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BIONX®PRO
Contact: Eric Redenius
+1 (760) 473-4503
eric.redenius@bionx.com
www.bionxpro.com
Purchase BIONX® PRO
NSF
Certified for Sport® verification for BIONX® PRO

BIONX® PRO Executive Summary
BIONX® PRO uses multiple, independent mechanisms
to achieve: (1) increased maximal aerobic power; (2)
glycogen-sparing effects (delayed fatigue observable
in the late stages of competitions); (3) accelerated
resynthesis of creatine phosphate (greater strength
for at-limit efforts); and (4) comprehensive management
of connective tissue repair/joint stiffness issues
(decreased recovery time given the trauma of training
and competition). At the organism level, using multiple,
independent mechanisms is the only approach to
create both a synergistic outcome where the net result
is greater than the result of each independent mechanism
and to produce the most robust and reliable performance
solution. Maximizing aerobic power, creating glycogen-sparing
effects, and enhancing cardiovascular function
and connective tissue repair and maintenance are mission-critical
objectives for elite performance in most athletic
endeavors. BIONX® PRO is the only product
available on the NSF Certified for Sport® roster
with these capabilities. BIONX® PRO integrates
these performance deliverables in a single product
in capsule form (360 capsules per container).
BIONX® PRO Application
Micronutritional and Nutraceutical Support
for Baseball's Achilles' Heel: Connective Tissue Vulnerability
In the last two years, three studies [24, 25, 26]
have been published regarding MLB injury prevalence including
one comprehensive epidemiological seven-year study
of all MLB injuries for fielders and pitchers [24].
To no one's surprise, pitchers suffered predominately
upper extremity injuries and fielders lower body injuries.
Between
2002 and 2007, 27% of pitchers were injured following
a season in which they pitched [25]. Examining
radiographic data for pitchers, evidence of findings
for the acromioclavicular joint in the shoulder
and radial head osteophytes and radioulnar joint in
the elbow increased in direct proportion to inning s
pitched but were not predictive of time spent
on the MLB disabled list [27]. MLB pitchers cumulatively
develop degenerative changes to connective tissue
in both their shoulder and elbow anatomies due
to repetitive use. To a lesser degree, damage accrues
to lower body anatomical structures in fielders
(as well as all athletes engaged in chronic
training and competition involving high force profiles).
To manage connective tissue wear and tear, MLB players
engage in off-season, pre-season, and in-season conditioning
programs including various forms of resistance training,
flexibility/mobility training, and physical therapy.
Playing baseball at the professional level imposes
stress profiles (intensity, frequency and specificity
of transient force spikes targeted on vulnerable anatomical
structures) that the human anatomy is evolutionarily
unfit to accommodate: training to become stronger
nonlinearly increases forces applied to anatomical
structures. Statistically,
MLB injury rates have increased 37% between 2005 and
2008 and from 2002 through the 2008 season an
average of 438.9 players per year were placed on the
disabled list [24]. In order to adapt to
stress at the highest feasible efficiency, all known
metabolic bottlenecks in the tissue repair process
(i.e. "healing") need to be identified
and then minimized. To achieve this, a broad repertoire
of micronutritional and nutraceutical components to
optimize adaptive response (i.e. to not only heal
but to supercompensate to the ravages of
repetitive, unabated stressors) that go beyond
essential nutrients are required. The optimal micronutritional solution
to address this vulnerability is a multifactorial,
systems biology approach composed of the following
three-pronged strategy: (1) prevention and damage
control; (2) management of anti-inflammatory processes;
and (3) construction of connective tissue. Before
this writing, no such serious, comprehensive offering
existed on the NSF Certified for Sport® roster:
until now.
