Discover the Advantages of HALO and HALO BioClass Fused-Core Columns
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1 Discover the Advantages of HALO and HALO BioClass Fused-Core Columns
2 Table of Contents M ilestones in the Development of Fused-Core Particles S uperior Performance of HALO Fused-Core Columns K ey Advantages of HALO Fused-Core Columns H ALO: Dependable Quality and Reproducibility S electing the Appropriate Pore Size H ALO Columns for Small Molecule Separations BIOCLASS COLUMNS MILESTONES IN THE DEVELOPMENT OF FUSED-CORE PARTICLES mid s approximately yrs Superficially porous particles (SPPs) were first proposed by Golay Horvath, Preiss, and Lipsky described a nucleotides separation using ~ µm cores with a thin layer of anion exchange resin; called the particles pellicular referring to the thin, skin-like coating Horvath pellicular Kirkland, Zipax - Silica sol on glass beads that were ~ µm particle size Kirkland, Permaphase permanently bonded stationary phase on SPP Zipax Interest in SPPs dwindled due to the low surface areas and lower efficiencies, slower speeds of these column supports compared to non-core particles that could be made in smaller sizes R eversed-phase Separations with HALO HILIC Separations with HALO Kirkland describes µm SPPs with Å pores Agilent introduces µm Poroshell based on Kirkland s work Kirkland, Langlois and DeStefano, working at Advanced Materials Technology, Inc. described HALO particles with a. µm core and a. µm thick shell for a total particle size of. µm Poroshell HALO Columns HALO. Columns HALO Columns HALO BioClass Columns HALO Protein Columns HALO Peptide Columns H ALO Glycan Columns H ALO UHPLC and HPLC Guard Columns C olumn Part Number Listing HALO and Fused-Core are registered trademarks of Advanced Materials Technology, Inc. Summary D r. Joseph (Jack) Kirkland has been intimately involved in the development of HPLC packings, including porous and Fused-Core (SPP), throughout his distinguished career SPPs were among the first packings developed for HPLC and have become important again after a -year hiatus HALO. Advanced Materials Technology (AMT) was the first company to commercialize Fused-Core particles smaller than µm in Columns packed with these. µm particles have created a revolution in HPLC technology - Performance is comparable to the performance of sub- µm non-core particles, but with half the back pressure HALO - Analysts can obtain very high efficiencies and faster separations using their existing HPLC instruments, which may be limited to bar AMT continues to be a leader in the development and commercialization of novel packing materials for small and large molecules (HALO, ; BioClass, ) Poroshell is a trademark of Agilent Technologies
3 SUPERIOR PERFORMANCE OF HALO FUSED-CORE COLUMNS: HALO FUSED-CORE COLUMNS HALO µm columns will deliver reliable high speed and high resolution separations at pressures lower than most non-core sub- µm columns. HALO. µm columns can meet or exceed the performance of most non-core sub- µm columns at pressures one-third to one-half the back pressure under the same conditions. Figure C. van Deemter Plot of Plate Height vs. Linear Velocity (flow rate) Figure A. Scanning Electron Microscope (SEM) image of HALO particles. The particle size distribution is very narrow due to the separate sizing steps for solid cores and finished Fused-Core silica particles. Effect of Particle Size and Type Columns: x. mm, Non-core C, µm; Non-core C,. µm; Non-core C,. µm; HALO C,. µm Solute: naphthalene; mobile phase: % ACN/% water, C HALO µm columns will match the performance of totally porous µm columns at roughly half the back pressure under the same conditions. Early Explanations for Superior Performance Faster Mass Transfer due to a thin porous bonded-phase layer exterior to particle s solid silica core More Uniform and Stable Column beds due to very narrow particle size distribution (~ % RSD vs. ~% RSD for non-core particles) Current Understanding of SPP Performance (Figure C) The superior performance of Fused-Core SPP columns is now believed to be due to: Reduction in eddy diffusion - % smaller van Deemter A term due to more uniform analyte flow paths through the column bed Figure B. SEM image of a focused-ion-beamcleaved HALO Protein. µm silica particle. This cut-away view shows the solid core with its very thin. µm outer porous layer. Plate Height, micrometers Some of the early and current explanations for the excellent performance of Fused-Core columns are described below. µm non-core. µm non-core Much lower longitudinal broadening, flat van Deemter plot and higher optimum linear velocity (flow rate) - D ue to the presence of the particle s solid core ( % smaller van Deemter B term ). µm Fused-Core. µm non-core Data fitted to Knox equation* Mobile Phase Velocity, mm/sec Much smaller reduced plate heights and high efficiencies for SPP columns due to smaller van Deemter A and B terms for SPP particles B + Cµ H= A+ µ H = height equivalent to theoretical plate A = eddy diffusion term B = longitudinal diffusion term C = resistance to mass transfer term µ = mobile phase linear velocity (L/t) van Deemter Equation *G.J. Kennedy, J.H. Knox, J. Chromatogr. Sci ().
4 High Speed Separations (Figures D and E) S maller reduced plate heights lead to high efficiencies; narrower and taller peaks, for improved resolution and lower detection limits (LODs and LOQs) F lat van Deemter plot and higher linear velocity optimum (Figure C, page ) allow higher flow rates with minimal column efficiency loss High Resolution Separations (Figure F) High efficiency with longer geometries (,, mm) provides greater resolving power for challenging applications L ower back pressure permits columns to be used in series for the most demanding UHPLC and HPLC separations Excellent Ruggedness and Reproducibility L ess plugging, longer usable column lifetime and greater uptime due to larger porosity frits (vs. sub- µm totally porous (non-core) columns) - µm frits for HALO. and HALO - µm frits for HALO vs... µm frits for sub- µm non-core columns Excellent column-to-column and lot-to-lot reproducibility (Page ) PERFORMANCE VS. NON-CORE COLUMNS HALO Superior efficiency compared to many popular sub- µm non-core columns Figure D. Separation of a -peptide mixture is accomplished in less than one minute using a. x mm, HALO. Peptide ES-C column using a delay-volumeminimized and-optimized Agilent system. ~ % lower back pressure than most commercially available sub- μm non-core columns HALO. Comparable resolution and peak capacity to sub- µm non-core columns at half of the back pressure under the same conditions, or HALO BioClass Comparable to or better than performance of sub- µm non-core columns for bioseparations at / to / of the back pressure Column:. x mm, HALO Peptide ES-C Part Number: - Mobile Phase A: water/.