Research & Development
RSO has established a solid scientific foundation for its potent pharmacological properties.
Its therapeutic efficacy has been rigorously validated through the significant reduction
of inflammatory cytokines and IgE levels in atopic dermatitis and ulcerative colitis models.
Beyond local treatment, RSO is gaining international recognition as a pioneering
pharmaceutical agent that optimizes the internal biological environment by modulating
the microbiome to strengthen immunity and promote hair growth.
Leveraging this unrivaled technology, we remain dedicated to advancing disease prevention
and treatment, consistently contributing to the betterment of human health and global well-being.
As a next-generation bio-material, RSO has scientifically proven its exceptional efficacy—ranging from the prevention of respiratory viral infections
to the treatment of systemic inflammatory diseases—through well known international scientific journals.
The exceptional efficacy of RSO has been rigorously validated through publications in numerous prestigious international journals (SCI-level).
For those who wish to explore more detailed research data and findings regarding RSO, please refer to the publication links provided below.
International Journals
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Therapeutic efficacy and mechanism of solubilized sturgeon oil in a mouse model of house dust mite-induced atopic dermatitis
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The preventice effect of solubilized sturgeon oil on dextran sulfate sodium-induced ulcereative colitis via inflammation attenuation and intestinal microbiota regulation
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Exploring the Preventive Potential of Solubillized Sturgeon Oil on Acute Infection with Respiratory Viruses
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Hair Growth Promoting Effects of Solubilized Sturgeon Oil and Its Correlation with the Gut Microbiome
” API ”
Active Pharmaceutical Ingredient
The API, is the substance utilized in the manufacture
of a finished pharmaceutical product.
It is the Active Biological Moiety that, upon administration, provides the intended
Pharmacological Activity or other direct effects within the human body, thus being
used in the diagnosis, cure, mitigation, treatment, or prevention of disease.
Essentially, the API is the key therapeutic component that determines
the efficacy of the medicine.
The API is the Chemical or Biological Entity that delivers the therapeutic effect
against a disease within the drug's Dosage Form (e.g., tablet, capsule, or injection).
Due to its critical importance, the API must be manufactured in accordance with
strict GMP(Good Manufacturing Practice) guidelines to maintain high purity and specific physicochemical characteristics (e.g., solubility, crystal form, and stability).
Consequently, it constitutes the central focus of Quality Control to ensure the safety,
efficacy, and quality of the finished drug product.
” FDA OTC ”
Food and Drug Administration Over the Counter
FDA OTC status designates pharmaceutical
products that are deemed safe and effective for consumer self-medication
without a prescription, and our commitment is to ensure these products,
primarily regulated via the rigorous OTC Monograph system, adhere to
the highest standards of safety, quality, and efficacy for broad public access.
” FDA NDA ”
Food and Drug Administration New Drug Application
The NDA is the rigorous and pivotal regulatory milestone submitted to
the U.S. FDA to formally seek market authorization. Successful NDA approval,
which demands exhaustive scientific validation of the drug's safety, therapeutic
efficacy, and manufacturing quality under strict GMP standards, serves
as the ultimate proof of global standard compliance, granting exclusive
access to the highly valuable U.S. pharmaceutical market.
