Sonics VC40 User Manual

USER’S GUIDE

HIGH INTENSITY ULTRASONIC

PROCESSOR

40 Watt Model

TABLE OF CONTENTS

Important Safeguards

SECTION 1 – INSTALLATION

Inspection
Electrical Requirements
Installing the Ultrasonic Processor

SECTION II – OPERATION

Principles of Ultrasonic Disruption
Functions of Controls, Indications, and Connectors
Preparations for Use
Tuning
Using the Ultrasonic Processor

SECTION III – SERVICE INFORMATION

Return of Equipment

SECTION IV – OPERATING SUGGESTIONS AND TECHNIQUES

The Ultrasonic Processor supplied with this instruction manual is constructed of the finest
material and the workmanship meets the highest standards. It has been thoroughly tested
and inspected before leaving the factory and when used in accordance with the
procedures outlined in this manual, will provide you with many years of safe and
dependable service.

Rev. 2003

IMPORTANT SAFEGUARDS

WARNING or CAUTION

READ BEFORE INSTALLING OR

USING THE EQUIPMENT

Your Ultrasonic Processor has been designed with safety in mind. However, no design
can completely protect against improper usage, which may result in bodily injury and/or
equipment damage. Please observe the following warnings at all times, read the operating
instructions carefully before operating the equipment, and retain this instruction manual
for future reference. If the Ultrasonic Processor is used in a manner contrary to that
specified in this instruction manual, the protection features designed into the unit may be
impaired.

When mounting the probe, always clamp the upper portion of the converter housing.

Never clamp the probe.

Make sure the Ultrasonic Processor is properly grounded via a 3-prong outlet.
High voltage is present in the power supply. Do not remove the cover. Refer all

servicing to qualified service personnel.

To avoid electric shock, disconnect the electrical power cord before removing the

cover prior to servicing.

Never operate the power supply unless it is connected to the converter.
Never secure anything to the probe, except at the nodal point (point of no activity).
Never touch a vibrating probe.
Never allow a microtip to vibrate in air for more than 10 seconds.
It is recommended that a sound abating enclosure or ear protection be used when

operating the Ultrasonic Processor.

2

Where you see this alert symbol and WARNING or

CAUTION heading, strictly follow the warning instructions

to avoid personal injury or equipment failure.

WARNING

SECTION 1 – INSTALLATION

INSPECTION

Prior to installing the Ultrasonic Processor, perform a visual inspection to detect any
evidence of damage, which might have occurred during shipment. Before disposing of
any packaging material, check it carefully for small items.

The Ultrasonic Processor was carefully packed and thoroughly inspected before leaving
our factory. The carrier, upon acceptance of the shipment, assumed responsibility for its
safe delivery. Claims for loss or damage sustained in transit must b e submitted to the
carrier.

If damage has occurred, contact your carrier within 48 hours of the delivery date. DO

NOT OPERATE DAMAGED EQUIPMENT. Retain all packing materials for future

shipment.

ELECTRICAL REQUIREMENTS

The Ultrasonic Processor requires a fused, single phrase 3-terminal grounding type
electrical outlet capable of supplying 50/ 60 Hz at 100 volts, 115 volts, 220 volts, or 240
volts, depending on the voltage option selected. For power requirements, check the label
on the back of the unit.

For your personal safety, do not, under any
circumstances, defeat the grounding feature of the

power cord by removing the grounding prong.

3

INSTALLING THE ULTRASONIC PROCESSOR

The Ultrasonic Processor should be installed in an area that is free from excessive dust,
dirt, explosive and corrosive fumes, and extremes of temperature and humidity.