% TFA; Mobile Phase B: / ACN/water/.% TFA Gradient: H old at.% B until. min.,.% to % B from.. min. Flow Rate:. ml/min. Temperature: C Pressure: bar LC System: Agilent SL Detection: nm Injection: µl. Gly-Tyr. Val-Tyr-Val. Angiotensin / (-) amide. Met-enk. Angiotensin / (-) amide. Angiotensin II. Leu-Enk. Ribonuclease A. Angiotensin (-) (mouse). Porcine Insulin ULTRAFAST BALLISTIC GRADIENT USING HALO Two-fold higher throughout at twice the flow rate vs. sub- µm non-core columns at similar pressures HALO Provides comparable efficiency and resolution to µm non-core columns for HPLC separations at % lower back pressure Figure E. Many researchers have found HALO columns in. mm ID to be very useful for highthroughout, ballistic separations by LC and LC-MS. Column:. x mm, HALO C Part Number: - Mobile Phase A: Water/.% TFA Mobile Phase B: Acetonitrile/.% TFA Gradient: -% B in sec. Flow Rate: ml/min. Pressure: bar. Atenolol. Pindolol. Propranolol. Indoprofen. Naproxen. Coumatetralyl Temperature: C Detection: UV nm, PDA Injection Volume:. µl Flow Cell: µl micro LC System: Shimadzu Nexera HALO FUSED-CORE PERFORMANCE ULTRAFAST PEPTIDE SEPARATION KEY ADVANTAGES OF HALO FUSED-CORE COLUMNS - Time (sec.) Outperforms legacy non-core columns in terms of peak shape, peak capacity and recovery CARBONYL-DNPH HIGH RESOLUTION SEPARATION Figure F. Environmental samples can be quite complex as demonstrated by this gradient separation dinitrophenylhydrazone (DNPH) carbonyl compound derivatives using a. x mm, HALO C column. Column:. x mm, HALO C, µm, Å Part Number: - Mobile Phase A: HO Mobile Phase B: / ACN/THF Gradient: Time %B - min. - min. - Flow Rate:. ml/min. Temperature: C Detection: nm Peak Capacity: Max. Pressure: bar Injection Volume:. µl. Formaldehyde-,-DNPH. Acetaldehyde-,-DNPH. Acetone-,-DNPH. Acrolein-,-DNPH. Propionaldehyde-,-DNPH. Crotonaldehyde-,-DNPH. Butyraldehyde-,-DNPH. Benzaldehyde-,-DNPH. Cyclohexanone-,-DNPH. Isovaleraldehyde-,-DNPH. Valeraldehyde-,-DNPH. o-tolualdehyde-,-dnph. m-tolualdehyde-,-dnph. p-tolualdehyde-,-dnph. Hexaldehyde-,-DNPH.,-Dimethylbenzaldehyde-,-DNPH. Heptaldehyde-,-DNPH. Octyl aldehyde-,-dnph. Nonanal-,-DNPH. Decyl aldehyde-,-dnph -,
5 HALO: DEPENDABLE QUALITY AND REPRODUCIBILITY HALO COLUMNS FOR SMALL AND LARGE MOLECULES: SELECTING THE APPROPRIATE PORE SIZE How to Choose the Right Pore Size? QA TEST QC TEST. x mm, HALO. µm : CHOH/ mm phosphate (ph ). ml/min., C phenol propranolol uracil - When an analyte is too large for the pores, restricted diffusion can occur, which can lead to peak broadening and reduced retention (Figure I) butyl paraben acenaphthene naphthalene amitriptyline. x mm, HALO. µm : CHCN/water. ml/min., C uracil HALO Column Family Products < Da HALO Å (small molecules) HALO HALO. HALO < kda* HALO BioClass HALO Glycan Da < MW < kda HALO BioClass HALO. Peptide HALO Peptide kda < MW < kda HALO BioClass HALO Protein For macrocyclic antibiotics and biomolecules such as peptides and proteins, use larger pore sizes such as Å HALO Peptide and Å HALO Protein columns (Page ) naphthalene Pore Size (Å) - Packing materials with smaller pores have greater surface area, which allows improved retention and loading capacity for lower MW analytes (Page ) -Cl--NO²-benzene MW Range Small molecules (< Da) are usually analyzed using HALO Ångstrom columns Advanced Materials Technology incorporates the know-how from its principal scientists, each with over years of experience in liquid chromatography, particle synthesis and column manufacturing to bring high quality, innovative products to our customers. Table A. Guidance for Pore Size Selection Match the column pore size according to the range of molecular weights (MWs) of the analytes in your sample (Table A) Figure G. Consistent reproducible performance from column to column and lot to lot is ensured because of well-designed processes and practices in the manufacture of HALO Fused-Core particles, HALO phases and HALO columns. Representative chromatograms of QA and QC tests are shown below, along with a historical plot of selectivity between a neutral and basic probe. * for glycans, glycopeptides and glycoproteins - RESTRICTED DIFFUSION FOR HIGHER MW POLYPEPTIDES ON HALO Å REPRODUCIBLE PERFORMANCE OVER TIME Selectivity for amitriptyline/acenaphthene ( ).. Alpha, Kami/Kacenaph Figure H. The selectivity value, alpha (kami/kacenaph) is plotted versus lot number for the amitriptyline/acenaphthene pair of individual HALO C lots from to. The vertical error bars show the bounds for two standard deviations about the mean value of.. The reproducible selectivity is indicative of processes that are well-controlled, which can produce reliable, high-quality columns Lot Number Figure I. In this example, broad peaks are observed in the upper chromatogram for bovine and human insulin, cytochrome C and lysozyme (MWs > ~ Da) chromatographed using a HALO Ångstrom column.this broadening is due to restricted diffusion using the smaller pore column. However, those same four peaks are much narrower and taller in the lower chromatogram using the Ångstrom HALO Peptide ES-C column. Peptide or Polypeptide PW. HALO Å PW. HALO Å MW (kda) Leucine enkephalin... Bovine insulin... Human insulin... Cytochrome C... Lysozyme... Halo. C Å Cyt C Lyso Lyso Cyt C Halo. Peptide ES-C Å Column:. x mm Part Number: HALO. C: - HALO. Peptide ES-C: - Mobile Phase A: / water/acetonitrile/.% TFA Mobile Phase B: / water/acetonitrile/.% TFA Gradient: % B to % B in min. Flow Rate:. ml/min. Temperature: C Detection: UV nm, VWD Injection Volume:. µl LC System: Agilent Peptides (in RT order): Leu-Enk, Bovine Insulin, Human Insulin, Cytochrome C, Lysozyme
