Research
Roundup
Surfactant
Curtails Nanotube Clumping in
Water
Scientists
have long touted carbon nanotubes as a futuristic means of delivering
drugs, fortifying brittle materials and conducting current in miniaturized
circuits. But attempts to introduce actual nanotubes into these roles
have often been stopped in their tracks by the slender filaments' stubborn
and unhelpful tendency to clump together in solution.
Now
scientists at Penn have found that
a readily available chemical, a surfactant
called sodium dodecylbenzene sulfonate
(NaDDBS), disperses nanotubes in water
with remarkable efficiency. The discovery,
described in a paper published in
January in the journal Nanoletters,
represents an important step towards
wider applications of nanotubes.
"Scientists
have suggested many possible applications
for carbon nanotubes, but tube aggregation
in solution has obstructed progress," said
lead author Dr. Mohammad F. Islam,
a postdoctoral researcher in Penn's
Department of Physics and Astronomy. "This
new approach improves our ability
to manipulate single tubes. Single
nanotubes can now participate in controlled
self-assembly, form fibers and composites,
and serve as microfluidic sensors
in water."
When
Dr. Islam and senior author Dr. Arjun
G. Yodh, professor of physics, added
NaDDBS to a cocktail of water and
nanotubes, the surfactant adhered
weakly to the nanotubes, preventing
the tubes from clinging to one another.
Dr. Islam, Dr. Yodh and colleagues
determined that NaDDBS increased the
concentration of single carbon nanotubes
in water up to 100-fold. Even at high
concentrations, roughly 63 percent
of nanotubes in aqueous solution remained
unbound.
"Sodium
dodecylbenzene sulfonate is pretty
non-invasive, so we expect that the
nanotubes' unique electronic, thermal,
optical and mechanical properties
will be preserved in suspension," said
Dr. Yodh. "An added bonus of
our complete solubilization approach
is that it is gentle. Mixing this
particular surfactant with nanotubes
and water in a low-power, high-frequency
sonicator, as we did, resulted in
very little breakage of the nanotubes,
which has been a problem with other
treatments."
Carbon
nanotubes tend to cling together because
they are subject to substantial van
der Waals attractions. While researchers
have explored numerous surfactants
to counter this attraction, Dr. Islam
and Dr. Yodh suggest that NaDDBS's
benzene ring, together with its long
alkane tail and charge group, conspire
to produce an unusual molecular arrangement
on the nanotube surface that reduces
aggregation.
Drs.
Islam and Yodh were joined on the Nanoletters paper
by co-authors Dr. Enrique Rojas, Dr.
D.M. Bergey and Dr. Alan T. "Charlie" Johnson,
all of the Department of Physics and
Astronomy and LRSM. The research was
funded by the NSF, NASA and the Petroleum
Research Fund.
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Dogs
Fed a Reduced-Calorie Diet Live
Longer
A
14-year study of canine diet and health has found that dogs fed a calorie-restricted
diet live a median 1.8 years longer than dogs allowed to eat more and
are slower to develop chronic diseases such as osteoarthritis.
The
findings add to the growing body of
evidence that caloric restriction
in a wide range of species significantly
boosts longevity. Dogs are the only
large mammals--and the closest human
relatives-- for which a diet-restriction
study has been completed. Similar
studies involving primates are ongoing.
The
results, from scientists at Penn's
School of Veterinary Medicine, Nestle
Purina PetCare Company, University
of Illinois, Cornell University and
Michigan State University, were the
subject of a September symposium in
St. Louis. Partial results were published
last May in the Journal of the
American Veterinary Medical Association.
The
study involved 48 labrador retrievers
from seven litters. Littermates were
paired, with one dog fed 25 percent
fewer calories than its sibling starting
at 8 weeks of age. The researchers
found a median life span of 13 years
among dogs whose food intake was reduced,
while dogs in the group fed a diet
higher in calories were uniformly
overweight and had a median life span
of 11.2 years.
"Impressive
as they are, the life span figures
are only part of the story," said
Dr. Gail K. Smith, professor of orthopedic
surgery at Penn and chair of the Department
of Clinical Studies at the School
of Veterinary Medicine. "The
study also showed that lean body conformation
forestalls some chronic illnesses,
most notably osteoarthritis, and that
diet can either mitigate or exacerbate
the expression of genetic diseases.
"This
study should reinforce for dog owners
the importance of keeping their dogs
lean, with palpable ribs and an obvious
waistline," Dr. Smith said. "Avoid
giving dogs too many high-calorie
treats and consider a brand of balanced
dog food formulated to be low in caloric
content while providing a sense of
satiety."