Reducing down-time due to injury and managing joint
stiffness is in the best interest of both baseball
teams and its players. Over the course of a baseball player's
career, ideally beginning years prior to
MLB play, there is no better investment than providing
a global collection of state-of-the-art forms of all
the mission-critical building blockers in clinically-determined
dosages to address all aspects demanded to support
connective tissue function, integrity, and reliability. Baseball
is a game defined by small margins. The team-performance
impact of even modest enhancement to tissue damage
prevention and accelerated connective tissue repair
and synthesis are powerfully leveraged: imagine
if during a full 162 game season there is a mere 2%
reduction in player-game count lost to injury? How
about 5% or more? It is often overlooked that nutrition
works synergistically with physical therapy in terms
of healing response. If there are metabolic bottlenecks
in the biochemical pathways responsible for healing,
then the efficacy of physical therapy is hampered
and, consequently, player down-time is extended. To
the player, the economic impact of extended career
longevity and the potential opportunity to improve
individual performance statistics due to
decreased injury down-time are paramount. In a game
where inches and milliseconds are the difference between
winning and losing, all avenues of safe and legal
performance enhancement need to be explored, integrated,
and evolved. Micronutritional support at the highest
level is a vital dimension of sustaining
performance at the limits of the human performance
envelope and the stresses of MLB play exceed the limits
of human connective tissue mechanical properties. BIONX® PRO
is the only offering on the NSF Certified for
Sport® roster to provide such an elegant
technical solution and is available for
the upcoming baseball season beginning with pre-season
play in the first quarter of 2013.
Strategy and Micronutritional Components
for Connective Tissue Repair and Maintenance:
A Multifactorial, Systems Biology Approach
1. Prevention and Damage Control
Bromelain, a proteolytic enzyme, blocks the early
cascade of inflammatory events to reduce recovery
time from the trauma of training and competition.
This inhibition of pro-inflammatory processes reduces
inflammatory symptoms like heat, swelling, and loss
of joint mobility [21]. SOD/CAT wheat sprouts
are not to be confused with “wheat sprouts”:
they are biodynamically grown using selective-induced
natural adaptation. This growing method maximizes
the sprout’s natural production of the primary
antioxidant enzymes superoxide dismutase (SOD) and
catalase (CAT). SOD and CAT are the most powerful
antioxidants in the body and serve a damage prevention
capacity in BIONX® PRO. Grape seed
extract is rich in powerful plant-based antioxidants
called oligomeric proanthocyanidin complexes or (OPCs).
OPCs have a wide range of effects including an ability
to increase intracellular levels of vitamin C, decrease
capillary fragility, scavenge free radicals, and inhibit
breakdown of collagen [22]. OPCs play an important
supporting role in the arrest of morning stiffness.
The antioxidant activity of OPCs is 50 times greater
than vitamin E and 20 times greater than vitamin C.
Grape seed extract primarily serves in an anti-catabolic
capacity (reduces the breakdown of connective tissue
structure) in BIONX® PRO. The goal
of the prevention strategy is to amplify the control
and reliability of the management of inflammation
and to reduce the demand for the synthesis of new
connective tissue structures. The execution of all
three phases of the strategy results in accelerated
recovery and an improvement in adaptive yield (the
purpose of training is supercompensation) from training
stress. BIONX® PRO is the only product
available on the NSF Certified for Sport® roster
with these capabilities.
2. Management of Inflammatory Processes
Curcumin and Boswellia serrata are the two
most efficacious, anti-inflammatory botanicals and
BIONX® PRO offers both at therapeutic levels
in their much more potent second-generation nutraceutical
forms as opposed to just the unmodified standardized
extracts. Meriva® curcumin
phytosome is a patented form of the botanical
curcumin that demonstrates a 29-fold increase
in absorption and a superior plasma curcuminoid profile
compared to conventional curcuminoid preparations.
Boswellia serrata (5-Loxin®)
is an Ayurvedic botanical possessing very powerful
anti-inflammatory actions and is a first tier tool
for the management of morning stiffness. 5-Loxin®
concentrates the most powerful Boswellia compound,
acetyl-11-keto-beta boswellic acid, or AKBA. The researchers
created a method using state-of-the-art manufacturing
practices to produce a Boswellia extract at a concentration
of 30% AKBA, ten times more concentrated than
ordinary Boswellia extracts. In clinical
research, a 250 mg daily dose of 5-Loxin® was
significantly better than a 100 mg dose for joint
stiffness and functional ability parameters. BIONX® PRO
at the recommended dosage of 24 capsules per day delivers
250 mg of 5-Loxin®. Many different signal
molecules that influence the behavior of signal networks
at the cellular level mediate inflammatory processes.
Meriva® and 5-Loxin® when used in
combination address inflammatory cascades more comprehensively
and robustly than either alone.
