Methanol Extract Of Rhizomes Research Articles

In-vitro antidiabetic activity of ethanolic extract from Khla (Schumannianthus dichotomus Roxb.) rhizome.

Schumannianthus dichotomus Roxb. in Thai, namely “Khla,” is notably distributed in South and South-East Asia regions. In Thai traditional medicine, rhizome has a bland taste, and after decoction, it is used to reduce body heat and fever and treatment of skin diseases. Recently, the methanolic extract of rhizome had reported the hepatoprotective and hypoglycemic activities in mice. Aims of this study were conducted to determine the nutritional value of rhizome and to evaluate α-glucosidase, and α-amylase inhibitory activities of ethanol extract from the rhizome (KE). The rhizome had a high content of dietary fiber and iron, while it was low in calories, fat, and carbohydrates. Thus, it can become an ingredient of a healthy diet. The total phenolic content of KE contained 229.8 ± 6.23 mg of gallic acid equivalent (GAE)/g. There was strongly inhibited α-glucosidase (IC50 = 0.11 ± 0.03 mg/mL) and comparable with the antidiabetic drug acarbose (IC50 = 0.10 ± 0.03 mg/mL). Therefore, KE was slightly inhibited by α-amylase (IC50 = 0.42 ± 0.05 mg/mL), when compared with acarbose (IC50 = 0.016 ± 0.001 mg/mL). Thus, the phytochemicals of different extracts are necessary to be identified. Therefore, the advance techniques were the limitation of our study.

A Review on Phytochemical Analysis and In-vitro Antioxidant Activity of Curcumin from Curcuma longa L. Rhizomes

This study focused on investigating the phytochemical composition and evaluating the antioxidant capability of an extract obtained from the rhizomes of Curcuma longa (turmeric). Preliminary screening tests revealed the presence of various bioactive compounds like alkaloids, flavonoids, phenolic substances, saponins, terpenoids, cardiac glycosides, and fixed oils/fatty acids in the methanolic rhizome extract. The antioxidant potential of the extract was assessed using the widely employed 1,1-diphenyl-2-picryl-hydrazyl (DPPH) free radical scavenging assay. The findings indicated a concentration-dependent enhancement in radical scavenging activity, reaching a maximum of around 81% at the highest concentration evaluated (3 mL). The remarkable antioxidant capacity can be attributed to the unique structural features of curcumin, the principal bioactive compound present, which contains methoxy, phenoxy, and carbon-carbon double bonds that enable efficient neutralization of free radicals and reactive oxygen species. Furthermore, curcumin has been reported to modulate the activity of transcription factors like Nrf2, thereby upregulating the expression of antioxidant enzymes and bolstering the body’s defense against oxidative stress. These findings offer empirical support for the historical use of C. longa and underscore the diverse potential uses of curcumin as a natural antioxidant across different sectors, including food, pharmaceuticals, and cosmetics

ANTISAPROLEGNIA ACTIVITY OF METHANOLIC EXTRACT OF ZINGIBER OFFICINALE IN BUNNEI (BARBUS SHARPEYI) HATCHERY

Usage of chemicals such as malachite green to disinfect fish eggs in aquaculture has been banned in many countries around the world due to its environmental negative impact. This study aimed to evaluate the Zingiber officinale rhizomes extract as an antifungal agent during incubation period of Bunnei eggs and comparison of its effects with malachite green. For this purpose 24 hours after fertilization, methanolic extract of Zingiber officinale rhizomes in four groups with a concentration of 500, 750, 1000, and 1250 mg/L and three replications per concentration in a (10 minute) bath every 12 hours and malachite green group with a concentration of 0.1 mg/L for (6 minutes) bath was used twice a day and control group without antifungal agents under the same physiochemical conditions as other treatments were tested. The present study showed that the highest percentage of fungal infection was 41.82±0.5 % for the control group and the lowest 0.3±0.5 % was obtained for the treatment of 1250 mg/L of Zingiber officinale rhizomes. Also, the results showed that there were significant differences between treatments of different concentrates of Zingiber officinale rhizomes and with malachite green group in fungal infection, percentage of fertilization and survival do not exist (P>0.05.) No apparent deformity and abnormality were observed in the hatched larvae of Bunnei, so the extract of Zingiber officinale rhizomes with concentration 500 mg /L can be used to disinfect Bunnei eggs during Incubation period and safe material for humans and the environment.

