ARK® is an autologous regenerative concentrate obtained from the patient's venous blood and/or adipose tissue immediately before the intervention. ARK® is applied when indicated and is part of the MIBRAR® protocol.
ARK® is created from the patient's own tissues and is used to support regenerative processes. Depending on the diagnosis and treatment goals, the doctor may recommend one fraction or a combination of fractions — this helps to more precisely select the biological component for the clinical situation.
AHF® is obtained by mechanical separation of venous blood using the CGF method (Concentrated Growth Factors). Contains plasma enriched with growth factors, anti-inflammatory factors and CD34+ stem cells. Separation is performed on Medifuge MF 200 equipment with disposable kits.
ALF® is obtained using the Lipogems® method — lipogenic separation of subcutaneous fat. Contains pluripotent mesenchymal stem cells with high differentiation potential. The concentration of beneficial cells in adipose tissue is 500–1,000 times higher than in bone marrow.
The combined option is used when it is advisable to combine the properties of both fractions. The specific scheme is chosen by the doctor after diagnosis.
The same name "plasma/concentrate" does not mean the same methodology and the same result. In the ARK® protocol, standards of obtaining and application are important because they directly affect material quality and safety.
ARK® is a powerful biological component, but its role is revealed precisely as part of the technology. In MIBRAR®, precise impact in the pathology zone and conditions created by specialized micro-invasive technique are important.
If everything is reduced to "just an injection," more often only short-term relief is achieved, not tissue structure restoration. Therefore, the doctor considers ARK® as part of a complete protocol, not as a standalone "universal procedure."
→ more often symptomatic effect
→ conditions for regenerative reconstruction (when indicated)
Since ARK® is obtained from the patient's own tissues, the probability of reactions associated with foreign substances is usually reduced. However, any medical procedure has limitations and potential risks — they can only be correctly assessed after diagnosis and in-person consultation.
In short: safety is not only "what is injected," but also how it is performed, who it is performed on, and which protocol is chosen.
Not always. Methods of obtaining, application standards, and clinical goals differ. In the MIBRAR® protocol, ARK® is part of a system, not a "standalone injection."
No. ARK® is applied fresh, immediately after obtaining.
No. The decision depends on the diagnosis, stage, contraindications, and treatment goal.
Structure restoration requires properly created conditions in the pathology zone. Therefore, ARK® is not used "in isolation" from the protocol.
There are no guarantees in medicine. The effect depends on many factors — from diagnosis to following recommendations.
ARK® is an autologous regenerative concentrate obtained from blood and/or adipose tissue. In everyday speech, patients often call this "stem cells," but more correctly — concentrate of own regenerative components.
Sensations depend on the method and material collection zone. During the consultation, the doctor will explain how this happens in your case.
No. ARK® is applied fresh, immediately after obtaining.
Because ARK® in MIBRAR® is considered part of a system: technique, precision of impact, and conditions for recovery are all important.
No. The option is chosen individually — based on diagnosis and treatment goal.
On the initial tissue condition, diagnosis, selected protocol, and adherence to recommendations during the recovery period.
During the consultation, the doctor will assess the diagnosis and offer a rational protocol: whether biological support is needed, which ARK® option is appropriate, and what the recovery plan will be.
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