Bio-Assisted Synthesis and Characterization of Zinc Oxide Nanoparticles from Lepidium sativum and Their Potent Antioxidant, Antibacterial and Anticancer Activities.

Nanotechnology is an emerging area of research that deals with the production, manipulation, and application of nanoscale materials. Bio-assisted synthesis is of particular interest nowadays, to overcome the limitations associated with the physical and chemical means. The aim of this study was to synthesize ZnO nanoparticles (NPs) for the first time, utilizing the seed extract of Lepidium sativum. The synthesized NPs were confirmed through various spectroscopy and imagining techniques, such as XRD, FTIR, HPLC, and SEM. The characterized NPs were then examined for various in vitro biological assays. Crystalline, hexagonal-structured NPs with an average particle size of 25.6 nm were obtained. Biosynthesized ZnO NPs exhibited potent antioxidant activities, effective α-amylase inhibition, moderate urease inhibition (56%), high lipase-inhibition (71%) activities, moderate cytotoxic potential, and significant antibacterial activity. Gene expression of caspase in HepG2 cells was enhanced along with elevated production of ROS/RNS, while membrane integrity was disturbed upon the exposure of NPs. Overall results indicated that bio-assisted ZnO NPs exhibit excellent biological potential and could be exploited for future biomedical applications. particularly in antimicrobial and cancer therapeutics. Moreover, this is the first comprehensive study on Lepidium sativum-mediated synthesis of ZnO nanoparticles and evaluation of their biological activities.

Antioxidative-, Antimicrobial-, Enzyme Inhibition-, and Cytotoxicity-Based Fractionation and Isolation of Active Components from Monotheca buxifolia (Falc.) A. DC. Stem Extracts.

The current study elaborates the pharmacological potential of the methanolic extract and its fractions of the stems of Monotheca buxifolia based on thin-layer chromatography and column chromatography analyses, exploiting biological and phytochemical assays. The results suggest that bioassay-guided isolation and fractionation led to the accumulation of biologically active components in the most active fractions that resulted in the isolation of different compounds. Structural elucidation of the purified compounds was accomplished using spectroscopic one-dimensional (1H, 13C) and two-dimensional NMR (heteronuclear multiple quantum coherence, heteronuclear multiple bond coherence, and correlation spectroscopy) and spectrometric (electron ionization mass spectrometry and high-resolution electron ionization mass spectrometry) techniques. The n-hexane, CHCl3, and EtAOc fractions led to the isolation of lupeol from different fractions. 1-Triacontanol was also isolated from the n-hexane fraction, while benzoic acid, methyl benzoate, ursolic acid, and 3-hydroxybenzoic acid were obtained from the EtOAc fraction. The compounds depicted good-to-moderate total antioxidative potential and total reducing power activity and significant free-radical scavenging activity. All the compounds showed significant urease and lipase inhibitory activity with poor-to-moderate amylase inhibition. Significant zone of inhibition was observed against different bacterial strains by the isolated compounds. This work therefore states that bioassay-guided isolation plays a vital role in the isolation of biologically active constituents that can be exploited for drug development.

Chemical composition, antibacterial and antioxidative activities of Monotheca buxifolia (Falc.) A. DC leaves essential oil.

Monotheca buxifolia (Sapotaceae) is used against different heath aliments due to auspicious biological properties. Essential oil was extracted from leaves of M. buxifolia through steam distillation. Gas chromatography coupled with mass spectrometry (GC-MS) showed presence of 34 compounds. Geranyl acetone (12.6%), nonanal (9.0%) and champhor (8.0%) were abundant while (E)-ß-ionone, cis-carvone oxide and caryophyllene oxide were also found. The oil presented 50.2% free radical scavenging activity while total antioxidant potential and total reducing power potential were 40.0 µg AAE/mL and 38.7 µg AAE/mL, respectively. The extracted oil presented moderate activity against Escherichia coli (14 mm) and Bacillus subtilis (11 mm). The study concludes that the essential oil of M. buxifolia leaves has diverse chemical composition and biological activities therefore can be explored for therapeutic potential.

Antioxidant, antimicrobial, enzyme inhibition, and cytotoxicity guided investigation of Sideroxylon mascatense (A.DC.) T.D. Penn. leaves extracts.

