Clinical studies are applied in the pharmaceutical industry, to specifically determine the action and evolution of the product and its final behavior in the body through pharmacokinetics and pharmacodynamics using a process where up to 4 phases of the drug are commonly involved with the end goal to develop a protocol and measure different interactions.
Biological products such as cell therapies have some characteristics compared to small molecule drugs. These products require novel study designs to address their uniqueness. Close attention to detail must be paid when defining critical endpoints. Special monitoring and reporting should also be considered due to the safety issues associated with these products, especially long-term monitoring, because cell therapies are even more complex and difficult to apply compared to conventional clinical studies as a consequence of the nature of the product. However, we must consider the importance that these therapies have contributed in the last 25 years, especially in revitalizing regenerative medicine, providing significant improvements in the quality of life of patients who have undergone these treatments for various causes and diseases. The mode of action is not always perfect, and the potency tests are still imprecise, hence the main concern when reviewing any clinical trial on allogeneic transplantation in autologous or donor cell therapies and also those of animal origin Xenotransplantation is that they all enjoy 100% biosecurity and with minimal risk of immune rejection.
The aforementioned does not relate to Biocell Ultravital products since they use peptides and cell extracts in their formulas that guarantee 100% safety without the possibility of immune rejection in patients. We have accumulated for more than 70 years of varied clinical expertise through specialized doctors mainly in Europe who have used Cellular Renovation Therapies for more than 3 generations to establish safety and efficacy parameters, mainly on patients for which an adequate evaluation is required to determine various aspects. Such as, their medical history, their family history, risks environmental conditions, and predisposition to degenerative diseases. In all the above parameters such as to time and dose to be applied are crucial be able to determine the therapeutic effectiveness. This is determined according to the type of trial or clinical expertise used to develop the application protocols focusing on the type of pathology. As of 2017 we had carried out 1,292 new observational tests in which the following criteria were evaluated:
Anti-inflammatory enzyme complex to treat acute inflammations and connective tissue.
Each cell and tissue have their own activity, one of which is enzymatic, which have the power to catalyze, facilitate and speed up certain synthetic and analytical processes. The genes themselves are regulators of the production of enzymes; Therefore, genes and enzymes can be considered as the fundamental units of life, which in synthesis is a chain of enzymatic processes, from the simplest, such as water (H2O) and carbon dioxide (CO2), present in plants to the formation of carbohydrates, to the most complicated ones that use very complex substrates. Enzymes carry out definitive functions related to health and disease.
Organic Aging and Cell Renewal Therapies
A set of rare, but often debilitating and often fatal genetic diseases provides other dramatic examples of the drastic physiological consequences that can follow deterioration of enzyme activity, even of a single enzyme. Therefore, the determination of these intracellular enzymes in the blood serum provides clinicians with valuable information for diagnosis and prognosis.
Bioenzym 4G is useful in chronic inflammatory processes such as: rheumatoid arthritis, osteoarthritis, chronic joint and soft tissue inflammatory processes, especially for those patients in whom the use of another type of steroidal anti-inflammatory is not possible.
What is Bioenzym 4G?
It is an anti-inflammatory therapy that contains cell extracts, lycopene, powerful antioxidants and enzymes that progressively act on the inflammatory processes caused by different genetic, mechanical and environmental factors without affecting other organ systems such as the digestive system.
Benefits of Bioenzym 4G
Bioenzym 4G is a new generation of anti-inflammatory steroid-free treatments. General anti-inflammatory activity (muscular, soft tissues, etc.)
How does it work?
The components of the formula reach the cells, directly or indirectly, in the case of oral products, through the bloodstream, and are selectively incorporated into the cells through various means of cellular transport. Enzymes help break down plasma proteins during acute inflammatory processes, facilitating their elimination through the circulatory or lymphatic system.
How should I take Bioenzym 4G?
Anti-inflammatory and preventive action:
One tablet in the morning and one in the evening for at least six months. As an adjunct in subclinical inflammations and postoperative inflammatory processes:
Two tablets in the morning and 2 in the evening for at least six months. In secondary inflammatory joint processes, trauma and benign prostatic hyperplasia.
Two tablets in the morning and 2 in the evening, for at least three months. The tablets are taken on an empty stomach and at night before dinner (30 minutes before meals).
What are the side or collateral effects associated with Bioenzym 4G?
This product has no side effects or contraindications with other medications. It lacks toxic properties due to its 100% natural organic components.
How does it feel to take Bioenzym 4G?
