The Discovery of Botox
The
discovery of Botox
the wonder product that turns back the clock - happened by accident.
In
the 1820s, a German doctor, Justinus Kerner began experimenting
with Botulinum toxin; a toxic protein produced by the bacterium,
Clostridium botulinum,
which causes botulism (a deadly form of food poisoning, that
thrives in home-canned food and has caused many deaths through
the centuries).
But
Kerner wanted to make use of the bacterium's muscle-weakening
qualities for therapeutic use. His work laid the foundation
for the discovery that the toxin could be used to relieve muscle
spasms -specifically, by blocking the release of acetylcholine,
a neurotransmitter that tells muscles when to contract.
Inspired
by this discovery, a dermatologist and ophthomologist, Alistair
and Jean Carruthers, began injecting patients mainly for muscular
disorders of the eye, and the results were successful.
When her assistant suggested she inject her pronounced frown
area, between the eyebrows, above the nose (referred to as 'glabellar
lines'). A phenomenon was born.
At
first people were horrified that a poison would be used to take
away their wrinkles. What were the risks? What needs to be clarified
is that you're injecting a product
of the botulism bacterium in the same way that
penicillin is a product of a mold.
Most antibiotics are natural products of other micro-organisms,
and Botox is no different.
The Treatment Approved
In
1989 the U.S. Food and Drug Administration had approved Botox®
for treatment of crossed eyes and uncontrollable
blinking (Blepharospams) and in 2000 for a neurological
movement disorder known as cervical
dystonia. In 2002 it was approved for a single
cosmetic procedure: reduction of glabellar lines (frown lines).
Botox® works for three to six months depending on the dosage
and physiology. But in tiny quantities, the toxin acts as a
muscle-relaxing agent by blocking the release of acetylcholine
in the nerve endings. It is administered by units, each equaling
precisely the dose it takes to kill a mouse. A typical cosmetic
treatment is 20 units per 'site'. Although, treating glabellar
lines constitutes the only cosmetic use indicated by the FDA
and Allergan, doctors routinely inject other facial areas: crow's
feet around the eyes, laugh lines, and creases near the nose.
Once injected, practitioners contend, the toxin 'spreads' by
no more than a quarter-inch.
Products
And Uses
Botox®
for aesthetic use is marketed as Botox/Botox
Cosmetic or Vistabel®
depending on the country of approval.
As
of March 2006,
Botox® from
Allergan, Inc. (Irvine, Calif., U.S.) received approval in the
U.K. for cosmetic use (glabellar/frown lines) and will be marketed
as Vistabel®,
following in the footsteps of other European countries including
France, Italy, Spain, Switzerland and most recently Germany
as well. Botox® or Vistabel® has cosmetic approval in
30 countries worldwide.
Another
development that is heating up among neurotoxins, is the introduction
of Xeomin®
(Merz Pharmaceuticals), another botulinum toxin type A, currently
approved across Europe for blepharospams
(a debilitating condition that causes patients to have uncontrolled
eyelid twitching and blinking) and cervical
dystonia (sustained contractions cause abnormal
posture of the head and neck, while periodic spasms produce
jerky head movements. The severity may vary from mild to severe.)
Xeomin was introduced in Germany in July 2005. There is also
an assortment of preparations from China and Korea flooding
the market.
Myobloc® from
Solstice Neurosciences (Malvern, Pa., U.S.) which is botulinum
toxin type B is currently approved in the U.S. and Canada for
the treatment of cervical dystonia.
It is marketed in Austria, France, Germany, Ireland, Italy,
Portugal, Spain and United Kingdom as NeuroBloc®.
Although considered effective, it has a more rapid onset of
action and a shorter duration of effect and is not widely used
for cosmetic uses.