6 HALO COLUMNS FOR SMALL MOLECULE ANALYSES Of the three variables in the general resolution equation, including efficiency (N) and retention(k), selectivity (α ) is the most powerful parameter for adjusting and improving resolution between peaks in a chromatographic separation. efficiency Rs = where selectivity retention ( )[ ][ ] N x (α-) x k α (+k) k = (k+k), α = k k and N= L = L H h x dp Moreover, column phase selectivity is one of the four most powerful and useful parameters for adjusting HPLC separation selectivity (see Table B). For ionizable analytes, mobile phase ph is, by far, the most effective parameter. However, column stationary phase is comparable to organic modifier choice (acetonitrile vs. methanol) and percent organic modifier/gradient steepness in its ability to change relative retention for UHPLC and HPLC separations. HALO columns are available in different stationary phases to use for method development and to apply for various types of analyses. The HALO phases that are available for reversedphase separations of small molecules are shown in Table C, and the phases are listed according to their differences in selectivity compared to HALO C at both ph. and ph. For example, if you were looking for a column with a different selectivity to a HALO C column at low ph, you might consider Table C and select a HALO PFP column as one most likely to be orthogonal to C. However, the other available HALO phases (Phenyl-Hexyl, RP-Amide, ) also retain and separate analytes via retention mechanisms different from HALO C and HALO C, so it might be prudent to consider one or more of the former phases as part of a comprehensive column screening or method development strategy (Figure J). HALO, HALO. and HALO columns for small molecule analyses are available in the following phases: Hydrophilic Interaction (HILIC) and Normal Phase Reversed Phase Penta-HILIC HILIC (silica) C Complete descriptions of the various phases are provided in Table D, along with physical and chemical properties, target analytes and best applications for each phase (Table E). C RP-Amide Phenyl-Hexyl See pages - for additional information about and applications for HALO HILIC and Penta-HILIC. PFP Table B. Parameters That Affect HPLC Selectivity in Order of Increasing Effectiveness (Refs. and ) HPLC Parameter Mobile phase ph (ionizable analytes only) Effectiveness for Changing Selectivity Most Effective Table C. Relative Reversed-Phase Orthogonality of HALO Phases vs. HALO C at Low and Mid ph (Refs. -) ph. ph HALO C HALO C HALO C HALO C HALO Phenyl-Hexyl HALO PFP HALO HALO Phenyl-Hexyl HALO RP-Amide HALO HALO PFP HALO RP-Amide Most Similar Organic modifier choice Percent organic modifier or gradient steepness Column stationary phase Column temperature Buffer choice Buffer concentration Least Effective Most Orthogonal Figure J. Example Strategy for Comprehensive Method Development Using Multiple HALO Stationary Phases and Column/Condition Screening, Followed by Optimization of Gradient Time, Temperature and ph HALO C HALO Screening gradients Select phase, ph, solvent Optimize tg, T, ph HALO RP-Amide -% CH CN, low ph ³ -% CH OH, low ph ³ -% CH CN, mid ph ³ -% CH OH, mid ph ³
7 HALO COLUMNS FOR SMALL MOLECULE SEPARATIONS HALO COLUMNS FOR SMALL MOLECULE SEPARATIONS Table D. HALO Small Molecule Column Specifications C C Phenyl-Hexyl Carbon Load (%) Surface Area (m/g) L.... L Yes Yes L High ph Limit Max. Temp. Upper ph Limit Yes L.... RP-Amide L.... Yes HILIC L. N.A. N.A. Pending.... C C C (octyldimethylsilane) Yes C C (octadecyldimethylsilane) Yes L Structure C Phenyl-Hexyl Phase Structure Excellent performance for broad range of analyte polarities Uncharged acids and bases, uncharged ion pairs Excellent performance for broad range of analyte polarities Complementary selectivity to alkyl phases Enhanced selectivity for aromatic compounds PFP (pentafluorophenylpropylsilane) Enhanced selectivity for stereoisomers Can be used in RPLC and HILIC modes Phenyl-Hexyl (phenylhexyldimethylsilane) (diisopropylcyanopropylsilane) No RP-Amide C Amide HILIC None (Bare Silica) Penta-HILIC proprietary penta-hydroxy ligand HILIC PFP Penta-HILIC Diverse analytes ranging from polar to non-polar Uncharged acids and bases, uncharged ion pairs Analytes differing by an aliphatic or aromatic group Analytes differing by an aliphatic or aromatic group Aromatic molecules with electron-withdrawing groups (NO, COOH, COOR, halogens), heterocycles, benzodiazepines, highly aqueous conditions Electron-rich compounds, aromatics, unsaturated compounds with double and/or triple bonds Basic analytes at low ph, stereoisomers, steroids, taxanes, substituted aromatics, highly aqueous conditions Polar and very polar bases, acids and neutrals More retention for polar analytes and much less retention for non-polar analytes Very hydrophobic analytes retained too strongly on C phase Complementary selectivity to alkyl phases Best Applications Electron-poor molecules, aromatic or unsaturated compounds (ketones, nitriles, alkenes) Complementary selectivity to alkyl phases Aromatic molecules with electron-withdrawing groups (NO, COOH, COOR, halogens), heterocycles, benzodiazepines, highly aqueous conditions Alcohols, Acids, Phenols, Catechins Acidic and basic analytes, heterocycles, proton donors and acceptors, highly aqueous conditions Can be used in HILIC and normal-phase modes Polar and very polar bases, acids and neutrals, especially with log P<. Enhanced sensitivity and peak shape for LC-MS, analyses of basic analytes in HILIC mode, normal-phase analysis with non-aqueous mobile phases Ideal for separation of highly polar compounds that are poorly retained in RPLC Polar analytes with log P values near or less than Polar acids, bases and zwitterions that are not retained or are poorly retained with RPLC Enhanced stability for minimum bleed and long life RP-Amide Phenyl-Hexyl Target Analytes Diverse analytes ranging from polar to non-polar Complementary selectivity to alkyl phases PFP Features and Benefits Endcapped PFP Phase Particle Size(s) (µm) Low ph Limit Max. Temp. Lower ph Limit Bonded Phase USP Designation. Penta-HILIC Table E. HALO Phases: Features and Benefits, Target Analytes and Best Applications