SECTION II – OPERATION

PRINCIPLES OF ULTRASONIC DISRUPTION

The ultrasonic power supply converts 50/60 Hz line voltage to high frequency electrical
energy. This high frequency electrical energy is transmitted to the piezoelectric
transducer within the converter, where it is changed to mechanical vibrations. The
vibrations from the converter are intensified by the probe, creating pressure waves in the
liquid. This action forms millions of microscopic bubbles (cavities) which expand during
the negative pressure excursion, and implode violently during the positive excursion.
This phenomenon, referred to as cavitation, creates millions of shock waves in the liquid,
as well as elevated pressures and temperatures at the implosion sites. Although the
cavitational collapse last but a few microseconds, and the amount of energy released by
each individual bubble is minute, the cumulative effect causes extremely high levels of
energy to be released into the liquid. The larger the probe tip, the larger the volume that
can be processed but at a lesser intensity. For information regarding the processing
capability of each probe, consult the tables below.

4

FUNCTIONS OF KEYS, CONTROLS, INDICATORS, AND CONNECTORS

ON / OFF SWITCH ON position – energizes the power supply.
POWER INDICATOR Illuminates when the power supply is energized.
OUTPUT CONTROL Controls the amplitude of vibrations at the probe tip.

POWER MONITOR

TUNE CONTROL

20-40 POWER MONITOR
SCALE SELECT SWITCH

FOOTSWITCH CONNECTOR Connects to footswitch cable.
PROBE CONNECTOR Connects to converter / probe assembly
POWER CORD – Rear Panel - Connects to power supply to electrical outlet.
FUSE(S) – Rear Panel - Protects against electrical overload.

Indicates in watts the amount of ultrasonic power delivered to the
probe.
Optimizes power supply performance by tuning the power supply to the
converter / probe assembly.
In the 20 position the POWER MONITOR indicates the percentage of
ultrasonic power delivered to the probe up to 20 watts.
In the 40 position the POWER MONITOR indicates the percentage of
the ultrasonic power delivered to the probe up to 40 watts.

5

CAUTION

CAUTION

Never place a washer between the probe and the converter.

Never apply grease to the mating surfaces or threads of the converter, probe, or

NOTE

Never grip the converter in the vise. Using a wrench, twist the converter off the

PREPARATION FOR USE

Do not operate an Ultrasonic Processor that has been in a very cold or hot
environment for a prolonged period of time. Wait until it has reached room

temperature

1. Ensure that the AMPLITUDE is set to OFF.

2. Plug the electrical line cord into the electrical outlet.

3. If the optional footswitch is used, insert the plug into the jack located on the rear

panel. Make sure that the plug is inserted forcefully all the way in.

4. If the converter / probe assembly is not already assembled; using the wrenches

provided, screw securely the probe into the converter.

microtip.

5. Mount the converter / probe assembly in a laboratory stand, secure the clamp to the

upper section of the converter housing only. Do not secure the clamp to any other
portion of the converter / probe assembly.

6. Connect the converter cable to the power supply.

Should it become necessary to remove a probe, use the wrenches supplied. If the
probe has been attached to the converter for a long period of time it might be
necessary to use a vise. Be sure the vise has soft jaws or other means to prevent
scratching. Secure the wide diameter portion of the probe in the jaws of the vise.

probe. A tap of a hammer may be applied to the end of the wrench. Never attempt
to remove the probe by twisting the converter housing, as this may damage the
electrical connections within the housing.

TUNING

CAUTION

The power supply should be tuned after the probe has reached operating temperature. When working with

Tune the power supply in accordance with the following procedures each time a new
converter or probe is used.

1. Ensure that the probe is not immersed in the liquid and that it does not come

in contact with anything.

2. Set OUTPUT CONTROL TO “60”.

3. Set 20-40 POWER MONITOR SCALE SELECT SWITCH to “20”.

4. Set POWER SWITCH to ON, and rotate the TUNE CONTROL clockwise or

counterclockwise until minimum (not maximum) reading (usually less than

30) is obtained on the POWER MONITOR. If minimum reading cannot be
obtained, make certain that the probe is tight. A loose probe will usually
generate a loud piercing sound.

5. Repeat step 4 with OUTPUT CONTROL set to “100”.

6. Set OUTPUT CONTROL to “60”.

7. Set POWER SWITCH to OFF.

low or high temperature liquids, immerse the probe in the liquid for a few minutes, withdraw the probe
out of the liquid, and then, tune the power supply.