3. Construction of Connective Tissue
Shark Cartilage contains glucosamine, chondroitin,
trace minerals, anti-inflammatory compounds, immune
support factors and other protein compounds required
for connective tissue repair and maintenance. OptiMSM® is
a source of biologically-available sulfur, a critical
mineral that is incorporated into connective tissue,
cell membranes, insulin, coenzyme A, hemoglobin and
muscle proteins. Manganese (from manganese ascorbate)
is a key trace mineral that is mandatory for connective
tissue synthesis [23]. Shark cartilage, OptiMSM®,
and manganese serve in a connective tissue, building-block
capacity in BIONX® PRO.
Amplifier to All Micronutritional Components
Black Pepper (Bioperine®)
is an extract from the fruit of black pepper that
increases the blood levels of nearly all of the nutrient
classes. For example, a 5 mg dose of Bioperine®
increases the blood level of CoQ10 by 31.8%, vitamin
C by 52.3%, selenium by 42.6% and beta-carotene by
61.2%.
Quality Control, Manufacturing, and Engineering of
BIONX® PRO
BIONX® PRO is manufactured at Douglas
Laboratories which is routinely inspected
by the FDA, is ISO 9001 certified, ISO 17025 accredited,
and is GMP Registered by NSF International. Douglas
Laboratories does not handle any substances that are
banned by the International Olympic Committee. Douglas
Laboratories uses blenders capable of homogeneously
blending nutrient concentrations as diverse as a 12,000:1
ratio so that BIONX® PRO assays within acceptable
tolerances of the label specifications. This is very
important as nutrient manufacturers are beginning
to require a label review to make sure their required
levels per serving are present to ensure nutrient
benefit. Douglas Laboratories uses low temperature
blending to improve disintegration thus ensuring maximal
absorption potential and to not denature the chemical
structure of thermally fragile botanical and connective
tissue components. Douglas Laboratories also tests
all in-bound ingredients for impurities like toxic
heavy metals (mercury, lead, cadmium, etc.) and virulent
bacteria and viruses. BIO NX®
PRO also meets or exceeds the quality standards established
by the U.S Pharmacopoeia 32 which addresses among
other things whether a capsule or tablet adequately
dissolves in time for it to be absorbed.
BIONX® PRO specification
Usage
for athletes under 180 pounds: 6 capsules taken twice
daily with meals (12 capsules per day).
Usage for athletes over 180 pounds: 12 capsules taken
twice daily with meals (24 capsules per day).
Note: BIONX® PRO is designed to
deliver maximal therapeutic benefit for connective
tissue management at 24 capsules per day. For
example, in clinical research, a 250 mg daily
dose of 5-Loxin® was significantly better
than a 100 mg dose for joint stiffness and functional
ability parameters. At the recommended dosage of 24
capsules per day, BIONX® PRO delivers
250 mg of 5-Loxin®, 600 mg of Meriva®
curcumin phytosome, 2000 mg of SOD/CAT wheat
sprouts, 6000 MCU of bromelain, and 1500
mg of shark cartilage.
Overview of the Strategy to Performance Enhancement
The application of increasing maximal aerobic power
and aerobic metabolic efficiency is unexplored territory
for "anaerobic/strength" sports such as football,
hockey, basketball and baseball. The reason for this
is that it has been believed for decades that aerobic
metabolism plays only a minor role in these sports and,
consequently, is ignored. The rationale for supporting
this belief is no longer valid; aerobic
metabolism has a much greater role than previously
understood [4, 5]. The consequences and opportunities
of these findings are large. It is self-evident that
increasing maximal aerobic power has direct benefit
for hockey, basketball, soccer and greater than marginal
benefit for football skill-position players like running
backs, receivers, kick returners and defensive backs,
but the principal benefit for these sports using this
approach, if taken to its practical and safe limit,
is primarily the conservation of intramuscular stores
of glycogen and, in a secondary role, increasing the
rate of creatine phosphate resynthesis. Even a slightly
enhanced shift of ATP generation in favor of aerobic
glycolysis versus anaerobic glycolysis (what actually
occurs is an extension of the aerobic glycolytic envelope
because these two processes are structurally-coupled
in sequential stages) produces a cumulative
glycogen
sparing effect resulting in an increased energy-reserve
capacity that matters greatly in the late phases of
these sports due to catastrophic fatigue ("running
out of gas", i.e. glycogen). Consuming carbohydrate
drinks and even an intravenous infusion do not compensate
for the extremely high rate of intramuscular glycogen
losses. Anaerobic glycolysis produces twice the rate
of ATP production (thus the high force/power production)
as aerobic glycolysis but at a glucose (glycogen)
cost of 18-fold (2 ATP/glucose vs. 36 ATP/glucose).
