Connecting Classical Phytotherapy to Molecular Receptors

Our research framework addresses the fundamental challenge in herbal medicine: standardizing heterogeneous plant materials into reproducible pharmaceutical candidates with quantified receptor affinities and validated pharmacokinetic exposure.

01

Classical Knowledge Base

Rigorous literature review across Charaka Samhita, Sushruta Samhita, and modern ethnobotanical reports to isolate traditional rationales.

02

Botanical Authentication

DNA barcoding, macroscopic identification, and species authentication to eliminate adulteration and ensure consistent raw-material sourcing.

03

Phytochemical Profiling

HPLC chromatography to quantify active therapeutic markers (Withanolides, Curcuminoids, Boswellic Acids, Cannabinoids).

04

Formulation Optimization

Designing advanced delivery matrices (SNEDDS, liposomes, modified-release) to overcome botanical bioavailability limits.

COLLABORATIVE RESEARCH VENTURE

Cannabinoid Research &
AYUSH Pharm Development

Nutrason Bioscience Pvt. Ltd., in strategic association with Sheen Biotech Pvt. Ltd., is engaged in research and early-stage product design involving cannabinoid-based ingredients, including non-intoxicating Cannabidiol (CBD), Cannabigerol (CBG), and THCA.

Interacting intimately with the human endocannabinoid system (ECS), these molecular compounds hold remarkable supportive promise for oncology-supportive wellness, restorative sleep architecture, stress regulation, neuromuscular comfort, and chronic inflammatory relief.

Alliance with Sheen Biotech Pvt. Ltd.

Combining Sheen Biotech's specialized capabilities in cannabinoid formulation design, novel delivery mechanisms, and analytical chromatography with Nutrason's deep AYUSH Pharm expertise to pioneer legally compliant, standardized cannabinoid science in India.

1

Raw-Material Authentication

Legally sourced, fully traceable botanical origin with strict screening for pesticides, heavy metals, residual solvents, and microbial safety.

2

Profiling & Standardization

Establishing rigorous specifications for CBD concentration, permitted legal THC limits, cannabinoid purity, and batch-to-batch uniformity.

3

Molecular & Bioavailability Synergy

Analyzing molecular receptor interactions and harmonizing cannabinoid isolates with synergistic Ayurvedic botanicals (Ashwagandha, Shallaki, Brahmi).

4

Dosage-Form Optimization

Formulating sublingual drops, tinctures, capsules, softgels, topical transdermal gels, ointments, and customized delivery solutions.

5

Quality Assurance & Stability

Accelerated climatic zone stability tests, packaging compatibility, shelf-life verification, and comprehensive pharmacovigilance.

Advanced Pharmaceutical Delivery Systems

Botanical actives often suffer from poor aqueous solubility, rapid first-pass hepatic metabolism, and low gastrointestinal permeability. Nutrason designs tailored pharmaceutical delivery systems to maximize therapeutic bioavailability and ensure clinical batch reproducibility.

Lipid Nano-Technology

Self-Nanoemulsifying Systems (SNEDDS & SEDDS)

Isotropic anhydrous mixtures of therapeutic oils, surfactants, and co-surfactants that spontaneously form fine oil-in-water nano-droplets (20–100 nm) upon contact with gastrointestinal fluids.

  • Target Actives: Highly lipophilic phytocannabinoids (CBD/CBG), Curcuminoids, Boswellic acids.
  • Pharmacokinetic Benefit: Bypasses intestinal P-glycoprotein efflux and increases lymphatic transport, elevating bioavailability by up to 400%.
  • Dosage Form: Liquid-filled hard gelatin or HPMC vegetarian capsules.
Quality Criteria: Thermodynamic stability, droplet size distribution (<50 nm PDI), zero phase separation across 24 months.
Solid Oral Dosage

Modified-Release & Gastro-Resistant Tablets

Polymeric hydrophilic matrix tablets and enteric film-coated solid platforms engineered to resist acidic gastric degradation (pH 1.2) and release standardized botanical actives selectively in the alkaline intestinal lumen (pH 6.8).