Ensure that the optional micro cup horn does not contain any liquid when tuning the power supply.

7

The speed control on an automobile, can, to a certain extent, be compared to an

Ultrasonic Processor. The speed control is designed to maintain the vehicles rate of

ower requirements. The speed

control senses these requirements, and automatically adjusts the amount of power

delivered by the engine in order to compensate for these ever changing conditions.

tance to the movement of

the vehicle, the greater the amount of power that will be delivered by the engine to

The Ultrasonic Processor is designed to deliver constant amplitude. As the

reases, additional power will be delivered

by the power supply to ensure that the excursion at the probe tip remains constant.

Using a more powerful power supply will not deliver more power into the liquid.

he probe that determines how much

The AMPLITUDE control allows the ultrasonic vibrations at the probe tip to be set

to any desired level. Although the degree of cavitation required to process the

y be determined by visual observation, the amount of power

required cannot be predetermined. A sensing network continuously monitors the

output requirements, and automatically adjusts the power to maintain the amplitude

ter the resistance to the movement of the probe due

to higher viscosity, deeper immersion of the probe into the sample, larger probe

diameter or higher pressure, the greater the amount of power that will be delivered to

trol fully clockwise will not cause the

maximum power to be delivered to the sample. The maximum power that the

Ultrasonic Processor is capable of delivering will only be delivered when the

ered by

USING THE ULTRASONIC PROCESSOR

travel constant. As the terrain changes, so do the p

The greater the terrain rate of incline and greater the resis

overcome that resistance.

resistance to the movement of the probe inc

Rather, it is the resistance to the movement of t
power will be delivered into the sample.

sample can readil

at the preselected level. The grea

the probe. Setting the AMPLITUDE con

resistance to the movement of the probe is high enough to draw maximum wattage.

This phenomenon can be demonstrated as follows: depress the probe down against a
piece of wood. The greater the down pressure, and consequent greater resistance to
the movement of the probe, the greater the amount of power that will be deliv

the power supply.

8

CAUTION

IMPORTANT

without showing up on the wattmeter. The smoother and shinie

Do not operate the power supply unless it is connected to the converter.
Never allow a microtip to vibrate in air for more than 10 seconds.
Do not allow the vibrating probe to come in contact with anything but the sample.

1. Ensure that the power supply is properly tuned.

2. Immerse the probe ½” (1 cm) into the liquid.

3. Set POWER SUPPLY to ON, if footswitch is used, depress footswitch. To use the

TIMER, select the time sequence desired, set TIMER ON/OFF switch to ON, and
depress TIMER START BUTTON. To energize the PULSER, select the pulse
duration desired.

4. Using OUTPUT CONTROL increase or decrease intensity as required.

Proper care of the probe is essential for dependable operation. The intense cavitation will,
after a prolonged period of time, cause the tip to erode, and the power output to decrease

be transmitted into the sample. Any erosion of the probe tip will increase the rate of future
erosion. For that reason it is recommended that after every 5 or 6 hours of use the tip be
examined, and if necessary, polished with emery cloth or an abrasive wheel. Since the probe
is tuned to vibrate at a specific frequency, it is most important that only the contaminated
surface be removed. This procedure can be repeated as long as the wattmeter reads less than
20 watts with the probe out of the sample, when the AMPLITUDE control is set at 100. If

the wattmeter reads over 20 watts the probe or replaceable tip should be changed.

9

r the tip, the more power will

SECTION III – SERVICE INFORMATION

Your Ultrasonic Processor was designed to provide you with years of safe and
dependable service. Nevertheless, because of component failure or improper usage, the
possibility does exist that it might not perform as it should, or that it will stop working all
together. The most probable causes for malfunction are listed below and should be
investigated.

The unit was plugged into an electrical outlet that provides a different voltage from that

required. See Electrical Requirements.