This 18-fold differential (not 10, 20, or 80% but
a 1800% difference) in fuel consumption is a remarkable
fact that can be exploited to create a distinct competitive
advantage.
Logic of Human Energy Production diagram
Visualization of Fuel Burn Rate
To put this in perspective, visualize an INDYCAR that
produces 1200 horsepower and goes 230 MPH with a burn
rate of 3 gallons per mile. If you had a 200 gallon
gas tank and the race were 50 miles you would logically
go flat out because you would have 50 gallons left at
the finish line. But given that you cannot refuel and
the race was 80 miles, would you go flat out? No, you
wouldn't because you couldn't. You would need an additional
car. Now imagine making a modification to the engine
where the maximal power output remained the same but
the burn rate from half-throttle to full-throttle dropped
8% or more. Wouldn't you be able to go full-throttle
longer after the modification and gain separation from
your flagging rivals?
BIONX® PRO Application: The Metabolic
Dimension of the New NFL Game Style
A vivid example of the metabolic consequences of increasing
the rate of play is the recent evolution and proliferation
of the 2-minute offense (circa Johnny Unitas era) to
the continuous use of a no-huddle offense: this has
changed the game far more than tactically and strategically.
With the duration of consecutive plays ("snaps")
falling below 30 seconds, the metabolic demand profile
of the NFL is converging on basketball. The impact of
this adaptation has not been recognized on the metabolic
level: reliance on anaerobic metabolism (both alactic
and lactic) is no longer a reliable strategy to win
football games even at the elite college level. Intramuscular
glycogen stores are decreased 36% with just 10
intervals of 6 second maximal bursts with 30 seconds
rest [5]. Once a large proportion of intramuscular
glycogen stores have been depleted the performance of
the athlete drastically declines from performance in
the first quarter (e.g. the 40 yard dash time increases
as a function of glycogen depletion but understand this
is a relative phenomenon: your opponent is slowing down
too). This is because high intensity exercise preferentially
depletes fast twitch fibers first [1]; production
of explosive power and top-end speed degrades during
the course of the game. For example, the Achilles' heel
of the highly-valued "shut-down" cover cornerback
is his gas tank. If he had to cover multiple deep "go"
routes in the first half his speed would degrade markedly
by the third quarter to the point he could no longer
prevent exploitable separation from a receiver having
blinding speed with a fuel tank of gas. Rotating
players (a second or third player on the depth chart
offer additional "gas tanks" although these
"cars" are not the same caliber as the "starting
car") and using exogenous oxygen on the sideline
marginally helps but the most direct solution is
conserving glycogen stores by modification of oxygen
transport (systemic cardiovascular) while simultaneously
enhancing the bottlenecks of metabolism (muscle biochemistry)
that exist between the integration of anaerobic and
aerobic glycolysis. Rotation of defensive linemen
on plays even of the same category of down-and-distance
is becoming more common in the NFL and even in NCAA
Division 1 (U. of Alabama) because of fatigue and performance
erosion (lower-body glycogen depletion). At higher altitude,
such as INVESCO Field ("Mile High Stadium"),
glycogen depletion is accelerated relative to sea-level
stadiums exacerbating the fatigue problem. Denver players
are acclimatized to the decreased ambient oxygen concentration
whereas their visiting opponents are not. This is a
distinct team-level competitive advantage due to the
differential in oxygen transport capacities*.
Alactic anaerobic metabolism (the phosphagen system)
has been partially addressed by supplemental oral creatine
monohydrate. Unfortunately, creatine
phosphate (CP) is resynthesized in muscle mitochondria
via aerobic metabolism (including fat oxidation) and
is rate-limited by oxygen availability [16].
Supplementing creatine monohydrate does help by increasing
the intramuscular creatine pool and to a limited degree
with resynthesis but its restoration (inside mitochondria:
C + P => CP) between plays is solely dependent on
aerobic metabolism; is rate-limited by oxygen availability
and pH (impaired by acidosis); is markedly slower
in fast twitch muscle than slow twitch (slow twitch
is nearly irrelevant to football performance); and can
take up to 50-60 seconds to recover just to 50% of baseline
[2, 3]. Free creatine (i.e. creatine not bound to a
phosphate group because it has been expended by alactic
anaerobic metabolism in a previous effort) is useless
for force production and athletic performance in subsequent
efforts (plays): it must be resynthesized between efforts.
