Rhizome Extract Research Articles

Green synthesis of silver nanoparticles using Houttuynia cordata Thunb rhizome extracts and their antibacterial potential against common foodborne pathogens

SummaryThe biological synthesis of functionalised nanoparticles using plant materials is considered more cost‐effective and eco‐friendly than chemical and physical methods. Hence, this study demonstrated the synthesis of silver nanoparticles (AgNPs) using Houttuynia cordata Thunb rhizome (HCR). The extract, prepared with distilled water, provided the required phytochemical components, such as flavonoids, terpenoids, phenols, proteins and other essential bio‐reducing agents. The AgNPs were exposed to reaction conditions, such as temperatures, pH values and AgNO3 concentrations, to identify the optimum synthesis condition and explore their impacts on particle size and antibacterial action against Gram‐positive (Staphylococcus aureus) and Gram‐negative (Salmonella enterica and Shigella dysenteriae) foodborne pathogens. The formation of AgNPs was indicated by specific surface plasmon resonance (SPR) intensity at 440–450 nm and colour changes under different reaction conditions. The structure and size distribution characterised by SEM and TEM revealed that the AgNPs exhibited a spherical‐shaped structure with irregular contours, regular distribution and aggregation. Although the average particle size ranged from 2 to 100 nm, relatively smaller sizes were detected at 10 mM (54.30), 80 °C (49.50 nm) and pH 6 (60.16 nm) conditions. The FTIR spectrum and EDX spectral signals affirmed the presence of reducing and stabilising agents in HCR extract, following the reduction of AgNPs from Ag+ to Ag0. AgNPs also exhibited excellent antibacterial activity against S. aureus, S. enterica and Sh. dysenteriae, indicating a broad spectrum for various applications in the food and pharmaceutical industries.

Influence of Thermal Treatment on the Composition of Alpinia officinarum Rhizome.

Alpinia officinarum is a representative of the Zingiberaceae family, which is known for its wide use in the food and pharmaceutical industries also due to its precious pharmacological potential. The major aim of the present study was to evaluate the influence of thermal treatment on the composition of the rhizome of Alpinia officinarum and its antioxidant activity. The fresh rhizome was subjected to various thermal treatment processes-boiling, frying and microwave heating during various time intervals-and their composition and antioxidant activity were determined using chromatographic (HPLC - High Performance Liquid Chromatography and HPLC-MS - High Performance Liquid Chromatography Mass Spectrometry) and spectrophotometric (DPPH and TPC - Total Phenolic Content) methods. Pinobanksin was the main compound found in the extract of the fresh rhizome (537.79 mg/kg), followed by galangin (197.7 mg/kg) and zingerone (185.5 mg/kg). The effect of thermal treatment on the rhizome composition was varied. In general, thermal processing significantly decreased the content of active compounds in the rhizome. However, there were some exceptions-boiling for 4 min significantly increased the content of pinobanksin (1162.4 mg/kg) and galangin (280.7 mg/kg), and microwave processing for 4 min increased the content of pinocembrin (213 mg/kg). It was found that boiling and microwave treatment significantly increased the antioxidant activity of the processed rhizomes.

Biological effects and phytochemical study of the underground part of Iris scariosa Willd. ex Link extract: A new source of bioactive constituents

