Are bioactive-rich fractions functionally richer?

Plant bioresources are relied upon as natural, inexpensive, and sustainable remedies for the management of several chronic diseases worldwide. Plants have historically been consumed for medicinal purposes based on traditional belief, but this trend is currently changing. The growing interest in the medicinal properties of plant bioresources stems from concerns of side effects and other adverse effects caused by synthetic drugs. This interest has yielded a better understanding of the roles of plant bioactive compounds in health promotion and disease prevention, including the underlying mechanisms involved in such functional effects. The desire to maximize the potential of phytochemicals has led to the development of "rich fractions," in which extracts contain bioactive compounds in addition to elevated levels of the primary compound. Although a rich fraction effectively increases the bioactivity of the extract, the standardization and quality assurance process can be challenging. However, the supercritical fluid extraction (SFE) system is a promising green technology in this regard. Future clinical and pharmacological studies are needed to fully elucidate the implications of these preparations in the management of human diseases, thereby fostering a move toward evidence-based medicine.

Impact of seawater on distribution of fluoride and other ions in groundwater of Diplo area, Thar Desert Pakistan.

The role of seawater dilution, along with other water-quality components, has been studied to determine the causes of spatial distribution of high fluoride concentrations in the groundwater of the Diplo sub-district, Thar Desert, Pakistan. Fluoride ion concentration ranges of up to 7.60 mg/L were discovered, with mean and median values of 1.66 and 1.34 mg/L, respectively. Estimates based on the total dissolved solid (TDS) ratio show the impact of seawater intrusion at a percentage of around 8.05% in the groundwater. The major ion chemistry of water in the central diamond shape of the Piper diagram precisely demarcates the phenomenon of the intrusion of seawater into the study area. The plots of Na+K vs. Ca+Mg (meq/L) and log C1 (mg/L) vs. log Ca+Mg/Na+K (meq/L) indicate a mixing of freshwater with seawater. The molar Na/Na+Cl and Ca/Ca+SO4 ratios of the groundwater, and correlation matrices of major ion chemistry, also show a blending of groundwater with seawater. Mutual relationships among Li+, Sr2+, and C1- ions further substantiate the marked influence of the marine environment on the groundwater in the study area.

Comparison of chemical composition of Aerva javanica seed essential oils obtained by different extraction methods.

Aerva javanica (Burm.f.) Juss. ex Schult. seed essential oils were obtained by hydrodistillation (HD) and dry steam distillation (SD) extracting methods and analyzed by using gas chromatography-mass spectrometry(GC-MS). Twenty and eighteen components representing 90.5% and 95.6% of the seed essential oil were identified, using hydrodistillation and dry steam distillation, respectively. The major constituent identified from seed essential oil obtained by HD were heptacosane (25.4%), 3-allyl-6-methoxyphenol (14.1%), pentacosane (12.1%), 6,10,14-trimethyl-2-pentade-canone (7.9%), nonacosane (7.1%), tricosane (3.6%), α-farnesene (3.5%), dodecanal (2.7%) and octacosane (2.1%). Whereas the major constituent identified from seed essential oil obtained by SD were heptacosane (41.4%), pentacosane (21.2%), nonacosane (14.8%), tricosane (6.3%), octacosane (4.2%) and tetracosane (3.0%).

Antidiabetic properties of germinated brown rice: a systematic review.

Diet is an important variable in the course of type 2 diabetes, which has generated interest in dietary options like germinated brown rice (GBR) for effective management of the disease among rice-consuming populations. In vitro data and animal experiments show that GBR has potentials as a functional diet for managing this disease, and short-term clinical studies indicate encouraging results. Mechanisms for antidiabetic effects of GBR due to bioactive compounds like γ-aminobutyric acid (GABA), γ-oryzanol, dietary fibre, phenolics, vitamins, acylated steryl ß-glucoside, and minerals include antihyperglycemia, low insulin index, antioxidative effect, antithrombosis, antihypertensive effect, hypocholesterolemia, and neuroprotective effects. The evidence so far suggests that there may be enormous benefits for diabetics in rice-consuming populations if white rice is replaced with GBR. However, long-term clinical studies are still needed to verify these findings on antidiabetic effects of GBR. Thus, we present a review on the antidiabetic properties of GBR from relevant preclinical and clinical studies, in order to provide detailed information on this subject for researchers to review the potential of GBR in combating this disease.

Development and implication of a capillary electrophoresis methodology for ciprofloxacin, paracetamol and diclofenac sodium in pharmaceutical formulations and simultaneously in human urine samples.