The probe is not secured properly.
If the probe has a replaceable tip, the tip is not secured properly, or the probe has been

used with low surface tension liquids.

A fuse(s) has failed. If a fuse(s) has failed, proceed as follows:

1. Ensure that the power switch is set to OFF.

2. Open the fuse holder cover(s).

3. Replace the fuse(s).

4. Set the AMPLITUDE control to 50 and the power switch to ON. With the probe

in air (out of sample), the wattmeter should read below 20 watts. If the reading
exceeds 20 watts, set the power switch to OFF, and disconnect the probe from the
converter.

5. Set the power switch back to ON. If the wattmeter reads below 20 watts, the

probe has failed or is out of tune due to excessive erosion, and should be replaced.
If the wattmeter reads above 20 watts, either the converter or power supp ly has
failed and the complete Ultrasonic Processor should be returned for repair.

10

IMPORTANT

NY BIOHAZARDOUS OR RADIOACTIVE MATERIAL AND ARE

RETURN OF EQUIPMENT

It is suggested that an Ultrasonic Processor in need of repair be sent back to the factory.

In order to receive prompt service; always contact the factory before returning any
instrument. Include date of purchase, model number and serial number. For instruments
not covered by the warranty, a purchase order should be forwarded to avoid unnecessary
delay. Care should be exercised to provide adequa te packing to insure against possible
damage in shipment. The Ultrasonic Processor should be sent to the “Service
Department” with all transportation charges prepaid and return of shipment indicated.

Please obtain a Return Authorization Number prior to re turning the instrument.

I CERTIFY THAT THE ULTRASONIC PROCESSOR AND / OR ACCESSORIES RETURNED
FOR REPAIR ARE FREE OF A
SAFE FOR HANDLING.

DO NOT RETURN ANY EQUIPMENT UNLESS SUCH CERTICATION CAN BE MADE.

11

OPERATING SUGGESTIONS AND TECHNIQUES

DISRUPTING CELLS

The disruption of cells is an important stage in the isolation and preparation of
intracellular products. From research levels through to production, many areas of
biotechnology, particularly recombinant technology, necessitate the use of ultrasonics for
cell disruption. Although some biological products are secreted from the cell or released
during autolysis, many others require sonication to release intracellular material. Cell
disruption focuses on obtaining the desired product from within the cell, and it is the cell
wall that must be disrupted to allow cell contents extraction.

Single-cell organisms (micro-organisms) consist of a semipermeable, tough, rigid outer
cell wall surrounding the protoplasmic membrane and cytoplasm. The cytoplasm is made
up of nucleic acid, protein, carbohydrates, lipids, enzymes, inorganic ions, vitamins,
pigments, inclusion bodies, and about 80% water. In order to isolate and extract any of
these substances from inside the cell, it is necessary to break the cell wall and
protoplasmic membrane. In some cases the cell may excrete the desired substance
without assistance, but in most cases, the cells must be lysed and sonicated in order for
these substances to be released. Breaking cell membranes and releasing the contents
present significant challenges. The process must be fast and thorough to maximize the
protein yield. Because the energy applied must be great enough to break the cell
membranes or walls, yet gentle enough to avoid physically or chemically damaging cell
contents, the Vibra-Cell with its variable intensity capability is ideally suited for this
application.

The level of intensity that should be used is application dependent. For example high
intensity might be recommended for the break up of cells, but should never be used when
the release of intracellular components might be objectionable e.g. Organelle isolation.

The ability to control the amplitude at the probe tip is a prerequisite for process
optimization. And because each application requires its own set of processing parameters,
due to variation in volume and composition, the optimum amplitude can only be
determined empirically. When processing a new sa mple, it is recommended that the
amplitude be set first at 50% (30% with a microtip) and then increased of decreased as
required.

Yeast, gram-positive bacteria, and to a lesser extent, gram-negative bacteria have
considerably harder cell walls in comparison to animal cells, and require relatively high
power for cell disruption.