8 REVERSED-PHASE SEPARATIONS WITH HALO To illustrate the selectivity differences among the various HALO RPLC phases, the following examples are provided. BENZODIAZEPINES ON HALO FUSED-CORE BONDED PHASES HALO C VS. RP-AMIDE FOR PHENOLICS Column:. x mm Part Numbers: -, -, -, - Mobile Phase A: mm Ammonium Acetate Mobile Phase B: Acetonitrile Gradient: - % B in. min. Flow Rate:. ml/min; Temperature: C Detection: UV nm Injection volume: µl Pressure: bar. Oxazepam. Lorazepam. Nitrazepam. Alprazolam. Clonazepam. Temazepam. Flunitrazepam. Diazepam Figure M. H ALO RP-Amide provides greater retention and resolution compared to HALO C for this phenol mixture. HALO RP-AMIDE HALO Phenyl-Hexyl HALO C,, Figure K. HALO Phenyl-Hexyl is the most retentive phase for these anti-anxiety drugs due to its propensity for π-π interactions. HALO C HALO RP-Amide. Uracil. Catechol.,,-Trinitrophenol.,,-Trichlorophenol., -Biphenol., -Dihydroxyacetophenone. -Chlorophenol Column:. x mm, HALO. µm RP-Amide and HALO C Part Number: - and - Mobile Phase: /: A/B A=. M Potassium phosphate, ph =. B= Acetonitrile Flow Rate:. ml/min. Temperature: ambient ( C), HALO PFP AROMATIC AND NITROAROMATIC COMPOUNDS DNT = dinitrotoluene i = impurity HALO C ii HALO, Figure N. HALO PFP delivers improved resolution and different elution order compared to HALO C for this mixture of steroids. HALO C. Prednisone Column:. x mm, HALO C. Cortisone. x mm, HALO PFP. Prednisolone Part Number: C: -. Hydrocortisone PFP: - Mobile Phase: /: water/methanol Flow Rate:. ml/min. Pressure: about bar Temperature: C Detection: UV nm, VWD Injection Volume:. μl Sample Solvent: % methanol in water Response Time:. sec. Flow Cell:. µl semi-micro LC System: Shimadzu Prominence UFLC XR ECV: about μl HALO PFP SEPARATION OF STRUCTURALLY SIMILAR STEROIDS ON HALO C AND PFP i. Resorcinol. Benzyl alcohol. Phenylacetonitrile. -Indanol.,-DNT.,-DNT.,-DNT. Anisole.-Chloro--nitrobenzene. Toluene Detection: UV mn, VWD Injection Volume:. μl Sample Solvent: water/methanol : (v/v) Response Time:. sec. Flow Cell:. μl semi-micro LC System: Shimadzu Prominence UFLC XR Extra Column Volume: about μl Figure L. HALO C and HALO columns may be used as orthogonal confirmatory columns for explosives analysis. Temperature: C Column:. x mm, HALO C, Part Numbers: C =-, =- Mobile Phase: /-A/B for C, /-A/B for A= water B= methanol Flow Rate:. ml/min. Pressure: About bar
9 HILIC SEPARATIONS WITH HALO NUCLEOSIDES AND NUCLEOBASES ON HALO PENTA-HILIC Figure P. These nucleosides and nucleobases are separated in under minutes using a HALO. Penta-HILIC column. Polar analytes that are poorly or not retained in RPLC Basic analytes that have poor peak shape (overloading) and/or poor retention at low ph in RPLC Some Typical Analytes for HILIC Separations Basic pharmaceuticals Analytes that have log P values near or less than zero Peptides When conditions orthogonal to RPLC mode are needed (elution order change) Polar organic acids Absorbance ( mm) HALO Penta-HILIC is a bonded silica phase, which has a highly polar ligand with hydroxyl groups tethered via novel proprietary linkage chemistry to Fused-Core silica particles. Hydrophilic interaction liquid chromatography (HILIC) is a useful UHPLC and HPLC mode for the following situations: Catecholamines and other neurotransmitters HALO columns are currently available in two different phases for HILIC separations (see Tables D and E, pages and, for properties, features and benefits): Nucleosides and nucleobases HALO HILIC Mono-, di-, tri- and other oligosaccharides HALO Penta-HILIC Opiates - CEPHALOSPORINS ON HALO PENTA-HILIC AND HALO HILIC Polar triazines and pyrimidines Analytes from metabolomic profiling HALO Penta-HILIC nm For more information on HILIC separations, please see references - on page. HALO HILIC, RETENTION ORDER REVERSAL AND IMPROVED RETENTION WITH HILIC adenosine + cytosine acenaphthene Column:. x mm Part Number: H ALO Penta-HILIC: - HALO HILIC: - Mobile Phase: A= / ACN/H with mm NHformate, ph=. (adj.) Mobile Phase: B= / ACN/H with mm NHformate, ph=. (adj.) Gradient: H ALO Penta-HILIC: -% B in min. HALO HILIC: -% B in min. Flow Rate:. ml/min. Pressure: bar with HALO Penta-HILIC bar with HALO HILIC Temperature: C Detection: UV nm, VWD Injection Volume:. µl Sample Solvent: / ACN/water Flow Cell: µl semi-micro LC System: Agilent. Cephalothin. Cefoxitin. Cefotaxime. Cefazolin. Cefaclor. Cephalexin. Cephradine. Cefadroxil. Ceftazidime. Cephalosporin C REVERSED-PHASE SEPARATION OF CEPHALOSPORINS USING HALO Column:. x mm Part Number:. µm HALO C: - Mobile Phase A: / ACN/. M Ammonium Formate Flow Rate:. ml/min. ph:. cytosine adenosine Figure R. HALO HILIC and Penta-HILIC columns often offer an orthogonal separation relative to reversed-phase separations, as shown here for HALO for a subset of the same cephalosporins shown in Figure Q. acenaphthene.. nm Column:. x mm Part Number:. µm HALO HILIC: - Mobile Phase A: / ACN/. M Ammonium Formate Flow Rate:. ml/min ph:. Figure Q. HALO Penta-HILIC shows increased retention and different selectivity vs. HALO HILIC for these cephalosporins. Glycosylceramides Figure O. You can often obtain a complete reversal in elution order and different selectivity using HILIC mode compared to reversed-phase mode under the same or appropriate conditions.. Thymine. Uracil. Thymidine. -Deoxyadenosine. Adenine. Uridine. Adenosine. Hypoxanthine. Xanthine. Cytosine. -Deoxycytidine. Guanine. -Deoxyguanosine. Cytidine. Guanosine Drug glycoside and glycuronide metabolites HALO HILIC is a Fused-Core silica phase that can be used either in HILIC mode or in normal-phase mode with waterimmiscible solvents (NPLC). Column:. x mm, HALO Penta-HILIC Part Number: - Mobile Phase A: mm Ammonium formate in % Acetonitrile/% water Mobile Phase B: mm Ammonium Formate in % Acetonitrile/% water Gradient: Time %B - min. - min. - Flow Rate:. ml/min. Temperature: C Detection: UV nm, VWD Injection volume:. µl Pressure: about bar.... Column:. x mm. µm HALO Part Number: - Mobile Phase A:. M Phosphate buffer, ph. (adj.) Mobile Phase B: Methanol Gradient: % B to % B in. min. Flow Rate:. ml/min. Temperature: C Detection: UV nm, VWD Injection Volume:. µl Sample Solvent: /: Water/Methanol Response Time:. sec. Flow Cell:. µl semi-micro LC System: Shimadzu Prominence UFLC XR ECV: about µl Pressure: bar at start of gradient. Cefadroxil. Ceftazidime. Cefaclor. Cephalexin. Cephradine. Cefotaxime. Cefoxitin. Cefazolin.