The expected toxicity and resistance of chemotherapeutic agents necessitate and encourage for the use of natural chemotherapeutic sources of plant origin in the clinical stage of cancer therapy. Plants of the genus Iris (Iridaceae) used by local populations for the treatment of cancer, bacterial and viral infections. In this study, an ethanol extract of rhizomes of I. scariosa was prepared and tested for the cytotoxicity using the MTT assay. The extract exhibited the most potent cytotoxicity against the breast cancer cell line MCF7 (IC50 = 9.28 ± 0.49 μg/ml, selectively index ˃5), and induced apoptosis in MCF7 lines. Notably, the extract significantly inhibited the colony formation of MCF7 and HepG2 cancer cells at a concentration range from 10.6 to 85.0 μg/ml, including non-toxic concentrations for HepG2 cells. The ethanol extract was analyzed by HPLC, revealed the identification of 5 secondary metabolites (quercetin, rutin, myricetin, apigenin, artemisetin), the content of which was shown to reach around 15% of the extract. The petroleum ether (PE) part of the extract (yield 2.62%) was analyzed by GC–MS. The composition of tert-butyl methyl ether (TBME) part of the extract (yield 23.72%) was studied. Total of 15 individual compounds: two benzophenones, eight isoflavones, four flavones and a (2R)-flavanone were isolated. The pentamethoxyflavone artemisetin and flavanone pinocembrin were isolated for the first from Iris sp. The readily available isoflavones from the TBME part of extract (irilone, iriflogenin, irigenin and tectorigenin) may serve as new leads for the discovery of anticancer drugs.

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 Anti--amylase and Anti--glucosidase Activity of Canna x Generalis L.H Bailey & E.Z Bailey Rhizome

Canna x generalis L.H Bailey & E.Z Bailey (CG) has been used as folk medicine to treat different diseases. However, scientific information about the pharmacological effects and chemical composition of this plant is still very limited. This study aims to evaluate for the first time the α-amylase and α-glucosidase inhibitory activity of CG rhizome extracts. The rhizome part of CG was extracted with ethanol and then fractionated with n-hexane, ethyl acetate, and water. The total extract and fractions were evaluated for their inhibitory effects on α-amylase and α-glucosidase enzymes in vitro. The results showed that the ethyl acetate fraction had the strongest inhibitory activity against α-amylase and α-glucosidase with IC50 values of 53.19 ± 2.79 and 95.83 ± 6.26 µg/mL, respectively. Therefore, the rhizome part of the CG plant, especially the ethyl acetate fraction, is a potential natural source for searching for active ingredients to prevent and treat diabetes.
 
 

Evaluation of Antiplatelet Aggregation and Anticoagulant Effects of Oxalis Debilis Kunth Rhizome Extracts

Cardiovascular disease is one of the leading causes of death globally. The discovery and use of natural products in the prevention and treatment of cardiovascular diseases have achieved great interest. Oxalis debilis is traditionally used for the treatment of various ailments. This study aimed to investigate the potential antiplatelet and anticoagulant properties of extracts derived from O. debilis rhizome. The rhizome of O. debilis was extracted with methanol and then fractionated to obtain four extracts: the total methanol extract, the n-hexane, ethyl acetate, and water fraction. These four extracts were then tested for their ability to inhibit platelet aggregation and blood coagulation in human blood samples. This report demonstrated for the first time that O. debilis had inhibitory effects on platelet aggregation induced by both adenosine diphosphate and collagen as well as blood coagulation. Moreover, the total methanol extract, the ethyl acetate, and the water fraction had strong antiplatelet aggregation effects. All tested extracts had mild anticoagulant activities. This plant could be a valuable natural source for searching for antithrombotic substances, or for the development of supplementary products for the treatment and prevention of heart diseases and thrombosis.

Antibacterial and anticancer activities of Nymphaea nauchali rhizome extracts

The present study was conducted to discover the antibacterial and anticancer activities of Nymphaea nauchali rhizome peel and core extracts. Antibacterial activity of ethanol, methanol, and acetone extracts of N. nauchali rhizome peel and inner core extracts has been tested against six biofilm-forming bacterial pathogens, E. coli, P. aeruginosa, E. faecalis, coagulase –ve Staph. aureus, Staph. aureus, and P. vulgaris by agar well diffusion assay. The size of inhibition zones around the wells in the presence of different extracts was used to determine the sensitivity of test bacteria. The anticancer activity of extracts was checked using the MCF-7 cell line, and potency was defined in terms of IC50 values. Methanol, ethanol, and acetone peel extracts showed more antibacterial activities against all test bacteria than inner core extracts. E. faecalis was highly resistant to acetone inner core extracts, and P. aeruginosa showed higher sensitivity to ethanol inner core extract. Ethanolic extracts of rhizome peel and inner core were more effective against the MCF-7 cell line than methanol and acetone extracts. IC50 values of 208.20 μgml−1and 136.16 μgml−1were noted for peel and inner core ethanol extracts, respectively. N. nauchali rhizome can be used as a potential entrant in developing novel antibacterial and anticancer phytoformulations.