Gram negative bacteria typically require 10 to 15 minutes of processing, while
staphylococcus requires 20 to 30 minutes.

12

Microorganisms differ greatly in their sensitivity to ultrasonic disintegration. For
example, the most readily disintegrated are the rod-like forms (bacilli), while the
spherical organisms (cocci) are much more resistant. The group Mycobacteria, to which
the tuberculosis organism belongs, is particularly difficult to disrupt. Generally, animal
cells are more easily disintegrated that plant cells, and red blood cells are more readily
disintegrated than muscle cells because they lack a protective cell wall.

Cellular disruption is the first step in RNA isolation and one of the most critical steps
affecting yield and quality of the isolated RNA. Typically, cell disruption needs to be fast
and thorough. Slow disruption, for example placing cells or tissue in guanidinium
isothiocyanate (GITC) lysis solution for a long t ime prior to sonication, may result in
RNA degradation by endogenous RNases released internally. This is especially a concern
when working with tissues high in endogenous RNase such as spleen and pancreas.

Disrupting frozen tissue is more time consuming a nd cumbersome that processing fresh
tissue, but freezing samples is sometimes necessary. Samples are usually frozen when, 1)
they are collected over a period of time and thus, cannot be processed simultaneously; 2)
there are many samples, 3) samples are co llected in the field, or 4) mechanical processing
of fresh samples is insufficient for thorough disruption. A mortar and pestle or bag and
hammer are typically used when the starting material is frozen. RNA will remain intact in
tissues for a day at 37ºC, a week at 25ºC a month at 4ºC and indefinitely at subzero
temperatures.

Ultrasonic processing will typically cause the temperature of the sample to increase
especially with small volumes. Since high temperatures inhibit cavitation, the sample
temperature should be kept as low as possible - preferably just above its freezing point.
This can be accomplished by immersing the sample vessel in an ice-salt-water bath.
Temperature elevation can also be minimized by using the pulser.

Increasing hydrostatic pressure (typically 15-60 psi) and viscosity can enhance cell
disruption. For microorganisms, the addition of glass beads in the 0.5 to 1mm size range
promotes cell disruption. Beads are almost a prerequisite when working with spores and
yeast. A good ratio is one volume of beads to two volumes of liquid. Glass beads are
available from Cataphote, Inc. P.O. Box 2369, Jackson, Mississippi 39225-2369 USA,
phone [phone] or [phone], FAX [phone], Jayco Inc. 675 Rahway
Ave., Union NJ 07083 USA, phone [phone], FAX [phone] or Sigmund
Lindner GmbH. P.O. Box 29. D-95483 Warmensteinach, Germany. Phone [phone]
94 10, FAX [phone].

When processing difficult cells such as yeast, pretreatment with an enzyme is beneficial.
Lysozyme, byaluronidase, glycosidase, glucalase, lyticase, zymolase and lysostaphin
digestion are among the enzymatic methods frequently used with yeast and Lysozyme
with bacteria. Enzymatic treatment is usually followed by sonication in a GITC lysis
buffer. Collogenase may be used with collogen, lysostaphin with staphylococcus, and
trypsin hyaluronidase with liver and kidney.

13

If enzymes cannot be used, the following procedures should be considered: Freezing the
sample at -70?C overnight, then thawing it in water immediately prior to ultrasonic
processing.

Most animal tissues can be processed fresh (unfrozen). It is important to keep fresh tissue
cold and to process it quickly (within 30 minutes) after dissection. When working with
fresh tissue, the cells must be sonicated immediately at the time the GITC lysis solution is
added. This can be done by dispensing the lysing solution in the tube, adding the tissue
and immediately sonicating. Samples should never be left sitting in lysis solution,
undisrupted. Large samples of hard tissues should be first treated in a blender or a
mechanical homogenizer.

Animal tissues that have been frozen after collection should be disrupted by grinding in
liquid nitrogen with a mortar and pestle. During this process, it is important that the
equipment and tissue remain at cryogenic temperatures. The tissue should be dry and
powdery after grinding. Grinding should be followed by thorough sonication in a GITC
lysis buffer. Processing frozen tissue in this way is cumbersome and time consuming, but
effective.

