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H Citoplacell ®

Antioxidant – Endocrine Function 60 Capsules This product is not intended to diagnose, treat, cure or prevent any disease.

H Citoplacell 4G therapy works naturally to induce the body to restructure its endocrine mechanisms by regulating the functions of the cells either water-soluble or fat-soluble, involved in hormonal order. Acting in both cases through different protein transports and by empathy to cells. Its action as a cellular stimulant exerts an efficacy relying on its powerful antioxidant components for the activation of the cycles and its structure in the cells.

Cellular Antioxidant.

Old age is mainly a process of cellular, natural and progressive oxidation, but this mechanism can be slowed down by effective antioxidant medications, which minimize its effects and mitigate the ravages of organic and physical aging to prolong the life expectancy of each individual.

The oxygen that we use to breathe is one of the main components responsible for cellular oxidation and serves to produce energy throughout the body, but small portions of this element produce free radicals, which are formed normally in the body when metabolized. The powerful action of H Citoplacell 4G achieves a therapeutic effect in addition to the endocrine one. It provides high antioxidant protection, with an increase in cellular energy, and the components in its formula stimulate the function of the pituitary to improve the production of (HGH) Hormone, which decreases with age and stress. Among other benefits HGH is called the hormone of youth.

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What is H Citoplacell 4G?

A 100% natural pharmaceutical quality treatment that does not contain synthetic hormones, but does contain components that are authentic hormonal precursors, so its indication is highly effective as an adjuvant therapy in endocrine functions, in addition to its powerful activity as a cellular antioxidant.

How does it work?

It works through cellular extracts and powerful 4th generation antioxidants. The synergy of amino acids and catalyst peptides in H Citoplacell 4G stimulates the pituitary gland to produce more HGH, the human growth hormone, better known as the “youth hormone”, it also promotes the production of testosterone or estrogens, depending on the sex of the patient.

What benefits does H Citoplacell 4G provide?:

  • Excellent antioxidant for optimal cellular function
  • Increased protein synthesis in almost every cell in the body.
  • Increased mobilization of fatty acids from adipose tissue for energy.
  • It increases the production of testosterone in men and estrogen in women because it contains DHEA and pregnenolone.
  • It promotes the development of muscle mass, increases strength, increases endurance, and contributes to a slimmer body.
  • Significantly improves cognitive functions and mood.
  • Cellular antioxidant.
  • Cardio-protective properties of its coenzyme Q-10 components.

How should I take H Citoplacell 4G?

As a preventive treatment for healthy people, one (1) capsule in the morning and one (1) capsule at night is recommended daily for six continuous or interleaved months. For people with 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 adjunct to the medications indicated by the treating physician.

Note:

The dose can be increased according to the clinical picture of the patient and the judgment of the doctor; the results depend on the completion of the treatment.

What are the side effects of H Citoplacell 4G?

This product has no side effects or contraindications with other medications. It lacks toxic properties due to its 100% natural organic components.

Is Citoplacell 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 ones such as:

Biopharmaxie y Schweizer Klinik Biocell.

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H Citoplacell

Indications:

  • Excellent antioxidant for optimal cellular function.
  •  Increased protein synthesis in almost every cell in the body.
  • Increased mobilization of fatty acids from adipose tissue for energy.
  • It increases the production of testosterone in men and estrogen in women because it contains DHEA and pregnenolone.
  • It promotes the development of muscle mass, increases strength, increases endurance, and contributes to a slimmer body.
  • Significantly improves cognitive functions and mood.
  • Cellular antioxidant. Cardio-protective properties of its coenzyme Q-10 components.

Composition:

Boxes of 30 capsules of 650 mg. / Boxes of 60 capsules of 650 mg. Each 650 mg capsule. contains:
Opotherapeutic extracts: Placenta, Pituitary Gland, Adrenal Gland.
Peptide Extracts: Placenta, Pituitary Gland, Adrenal Gland.
Other Actives: Superoxide Dismutase, Glutathione Peroxidase, Glutathione Reductase, Glutathione Transferase, Adenosine Triphosphate (ATP) Ginkgo Biloba, Tecoma Curialis, Co enzyme Q10, Royal Jelly, Hydrolyzed soybean albumin, DHEA, KH3, Riboflavin, Pretinolone, Thiamine, Huperzine, Vinpocetine.
Stabilizers and Excipients.

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.

Administration:

Oral use, consume before taking food to improve absorption, preferably with water.

Dosage:

As a preventive treatment for healthy people, one (1) capsule 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.

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:

Contains a box with two (2) blisters of 15 capsules 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.

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.

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.

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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.


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.

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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.

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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.


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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:


Scientific bibliographies.


In 1980 Jean Dausset was awarded the Nobel Prize in Medicine for demonstrating that genetically determined cell surface structures regulate immunological reactions, inspiring in this scientific contribution Wagman decided to incorporate immunological extracts into the formulas of all first-generation Biocell Ultravital products in order to strengthen the immune system.


In 1999, Günter Blobel won the Nobel Prize in Medicine for his work in the 1970s, discovering that proteins have intrinsic signals that govern their transport and location in the cell.


In 2001 Paul Maxime Nurse was the winner of the Nobel Prize in Physiology or Medicine for his discoveries of key regulators of the cell cycle.


In 2007 Martin John Evans was awarded the Nobel Prize in Medicine for his work on stem cells and genetic manipulation in animal models.


In 2016 Yoshinori Ōsumi received the Nobel Prize in Medicine” for his discoveries on the mechanisms of autophagy for survival of mitochondrial energy in cells.


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Dr. Freddie Ulan

Chiropractor, Certified Clinical Nutritionist