Phytochemical Profiling and Assessment of Antidiabetic Activity of Curcuma Angustifolia Rhizome Methanolic Extract: An In Vitro and In Silico Analysis.

Curcuma angustifolia Roxb. is a plant with medicinal potential, traditionally used to treat different diseases. The present study aimed to determine the antidiabetic activity of C. angustifolia rhizome in vitro and in silico. The methanolic extract of C. angustifolia rhizome was analyzed by FTIR and GC-MS to determine the phytochemicals present. The antidiabetic potential of the extract was evaluated by different assays in vitro. The extract inhibited both α-amylase and α-glucosidase enzymes and the glucose diffusion through the dialysis membrane in a concentration-dependent manner with IC50 values of 530.39±0.09, 293.75±0.11, and 551.74±0.3 μg/ml respectively. The methanolic extract also improved yeast cell's ability to take up glucose across plasma membranes and the adsorption of glucose. The findings were supported by molecular docking studies. The results showed that the methanol extract of C. angustifolia rhizome has significant antidiabetic activity and thus can be also studied to isolate the potential compound with antidiabetic activities.

ANTI INFLAMMATORY EFFECT AND GC-MS METABOLOME PROFILING OF Curcuma haritha Mangaly and M. Sabu – AN ENDEMIC HERB OF KERALA, SOUTH INDIA

Curcuma haritha (Zingiberaceae) is a less explored endemic ethnomedicinal herb of north Kerala (India). The aim of present study was to evaluate the anti inflammatory potential and phytochemical profile of methanolic rhizome extract of C. haritha. The preliminary assays performed were, the proteinase inhibition and the protein denaturation inhibition tests, followed by cyclooxygenase, lipoxygenase, iNOS and cellular nitrite activity/expression assays in LPS stimulated RAW 264.7 cells. The toxicity of the extract was studied using MTT assay and the expression of COX-2 inflammatory protein in treated cells was determined by indirect ELISA. The phytochemical profiling was done by GC-MS analysis. All the assays revealed a dose-dependent anti-inflammatory effect in vitro. The inhibition of inflammatory enzymes, COX-2, Lox and iNOS were observed as 62.16 ± 0.49, 57.25 ± 1.98 and 56.74 ± 2.73%, respectively, at maximum concentration (100 µg mL-1). The cellular nitrite levels and expression of COX-2 mediator protein also decreased in treated cells proving the anti inflammatory effect of the extract. GC-MS screening revealed the presence of 54 phytoconstituents including anti-inflammatory compounds like curcumenol, chamazulene, etc., Therefore, in the light of above results, C. haritha can be considered as a potential anti-inflammatory drug source plant.

Evaluation of Anxiolytic Activity of Methanolic Extract of Rhizome of Bergenia ciliata (Pashanbheda) in Swiss Albino Mice

Evaluation of Anxiolytic Activity of Methanolic Extract of Rhizome of Bergenia ciliata (Pashanbheda) in Swiss Albino Mice

CHARACTERIZATION OF FRACTION CONTAINING BETA ASARONE ISOLATED FROM ACORUS CALAMUS LINN. RHI- ZOMES AND STUDYING THE AMELIORATIVE EFFECT OF JUGLANS REGIA KERNEL OIL ON ITS ANTIEPILEPTIC PO- TENTIAL

Sweet flag (Acorus calamus) has a long history of use in the treatment of a range of diseases, including inflammatory response, chest pain, digestive problems, and neurological disorders. The prime objective of the study is to isolate newer moieties from Acorus calamus (AC) rhizomes and to test their anticonvulsant potential with Juglans Regia Kernel Oil (Walnut Oil). Pharmacognostic standardization of AC rhizomes have been performed as per WHO guidelines of standardization. Methanolic extract of AC rhizomes was used for isolation of active moieties using column chromatography. Further, characterization of isolated moieties has been performed using UV, IR, 1H-NMR, C13- NMR and LCMS data. OECD 423 guidelines have been fol- lowed for the determination of oral acute toxicity. Swiss albino mice(n=6) were used for in-vivo studies. An- ticonvulsant study of isolated and characterized fraction of Beta Asarone was performed using scPTZ in- duced convulsion model. Pharmacognostic standardization of rhizomes showed results that fall within the pharmacopoeial limits. Spectral details of the fraction confirmed the identity as Beta Asarone. Juglans Regia Kernel oil and AC isolated fraction has shown a better ameliorative antiepileptic effect with prolonged time for seizure onset. Percentage protection has also been enhanced as compared to standard drug.