Cultured cells are normally easy to disrupt. Cells grown in suspension are collected by
centrifugation, rinsed with PBS to remove culture medium, and then lysed by sonicating
in a GITC lysis buffer. Placement of the vessel on ice while washing and lysing the cells
will further protect the RNA from endogenous RNases released during the disruption
process.

Soft, fresh plant tissue can often be disrupted by sonicating in a lysis buffer. Other plant
tissues, like pine needles, need to be ground dry, without liquid nitrogen. Some hard,
woody plant materials require freezing and grinding in liquid nitrogen prior to being
ultrasonically processed. Plant cell suspension cultures and calluses can typically be
sonicated in a lysis buffer within 2 minutes. The diversity of plants and plant tissue make
it impossible to give a single recommendation for all. However, most plant tissues
typically contain polysaccharides and polyphenols that can coprecipitate with RNA and
inhibit downstream assays. Treating a plant tissue lysate with polyvinylpyrrolidone
(PVP) will precipitate such problematic components from the lysate before the actual
RNA isolation is carried out.

Whenever possible, the tissues should be diced very small to permit movement within the
liquid. Tough tissues such as skin and muscle should be macerated first in a blender or
the like for about 10 seconds, and confined to a small vessel during ultrasonic treatment.
If sub-cellular particles are desired intact, the amplitude should be kept low, and the
processing time increased.

Yeast can be extremely difficult to disrupt because their cell walls may form capsules or
nearly indestructible spores. To process yeast, sonicate in a tube containing the sample,
guanidinium-based lysis buffer and small glass beads (0.5 – 1 mm). Pretreatment with

14

zymolase, glucalase and / or lyticase to produce spheroplasts that are readily lysed may
also be useful.

To disrupt filamentous fungi, scrape the mycelial mat into a cold mortar, add liquid
nitrogen and grind to a fine powder with a pestle. The powder can then be thoroughly
sonicated in lysis buffer to solubilize completely. As fungi may also be rich in
polysaccharides, pretreatment with polyvinylpyrrolidone (PVP) may be beneficial.

Bacteria, like plants, are extremely diverse; therefore, it is difficult to make one
recommendation for all bacteria. Ultrasonic processing will lyse most Gram positive and
Gram negative bacteria, including mycobacteria. Although it is recommended that glass
beads and lysis solution be used; it is possible to lyse some Gram negative bacteria by
sonicating in lysis solution without beads. Bacteria cell walls can be digested with
lysozyme to form spheroplasts. Gram positive bacteria usually require more rigorous
digestion and longer processing time. The spheroplasts are then lysed with sonication in
GITC lysis buffer.

Disruption of cells found in soil and sediments is accomplished one of two ways. One
technique isolates the bacterial cells from the material prior to the RN A isolation
procedure. This is accomplished by homogenization of wet soil in a mechanical blender
followed by a slow speed centrifugation to remove fungal biomass and soil debris. The
supernatant is centrifuged again at a higher speed to pellet the bacteria cells. Cells can
then be lysed as described above for bacteria. Other techniques describe RNA isolation
from the soil or sediment directly. For example, one method requires soil to be added to a
diatomaceous earth and lysis buffer, and then sonicated. The sample is then centrifuged
to remove solid debris.

Always immerse the probe deep enough below the surface of the sample to inhibit
aerosoling or foaming, foaming substantially reduces cavitation. Processing at a lower
power setting without foam is much more effective than processing at a higher power
setting with foam. Decreasing the power, increasing processing time and lowering the
temperature of the sample will usually prevent aerosoling and foaming. Do not use any
antifoaming agents or surfactants.

