Mahayograj Guggul
Mahayograj Guggul is a classical Ayurvedic guggulu, a resin-based preparation. Listed in Ayurvedic Formulary of India (AFI) Part I; quality standards established by CCRAS; UHPLC/HPTLC validated quality control methods published (2022).
| Also known as | Mahayograj Guggul, MahayograjGuggul |
|---|---|
| Pharmacopoeia status | Listed in Ayurvedic Formulary of India (AFI) Part I; quality standards established by CCRAS; UHPLC/HPTLC validated quality control methods published (2022) |
Names and identification
| Language | Name |
|---|---|
| English | Mahayograj Guggul |
Where is it described in the classical texts?
Bhaishajya Ratnavali (Amavata Chikitsa); also referenced in Sharangdhara Samhita and Yoga Ratnakara
How does it work?
- Anti-inflammatory action: Guggulsterones (E and Z) reduce joint inflammation by inhibiting NF-kB pathway and modulating pro-inflammatory cytokines (TNF-alpha, IL-6, IL-1beta)
- Ama digestion and metabolic correction: The formulation’s primary action is on Ama (metabolic toxins); it digests Ama and prevents further formation by rectifying digestive processes and metabolic activities
- Lipid metabolism modulation: Guggulsterones act as FXR antagonists, promoting bile acid synthesis and cholesterol excretion
- Mineral supplementation via bhasma: Processed metallic calx (iron, tin) provide bioavailable trace minerals that support enzymatic processes and tissue repair in musculoskeletal system
- Bioavailability enhancement: Piperine from Trikatu inhibits hepatic and intestinal glucuronidation and P-glycoprotein efflux, enhancing absorption of all active phytoconstituents
Which traditional uses are supported by research?
- Rheumatoid arthritis (Amavata) management validated in double-blind clinical study showing 30% greater DAS28 score reduction than standard guggul extract
- Comprehensive joint disorder relief validated through broad anti-inflammatory and analgesic mechanisms across multiple pharmacological studies
- Gout management supported by uric acid reduction and anti-inflammatory mechanisms validated in clinical observations
- Neurological and musculoskeletal pain relief supported by Vata-pacifying and nervine properties confirmed in traditional prescribing data
What do recent clinical trials show?
3 further claims previously listed here could not be traced to a published paper and have been removed. Classical formulations are researched largely in journals that PubMed does not index, so an absence here reflects the reach of the index rather than the state of the evidence.
Recent safety updates
- Contains processed heavy metals (Vanga, Naga, Rasa Sindhura) - must be prepared strictly according to classical Shodhana (purification) protocols; self-medication strongly discouraged; use only under qualified Ayurvedic physician supervision
- Not recommended in pregnancy, lactation, or children; periodic monitoring of liver and kidney function advised for use beyond 3 months; may interact with anticoagulants, thyroid medications, and NSAIDs
What is it made of?
Mineral/Elemental Profile
- Primary component: Mineral-derived preparation
- Note: Composition varies by specific preparation method
Analytical Methods: XRD, ICP-OES, SEM-EDS
Dosage forms and preparation
Dosage Forms: Vati (pill/tablet), Capsule
Standard Dosage: 2 tablets twice daily
Bioavailability: Guggulu resin acts as natural bioenhancer; guggulsterones have moderate oral bioavailability (~40%); lipophilic matrix aids absorption of co-formulated herbs
Optimal Timing: After meals, twice daily
Shelf Life: 2 years (guggulu preparations per ASU); potency may decrease after 1 year
Storage: Airtight container, cool dry place; guggulu preparations are hygroscopic
Marker Compounds: Guggulsterone Z, Guggulsterone E, Piperine
Quality Parameters: Weight variation ±5%, disintegration <60 min, hardness 4-8 kP, assay: Guggulsterone Z, Guggulsterone E, Piperine, guggulsterone content
Vehicle (Anupana): Warm water
Synergistic Combinations
- Key herbs: Guggulu with Triphala, Trikatu, Vidanga + 20 herbs and bhasmas; guggulu potentiates anti-inflammatory and hypolipidemic actions
Composition
As given in the Ayurvedic Formulary of India, Part I, entry 5:6 (MAHA YOGARAJA GUGGULU), which cites Sarmngadharasamhita, Madhyamakhanda, Adhyaya 7; 56-60. (Printed thus at lines 10888-10889; "Sarmngadhara" is the OCR of Sarngadhara. The Devanagari colophon at line 10916 prints "(शार्धधरसंहिता, मध्यमखण्ड, अध्याय, 7; 56-60)".. Names, parts and quantities are transcribed as printed and checked row by row against the book. Manufacturers' versions of a classical formulation can differ from the formulary.
| # | Ingredient | Part | Quantity |
|---|---|---|---|
| 1 | Nagara (Sunthi) (sunthi) | rhizome | 3 g. |
| 2 | Pippali * | fruit | 3 g. |
| 3 | Cavya * | stem | 3 g. |
| 4 | Pippalimula (pippali) (pippali) * | root | 3 g. |
| 5 | Citraka * | root | 3 g. |
| 6 | Hingu-bhrsta | exudate | 3 g. |
| 7 | Ajamoda | fruit | 3 g. |
| 8 | Sarsapa * | 3 g. | |
| 9 | [illegible] | illegible | |
| 10 | [illegible] | illegible | |
| 11 | Renuka | seed | 3 g. |
| 12 | Indrayava (kutaja) (kutaja) | seed | 3 g. |
| 13 | Patha * | root | 3 g. |
| 14 | [illegible] * | fruit | 3 g. |
| 15 | Gajapippali * | fruit | 3 g. |
| 16 | Katuka * | Rt/Rz. | 3 g. |
| 17 | Ativisa * | root tuber | 3 g. |
| 18 | Bharngi | root | 3 g. |
| 19 | Vaca | rhizome | 3 g. |
| 20 | Murva * | root | 3 g. |
| 21 | Haritaki | pericarp | 40 g. |
| 22 | Bibhitaka | pericarp | 40 g. |
| 23 | Amalaki | pericarp | 40 g. |
| 24 | Guggulu-sodhita * | exudate | 180 g. |
| 25 | Vanga-bhasma * | 48 g. | |
| 26 | Raupya (rajata) bhasma (rajata) * | 48 g. | |
| 27 | Naga-bhasma * | 48 g. | |
| 28 | Loha sara (lauha) bhasma (lauha) * | 48 g. | |
| 29 | Abhraka-bhasma * | 48 g. | |
| 30 | Mandura-bhasma * | 48 g. | |
| 31 | Rasa Sindura (parada) (parada) * | 48 g. |
Cells marked illegible are damaged in the source scan. The ingredient name is shown where it was readable, and nothing is inferred to fill a gap.
* The scanned text was damaged at this row and the name was read from the entry's own Sanskrit verse.
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