution, the surface composition and
charge, and the molecular weight and chemical composition of the constituting molecules including
its active‐ingredient if applicable. A successful technique for the separation of complex mixtures is
comprehensive two‐dimensional liquid chromatography (LC×LC).
Comprehensive two‐dimensional liquid chromatography is indispensable for the separation of
complex mixtures. In principle, the development of an LC×LC method requires establishing two
separation dimensions with vastly different (“orthogonal”) selectivities. However, with the advent
of
state‐of‐the‐art instrumentation for LC×LC, the number of options to realize and optimize LC×LC
separations is increasing dramatically. Advanced modulation interfaces have significantly reduced
the
threats of solvent incompatibility and limited detector sensitivity in the comprehensive mode
(LC×LC). However, these developments are accompanied by an increase in the complexity of the
system and, thus, the time required for method development.
We recently demonstrated a proof‐of‐principle MANIAC system, which combined a separation of
particles in aqueous hydrodynamic chromatography with a fast separation of the constituting
polymers by organic size‐exclusion chromatography. The developed method featured a novel
implementation of intermediate sample transformation and now has been expanded to allow even
hydrophilic and charged particles to be modulated. In addition, we focus on the use of capillary and
chip‐based microreactors to improve the applicability and flexibility of the overall potential of
LC×LC separations towards drug‐delivery particles.
In this presentation, these and other developed methods for large and small molecules will be
shown.
Moreover, great attention will be given to the feasibility of 2D‐LC as a technique in the industrial
routine lab. The development and application of method‐development and data‐analysis tools to
facilitate easy and flexible use of 2D‐LC will be demonstrated.
“2D‐LC in Pharmaceutical R&D. Applications beyond increasing peak capacity”
Adrian Clarke
TRD and CHAD Analytical Network Leader
Novartis Pharmaceuticals, Basel, Switzerland
Abstract
Conventional liquid chromatography (1D‐LC) is not always capable of effectively resolving complex
samples. This limitation is not solely due to the lack of column efficiency, but is pre‐dominantly due
to insufficient chromatography selectivity and the need to separate the analytes of interest by
utilising orthogonal retention mechanisms. These limitations are the main reason, two‐dimensional
liquid chromatography (2D‐LC) is continuing to attract much interest for its markedly higher
resolving power compared to 1‐D separations. This presentation will discuss the benefits of 2D‐LC,
and show examples of multiple applications of (multiple heart‐cutting) 2D‐LC in pharmaceutical
analysis. The presentation will demonstrate 2D‐LC is not only beneficial to increase peak capacity,
but also to support process and product development and investigations. Applications include:
tracking of the various peaks of interest across 2 different methods (e.g. method transfer from an
MS incompatible buffer to an MS compatible buffer). A second application using 2D‐LC‐SPE‐MS for
on‐line enrichment of impurities peaks to facilitate improved impurity identification. The third
application supports method development by confirming peak purity using orthogonal stationary
phases in the 1st and 2nd dimensions and can be was used to investigate mass balance. Further
applications demonstrate the use for the analysis complex pharmaceutical molecules and drug
delivery systems (e.g. new modalities). The talk will finish with a summary on the
challenges and future outlook for 2D‐LC in the regulated pharmaceutical industry.
PROPOSED EXHIBITOR ROOM LAYOUTS IN ELEMENTS BUILDING
EGRET ROOMS 1+2. AGILENT
4 GOLD EXHIBITORS ON 4 DOUBLE TABLES.
FOOD ON CENTRE LINE
SHIMADZU
THERMO
SCIEX
EIDER ROOM.
4 SILVER EXHIBITORS ON 4 TABLES +FOOD
RSSL
SEPSOLVE
ANATUNE
[HICHROM‐DAICEL CHIRAL TECH EURO]
REAR FOYER AREA
3 BRONZE EXHIBITORS ON 3
TABLES + FOOD
ATG
BIOPHARMA
CRAWFORD
SPONSORS & EXHIBITORS TABLE NAME PLATES
‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐
SHIMADZU
AGILENT
THERMO
SCIEX
‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐
RSSL
SEPSOLVE
ANATUNE
HICHROM+DAICEL/CHIRALTECH SHARE
‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐
ATG
BIOPHARMA
CRAWFORD SCI
A full timetabled programme will be displayed prominently.