During cavitation, free radicals are formed which, if they are allowed to accumulate, can
greatly affect the biological integrity of the sample by reacting with proteins,
polysaccharides, or nucleic acids. Although during short periods of processing their
formation is not normally considered a problem; for longer durations, the addition of free
radical scavengers such as, carbon dioxide, N2O, cysteine, reduced glutahione,
dithiothreitol or other SH compounds, might be beneficial. Saturating the sample with a
protective atmosphere of helium or nitrogen gas, or dropping a small pellet of dry ice in
the sample, will also inhibit free radical formation. Whereas it is true that gas is required
for effective cellular disruption, it is not necessary that the vapor phase be oxygen or air
since any gas except carbon dioxide will work just as well.

15

Various methods can be used to measure the efficiency of the disruption. For example, a
visual count can be made using a microscope.
For greater accuracy, a protein assay could be used. This procedure is widely recognized
as a good method for measuring cell disruption by taking into account the amount of
protein released after disruption. The disrupted cells are then tested and checked against
this number for percentage bre akage.
There are several types of protein assays. One commonly used is the Folin Reaction
(Lowry Assay) method, as it is comparatively simple and provides consistent results.
This colorimetric method has a sensitivity to protein of around 8 µg / mL in the assay
solution.
The assay turns blue in the presence of proteins due to the reaction of copper ions in the
alkaline solution with protein and the reduction of phosphomolybdate- phosphotungstic
acid in the Folin reagent by aromatic amino acids in the treated protein.
Fractional protein release, Rp, is calculated using the following equation and multiplying
the result by 100:

Rp = Cf – Cb

Ct – Cb

Cf = Free protein
Ct = total protein
Cb = Background protein

This gives the actual disruption percentage, taking into account the background levels of
protein before disruption.

Since the greatest concentration of energy is beneath the probe, it is imperative that the
sample be kept as close to the tip as possible, liquids are easily processed because the free
moving cells circulate repeatedly below the probe. Solid materials however have a
tendency to be repelled by the ultrasonic, and should be processed in a vessel large
enough to accommodate the probe, yet small enough to restrict sample movement. For
small samples, conical shaped test tubes are recommended.

Allowing the probe to contact the vessel will decrease the power output, and cause
minute grey glass particles to migrate into the sample. Although these glass particles will
not adversely affect the chemical composition of the sample, they will form a thin grey
layer on centrifuging. If the probe has to come in contact with a solid sample, use a
standard 20mm (3/4”) diameter stainless steel centrifuge tube cut to 70mm (3”) length.
Do not use a glass tube. Microtips must never allowed to come in contact with anything
but the liquid, because the stress resulting at the point of contact with a hard surface will
cause the microtip to fracture. Although larger probes will not fracture if they co me in
contact with a glass vessel, they may cause the vessel to fracture.

Before each application, place the tip in water or alcohol and energize the power supply
for a few seconds to remove any residual substances. If concerned about contamination
from previous use, clean the probe with a 20% Virkon solution and rinse with distilled
water. For critical application, probes may be autoclaved.

16

To inhibit sample loss in test tube due to sticking, siliconize the test tube as follows:
Wash and dry the test tub e thoroughly, coat with silicone, then air dry. “Sigmacote”
manufactured by Sigma Chemical Co., 3050 Spruce Street, St. Louis, Missouri 63103,
USA, phone [phone], is ideally suited for that purpose.

High viscosity and concentration are problematic . 2,000 cps and 15% concentration by
weight are maximum limits. Because with ultrasonics the sound waves are propagated
through the sample, if the sample is so thick that it will not pour or circulate easily, it is
too thick for ultrasonic processing.

Use the Cup Horn for processing pathogenic, radioactive, and biohazardous materials in
complete isolation without probe intrusion. Because plastic tubes have a tendency to
absorb vibrations, it is preferable, whenever possible, to contain the sample in a stainless
steel tubes or glass tubes when working with a cup horn. To expedite processing, add
glass beads to the sample. If desired, crushed ice can also be added to the water inside the
cup horn, in order to optimize cooling. Processing samples in a Cup Horn will usually
take 4 times longer than processing with the direct probe intrusion method

17