2. OVERVIEW
• INTRODUCTION
• INSTRUMENTATION
• PRINCIPLE
Sample introduction
Ion source
Mass analysers
Detection unit
Peak measurement
Methods of quantitation
Interferences
• PHARMACEUTICAL APPLICATIONS
• NEXT GENERATION OF ICP-MS
• CONCLUSIONS
3. INTRODUCTION
What is ICP-MS?
Inductively Coupled Plasma Mass Spectrometry
Elemental analysis with:
• Wide elemental coverage
• Very low detection limits(ppt /ppm)
• Fast analysis times (all elements at once)
• Simple spectra
• Isotopic information
5. Why is ICP-MS unique?
ICP-MS can:
• measure almost any element at ppt to ppm levels in almost any material.
• measure all elements in a single analysis.
• distinguish different element species (speciation).
Main requirements in pharmaceutical analysis are:
• high sensitivity
• good matrix tolerance
• low levels of interferences
• ease of coupling to speciation techniques ( LA, LC and maybe GC)
6. INSTRUMENTATION
2 METALLIC CONES (SAMPLER AND
SKIMMER CONE ( 0.6-1.2mm ORIFICE, AT
760 TORR) TO SEPARATE FINE DROPLETS
(1-2%)FROM LARGER ONES
USING PERISTALTIC
PUMP(1ml/min)
750-1500W
7.
8. PRINCIPLE
• Liquid samples to form aerosol in nebulizer.
• Introduction of Argon to the ICP torch, which is located in center of a radio
frequency (RF) coil for energy supply.
• RF field causes collisions of Ar atoms, generating a high-energy plasma.
• Sample aerosol decomposed in plasma (6000 - 10000 K) to form analyte atoms
which are simultaneously ionized.
• Ions extracted from the plasma into mass spectrometer region.
14. MASS
ANALYSERS
1.QUADRUPOLE MASS SPECTROMETER
• dc field on one pair of opposite rods and RF field on the
other pair.
• Ions of a selected m/z ratio are allowed to pass through
the rods of the detector.
16. 3.DOBLE FOCUSSING SECTOR MS
• ESA- kinetic energy focusing
• Magnet : ions travel in a curved path and are
separated according to their m/z.
17.
18. DETECTION
UNIT
1.SECONDARY ELECTRON MULTIPLIER
• Incoming ion creates an electron.
• Acceleration of electron towards the second dynode.
• Electron cascade is analysed as pulse or current.
19. 2.FARADAY CUP
• Incoming ion draw an electron from the ground to neutralize the positive
charge of the incoming ion.
• A voltage is measured.
20. 3.MULTIPLE COLLECTOR DEVICES
• Multiple detectors are aligned parallel.
• Nuclides are measured simultaneously.
• Prerequisite for precise isotopic ratio measurement.
22. PEAK MEASUREMENT
MEASUREMENT VARIABLES:
• Whether it is a continuous or transient signal.
• The temporal length of the sampling event.
• Volume of sample available.
• Number of samples being analyzed.
• Number of replicates per sample.
• Number of elements being determined.
• Detection limits required.
• Precision/accuracy expected.
• Dynamic range needed.
• Integration time used.
23. METHODS OF QUANTITATION
• Quantitative analysis
• Semiquantitative routine
• Isotope dilution
• Isotope ratio
• Internal standardization
24. INTERFERENCES
• Polyatomic Interferences
Minimized by:
1. Optimization of nebulizer gas flow (1.5-1.8ml/min).
2. RF power adjustment (500-800W).
3. Sampling position within plasma.
• Isobaric Interferences
Minimized by:
1. cold plasma technique
2. collision/reaction cell
3. High resolution mass analysers as double focussing magnetic field sector.
• Matrix Interferences
Minimized by: use internal standardization
26. FIELDS OF APPLICATIONS
• Qualitative and Quantitative (simultaneous multi element
analysis).
• Isotope ratio measurement
• Coupling techniques:
Chromatographic system
Laser ablation
27. LC-ICP-MS
Advantages of HPLC ICP-MS as detector
• Wide applicability • Selective for the element
• High resolution • Provide isotopic information
• Rapid analysis • Determination of multiple
• High sensitivity elements simultaneously
• High reproducibility • Universal ,regardless the mode of
• Quantitative chromatography
• Easily automated • Extremely sensitive
• Detection limits in ppt range
28. ABLATION ICP-MS
Analysis of solid sample surfaces
Procedure:
• Laser beam focused onto sample surface in ablation
chamber or cell.