This work studies the development of a simple and fairly rapid methodology for simultaneous determination/separation of three frequently co-administered drugs; ciprofloxacin (CIP), paracetamol (PCT) and diclofenac sodium (DIC) using capillary electrophoresis (CE) with UV detection at 260 nm. Separation was achieved in only 6.5 min with a simple buffer of sodium tetraborate (50 mM) at pH 9.0. The Parameters affecting the separation and detection were optimized. The calibration curves were linear in the range of 5-500 µg/mL for CIP, 5-250 µg/mL for PCT and 1-125 µg/mL for DIC sodium under the optimized conditions. The lower limit of detection (LOD) was found to be 1 µg/mL for CIP & PCT and 0.5 µg/mL for DIC. The method was successfully used for the analysis of drugs in commercial pharmaceutical formulations and simultaneously from patient's urine sample with RSD 0.5-2.4%. Results obtained with CE method are compared with standard HPLC procedure and were found in good agreement.

Colorimetric sensing of cephradine through polypropylene glycol functionalized gold nanoparticles.

The development of metal nanoparticle-based facile colorimetric assays for drugs and insecticides is an emerging area of current scientific research. In the present work, polypropylene glycol was used for stabilization of gold nanoparticles (AuNPs) in a simple one-pot two-phase process and subsequently employed it for the specific detection of cephradine (CPH). The characterization of the prepared PPG-AuNPs was conducted through various analytical techniques such as UV-visible spectrophotometry, Fourier transform infrared spectroscopy, atomic force microscopy (AFM), zeta potential and zetasizer techniques. As the major target of the study, the stabilized PPG-AuNPs were employed for colorimetric detection of CPH and other drugs. Typical wine-red colour of PPG-AuNPs disappeared immediately and surface plasmon resonance band quenched by addition of CPH in the presence of several other interferents (drugs and salts) and in real samples. PPG-AuNPs permitted efficient, selective, reliable and rapid determination in a concentration range of 0.01-120 mM with a detection limit (LoD) of 11.0 mM. The developed sensor has the potential to be used for fast scanning of pharmaceutical formulations for quantification of CPH at production facilities.

A review on detection of heavy metals from aqueous media using nanomaterial-based sensors.

The extensive release of heavy metals into the natural water bodies has become globally prevalent from past few decades. Heavy metal toxicity is becoming a serious threat to human and the environment. Due to their prolonged half-life, potential accumulation in different parts of body, and non-biodegradability, metal ions are being obvious entities that can cause several hazardous health risks. A number of methods have been developed for the detection of heavy/toxic metals based on sensors. Among the various new technologies, chemical and optical nano sensors are emerging technology to detect toxic heavy metals. Several nano sensors have been developed using nano materials, synthesized from green or chemical methods. The nano sensors are convenient to prepare and provide enhanced limit of detection, limit of quantification, and onsite detection. This review covers the recent work reported from 2013 to 2019 for the detection of heavy metals using sensors based on nano materials synthesized by different routes. Graphical abstract.

Salicylaldehyde derivative of nano-chitosan as an efficient adsorbent for lead(II), copper(II), and cadmium(II) ions.

In this study, a biodegradable natural polymer chitosan was modified with salicylaldehyde to prepare salicylaldehyde functionalized chitosan nanoparticles (N-Ch-Sal). The N-Ch-Sal was characterized by atomic force microscopy (AFM), scanning electron microscopy-energy-dispersive X-ray (SEM-EDX), Fourier transform infrared spectroscopy (FT-IR) and thermogravimetric analysis (TGA). The salicylaldehyde functionalized chitosan nanoparticles (N-Ch-Sal) (~80 nm) were then used for the adsorption of three heavy metals viz., Cu(II), Cd(II) and Pb(II) ions. The above-mentioned techniques were also employed for evaluation of changes in N-Ch-Sal after metal adsorption. The parameters affecting the adsorption of metal ions including pH, contact time, amount of adsorbent, initial metal ion concentration and the effect of interfering ions, were studied thoroughly and optimized. The concentration of metal ions remaining in the aqueous system after adsorption experiments was analyzed by ICP-MS. At optimal conditions, sorption capacity of Pb(II) ion was found to be highest i.e., 123.67 followed by Cu(II) (84.60) and Cd(II) (63.71 mg/g). The adsorption process followed the pseudo-second-order kinetic model and fitted well with the Langmuir adsorption isotherm. The adsorption method was applied to a real tap water sample for the quantification and removal of Pb(II) ions. The concentration of Pb(II) ions in the tested sample was 4.88 ppb.