The present study demonstrates the pharmacological tendency of Sideroxylon mascatense leaves extracts, fractions and sub-fractions using thin layer chromatography, column chromatography, and phytochemical (phenolics, flavonoids) and biological assays (free radical scavenging, antioxidative, antimicrobial, enzyme inhibition). The results disclosed that fractionation practice accumulated the active phytochemicals in few fractions and finally leads to the isolation of active compounds. The structural elucidation was carried out using spectroscopic 1D (1H, 13C) 2D NMR and spectrometric techniques. The n-hexane fraction led to isolation of lupeol. From the CHCl3 and EtOAc fractions, two compounds were isolated, hentriacontanol, and lupeol, respectively. The isolated compounds were also characterized for biological activities. This study concludes that bioactivity guided isolation can be performed for isolation of active constituents from S. mascatense which can be further explored for drug development.

Metabolic fingerprinting, antioxidant characterization, and enzyme-inhibitory response of Monotheca buxifolia (Falc.) A. DC. extracts.

BACKGROUND: Ethnobotanical and plant-based products allow for the isolation of active constituents against a number of maladies. Monotheca buxifolia is used by local communities due to its digestive and laxative properties, as well as its ability to cure liver, kidney, and urinary diseases. There is a need to explore the biological activities and chemical constituents of this medicinal plant. METHODS: In this work, the biochemical potential of M. buxifolia (Falc.) A. DC was explored and linked with its biological activities. Methanol and chloroform extracts from leaves and stems were investigated for total phenolic and flavonoid contents. Ultrahigh-performance liquid chromatography coupled with mass spectrometry (UHPLC-MS) was used to determine secondary-metabolite composition, while high-performance liquid chromatography coupled with photodiode array detection (HPLC-PDA) was used for polyphenolic quantification. In addition, we carried out in vitro assays to determine antioxidant potential and the enzyme-inhibitory response of M. buxifolia extracts. RESULTS: Phenolics (91 mg gallic-acid equivalent (GAE)/g) and flavonoids (48.86 mg quercetin equivalent (QE)/g) exhibited their highest concentration in the methanol extract of stems and the chloroform extract of leaves, respectively. UHPLC-MS analysis identified a number of important phytochemicals, belonging to the flavonoid, phenolic, alkaloid, and terpenoid classes of secondary metabolites. The methanol extract of leaves contained a diosgenin derivative and polygalacin D, while kaempferol and robinin were most abundant in the chloroform extract. The methanol extract of stems contained a greater peak area for diosgenin and kaempferol, whereas this was true for lucidumol A and 3-O-cis-coumaroyl maslinic acid in the chloroform extract. Rutin, epicatechin, and catechin were the main phenolics identified by HPLC-PDA analysis. The methanol extract of stems exhibited significant 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid (ABTS) radical-scavenging activities (145.18 and 279.04 mmol Trolox equivalent (TE)/g, respectively). The maximum cupric reducing antioxidant capacity (CUPRAC) (361.4 mg TE/g), ferric-reducing antioxidant power (FRAP) (247.19 mg TE/g), and total antioxidant potential (2.75 mmol TE/g) were depicted by the methanol extract of stems. The methanol extract of leaves exhibited stronger inhibition against acetylcholinesterase (AChE) and glucosidase, while the chloroform extract of stems was most active against butyrylcholinesterase (BChE) (4.27 mg galantamine equivalent (GALAE)/g). Similarly, the highest tyrosinase (140 mg kojic-acid equivalent (KAE)/g) and amylase (0.67 mmol acarbose equivalent (ACAE)/g) inhibition was observed for the methanol extract of stems. CONCLUSIONS: UHPLC-MS analysis and HPLC-PDA quantification identified a number of bioactive secondary metabolites of M. buxifolia, which may be responsible for its antioxidant potential and enzyme-inhibitory response. M. buxifolia can be further explored for the isolation of its active components to be used as a drug.

Green and Chemical Syntheses of CdO NPs: A Comparative Study for Yield Attributes, Biological Characteristics, and Toxicity Concerns.