• Miniature plasma above sample ablates material from
surface.
• Resultant particulate material is transported to ICP-MS
with carrier gas stream (e.g. Ar)
• Sample is decomposed, atomised and ionized in ICP
plasma and analyzed in mass spectrometer.
Applications for LA-ICP-MS:
• Monitor distribution of administered drugs among different tissues and body
compartments.
• In-situ analysis of metals and other elements in samples separated using PAGE,
e.g.:
– Au and Pt drug metabolite identification.
– Determine degree of phosphorylation of different separated proteins.
29. PHARMACEUTICAL APPLICATIONS
• Pharmaceutical waste water
• Drug discovery / drug development:
Analysis of individual forms of drug compounds using target element
analysis
Simple metal analysis during development of metal-based drugs
• QA/QC and process development:
National Pharmacopeia (e.g. USP, EP, JP) Testing
Impurity limit tests
Metals in active pharmaceutical ingredients (API)
QC of natural products – toxic impurities
Toxic element impurities (e.g. heavy metals)
• Clinical trials:
Simple metal analysis for active component confirmation
Monitoring of the metabolites of an administered drug
30. • Metal impurities – Leachables from pharmaceutical packaging materials
1. Interaction between formulation and packaging material results in
components migrating into the drug product.
2. These components may be toxic or affect the stability of the drug product
3. Storage conditions impact leaching (heat, UV radiation, storage time)
Typical leachables are:
• Small organic molecules [monomers, excipients, reaction by-products],
• Metal ions and trace elements (e.g. aluminum, cadmium, chromium, copper, lead,
manganese, and zinc)
• Metal ions can affect the stability of the formulation, catalyze the degradation
of the active pharmaceutical ingredient (API) and cause unqualified degrades to
form, or pose a toxicity threat on their own.
31. NEXT GENERATION OF ICP-MS
(NexION 300 ICP-MS Instruments)
• Engineered to deliver a level of stability, flexibility and performance never
before seen in an ICP-MS instrument, PerkinElmer's NexION® 300 is the
first truly significant and revolutionary industry advancement in recent
years.
32. The NexION 300 offers:
• 3 modes of operation (Standard, Collision and Reaction) and can be quickly
switched from 1 mode to another.
• So, every analysis can be performed on the same instrument.
• It's the only ICP-MS that lets you maximize productivity without compromising
sensitivity or performance.
• A single ICP-MS instrument offers both the simplicity and convenience of a
collision cell and the exceptional detection limits of a true reaction cell.
• Stability is optimized by incorporating a unique Triple Cone Interface and
Quadrupole Ion Deflector. Designed to remove an unprecedented level of un-
ionized material (and preventing it from entering the Universal Cell), this
innovative ion path keeps the instrument clean, minimizing drift and eliminating
the need for cell cleanings.
33. Features/Benefits
• Large, accessible sample introduction system
• Low liquid uptake nebulizer
• Free-running RF plasma generator
• Automated X, Y, Z torch positioning
• Patented PlasmaLok® technology
• Fastest scanning quadrupole in the industry
• Quadrupole Ion Deflector
• Triple Cone Interface
• Plasma View window
• Four-stage vacuum system
• Benchtop design
34. APPLICATIONS
• Gold Nanoparticles Reference Materials Using the NexION 300 ICP-MS in
Single Particle Mode.
• Coupling Flow Field Flow Fractionation to ICP-MS for the Detection and
Characterization of Silver Nanoparticles.
• The Determination of Lead in Calcium-Based Antacid and Dietary
Supplements.
• The Determination of Metals in Cosmetics.
• Assuring safety of traditional Chinese herbal medicines by monitoring
inorganic impurities using ICP-MS.
35. CONCLUSIONS
• ICP-MS is excellent detector for HPLC in bioanalysis.
• Orthogonal to other detectors.
• Rapid and efficient method for metabolism studies
/speciation.
• Polyatomic interferences from high matrix samples are a
major challenge.
• Room for instruments improvements.