Preparation, characterization, and binding profile of imprinted semi-IPN cryogel composite for aluminum.

Human body is greatly exposed to aluminum due to its high abundance in the environment. This nonessential metal is a threat to the patients of chronic renal disorders, as it is easily retained in their plasma and quickly accumulates in different tissues. Thus, there is great need to remove it from the aqueous environment. In this study, Al3+ imprinted semiinterpenetrating polymer network (semi-IPN)-based cryogel composite was prepared and applied for the purification of environmental and drinking water samples from aluminum. Poly (2-hydroxyethyl methacrylate) (pHEMA) discs were produced via cryogenic treatment and imprinted semi-IPN was introduced to the 3-(trimethoxysilyl) propyl acrylatemodified macroporous cryogel discs. The adsorption properties and selectivity of the aluminum (III) imprinted semi-IPN cryogel composite were studied in detail. The imprinted semi-IPN cryogel composite showed good selectivity towards aluminum (III) ions with the imprinting factor (IF) of 76.4 in the presence of competing copper (II), nickle (II), and iron (III) ions. The maximum adsorption capacity of 271 µmol g-1 was obtained for aluminum (III) at pH 7.0 within 10 min using imprinted semi-IPN cryogel composite. The good selectivity and reusability of aluminum (III)-imprinted semi-IPN cryogel composite makes this material an eligible candidate for the purification of drinking water from aluminum (III) leaving important minerals remained in the water.

Electrolytic recovery of chromium salts from tannery wastewater.

Tannery wastewater collected from a local leather industry in Peshawar, Pakistan was subjected to DC electrolysis in a simple cell having two static sheet electrodes and stirring assembly after proper dilution and adjustment to desired conditions. One percent HNO(3) and 1% NaHCO(3) were used as electrolytes and pH adjusters. The latter salt also worked as sodium source for anodic deposition of Na(2)Cr(2)O(7). Various combinations of electrodes were tested and conditions optimized for best electrode couple with increased recovery and removal of chromium in the form of Cr(OH)(3) and/or Na(2)Cr(2)O(7) at cathode and anode, respectively. The recovery of 99% chromium was achieved after 2h electrolysis at a cell potential of 1.0 V, pH 5.0 and stirring rate of 500 rpm using Pb sheet as anode and Cu sheet as cathode. The most interesting and novel finding of this work was the recovery of the mentioned salt(s) alone at Cu cathode or Pb anode or collectively at both electrodes by proper control of pH. Such treatment not only minimizes the environmental water pollution, but results in the formation of useful products employed for recycling purpose in tannery or other related industry to make the process economical.

Simpler spectrophotometric assay of paracetamol in tablets and urine samples.

A very fast, economical and simpler direct spectrophotometric method was investigated for paracetamol (PC) determination in aqueous medium without using any chemical reagents. The method is based on the photo-absorption of the analyte at 243 nm after dissolution in water. The change in structure of PC after addition of water was studied by comparing the corresponding FTIR spectra. Optimization studies were conducted by using a 5 microg ml(-1) standard solution of the analyte. Various parameters studied include, time for stability and measurement of spectra, effect of HCl, NaOH, CH(3)COOH and NH(3) for change in absorbance and shift in spectra, interference by some analgesic drugs and some polar solvents and temperature effect. After optimization, Beer's law was obeyed in the range of 0.3-20 microg ml(-1) PC solution with a correlation coefficient of 0.9999 and detection limit of 0.1 microg ml(-1). The newly developed method was successfully applied for PC determination in some locally available tablets and urine samples. The proposed method is very useful for quick analysis of various types of solid and liquid samples containing PC.

Banana peel: an effective biosorbent for aflatoxins.

This work reports the application of banana peel as a novel bioadsorbent for in vitro removal of five mycotoxins (aflatoxins (AFB1, AFB2, AFG1, AFG2) and ochratoxin A). The effect of operational parameters including initial pH, adsorbent dose, contact time and temperature were studied in batch adsorption experiments. Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and point of zero charge (pHpzc) analysis were used to characterise the adsorbent material. Aflatoxins' adsorption equilibrium was achieved in 15 min, with highest adsorption at alkaline pH (6-8), while ochratoxin has not shown any significant adsorption due to surface charge repulsion. The experimental equilibrium data were tested by Langmuir, Freundlich and Hill isotherms. The Langmuir isotherm was found to be the best fitted model for aflatoxins, and the maximum monolayer coverage (Q0) was determined to be 8.4, 9.5, 0.4 and 1.1 ng mg(-1) for AFB1, AFB2, AFG1 and AFG2 respectively. Thermodynamic parameters including changes in free energy (ΔG), enthalpy (ΔH) and entropy (ΔS) were determined for the four aflatoxins. Free energy change and enthalpy change demonstrated that the adsorption process was exothermic and spontaneous. Adsorption and desorption study at different pH further demonstrated that the sorption of toxins was strong enough to sustain pH changes that would be experienced in the gastrointestinal tract. This study suggests that biosorption of aflatoxins by dried banana peel may be an effective low-cost decontamination method for incorporation in animal feed diets.

