Sementex (Solution, Cream) Instructions for Use
ATC Code
D03AX (Other drugs that promote normal scarring)
Clinical-Pharmacological Group
Drug that activates tissue metabolism, improves trophism and stimulates the regeneration process
Pharmacotherapeutic Group
Tissue regeneration stimulant
Pharmacological Action
Polydeoxyribonucleotide, obtained from trout milt.
It activates DNA synthesis, stimulates A-2 type receptors in the cell, enhances cellular proliferation and tissue metabolism, and activates the pentose phosphate pathway involved in cellular energy metabolism, which ensures the restoration of the structure and trophism of connective tissue, stimulation of collagen synthesis, and the formation of new tissue structure in scars of various etiologies.
It activates the engraftment processes of autografts during skin transplantation.
Pharmacokinetics
After intramuscular administration, Tmax is 1 hour. Cmax is 6.28 µg/ml.
It does not bind to plasma proteins.
It is metabolized at the plasma level by nonspecific DNases that adhere to the membranes of various cellular structures and break down Polydeoxyribonucleotide into oligo- and mononucleotides.
T1/2 is 3 hours. T1/2 of the α-phase is 24 minutes, of the β-phase is 150 minutes.
It is excreted mainly in the urine (65%) and in the feces. It does not accumulate.
Indications
Mechanical injuries with violation of the integrity of the skin; trophic ulcers; thermal burns of II-III degree; anal fissures and fissures of the mammary gland nipples; engraftment of skin grafts.
Aesthetic medicine: rejuvenation of the skin of the face and neck; skin restoration in the post-peeling period; stimulation of collagen synthesis in fine wrinkles; elimination of striae by the method of local infiltration.
ICD codes
| ICD-10 code | Indication |
| K60 | Fissure and fistula of anus and rectum |
| L90.6 | Atrophic striae |
| L90.9 | Unspecified atrophic skin change |
| L98.4 | Chronic skin ulcer, not elsewhere classified |
| N64.0 | Fissure and fistula of nipple |
| T14 | Injuries to unspecified parts of body |
| T30 | Burns and corrosions of unspecified body region |
| Z94.6 | Presence of transplanted bone |
| ICD-11 code | Indication |
| DB50.Z | Fissure or fistula of anal region, unspecified |
| DE2Z | Diseases of the digestive system, unspecified |
| EA40 | Tropical phagedenic ulcer |
| EE40.1Z | Striae of skin, unspecified |
| EE40.Z | Atrophy or degeneration of connective tissue of dermis or subcutaneous fat, unspecified |
| EF60 | Ischemic ulceration of the skin |
| EM0Z | Unspecified skin disorder |
| GB23.1 | Fissure or fistula of nipple |
| ME60.2 | Ulcerative skin lesion of unspecified nature |
| ND56.Z | Unspecified injury of unspecified part of trunk, limb or body region |
| NE11 | Burn of unspecified body region |
| QB63.5 | Presence of transplanted bone |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Solution, Cream
Intramuscularly, subcutaneously, externally.
Intramuscularly and subcutaneously, 3 ml every other day. The course of treatment is 15-20 days.
When using the local infiltration method: 3 ml once a day. The course is 5-7 procedures.
Externally: apply a thin layer to the affected surface 1-2 times a day. The duration of treatment is determined by the clinical picture.
Adverse Reactions
Allergic reactions.
Contraindications
Hypersensitivity; children under 16 years of age.
Use in Pregnancy and Lactation
Use with caution during pregnancy and lactation (breastfeeding).
Pediatric Use
Contraindicated in children under 16 years of age.
Special Precautions
It is recommended to combine the use of the injectable form of the drug with the external use of the cream. When treating contaminated and infected wounds, the drug should be used in complex therapy with antiseptics and/or antibiotics.
Drug Interactions
It enhances the action of hyaluronic acid.
Storage Conditions
Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.
Dispensing Status
Rx Only
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical DisclaimerBrand (or Active Substance), Marketing Authorisation Holder, Dosage Form
Cream for external use 80 mg/25 g: tube
Marketing Authorization Holder
Mastelli, S.r.l. (Italy)
Dosage Form
| Sementex | Cream for external use 80 mg/25 g: tube |
Dosage Form, Packaging, and Composition
| Cream for external use | 25 g |
| Polydeoxyribonucleotide | 80 mg |
25 g – aluminum tubes (1) – cardboard packs.
Solution for intramuscular and subcutaneous administration 5.625 mg/3 ml: amp. 5 pcs.
Marketing Authorization Holder
Mastelli, S.r.l. (Italy)
Dosage Form
| Sementex | Solution for intramuscular and subcutaneous administration 5.625 mg/3 ml: amp. 5 pcs. |
Dosage Form, Packaging, and Composition
| Solution for intramuscular and subcutaneous administration | 1 amp. |
| Polydeoxyribonucleotide | 5.625 mg |
3 ml – ampoules (5) – cardboard packs.