10 HALO (UHPLC) FAST LOCAL ANESTHETIC SEPARATION USING HALO PENTA-HILIC HALO Highest UHPLC performance possible without the disadvantages of sub- µ m columns Figure T. This mixture of five local anesthetics is resolved isocratically in. minutes using a HALO Penta-HILIC column. Use when the highest efficiency is needed E xcellent for fast method development and column/ condition screening Solid Core. µm µm B est performance obtained with instrumentation having extracolumn volume (IBW< µl) Ruggedness for R&D. µm µm inlet frit Shell with Å pores Pressure limit, bar/, psi mm (mau) Column:. x mm, HALO Penta-HILIC Part Number: - Isocratic: /: ACN/water with mm Ammonium Formate buffer, ph Flow Rate:. ml/min. Temperature: C Detection: UV nm, photodiode array detector Injection Volume:. µl Sample Solvent: / ACN/. M ammonium formate buffer ph Data Rate: Hz Response Time:. sec. Flow Cell:. µl semi-micro Pressure: bar LC System: Agilent SL Note: IBW is instrumental band width and is a measure of extracolumn dispersion.. Benzocaine. Lidocaine. Tetracaine. Procaine. Procainamide - ULTRA-FAST SEPARATION OF ANTICOAGULANTS USING HALO C..... Figure S. This separation of anticoagulants is completed in one minute using a short. x mm HALO C column using a Shimadzu Nexera UHPLC system. STEROID SEPARATION USING HALO PFP Absorbance ( mm) Column:. x mm, HALO C Part Number: - Mobile Phase A: mm Formic acid Mobile Phase B: / Acetonitrile/Methanol Gradient: Time %B Flow Rate:. ml/min. Temperature: C Detection: nm Injection Volume:. µl Maximum Pressure: bar Uracil (t).,-dihdroxycoumarin. -Hydroxycoumarin. Coumarin. -Chloro--hydroxycoumarin. Warfarin. Coumatetralyl. Coumachlor mm (mau) Figure U. HALO PFP columns often show excellent selectivity for steroids. HALO PFP is able to readily separate a mixture of steroids in less than minutes in gradient mode. Column:. x mm, HALO PFP Part Number: - Mobile Phase A: water Mobile Phase B: methanol Gradient: Time %B min. min. min. Flow Rate:. ml/min. Temperature: C Pressure: bar initial Detection: UV nm, VWD Injection volume: μl Sample Solvent: methanol Response Time:. sec. Flow Cell:. μl semi-micro ECV: about μl LC System: Shimadzu Prominence UFLC XR. Uracil. Hydrocortisone. Prednisolone. Cortisone. Prednisone. Dexamethasone. ß-Estradiol. Estrone. Halcinonide See page for full list of HALO part numbers.
11 HALO. HALO. (UHPLC AND HPLC) Reliable, efficient performance with lower back pressure compared to all sub- µ m columns ULTRAFAST SEPARATION OF TRICYCLIC ANTIDEPRESSANTS Use for high speed or high resolution with UHPLC or HPLC applications Solid Core Excellent for R&D and routine analyses. µm. µm Figure X. These basic tricyclic antidepressants are separated in less than two minutes, with excellent peak shape, using a HALO Penta-HILIC column. µm inlet frit Pressure limit, bar/ psi Figure V. These common statin drugs are separated in minute using a -mm HALO Phenyl-Hexyl column Column:. x mm, HALO. Phenyl-Hexyl Part Number: - Mobile Phase: /: A/B A:. M formic acid in water B: Acetonitrile Flow Rate:. ml/min. Pressure: Bar Temperature: C Detection: UV nm, VWD Injection Volume:. µl Sample Solvent: / methanol/water ( mm formic acid) Response Time:. sec. Flow Cell:. µl semi-micro LC System: Shimadzu Prominence UFLC XR ECV: ~ μl.... nm ULTRAFAST SEPARATION OF STATIN DRUGS.. µm Shell with Å pores Pravastatin Atorvastatin Mevastatin Simvastatin.... Figure Y. Six neonicotinoids are separated using a HALO. column. The sub- µm Fused-Core silica-based packing allows rapid separations at modest pressures. nm - Column:. x mm, HALO C,. µm Part Number: - Mobile Phase A: Water Mobile Phase B: Methanol Gradient: Time %B... Flow Rate:. ml/min. Temperature: C Detection: UV nm, VWD Injection Volume: µl Sample Solvent: /: Water/methanol Response Time:. sec. Data rate: Hz Pressure: bar to start, max. bar Flow Cell:. µl semi-micro LC System: Shimadzu Prominence UFLC XR ECV: about µl. HMX. RDX.,,-Trinitrotoluene.,-Dinitrotoluene.,-Dinitroaniline. Nitrobenzene. Nitroglycerin. Tetryl. -Amino-,-Dinitrotoluene. -Amino-,-Dinitrotoluene.,-Dinitrotoluene.,-Dinitrotoluene. -Nitrotoluene. -Nitrotoluene. -Nitrotoluene. PETN (pentaerythritol tetranitrate) nm Figure W. In this example, a. x mm HALO. C column is used to resolve explosives in minutes. This separation is quite sensitive to temperature, and was optimized using gradient time x temperature (tg x T) computer modelingand simulation using DryLab software.. Trimipramine. Amitriptyline. Doxepin. Nortriptyline. Amoxapine HIGH RESOLUTION OF NEONICOTINOIDS ON HALO. HIGH RESOLUTION SEPARATION OF EXPLOSIVES Column:. x mm, HALO Penta HILIC Part Number: - Mobile Phase: /: A/B A:. M Ammonium formate, ph=. (adj.) B: Acetonitrile Flow Rate:. ml/min. Temperature: C Detection: UV nm, VWD Injection Volume:. µl Sample Solvent: /: Water/acetonitrile Response Time:. sec. Maximum Pressure: Bar Flow Cell:. µl semi-micro LC System: Shimadzu Prominence UFLC XR ECV: about µl Column:. x mm, HALO Part Number: - Mobile Phase: /: A/B A:.% Formic acid in water B: Acetonitrile Flow Rate:. ml/min. Pressure: Bar Temperature: C Detection: UV nm, VWD Injection Volume:. µl Sample Solvent: A cetonitrile Response Time:. sec. Flow Cell:. µl semi-micro LC System: Shimadzu Prominence UFLC XR ECV: ~ μl. Nitenpyram. Thiamethoxam. Clothianidin. Imidacloprid. Acetamiprid. Thiacloprid See page for full list of HALO. part numbers.