A rapid Fourier-transform infrared (FTIR) spectroscopic method for direct quantification of paracetamol content in solid pharmaceutical formulations.

A transmission FTIR spectroscopic method was developed for direct, inexpensive and fast quantification of paracetamol content in solid pharmaceutical formulations. In this method paracetamol content is directly analyzed without solvent extraction. KBr pellets were formulated for the acquisition of FTIR spectra in transmission mode. Two chemometric models: simple Beer's law and partial least squares employed over the spectral region of 1800-1000 cm(-1) for quantification of paracetamol content had a regression coefficient of (R(2)) of 0.999. The limits of detection and quantification using FTIR spectroscopy were 0.005 mg g(-(1) and 0.018 mg g(-1), respectively. Study for interference was also done to check effect of the excipients. There was no significant interference from the sample matrix. The results obviously showed the sensitivity of transmission FTIR spectroscopic method for pharmaceutical analysis. This method is green in the sense that it does not require large volumes of hazardous solvents or long run times and avoids prior sample preparation.

Geochemical controls of high fluoride groundwater in Umarkot Sub-District, Thar Desert, Pakistan.

Groundwater samples (n=152) were collected in the Thar Desert of the Umarkot Sub-District, Pakistan to evaluate the geochemical controls on the occurrence of high fluoride (F(-)) levels within the study area. Fluoride concentrations range from 0.06 to 44.4 mg/L, with mean and median values of 5.22 and 4.09 mg/L, respectively; and roughly 84% of the samples contain fluoride concentrations that exceed the 1.5mg/L drinking water standard set by WHO. The overall groundwater quality reflects the influences of silicate mineral weathering and evaporation. Fluoride originates from the weathering of minerals derived from Type-A granite and possibly anion exchange (OH(-) for F(-)) on clays and weathered micas under high pH conditions. High fluoride levels are associated with Na-HCO3 type water produced by calcite precipitation and/or base ion exchange. Depleted calcium levels in groundwater allow higher fluoride concentrations to occur before the solubility limit for fluoride is reached.

Assay of phenolic compounds from four species of ber (Ziziphus mauritiana L.) fruits: comparison of three base hydrolysis procedure for quantification of total phenolic acids.

The present study was undertaken to investigate the flavonoid profile in four species of ber (Ziziphus mauritiana Lamk.) fruit. The 12 flavonoids identified were quercetin 3-O-robinobioside, quercetin 3-O-rutinoside, quercetin 3'-O-galactoside, quercetin 3'-O-glucoside, quercetin 3'-O-rhamnoside, quercetin 3'-O-pentosylhexoside, quercetin 3-O-6'malonylglucoside, quercetin 3'-O-malonylglucoside, luteolin 7-O-6'malonylglucoside, luteolin 7-O-malonylglucoside, myricetin 3-O-galactoside, and naringenin tri glycoside. This is the first report on extraction of nine additional flavonoids from the ber fruits. In addition, we also compared the impact of three different base hydrolysis techniques namely ultrasonic assisted base hydrolysis (UABH), microwave assisted base hydrolysis (MWABH), and pressurised liquid assisted base hydrolysis (PLABH) for the quantification of total phenolic acids. Nine phenolic acids, protocatechuic acid, p-hydroxybenzoic acid, ferulic acid, chlorogenic acid, vanillic acid, caffeic acid, vanillin, ortho- and para-coumaric acids, were identified and quantified. The three major phenolic acids identified in all four ber species were p-coumaric acid, vanillin and ferulic acids. Higher amounts (p<0.05) of total phenolic acids in all cultivars were obtained with the PLABH technique as compared to other two procedures (UABH and MWABH).

Chemical composition of essential oil from Calligonum polygonoides Linn.