Hepatoprotective Principles from the Rhizomes of Picrorhiza kurroa.

A methanol extract of rhizomes of Picrorhiza kurroa Royle ex Benth. (Plantaginaceae) showed hepatoprotective effects against D-galactosamine (D-GalN)/lipopolysaccharide (LPS)-induced liver injury in mice. We had previously isolated 46 compounds, including several types of iridoid glycosides, phenylethanoid glycosides, and aromatics, etc., from the extract. Among them, picroside II, androsin, and 4-hydroxy-3-methoxyacetophenone exhibited active hepatoprotective effects at doses of 50-100 mg/kg, per os (p.o.) To characterize the mechanisms of action of these isolates and to clarify the structural requirements of phenylethanoid glycosides for their hepatoprotective effects, their effects were assessed in in vitro studies on (i) D-GalN-induced cytotoxicity in mouse primary hepatocytes, (ii) LPS-induced nitric oxide (NO) production in mouse peritoneal macrophages, and (iii) tumor necrosis factor-α (TNF-α)-induced cytotoxicity in L929 cells. These isolates decreased the cytotoxicity caused by D-GalN without inhibiting LPS-induced macrophage activation and also reduced the sensitivity of hepatocytes to TNF-α. In addition, the structural requirements of phenylethanoids for the protective effects of D-GalN-induced cytotoxicity in mouse primary hepatocytes were evaluated.

Study of Phytochemical Constituent and Biological Activities of Methanolic Extract of Rhizomes of Neopicrorhiza scrophulariiflora and Roots of Rheum australe collected from the Alpine Region of Nepal

Rhizomes of Neopicrorhiza scrophularii flora and roots of Rheum australe were collected from the alpine regions of the Jumla district of Nepal. The phytochemical analysis of the methanolic extract of these plants revealed the presence of polyphenols, flavonoids, quinones, saponins, and tannins. The total phenolic and flavonoid content in the extracts of N. scrophulariiflora were estimated to be 141.27±1.414 mg GAE/gm and 43.48±5.476 QE/gm respectively and that in the extracts of R. austral were estimated to be 101.54±4.061 mg GAE/gm and 24.97±2.857 mg QE/gm respectively. A brine shrimp lethality test was performed with the extracts of N. scrophulariiflora and R. austral against brine shrimp nauplii and results revealed high toxicity of the extracts towards nauplii with LC50 values 173.78μg/mL and 257.03μg/mL respectively. N. scrophulariiflora showed the strongest DPPH radical scavenging activity with IC50 value of 57.49 μg/mL in comparison to R. austral whose IC50 was determined to be 68.91μg/mL, ascorbic acid taken as standard with IC50 value 49.05μg/ml. In α-amylase inhibition assay, N. scrophulariiflora extract exhibited strong activity with IC50 value 140.67μg/mL while that of R. austral extract showed mild activity with IC50 value 192.88μg/mL. All the biological studies revealed that N. scrophulariiflora extract is more active than that R. austral extract. Column chromatography of the extract of N. scrophulariiflora was performed and 50 % methanolic fraction was further subjected to FTIR and GC-MS analysis. The GC-MS analysis showed various compounds and among them, 13 major compounds were identified.

Analysis of phytochemicals and biological activities of rhizome of Curcuma longa, aerial parts of Centella asiatica, and corn silk of Zea mays

Nepal is a storehouse of medicinal plants. Medicinal plants like the rhizome of Curcuma longa, the aerial part of Centella asiatica, and corn silk of Zea mays were used traditionally as medicine for diseases like inflammation, hepatic disorders, cough, etc. In this study, these selected plants were subjected to the analysis of phytochemical constituents, and biological activities following standard methods. Phytochemical analysis of the methanolic extract of these selected plants revealed the presence of different chemical constituents such as polyphenols, flavonoids, glycosides, quinones, saponins, and tannins. C. longa rhizomes also showed the strongest DPPH radical scavenging activity with IC50 of 55.06 µg/mL which was very close to standard ascorbic acid (49.09 µg/mL) than that of the aerial part of C. asiatica (72.56µg/mL) and corn silk of Z. mays (131.96 µg/mL). Total phenolic and total flavonoid content was found highest in C. longa with the values of 195.95 ± 0.899 mg GEA/g and 56.45 ±4.056 mg QE/g respectively. The phenolic and flavonoid content of methanolic extract of aerial parts of C. asiatica was found to be 110.78 ± 1.984 mg GEA/g and 30.00 ± 2.358 mg QE/g and corn silk of Z. mays were found to be 65.92 ± 1.244 mg GEA/g and 18.50 ±1.424 mg QE/g respectively. The methanolic extract of rhizomes of C. longa exhibited high α-amylase inhibitory activity with IC50 values of 382.30 µg/mL than that of C. asiatica with IC50 value of 520.48 µg/mL and Z. mays with IC50 value 593.09 µg/mL.