12 BENZODIAZEPINE SEPARATION USING HALO PFP HALO Column:. x mm, HALO PFP Part Number: - Mobile Phase A: mm Ammonium Acetate, ph. Mobile Phase B: ACN, -% B in min. Temperature: C Flow:.mL/min. Detector: UV at nm Injection: μl... HALO (HPLC) Performance of µ m non-core column at µ m column pressures Ideal for: QC laboratories HALO PFP (µm) P= bar. µm PFP P= bar High throughout, ballistic gradient and isocratic applications NOTE: Peak widths at half height are labeled for comparable peaks on both columns. Comparative results presented here may not be representative for all applications. High resolution at HPLC back pressures (using columns in series) LC-MS ANALYSIS OF STEVIA GLYCOSIDES USING HALO PENTA-HILIC µm inlet frit FAST, HIGH RESOLUTION GRADIENT FLAVONOID SEPARATION SAMPLE: Mixture of flavonoids, μl in MeOH,,,,, POLAR AROMATIC COMPOUNDS ON HALO RP-AMIDE ANALYTES:. Hesperidin. Myricetin. Quercetin. Naringenin. Apigenin. Hesperetin. Kaempferol. Biochanin. Steviolbioside or rubusoside. (+),, Rebaudioside A. (+) Dulcoside A. (+),, Figure CC. HALO RP-Amide shows excellent resolution and peak shape for this mixture of polar aromatic compounds. nm (mau)..... Volts. Stevioside. (+),, - Column:. x mm, HALO C Part Number: - Flow Rate:. ml/min. Temperature: C Gradient: % CHCN for. min. -% CHCN/ mm NHCOO (.% HCOOH) in min. Max. Pressure: bar SIM (+),,. ESI: +. kv Scan Range: - m/z Scan Rate: pps Capillary: C Heat Block: C Nebulizing Gas Flow:. L/min. Drying Gas Flow: L/min.,, Intensity Shell with Å pores Figure BB. LC-MS analysis of stevia glycosides from a Stevia natural sweetener extract is easily accomplished using the HALO Penta-HILIC column due to its unique bonded phase containing five OH groups. Flow Rate:. ml/min. Pressure: bar Temperature: Ambient Injection Volume: μl Sample Solvent: /: Acetonitrile/water LC System: Shimadzu Nexera MS: Shimadzu LCMS (single quadrupole) Column:. x mm, HALO Penta-HILIC Part Number: - Mobile Phase A: / Water/acetonitrile with mm Ammonium formate, ph Mobile Phase B: / Water/acetonitrile with mm Ammonium formate, ph Gradient: % B to % B over min.. µm Pressure limit, bar/ psi Figure Z. This mixture of flavonoids is baseline resolved in less than minutes using a. x mm HALO C column with a fast.-ml/min. flow rate with an LC-MS-compatible mobile phase.. Oxazepam. Lorazepam. Nitrazepam. Clonazeparm. Flunitrazepam. Diazepam... µm. µm Solid Core Dirty samples Figure AA. These six benzodiazepine drugs are separated in minutes with better performance than a µm non-core column at ½ the pressure. Column:. x mm, HALO- RP-Amide Part Number: - Mobile Phase: /: A/B A: mm Potassium Phosphate, ph B: Acetonitrile Flow Rate:. ml/min Pressure: bar Temperature: C Detection: UV nm, VWD Injection Volume:. μl Sample Solvent: /: Water/Acetonitrile Response Time:. sec. Flow Cell: μl semi-micro LC System: Optimized Agilent. Uracil. Benzamide. Aniline. Cinnamyl Alcohol. Dimethyl Phthalate. -Nitroaniline. -Bromoacetanilide., -Biphenol., -Biphenol See page for full list of HALO part numbers.
13 Table F. HALO BioClass Column Specifications Particle Size(s) (µm) Pore Size (Å) Carbon Load (%) Surface Area (m/g) Low ph Limit High ph Limit Max. Temp. Lower ph Limit Max. Temp. Upper ph Limit Endcapped HALO Protein C.. Yes HALO Protein ES-C.. Yes HALO Peptide ES-C... No HALO Peptide... Yes HALO Glycan.. No HALO PROTEIN, PEPTIDE AND GLYCAN Today, researchers are keenly interested in both fast and high resolution separations of numerous biomolecules to support the development of novel therapeutic proteins and peptides in pharmaceutical drug development, to advance understanding in modern university laboratories, to characterize protein post-translation modifications, and to fully assess subtle differences in biosimilars and other products of bioengineering and manufacture. HALO BioClass columns have been developed to make such tasks easier and more effective, and are aimed at the following areas of bioseparations: I ntact proteins, monoclonal antibodies (mabs), biosimilars, and other large biomolecules such as pegylated proteins, antibody drug conjugates (ADCs), etc. Peptide mapping (analysis of enzyme digests) for characterization and monitoring of synthetic protein drugs Analysis of therapeutic peptides and peptide biomarkers (protein surrogates) H igh resolution separations of complex mixtures of glycans released from N- and O-linked glycoproteins Currently, the HALO BioClass column family is comprised of the following products. Their features and benefits are described below, and their specifications are shown in Table F. HALO Protein C Stability up to C HALO Peptide ES-C Fast, high resolution separations C an elute very large proteins with good peak shape and recovery Extremely stable up to C Compatible with UHPLC and HPLC Rugged, reliable performance Low LC-MS bleed Use with either UHPLC or HPLC HALO Protein ES-C Extremely stable up to C HALO Peptide Same benefits as Peptide ES-C C an elute very large proteins with good peak shape and recovery Alternative selectivity to Peptide ES-C for peptide mapping and proteomic applications Compatible with UHPLC and HPLC High peak capacity HALO Glycan Improved retention of acidic and zwitterionic analytes Very low sensitivity to buffer concentration Structure of an antibody showing its heavy chain in blue and its light chain in green. Able to separate isobaric oligosaccharides with different linkages Very low LC-MS bleed
14 HIGH RESOLUTION OF LIGHT AND HEAVY CHAIN VARIANTS OF IgG Masses deconvoluted using MagTran software*. Column:. x mm,. μm HALO Protein C Part Number: - Mobile Phase A:.% formic acid with mm Ammonium Formate Mobile Phase B: % ACN/% IPA/% A solvent Gradient: % B in min. Temperature: C Detection: nm and MS using pps scan rate from to m/z Injection Volume: μl of μg/μl reduced and alkylated lgg Sample Solvent:.% (v/v) formic acid in water MS Parameters: P ositive ion mode, ESI at +. kv, C heatblock, C capillary LC-MS System: S himadzu Nexera and LCMS- (single quadrupole MS) m/z LC= light chain HC= heavy chain -. µm.. HC:,.... Shell with Å pores µm inlet frit.. C and sterically-protected ES-C phases - Excellent high temperature stability (up to C) for improved peak shape and recovery. HC:, - Allows HALO Protein columns to be used with both UHPLC and HPLC instrumentation for fast bioseparations at moderate back pressures. µm LC:,. µm.. LC:, Solid Core.. LC:,. µm Fused-Core particles with a very thin. µm outer porous shell Figure EE. Very high resolution is obtained between variants of light and heavy chains of a reduced and alkylated monoclonal antibody (IgG) sample using a HALO Protein C column. nm Ångstrom pores to provide unrestricted pore access for polypeptides and proteins as large as kda - Provides narrower peaks and better recoveries for large biomolecules (vs. smaller pore sizes and non-core particles). HC:, HC:, HC:, HALO Protein ULTRAFAST PROTEIN SEPARATION USING HALO PROTEIN ES-C. Pressure limit, bar/ psi HALO Protein ES-C,. µm, Å Pressure: bar LARGE PROTEIN SEPARATION USING HALO PROTEIN C FUSED-CORE COLUMN Figure DD. High resolution separation of light and heavy chains of a denatured contractile protein (whole myosin from purified rabbit skeletal muscle) using HALO Protein C at C... Figure FF. An ultrafast protein separation is achieved on a HALO Protein ES-C Ångstrom column in less than minute Non-core C, µm, Å Pressure: bar Column:. x mm HALO Protein ES-C Part Number: - Instrument: Agilent SL Injection Volume: μl Detection: nm Temperature: C Flow Rate: ml/min. Mobile Phase A: water/.% TFA Mobile Phase B: acetonitrile/.% TFA Gradient: % B in min. Using and µl heat exchangers in column compartment PEAK IDENTITIES. Ribonuclease A. Cytochrome c. Lysozyme. α-lactalbumin. Catalase NOTE: Peak widths at half height are shown above respective peaks. Comparative results presented here may not be representative for all applications. Heavy chain subunits ~ kda Column:. x mm, HALO. µm Protein C Part Number: - Instrument: Agilent SL Injection Volume: µl Sample: denatured myosin Detection: nm Flow Rate:. ml/min. Mobile Phase A: water/.% TFA Mobile Phase B: acetonitrile/.% TFA Gradient: % B in min. Temperature: C - Expanded view.... HALO PROTEIN C PROVIDES NARROWER AND TALLER PEAKS THAN TOTALLY POROUS COLUMN Figure GG. HALO Protein C dramatically outperforms a conventional non-core C column,delivering narrower and taller peaks with improved recovery of holotransferrin, apomyoglobin, catalase and enolase. HALO Protein C,. µm, Å Pressure: bar Light chain subunits ~- kda - Non-core C, µm, Å Pressure: bar PEAK IDENTITIES - Column:. x mm HALO Protein C Part Number: - Instrument: Agilent SL Injection Volume: μl Detection: nm Temperature: C Flow Rate:. ml/min. Mobile Phase A: water/.% TFA Mobile Phase B: acetonitrile/.% TFA Gradient: % B in min.. Ribonuclease A. Cytochrome c. Lysozyme. Holotransterrin. Apomyoglobin. Catalase. Enolase Comparative results presented here may not be representative for all applications. See page for full list of HALO Protein part numbers.