The essential oil from air dried buds and roots of Calligonum polygonoides Linn., has been extracted from dry steam distillation and analysed for chemical composition by gas chromatography-mass spectrometry. In total, 27 and 10 compounds were analysed qualitatively and quantitatively, accounting for 68.42% and 82.12% total contents of the essential oils of buds and roots, respectively. It contains a complex mixture of terpenoids, hydrocarbons, phenolic compounds, acid derivatives and ketones. The main component of essential oil was ethyl homovanillate (11.79%) in buds and drimenol (29.42%) in roots.

Lithological influences on occurrence of high-fluoride groundwater in Nagar Parkar area, Thar Desert, Pakistan.

Factors regulating the occurrence of high fluoride (F(-)) concentrations in groundwater near Nagar Parkar Town, SE corner of Pakistan have been investigated considering lithological influences. F(-) ion concentrations in groundwater range up to 7.85 with mean value of 3.33 mg L(-1). Plots of major elements and their normative mineral composition reflect granitic composition of the rocks in the study area. Modal mineralogical analysis show high perthite, plagioclase feldspars and quartz, while micas, amphiboles and pyroxenes occur in minor quantities. Water-rock interactions, based on dissolved ions of F(-), SiO(2), Na(+), K(+), Mg(2+), Li(+) and Sr(2+) suggest that fluoriferous groundwater originates from granitic rocks, typically from albite, biotite, hornblende and pyroxene and its alteration products such as kaolin and soil. The Log TDS, Na/Na+Ca ratio, Mg/Ca+Mg and Cl/Sigma anions are significant to review the impact of weathering processes which promote the availability of F(-) ions in the groundwater of study area. Principal component analysis (PCA) also renders close association among F(-) ions and other elements in the rocks and groundwater. Studies on F(-) estimation in the granite rock, china clay, soil and sand samples also indicate the presence of high F(-) concentration in these materials and average values have been found to be 1939, 710, 254 and 16 mg kg(-1), respectively.

Geochemical factors controlling the occurrence of high fluoride groundwater in the Nagar Parkar area, Sindh, Pakistan.

Fluoride concentrations in groundwater near Nagar Parkar in the Thar Desert of southeastern Pakistan range from 1.13 to 7.85 mg/l, and roughly 78% of the samples contain fluoride in concentrations that exceed the drinking water standard of 1.5mg/l set by WHO. The groundwater is alkaline (pH 7.1-8.4), brackish (TDS 449-15,933 mg/l), and classified as Na-Cl type water. This prevailing chemical character reflects the influence of saltwater intrusion, high evaporation rates, and ion exchange. Groundwater is also supersaturated with respect to calcite, which promotes the removal of Ca(2+) and HCO(3)(-) from solution. As a result, groundwater is generally undersaturated with respect to fluorite, the mineral that typically controls the upper limit of fluoride concentrations. This study examines a number of geochemical parameters in an effort to discover the controls on fluoride concentrations in groundwater. High fluoride concentrations are associated with high TDS, high pH, high Na concentrations, and high sodium absorption ratios (SAR). This suggests that elevated fluoride levels are the result of enhanced fluorite solubility due to Ca depletion and high ionic strength and the release of fluoride from colloid surfaces under high pH conditions. Contrary to what has been found in other studies, sample depth and water temperature do not appear to have a significant role in the distribution of fluoride within the groundwater.

A new simple sensitive differential pulse polarographic method for the determination of acrylamide in aqueous solution.

A new simple sensitive differential pulse polarographic (DPP) method was investigated for the determination of acrylamide (AA) directly in a neutral aqueous solution. The AA showed a well-defined and well-resolved peak in pure aqueous LiCl at -1.84V in the potential range from -1.6V to -1.97V at nitrogen pressure of 0.5kgcm(-2). Among the various electrolytes studied, the AA showed good DPP response in the presence of LiCl and tetra methyl ammonium iodide, while it showed poor response in the presence of tetra butyl ammonium hydroxide and tetra butyl ammonium bromide due to their strong adsorption on the surface of electrode which hindered its reduction. The effect of LiCl concentration, the cyclic voltammetric response and the drop time study showed that AA exhibited an irreversible adsorptive electrochemical behavior. The good electrochemical response in pure aqueous medium suggested that hydrogen bonding might be involved which may favor the electrode reaction. Under optimized conditions, the peak current was linear in the entire concentration range from 0.2 mgL(-1) to 20 mgL(-1) with the correlation coefficient of R(2)=0.9998. The method showed good reproducible results with R.S.D. of 0.3% (n=16). The detection limit (LOD) was 27 microgL(-1). The influence of various interfering agents was also studied. The method was applied successfully for the quantification of AA in water samples without any interference effect from alkali metals.