Antioxidant activities (DPPH and ABTS method) from extract of Bangle rhizome (Zingiber cassumunar) using different method of extraction

Antioxidants are important for the prevention of oxidative stress, which can cause various degenerative diseases. Bangles contain bioactive components with antioxidant potential. Processing affects the active compounds in food, including angle. This study aimed to determine the effects of the blanching and extraction methods on the antioxidant activity of Bangle. This study focused on three factors: blanching treatment extraction technique, time, and type of extraction solvent. Analyses of antioxidants using the DPPH and ABTS methods were conducted in triplicate for each sample. Data were analyzed using ANOVA. The results of this study show that the method, time, and type of solvent significantly affect the antioxidant activity of bangle rhizome extracts. The best treatment for antioxidant activity of Bangle rhizome was blanching treatment by adding 0,05% citric acid solution in the sonication extraction method for 30 min with ethanol as the solvent. The IC50 value on the DPPH method was 20,61±0,76 mg/g, and the percent free radical scavenging value was 87,11±3,04%. The IC50 value on the ABTS method is 20,79±0,29 mg/g and a percent free radical scavenging activity value of 92,75±0,13%. This study provides key insights for choosing effective extraction methods to increase antioxidant activity in natural materials, such as Bangle rhizomes.

Pharmacological Activities of Six Species of Hedychium J. Koenig from Nepal

Species of Hedychium Koenig are perennial herbs. Some of the species like H. ellipticum, H. spicatum, H. coronarium are traditionally used as medicinal plants. In the present study, methanolic rhizome extracts of six different species of Hedychium namely H. spicatum, H. ellipticum, H. thyrsiforme, H. coccineum, H. gardnerianum and H. coronarium were analysed for their antioxidant, antidiabetic and antibacterial activities. The antioxidant activity analysed by DPPH assay showed the highest potential (lowest IC50 value) in H. coccineum (148.82±2.83 µg/ml) and lowest potential (maximum IC50 value) in H. thyrsiforme (996.55±9.42 µg/ml). The rhizome extracts of different species showed moderate α-amylase inhibition activity in vitro. The highest α-amylase inhibition (79.67%) was observed for H. coronarium while the lowest inhibition (64.0%) was observed in H. thyrsiforme. However, these values were found lower than the value (92.37%) obtained for positive control, i.e., Acarbose. The antibacterial activity was determined against two Gram-positive (Bacillus subtilis and Staphylococcus aureus) and two Gram-negative (Klebsiella pneumoniae and Pseudomonas aeruginosa) bacterial strains by agar well diffusion method. Except for H. ellipticum the extracts of all other species showed antibacterial activity against all the bacterial strains tested. The extracts of H. ellipticum showed antibacterial activity only against B. subtilis and K. pneumoniae. The extract of H. coronarium showed the highest zone of inhibition (16.67±1.15 mm) against B. subtilis. However, the antibacterial activity was weak compared to standard antibiotics for all the extracts and at all concentration tested. These results show that rhizomes of other species can also be used in the same manner as that of H. coronarium and H. spicatum, two species most used in various ethnomedicinal applications.