This problem is non-linearly amplified as the duration
between plays decreases (i.e. the work to rest ratio
skyrockets: there is a huge game-changing difference
between snap counts in 20 vs. 30 vs. 40 second intervals
relative to fatigue acceleration; think "Super
no huddle"). In sports like football that demand
constant CP resynthesis as opposed to sports like Olympic
lifting or the 100 meter dash which do not, enhancement
of resynthesis is theoretically more important than
increasing the CP pool but executing both is optimal.
Players cannot use their oxygen tanks between plays
on the field but they can improve oxygen transport by
other means while on the field via the
approach described here.
To fully execute this strategy, a multifactorial,
systems biology approach is obligatory. BIONX® PRO
is the only product available on the NSF Certified for
Sport® roster with these capabilities.
BIONX® PRO specification
Usage
for athletes under 180 pounds: 6 capsules taken twice
daily with meals (12 capsules per day).
Usage for athletes over 180 pounds: 12 capsules taken
twice daily with meals (24 capsules per day).
Note: BIONX® PRO is designed to
deliver maximal therapeutic benefit for connective
tissue management at 24 capsules per day. For
example, in clinical research, a 250 mg daily
dose of 5-Loxin® was significantly better
than a 100 mg dose for joint stiffness and functional
ability parameters. At the recommended dosage of 24
capsules per day, BIONX® PRO delivers
250 mg of 5-Loxin®, 600 mg of Meriva®
curcumin phytosome, 2000 mg of SOD/CAT wheat
sprouts, 6000 MCU of bromelain, and 1500
mg of shark cartilage.
Micronutritional
Components for Aerobic Power, Glycogen-Sparing and Cardiovascular
Function:
A Multifactorial, Systems Biology Approach
1. Cardiovascular Modification: Deliver More
Oxygen to Working Muscles
At the organism level, the objective is to increase
the oxygen carrying capacity of the arterial blood supply.
BIONX® PRO achieves the objective via three
degenerate (independent) approaches that target heart
metabolic and myocardial (mechanical/inotropic effects)
function [17]. Trisodium phosphate on the organism level
increases VO2 max by 9-10% [6, 7, 8] and increases
oxygen pulse (amount of oxygen in arterial blood per
heart beat [ml O2/HR]) by 15% [7]. Trisodium phosphate
on the myocardial level increases ejection fraction
by 5% under maximal conditions (volume of blood ejected
from left ventricle per contraction as measured by 2D
echocardiogram) [6].
Hawthorn extract (Crataegus oxycantha, standardized
to 2% vitexin-2"-rhamnoside) is the most potent
inotropic cardiotonic agent in the global botanical
repertoire. Inotropy refers to effects on the force
with which the heart muscle contracts and is measured
by changes in stroke volume and/or ejection fraction
that are parameters of cardiac output. Hawthorn
is inotropic by means independent from trisodium phosphate.
Hawthorn increases coronary and myocardial circulation
and improves systolic contraction and ejection fraction
[9, 10, 11, 12]. In addition to trisodium phosphate
and hawthorn, magnesium orotate has been used to enhance
myocardial contractility and improve exercise tolerance
in trained athletes [13, 14]. Magnesium orotate enhances
the functional reserves of the trained heart and accounts
for its use in sport applications [15].
2. Muscle Metabolism Modification: Amplify the
Utilization of Available Oxygen Supply
At the local level (i.e. within working muscle), the
objective is to increase the availability of oxygen
in order to extend the aerobic glycolytic envelope and
increase the anaerobic threshold. Under all but the
most intense, intermittent burst activities, if more
intramuscular oxygen is available, it will be consumed
and this has a dramatic impact on the conservation of
precious glycogen supply and will impact PC recycling
because of oxygen availability and increased pH. This
is most relevant to the lower body since these large
muscles are active on much closer to a continuous "non-spiky"
basis (a much higher duty cycle than the upper body)
and operate with aerobic enzyme systems at maximal activity.
Late in games it is "heavy legs", not "heavy
arms" that define fatigue and performance erosion.