  • Target Actives: Acid-sensitive withanolides, saponin glycosides, and therapeutic enzymes.
  • Pharmacokinetic Benefit: Prevents premature gastric hydrolysis and extends therapeutic plasma concentration over an 8 to 12-hour window.
  • Dosage Form: Bi-layer compressed tablets, enteric film-coated caplets.
Quality Criteria: USP/IP Dissolution apparatus testing (<10% release in 0.1N HCl, >80% in buffer pH 6.8 within 45 mins).
Molecular Complexation

Phytosome & Phospholipid Complexation

Patented stoichiometric molecular complexes wherein individual polyphenolic molecules are chemically bonded to dietary phospholipids (phosphatidylcholine), transforming poorly absorbed hydrophilic/lipophilic phytocomplexes into highly permeable lipid-compatible vesicles.

  • Target Actives: Curcumin C3, Boswellia AKBA, Green Tea EGCG, Silymarin.
  • Pharmacokinetic Benefit: Drastically accelerates passive enterocyte absorption; achieves up to 5-fold higher peak plasma concentration (Cmax).
  • Dosage Form: Standardized powder suspensions, high-potency capsules.
Quality Criteria: Nuclear Magnetic Resonance (NMR) confirmation of hydrogen bonding between flavonoid OH groups and phosphatidylcholine head.
Mucosal Absorption

Sublingual & Buccal Mucosal Droppers

Micronized tincture droppers and hydro-ethanolic botanical solutions formulated for sublingual capillary plexus absorption directly into systemic circulation via the jugular vein.

  • Target Actives: Pure CBD/CBG isolates, Valeriana (Tagara), Jatamansi, Shankhpushpi.
  • Pharmacokinetic Benefit: Completely circumvents liver first-pass metabolism; delivers rapid onset of action within 15–25 minutes for acute palliative pain and sleep latency.
  • Dosage Form: Calibrated medical dropper bottles with tamper-evident pipettes.
Quality Criteria: Mucosal non-irritancy index, microbial sterility, precise volumetric dosing accuracy (±2%).
Dermatological & Transdermal

Penetration-Enhanced Hydrogels & Emulsions

Non-greasy, biomimetic topical lipid emulsions and aqueous hydrogels engineered with natural terpenes (menthol, cineole) and cold-pressed seed oils that reversibly fluidize stratum corneum lipids.

  • Target Actives: Nirgundi extract, Shallaki, Aloe barbadensis inner fillet, Yashad Bhasma.
  • Pharmacokinetic Benefit: Delivers concentrated anti-nociceptive actives directly to deep articular tissues without systemic gastric exposure.
  • Dosage Form: Airless pump dispensers, laminate tubes.
Quality Criteria: Franz cell transdermal flux rate testing, pH compatibility (5.5±0.3), epidermal hydration index.
Micro-Encapsulation

Micro-Encapsulated Dry Suspensions & Granules

Spray-dried polymeric encapsulation utilizing maltodextrin and modified acacia gum matrices to protect volatile phytoconstituents (essential terpenes, monoterpenes) against thermal degradation and oxidation.

  • Target Actives: Aromatic digestive bitters, volatile monoterpenes, pediatric nutraceutical matrices.
  • Pharmacokinetic Benefit: Masks intense bitterness and enables instantaneous, clump-free aqueous dispersion for pediatric and convalescent consumption.
  • Dosage Form: Moisture-sealed sachets, dispersible oral granules.
Quality Criteria: Particle size distribution (50–150 μm), moisture content (<3.5%), reconstitution time under 10 seconds.

Investigational Molecules & Cellular Pathways

Nutrason investigates characterized botanical single molecules and standardized multi-compound complexes across documented cellular signaling pathways.

Withaferin A

Withania somnifera (Ashwagandha)
Preclinical Oncology Signal

Steroidal lactone investigated for binding to heat-shock protein 90 (HSP90), downregulating NF-κB, and modulating cytoskeletal vimentin in breast cancer and lymphoma models.

