Polydeoxyribonucleotide Powder
Description
Premium Polydeoxyribonucleotide Powder - Clinical-Grade Regenerative Ingredient
With over 25 years of experience in the biotech industry and an annual production capacity of more than 5,000 tons, Hunan Clover Origins Biotech provides Polydeoxyribonucleotide Powder of pharmaceutical grade with a purity of 99%. Our product is obtained from sustainable salmon DNA, with a uniform molecular weight distribution (50-1,500 kDa) by controlled extraction techniques. DNA content >95%, A260/A280 ratio between 1.8 and 2.0 and endotoxin levels <0.5 EU/mg. This product is compliant with FDA, ISO 9001, HACCP and FSSC 22000. We offer flexible MOQ, fast 5-10 day bespoke production and full documentation assistance for medical esthetics, wound care and regenerative medicine applications world-wide.
What Makes Our Polydeoxyribonucleotide Powder Different?
The PDRN is a high dimensional biomaterial, specifically developed for tissue regeneration purposes. This uniform mixture of deoxyribonucleotide polymers is an adenosine A2A receptor agonist that induces a cascade of regeneration responses at the cellular level.
Our bio-extracted powder is more biocompatible than synthetic equivalents. The particular range of molecular weights allows the rapid synthesis of DNA via the 'salvage pathway'. This greatly minimizes the metabolic expenditures in the processes of tissue repair.
You will benefit from our controlled purifying process that maintains structural integrity. The resulting white to off white lyophilized powder is highly soluble in physiological saline and aqueous buffers. This provides an easy formulation for your manufacturing needs.
We have a thermal stability advantage over protein-based compounds ; therefore, we deliver constant performance. When properly prepared, this powder is resistant to enzymatic degradation, providing you with a stable shelf life for your completed products.
Technical Specifications & Quality Parameters
| Parameter | Specification | Test Method |
|---|---|---|
| Purity | 99% | HPLC |
| DNA Content | ≥95% | UV Spectroscopy |
| Molecular Weight Range | 50-1,500 kDa | GPC/SEC |
| A260/A280 Ratio | 1.8-2.0 | UV Spectrophotometry |
| Endotoxin Level | <0.5 EU/mg | LAL Test |
| Residual Protein | <0.1% | BCA/Lowry Method |
| Appearance | White to off-white powder | Visual |
| Solubility | Soluble in physiological saline | Dissolution Test |
| Heavy Metals | Meets EP/USP standards | ICP-MS |
| Residual Solvents | Compliant | GC-HS |
| Source | Salmon DNA (Oncorhynchus spp.) | Documented |
Core Regenerative Benefits for Your Formulations
Tissue Regeneration Support
Our powder supports cell repair and accelerates wound healing. It boosts fibroblast activity and increases synthesis of collagen type I. This is why it is perfect for post-procedure healing products.
You are able to harness it to induce natural restorative mechanisms. The nucleotide fragments serve as building blocks for cellular DNA synthesis. This is conducive to fast turn-over of tissue in aging or injured skin.
Anti-Inflammatory Performance
The chemical serves to regulate pathways of the inflammatory response. It decreases major inflammatory cytokines such as IL-1β and TNF-α. This characteristic is useful for orthopedic and dermatological applications.
When you use this ingredient, you will get two benefits: regeneration and inflammation control. This duo provides a more effective approach to chronic problems than single mechanism substances.
Angiogenesis & Vascularization
PDRN induces the formation of VEGF (Vascular Endothelial Growth Factor). This leads to improved development of blood vessels in areas with poor circulation. Better results are seen in wound healing and ischemia problems.
The increased vascularization brings the nutrients to the areas of healing. This speeds up the recovery times for your end users.