In fact, the discovery and exploitation of the starkly
different fatigue profiles between upper and lower body
in football is virgin territory to disrupt the delicate
parity in the NFL. Tactically, specific high-value players
that can be exposed to multiple 5-second sprints can
be targeted and neutralized metabolically by depleting
a large proportion of their fast-twitch, lower body
glycogen stores over the course of a few drives or by
half time. Strategically, the exploited vulnerability
creates offensive "big play" opportunities
by late third quarter due to erosion of peak speed,
explosive power and agility.
Using a systems biologic approach, intramuscular oxygen
flow rate is enhanced by cardiovascular measures (systemically/globally)
and aerobic metabolic efficiency is addressed by reducing
the impact of the bottleneck enzymes (pyruvate dehydrogenase
complex (PDC: EC
1.2.4.1; EC
2.3.1.12; EC
1.8.1.4) linking the output (pyruvate) from anaerobic
glycolysis with its input for aerobic glycolysis (locally
within recruited muscle). Both these strategies increase
maximal oxygen uptake but do so through degenerate (independent)
pathways [17]. As an additional degenerate measure,
high levels of pantothenic acid, which is a direct precursor
of acetyl coenzyme-A (a potential rate-limiting metabolite
in aerobic glycolysis), is loaded to cellular saturation.
High-dose oral loading of pantothenic acid increases
aerobic efficiency at 75% of VO2 max while decreasing
lactate production [19, 20]. The PDC catalyzes
by oxidative decarboxylation pyruvate to acetyl coenzyme-A,
the input to aerobic glycolysis. Given sufficient oxygen,
ATP (energy for muscular contraction) is produced aerobically
in lieu of pure anaerobic processes at a greatly reduced
glycogen cost.
Independent of cardiovascular modification (i.e. without
effect on oxygen pulse), the use of pyridoxine alpha-ketoglutaric
acid at physiologic significant dose increases VO2 max
by 6% and significantly reduces lactate production at
supramaximal loads [18]. In other words, scientific
studies verify that both of these degenerate, independent
pathways significantly increase VO2 max under supramaximal
loads. Given systems biology, there is a high likelihood
that these two approaches implemented simultaneously
are not only degenerate but also synergistic since multiple,
independent, potential, rate-limiting targets are addressed.
Strategy and Micronutritional Components
for Connective Tissue Repair and Maintenance:
A Multifactorial, Systems Biology Approach
1. Prevention and Damage Control
Bromelain, a proteolytic enzyme, blocks the early cascade
of inflammatory events to reduce recovery time from
the trauma of training and competition. This inhibition
of pro-inflammatory processes reduces inflammatory symptoms
like heat, swelling, and loss of joint mobility [21]. SOD/CAT
wheat sprouts are not to be confused with “wheat
sprouts”: they are biodynamically grown using
selective-induced natural adaptation. This growing method
maximizes the sprout’s natural production of the
primary antioxidant enzymes superoxide dismutase (SOD)
and catalase (CAT). SOD and CAT are the most powerful
antioxidants in the body and serve a damage prevention
capacity in BIONX® PRO. Grape seed
extract is rich in powerful plant-based antioxidants
called oligomeric proanthocyanidin complexes or (OPCs).
OPCs have a wide range of effects including an ability
to increase intracellular levels of vitamin C, decrease
capillary fragility, scavenge free radicals, and inhibit
breakdown of collagen [22]. OPCs play an important supporting
role in the arrest of morning stiffness. The antioxidant
activity of OPCs is 50 times greater than vitamin E
and 20 times greater than vitamin C. Grape seed extract
primarily serves in an anti-catabolic capacity (reduces
the breakdown of connective tissue structure) in BIONX® PRO.
The goal of the prevention strategy is to amplify the
control and reliability of the management of inflammation
and to reduce the demand for the synthesis of new connective
tissue structures. The execution of all three phases
of the strategy results in accelerated recovery and
an improvement in adaptive yield (the purpose of training
is supercompensation) from training stress. BIONX® PRO
is the only product available on the NSF Certified for
Sport® roster with these capabilities.