Amylolytic-dependent biofilm inhibition of H. forrestti var. forrestii rhizome extract against S.aureus pathogens

Rhizosphere bacterial infections are studied with great interest as it enlightens the idea of host-pathogen interaction combined with host defence adaptations. In this study, we are studying the ability of Hedychium forrestti var. forrestii rhizome against rhizosphere bacterial colonialization. It is understood that bacterial colonialization is immensely supported by biofilm production. We analyzed the biofilm inhibition efficacy of the plant rhizome extract, which suggested that the presence of plant rhizome extract could successfully downregulate the rate of bacterial adherence. The Spectrophotometrical data indicated that about 80% of biofilm production by Staphylococcus aureus can be inhibited by administering 500 µg/ml plant rhizome extract. The microscopic studies pointed out that antagonist-disabled bacteria form a film upon a given surface compared to untreated conditions. Fluorescence microscopy also identified that biofilm inhibition made bacteria more vulnerable. It was observed that the biofilm inhibition by plant rhizome extract is complimented by the amylolytic property of plant rhizome extract, verified by the enzyme kinetics studies. The plant rhizome extract process suggested a notable amylolytic action by Michaelis–Menten kinetics.

Antimicrobial Activity on Streptococcus mutans and Enterococcus faecalis of Cyperus articulatus Ethanolic Extracts.

Oral diseases are one of the biggest public health problems worldwide, caused by opportunistic pathogens such as Streptococcus mutans and Enterococcus faecalis. Cyperus articulatus (priprioca) is a plant conventionally used in traditional medicine in the Amazon region. However, little is known about the possible dentistry-related uses of extracts from the rhizomes and solid waste generated by the extraction of essential oils from this vegetable. This study aimed to investigate the chemical composition of volatile compounds and antimicrobial activity through the Minimum Inhibitory Concentration test (MIC and assessment of the toxicity by Hens Egg Test-Chorion Allantoic Membrane (HET-CAM) of the ethanolic extracts from Cyperus articulatus intact rhizomes and solid waste. We identified sesquiterpenes as the main constituents, strong antimicrobial activity of the ethanolic extract of intact rhizomes against S. mutans (MIC = 0.29 mg/mL), moderate antimicrobial activity against E. faecalis of the extract obtained from the solid waste (MIC = 1.17 mg/mL), and absence of toxicity for both tested extracts. The absence of irritation and the antibacterial activity of the ethanolic extract from C. articulatus rhizomes and solid waste reveal its potential for use in the alternative control of bacteria that cause oral infections and may present economic viability as a raw material for dental products.

Antifungal evaluation of turmeric rhizome extract against Colletotrichum capsici, the causal agent of anthracnose on red-chili peppers (Capsicum annum L.)

This study was conducted to evaluate the antifungal activity of the ethanolic extract of turmeric rhizome against Colletotrichum capsici Syd. and its efficacy in reducing anthracnose disease development on red chili peppers. The in vitro experiment aimed to determine the effect of the extract on inhibiting C. capsici growth in potato sucrose agar (PSA) medium incorporating the turmeric rhizome extract. The variables examined were mycelial growth, fungal sporulation, and spore germination. The in vivo experiment aimed to evaluate the effectiveness of the extract in reducing disease development on red chili peppers. The treatments were conducted using a completely randomized design with five concentration treatments and three replicates. The variables examined were radial mycelial growth zone diameter, fungal sporulation, spore germination, and disease intensity. Data were analyzed by analysis of variance, and the least significant difference was used for comparing means between treatments. The results of these experiments showed that ethanolic turmeric rhizome extract exhibited antifungal activity against C. capsici both in vitro and in vivo conditions. Turmeric rhizome extracts with concentrations of 1%, 2%, 3%, and 4% significantly inhibited mycelial growth, and even at a 4% concentration, C. capsici fungal colonies did not grow. Evaluation of the effect of the extract on fungal sporulation showed that inhibition occurred at a concentration of 3%, while inhibition of spore germination occurred at concentrations of 1%, 2%, and 3%. Application of turmeric extract at concentrations of 1%, 2%, 3%, and 4% effectively reduced the intensity of anthracnose on red chili.