"Dogs
in the calorie-restricted group didn't
require treatment for osteoarthritis
until a mean age of 13.3 years, fully
three years later than the dogs in
the control group," Smith said. "Because
osteoarthritis is painful, this deferral
represents a substantial boost in
quality of life."
Dr.
Smith was joined in the study, funded
and conducted by Nestle Purina PetCare,
by Darryl N. Biery at Penn; Richard
D. Kealy, Dennis F. Lawler and Joan
M. Ballam at Nestle Purina; Elizabeth
H. Greeley and Mariangela Segre at
Illinois; George Lust at Cornell;
and Howard D. Stowe at Michigan State.
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"Jumping
Genes" May Aid in Discovery
of Gene Function
Researchers
at Penn's School of Medicine have bred a mouse to model human L1 retrotransposons,
the so-called "jumping genes." Retrotransposons are small stretches
of DNA that are copied from one location in the genome and inserted elsewhere,
typically during the genesis of sperm and egg cells. The L1 variety of
retrotransposons, in particular, are responsible for about one third of
the human genome.
The
mouse model of L1 retrotransposition
is expected to increase our understanding
of the nature of jumping genes and
their implication in disease. According
to the Penn researchers, the mouse
model may also prove to be a useful
tool for studying how a gene functions
by knocking it out through L1 insertion.
Their report was in the December,
2002 issue of Nature Genetics.
"There
are about a half million L1 sequences
in the human genome, of which 80 to
100 remain an active source of mutation," said
Dr. Haig H. Kazazian, Jr., chair of
the Department of Genetics and senior
author in the study. "This animal
model will help us better understand
how this happens, as well as provide
a useful tool for discovering the
function of known genes."
In
humans, retrotransposons cause mutations
in germ line cells, such as sperm,
which continually divide and multiply.
Like an errant bit of computer code
that gets reproduced and spread online,
retrotransposons are adept at being
copied from one location and placed
elsewhere in the chromosomes. When
retrotransposons are inserted into
important genes, they can cause disease,
such as hemophilia and muscular dystrophy.
On the other hand, retrotransposons
have been around for 500 to 600 million
years, and have contributed a lot
to evolutionary change.
For
some time, researchers have been trying
to understand how retrotransposons
affect the genome and, in addition,
what science may learn from the techniques
they employ. According to Dr. Kazazian
and his colleagues, the mouse model
displays high-frequency chromosome
to chromosome retrotransposition of
human L1s, which behave in exactly
the same way as they do in humans.
While the current tissue culture model
works well, it does not mimic the
way retrotransposons jump in chromosomes.
The
researchers believe that by understanding
the mechanics of retrotransposition,
they might be able to use similar
techniques for genetic therapies in
humans. They also hope to learn more
about the basic mysteries behind retrotransposition,
such as why L1 retrotransposons only
seem to effect the germ line and not
any other type of cell in the body.
Funding
for this research was provided by
grants from the NIH.
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Optimism
in HIV-Positive Patients May
Lead to Risky Moves
New
study findings suggest that HIV-positive patients who believe they will
live for many years are more likely to miss medication doses and to not
practice safe sex than their peers who are less hopeful. Optimism can
often help patients cope with a medical condition; but these findings
indicate that in the context of HIV, there can be negative consequences
to a positive outlook, according to Dr. William C. Holmes, assistant professor
of medicine and epidemiology, and medical student Joseph L. Pace.
The
authors surveyed 220 HIV-positive
people about their backgrounds, disease
history, attitude about their illness
and health behaviors. The investigators
found that people were more likely
to use negative words about being
HIV-positive when they were first
diagnosed than at the time they completed
the surveys. Most of the patients
said they thought they would live
for many years, and 27 percent said
they expected to reach old age. White
respondents, those with less education,
and patients with relatively low levels
of CD4 cells were less likely to hold
out hope for the future.
Those
patients who said they were relatively
optimistic about the future were twice
as likely as those with relatively
pessimistic outlooks to sometimes
forget to take their medications,
and they were almost twice as likely
to report not practicing safe sex.
About 26 percent of optimists and
13 percent of pessimists occasionally
forgot to take their medications;
57 percent of optimists and 29 percent
of pessimists said they did not always
practice safe sex.
The
full report, "HIV-Seropositive
Individuals' Optimistic Beliefs About
Prognosis and Relation to Medication
and Safe Sex Adherence" was published
in the September issue of the Journal
of General Internal Medicine.
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