2. Management of Inflammatory Processes
Curcumin and Boswellia serrata are the two
most efficacious, anti-inflammatory botanicals and BIONX® PRO
offers both at therapeutic levels in their much more
potent second-generation nutraceutical forms as opposed
to just the unmodified standardized extracts. Meriva® curcumin
phytosome is a patented form of the botanical curcumin
that demonstrates a 29-fold increase in absorption
and a superior plasma curcuminoid profile compared to
conventional curcuminoid preparations. Boswellia serrata
(5-Loxin®)
is an Ayurvedic botanical possessing very powerful anti-inflammatory
actions and is a first tier tool for the management
of morning stiffness. 5-Loxin® concentrates the
most powerful Boswellia compound, acetyl-11-keto-beta
boswellic acid, or AKBA. The researchers created a method
using state-of-the-art manufacturing practices to produce
a Boswellia extract at a concentration of 30% AKBA,
ten times more concentrated than ordinary Boswellia
extracts. In clinical
research, a 250 mg daily dose of 5-Loxin® was
significantly better than a 100 mg dose for joint stiffness
and functional ability parameters. BIONX® PRO
at the recommended dosage of 24 capsules per day delivers
250 mg of 5-Loxin®. Many different signal
molecules that influence the behavior of signal networks
at the cellular level mediate inflammatory processes.
Meriva® and 5-Loxin® when used in
combination address inflammatory cascades more comprehensively
and robustly than either alone.
3. Construction of Connective Tissue
Shark Cartilage contains glucosamine, chondroitin, trace
minerals, anti-inflammatory compounds, immune support
factors and other protein compounds required for connective
tissue repair and maintenance. OptiMSM® is
a source of biologically-available sulfur, a critical
mineral that is incorporated into connective tissue,
cell membranes, insulin, coenzyme A, hemoglobin and
muscle proteins. Manganese (from manganese ascorbate)
is a key trace mineral that is mandatory for connective
tissue synthesis [23]. Shark cartilage, OptiMSM®,
and manganese serve in a connective tissue, building-block
capacity in BIONX® PRO.
Amplifier to All Micronutritional Components
Black Pepper (Bioperine®)
is an extract from the fruit of black pepper that increases
the blood levels of nearly all of the nutrient classes.
For example, a 5 mg dose of Bioperine® increases
the blood level of CoQ10 by 31.8%, vitamin C by 52.3%,
selenium by 42.6% and beta-carotene by 61.2%.
Quality Control, Manufacturing, and Engineering
of BIONX® PRO
BIONX® PRO is manufactured at Douglas
Laboratories which is routinely inspected by
the FDA, is ISO 9001 certified, ISO 17025 accredited,
and is GMP Registered by NSF International. Douglas
Laboratories does not handle any substances that are
banned by the International Olympic Committee. Douglas
Laboratories uses blenders capable of homogeneously
blending nutrient concentrations as diverse as a 12,000:1
ratio so that BIONX® PRO assays within acceptable
tolerances of the label specifications. This is very
important as nutrient manufacturers are beginning to
require a label review to make sure their required levels
per serving are present to ensure nutrient benefit.
Douglas Laboratories uses low temperature blending to
improve disintegration thus ensuring maximal absorption
potential and to not denature the chemical structure
of thermally fragile botanical and connective tissue
components. Douglas Laboratories also tests all in-bound
ingredients for impurities like toxic heavy metals (mercury,
lead, cadmium, etc.) and virulent bacteria and viruses.
BIONX® PRO also meets or exceeds the quality standards
established by the U.S Pharmacopoeia 32 which addresses
among other things whether a capsule or tablet adequately
dissolves in time for it to be absorbed.
References
[1] Gollnick, P.D., Armstrong, R.B.,
Sembrowich, W.L., Shepherd, R.E., and Saltin, B.,
Glycogen depletion pattern in human skeletal muscle
fibers after heavy exercise, J. Appl. Physiology,
34(5): 615-618, 1973
[2] Kjaer, M., Krogsgaard, M., Magnusson, P., Engebretsen,
L., Roos, H., Takala, T., and Woo, S.L., Textbook
of Sports Medicine: Basic Science and Clinical Aspects
of Sports Injury and Physical Activity, Blackwell
Science Ltd., 2003, p. 192
[3] Maughan, R. and Gleeson, M., The Biochemical Basis
of Sports Performance, Oxford University Press, 2004,
pp. 84-86
[4] Parloin, M.L., Chesley, A., Matsos, M.P., Spriet,
L.L., Jones, N.L., and Heigenhauser, J.F., Regulation
of skeletal muscle glycogen phosphorylase and PDH
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