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Use of abundant indigenous energy crops for biofuel production contributes to enhance the economy and reduce the dependence on fossil fuels. This article aims to shed light on two energy crops available in Pakistan; castor (Ricinus communis L.) and cottonseed (Gossypium hirsutum L.). Although castor has excellent oil content (54%), its high viscosity is not acceptable. Therefore, pre-blending with cottonseed oil was proposed. Physical and chemical properties of crude oils, pure biodiesels and binary blends besides fatty acid composition and degree of unsaturation were analyzed. Biodiesels were checked for quality parameters within limits of American Society for Testing Materials (ASTM) and European Standards. Improvement in kinematic viscosity and density of castor biodiesel were noticed following this concept. Moreover, the developed empirical formula indicated that an optimized blending ratio of 93.86% cottonseed oil and 6.14% castor oil accomplished biodiesel yield of 91.12%, kinematic viscosity of 6 mm(2)/s and cetane number of 48.79, respectively, which all satisfy ASTM D6751. This technique also indicated that pre-blending can raise the ester content of castor biodiesel. In conclusion, it is recommended to adopt the concept of pre-blending to improve the quality of biodiesel and thus the engine and emission performance in compression ignition engines.

Selectivity of gold nanoparticles (AuNPs) depends upon surface functionality; small changes in structure or concentration bring significant changes in the behavior of AuNPs. In this study, citrate-capped AuNPs were functionalized with ortho-dicarboxylate substituted pyridine (2,3-PDCA) and detailed studies on experimental conditions were carried out to check the stability of AuNPs and response for Cr3+. Stability of PDCA-AuNPs was found sensitive to the pH, ionic strength of buffer and its type. Capping behavior of PDCA on C-AuNPs was examined by FTIR spectroscopy. Surface morphology and size of synthesized AuNPs were confirmed by AFM, XRD, and DLS techniques where particles were found 11nm in size, monodisperse and spherical in shape. Interaction of stabilized AuNPs was tested with various metal ions; where Cr3+ induced the changes in localized surface plasmon band (LSPR) of PDCA-AuNPs which leads to a color change from wine red to violet blue. The phenomenon is explained as cooperative effect of citrate and pyridine nitrogen on surface of AuNPs in contrary to meta-dicarboxylate substituted pyridine derivatives. Further, under optimized and controlled conditions Cr3+ shows linear response with decrease in absorbance at LSPR intensity of AuNPs (518nm). Moreover, to demonstrate the applicability of method, Cr3+ was determined in the presence of Cr (VI) which shows 96% recovery.

The aim of this study was to quantify free fatty acid in cottonseed oil (Gossypium) variety by a chemometric approach using Fourier transform infrared spectroscopy. Calibration standards were prepared by gravimetrical mixing of oleic acid (0.1–40 g/100 g) in neutralized cottonseed oil containing

Pomegranate is an earliest and holy fruit affectionately known as the “jewel of winter” belongs to the Punicaceae family. Throughout the world, ~500 known pomegranate varieties available which reveal different quality characteristics of fruit such as size, shape, color, flavor and taste and seed hardness. The pomegranate seeds contain approximately 3% of total fruit weight, which contains typically oil in the range of 12–20%. Conjugated fatty acids are present in many plant oils with varying concentrations including pomegranate seed oil. Conjugated fatty acids are the geometric and positional isomers of polyunsaturated fatty acids with alternate double bonds. These fatty acids received remarkable interest due to valuable physiological effects on various diseases. The pomegranate seed oil contains higher concentration (>70%) of conjugated fatty acids in the form of punicic acid (9cis, 11trans, 13cis-conjugated linolenic acid). In the present chapter, chemistry and functionality of pomegranate fruit and seed oil especially conjugated fatty acids are reviewed.