A Review of the Pharmacological effects of Alpinia galanga Linn. and it’s Phytoconstituents

Middle class people who live in rural or urban areas often find it difficult to get modern health services, so they more often use traditional medicines obtained from herbal plants that grow around them. From the ancient Vedic era, green plants are being used for their medicinal properties to treat several diseases. Green plants represent a big source of bioactive compounds. Alpinia galanga (Linn.) of Zingiberaceae family is one amongst those medicinally important plants. Alpinia galanga plant is used in medicine and in food preparation. Rhizome extract of Alpinia galanga have high phenolic and flavonoid contents when compared to leaf extract. Because of elevated phenolic and flavonoid content in rhizome extract of Alpinia galanga there is noticeable antimicrobial as well as radical scavenging potential. It is a well-known official drug thought out the country as integrated contribution of nature. It is commonly used for the management of eczema, coryza, bronchitis, otitis interna, gastritis, ulcers, morbilli and cholera, pityriasis versicolor, to clear the mouth, emaciation. The different parts of the plant have various effects like antifungal, antiprotozoal, antiplatelet, antiviral, antidiabetic, immunomodulatory, antibacterial, anti-oxidant effects, hypolipidemic and many others. The current review add significant information about its, pharmacological activities, medicinal properties and phytochemical investigations as a traditional drug to cure for a number of diseases. Every fraction of the plant has valuable properties that can deliver humanity. The complete plant will be broadly investigated for further future prospective.

Antibacterial Effectiveness Test of Methanol Extract of Red Galangal Rhizome (Alpinia purpurata (Vieill) K. Schum) Against Streptococcus pyogenes and Klebsiella pneumonia Bacteria

Red galangal rhizome (Alpinia purpurata (Vieill) K. Schum) is a medicinal plant belonging to the family Zingiberaceae. Red galangal rhizomes have antibacterial benefits because they contain active substances such as flavonoids, saponins, triterpenoids, alkaloids, and tannins. Streptococcus pyogenes causes bacterial infections of the skin and upper respiratory tract, while Klebsiella pneumonia is the bacteria that causes pneumonia. This study aims to determine the antibacterial effectiveness of methanol extract of red galangal rhizomes (Alpinia purpurata (Vieill) K. Schum) against Streptococcus pyogenes and Klebsiella pneumonia bacteria. This research is an experimental laboratory with a post-test-only controlled group design. Red galangal rhizomes were extracted using methanol solvent and tested for antibacterial effectiveness using the well method. There were 6 groups in the study, namely the chloramphenicol positive control group, the distilled water negative control group, and the 20%, 40%, 60%, and 80% concentration groups. The largest inhibition zone diameter was found at a concentration of 80%, with an average of 25.50 mm in Streptococcus pyogenes bacteria and 28.73 mm in Klebsiella pneumonia bacteria. In conclusion, methanol extract of red galangal rhizome (Alpinia purpurata (Vieill) K. Schum) effective against bacteria Streptococcus pyogenes and Klebsiella pneumonia.

Preliminary Qualitative Analysis of Plant Samples by High-performance Thin-layer Chromatography for the Presence of Steroid Sapogenins of Some Representatives of the Dioscoreacae, Fabaceae, Ranunculaceae, Melanthiaceae, Scrophulariaceae