Downregulation of pro-inflammatory markers NF-κB1, RelA and COX-2 using Aconitum chasmanthum Stapf ex Holmes -in vitro and in-silico study

Nuclear factor kappa B signaling pathway and cyclooxygenase-2 are considered molecular prototypes for targeting various diseases including inflammation. Aconitum chasmanthum has been used for decades to cure different ailments as its anti-inflammatory and anti-analgesic effects are well documented, but the mechanism remains unknown. Thus, in current study, we attempted to assess the anti-inflammatory characteristics of Aconitum chasmanthum which can be regarded as an appealing therapeutic candidate. In present study, High-Resolution Liquid Chromatography and Mass Spectrophotometry (HRLCMS-QTOF-MS) method were used to determine the phytoconstituents in the methanolic extract of wild rhizome of Aconitum chasmanthum. The in vitro studies were done on HCT-116 cell line and an MTT assay was used to assess the cell viability (IC50 value). In the present study, mRNA expression of pro-inflammatory genes (nuclear factor kappa B1, nuclear factor kappa B3 (RelA), and cyclooxygenase-2) was determined via quantitative polymerase chain reaction and western blot. Molecular docking analysis was performed by Auto Dock Vina to find potential compounds having anti-cyclooxygenase-2 activity. The current investigations found that methanolic extract strongly downregulates the gene expression of pro-inflammatory genes at a concentration of 200 μg/mL. While as western blot results showed a significant decrease in cyclooxygenase-2 protein level at 200 μg/mL concentration for 48 hrs. ADMET analysis revealed the physiochemical properties of bioactives and a drug. Molecular docking revealed staurosporine was the most effective compound against COX-2 with the highest binding affinity of − 9.7 kcal/mol. Thus the findings of current study reveal that Aconitum chasmanthum possesses substantial anti-inflammatory/anti-analgesic properties and therefore can be used to develop novel anti-inflammatory and anti-analgesic drugs in future.

Evaluation of in vitro anti-acne activity of methanolic extracts of Cyperus rotundus and Nymphaea nouchali

Background: The objective of this study was to evaluate in vitro anti-acne activity against Staphylococcus aureus (S. aureus), Staphylococcus epidermidis (S. epidermidis), and Escherichia coli (E. coli) using the agar well diffusion method. Methods: Air-dried and ground, matured rhizomes of Cyperus rotundus (CR), petals and pollen of Nymphaea nouchali (NN) were macerated in methanol. The resultant extracts were concentrated using a rotary evaporator. The anti-bacterial activity was performed against Staphylococcus aureus (ATCC 25923), Staphylococcus epidermidis (ATCC12228), and Escherichia coli (ATCC 25922) using the agar well diffusion method, and gentamicin was used as a positive control. The whole experiment was done in triplicates. Results: The data obtained from dose-response curves, methanolic extracts of Cyperus rotundus rhizomes against staphylococcus aureus (IC50=819.2 µg/ml), Nymphaea nouchali pollens against Staphylococcus epidermidis (IC50=787.7 µg/ml) and combination against Escherichia coli (IC50=813.6 µg/ml) were exhibited the highest potency. A strong positive statistically significant correlation was exhibited between the zone of inhibition and the concentrations of all plant extracts. The p value was less than 0.05 (p<0.05) and all the R2 values were around 1. Conclusions: The maximum anti-bacterial potency against gentamicin equivalent was observed in S. aureus, S. epidermidis, and E. coli at the concentration of 15625 µg/ml in combination. The present study might bring progress in the treatment of acne using herbs and in developing herbal formulations for safe and effective management of the disease.