Because it is an enzyme therapy, the first thing that is perceived is joint de-inflammation, since its components dissolve excessive fibrin obstructions formed at the site of inflammation, restoring circulation in the area.
What is the price of the Bioenzym 4G product?
The price will depend on the number of doses that your doctor prescribes, but what value do you place on your health? We must remember that the most important thing in life is not to survive, whilst living with chronic diseases and ailments, but to live a long and full life whilst remaining healthy.
If we could buy insurance that guaranteed health, would we do it?
If we reflect on the purchase of life insurance, this only gives us peace of mind, because we have our family protected, but it does not protect our health or our future physical well-being.
Is Bioenzym 4G available in pharmacies?
Because it is a product of biological and non-pharmaceutical origin, it is not for sale in traditional pharmacies, only in some specialized.
Biopharmaxie and
Schweizer Klinik Biocell
Bioenzym
Indications:
- Anti-inflammatory activity.
- Bone-joint inflammatory processes.
- Antiviral activity.
- Post-surgical inflammatory processes.
- Strengthening of the immune defense.
- Adjuvant action in prostatic hyperplasia.
- Main indications acute inflammation
Preventive action in subclinical inflammation.
- Osteoarticular inflammatory processes secondary to trauma or autoimmune.
- Post-surgical inflammatory processes without complications.
- Helping action in all inflammatory processes.
Preventive action in all conditions due to acute inflammation.
- Indications in chronic inflammation diseases.
- Post-surgical inflammatory processes without complications.
- Helping action in all inflammatory processes.
Indications in chronic inflammation diseases.
- Stroke.
- Multiple sclerosis.
- Diabetic neuropathies and other metabolic disorders.
- Mellitus diabetes.
- Neurodegenerative diseases.
Action mechanism for 4th cellular generation
The mechanism of action of peptides is similar to that of drugs, since the last three amino acid residues adjacent to the C-terminal region of peptides that have therapeutic activity are strongly linked to the active site where they have a higher inhibition specificity. The biopeptides are protected in enteric-coated tablets and capsules to prevent their degradation in the GI and seek their best absorption in the intestinal tract, thus benefiting the percentage of absorption in blood and to achieve this we have incorporated catalysts in each formula, as well as, three amino acids arginine, glycine and aspartic acid to increase the body’s chemical reaction for coupling and subsequent absorption. By incorporating this sequence into the different peptide chains at different positions in the standard formula, it allows new variants both in the negatively charged aspartic acid side chain like arginine, (positively charged). The formula and methods obey an exclusive patent of
Biocell Ultravital 4th generation products to improve their absorption when they are administered orally to bind to the target molecule and its therapeutic effect is restored when it reaches its destination.
Pharmacokinetics and Pharmacodynamics
The components of the various formulas reach the cells, either directly or indirectly by blood in the case of oral products, and are incorporated by them, through the various means of cellular transport, depending on the size of the cells and molecules in question. In the case of large molecules, their incorporation into cells will be by receptor-mediated endocytosis, following the chain: vesicle, endosome and lysosome. In the case of smaller molecules, their incorporation will be by simple diffusion or protein-facilitated diffusion, depending on the case.
The cellular extracts that have entered the cells by endocytosis, are made up of molecules whose atoms are linked together by chemical bonds, in which energy is retained. Both matter and energy are used by the cell, through a process called cellular digestion, which breaks down the molecules by the action of the hydrolase enzymes contained in the lysosomes.
Composition:
Boxes of 30 tablets of 650 mg. / Boxes of 60 tablets of 650 mg.
Each 650 mg tablet contains:
Opotherapy Extracts: Embryo, Thymus Gland.
Peptide Extracts: Embryo, Thymus Gland.
Enzyme Complexes: Glutathione Transferase, Glutathione Peroxidase, Superoxide Dismutase, Glutathione Reductase, Adenosín Trifosfato(ATP),
Other actives: Lycopene, Pancreatin 7NF, Pure Papain, Bromelain 2500 GDU. Trypsin 2, 160FIP-Uds Sus Scrofa, Chymotrypsin, Rutoside, Sophora Japonica., Calcium Phosphate, Gamma-Tocopherol, Cholecalciferol, Ascorbic Acid, Calcium, Zinc, Selenium, Genistein.
Other Ingredients: Stabilizers and Excipients.
Oral use, consume before taking food to improve absorption, preferably with water.
Dosage:
As a preventive treatment for healthy people, one (1) tablet is recommended in the morning and one (1) at night daily for six intercalated months.
For people who have any condition or disease indicated here, it is recommended to consume two (2) capsules in the morning and two (2) capsules at night daily for twelve (12) months as an adjunctive reinforcement to the medications indicated by the treating physician.