Keeping in view the versatile applications of castor oil in cosmetic, pharmaceutical and recently as renewable source, the present work is a step towards the commercialization of castor on large scale in Pakistan. The current study introduces a castor variety with high oil content. Initially seeds were physically examined for some physical parameters. Seed moisture, ash content and linear dimensions such as length, width and thickness were found to be 4.53%, 6.44%, 12.24 mm, 8.31 mm and 5.67 mm, respectively. For oil extraction, Soxhlet method was used which resulted in the high oil content 54.0%. For quality assessment of oil, physicochemical parameters were checked according to official standard AOCS methods and compared with ASTM specifications. The determined parameters were as follows; specific gravity 0.953 g/cm(-3), refractive index 1.431, viscosity 672.0 mPas.s, moisture content 0.32%, FFA 0.14%, IV 83.61 gI2/100 g, PV 2.25 meq/Kg and SV 186.0 mgKOH/g. Furthermore, fatty acid analysis of oil showed that, most abundant fatty acid was ricinoleic acid 94.59%, followed by palmitic 0.31%, linoleic 1.84%, oleic (n-9) 2.05%, oleic (n-10) 0.22%, stearic 0.45% and eicosenoic acid 0.53%. The detected fatty acids were compared with registered variety and varieties of other regions.

Calixarenes are well known for their molecular recognition properties. Thus, the present study was carried out to explore their usage in the isolation of flavonoids [i.e. quercetin (I) and catechin (II)] from plant extracts, e.g. Alhagi camelorum through metal complexation. The synthesis of flavonoid metal complexes from plant extracts through direct complexation and their purification by using calix[4]arene based resin (R-1) was carried out simultaneously to ensure the separation efficiency of R-1. It was observed that the direct complexation of flavonoids present in plant extracts and purification using a column loaded with R-1 could be the best choice for industries requiring the isolation and purification of flavonoids or their complexes from plants.

Free fatty acids (FFA) are produced by the hydrolysis of oils and fats. The level of FFA depends on time, temperature and moisture content because the oils and fats are exposed to various environments such as storage, processing, heating or frying. Since FFA are less stable than neutral oil, they are more prone to oxidation and to turning rancid. Thus, FFA is a key feature linked with the quality and commercial value of oils and fats. The American Oil Chemists' Society (AOCS), the Association of Official Analytical Chemists (AOAC) and the European Commission (EC) Regulations have established almost identical standard methods for the assessment of FFA. These methods are based on titration, where oils or fats need to be dissolved in hot neutralized ethanol or ethanol/diethyl ether using phenolphthalein as an end point indicator. Titrimetric procedures are, however, laborious and need large amounts of chemicals and solvents. The cost of chemicals and environmental issues further limit these procedures. In addition, accurate detection of end points, especially for highly colored crude oil using a colorimetric indicator, is a difficult task. Despite these disadvantages, the titration method is unfortunately still being used in most of the edible-oil industries for the determination of FFA. Because of a lack of any comprehensive review on this very important topic, we have made an attempt to present a review in order to discuss the various methods available with special emphasis on the instrumental methods because of their high sensitivity, accuracy and rapidity.

Palm fatty acid distillate (PFAD) is cheap and valuable byproduct of edible oil processing industries. This study was designed to characterize PFAD collected from different local oil industries. AOCS methods were used for the determination of physicochemical parameters such as free fatty acid (FFA), saponification value (SV), iodine value (IV), peroxide value (PV) and moisture content. Fatty acid composition was analyzed using GC-MS. Moisture content of samples was found to be in the range between 0.06-7.50%, while FFA, SV, IV and PV were found to be 65.70-94.68%, 195.23-219.64 mg KOH/g, 38.49- 63.10 g I2/100 g, 1.09-16.50 meq/kg, respectively. Mean value of fatty acids in PFAD was found as 0.04% lauric, 0.42% myristic, 41.25% palmitic, 7.29% stearic, 41.58% oleic, 8.95 % linoleic, 0.04% eicosenoic, 0.27% arachidic, 0.07% docosanoic, and 0.05% tetracosanoic acid, respectively. Palmitic acid was found as dominant saturated fatty acid 38.63-45.30%, whereas oleic acid C18:1 n9 was major unsaturated fatty acid 33.54-44.05 % in PFAD.