Introduction. Results of original research carried out by means of high performance thin layer chromatography (HPTLC) of various plant samples (air-dry raw material) of Dioscoreaceae, Ranunculaceae, Fabaceae, Melanthiaceae, Scrophulariaceae families are presented in this article.Aim. To carry out preliminary qualitative analysis by HPTLC method of steroidal sapogenins composition in hydrolyzed extracts, obtained from vegetative samples of above-ground and underground organs of some Dioscoreaceae, Ranunculaceae, Fabaceae, Melanthiaceae, Scrophulariaceae families.Materials and methods. Extraction from pre-dehydrated raw materials was carried out with 50 % aqueous isopropanol (c.p.) in an ultrasonic bath, followed by acidic hydrolysis of O-glycoside bonds, evaporation and redissolution of dry residue in 99 % methanol (c.p.); purification from suspended solids by filtering through filters with 20 µm perforation diameter. HPTLC was performed on apparatus complex CAMAG (Switzerland) using HPTLC Aluminium sheets Silica gel 60 F254 plates 20 × 20 cm, which were cut to the size 20 × 10 cm.Results and discussion. After scanning densitometry at 254 nm, we found that the separation of isopropanol extracts, followed by redissolution in strong methanol in this solvent system allows a fairly acceptable separation and identification of the compounds studied. Comparison of the tracks of plant extracts was performed with standard samples of steroid sapogenins, whose methanol solutions were applied to one stain-strobe of track 1, provided that they had different Rf indices and coloration after derivatization.Conclusion. Diosgenin was identified in plant extracts of rhizomes and roots of Dioscorea nipponica and Dioscorea caucasica and in seeds of Trigonella foenum-graecum preliminarily. Sarsasapogenin was verified in extracts of fruits of Sophora japonica, tigogenin in extracts of seeds of Trigonella foenum-graecum, herb of Pulsatilla patens and herb of Veronica officinalis. Yamogenin was detected in extracts of seeds of Trigonella foenum-graecum and herb of Veronica officinalis. This work is exploratory in nature, assessing the presence of certain saponins by their sapogenins in selected extracts. We will optimize the HPLC separation procedure and choose other detection methods to unambiguously assess the co-presence of the studied sapogenins with approximately the same staining shades after derivatization and matching retention indices: there are pairs of steroidal sapogenins that have the same retention, we decided to group them in mixtures so that there would be separation within the group and subsequent comparison with the original extracts would make it possible to identify those or other sapogenins in such extracts.

Effect of pH, Amount of Metal Precursor, and Reduction Time on The Optical Properties and Size of Zinc Oxide Nanoparticles Synthesized Using Aqueous Extract of Rhizomes of Acorus calamus

Nanoparticles possess various unique characteristics compared to the corresponding bulk materials. Large band gap, non-toxic nature, and multi-applicability are the worthwhile characteristics of zinc oxide to be synthesized and studied. The size of nanoparticles can be controlled by varying the different experimental conditions. This paper reports the synthesis of zinc oxide nanoparticles by using an aqueous extract of rhizomes of Acorus calamus, where the bio-components present in aqueous extract acted as reducing agents. The size and band gap energy of zinc oxide nanoparticles were studied by varying different parameters such as pH, concentration of the metal precursor, and reduction time. The variations in the size of nanoparticles were studied by UV-visible spectroscopy. FTIR showed phenolic compounds, primary amines, and amides (proteins/enzymes) as the functional groups responsible for the reduction of metal precursors to form nanoparticles. The surface morphology of nanoparticles was studied by FE-SEM image. The FE-SEM image displayed the formation of various shapes and agglomeration of the nanoparticles. XRD pattern revealed that the average size of zinc nanoparticles is 10 nm. In vitro antibacterial activity of ZnO nanoparticles has been assayed against gram-positive and gram-negative bacteria. The growth inhibitory activity of nanoparticles against different bacterial pathogens has also been determined

Phytochemical Profile and In Vitro Bioactivities of Wild Asparagus stipularis.

In this study, Asparagus stipularis was characterized concerning its phytochemical composition, antioxidant potential, cytotoxicity, and pancreatic lipase inhibitory activities. Twenty-seven compounds were identified and quantified by HPLC-DAD-MS in the leaf, stem, pericarp, and rhizome of ethanolic extracts. Seven steroidal saponins were detected, and the highest content was quantified in rhizome and pericap. A. stipularis also contained significant amounts of flavonoids in the aerial part. Isorhamnetin tetra-glycoside, quercetin-3-glucosyl-rutinoside, and rutin were the main flavonoid derivatives in leaf, stem, and pericarp extracts, respectively. In addition, eleven phenolic acids were also detected; among them, caffeic acid, protocatechuic acid, p-hydroxybenzoic acid, and ferulic acid were the predominant phenolics, with these having the highest amounts quantified in the rhizome extracts. All the tested extracts possessed antioxidant capacities, with pericarp and rhizome extracts exhibiting the highest activity in DPPH, ABTS, and FRAP assays. The extracts from pericarp and rhizome were revealed to also be the strongest inhibitors of pancreatic lipase. The rhizome extracts exhibited potent cytotoxic activity against HCT-116 and HepG2 with IC50 values of 30 and 54 µg/mL after 48 h of treatment. The present study demonstrated that A. stipularis can be used as a new source of natural antioxidants and potential anticancer and antiobesity compounds.

