Lavanga: Difference between revisions
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|title = Lavanga | |title = Lavanga | ||
|label1 = Section/Chapter | |label1 = Section/Chapter | ||
|data1 = Herb database/ | |data1 = Herb database/Lavanga | ||
|label2 = Botanical name(s) | |label2 = Botanical name(s) | ||
|data2 = Syzygium aromaticum (L.) Merr. & L.M.Perry | |data2 = Syzygium aromaticum (L.) Merr. & L.M.Perry | ||
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|data7 = [[Charak Samhita Research, Training and Skill Development Centre]] | |data7 = [[Charak Samhita Research, Training and Skill Development Centre]] | ||
|label8 = DOI | |label8 = DOI | ||
|data8 = | |data8 = {{DoiWithLink}} | ||
}} | }} | ||
[[File:Lavanga.jpg|thumb|'''Lavanga (''Syzygium aromaticum'')''']] | |||
== Botanical & Vernacular Names == | == Botanical & Vernacular Names == | ||
* '''Latin Name:''' ''Syzygium aromaticum'' | * '''Latin Name:''' ''Syzygium aromaticum'' | ||
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The primary therapeutic potential of Lavanga resides in its volatile essential oil ('''Clove Oil'''), which yields 15% to 20% of the dried flower bud weight. The volatile profile is dominated by phenylpropanoids and sesquiterpenes:<ref name="AbdulAziz2023">{{cite journal |vauthors=Abdul Aziz AH, Rizkiyah DN, Qomariyah L, Irianto I, Che Yunus MA, Putra NR |title=Unlocking the Full Potential of Clove (Syzygium aromaticum) Spice: An Overview of Extraction Techniques, Bioactivity, and Future Opportunities in the Food and Beverage Industry |journal=Processes |volume=11 |issue=8 |pages=2453 |year=2023 |doi=10.3390/pr11082453}}</ref> | The primary therapeutic potential of Lavanga resides in its volatile essential oil ('''Clove Oil'''), which yields 15% to 20% of the dried flower bud weight. The volatile profile is dominated by phenylpropanoids and sesquiterpenes:<ref name="AbdulAziz2023">{{cite journal |vauthors=Abdul Aziz AH, Rizkiyah DN, Qomariyah L, Irianto I, Che Yunus MA, Putra NR |title=Unlocking the Full Potential of Clove (Syzygium aromaticum) Spice: An Overview of Extraction Techniques, Bioactivity, and Future Opportunities in the Food and Beverage Industry |journal=Processes |volume=11 |issue=8 |pages=2453 |year=2023 |doi=10.3390/pr11082453}}</ref> | ||
* ''' | * '''Eugenol (4-allyl-2-methoxyphenol):''' Accounts for 70–90% of the total essential oil content. It functions as the primary bioactive constituent responsible for analgesic, anti-inflammatory, and antimicrobial actions. | ||
* '''Eugenyl Acetate:''' Comprises 2–15% of the oil, contributing to the sedative, anti-inflammatory, and antispasmodic profile. | * '''Eugenyl Acetate:''' Comprises 2–15% of the oil, contributing to the sedative, anti-inflammatory, and antispasmodic profile. | ||
* ''' | * '''β-Caryophyllene:''' Represents 5–12% of the oil, acting as a selective cannabinoid receptor type-2 (CB<sub>2</sub>) agonist with anti-inflammatory properties. | ||
* '''Polyphenols & Tannins:''' Contains gallic acid, ellagic acid, and flavonoids (quercetin, kaempferol) providing antioxidant protection. | * '''Polyphenols & Tannins:''' Contains gallic acid, ellagic acid, and flavonoids (quercetin, kaempferol) providing antioxidant protection. | ||
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== Safety Profile, Toxicology, & Contraindications == | == Safety Profile, Toxicology, & Contraindications == | ||
* '''Toxicity:''' | * '''Toxicity:''' Generally Recognized As Safe (GRAS) by the FDA as a food additive. However, concentrated clove oil applied undiluted can cause mucosal irritation, tissue necrosis, or contact dermatitis. | ||
* '''Overdose Risk:''' Oral ingestion of concentrated eugenol in high doses (>10–12 mL) can induce systemic toxicity characterized by acute liver injury, disseminated intravascular coagulation (DIC), metabolic acidosis, and central nervous system depression. | * '''Overdose Risk:''' Oral ingestion of concentrated eugenol in high doses (>10–12 mL) can induce systemic toxicity characterized by acute liver injury, disseminated intravascular coagulation (DIC), metabolic acidosis, and central nervous system depression. | ||
* '''Drug Interactions:''' Due to antiplatelet effects mediated through thromboxane A<sub>2</sub> inhibition, caution is warranted when co-administered with oral anticoagulants (e.g., [[Warfarin]]) or antiplatelet agents (e.g., | * '''Drug Interactions:''' Due to antiplatelet effects mediated through thromboxane A<sub>2</sub> inhibition, caution is warranted when co-administered with oral anticoagulants (e.g., [[Warfarin]]) or antiplatelet agents (e.g., Aspirin, Clopidogrel). | ||
== References == | == References == | ||