A quick and reliable analytical method for the quantitative assessment of cefixime in orally administered pharmaceutical formulations is developed by using diamond cell attenuated total reflectance (ATR) Fourier transform infrared (FT-IR) spectroscopy as an easy procedure for quality control laboratories. The standards for calibration were prepared in aqueous medium ranging from 350 to 6000 mg/kg. The calibration model was developed based on partial least square (PLS) using finger print region of FT-IR spectrum in the range from 1485 to 887 cm−1. Excellent coefficient of determination (R2) was achieved as high as 0.99976 with root mean square error of 44.8 for calibration. The application of diamond cell (smart accessory) ATR FT-IR proves a reliable determination of cefixime in pharmaceutical formulations to assess the quality of the final product.

A rapid, simple and reproducible single bounce attenuated total reflectance (SB-ATR) Fourier transform infrared (FTIR) spectroscopic method was developed for determination of the n − 6, n − 3 and ratio of n − 6: n − 3 polyunsaturated fatty acids (PUFAs) in poultry feed lipids using partial least squares (PLS) regression. Data for n − 6, n − 3 and ratio of n − 6: n − 3 was acquired by gas chromatography (GC) and used as a standard values for FTIR calibration. The best regression results were achieved using first derivatives of the 1475–650 cm −1 spectral region for n − 6, n − 3 and ratio of n − 6: n − 3 with high regression coefficients ( R 2 ) of 0.999, 0.994 and 0.998, respectively and low RMSEP values of 1, 0.06 and 0.83, respectively. The results of the present study revealed that FTIR could be used for rapid and accurate determination of n − 6, n − 3 and ratio of n − 6: n − 3 PUFAs present in poultry feed lipids.

In the present study, the quality of frying oil, as affected by commercial pan fish frying, was investigated. The quality of fresh frying oil, null replenishment (NR) oil, and discarded frying oil were evaluated by drawing out the oil samples from the fryer at the initial stage, just before the addition of new frying oil for level make-up and used oil of the last frying cycle, respectively. The parameters used to assess the quality were the fatty acid composition including trans fatty acid (TFA), free fatty acid, and peroxide values of frying oil. Gas chromatography-mass spectroscopy (GC-MS) was used to examine fatty acids profiles of the frying oils. Trans fatty acid in fresh oils varied from 2.5%–3.8% (except oil-6, which contained 13%), whereas NR oils and discarded oils contained 5.6%–14.8% and 7.3%–20.8% trans fatty acids, correspondingly. Free fatty acid in fresh, NR, and discarded oils were 0.12%–0.24%, 0.22%–1.74%, and 0.80%–3.39%, respectively. Peroxide value in fresh, NR, and discarded oils were...

The purpose of this study was to determine the total trans fat content from the Fourier transform infrared (FT-IR) spectra of neat fats extracted from cereal-based foods using a single-bounce horizontal attenuated total reflectance (SB-HATR) sampling accessory. Partial least squares (PLS) regression was employed for the development of calibration models. A trans fat calibration curve was prepared by adding trielaidine gravimetrically to trans free canola oil. Regression of the FT-IR/PLS-predicted trans contents was 0.999 with a root-mean-square error of calibration (RMSEC) and root-mean-square error of prediction (RMSEP) 0.07% and 0.07%, respectively. Amongst the samples examined, the fat content was in the range of 8.2–27.2%, whilst most samples contained more than 10% trans fat; the highest trans fat content was 16.3%. The FT-IR results were comparable with gas chromatography (GC).

The amount of trans fatty acids (TFA) in fourteen industrially hydrogenated and deodorized oils was determined. To achieve better sensitivity 200 μm KCl cell was used in transmission Fourier transform infrared (FT-IR) spectroscopy. The results of transmission FT-IR spectroscopy were evaluated by gas chromatography (GC) with flame ionization detector (FID), and found to be comparable. All analyzed cooking oil samples had a lower trans content of 0.4–1.8%. Trans fatty acid contents of partially hydrogenated oil samples were relatively higher as comparable to those of the cooking oils. Among the samples examined, the highest level was found to be at 26.5% and 25.7% by the GC–FID and FT-IR spectroscopy, respectively. Due to harmful effects, high amounts of trans fatty acids in partially hydrogenated oils is an alarming issue for the consumer’s health and quality control authorities.

