PATHELEN®Hybrid Vet
A new innovative doping safe treatment for wound care in animals that works by eliminating the biofilm
PATHELEN® Hybrid Vet is a new microporous silica powder, that adsorbs wound exudate, reducing the healing time of chronic wounds and offers a cost-effective alternative to the current treatment options for wounds.
PATHELEN® is a pioneering European Class I Certified, U.S.FDA approved medical device without side effects and antimicrobial resistant safe.
PATHELEN® Hybrid Vet is an effective and powerful replacement for all other currently available antimicrobial wound treatments for animals
PATHELEN® Hybrid Vet is a wound powder which contains both hydrophilic and hydrophobic silicas in a highly porous structure. Through capillary action, these silicas
act to irreversibly adsorb wound exudative material (including bacterial toxins) to the upper surface of the layers of the powder from where it effectively evaporates.
PATHELEN® Hybrid Vet thus “de-toxifies” and cleans the wound.
PATHELEN® Hybrid Vet is not antibacterial but withdraws water from a bacterial biofilm, disrupting its structure and allowing the host’s immune system to gain entry and destroy the microorganisms present.
Due to its mode of action, PATHELEN® Hybrid Vet is able to treat a WIDE range of acute and chronic wounds.
Infected wounds*
Exuding Wounds
Wounds with resistant nuclei
Traumatic wounds
Any open wounds with a biofilm
PATHELEN® Hybrid Vet works most efficiently when a biofilm is present on the wound. It should not be used if there are obvious signs of infection i.e., erythema, swelling, warmth, beyond the wound.
*Based on independent case study (Italy 2020)
INGREDIENTS DESCRIPTION
Aerosil 300 Pharma
- Hydrophilic highly dispersed silica with an ability to absorb pathogenic protein substances (up to 800 mg/g) including microbial enzymes and toxins.
- The high level of hydroxyl (-OH) groups on the silica attract water and produce a dehydrating effect on the wound, removing oedematous fluid
Aerosil R972 Pharma
- Hydrophobic highly dispersed silica which absorbs low and middle molecular metabolites via capillary action
- Combing hydrophilic and hydrophobic silica therefore allows absorption of a much wider range of substances and pathogenic organisms within wounds
Benzalkonium Chloride
- Forms a molecular layer over the surface of the silica and serves as a surfactant and disinfectant
By disrupting the wound’s biofilm, it allows entry of the animal's body’s own immune cells, which destroy microorganisms within the biofilm, promoting the natural healing process and reducing the need for antibiotics.
PATHELEN® Hybrid Vet is an effective and powerful replacement for all other currently available antimicrobial wound treatment devices.
Clinical practice shows that the current, individual use of other antimicrobial agents in the treatment of purulo-inflammatory diseases and purulent wounds, does not always lead to the desired result. Additionally, misuse of antibiotics has contributed to the emergence of resistant (hospital) strains of pathogenic microorganisms, including methicillin-resistant Staphylococcus aureus (MRSA), and become a serious challenge for modern medicine.
PATHELEN® Hybrid can solve this problem, utilising new compositions based on highly dispersed silicas and which have enhanced absorptive, anti-inflammatory and wound-healing abilities for the treatment of a wide range of diseases caused by pathogenic microorganisms, in particular, purulent wounds. The intensity of the regeneration process and healing of infected ulcers and wounds depends largely on the speed with which they are cleared of pus and necrotic tissues. Applique sorption, a method of wound healing in which an absorbent in powder form is applied to the wound as a dressing, greatly accelerates this process. This absorption detoxification restores the integrity of the skin and mucous membranes by the removal of microbial cells, bacterial toxins and toxic metabolites of wound fluid and wound cavities in direct contact with the surface of PATHELEN®.
Another important therapeutic factor in the first phase of wound healing is dehydration, i.e. absorption of fluid from the wound cavity and perifocal tissues. Hydrophilic highly dispersed silica (HDS) can be used in the first phase of wound healing. Its detoxifying action is due to the absorption of pathogenic protein substances (up to 800 mg/g), including microbial enzymes, exo-and endotoxins (Lipopolysaccharides) and micro-organisms.
What is PATHELEN®
Does PATHELEN® stick on the wound when the dressing is removed?
Is PATHELEN® a licensed Medical Device or Medicine?
What does it do?
How do I use PATHELEN®?
How fast does it work?
Can PATHELEN® be used on dried wounds (once granulating Tissue has formed)?
Is there a restriction on how often it can be used?
Are there any side-effects from PATHELEN®?
What are PATHELEN® Ingredients?
35.9% Aerosil R972 Pharma
0.1% Benzalkonium chloride
Can PATHELEN® be used safely on young or pregnant animals?
Can PATHELEN® still be used once opened?
Can PATHELEN® be used alongside other drugs?
Is PATHELEN® protected by a Trademark and Patent?
Can PATHELEN® be administered without specialist training?
Has PATHELEN® been proven to work?
Female Pony, 3 years old
- Lacero contusion wound in the lumbar sacral region with exposure of the muscular masses of the rump and spinous processes of the last lumbar vertebrae.
- Given the considerable extent of the wound and the application of bandages in the affected area being possible, local dressings with 7.5% iodine solution, application of antibiotic spray and administration of systemic antibiotic for 7 days are carried out.
- From the seventh day, systemic therapy is suspended and the application of Pathelen is started; after thorough cleansing of the area and disinfection with a 7.5% iodine solution, rinse and apply the product over the entire area.
- Neo formation of granulation tissue and peripheral vascularity is observed.
Dott.ssa Concetta Molè
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Medical Device Class I - EMA European Medicine Agency (CE) Swissmedic registered under CH-201805-0002
U.S. FDA Regulation Number 3017399130
Nigerian NAFDAC 03-6974
Ghana FDA FDA/D.19-3044
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