| Customization: | Available |
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| CAS No.: | 2381089-83-2 |
| Formula: | C18h3on4og |
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BRONCHOGEN® is a dietary supplement with а synthesized Khavinson's bronchial peptide. It normalises the function of the bronchi by reducing peptide deficiency and restoring protein synthesis inside a cell.
Peptide complex for the broncho-pulmonary system, is used treating acute and chronic bronchitis, chronic obstructive pulmonary disease (COPD).
Bronchogen is recommended for patients suffering from chronic bronchitis to increase immune system and endurance of the respiratory system. Bronchogen is prescribed to prevent exacerbation of bronchopulmonary system chronic diseases and to increase the overall effectiveness of bronchitis, COPD and asthma treatment.
Indications for use:
Bronchogen can be easily combined with other supplements and medicines and should be used in addition to conventional medical treatments. Bronchogen does not have any side effects, does not cause allergic reactions and addiction.
Ingredients:
Peptidе AKS-B (L- alanin; L- aspartic acid; L- glutamic acid; L- arginine). Inactive ingredients: microcrystalline cellulose (E460), beet root sugar, lactose, starch, Tween-80.
Recommendation for application:
Adults: 2 capsules twice a day, with food, during 1 month. After 3-6 months it is advisable to repeat the course to achieve the best results.
After the course of Chonluten it is recommended to take natural lungs and bronchi peptide TAXOREST® (2 capsules before meal every morning during 1-2 months).
Contraindications:
individual intolerance of components, pregnancy, lactation.
Form of production:
60 capsules of 0.275 g.
Storage conditions:
store at a temperature between +5°C and +25°C in a dark place
| Items | Specifications |
| Business Type | We are a manufacturer of GMP peptide and provide OEM service. The lid also can be customized |
| Filling amount | The filling amount is 2-5mg extra per bottle. |
| Purity | The purity is above 99% |
| Price | Competitive price |
| Delivery time | The delivery time is stable and short. If you pay before 12 a.m,the goods can be shipped on the same day. |
| Shipping risk | If the package was lost we will resend the goods to you,so you won't suffer a loss if you buy it. |
Zhaobo Bio acquired early mastery of development and manufacturing of peptides, the short chain amino acids linked by peptide bonds that have enabled new generations of small molecule drugs that closely mimic the body's natural pathways.
Now Zhaobo Bio possesses first-class capabilities to manufacture peptides at industrial scale and in full compliance with the strictest Good Manufacturing Practice (GMP) standards.
Upstream peptide synthesis
Zhaobo Bio production plants are endowed with state-of-the-art equipment for solvent supply, peptide synthesis, purification and isolation of active ingredients and intermediates. All equipment and containment is GMP qualified and cleaning validated. Overlapping capacities and sizes of different equipment trains facilitate a smooth scale-up for increases in demand within the product life cycle.
Downstream purification and isolation of peptides
Zhaobo Bio is committed to the systematic expansion and modernization of its purification equipment in order to ensure the efficient production of ever-increasing amounts of bulk peptide pharmaceuticals.
It uses sophisticated methods for large scale purification campaigns such as preparative high performance liquid chromatography (HPLC), ion exchange (IEX), size-exclusion chromatography (SEC), and ultra-filtration (UF/TFF). The equipment in place permits highly efficient or even continuous manufacturing of extremely pure products up to multi-kg quantities per lot.
For preparative HPLC, dynamic axial compression (DAC) stainless steel columns of up to 60 cm diameter both in batch and continuous mode are packed with the appropriate high performance silica separation phase. For low-pressure chromatography columns up to 80 cm diameter are available. Solvent delivery is ensured from eluent tank farms and containers.
The control of microbiological contamination is a prerequisite for API manufacturing. Class D (ISO 8) and C (ISO 7) clean rooms are supplied via HEPA-filtered, temperature and humidity controlled air, down-flow booths are used for minimizing microbial contamination and protecting operators. Highly active pharmaceutical ingredients are handled in integrated safety workbenches or flexible isolators reaching OEB level 4 (1-10 µg/m3).
Predefined physicochemical properties of the API can only be achieved by a carefully controlled isolation process. Besides precipitation and crystallization, lyophilization of intermediates and final API is a standard unit operation. LaixingPharma have multiple lyophilizers in different sizes (up to 300 liters) located in clean rooms.
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