It can be taken indefinitely as its components do not create a deposit.
Side effects:
Due to its peptide and opotherapeutic content in its formula, it could in some cases cause a slight headache, which disappears after a few minutes, nausea is very occasional and disappears in a few hours.
Extraction and obtaining of biopeptides and cellular extracts
It should be noted that the formulas contain biological components of animal origin in combination with other compounds that enhance the therapeutic action and are extracted especially in the embryonic stage and processed during the second month of gestation, these components that are part of the formulas of some of Our products are obtained after a long biochemical process and are certified free of prions, pyrogens, bacteria, nano-bacteria, fungi, viruses and after many controls, the risks of an immune reaction in Humans are 100% eliminated.
Many years of clinical experience has shown that pigs and sheep are the best donors, because they are strong and immunologically resistant. Proof of this is that even in the 21st century, most heart valve transplants for humans are derived from pigs, in addition to insulin and many derived products for therapeutic purposes, come from these. These methods are continuously monitored to determine that they meet the strictest standards required by biosafety for therapeutic purposes. All the components and other active ingredients of the formulas are also approved by the Federal Food and Drug Agency (FDA) and are manufactured in the USA by BIOCELL ULTRAVITAL USA under Swiss license from Biocell Ultravital.
Contraindication.
It can be safely combined with other medications.
In the recommended doses, no adverse reactions have been observed in any case.
Those who have diabetes must first be controlled.
Presentation and packaging.
A box with two (2) blisters of 15 tablets / four (4) blisters of 15 tablets of 650 mg each, and its manufacture is carried out in a sterile atmosphere according to the international regulations of the European Pharmacopoeia. Do not use after the expiration date, or when the blister is perforated or a capsule is broken, or when the security packaging is open or forced.
Conservation:
Keep in a dry and cool place at room temperature between 5 ° C and 40 ° C. Do not use after the expiration date, nor when the present vial has broken the safety cap, nor when the outer packaging is open or forced.
Control of finished product:
Two (2) independent laboratories perform various tests and mycotic controls, biological, bacteriological type 5 analyzes, multicenter immunocellular tests, Anti brucellosis, Virological controls, multiple anti-prion tests, Bacteriosis, Cyclospores, Mycobacteria, Salmonellosis in accordance with the subject of biology for therapeutic purposes for human consumption according to current EC regulations
Warning:
Biocell Ultravital guarantees the purity and quality of its products and is not responsible for damage to third parties that may cause malpractice.
How Does it Work?
How the Formulas are Developed?
All our products have been formulated to optimize cell function because if we have healthy cells, we will be healthier every day, and they are based on our 4 pillars of cellular longevity. They work together as a whole to promote energy production and cell growth.
We strive to achieve perfection for each of our therapeutic categories, since they are formulated by carefully selecting each component after confirming its characteristics and clinical trials that positively compromise the efficacy in each formula, this is basically the science on which our products and therapies are based.
Biocell Ultravital products are formulated with ingredients that are 100% natural biological substances, with the highest quality standards, containing cellular extracts of animal origin and peptide hydrolysates extracted from plant extracts and glands of young animals in combination with antioxidants, enzymes and vitamins we managed to optimize the formulas and their therapeutic scope.
All raw material sources are carefully selected from organic plants and organs of pigs and sheep less than one year old and undergo a prion and decontaminated pharmaceutical standardization process that meets high biosecurity standards for reach specific concentrations of high purity and are processed under strict controls to guarantee the high quality and purity of their products.
No chemicals, other harmful or unwanted substances are used in the extraction. Modern technology ensures the recovery of assets in a biologically natural way, without changes. This is very important for the safety of each formula. None of the components in Biocell Ultravital formulas are genetically modified. (NON GMO)
Production and Extraction of Bio Peptides 4th Cellular Generation
The chemical synthesis to produce bioactive peptides of the 4th cell generation of
Biocell Ultravital are obtained using combined methods of enzymatic hydrolysis through proteolytic enzymes and by fermentation using starter cultures. This combination of both methods gives origin to peptides with a safer biological activity due to the fact that in one all the contaminating traces are eliminated and the other facilitates the absorption through the intestinal tract. An additional advantage of enzymatic hydrolysis is the reduction of allergens. The procedure to obtain, isolate and identify biopeptides with specific biological activity, is obtained with the solution of the gland or organ to extract biopeptides, to which papain, pepsin, trypsin are added, the application of different enzymes pursue the formation of a mixture with different ranges of biological activity and incubated for a certain time to obtain the desired degree of hydrolysis.