Phytochemical analysis, antioxidant and antibacterial activities of methanolic rhizome extract of Bergenia pacumbis: A valuable medicinal herb

Bergenia pacumbis, a perennial herb of the Saxifragaceae family, usually referred to as ‘Pashanbheda’ is geographically distributed within the temperate Himalaya including Nepal. The purpose of this study was to evaluate the phytochemical analysis as well as in vitro antioxidant and antibacterial activities of methanolic rhizome extract of B. pacumbis. The rhizome of B. pacumbis was extracted in methanol using the Soxhlet apparatus and then the extract was concentrated. The rhizome extract was tested for phytochemicals using the standard protocol. The in vitro antioxidant activity of the extract was evaluated using the 2, 2- diphenyl-1-picrylhydrazyl free radical scavenging assay. The 50 % inhibitory concentration (IC50) values of ascorbic acid and B. pacumbis were found to be 11.91 ± 0.03 μg/mL and 11.99 ± 0.05 μg/mL respectively that indicate B. pacumbis is a good source of antioxidant agents. The extract was further tested for antibacterial activity through the agar well diffusion method and found to be effective against Staphylococcus aureus (16 mm) and Klebsiella pneumoniae (12 mm). The present study validates the traditional use of B. pacumbis. BIBECHANA 19 (2022) 14-26

Methanolic rhizome extract of Trillium govanianum coated gold nanoparticles: Facile biogenic synthesis, their characterisation, and potential antimicrobial study

Methanolic rhizome extract of <i>Trillium govanianum</i> coated gold nanoparticles: Facile biogenic synthesis, their characterisation, and potential antimicrobial study

Study of anti-inflammatory activity of aqueous and methanolic extracts of fresh rhizome of Zingiber Officinale in Wistar rats

To evaluate the anti-inflammatory activity of aqueous and methanolic extracts of fresh rhizome of plant Zingiber officinale: 1. To evaluate anti-inflammatory activity of all extracts in two doses and the standard drug in wistar rats by using Carrageenan induced paw edema method. 2. To compare anti-inflammatory activity of both extracts with that of standard drug. The study was conducted after animal ethics committee approval. Animals were divided into six groups. Control group received 0.2ml NS IP while test groups received aspirin (150mg/kg) , Aqueous extract of fresh rhizome of Z. officinale (100 and 200mg/kg) , Methanolic extract of fresh rhizome of Z. officinale (100 and 200 mg/kg). Acute model of inflammation consisting of carrageenan induced rat paw edema method was used to investigate anti-inflammatory activity of Ginger. The present study clearly showed significant anti-inflammatory activity of aqueous and methanolic extracts of fresh rhizome (p &lt; 0.05) in acute model of inflammation when compared to control and its activity was comparable to aspirin at all time interval. Aqueous and methanolic extracts of gingiber officinale have significant anti‑inflammatory property.

Evaluation of the inhibitory effect of Zingiber officinale rhizome on Babesia and Theileria parasites.

The effect of Zingiber officinale rhizome methanolic extract (ZOR) on the in vitro growth of bovine Babesia (B. bovis, B. bigemina, and B. divergens) and equine piroplasm (B. caballi, and Theileria equi) parasites and on the growth of B. microti in mice was evaluated in this study. The possible in vitro synergistic interaction between ZOR and either diminazene aceturate (DA) or potent Medicines for Malaria Venture (MMV) hits from the malaria box was also investigated. In vitro, ZOR reduced the growth of B. bovis, B. bigemina, T. equi, and B. caballi in a dose-dependent manner. B. divergens was the most susceptible parasite to the in vitro inhibitory effect of ZOR. DA and MMV compounds enhanced the in vitro inhibitory antibabesial activity of ZOR. 12.5mg/kg DA when administrated in combination with ZOR in mice exhibited a significant inhibition (P<0.05) in B. microti growth better than those observed after treatment with 25mg/kg DA monotherapy. These findings suggest that ZOR could be a viable medicinal plant for babesiosis treatment, particularly when combined with a modest dose of either DA or powerful anti-B. bigemina MMV hits.

Geographical Discrimination of Curcuma longa L. in Vietnam Based on LC-HRMS Metabolomics

Curcuma longa L. has been used as a food, cosmetic, traditional medicine, and natural dye for a long time in tropical and subtropical regions such as India, China, and Vietnam. Curcuminoids are considered the main bioactive compounds in this plant. This study focuses on metabolites profiling of the rhizome methanolic extract of C longa samples collected in 6 different provinces in Vietnam using liquid chromatography coupled with high-resolution mass spectrometry. The partial least-squares discriminant analysis model was then established to discriminate its metabolomes and identify the chemomarkers that help to distinguish C longa from 6 geographical locations. Consequently, collected samples were segregated into 3 main groups: northern (Lang Son, with typical content of 2 terpenoids), center (Nghe An), and southern highland (Lam Dong, with distinctive profile of 3 curcuminoids). The absolute curcuminoids’ amount was also measured based on the calibration curve of reference standards. The differential metabolites including curcumin, demethoxycurcumin, and bisdemethoxycurcumin were found with the highest range in samples from Lang Son, indicating the excellent quality of turmeric cultivated in this area.