The fat contents of 12 brands of biscuits were extracted and evaluated for free fatty acids (FFA) and their fatty acid composition (FAC). The oil content and FFA varied from 13.7 to 27.6% and 0.2 to 1.0%, respectively. The FAC was analyzed by gas chromatography–mass spectroscopy with particular emphasis on trans fatty acids (TFA). Total saturated, unsaturated, cis-monounsaturated and polyunsaturated fatty acids were determined in the range of 37.9–46.9, 53.0–62.0, 12.3–43.7 and 0.1–9.2%, respectively. The high amount of TFA was observed in all biscuit samples and varied from 9.3 to 34.9%. The quantity and quality of the lipid fraction of the biscuits indicated that the all analyzed biscuits are a rich source of fat, saturated fatty acids and trans fatty acids, consequently not suitable for the health of consumers. The high content of trans fatty acids and palmitic acid also indicated that blends of RBD palm oil and partially hydrogenated oil had been used in the biscuit manufacturing.

Ten margarine brands of Pakistan were analyzed for their fatty acid composition with emphasis on trans fatty acids (TFA) using GC-MS. Saturated, cis-monounsaturated and polyunsaturated fatty acids were present at 24.2-58.1, 5.7-35.4 and 3.8-37.4% of total fatty acids, respectively. Among the saturated fatty acids, palmitic acid (16.9-33.8%) was dominant in all analyzed margarine brands and its higher amount indicates that palm oil was a major contributor in the margarine manufacturing. Among samples tested only one contained a low level of TFA (2.2%) while the rest contained very high amounts of TFA (11.5-34.8%) which clearly shows that hydrogenated oils were used in the formulation of margarines. Fatty acid profiles demonstrated that all samples belong to the hard margarine category containing high amounts of trans and saturated fatty acids which is an alarming issue for the health of consumers.

A rapid method has been developed to extract and quantitatively measure the total oil content in poultry feeds using a domestic microwave oven. The optimized extraction procedure involves the replicate (6×) extraction of 5 g of ground feed with 12 ml of hexane for 20 s in a 900 W oven. Each replicate involves the collection of the resulting miscella and its replacement with fresh solvent for re-extraction. The collected extracts were centrifuged and transferred to a vial. The solvent was evaporated to a constant weight and the residual lipid weighed. In comparison to conventional Soxhlet extraction method, lipid contents obtained using the optimized microwave procedure was not significantly different. However, FTIR analysis indicated that the microwave procedure was superior in minimizing the formation of free fatty acids (FFA) relative to the Soxhlet procedure if the temperature of the sample was kept within the range of 45–50 °C. This simple, sequential extraction procedure is rapid, highly efficient and provides a simple mean of quantitating the lipid content of poultry feed in less than 40 min without the need for specialized microwave oven.

Transmission Fourier transform infrared (FTIR) spectroscopic method using 100 μm KCl cell was applied for the determination of total polar compounds (TPC), carbonyl value (CV), conjugated diene (CD) and conjugated triene (CT) in canola oil (CLO) during potato chips frying at 180 °C. The calibration models were developed for TPC, CV, CD and CT using partial least square (PLS) chemometric technique. Excellent regression coefficients (R(2)) and root mean square error of prediction values for TPC, CV, CD and CT were found to be 0.999, 0.992, 0.998 and 0.999 and 0.809, 0.690, 1.26 and 0.735, respectively. The developed calibration models were applied on samples of canola oil drawn during potato chips frying process. A linear relationship was obtained between CD and TPC with a good correlation of coefficient (R(2)=0.9816). Results of the study clearly indicated that transmission FTIR-PLS method could be used for quick and precise evaluation of oxidative changes during the frying process without using any organic solvent.

Free fatty acids (FFA) inNigella sativa(N. sativa) commercial and seed oil were determined using single-bounce attenuated total reflectance (SB-ATR) Fourier transform infrared (FTIR) spectroscopy. Gravimetrical mixing was done by adding 0.1–40% oleic acids in neutralizedN. sativaoil containing 0.1% FFA. FTIR spectroscopy technique and partial least square (PLS) calibration were used to detect the absorption region of carbonyl (C=O) which is in the range of 1690–1727 cm−1. The results of PLS calibration model and root mean square error of calibration (RMSEC) are 0.999 and 0.449, respectively. Comparing the FFA obtained inN. sativaoil by using FTIR with the FFA obtained using AOCS titrimetric method shows a positive correlation and confirms that the described method is a useful procedure.