High-Performance Application Scenarios
Medical Esthetics and Skin Boosters
In the esthetic medicine field our Polydeoxyribonucleotide Powder is the active core of the solutions for micro-injections. It is beneficial in treating dermal atrophy in combination with non-crosslinked hyaluronic acid.
The powder is active in complicated dermal microenvironment. It speeds up recovery after laser resurfacing and microneedling. Your clinic partners will like the less downtime for their patients.
A uniform molecular weight distribution is beneficial for mesotherapy products. This allows for consistent pharmacokinetics and predictable regeneration outcomes between treatments.
Orthopedics & Sports Medicine
High concentration PDRN may be formulated for intra-articular injection. This chemical serves as a tissue healing agent in the treatment of tendinitis and osteoarthritis management.
It has anti-inflammatory effects on cytokines and stimulates the growth of chondrocytes in the synovial fluid milieu. Doing both will give you pain relief and structural progress.
Better results have been shown for tendon and ligament restoration in regenerative sports medicine applications. The substance helps get athletes back to action faster.
Applications in Clinical Wound Care
Our powder is used in sterile preparations for hospital-grade formulations. These include eye drops to treat corneal ulcers and topical gels for diabetic foot ulcers.
The ability to induce angiogenesis is important in inadequately vascularized tissues. This mechanism will solve a major challenge in chronic wound care.
Deficits in peripheral circulation react especially well to PDRN's encouragement of vascular development. It is hence well suited for problematic patient populations.
Advanced Cosmeceutical Development
Formulate high-end barrier repair serums with medical-level positioning. Anti-inflammatory activity and protection against UV-related DNA damage.
Your products benefit from a competitive edge in the premium skin care segment. The substance is reliable in complex multi-active compositions.
Visible benefits of skin quality enhancement and dermal recovery support. This results in client happiness and repeat sales for your brand.
Rigorous Quality Control Protocol
Multi-Tiered Testing Standards
We do thorough quality checks at all stages of production. Molecular weight distribution is confirmed by Gel Permeation Chromatography (GPC/SEC) to be in the physiologically active range of 50-1,500 kDa.
BCA or Lowry techniques for residual protein analysis reduce immunogenicity risk. Our limits are below 0.1%, ensuring your injectable formulations are safe for patients.
All batches should be tested for endotoxin by LAL assay. This inhibits pyrogenic reactions in delicate medicinal applications. Certificates of analysis are provided with every order.
Heavy Metal and Contaminant Screening
ICP-MS screening demonstrates conformity with EP/USP heavy metal standards. We regularly test for lead, arsenic, cadmium and mercury.
GC-HS residual solvent testing shows no hazardous extraction compounds are left. This is to ensure the integrity of the formulation and safety of the end-user.
We have a thorough traceability system that traces each batch from the source ingredient to the finished powder. Ensure total visibility into supply chain for regulatory filings.
Third Party Verification
We work with globally known labs such as Eurofins, SGS and Alkemist Labs. Quality claims are independently validated by third-party independent testing .
They assist your regulatory filings with certificates from these trusted sources. They boost customer confidence in your end products.
On request, testing documentation for a given batch can be provided within 12 hours. This quick turnaround will assist you in your production scheduling.

Why Partner With Clover Origins?
Manufacturing Excellence
Our 3 advanced facilities maintain GMP standards throughout production. Annual capacity over 5,000 tons ensures stable supply for your growing business.
We provide flexible MOQ options that allow for both small-scale testing and large-scale commercial production. Standard products ship within 1-2 days from our existing inventory.
Custom details are completed within production times of 5-10 days. Quick turnaround means your product development stays on track.
Technical Support & Customization
Our R&D department provides custom solutions tailored to your specific formulation needs. Our services include premix enhancement and compound development.
OEM/ODM manufacturing supports various dosage forms. These include capsules, gummies, liquids and powder blends for finished product demands.
Technical documentation is available within 12 hours of the request. Sample development is completed within 7 working days for your evaluation.
Global Compliance Administration
We are FDA registered and certified to ISO 9001, FSSC 22000, HACCP, Kosher and Halal standards. This broad scope is the basis for operations in highly regulated markets.
Quality parameters are equal to or better than those of China, the EU and the USA. Our compliance-focused manufacturing method gives you confidence in your exports.
We offer complete documentation packages for your regulatory submissions. This includes CoA, allergen statements, BSE/TSE certificates and stability data.
Dependable International Logistics
We rely on long-standing relationships with DHL, FedEx, UPS and TNT to guarantee reliable delivery. Same-day pickups are available for urgent shipments.
Our extensive customs clearance experience reduces border delays. Ocean and air cargo options offer economical solutions for different shipment sizes.
Real-time tracking keeps you informed throughout your shipment. We provide coordination support until your package is safely delivered.


FAQ
Q: What is the typical molecular weight range of your product?
A: Our PDRN maintains a standardized range of 50-1,500 kDa. This specific distribution optimizes biological activity for tissue regeneration. GPC/SEC testing verifies each batch meets these parameters before release.
Q: Is your powder suitable for injectable formulations?
A: Yes, our pharmaceutical-grade powder meets injectable standards. Endotoxin levels stay below 0.5 EU/mg, and residual protein content remains under 0.1%. These specifications support sterile manufacturing requirements.
Q: What documentation do you provide for regulatory submissions?
A: We supply comprehensive packages including CoA, manufacturing flow charts, allergen statements, BSE/TSE certificates, heavy metal test reports, and stability data. Third-party testing certificates from Eurofins or SGS are available upon request.
Q: Can you customize the molecular weight distribution?
A: Our R&D team can adjust specifications within feasible ranges. Custom development requires 7 days for sample preparation and validation testing. Contact us with your specific requirements for evaluation.
Q: How do you ensure batch-to-batch consistency?
A: We implement full-process traceability and standardized extraction protocols. Each batch undergoes identical testing sequences. Statistical process control monitors critical parameters to maintain consistency.
Q: What is your minimum order quantity?
A: MOQ varies based on specification requirements. Standard 99% purity powder typically starts at 1 kg for initial trials. We offer flexibility for R&D quantities and scale up as your needs grow.
Q: How should the powder be stored?
A: Store in tightly sealed containers at 2-8°C in a dry environment. Avoid repeated freeze-thaw cycles. Under proper conditions, shelf life extends to 24 months from manufacturing date.
Q: Do you provide samples for formulation testing?
A: Yes, we offer free samples (typically 10-50g) for qualified partners. Sample requests receive response within 1 hour, with shipment within 24-48 hours for stock items.
Start Your Regenerative Product Development Today
Partner with Hunan Clover Origins Biotech for reliable supply of premium Polydeoxyribonucleotide Powder. Contact our team at info@cloverorigins.com for specifications, samples, or technical consultation.
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