15 COUPLED HALO PEPTIDE COLUMNS FOR MAXIMUM PEAK CAPACITY Figure II. Three HALO Peptide ES-C -mm columns ( mm total length) were connected in series to achieve a peak capacity of for this mixture of tryptic digests of α--glycoprotein and apotransferrin. HALO. Peptide HALO Ångstrom columns currently available in two particle sizes (. and µm) and in two stericallyprotected phases: ES-C and (Table F)... µm Ideal for both ultrafast and ultrahigh resolution separations of peptides and polypeptides up to kda. µm Outperforms non-core µm, Ångstrom columns in terms of peak width, peak capacity and peak height (Figure HH).. µm Solid Core Shell with Å pores. Columns: Three -mm. mm HALO Peptide. ES-C columns Part Number: of - Mobile Phase A: water/.% formic acid/ mm ammonium formate Mobile Phase B: A with % acetonitrile Gradient: % B in min. Flow Rate:. ml/min. Temperature: C Detection: nm Injection Volume: μl [ μg each] of α--glycoprotein tryptic digest and apotransferrin tryptic digest HALO Peptide Offers comparable peak capacity to sub- µm non-core columns at % back pressure. µm Solid Core HALO Peptide ES-C. µm, Å Pmax = bar. Columns:. x mm, HALO. Peptide ES-C and. x mm, non-core µm C column Part Number: - Mobile Phase A: % water/% ACN/.% TFA Mobile Phase B: % water/% ACN/.% TFA Gradient: -.% B in min. Flow Rate:. ml/min. Temperature: C Injection Volume: μl LC System: Agilent - Column:. x mm Part Numbers: HALO Peptide : - HALO Peptide ES-C: - Instrument: Optimized Agilent Injection Volume: μl Detection: nm Temperature: C Flow Rate:. ml/min Mobile Phase A: water/.% TFA Mobile Phase B: ACN/.% TFA Gradient: % B in min. HALO Peptide ES-C - Figure HH. HALO Peptide. column produces significantly taller peaks and higher peak capacity than a non-core µm column. Shell with Å pores COMPARISON OF FUSED-CORE TO NON-CORE COLUMNS FOR PEPTIDE SEPARATIONS. µm Non-core C µm, Å Pmax = bar HALO Peptide.. µm µm inlet frit Figure JJ. HALO Peptide offers alternative selectivity to HALO ES-C for this mixture of peptides and polypeptides. ALTERNATE SELECTIVITY USING HALO PEPTIDE HALO Peptide offers different selectivity and improved retention for polar peptides (Figure JJ) Columns (Peptide. and µm) can be used in series to increase peak capacity for UHPLC and HPLC analyses of complex tryptic digest samples (Figure II) Pressure limit, bar/ psi. Asp-Phe. Angiotensin (-) amide. Tyr-Tyr-Tyr. Bradykinin. Leu-Enk. Angiotensin II. Neurotensin. ß endorphin. Sauvagine. Mellitin Graphical representation of a polypeptide structure having beta-pleated sheet and alpha-helical regions. Gly-Tyr. Angiotensin / (-) amide. Val-Tyr-Val. Met-Enk. Angiotensin / (-) amide. Angiotensin II. Leu-Enk. Angiotensin (-) human. Angiotensin (-) mouse Comparative results presented here may not be representative for all applications.. NOTE: Peak widths at half height are shown above respective peaks. See page for full list of HALO Peptide part numbers.
16 SEPARATION OF N-LINKED GLYCANS FROM RIBONUCLEASE B Figure LL. Gradient HILIC-MS separation of N-linked glycans, which had been released using PNGase from ribonuclease B, using the HALO Glycan column. HALO Glycan Ångstrom pore size Incorporates a highly polar ligand that contains hydroxyl groups tethered to. µm Fused-Core silica particles via novel, proprietary linkage chemistry (Table F). µm. µm Solid Core Ideal for hydrophilic interaction liquid chromatography (HILIC) separations of oligosaccharides, and particularly, of released and labeled glycans from glycoproteins and proteoglycans Man Man Shell with Å pores Man.... nm Column:. x mm,. μm HALO Glycan Part Number: - Mobile Phase A: mm Ammonium Formate, ph. Mobile Phase B: Acetonitrile Gradient: -% B in min. Flow Rate:. ml/min. Pressure: bar Temperature: C Detection: UV nm Injection Volume: μl Sample Solvent: / ACN/water Response Time:. sec. Data Rate:. Hz Flow Cell:. μl semi-micro LC System: Shimadzu Nexera G G G G G G G :.(+) :.(+) :.(+) :.(+) :.(+) :.(+) :.(+) :.(+) :.(+) :.(+) :.(+) :.(+) :.(+) :.(+) :.(+) :.(+) :.(+),,,,, UV.. GF GF GF MS GF GFB Column:. x mm, HALO. µm Glycan Part Number: - Mobile Phase A: mm Ammonium Formate, ph. Mobile Phase B: Acetonitrile Gradient:. % B in min Flow Rate:. ml/min. Temperature: C Detection: UV nm Injection Volume: μl LC System: Shimadzu Nexera MS: S himadzu LCMS (single quadrupole) ESI: +. kv Scan range: - m/z Scan rate: pps GF+NeuAc GF-N G G G. -., G G.... Figure KK. Example QA Chromatogram for HALO Glycan column. Each HALO Glycan packing lot is tested using this glycan ladder mixture to assess and ensure lot-to-lot reproducibility QA ANALYSIS OF HALO GLYCAN GF.... GF. Pressure limit, bar/ psi Figure MM. Released- and procainamide-labeled glycans from human IgG were separated using a. x mm HALO Glycan column and detected using UV and selected-ion-monitoring MS detection. µm inlet frit SEPARATION OF N-LINKED GLYCANS FROM HUMAN IgG - Peaks for oligosaccharides composed of and GU must meet tight specifications for retention and peak width before lot is approved for glycan analysis. Each lot of HALO Glycan material is tested for quality assurance (Figure KK) by separation of a procainamidereducing-end-labeled glycan ladder of oligosaccharides having glucose units (GU). G# = DP of maltooligosaccharide For example, G = maltotriose Column:. x mm,. µm HALO Glycan Part Number: - Mobile Phase A: mm Ammonium Formate, ph. Mobile Phase B: Acetonitrile Gradient:..% B in. min Flow Rate:. ml/min. Temperature: C Detection: UV nm Injection Volume: μl Man. µm Mobile phases typically consist of acetonitrile and aqueous ammonium formate buffer ( mm, ph.) used to form a gradient of increasing water content during elution Ribonuclease B N-Linked Glycans Man GFB G+NeuAc GF+NeuAc GFB+NeuAc GFB+NeuAc See page for full list of HALO Glycan part numbers.