A rapid, reliable and cost effective analytical procedure for the estimation of ibuprofen in pharmaceutical formulations and human urine samples was developed using transmission Fourier Transform Infrared (FT-IR) spectroscopy. For the determination of ibuprofen, a KBr window with 500 μm spacer was used to acquire the FT-IR spectra of standards, pharmaceuticals as well as urine samples. Partial least square (PLS) calibration model was developed based on region from 1807 to 1,461 cm(-1) using ibuprofen standards ranging from 10 to 100 μg ml(-1). The developed model was evaluated by cross-validation to determine standard error of the models such as root mean square error of calibration (RMSEC), root mean square error of cross validation (RMSECV) and root mean square error of prediction (RMSEP). The coefficient of determination (R(2)) achieved was 0.998 with minimum errors in RMSEC, RMSECV and RMSEP with the value of 1.89%, 1.63% and 4.07%, respectively. The method was successfully applied to urine and pharmaceutical samples and obtained good recovery (98-102%).

The purpose of this study was to develop a rapid, simple and sensitive quantitation method for pseudoephedrine (PSE), paracetamol (PAR) and loratadine (LOR) in plasma and pharmaceuticals using liquid chromatography-tandem mass spectrometry with a monolithic column. Separation was achieved using a gradient composition of methanol-0.1% formic acid at a flow rate of 1.0 mL min-1. Mass spectral transitions were recorded in SRM mode. System validation was evaluated for precision, specificity and linearity. Limit of detection for pseudoephedrine, paracetamol, and loratadine were determined to be 3.14, 1.86 and 1.44 ng mL-1, respectively, allowing easy determination in plasma with % recovery of 93.12 to 101.56%.

In present work, the concentration of essential elements, copper (Cu), iron (Fe) and zinc (Zn) were measured in ten different juices, to evaluate whether the intakes of under study nutrients accomplished within recommended permissible levels. Flame atomic absorption spectrometry (FAAS) was used to estimate and evaluate the levels of essential elements such as Cu, Fe and Zn in ten juice samples. The elements were analyzed prior to microwave assisted acid digestion (MAD). For comparison purpose, wet acid digestion (CAD) method was used for determination of essential elements. The accuracy of proposed method was evaluated by performing addition-recovery experiments to prove the reliability of the method. All obtained analytical results by MAD and CAD showed a good agreement at a 95% confidence level. The detection limits of Cu, Fe and Zn were 22.7 microg/L, 3.85 microg/L and 3.05 microg/L. The dietary intakes of all three studied elements have also been estimated.

The prospect of using single bounce attenuated total reflectance (SB-ATR)-Fourier transform infrared (FTIR) spectroscopy as a rapid quantitative tool to determine the main fatty acid groups present in different edible oils was investigated. Partial least squares (PLS) calibrations were developed using SB-ATR-FTIR spectra which were associated with fatty acid groups (saturated, trans, mono- and polyunsaturated) using quantitative data obtained by gas chromatography (GC). Good calibrations were obtained for all main four fat groups (saturated, mono, trans and polyunsaturated) with excellent precision. The coefficient of determination (R(2)), root mean square error of prediction (RMSEP) and bias for validation set were obtained as 0.999, 2.43 and 0.998 for saturated; 0.999, 1.850 and 0.003 for mono; 0.999, 0.625 and -0.001 for trans while for poly the values were 0.999, 1.170 and 0.003, respectively. The results of 13 validation samples for total saturated, mono, trans and polyunsaturated fats by FI-IR were found in the range of 8.16-55.16, 37.62-74.75, 0.20-18.16 and 1.36-62.35%, respectively. The present study shows that it may well be possible to expand the utility of SB-ATR-FTIR spectroscopy not only to provide isolated trans data, but also serve as a simple, rapid and quantitative means of categorizing the main groups present in the edible oils. The information obtained would be useful for meeting the new lipid nutritional labeling requirements.