Kigelia africana fruit biofibre polysaccharide extraction and biofibre development by silane chemical treatment.

Silane-treated natural cellulosic Kigelia africana fruit fibre (KAF) was experimentally established to have strong strength after removing hydrophilic materials. Silane treatment makes it compatible with hydrophobic biopolymeric materials than existing non-grafted KA fibre. In this work, the polysaccharide was extracted from the KAF and found to have all the essential compounds. KA fruit-based cellulosic fibre was extracted and treated with different concentrations of silane solution. Silane-treated (13%) KAF has a cellulose content of about 76.86%. The peak found at 1734 cm-1 shows the hemicellulose in untreated fibres, and its intensity decreased after silane treatment, as confirmed by FTIR. X-ray diffraction investigation indicated that silane-treated (5%) KAF has a crystallinity index of 70.22%. After treatment, the tensile strength of 5% silane-treated KAF shows a tensile strength of 490.77 MPa, giving more viability to biofibre reinforcement.

MPdb: Melghat Plant databank.

Melghat Plant databank (MPdb) is the first attempt to review all the past floristic documents and medicinal plants and digitize the Melghat Flora. This curated database contains compiled information about 1028 plants from 139 plant families and 537 genera. Curated medicinal plant information gathered 660 medicinal species records from 128 plant families and 421 genera in MPdb for Melghat Flora. Each plant record is reviewed, scrutinizes, and recorded. More than 9000 records for medicinal uses for nearly 140 diseases, reported phytochemicals, and published cross references. MPdb will serve as a valuable information resource for students, researchers, and aboriginal communities to explore Melghat Flora for better-applied prospects in herbal drug research.

Transparent magnesium aluminate spinel: a prospective biomaterial for esthetic orthodontic brackets.

Adult orthodontics is recently gaining popularity due to its importance in esthetics, oral and general health. However, none of the currently available alumina or zirconia based ceramic orthodontic brackets meet the esthetic demands of adult patients. Inherent hexagonal lattice structure and associated birefringence limits the visible light transmission in polycrystalline alumina and make them appear white and non transparent. Hence focus of the present study was to assess the feasibility of using magnesium aluminate (MgAl2O4) spinel; a member of the transparent ceramic family for esthetic orthodontic brackets. Transparent spinel specimens were developed from commercially available white spinel powder through colloidal shaping followed by pressureless sintering and hot isostatic pressing at optimum conditions of temperature and pressure. Samples were characterized for chemical composition, phases, density, hardness, flexural strength, fracture toughness and optical transmission. Biocompatibility was evaluated with in-vitro cell line experiments for cytotoxicity, apoptosis and genotoxicity. Results showed that transparent spinel samples had requisite physico-chemical, mechanical, optical and excellent biocompatibility for fabricating orthodontic brackets. Transparent spinel developed through this method demonstrated its possibility as a prospective biomaterial for developing esthetic orthodontic brackets.

Basti: Does the equipment and method of administration matter?

Basti is one of the five procedures of panchakarma in Ayurveda. Classically, it is advocated in the diseases of vata. It is mainly of two types viz. asthapana and anuvasana. According to the classical texts basti administration is done with the help of animal bladder (bastiputaka) and specially prepared metal/wooden nozzle/catheter (bastinetra), the whole assembly is called as bastiyantra. Nowadays, except in some of the Vaidya traditions in Kerala, basti administration is often done using enema-can or douche-set. In the aforesaid classical procedure active pressure is expected to be given on the bastiputaka whereas, in conventionally used enema-can only passive or gravitational force plays a role. This is important in the context of 'basti danakala or pidanakala i.e. time for basti administration'.

A sensitive and selective LC-MS-MS method for simultaneous determination of picroside-I and kutkoside (active principles of herbal preparation picroliv) using solid phase extraction in rabbit plasma: application to pharmacokinetic study.

A rapid, sensitive and selective LC-MS-MS method for the simultaneous quantitation of picroside-I and kutkoside (active constituents of herbal hepatoprotectant picroliv) was developed and validated in rabbit plasma. The analytes and internal standard (Amarogentin) were extracted using Oasis HLB solid phase extraction cartridges. Analysis was performed on Spheri RP-18 column (10 microm, 100 mm x 4.6 mm i.d.) coupled with guard column using acetonitrile:MilliQ water (50:50, %v/v) as mobile phase at a flow rate of 1 ml/min with a retention time of 1.39, 1.33 and 1.42 min for picroside-I, kutkoside and amarogentin, respectively. The quantitation was carried out using an API-4000 LC-MS-MS with negative electro spray ionization in multiple reaction monitoring (MRM) mode. The precursor to product ion transitions for picroside-I, kutkoside and amarogentin were m/z 491 > 147, 199; 511 > 167, 235; 585 > 227, respectively. The method was validated in terms of establishing linearity, specificity, sensitivity, recovery, accuracy and precision (within- and between-assay variation), freeze-thaw (f-t), auto injector and dry residue stability. Linearity in plasma was observed over a concentration range of 1.56-400 ng/ml with a limit of detection (LOD) of 0.5 ng/ml for both analytes. The recoveries from spiked control samples were > 60 and > 70% for picroside-I and kutkoside, respectively. Accuracy and precision of the validated method were within the acceptable limits of < 20% at low and < 15% at other concentrations. The analytes were stable after three freeze-thaw cycles and their dry residues were stable at -60 degrees C for 15 days. The method was successfully applied to determine concentrations of picroside-I and kutkoside post i.v. bolus administration of picroliv in rabbit.