17 HALO UHPLC AND HPLC GUARD COLUMNS Collect strongly retained compounds from the sample and minimizes column fouling Finger-tight, direct-connect units that auto-adjust to any column with a inlet port U ltra-low dispersion, easy to use, operate at pressures up to bar Easily replace guard cartridge without removing guard holder from the flow path A vailable for all HALO analytical geometries (.,. and. mm ID) and phases HALO GUARD COLUMNS: PROTECTION + PERFORMANCE with guard column See figure below for an exploded view of the HALO guard cartridge and guard holder. Please see pages for ordering information. Titanium hybrid ferrule Adds durability for multiple connections Figure NN. HALO guard columns provide optimum protection for your HALO HPLC and UHPLCcolumn without sacrificing column efficiency. nm Finger-tight guard cartridge holder, Inlet Provides easy replacement of guard cartridge Finger-tight guard cartridge holder, Outlet Allows for replacement of guard cartridge without removing the guard holder from the flow path no guard column Column:. x mm. µm HALO C Mobile Phase: / ACN/water Flow Rate:. ml/min. Temperature: C Detection: nm Injection Volume: µl Pressure: bar with guard column bar without guard column Instrument: Optimized Agilent bypassed semi-micro flow cell. ID tubing Hz data rate HALO guard cartridge All HALO phases available Auto-adjusting zero dead volume (ZDV) end fitting Ensures optimum, ZDV connection to the analytical column The Optimize Technologies EXP Titanium Hybrid Ferrule is Patent Pending. The EXP Holder is patented under Patent No.,, B. The OPTI- prefix is a registered trademark of Optimize Technologies, Inc.
18 HALO COLUMNS HALO. COLUMNS The part numbers for HALO columns are presented below. HALO columns are available in the following analytical internal diameters (. and. mm). Guard columns are also available for HALO columns for these IDs for UHPLC to provide additional protection when necessary. HALO. columns are available in nano, capillary and analytical diameters, as well as in a mm semi-preparative diameter. Guard columns are available for analytical diameters of.,., and. mm.. µm, Å µm, Å ID x Length (in mm). x. x. x. x. x. x. x. x. x. x. x. x (in mm) C μm Guard columns, -pack C ID x Length (in mm). x. x - - Guard Column Holder C Phenyl Hexyl RP-Amide PFP Penta-HILIC HILIC C - - Phenyl Hexyl - - RP-Amide - - PFP Penta-HILIC - - HILIC Visit our web site.. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x C C Phenyl Hexyl RP-Amide PFP Penta-HILIC HILIC Phenyl Hexyl RP-Amide PFP Penta-HILIC HILIC µm, Å Guard columns, -pack (in mm). x. x. x C Guard Column Holder C
19 HALO COLUMNS HALO PROTEIN COLUMNS HALO GLYCAN COLUMNS HALO columns are available in nano, capillary and analytical diameters, and in a mm semi-preparative diameter. HALO Guard columns are available for analytical diameters of.,. and. mm. Part numbers for nano, capillary, analytical and semipreparative HALO Protein columns in both C and ES-C phases are provided below. Guard columns are available for HALO Protein columns in.,. and. mm IDs for UHPLC and HPLC applications to provide additional column protection when desired. HALO Glycan columns are available in. and. mm diameters in the following lengths in. µm particle sizes. Guard columns are available for UHPLC and HPLC applications if additional protection is desired. µm, Å (in mm). x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x C C Phenyl Hexyl RP-Amide PFP Penta-HILIC HILIC x. x. x Guard Column Holder C x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x C Phenyl Hexyl RP-Amide PFP Penta-HILIC HILIC HALO Protein C HALO Protein ES-C HALO Protein C HALO Protein ES-C (in mm). x. x. x. x. x. x HALO Glycan Guard Columns, -pack (in mm). x. x Guard Column Holder HALO Glycan Visit our web site. Guard Columns, -pack (in mm) µm, Å Guard columns, -pack (in mm) (in mm). x. x. x Guard Column Holder - -
20 HALO PEPTIDE COLUMNS The part numbers are provided below for the nano, capillary, analytical and semi-preparative HALO. and HALO Peptide columns in both ES-C and phases. Guard columns are available for.,. and. mm internal diameters for UHPLC and HPLC applications, if additional protection is desired. ID x Length (in mm). x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x. x HALO. Peptide ES-C HALO. Peptide HALO- Peptide ES-C HALO- Peptide HALO- Peptide ES-C HALO- Peptide REFERENCES. A dapted from book, Introduction to Modern Liquid Chromatography, rd Edition, L. R. Snyder, J. J. Kirkland and J. W. Dolan,, p., Wiley & Sons.. Orthogonal separations for reversed-phase liquid chromatography; J. Pellett, P. Lukulay, Y. Mao, W. Bowen, R. Reed, M. Ma, R.C. Munger, J.W. Dolan, L. Wrisley, K. Medwid, N.P. Toltl, C.C. Chan, M. Skibic, K. Biswas, K. A. Wells, and L.R. Snyder; Journal of Chromatography A, ().. C olumn selectivity in reversed-phase liquid chromatography I. A general quantitative relationship; N.S. Wilson, M.D. Nelson, J.W. Dolan, L.R. Snyder, R.G. Wolcott and P.W. Carr; Journal of Chromatography A, ().. C olumn selectivity in reversed-phase liquid chromatography IV. Type-B alkyl-silica columns; J. J. Gilroy, J. W. Dolan and L. R. Snyder; Journal of Chromatography A, () ( ColumnMatch ).. D.V. McCalley and U.D. Neue, J. Chromatogr. A, ().. A.J. Alpert. Anal. Chem., ().. D.V. McCalley, J. Chromatogr. A, ().. A.J. Alpert et al., Anal. Chem., (). Guard Columns, -pack ID x Length (in mm). x. x. x Guard Columns HALO. Peptide ES-C HALO. Peptide Visit our web site. info@advanced-materials-tech.com
21 Halo and Fused-Core are registered trademarks of Advanced Materials Technology, Inc.
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