After this, the hydrolyzate is fractionated by exclusion chromatography and semi-preparative liquid chromatography in reverse phase, selecting the fraction with the highest activity as a result of the first invitro tests, and finally the sequence of the peptides responsible for generating the activity is identified. The desired therapy is obtained by applying mass spectrometry and / or N-terminal sequencing. However, hydrolysates are complex mixtures and can contain up to hundreds of different molecules, therefore, locating bioactive peptides in these procedures is a biochemical work of constant expertise that results in a difficult task and requires a lot of time and dedication. The fractions usually still contain multiple compounds that require additional cycles of fractionation, concentration and evaluation of bioactivity to be able to identify the molecule responsible for the activity in the formulas of each product according to the therapeutic indication.
Consequently, the enzymatic hydrolysis used offers undoubted advantages, such as the absence of substrate degradation processes since the enzymes are selective for a type of bond, pH values between 5 to 10 and the temperatures between 40 to 60ºC, thus maintaining or improving the nutritional value of the protein. The specificity of the enzyme affects the size, quantity, and composition of free peptides and amino acids, as well as their amino acid sequence.
Safety in Therapies
Safety control is a very important factor, especially when it comes to high quality health products, which is why at
Biocell Ultravital in France, which is the main headquarters where all the research and development of the formulas take place, we have monitoring and follow-up mechanisms for each product, this to prevent any error in the next production, that is why we are continuously implementing software for the detection of technical failures of the human team in charge of production. This translates into maximum safety controls that guarantee the complete quality of the production, eliminating 100% possible adverse reactions due to the indication of some of our products that does not correspond to a contraindication already described.
This discipline has become responsible for quality control in the formulation and manufacturing phases thanks to the detection, evaluation, knowledge and analysis for the prevention of adverse reactions and other possible problems related to the products, covering a wide spectrum of continuous analysis so that they do not cause any harm to the patient. We actively participate in decision-making when manufacturing to prevent possible complications in any of the production stages. Thanks to the standardization and development of specific protocols established for each production and subjected to continuous analysis adhering to very specific guidelines we are able to prevent these unwanted complications. We are mandated by compliance with the European Pharmacopoeia in Europe and adhere to current FDA regulations when manufacturing the different products corresponding to Biocell Ultravital Cellular Renovation Therapies.
Research and Development
When
Biocell Ultravital incorporates products with new formulas and they reach the market, at least an average of 5 to 7 years have elapsed, consumed in the different phases of research and development. This journey requires a scientific and economic effort, for this reason we say that out of every 300 new formulas that are beginning to be investigated, only 20 end up becoming treatments available to patients either as an adjunct or preventive of cellular function and the immune system.
Working in the context of formulas based on opotherapeutic extracts or cells of xenogeneic origin, they aim to support the expansion of products for basically strengthening the immune system.
Cellular Renovation Therapy may contribute as reinforcement to the primary treatment to treat the various human diseases that are associated with failures of the immune system. In order to achieve this purpose the continuous efforts of a scientific committee structured by various institutions in the field biology headed by Prof. Dr. Ben L Pfizer is needed. These contributions guide new formulations that improve the components has been allocated to four fundamental guidelines with specific objectives corresponding to the 4th generation cellular products by Biocell Ultravital: Protection, Repair, Revitalization and Regeneration properties. These therapeutic lines are developed with a common research and development strategic plan for each product category.
Manufacturing Plants and Procedures
In Europe, research, production and development is carried out at Biocell Ultravital, France, and we share part of the manufacturing in two other associated plants, mainly for the production of some raw materials, between Germany and the Netherlands.
We also manufacture our products in the USA, BIOCELL ULTRAVITAL USA Laboratories, where we have a modern production factory especially for manufacturing formulas and products for oral presentation.
Since our products formulas require components be extracted from a biological source, in all manufacturing plants we have ensured that they are manufactured in production rooms that have state-of-the-art equipment controlled by software that manages the procedures monitoring each phase of the process. Development with the latest air conditioning, quality and safety systems, to ensure that the final product does not lose its therapeutic potency, for this reason the active ingredients of each formula and the preparation in the initial phase are conditioned in isolated clean rooms and by specialized professionals trained to measure and control the production process from the moment this first manufacturing phase begins and continuing these quality controls through each phase of production until the final product is approved.
Each manufacturing plant, although with different facilities, produces with the same manufacturing procedures, efficiently following the highest quality standards that comply with all the regulations established by the European Pharmacopoeia and the FDA.