Screening and characterization of phytochemical content of methanolic extract of Rhizome of Curcuma amada and their antibacterial activity against MRSA

Screening and characterization of phytochemical content of methanolic extract of Rhizome of Curcuma amada and their antibacterial activity against MRSA

Variable Secondary Metabolite Profiles Across Cultivars of Curcuma longa L. and C. aromatica Salisb.

Background: Curcuma spp. (Zingiberaceae) are used as a spice and coloring agent. Their rhizomes and essential oils are known for medicinal properties, besides their use in the flavoring and cosmetic industry. Most of these biological activities were attributed to volatile and nonvolatile secondary metabolites present in the rhizomes of Curcuma spp. The metabolite variations among the species and even cultivars need to be established for optimized use of Curcuma spp. Objectives: We compared the phytochemical profiles of rhizomes and their essential oils to establish the variability among seven cultivars: five of Curcuma longa L. (Alleppey Supreme, Duggirala Red, Prathibha, Salem, Suguna) and two of C. aromatica Salisb. (Kasturi Araku, Kasturi Avidi). The GC-MS and LC-MS-based analyses were employed to profile secondary metabolites of these selected cultivars. Methods: Rhizomes of Curcuma spp. were subjected to hydro-distillation to collect essential oil and analyzed by GC-MS. The methanol extracts of fresh rhizomes were subjected to LC-MS analyses. The compounds were identified by using the relevant MS library databases as many compounds as possible. Results: The essential oil content of the cultivars was in the range of 0.74–1.62%. Several compounds were detected from the essential oils and rhizome extracts by GC-MS and LC-MS, respectively. Of these, 28 compounds (13 from GCMS and 15 from LCMS) were common in all seven cultivars, e.g., α-thujene, and diarylheptanoids like curcumin. Furthermore, a total of 39 new compounds were identified from C. longa L. and/or C. aromatica Salisb., most of them being cultivar-specific. Of these compounds, 35 were detected by GC-MS analyses of essential oils, 1,2-cyclohexanediol, 1-methyl-4-(1-methylethyl)-, and santolina alcohol, to name a few. The other four compounds were detected by LC-MS of the methanolic extracts of the rhizomes, e.g., kaempferol-3,7-O-dimethyl ether and 5,7,8-trihydroxy-2′,5′-dimethoxy-3′,4′-methylene dioxyisoflavanone. Conclusions: We identified and recorded the variability in the metabolite profiles of essential oils and whole rhizome extracts from the seven cultivars of Curcuma longa L. and C. aromatica Salisb. As many as 39 new metabolites were detected in these seven Indian cultivars of Curcuma spp. Many of these compounds have health benefits.

Determination of Bergenin in Different Parts of Bergenia ciliata using a Validated RP-HPLC Method

Bergenia ciliata (Family: Saxifragaceae) is a folklore remedy for the treatment of various ailments in Asian countries. Bergenin (1) has been isolated as an active constituent in many studies, however, the amount of bergenin has not been determined in all parts of the plant. A simple RP-HPLC method was developed to determine the amount of bergenin in methanol extracts of leaves, rhizomes and roots of the plant. Separation was achieved on an Agilent Eclipse XDB-C18 column maintained at 25 ℃ using isocratic solvent system (water: methanol: acetic acid; 62.5:37:0.5 v/v/v) adjusted at pH 2 0 at a flow rate of 1.0 mL/min. and detected at 275 nm. Correlation coefficient (0.9952) showed linearity of concentration (5-200 μg/mL) and response. The values of LOD (0.00947 μg/mL) and LOQ (0.02869 μg/mL) indicated that method was sensitive. The recovery of bergenin was 99.99-100% indicating accuracy of method. The methanol extract of rhizomes contained higher amount of bergenin (19.4%) than roots (9.2%) and leaves (6.9%). It is concluded that methanol extract of rhizomes is a better source of bergenin than other parts of the plant. The findings are useful for standardization of bergenin containing extracts and herbal preparations.