Green Synthesis and Biological Activities of Zinc Oxide Nanoparticles using Ampelocissus martini Rhizome Extract

AbstractZinc oxide nanoparticles (ZnO NPs) were prepared by co‐precipitation of zinc acetate with Ampelocissus martini rhizome extract (AM). Four conformations of ZnO NPs were obtained by conjoined precipitation of sodium hydroxide, zinc acetate dihydrate, and AM: ZnO NPs‐01, ZnO NPs‐02, ZnO NPs‐03, and ZnO NPs‐04. The structure of ZnO NPs was confirmed by X‐Ray diffraction (XRD). Fourier transform infrared (FTIR) analysis was conducted to identify functional groups. The formation and morphology of the synthesized ZnO NPs were confirmed by field emission scanning electron microscopy (FE‐SEM) with Energy dispersive X‐ray spectroscopy (EDS) mapping, and transmission electron microscopy (TEM). Free radical scavenging activity was determined by 2,2‐diphenyl‐1‐picryl‐hydazyl‐hydrate (DPPH) and 2,2/‐azino‐bis‐(3‐ethylbenzothi‐azoline‐6‐sulfonic acid (ABTS) assays. Antibacterial activity was examined by disc diffusion analysis together with minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC). ZnO NPs‐04 showed the highest inhibition in DPPH and ABTS assays and was active against E. coli and S. aureus with MICs=10 mg/mL and 5 mg/mL, respectively. These findings indicated that synthesized NPs could be utilized for several medicinal applications.

Effects of Hydroethanolic Rhizome Extract of Anchomanes difformis (Blume) in Type 2 (Streptozocin-Nicotinamide-Induced) Diabetic Rats

Effects of Hydroethanolic Rhizome Extract of Anchomanes difformis (Blume) in Type 2 (Streptozocin-Nicotinamide-Induced) Diabetic Rats

Oral sub-chronic toxicity of fingerroot (Boesenbergia rotunda) rhizome extract formulation in Wistar rats

BackgroundBoesenbergia rotunda (fingerroot) rhizome extract contains two major bioactive components, panduratin A and pinostrobin. In our previous study, we found the anti-inflammatory effects of the fingerroot extract against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in golden Syrian hamsters. In the present study, we evaluated the sub-chronic toxicity of a fingerroot extract formulation over 90 consecutive days of oral administration. MethodsWe enhanced the water solubility of a fingerroot extract by formulating it with cyclodextrin, containing panduratin A (29% w/w) and pinostrobin (32% w/w). This formulation was administered to male and female Wistar rats at doses of 25, 50, or 100 mg/kg/day for a duration of 90 days. Additionally, two recovery groups, comprising a control group and a high-dose group, were designated for a 14-day observation period to assess the persistence and reversibility of potential adverse effects. Throughout the experiment, we performed clinical and health observations, followed by hematological testing, clinical biochemistry analysis, necropsy examination, and histopathological evaluation at the end of the experiment. ResultsThe administration of the fingerroot extract formulation at doses of 25, 50, or 100 mg/kg/day did not result in mortality or clinical signs of toxicity. No clinically significant findings were associated with the oral administration of the fingerroot extract formulation. ConclusionThe fingerroot extract formulation showed no serious adverse effects at doses up to 100 mg/kg/day in Wistar rats under the experimental condition. Consequently, the No Observed Adverse Effect Level (NOAEL) was considered to be 100 mg/kg/day. This finding contributes significance for future developments involving fingerroot extract in herbal medicinal products targeting chronic inflammation.