Products that Improve Cellular Renovation
Currently there is a growing interest in cell therapy extracted from the patient’s own stem cells, unlike our products,
Cellular renovation therapies (CRT) provide sustained results without complications and represent a great economic saving in comparison. The products in the Biocell Ultravital line of
Cell Renewal Therapies are divided into 5 main groups that include:
Regeneration, Revitalization, Detoxification, De-inflammatory and Hormonal.
CRT have worked with great success in recent years as a preventive treatment, without discarding its effective action as a primary therapeutic. The treatment benefits are notorious for their adjuvant action in allopathic medicine. CRT, through their formulas, exclusively allow us to transform diseased or aging organs into healthy organs with a highly functional capacity. Their components activate a series of stimuli that cells need for a normal cycle of continuous renewal, and they can be incorporated into the body through injections or orally. These various components are assimilated by the body through endocytosis and a good part is introduced into the cells. This is produced by the emission of pseudopods until they completely encompass it to form a vacuole, which then fuses with the lysosomes to degrade the phagocytosed substance, which is known by the name of phagosome. This method is characterized by being the mode of nutrition used by cells through ingestion of foreign matter. In addition, it is one of the greater means of transport that they use to defend themselves against some cells of multicellular organisms.
From this mechanism and many other stimulating biochemical changes, nutrition begins for an effective CELLULAR RENOVATION. CRT brings a fresh genetic information contained in DNA and RNA, stimulating secretion inducing old or sick cells and reprogramming to operate properly, providing the recipient bodies, a large number of biochemical and enzyme substrates containing information needed to revitalize an organ, or a gland. CRT contains various compounds that are primarily responsible for properly nourishing cells, but, moreover, each of the formulas in a CRT contains cells and embryonal tissues that increase positive changes in cell cycle complementing in part dysfunctional lapses. This is how the different components are first incorporated as essential nutrients and as well, how the embryonic tissues reach the organ with low vitality and that need to be dynamized. This process is called CELLULAR RENOVATION and its benefits are perceived after several weeks, as it passes slowly from the cell to the tissue, from the tissue to the organ and from the organ to the system. Some specialists feel that the most important result of using CRT is the revitalization of the body’s immune defense mechanisms. When damage occurs to the cells that make up the different tissues and organs involved in the immune system, either through aging or environmental poisoning, the body becomes defenseless from both external invasion and internal degeneration. The damage caused to the organs of the immune system can be reversed by stimulating the body’s defense mechanisms to boost the health of the weakened organ.
Security System to Prevent Falsification
Biocell Ultravital has developed for the
4th generation a sophisticated security system for its products to prevent the repetition of copies and / or counterfeiting of our products. Moving forward, we will invest a great technological effort in each package to ensure that you will have an original product in your hand.
This security system is applied to new packaging that have a QR Scan code applied to a double security system, a first physical stage in the packaging that will reveal through a security tab if the product has been violated and a second with an implantation of sophisticated software that will allow you to check if the product you purchased is original through our website, or by downloading the new BIOCELL APP for Android and IOS for free.
The falsification of ethical and health products is a problem that is becoming increasingly important, and all the different therapeutic areas may be affected.
These counterfeits seek to pass for authentic products, copying the packaging material, the commercial image, the logo, the information brochures, as well as the shape and colors of the original product.
In addition, they use the same lot number, expiration date and other identifying elements of the authentic product. However, they are manufactured and placed on the market without the authorization of any health authority. These original and generic medicines, as well as vitamins are also falsified and even more so those products that enjoy prestige are the most vulnerable and these falsifications may contain active ingredients in incorrect doses or lower doses than those authorized, or the absence of active ingredients and even include some toxic elements. Many may even be manufactured under dangerous conditions that are not controlled. Thus, they can pose a significant risk to health and are sometimes especially difficult to identify.
In short, they look identical to the original product, but contain “uncontrolled” components that are life threatening.
he trade in counterfeit medicines is controlled by international criminal networks, and no region is exempt. Those countries with less controlled drug distribution systems are more vulnerable to this type of practice; However, the most developed countries are not spared from this evil, especially when patients purchase drugs on the internet or unauthorized websites. Unfortunately, in the past we have been victims of these unethical organizations and have had to report these facts to the authorities since many people especially in Asian countries, as well as Mexico and others in Central and South America are victims of misleading offers of therapies, even by unethical doctors who offer the products at prices lower than the real cost. However, in the end they spend more money due to the need to seek immediate clinical help as demonstrated on several occasions reported by us through our attorneys around the world from patients who were treated clinically for administering fake products.