Key Pathways: Cellular stress response, apoptosis induction, proteasome inhibition.

Curcuminoids C3 Complex

Curcuma longa (Haridra)
Clinical Supportive Care

Standardized tricurcuminoid mixture (Curcumin, Demethoxycurcumin, Bisdemethoxycurcumin) inhibiting COX-2, 5-LOX, TNF-α, and downstream pro-inflammatory interleukins.

Key Pathways: NF-κB suppression, systemic cytokine dampening, antioxidant scavenging.

Thymoquinone

Nigella sativa (Kalonji)
Preclinical Pancreatic Models

Bioactive quinone investigated in cell and animal models for mitochondrial apoptosis induction and potentiation of conventional chemotherapeutic sensitivity.

Key Pathways: Reactive oxygen species (ROS) regulation, p53 upregulation, cell cycle arrest.

Berberine Hydrochloride

Berberis aristata (Daruharidra)
Human Trial Signal (Adenoma)

Isoquinoline alkaloid with documented clinical trial evidence for reducing colorectal adenoma recurrence through AMP-activated protein kinase (AMPK) activation.

Key Pathways: AMPK phosphorylation, intestinal mucosal barrier preservation, glucose homeostasis.

Acetyl-11-Keto-β-Boswellic Acid

Boswellia serrata (Shallaki)
Arthritis & Neuropathy

Pentacyclic triterpene that acts as a non-redox, allosteric inhibitor of 5-lipoxygenase (5-LOX), selectively blocking leukotriene B4 synthesis without gastric ulceration.

Key Pathways: 5-LOX inhibition, cartilage matrix degradation protection, cerebral edema reduction.

Cannabidiol & Cannabigerol (CBD/CBG)

Cannabis sativa (Licensed Sourcing)
Supportive Care & Neuro

Non-intoxicating phytocannabinoids with diverse multi-target pharmacology across the endocannabinoid system, TRPV1 vanilloid receptors, and 5-HT1A serotonergic pathways.

Key Pathways: Negative allosteric modulation of CB1, GABAergic tone support, FAAH enzyme inhibition.

6-Stage Analytical Quality Protocol

Every investigational formulation developed by Nutrason undergoes strict analytical screening to ensure zero heavy metal contamination, zero solvent residues, and exact phytochemical marker quantification.

1

DNA Barcoding & Identity

Verification of exact botanical species and taxonomic authenticity to eliminate cross-species contamination.

2

HPLC/HPTLC Fingerprint

High-Performance Thin-Layer and Liquid Chromatography to quantify active marker peaks against primary reference standards.

3

GC-MS Residual Solvents

Gas Chromatography-Mass Spectrometry confirming compliance with ICH Q3C limits for extraction solvents.

4

ICP-MS Heavy Metals

Inductively Coupled Plasma Mass Spectrometry quantifying Lead, Arsenic, Cadmium, and Mercury down to parts-per-billion (ppb).

Research Governance & CYP450 Interaction Screening

In accordance with ethical hospital collaboration guidelines, Nutrason screens all botanical candidates for potential interactions with Cytochrome P450 enzymes (CYP3A4, CYP2C9, CYP2D6). This protects patients undergoing chemotherapy or taking conventional cardiovascular/neurological medications from unanticipated pharmacokinetic fluctuations.

Nutrason High-Tech Cleanroom Analytical Facility
Analytical Quality Standards

HPLC Chromatography & Phytochemical Standardization Facility

Operating in full compliance with cGMP, WHO-GMP, and AYUSH Pharmacopoeial monographs. Our facility in Noida, UP executes batch-to-batch standardization, accelerated climatic zone IVB stability testing, and full analytical dossier compilation.

Scientist & Hospital Inquiries

Collaborate With Our Molecular R&D Team

Connect with our pharmacologists and formulation scientists to discuss investigational delivery systems, hospital clinical protocols, or customized AYUSH proprietary medicine supply.

Inquire on WhatsApp (+91-7303590059) Visit Contact Desk
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