Metallic nanoparticles (NPs) have enormous applications due to their remarkable physical and chemical properties. The synthesis of NPs has been a matter of concern because chemical methods are toxic. On the contrary, biological methods are considered eco-friendly. To compare the toxicity and the environment-friendly nature of the synthesis methodologies, cadmium NPs were synthesized through chemical (Ch) (co-precipitation) and biological (plant extracts as reducing agent) methods. Cadmium nitrate was reduced with NaOH, while in the biological method, the Cd ions were reduced by Artemisia scoparia (As) and Cannabis sativa (Cs) extracts. X-ray diffraction (XRD) analysis confirmed the pure single-phase cubic structure of green and chemically synthesized CdO NPs except As-CdO NPs that were crystalline cum amorphous in nature. The size of nanoparticles was 84 nm (Cs-CdO NPs) and 42.2 nm (Ch-CdO NPs). The scanning electron microscope (SEM) images exhibited an irregular disklike morphology of nanoparticles that agglomerated more in the case of green synthesis. The antioxidant and antimicrobial potential of NPs revealed that chemically synthesized NPs have better antimicrobial capability, while the antioxidative activities were better for green-synthesized NPs. However, the low yield, high ion disassociation, and waste (unreacted metal) production in the green synthesis of CdO NPs increase the risk of contamination to biosphere. Both types of NPs did not affect the seed germination of Dodonaea viscosa. However, chemically synthesized NPs were less toxic on plant morphological response. The study concludes that the chemically synthesized CdO NPs have better morphology, significant antimicrobial activity, and less toxicity to plant species compared to green-synthesized NPs. Moreover, during the green synthesis, unreacted metals are drained, which causes contamination to the ecosystem.

Antioxidative, protein kinase inhibition and antibacterial potential of seven mango varieties cultivated in Pakistan.

Peel, pulp and kernel extracts of seven mango fruit (varieties) were analyzedsubjected for antibacterial and antioxidative potential. Langra peel showed good activity against B. subtilis, S. aureus and E. aerogenes. Good zone of inhibition by chaunsa kernel (28mm) and pulp (22mm) against Streptomyces stipulate its potential as anticarcinogencancerous. Dosehri and almashil pulp and sindhri peel asserted free radical scavenger (upto 79%) determined through DPPH assay. The peel and kernel of almashil contained maximum (total) flavonoids contents (58 & 43µgQE/100mg, respectively) while; total phenolics were higher in kernel of sindhri, chaunsa, langra and hujra and almashil pulp. Reducing power potential demonstrated variation from 300 to 554µgAAE/100mg. Total antioxidant potential was maximum in hujra pulp (512µg AAE/100mg). Concluded This study concludes that mango has vast beneficial potential for prone to human health and may also be used for isolation of antioxidative and antimicrobial as well as a protein kinase inhibition agent.

Synthesis, characterization and biological activities of monometallic and bimetallic nanoparticles using Mirabilis jalapa leaf extract.

Monometallic ZnO and Ag nanoparticles (NPs) and bimetallic ZnO/Ag NPs were synthesized using leaves extract of Mirabilis jalapa. XRD analysis confirmed the crystalline nature of NPs with size range from 19.3 to 67.4 nm for bimetallic, and 12.9 and 32.8 nm for monometallic NPs. SEM images reveal varying shapes of the monometallic (needle like and spherical for ZnO and Ag, respectively) and bimetallic (plates, sheets, and spherical) NPs depending upon concentration of salts used. Biological characterization reveals that both mono and bi metallic nanoparticles demonstrate free radical scavenging, total antioxidant, and reducing power potentials. Phenolic and flavonoid like properties of NPs were also observed might be due to presence of different functional groups on the particles surface. Bimetallic NPs displayed astonishing antibacterial (up to 25 mm zone of inhibition) and antileishmanial properties. The results suggest that bimetallic ZnO/Ag nanoparticles hold greater potential then monometallic against bacteria and Leishmania. Other biomedical applications also varied depending upon concentration of precursors. Furthermore, ratio of salt concentrations used for synthesis of bimetallic NPs affect morphological and biochemical characteristics of NPs.

Synthesis, characterization, applications, and challenges of iron oxide nanoparticles.

Recently, iron oxide nanoparticles (NPs) have attracted much consideration due to their unique properties, such as superparamagnetism, surface-to-volume ratio, greater surface area, and easy separation methodology. Various physical, chemical, and biological methods have been adopted to synthesize magnetic NPs with suitable surface chemistry. This review summarizes the methods for the preparation of iron oxide NPs, size and morphology control, and magnetic properties with recent bioengineering, commercial, and industrial applications. Iron oxides exhibit great potential in the fields of life sciences such as biomedicine, agriculture, and environment. Nontoxic conduct and biocompatible applications of magnetic NPs can be enriched further by special surface coating with organic or inorganic molecules, including surfactants, drugs, proteins, starches, enzymes, antibodies, nucleotides, nonionic detergents, and polyelectrolytes. Magnetic NPs can also be directed to an organ, tissue, or tumor using an external magnetic field for hyperthermic treatment of patients. Keeping in mind the current interest in iron NPs, this review is designed to report recent information from synthesis to characterization, and applications of iron NPs.